BETA


2012/2041(INI) Microbial challenge - rising threats from antimicrobial resistance

Progress: Procedure completed

RoleCommitteeRapporteurShadows
Lead ENVI ROSBACH Anna (icon: ECR ECR) MAZEJ KUKOVIČ Zofija (icon: PPE PPE), KADENBACH Karin (icon: S&D S&D), SKYLAKAKIS Theodoros (icon: ALDE ALDE), STAES Bart (icon: Verts/ALE Verts/ALE)
Committee Opinion AGRI HÄUSLING Martin (icon: Verts/ALE Verts/ALE)
Committee Opinion ITRE
Lead committee dossier:
Legal Basis:
RoP 54

Events

2016/10/24
   EC - Follow-up document
Documents
2016/10/24
   EC - Follow-up document
Documents
2015/03/11
   EC - Follow-up document
Details

This Commission staff working document concerns the progress made so far against the rising threats from Antimicrobial Resistance.

To recall, in 2011, the Commission launched a 5-year Action Plan against Antimicrobial Resistance. The progress made under the specific actions may be summarised as follows:

Action n° 1: Strengthen the promotion of the appropriate use of antimicrobials in all Member States : t he European Parliament has allocated funds for a preparatory action to promote the appropriate use of antimicrobials in human medicine. The Antibiotic Resistance and Prescribing in European children (ARPEC) project funded under the Health Programme (2010-2013), aims at improving the quality of antibiotic prescribing for children in Europe and to reduce the prevalence of antimicrobial resistance in bacterial infections in children. The Commission services will publish later in 2015 data and information provided by the Member States in order to further strengthen the prudent use of antimicrobials in human medicines in the EU.

Action n° 2: Strengthen the regulatory framework on veterinary medicines and on medicated feed : the current veterinary medicines legislation does not provide sufficient tools to ensure that risks to human health arising from the use of antimicrobials in animals are adequately managed. In 2014, the Commission adopted proposals for veterinary medicinal products and medicated feed . They are currently undergoing the ordinary legislative procedure in the European Parliament and the Council.

Action n° 3: Introduce recommendations for prudent use in veterinary medicine, including follow-up reports : regardless of the efforts carried out to improve the prudent use of veterinary antimicrobials it is also necessary to update marketing authorisations to take into account of the latest scientific developments. The Commission services are finalising the drafting of Guidelines for prudent use of antimicrobials in veterinary medicine.

Action n° 4: Strengthen infection prevention and control in healthcare settings : the report showed that in the area of prevention and control of healthcare associated infections (HAI), 26 out of 28 responding countries implemented a combination of actions to prevent and control such infections. More efforts are needed to ensure adequate numbers of specialised infection control staff, receiving regular training, and with dedicated time for this task in hospitals and other healthcare settings. Tailored basic infection prevention and control structures and practices in nursing homes and other long term care facilities should be reinforced. Information on HAI to patients should be improved.

Action n° 5: Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law : t he Commission proposal for a Regulation on animal health was adopted in May 2013. It is currently undergoing the ordinary legislative procedure in the European Parliament and in the Council. Its objective is to create an EU animal health legal framework for the control of major transmissible animal diseases.

Action n° 6: Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients : as rapid response, the New Drugs for Bad Bugs (ND4BB) programme was launched in May 2012. A new model for open innovation in the pharmaceutical research area has been created to spur the development of new antibiotics . This model means that research sectors and individual companies now provide unprecedented access to each other’s data and collaborate on solving problems of public health concern.

The Commission and the European Investment Bank are jointly developing a pilot financial facility which aims to target Infectious Diseases (ID). It is expected to be launched in 2015.

Action n° 7: Promote efforts to analyse the need for new antibiotics into veterinary medicine : the report acknowledged that there are certain gaps between the approved indications for veterinary antimicrobials and the needs of veterinarians. This area needs to be improved.

Action n° 8: Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors : the Commission services are supporting and actively cooperating with the WHO in this field. Cooperation with China has started and possible cooperation with Russian is imminent. The Commission services are also contributing to the work against antimicrobial resistance in developing countries. They have also begun to develop a strategic approach to the pollution of water by pharmaceuticals . Proposals are awaited in 2017.

Action n° 9: Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine : t ransfer of the European system for surveillance of antimicrobial consumption in human medicine to ECDC was completed in 2012. The system is now integrated as part of ECDC surveillance as the European Surveillance of Antimicrobial Consumption Network (ESAC-Net).

Action n° 10: Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine : t he information collected by the three agencies: the European Food Safety Authority (EFSA), the European Medicines Agency (EMA) and the European Centre for Disease Prevention and Control (ECDC) on antimicrobial resistance and antimicrobial consumption needs to be combined and jointly analysed in order to assess the relationship between use of antimicrobials and antimicrobial resistance in animals and in humans at the European level.

Action n° 11: Reinforce and co-ordinate research efforts : af ter the launch of the Action Plan, research on AMR has been further supported by the Commission services with a total budget of approx. €130 million under the EU’s Seventh Framework Programme for Research and Technological Development. The new EU framework programme Horizon 2020 continues to give research on infectious diseases including AMR a high priority. In 2014, the European Commission devoted €28 million to the development of new vaccines candidates against tuberculosis, and has earmarked €25 million for HIV vaccine research in 2015.

Action n° 12: Survey and comparative effectiveness research : e ach year, the European Antibiotic Awareness Day (EAAD) attracts strong media interest across Europe. In July 2013, ECDC provided training on the development, implementation and evaluation of prudent antibiotic use campaigns to 29 participants from 20 Member States and Norway.

Documents
2013/05/13
   EC - Commission response to text adopted in plenary
Documents
2012/12/12
   PT_PARLIAMENT - Contribution
Documents
2012/12/11
   EP - Results of vote in Parliament
2012/12/11
   EP - Decision by Parliament
Details

The European Parliament adopted by 588 votes to 16, with 23 abstentions, a resolution on “the Microbial Challenge – Rising threats from Antimicrobial Resistance”.

Parliament recalls that resistance to antibiotics for certain bacteria is as high as 25 % or more in several Member States and that much of the antimicrobial resistance (AMR) problem stems from the misuse – in particular the excessive use – of antibiotics. It recalls that in the EU, Iceland and Norway alone, antimicrobial resistant bacteria cause some 400 000 infections and 25 000 deaths annually, with at least EUR 1.5 billion spent on extra healthcare costs and productivity losses. It also highlights the fact that many Member States do not have a solid legal and regulatory framework to mandate and support the rational use of medicines. As a result, Parliament calls for the complete and rapid implementation of measures in this area.

Although welcoming the Commission’s five-year strategic Action Plan on tackling AMR and viewing it as generally going in the right direction, Parliament notes that many of the action points reiterate measures prescribed over a decade ago, and that it is not sufficient for tackling the growing risk presented by AMR at international level .

In this context, Members call for an integrated roadmap outlining relevant policy responses, including possible legislative action.

Parliament calls in particular for the Action Plan to:

cover all animals under the EU animal welfare strategy, including, for instance, companion animals and animals used for sports, and emphasise the logical connection between animal health and the use of antimicrobials, as well as the link between animal health and human health.

Prudent use of antimicrobials in human and veterinary medicine: Parliament calls for the prudent use of antimicrobials. The key objective of any AMR strategy is to maintain the efficiency of existing antimicrobials by using them responsibly at the correct therapeutic level only when strictly necessary and prescribed over a specific time at the appropriate dosage (and not for treating viral infections). Similar prudence needs to be exercised in veterinary medicine. Parliament calls on the Member States to use electronic recording systems to ensure that usage patterns on individual farms are appropriate, thus ensuring responsible and minimal use. It also suggests to the Commission that current provisions on maximum animal density in livestock farming be re-evaluated as herd sizes today often present obstacles to the treatment of individual or smaller groups of animals, providing incentives for the prophylactic use of antimicrobials. It calls for a legislative proposal to be presented for the veterinary sector to limit its use of third- and fourth-generation Critically Important Antimicrobials (CIAs) for humans.

Parliament considers that the pending revision of Directive 2001/82/EC offers an important opportunity to take effective measures to reduce AMR through strengthening the provisions for veterinary medicines, such as:

limiting the right to prescribe antimicrobials to professionally qualified veterinarians only; separating the right to prescribe from the right to sell antimicrobials, thereby eradicating economic incentives to prescribe.

Measures are called for to encourage efforts to study hospital outbreaks, to improve diagnostics but also to assess and monitor the Member States' implementation of relevant EU legislation on antimicrobials, in particular with regard to the prescription-only use of antibiotics in the human health and veterinary sectors.

Prevention: Parliament calls for more effective measures to be introduced to prevent both the appearance and the spread of antimicrobial resistance. These measures include better monitoring and better notification of micro-organisms resistant to antimicrobials, as well as a more effective combating of infections, in particular by means of vaccinations. Among other measures that it calls for are limits on uncontrolled access to antimicrobial agents, in particular via the growing number of illegal sales on the internet, and their inappropriate use. It calls on the Member States to improve infection control, and to raise and promote good standards of hygiene – especially hand hygiene, – in order to prevent the spread of infections and reduce the need for antibiotics.

Parliament also invites the Commission to classify, in the forthcoming review of the European veterinary pharmaceuticals legislation, medicated feeding stuffs as ‘pharmaceuticals’ and not as ‘feeding stuffs’, in order to ensure that, in future, the sensitive area of medicated foodstuffs is monitored under pharmaceuticals legislation and that official inspections are carried out accordingly, while ensuring that medicated foodstuffs fall into the ‘prescription only’ category .

Development of new antimicrobials or alternatives for treatment: Parliament considers it vital to limit the emergence of bacteria that are resistant to antimicrobials . In this context, it is necessary to develop new antimicrobial agents. In parallel, it stresses the advantages of public-private partnerships because these can contribute to reaching this objective by dissociating sales transactions from investment in research and development. In this area, Parliament calls on the Commission and the Member States to accelerate R&D activities in order to provide new tools to fight tuberculosis and drug-resistant tuberculosis.

Parliament also underlines the need to examine new regulatory approaches that would result in stimulating industrial research and the development of new antimicrobials while safeguarding patient safety. It also calls on the Commission to ensure the development and availability of more on-farm tools for early, rapid diagnosis and control of diseases, as well as for a broad and effective diagnostic system at Member State level.

Monitoring and reporting: in this regard, Parliament calls on the Commission and the Member States to seek greater cooperation and coordination on early detection, alert and coordinated response procedures regarding pathogenic antimicrobial resistant bacteria in humans, animals, fish and foodstuffs. It calls on Member States to compile clear, comparable, transparent and timely reference data on antimicrobial drug usage so that effective action can be undertaken. It considers, however, that data gathered on the use of antibiotics should be made accessible only to the experts, authorities and decision-makers concerned. It calls on the Member States to ensure separate monitoring and control of resistance among livestock, domestic animals and racing animals.

Communication, education and training: Parliament notes that one of the most common uses for antibiotics is as treatment against the common cold , and that much would be gained if the public could be made aware of the fact that the common cold is a viral infection whereas antibiotics only provide protection against bacterial infections. It calls on the Commission to compile a best practice list with regard to the implementation of effective communication campaigns and professional training courses aimed at raising AMR awareness. It believes that effective information and awareness campaigns must be developed with a view to heightening awareness of the dangers of the unintentional spread of antimicrobial pathogens in hospitals and in the home, and awareness of the means of avoiding this. Campaigns along the lines of "Please take this antibiotic medicine only if it is prescribed by a doctor to you and take it as prescribed” should be promoted and included in the package leaflet.

International cooperation: lastly, Parliament believes that concerted and timely international action that avoids overlap and builds critical mass is the only way forward in minimising the threat to public health that AMR poses globally. It considers that the work undertaken by the Transatlantic Task Force on Antimicrobial Resistance (TATFAR) should be used as a model for international cooperation on antimicrobial resistance. Other similar multilateral and bilateral commitments for the prevention and control of AMR should also be encouraged, in accordance with the guidelines laid down by the WHO (in particular in regard to the control of counterfeit antimicrobials).

Documents
2012/12/11
   EP - End of procedure in Parliament
2012/12/10
   EP - Debate in Parliament
2012/11/15
   EP - Committee report tabled for plenary, single reading
Documents
2012/11/14
   EP - Committee report tabled for plenary
Documents
2012/11/06
   EP - Vote in committee
2012/10/16
   EP - Amendments tabled in committee
Documents
2012/10/15
   EP - Committee opinion
Documents
2012/09/19
   EP - Amendments tabled in committee
Documents
2012/07/12
   EP - Committee draft report
Documents
2012/06/21
   CSL - Resolution/conclusions adopted by Council
Details

The Council adopted conclusions on the impact of antimicrobial resistance (AMR) in the human health sector and in the veterinary sector , calling upon member states to develop and implement national strategies or action plans for countering AMR.

These national strategies or action plans should, amongst others, include the following elements:

national guidelines on the treatment of humans and animals with antimicrobial agents; communication guidelines and programmes for education and training of professionals; enforcement of national legislation preventing all illegal sales of antimicrobials including illegal sales over the internet; limitation of the use of critically important antibiotics to cases where microbiological diagnosis and susceptibility testing has determined that no other type of antimicrobials will be effective; limitation of prophylactic use of antimicrobials to cases with defined clinical needs; limitation of prescription and use of antimicrobials for herd treatment of animals to cases with a clear clinical or epidemiological justification.

The conclusions also call upon the member states and the Commission to examine the conditions of prescription and sale of antimicrobials in order to ascertain whether practices in human and animals healthcare may lead to over-prescription, overuse or misuse of antimicrobials.

The Commission is invited to expedite the review of legislative acts in order to take antimicrobial resistance better into account. This applies notably to directive 90/167 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the EU and directive 2001/82 on the EU code relating to veterinary medicinal products.

The Commission informed that preparatory work for some of the actions to which it is invited has already been started.

According to the World Health Organisation (WHO) about 440 000 new cases of multidrugresistant tuberculosis (MDR-TB) emerge annually, causing at least 150 000 deaths. A high percentage of hospital-acquired infections are caused by highly resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA).

2012/06/21
   CSL - Council Meeting
2012/03/23
   EP - ROSBACH Anna (ECR) appointed as rapporteur in ENVI
2012/03/15
   EP - Committee referral announced in Parliament
2012/02/29
   EP - HÄUSLING Martin (Verts/ALE) appointed as rapporteur in AGRI
2011/11/15
   EC - Non-legislative basic document
Details

PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR).

BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives).

Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe.

The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion.

For their part, the Council and the European Parliament have already examined this issue and on 12 May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR.

This Communication responds to this request.

CONTENT: in this regard, the Commission has taken a number of important actions:

in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR; in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella; in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals; the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas; AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States; scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage.

Based on such holistic approach, the new actions put forward in this Action Plan aim at:

mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR.

mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR.

The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions:

Action n° 1 : Strengthen the promotion of the appropriate use of antimicrobials in all Member States. Action n° 2 : Strengthen the regulatory framework on veterinary medicines and on medicated feed. Action n° 3 : Introduce recommendations for prudent use in veterinary medicine, including follow-up reports. Action n° 4 : Strengthen infection prevention and control in healthcare settings. Action n° 5 : Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law. Action n° 6 : Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients. Action n° 7 : Promote efforts to analyse the need for new antibiotics into veterinary medicine. Action n° 8 : Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors. Action n° 9 : Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine. Action n° 10 : Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine. Action n° 11 : Reinforce and co-ordinate research efforts. Action n° 12 : Survey and comparative effectiveness research.

Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.

2011/11/15
   EC - Non-legislative basic document published
Details

PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR).

BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives).

Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe.

The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion.

For their part, the Council and the European Parliament have already examined this issue and on 12 May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR.

This Communication responds to this request.

CONTENT: in this regard, the Commission has taken a number of important actions:

in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR; in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella; in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals; the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas; AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States; scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage.

Based on such holistic approach, the new actions put forward in this Action Plan aim at:

mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR.

mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR.

The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions:

Action n° 1 : Strengthen the promotion of the appropriate use of antimicrobials in all Member States. Action n° 2 : Strengthen the regulatory framework on veterinary medicines and on medicated feed. Action n° 3 : Introduce recommendations for prudent use in veterinary medicine, including follow-up reports. Action n° 4 : Strengthen infection prevention and control in healthcare settings. Action n° 5 : Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law. Action n° 6 : Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients. Action n° 7 : Promote efforts to analyse the need for new antibiotics into veterinary medicine. Action n° 8 : Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors. Action n° 9 : Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine. Action n° 10 : Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine. Action n° 11 : Reinforce and co-ordinate research efforts. Action n° 12 : Survey and comparative effectiveness research.

Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.

Documents

Activities

AmendmentsDossier
187 2012/2041(INI)
2012/09/19 ENVI 125 amendments...
source: PE-496.371
2012/09/20 AGRI 52 amendments...
source: PE-496.440
2012/10/26 ENVI 10 amendments...
source: PE-496.577

History

(these mark the time of scraping, not the official date of the change)

docs/0
date
2011-11-15T00:00:00
docs
summary
type
Non-legislative basic document
body
EC
docs/5
date
2012-11-15T00:00:00
docs
url: https://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html title: A7-0373/2012
type
Committee report tabled for plenary, single reading
body
EP
docs/8
date
2012-12-13T00:00:00
docs
url: http://www.connefof.europarl.europa.eu/connefof/app/exp/COM(2011)0748 title: COM(2011)0748
type
Contribution
body
PT_PARLIAMENT
docs/10
date
2012-12-12T00:00:00
docs
url: https://connectfolx.europarl.europa.eu/connefof/app/exp/COM(2011)0748 title: COM(2011)0748
type
Contribution
body
PT_PARLIAMENT
events/0/docs/1/url
Old
https://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
New
https://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=0748
events/4
date
2012-11-14T00:00:00
type
Committee report tabled for plenary
body
EP
docs
url: https://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html title: A7-0373/2012
events/4
date
2012-11-15T00:00:00
type
Committee report tabled for plenary
body
EP
docs
url: https://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html title: A7-0373/2012
summary
committees/0/shadows/4
name
MATIAS Marisa
group
European United Left - Nordic Green Left
abbr
GUE/NGL
docs/0/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077
New
https://www.europarl.europa.eu/doceo/document/ENVI-PR-486077_EN.html
docs/1/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.371
New
https://www.europarl.europa.eu/doceo/document/ENVI-AM-496371_EN.html
docs/2/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE494.678&secondRef=02
New
https://www.europarl.europa.eu/doceo/document/AGRI-AD-494678_EN.html
docs/3/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577
New
https://www.europarl.europa.eu/doceo/document/ENVI-AM-496577_EN.html
events/0
date
2011-11-15T00:00:00
type
Non-legislative basic document published
body
EC
docs
summary
events/0
date
2011-11-15T00:00:00
type
Non-legislative basic document published
body
EC
docs
summary
events/1/type
Old
Committee referral announced in Parliament, 1st reading/single reading
New
Committee referral announced in Parliament
events/3/type
Old
Vote in committee, 1st reading/single reading
New
Vote in committee
events/4
date
2012-11-15T00:00:00
type
Committee report tabled for plenary
body
EP
docs
url: https://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html title: A7-0373/2012
summary
events/4
date
2012-11-15T00:00:00
type
Committee report tabled for plenary, single reading
body
EP
docs
url: http://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html title: A7-0373/2012
summary
events/5/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?secondRef=TOC&language=EN&reference=20121210&type=CRE
New
https://www.europarl.europa.eu/doceo/document/CRE-7-2012-12-10-TOC_EN.html
events/7
date
2012-12-11T00:00:00
type
Decision by Parliament
body
EP
docs
url: https://www.europarl.europa.eu/doceo/document/TA-7-2012-0483_EN.html title: T7-0483/2012
summary
events/7
date
2012-12-11T00:00:00
type
Decision by Parliament, 1st reading/single reading
body
EP
docs
url: http://www.europarl.europa.eu/doceo/document/TA-7-2012-0483_EN.html title: T7-0483/2012
summary
procedure/Modified legal basis
Rules of Procedure EP 150
procedure/Other legal basis
Rules of Procedure EP 159
procedure/legal_basis/0
Rules of Procedure EP 54
procedure/legal_basis/0
Rules of Procedure EP 52
committees/0
type
Responsible Committee
body
EP
associated
False
committee_full
Environment, Public Health and Food Safety
committee
ENVI
rapporteur
name: ROSBACH Anna date: 2012-03-23T00:00:00 group: European Conservatives and Reformists abbr: ECR
shadows
committees/0
type
Responsible Committee
body
EP
associated
False
committee_full
Environment, Public Health and Food Safety
committee
ENVI
date
2012-03-23T00:00:00
rapporteur
name: ROSBACH Anna group: European Conservatives and Reformists abbr: ECR
shadows
committees/2
type
Committee Opinion
body
EP
associated
False
committee_full
Agriculture and Rural Development
committee
AGRI
rapporteur
name: HÄUSLING Martin date: 2012-02-29T00:00:00 group: Greens/European Free Alliance abbr: Verts/ALE
committees/2
type
Committee Opinion
body
EP
associated
False
committee_full
Agriculture and Rural Development
committee
AGRI
date
2012-02-29T00:00:00
rapporteur
name: HÄUSLING Martin group: Greens/European Free Alliance abbr: Verts/ALE
docs/4/body
EC
events/0/docs/1/url
Old
https://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
New
https://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=0748
events/4/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN
New
http://www.europarl.europa.eu/doceo/document/A-7-2012-0373_EN.html
events/7/docs/0/url
Old
http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483
New
http://www.europarl.europa.eu/doceo/document/TA-7-2012-0483_EN.html
activities
  • date: 2011-11-15T00:00:00 docs: url: http://www.europarl.europa.eu/RegData/docs_autres_institutions/commission_europeenne/com/2011/0748/COM_COM(2011)0748_EN.pdf title: COM(2011)0748 type: Non-legislative basic document published celexid: CELEX:52011DC0748:EN body: EC commission: DG: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers Commissioner: BORG Tonio type: Non-legislative basic document published
  • date: 2012-03-15T00:00:00 body: EP type: Committee referral announced in Parliament, 1st reading/single reading committees: body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin body: EP shadows: group: PPE name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: ECR name: ROSBACH Anna body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
  • body: CSL meeting_id: 3177 council: Employment, Social Policy, Health and Consumer Affairs date: 2012-06-21T00:00:00 type: Council Meeting
  • date: 2012-11-06T00:00:00 body: EP type: Vote in committee, 1st reading/single reading committees: body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin body: EP shadows: group: PPE name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: ECR name: ROSBACH Anna body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
  • date: 2012-11-15T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN type: Committee report tabled for plenary, single reading title: A7-0373/2012 body: EP type: Committee report tabled for plenary, single reading
  • date: 2012-12-10T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?secondRef=TOC&language=EN&reference=20121210&type=CRE type: Debate in Parliament title: Debate in Parliament body: EP type: Debate in Parliament
  • date: 2012-12-11T00:00:00 docs: url: http://www.europarl.europa.eu/oeil/popups/sda.do?id=22191&l=en type: Results of vote in Parliament title: Results of vote in Parliament url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483 type: Decision by Parliament, 1st reading/single reading title: T7-0483/2012 body: EP type: Results of vote in Parliament
commission
  • body: EC dg: Health and Food Safety commissioner: BORG Tonio
committees/0
type
Responsible Committee
body
EP
associated
False
committee_full
Environment, Public Health and Food Safety
committee
ENVI
date
2012-03-23T00:00:00
rapporteur
name: ROSBACH Anna group: European Conservatives and Reformists abbr: ECR
shadows
committees/0
body
EP
responsible
False
committee
AGRI
date
2012-02-29T00:00:00
committee_full
Agriculture and Rural Development
rapporteur
group: Verts/ALE name: HÄUSLING Martin
committees/1
type
Committee Opinion
body
EP
associated
False
committee_full
Industry, Research and Energy
committee
ITRE
opinion
False
committees/1
body
EP
shadows
responsible
True
committee
ENVI
date
2012-03-23T00:00:00
committee_full
Environment, Public Health and Food Safety
rapporteur
group: ECR name: ROSBACH Anna
committees/2
type
Committee Opinion
body
EP
associated
False
committee_full
Agriculture and Rural Development
committee
AGRI
date
2012-02-29T00:00:00
rapporteur
name: HÄUSLING Martin group: Greens/European Free Alliance abbr: Verts/ALE
committees/2
body
EP
responsible
False
committee_full
Industry, Research and Energy
committee
ITRE
council
  • body: CSL type: Council Meeting council: Employment, Social Policy, Health and Consumer Affairs meeting_id: 3177 url: http://register.consilium.europa.eu/content/out?lang=EN&typ=SET&i=SMPL&ROWSPP=25&RESULTSET=1&NRROWS=500&DOC_LANCD=EN&ORDERBY=DOC_DATE+DESC&CONTENTS=3177*&MEET_DATE=21/06/2012 date: 2012-06-21T00:00:00
docs
  • date: 2012-07-12T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077 title: PE486.077 type: Committee draft report body: EP
  • date: 2012-09-19T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.371 title: PE496.371 type: Amendments tabled in committee body: EP
  • date: 2012-10-15T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE494.678&secondRef=02 title: PE494.678 committee: AGRI type: Committee opinion body: EP
  • date: 2012-10-16T00:00:00 docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577 title: PE496.577 type: Amendments tabled in committee body: EP
  • date: 2013-05-13T00:00:00 docs: url: /oeil/spdoc.do?i=22191&j=0&l=en title: SP(2013)175 type: Commission response to text adopted in plenary
  • date: 2015-03-11T00:00:00 docs: title: SWD(2015)0059 summary: This Commission staff working document concerns the progress made so far against the rising threats from Antimicrobial Resistance. To recall, in 2011, the Commission launched a 5-year Action Plan against Antimicrobial Resistance. The progress made under the specific actions may be summarised as follows: Action n° 1: Strengthen the promotion of the appropriate use of antimicrobials in all Member States : t he European Parliament has allocated funds for a preparatory action to promote the appropriate use of antimicrobials in human medicine. The Antibiotic Resistance and Prescribing in European children (ARPEC) project funded under the Health Programme (2010-2013), aims at improving the quality of antibiotic prescribing for children in Europe and to reduce the prevalence of antimicrobial resistance in bacterial infections in children. The Commission services will publish later in 2015 data and information provided by the Member States in order to further strengthen the prudent use of antimicrobials in human medicines in the EU. Action n° 2: Strengthen the regulatory framework on veterinary medicines and on medicated feed : the current veterinary medicines legislation does not provide sufficient tools to ensure that risks to human health arising from the use of antimicrobials in animals are adequately managed. In 2014, the Commission adopted proposals for veterinary medicinal products and medicated feed . They are currently undergoing the ordinary legislative procedure in the European Parliament and the Council. Action n° 3: Introduce recommendations for prudent use in veterinary medicine, including follow-up reports : regardless of the efforts carried out to improve the prudent use of veterinary antimicrobials it is also necessary to update marketing authorisations to take into account of the latest scientific developments. The Commission services are finalising the drafting of Guidelines for prudent use of antimicrobials in veterinary medicine. Action n° 4: Strengthen infection prevention and control in healthcare settings : the report showed that in the area of prevention and control of healthcare associated infections (HAI), 26 out of 28 responding countries implemented a combination of actions to prevent and control such infections. More efforts are needed to ensure adequate numbers of specialised infection control staff, receiving regular training, and with dedicated time for this task in hospitals and other healthcare settings. Tailored basic infection prevention and control structures and practices in nursing homes and other long term care facilities should be reinforced. Information on HAI to patients should be improved. Action n° 5: Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law : t he Commission proposal for a Regulation on animal health was adopted in May 2013. It is currently undergoing the ordinary legislative procedure in the European Parliament and in the Council. Its objective is to create an EU animal health legal framework for the control of major transmissible animal diseases. Action n° 6: Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients : as rapid response, the New Drugs for Bad Bugs (ND4BB) programme was launched in May 2012. A new model for open innovation in the pharmaceutical research area has been created to spur the development of new antibiotics . This model means that research sectors and individual companies now provide unprecedented access to each other’s data and collaborate on solving problems of public health concern. The Commission and the European Investment Bank are jointly developing a pilot financial facility which aims to target Infectious Diseases (ID). It is expected to be launched in 2015. Action n° 7: Promote efforts to analyse the need for new antibiotics into veterinary medicine : the report acknowledged that there are certain gaps between the approved indications for veterinary antimicrobials and the needs of veterinarians. This area needs to be improved. Action n° 8: Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors : the Commission services are supporting and actively cooperating with the WHO in this field. Cooperation with China has started and possible cooperation with Russian is imminent. The Commission services are also contributing to the work against antimicrobial resistance in developing countries. They have also begun to develop a strategic approach to the pollution of water by pharmaceuticals . Proposals are awaited in 2017. Action n° 9: Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine : t ransfer of the European system for surveillance of antimicrobial consumption in human medicine to ECDC was completed in 2012. The system is now integrated as part of ECDC surveillance as the European Surveillance of Antimicrobial Consumption Network (ESAC-Net). Action n° 10: Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine : t he information collected by the three agencies: the European Food Safety Authority (EFSA), the European Medicines Agency (EMA) and the European Centre for Disease Prevention and Control (ECDC) on antimicrobial resistance and antimicrobial consumption needs to be combined and jointly analysed in order to assess the relationship between use of antimicrobials and antimicrobial resistance in animals and in humans at the European level. Action n° 11: Reinforce and co-ordinate research efforts : af ter the launch of the Action Plan, research on AMR has been further supported by the Commission services with a total budget of approx. €130 million under the EU’s Seventh Framework Programme for Research and Technological Development. The new EU framework programme Horizon 2020 continues to give research on infectious diseases including AMR a high priority. In 2014, the European Commission devoted €28 million to the development of new vaccines candidates against tuberculosis, and has earmarked €25 million for HIV vaccine research in 2015. Action n° 12: Survey and comparative effectiveness research : e ach year, the European Antibiotic Awareness Day (EAAD) attracts strong media interest across Europe. In July 2013, ECDC provided training on the development, implementation and evaluation of prudent antibiotic use campaigns to 29 participants from 20 Member States and Norway. type: Follow-up document body: EC
  • date: 2016-10-24T00:00:00 docs: title: SWD(2016)0347 type: Follow-up document body: EC
  • date: 2016-10-24T00:00:00 docs: title: SWD(2016)0348 type: Follow-up document body: EC
  • date: 2012-12-13T00:00:00 docs: url: http://www.connefof.europarl.europa.eu/connefof/app/exp/COM(2011)0748 title: COM(2011)0748 type: Contribution body: PT_PARLIAMENT
events
  • date: 2011-11-15T00:00:00 type: Non-legislative basic document published body: EC docs: url: http://www.europarl.europa.eu/registre/docs_autres_institutions/commission_europeenne/com/2011/0748/COM_COM(2011)0748_EN.pdf title: COM(2011)0748 url: https://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748 title: EUR-Lex summary: PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR). BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives). Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe. The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion. For their part, the Council and the European Parliament have already examined this issue and on 12 May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR. This Communication responds to this request. CONTENT: in this regard, the Commission has taken a number of important actions: in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR; in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella; in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals; the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas; AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States; scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage. Based on such holistic approach, the new actions put forward in this Action Plan aim at: mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR. mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials; putting in place effective ways to prevent microbial infections and their spread; developing effective antimicrobials or alternatives for treatment of human and animal infections; joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment; reinforcing research to develop the scientific basis and innovative means to combat AMR. The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions: Action n° 1 : Strengthen the promotion of the appropriate use of antimicrobials in all Member States. Action n° 2 : Strengthen the regulatory framework on veterinary medicines and on medicated feed. Action n° 3 : Introduce recommendations for prudent use in veterinary medicine, including follow-up reports. Action n° 4 : Strengthen infection prevention and control in healthcare settings. Action n° 5 : Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law. Action n° 6 : Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients. Action n° 7 : Promote efforts to analyse the need for new antibiotics into veterinary medicine. Action n° 8 : Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors. Action n° 9 : Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine. Action n° 10 : Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine. Action n° 11 : Reinforce and co-ordinate research efforts. Action n° 12 : Survey and comparative effectiveness research. Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.
  • date: 2012-03-15T00:00:00 type: Committee referral announced in Parliament, 1st reading/single reading body: EP
  • date: 2012-06-21T00:00:00 type: Resolution/conclusions adopted by Council body: CSL summary: The Council adopted conclusions on the impact of antimicrobial resistance (AMR) in the human health sector and in the veterinary sector , calling upon member states to develop and implement national strategies or action plans for countering AMR. These national strategies or action plans should, amongst others, include the following elements: national guidelines on the treatment of humans and animals with antimicrobial agents; communication guidelines and programmes for education and training of professionals; enforcement of national legislation preventing all illegal sales of antimicrobials including illegal sales over the internet; limitation of the use of critically important antibiotics to cases where microbiological diagnosis and susceptibility testing has determined that no other type of antimicrobials will be effective; limitation of prophylactic use of antimicrobials to cases with defined clinical needs; limitation of prescription and use of antimicrobials for herd treatment of animals to cases with a clear clinical or epidemiological justification. The conclusions also call upon the member states and the Commission to examine the conditions of prescription and sale of antimicrobials in order to ascertain whether practices in human and animals healthcare may lead to over-prescription, overuse or misuse of antimicrobials. The Commission is invited to expedite the review of legislative acts in order to take antimicrobial resistance better into account. This applies notably to directive 90/167 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the EU and directive 2001/82 on the EU code relating to veterinary medicinal products. The Commission informed that preparatory work for some of the actions to which it is invited has already been started. According to the World Health Organisation (WHO) about 440 000 new cases of multidrugresistant tuberculosis (MDR-TB) emerge annually, causing at least 150 000 deaths. A high percentage of hospital-acquired infections are caused by highly resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA).
  • date: 2012-11-06T00:00:00 type: Vote in committee, 1st reading/single reading body: EP
  • date: 2012-11-15T00:00:00 type: Committee report tabled for plenary, single reading body: EP docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN title: A7-0373/2012 summary: The Committee on the Environment, Public Health and Food Safety unanimously adopted the initiative report by Anna ROSBACH (ECR, DK) on “the Microbial Challenge – Rising threats from Antimicrobial Resistance”. Members recall that resistance to antibiotics for certain bacteria is as high as 25 % or more in several Member States and that much of the antimicrobial resistance (AMR) problem stems from the misuse – in particular excessive use – of antibiotics. They also highlight the fact that many Member States do not have a solid legal and regulatory framework to mandate and support the rational use of medicines. As a result, Members call for the complete and rapid implementation of measures in this area. Although they welcome the Commission’s five-year plan strategic Action Plan on tackling AMR and view it as generally going in the right direction, Members note that many of the action points reiterate measures prescribed over a decade ago, it is not sufficient for tackling the growing risk presented by AMR at international level . In this context, Members call for an integrated roadmap outlining relevant policy responses, including possible legislative action. Members call in particular for the Action Plan to: cover all animals under the EU animal welfare strategy, including, for instance, companion animals and animals used for sports, and emphasise the logical connection between animal health and the use of antimicrobials, as well as the link between animal health and human health. Prudent use of antimicrobials in human and veterinary medicine: Members call for the prudent use of antimicrobials. The key objective of any AMR strategy is to maintain the efficiency of existing antimicrobials by using them responsibly at the correct therapeutic level only when strictly necessary and prescribed over a specific time at the appropriate dosage (and not for treating viral infections). Similar prudence needs to be exercised in veterinary medicine. Members call on the Member States to use electronic recording systems to ensure that usage patterns on individual farms are appropriate, thus ensuring responsible and minimal use. They also suggest to the Commission that current provisions on maximum animal density in livestock farming be re-evaluated as herd sizes today often present obstacles to the treatment of individual or smaller groups of animals, providing incentives for the prophylactic use of antimicrobials. They also call for a legislative proposal to be presented for the veterinary sector to limit its use of third- and fourth-generation Critically Important Antimicrobials (CIAs) for humans . The Commission and the Member States are also invited to encourage efforts to study hospital outbreaks, to improve diagnostics but also to assess and monitor the Member States' implementation of relevant EU legislation on antimicrobials, in particular with regard to the prescription-only use of antibiotics in the human health and veterinary sectors. Prevention: Members call for more effective measures to be introduced to prevent both the appearance and the spread of antimicrobial resistance. These measures include better monitoring and better notification of micro-organisms resistant to antimicrobials, as well as a more effective combating of infections, in particular by means of vaccinations. Among other measures they call for limits on uncontrolled access to antimicrobial agents, in particular via the growing number of illegal sales on the internet, and their inappropriate use. They call on the Member States to improve infection control, and to raise and promote good standards of hygiene – especially hand hygiene, – in order to prevent the spread of infections and reduce the need for antibiotics. Development of new antimicrobials or alternatives for treatment: Members consider it vital to limit the emergence of bacteria that are resistant to antimicrobials. In this context, it is necessary to develop new antimicrobial agents. In parallel, Members stress the advantages of public-private partnerships because these can contribute to reaching this objective by dissociating sales transactions from investment in research and development. In this area, Members call on the Commission and the Member States to accelerate R&D activities in order to provide new tools to fight tuberculosis and drug-resistant tuberculosis. Members also underline the need to examine new regulatory approaches that would result in stimulating industrial research and the development of new antimicrobials while safeguarding patient safety. They also call on the Commission to ensure the development and availability of more on-farm tools for early, rapid diagnosis and control of diseases, as well as for a broad and effective diagnostic system at Member State level. Monitoring and reporting: in this field, Members call on the Commission and the Member States to seek greater cooperation and coordination on early detection, alert and coordinated response procedures regarding pathogenic antimicrobial resistant bacteria in humans, animals, fish and foodstuffs. They call on Member States to compile clear, comparable, transparent and timely reference data on antimicrobial drug usage so that effective action can be undertaken. They consider, however, that data gathered on the use of antibiotics should be made accessible only to the experts, authorities and decision-makers concerned. They call on the Member States to ensure separate monitoring and control of resistance among livestock, domestic animals and racing animals. Communication, education and training: Members note that one of the most common uses for antibiotics is as treatment against the common cold , and that much would be gained if the public could be made aware of the fact that the common cold is a viral infection whereas antibiotics only provide protection against bacterial infections. They call on the Commission to compile a best practice list with regard to the implementation of effective communication campaigns and professional training courses aimed at raising AMR awareness. They believe that effective information and awareness campaigns must be developed with a view to heightening awareness of the dangers of the unintentional spread of antimicrobial pathogens in hospitals and in the home, and awareness of the means of avoiding this. Campaigns along the lines of "Please take this antibiotic medicine only if it is prescribed by a doctor to you and take it as prescribed” should be promoted and included in the package leaflet. International cooperation: lastly, Members believe that concerted and timely international action that avoids overlap and builds critical mass is the only way forward in minimising the threat to public health that AMR poses globally.They consider that the work undertaken by the Transatlantic Task Force on Antimicrobial Resistance (TATFAR) should be used as a model for international cooperation on antimicrobial resistance. Other similar multilateral and bilateral commitments for the prevention and control of AMR should also be encouraged, in accordance with the guidelines laid down by the WHO (in particular in regard to the control of counterfeit antimicrobials).
  • date: 2012-12-10T00:00:00 type: Debate in Parliament body: EP docs: url: http://www.europarl.europa.eu/sides/getDoc.do?secondRef=TOC&language=EN&reference=20121210&type=CRE title: Debate in Parliament
  • date: 2012-12-11T00:00:00 type: Results of vote in Parliament body: EP docs: url: https://oeil.secure.europarl.europa.eu/oeil/popups/sda.do?id=22191&l=en title: Results of vote in Parliament
  • date: 2012-12-11T00:00:00 type: Decision by Parliament, 1st reading/single reading body: EP docs: url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483 title: T7-0483/2012 summary: The European Parliament adopted by 588 votes to 16, with 23 abstentions, a resolution on “the Microbial Challenge – Rising threats from Antimicrobial Resistance”. Parliament recalls that resistance to antibiotics for certain bacteria is as high as 25 % or more in several Member States and that much of the antimicrobial resistance (AMR) problem stems from the misuse – in particular the excessive use – of antibiotics. It recalls that in the EU, Iceland and Norway alone, antimicrobial resistant bacteria cause some 400 000 infections and 25 000 deaths annually, with at least EUR 1.5 billion spent on extra healthcare costs and productivity losses. It also highlights the fact that many Member States do not have a solid legal and regulatory framework to mandate and support the rational use of medicines. As a result, Parliament calls for the complete and rapid implementation of measures in this area. Although welcoming the Commission’s five-year strategic Action Plan on tackling AMR and viewing it as generally going in the right direction, Parliament notes that many of the action points reiterate measures prescribed over a decade ago, and that it is not sufficient for tackling the growing risk presented by AMR at international level . In this context, Members call for an integrated roadmap outlining relevant policy responses, including possible legislative action. Parliament calls in particular for the Action Plan to: cover all animals under the EU animal welfare strategy, including, for instance, companion animals and animals used for sports, and emphasise the logical connection between animal health and the use of antimicrobials, as well as the link between animal health and human health. Prudent use of antimicrobials in human and veterinary medicine: Parliament calls for the prudent use of antimicrobials. The key objective of any AMR strategy is to maintain the efficiency of existing antimicrobials by using them responsibly at the correct therapeutic level only when strictly necessary and prescribed over a specific time at the appropriate dosage (and not for treating viral infections). Similar prudence needs to be exercised in veterinary medicine. Parliament calls on the Member States to use electronic recording systems to ensure that usage patterns on individual farms are appropriate, thus ensuring responsible and minimal use. It also suggests to the Commission that current provisions on maximum animal density in livestock farming be re-evaluated as herd sizes today often present obstacles to the treatment of individual or smaller groups of animals, providing incentives for the prophylactic use of antimicrobials. It calls for a legislative proposal to be presented for the veterinary sector to limit its use of third- and fourth-generation Critically Important Antimicrobials (CIAs) for humans. Parliament considers that the pending revision of Directive 2001/82/EC offers an important opportunity to take effective measures to reduce AMR through strengthening the provisions for veterinary medicines, such as: limiting the right to prescribe antimicrobials to professionally qualified veterinarians only; separating the right to prescribe from the right to sell antimicrobials, thereby eradicating economic incentives to prescribe. Measures are called for to encourage efforts to study hospital outbreaks, to improve diagnostics but also to assess and monitor the Member States' implementation of relevant EU legislation on antimicrobials, in particular with regard to the prescription-only use of antibiotics in the human health and veterinary sectors. Prevention: Parliament calls for more effective measures to be introduced to prevent both the appearance and the spread of antimicrobial resistance. These measures include better monitoring and better notification of micro-organisms resistant to antimicrobials, as well as a more effective combating of infections, in particular by means of vaccinations. Among other measures that it calls for are limits on uncontrolled access to antimicrobial agents, in particular via the growing number of illegal sales on the internet, and their inappropriate use. It calls on the Member States to improve infection control, and to raise and promote good standards of hygiene – especially hand hygiene, – in order to prevent the spread of infections and reduce the need for antibiotics. Parliament also invites the Commission to classify, in the forthcoming review of the European veterinary pharmaceuticals legislation, medicated feeding stuffs as ‘pharmaceuticals’ and not as ‘feeding stuffs’, in order to ensure that, in future, the sensitive area of medicated foodstuffs is monitored under pharmaceuticals legislation and that official inspections are carried out accordingly, while ensuring that medicated foodstuffs fall into the ‘prescription only’ category . Development of new antimicrobials or alternatives for treatment: Parliament considers it vital to limit the emergence of bacteria that are resistant to antimicrobials . In this context, it is necessary to develop new antimicrobial agents. In parallel, it stresses the advantages of public-private partnerships because these can contribute to reaching this objective by dissociating sales transactions from investment in research and development. In this area, Parliament calls on the Commission and the Member States to accelerate R&D activities in order to provide new tools to fight tuberculosis and drug-resistant tuberculosis. Parliament also underlines the need to examine new regulatory approaches that would result in stimulating industrial research and the development of new antimicrobials while safeguarding patient safety. It also calls on the Commission to ensure the development and availability of more on-farm tools for early, rapid diagnosis and control of diseases, as well as for a broad and effective diagnostic system at Member State level. Monitoring and reporting: in this regard, Parliament calls on the Commission and the Member States to seek greater cooperation and coordination on early detection, alert and coordinated response procedures regarding pathogenic antimicrobial resistant bacteria in humans, animals, fish and foodstuffs. It calls on Member States to compile clear, comparable, transparent and timely reference data on antimicrobial drug usage so that effective action can be undertaken. It considers, however, that data gathered on the use of antibiotics should be made accessible only to the experts, authorities and decision-makers concerned. It calls on the Member States to ensure separate monitoring and control of resistance among livestock, domestic animals and racing animals. Communication, education and training: Parliament notes that one of the most common uses for antibiotics is as treatment against the common cold , and that much would be gained if the public could be made aware of the fact that the common cold is a viral infection whereas antibiotics only provide protection against bacterial infections. It calls on the Commission to compile a best practice list with regard to the implementation of effective communication campaigns and professional training courses aimed at raising AMR awareness. It believes that effective information and awareness campaigns must be developed with a view to heightening awareness of the dangers of the unintentional spread of antimicrobial pathogens in hospitals and in the home, and awareness of the means of avoiding this. Campaigns along the lines of "Please take this antibiotic medicine only if it is prescribed by a doctor to you and take it as prescribed” should be promoted and included in the package leaflet. International cooperation: lastly, Parliament believes that concerted and timely international action that avoids overlap and builds critical mass is the only way forward in minimising the threat to public health that AMR poses globally. It considers that the work undertaken by the Transatlantic Task Force on Antimicrobial Resistance (TATFAR) should be used as a model for international cooperation on antimicrobial resistance. Other similar multilateral and bilateral commitments for the prevention and control of AMR should also be encouraged, in accordance with the guidelines laid down by the WHO (in particular in regard to the control of counterfeit antimicrobials).
  • date: 2012-12-11T00:00:00 type: End of procedure in Parliament body: EP
links
other
  • body: EC dg: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers commissioner: BORG Tonio
procedure/Modified legal basis
Old
Rules of Procedure of the European Parliament EP 150
New
Rules of Procedure EP 150
procedure/dossier_of_the_committee
Old
ENVI/7/08364
New
  • ENVI/7/08364
procedure/legal_basis/0
Rules of Procedure EP 52
procedure/legal_basis/0
Rules of Procedure of the European Parliament EP 052
procedure/subject
Old
  • 3.10.08 Animal health requirements, veterinary legislation and pharmacy
  • 4.20 Public health
  • 4.20.01 Medicine, diseases
  • 4.20.02 Medical research
New
3.10.08
Animal health requirements, veterinary legislation and pharmacy
4.20
Public health
4.20.01
Medicine, diseases
4.20.02
Medical research
activities/0/docs/0/celexid
CELEX:52011DC0748:EN
activities/0/docs/0/url
Old
http://www.europarl.europa.eu/registre/docs_autres_institutions/commission_europeenne/com/2011/0748/COM_COM(2011)0748_EN.pdf
New
http://www.europarl.europa.eu/RegData/docs_autres_institutions/commission_europeenne/com/2011/0748/COM_COM(2011)0748_EN.pdf
activities/0/docs/0/celexid
CELEX:52011DC0748:EN
activities/0/docs/0/text/0
Old

PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR).

BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives).

Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe.

The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion.

For their part, the Council and the European Parliament have already examined this issue and on 12May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR.

This Communication responds to this request.

CONTENT: in this regard, the Commission has taken a number of important actions:

  • in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR;
  • in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella;
  • in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals;
  • the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas;
  • AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States;
  • scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage.

Based on such holistic approach, the new actions put forward in this Action Plan aim at:

  1. mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials;
  2. putting in place effective ways to prevent microbial infections and their spread;
  3. developing effective antimicrobials or alternatives for treatment of human and animal infections;
  4. joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment;
  5. reinforcing research to develop the scientific basis and innovative means to combat AMR.

The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions:

  • Action n° 1: Strengthen the promotion of the appropriate use of antimicrobials in all Member States.
  • Action n° 2: Strengthen the regulatory framework on veterinary medicines and on medicated feed.
  • Action n° 3: Introduce recommendations for prudent use in veterinary medicine, including follow-up reports.
  • Action n° 4: Strengthen infection prevention and control in healthcare settings.
  • Action n° 5: Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law.
  • Action n° 6: Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients.
  • Action n° 7: Promote efforts to analyse the need for new antibiotics into veterinary medicine.
  • Action n° 8: Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors.
  • Action n° 9: Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine.
  • Action n° 10: Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine.
  • Action n° 11: Reinforce and co-ordinate research efforts.
  • Action n° 12: Survey and comparative effectiveness research.

Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.

New

PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR).

BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives).

Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe.

The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion.

For their part, the Council and the European Parliament have already examined this issue and on 12May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR.

This Communication responds to this request.

CONTENT: in this regard, the Commission has taken a number of important actions:

  • in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR;
  • in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella;
  • in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals;
  • the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas;
  • AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States;
  • scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage.

Based on such holistic approach, the new actions put forward in this Action Plan aim at:

  1. mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials;
  2. putting in place effective ways to prevent microbial infections and their spread;
  3. developing effective antimicrobials or alternatives for treatment of human and animal infections;
  4. joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment;
  5. reinforcing research to develop the scientific basis and innovative means to combat AMR.

The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions:

  • Action n° 1: Strengthen the promotion of the appropriate use of antimicrobials in all Member States.
  • Action n° 2: Strengthen the regulatory framework on veterinary medicines and on medicated feed.
  • Action n° 3: Introduce recommendations for prudent use in veterinary medicine, including follow-up reports.
  • Action n° 4: Strengthen infection prevention and control in healthcare settings.
  • Action n° 5: Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law.
  • Action n° 6: Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients.
  • Action n° 7: Promote efforts to analyse the need for new antibiotics into veterinary medicine.
  • Action n° 8: Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors.
  • Action n° 9: Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine.
  • Action n° 10: Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine.
  • Action n° 11: Reinforce and co-ordinate research efforts.
  • Action n° 12: Survey and comparative effectiveness research.

Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.

activities/0/type
Old
Non-legislative basic document
New
Non-legislative basic document published
activities/1/committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: PPE name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: ECR name: ROSBACH Anna
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
activities/1/date
Old
2012-12-11T00:00:00
New
2012-03-15T00:00:00
activities/1/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483 type: Decision by Parliament, 1st reading/single reading title: T7-0483/2012
activities/1/type
Old
Text adopted by Parliament, single reading
New
Committee referral announced in Parliament, 1st reading/single reading
activities/2/text/0
Old

The Council adopted conclusions on the impact of antimicrobial resistance (AMR) in the human health sector and in the veterinary sector, calling upon member states to develop and implement national strategies or action plans for countering AMR.

These national strategies or action plans should, amongst others, include the following elements:

  • national guidelines on the treatment of humans and animals with antimicrobial agents;
  • communication guidelines and programmes for education and training of professionals;
  • enforcement of national legislation preventing all illegal sales of antimicrobials including illegal sales over the internet;
  • limitation of the use of critically important antibiotics to cases where microbiological diagnosis and susceptibility testing has determined that no other type of antimicrobials will be effective;
  • limitation of prophylactic use of antimicrobials to cases with defined clinical needs;
  • limitation of prescription and use of antimicrobials for herd treatment of animals to cases with a clear clinical or epidemiological justification.

The conclusions also call upon the member states and the Commission to examine the conditions of prescription and sale of antimicrobials in order to ascertain whether practices in human and animals healthcare may lead to over-prescription, overuse or misuse of antimicrobials.

The Commission is invited to expedite the review of legislative acts in order to take antimicrobial resistance better into account. This applies notably to directive 90/167 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the EU and directive 2001/82 on the EU code relating to veterinary medicinal products.

The Commission informed that preparatory work for some of the actions to which it is invited has already been started.

According to the World Health Organisation (WHO) about 440 000 new cases of multidrugresistant tuberculosis (MDR-TB) emerge annually, causing at least 150 000 deaths. A high percentage of hospital-acquired infections are caused by highly resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA).

New

The Council adopted conclusions on the impact of antimicrobial resistance (AMR) in the human health sector and in the veterinary sector, calling upon member states to develop and implement national strategies or action plans for countering AMR.

These national strategies or action plans should, amongst others, include the following elements:

  • national guidelines on the treatment of humans and animals with antimicrobial agents;
  • communication guidelines and programmes for education and training of professionals;
  • enforcement of national legislation preventing all illegal sales of antimicrobials including illegal sales over the internet;
  • limitation of the use of critically important antibiotics to cases where microbiological diagnosis and susceptibility testing has determined that no other type of antimicrobials will be effective;
  • limitation of prophylactic use of antimicrobials to cases with defined clinical needs;
  • limitation of prescription and use of antimicrobials for herd treatment of animals to cases with a clear clinical or epidemiological justification.

The conclusions also call upon the member states and the Commission to examine the conditions of prescription and sale of antimicrobials in order to ascertain whether practices in human and animals healthcare may lead to over-prescription, overuse or misuse of antimicrobials.

The Commission is invited to expedite the review of legislative acts in order to take antimicrobial resistance better into account. This applies notably to directive 90/167 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the EU and directive 2001/82 on the EU code relating to veterinary medicinal products.

The Commission informed that preparatory work for some of the actions to which it is invited has already been started.

According to the World Health Organisation (WHO) about 440 000 new cases of multidrugresistant tuberculosis (MDR-TB) emerge annually, causing at least 150 000 deaths. A high percentage of hospital-acquired infections are caused by highly resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA).

activities/3
date
2012-07-12T00:00:00
docs
url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077 type: Committee draft report title: PE486.077
body
EP
type
Committee draft report
activities/3/committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: PPE name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: ECR name: ROSBACH Anna
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
activities/3/date
Old
2012-09-19T00:00:00
New
2012-11-06T00:00:00
activities/3/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.371 type: Amendments tabled in committee title: PE496.371
activities/3/type
Old
Amendments tabled in committee
New
Vote in committee, 1st reading/single reading
activities/4/committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: EPP name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: EFD name: ROSBACH Anna
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
activities/4/date
Old
2012-03-15T00:00:00
New
2012-11-15T00:00:00
activities/4/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN type: Committee report tabled for plenary, single reading title: A7-0373/2012
activities/4/type
Old
Committee referral announced in Parliament, 1st reading/single reading
New
Committee report tabled for plenary, single reading
activities/5
date
2012-10-16T00:00:00
docs
url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577 type: Amendments tabled in committee title: PE496.577
body
EP
type
Amendments tabled in committee
activities/5/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?secondRef=TOC&language=EN&reference=20121210&type=CRE type: Debate in Parliament title: Debate in Parliament
activities/6/committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: EPP name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: EFD name: ROSBACH Anna
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
activities/6/date
Old
2012-11-06T00:00:00
New
2012-12-11T00:00:00
activities/6/docs
  • url: http://www.europarl.europa.eu/oeil/popups/sda.do?id=22191&l=en type: Results of vote in Parliament title: Results of vote in Parliament
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483 type: Decision by Parliament, 1st reading/single reading title: T7-0483/2012
activities/6/type
Old
Vote in committee, 1st reading/single reading
New
Results of vote in Parliament
activities/7
date
2012-11-15T00:00:00
docs
url: http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN type: Committee report tabled for plenary, single reading title: A7-0373/2012
body
EP
type
Committee report tabled for plenary, single reading
committees/0/rapporteur/0/mepref
Old
4de185720fb8127435bdbeff
New
4f1ac8f9b819f25efd000103
committees/1/rapporteur/0/group
Old
EFD
New
ECR
committees/1/rapporteur/0/mepref
Old
4de188070fb8127435bdc2a3
New
4f1adadcb819f207b3000095
committees/1/shadows/0/group
Old
EPP
New
PPE
committees/1/shadows/1/mepref
Old
4de185fc0fb8127435bdbfbf
New
4f1ac963b819f25efd000132
committees/1/shadows/2/mepref
Old
4dee5a2d0fb8127435be059f
New
4f1adb75b819f207b30000c6
committees/1/shadows/3/mepref
Old
4de188650fb8127435bdc331
New
4f1adb8fb819f207b30000cf
committees/1/shadows/4/mepref
Old
4de186f60fb8127435bdc122
New
4f1ad983b819f207b300001f
procedure/Modified legal basis
Rules of Procedure of the European Parliament EP 150
procedure/legal_basis/0
Old
Rules of Procedure of the European Parliament EP 048
New
Rules of Procedure of the European Parliament EP 052
procedure/subject/2
Old
4.20.01 Medicine, diseases, AIDS
New
4.20.01 Medicine, diseases
activities/8/type
Old
Debate scheduled
New
Debate in Parliament
activities/9/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=TA&language=EN&reference=P7-TA-2012-483 type: Decision by Parliament, 1st reading/single reading title: T7-0483/2012
activities/9/type
Old
Vote scheduled
New
Text adopted by Parliament, single reading
procedure/stage_reached
Old
Awaiting Parliament 1st reading / single reading / budget 1st stage
New
Procedure completed
activities/7/docs/0/text
  • The Committee on the Environment, Public Health and Food Safety unanimously adopted the initiative report by Anna ROSBACH (ECR, DK) on “the Microbial Challenge – Rising threats from Antimicrobial Resistance”.

    Members recall that resistance to antibiotics for certain bacteria is as high as 25 % or more in several Member States and that much of the antimicrobial resistance (AMR) problem stems from the misuse – in particular excessive use – of antibiotics. They also highlight the fact that many Member States do not have a solid legal and regulatory framework to mandate and support the rational use of medicines. As a result, Members call for the complete and rapid implementation of measures in this area.

    Although they welcome the Commission’s five-year planstrategic Action Plan on tackling AMR and view it as generally going in the right direction, Members note that many of the action points reiterate measures prescribed over a decade ago, it is not sufficient for tackling the growing risk presented by AMR at international level.

    In this context, Members call for an integrated roadmap outlining relevant policy responses, including possible legislative action.

    Members call in particular for the Action Plan to:

    • cover all animals under the EU animal welfare strategy, including, for instance, companion animals and animals used for sports, and
    • emphasise the logical connection between animal health and the use of antimicrobials, as well as the link between animal health and human health.

    Prudent use of antimicrobials in human and veterinary medicine: Members call for the prudent use of antimicrobials. The key objective of any AMR strategy is to maintain the efficiency of existing antimicrobials by using them responsibly at the correct therapeutic level only when strictly necessary and prescribed over a specific time at the appropriate dosage (and not for treating viral infections). Similar prudence needs to be exercised in veterinary medicine. Members call on the Member States to use electronic recording systems to ensure that usage patterns on individual farms are appropriate, thus ensuring responsible and minimal use. They also suggest to the Commission that current provisions on maximum animal density in livestock farming be re-evaluated as herd sizes today often present obstacles to the treatment of individual or smaller groups of animals, providing incentives for the prophylactic use of antimicrobials. They also call for a legislative proposal to be presented for the veterinary sector to limit its use of third- and fourth-generation Critically Important Antimicrobials (CIAs) for humans.

    The Commission and the Member States are also invited to encourage efforts to study hospital outbreaks, to improve diagnostics but also to assess and monitor the Member States' implementation of relevant EU legislation on antimicrobials, in particular with regard to the prescription-only use of antibiotics in the human health and veterinary sectors.

    Prevention: Members call for more effective measures to be introduced to prevent both the appearance and the spread of antimicrobial resistance. These measures include better monitoring and better notification of micro-organisms resistant to antimicrobials, as well as a more effective combating of infections, in particular by means of vaccinations. Among other measures they call for limits on uncontrolled access to antimicrobial agents, in particular via the growing number of illegal sales on the internet, and their inappropriate use. They call on the Member States to improve infection control, and to raise and promote good standards of hygiene – especially hand hygiene, – in order to prevent the spread of infections and reduce the need for antibiotics.

    Development of new antimicrobials or alternatives for treatment: Members consider it vital to limit the emergence of bacteria that are resistant to antimicrobials. In this context, it is necessary to develop new antimicrobial agents. In parallel, Members stress the advantages of public-private partnerships because these can contribute to reaching this objective by dissociating sales transactions from investment in research and development. In this area, Members call on the Commission and the Member States to accelerate R&D activities in order to provide new tools to fight tuberculosis and drug-resistant tuberculosis.

    Members also underline the need to examine new regulatory approaches that would result in stimulating industrial research and the development of new antimicrobials while safeguarding patient safety. They also call on the Commission to ensure the development and availability of more on-farm tools for early, rapid diagnosis and control of diseases, as well as for a broad and effective diagnostic system at Member State level.

    Monitoring and reporting: in this field, Members call on the Commission and the Member States to seek greater cooperation and coordination on early detection, alert and coordinated response procedures regarding pathogenic antimicrobial resistant bacteria in humans, animals, fish and foodstuffs. They call on Member States to compile clear, comparable, transparent and timely reference data on antimicrobial drug usage so that effective action can be undertaken. They consider, however, that data gathered on the use of antibiotics should be made accessible only to the experts, authorities and decision-makers concerned. They call on the Member States to ensure separate monitoring and control of resistance among livestock, domestic animals and racing animals.

    Communication, education and training: Members note that one of the most common uses for antibiotics is as treatment against the common cold, and that much would be gained if the public could be made aware of the fact that the common cold is a viral infection whereas antibiotics only provide protection against bacterial infections. They call on the Commission to compile a best practice list with regard to the implementation of effective communication campaigns and professional training courses aimed at raising AMR awareness. They believe that effective information and awareness campaigns must be developed with a view to heightening awareness of the dangers of the unintentional spread of antimicrobial pathogens in hospitals and in the home, and awareness of the means of avoiding this. Campaigns along the lines of "Please take this antibiotic medicine only if it is prescribed by a doctor to you and take it as prescribed” should be promoted and included in the package leaflet.

    International cooperation: lastly, Members believe that concerted and timely international action that avoids overlap and builds critical mass is the only way forward in minimising the threat to public health that AMR poses globally.They consider that the work undertaken by the Transatlantic Task Force on Antimicrobial Resistance (TATFAR) should be used as a model for international cooperation on antimicrobial resistance. Other similar multilateral and bilateral commitments for the prevention and control of AMR should also be encouraged, in accordance with the guidelines laid down by the WHO (in particular in regard to the control of counterfeit antimicrobials).

activities/3/date
Old
2011-11-15T00:00:00
New
2012-07-12T00:00:00
activities/3/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077 type: Committee draft report title: PE486.077
activities/3/type
Old
Date
New
Committee draft report
activities/5
date
2012-07-12T00:00:00
docs
url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077 type: Committee draft report title: PE486.077
body
EP
type
Committee draft report
activities/5/date
Old
2012-03-08T00:00:00
New
2012-10-16T00:00:00
activities/5/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577 type: Amendments tabled in committee title: PE496.577
activities/5/type
Old
EP officialisation
New
Amendments tabled in committee
activities/7/date
Old
2012-09-14T00:00:00
New
2012-11-15T00:00:00
activities/7/docs
  • url: http://www.europarl.europa.eu/sides/getDoc.do?type=REPORT&mode=XML&reference=A7-2012-373&language=EN type: Committee report tabled for plenary, single reading title: A7-0373/2012
activities/7/type
Old
Deadline Amendments
New
Committee report tabled for plenary, single reading
activities/8
date
2012-10-16T00:00:00
docs
url: http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577 type: Amendments tabled in committee title: PE496.577
body
EP
type
Amendments tabled in committee
activities/10
date
2012-11-15T00:00:00
docs
type: Committee report tabled for plenary, single reading title: A7-0373/2012
body
EP
type
Committee report tabled for plenary, single reading
activities/12
body
EC
date
2012-12-10T00:00:00
type
Prev DG PRES
commission
DG: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers Commissioner: BORG Tonio
activities/1/commission/0/Commissioner
Old
DALLI John
New
BORG Tonio
activities/12/commission/0/Commissioner
Old
DALLI John
New
BORG Tonio
other/0/commissioner
Old
DALLI John
New
BORG Tonio
activities/11/type
Old
Indicative plenary sitting date, 1st reading/single reading
New
Debate scheduled
activities/12
body
EC
date
2012-12-10T00:00:00
type
Prev DG PRES
commission
DG: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers Commissioner: DALLI John
activities/13
date
2012-12-11T00:00:00
body
EP
type
Vote scheduled
activities/10/date
Old
2012-11-14T00:00:00
New
2012-11-15T00:00:00
activities/1/docs/0/url
Old
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
New
http://www.europarl.europa.eu/registre/docs_autres_institutions/commission_europeenne/com/2011/0748/COM_COM(2011)0748_EN.pdf
activities/10
date
2012-11-14T00:00:00
docs
type: Committee report tabled for plenary, single reading title: A7-0373/2012
body
EP
type
Committee report tabled for plenary, single reading
activities/9/committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: EPP name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin group: ALDE name: SKYLAKAKIS Theodoros group: Verts/ALE name: STAES Bart group: GUE/NGL name: MATIAS Marisa responsible: True committee: ENVI date: 2012-03-23T00:00:00 committee_full: Environment, Public Health and Food Safety rapporteur: group: EFD name: ROSBACH Anna
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
activities/9/type
Old
Vote scheduled in committee, 1st reading/single reading
New
Vote in committee, 1st reading/single reading
activities/8/docs/0/url
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.577
activities/8
date
2012-10-16T00:00:00
docs
type: Amendments tabled in committee title: PE496.577
body
EP
type
Amendments tabled in committee
activities/7/docs/0/url
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE496.371
activities/7
date
2012-09-19T00:00:00
docs
type: Amendments tabled in committee title: PE496.371
body
EP
type
Amendments tabled in committee
activities/3/committees/1/rapporteur/0/group
Old
ECR
New
EFD
activities/3/committees/1/shadows/4
group
GUE/NGL
name
MATIAS Marisa
committees/1/rapporteur/0/group
Old
ECR
New
EFD
committees/1/shadows/4
group
GUE/NGL
name
MATIAS Marisa
activities/4/text
  • The Council adopted conclusions on the impact of antimicrobial resistance (AMR) in the human health sector and in the veterinary sector, calling upon member states to develop and implement national strategies or action plans for countering AMR.

    These national strategies or action plans should, amongst others, include the following elements:

    • national guidelines on the treatment of humans and animals with antimicrobial agents;
    • communication guidelines and programmes for education and training of professionals;
    • enforcement of national legislation preventing all illegal sales of antimicrobials including illegal sales over the internet;
    • limitation of the use of critically important antibiotics to cases where microbiological diagnosis and susceptibility testing has determined that no other type of antimicrobials will be effective;
    • limitation of prophylactic use of antimicrobials to cases with defined clinical needs;
    • limitation of prescription and use of antimicrobials for herd treatment of animals to cases with a clear clinical or epidemiological justification.

    The conclusions also call upon the member states and the Commission to examine the conditions of prescription and sale of antimicrobials in order to ascertain whether practices in human and animals healthcare may lead to over-prescription, overuse or misuse of antimicrobials.

    The Commission is invited to expedite the review of legislative acts in order to take antimicrobial resistance better into account. This applies notably to directive 90/167 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the EU and directive 2001/82 on the EU code relating to veterinary medicinal products.

    The Commission informed that preparatory work for some of the actions to which it is invited has already been started.

    According to the World Health Organisation (WHO) about 440 000 new cases of multidrugresistant tuberculosis (MDR-TB) emerge annually, causing at least 150 000 deaths. A high percentage of hospital-acquired infections are caused by highly resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA).

activities/5/docs/0/url
http://www.europarl.europa.eu/sides/getDoc.do?type=COMPARL&mode=XML&language=EN&reference=PE486.077
activities/5
date
2012-07-12T00:00:00
docs
type: Committee draft report title: PE486.077
body
EP
type
Committee draft report
procedure/legal_basis
  • Rules of Procedure of the European Parliament EP 048
activities/4
date
2012-06-21T00:00:00
body
CSL
type
Council Meeting
council
Employment, Social Policy, Health and Consumer Affairs
meeting_id
3177
activities/3/committees/1/shadows/2
group
ALDE
name
SKYLAKAKIS Theodoros
activities/3/committees/1/shadows/3
group
Verts/ALE
name
STAES Bart
activities/4/date
Old
2012-09-11T00:00:00
New
2012-09-14T00:00:00
committees/1/shadows/2
group
ALDE
name
SKYLAKAKIS Theodoros
committees/1/shadows/3
group
Verts/ALE
name
STAES Bart
procedure/legal_basis
  • Rules of Procedure of the European Parliament EP 048
activities/1/docs/0/url
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
activities/1/docs/0/text
  • PURPOSE: to establish an action plan against the rising threats from Antimicrobial Resistance (AMR).

    BACKGROUND: since the introduction of penicillin in the 1940s antimicrobial medicines, such as antibiotics, have become essential for the treatment of many microbial infections in humans and animals. In addition to the treatment of infectious diseases (e.g. pneumonia, tuberculosis, malaria, HIV/AIDS) and hospital-acquired infections (e.g. methicilin resistant Staphylococcus aureus (MRSA), antimicrobials are vital for reducing the risk of complications in relation to complex medical interventions, such as hip replacements, organ transplants, cancer chemotherapy and the care of premature babies. In addition, antimicrobials are used in veterinary medicine and for non-therapeutic purposes (e.g. disinfectants, preservatives, and food and feed additives).

    Seventy years later, these applications are now seriously jeopardized by the emergence and spread of microbes that are resistant to affordable and effective firstchoice, or "first-line" medicines, rendering the drugs concerned ineffective for the treatment of the infection. This resistance is a natural biological phenomenon but is amplified by a variety of factors. The inappropriate use of therapeutic antimicrobials in human and veterinary medicine, the use of antimicrobials for non-therapeutic purposes as well as the pollution of the environment by antimicrobials is accelerating the emergence and spread of resistant microorganisms. The consequences are severe.

    The Commission recall that a subset of drug-resistant bacteria is responsible for about 25 000 human deaths annually. In addition to avoidable death, this also translates into extra healthcare costs and productivity losses of at least EUR 1.5 billion.

    For their part, the Council and the European Parliament have already examined this issue and on 12May 2011 the European Parliament adopted a non-legislative resolution on antibiotic resistance in which it stresses that AMR has become a huge issue in recent years. To cope with this growing problem and the consequent treatment failures, the EP calls on the Commission to establish an EU-wide plan to combat AMR.

    This Communication responds to this request.

    CONTENT: in this regard, the Commission has taken a number of important actions:

    • in the field of human medicine, the 2001 Community Strategy against AMR called for EU actions against AMR in the fields of surveillance, research, prevention and international cooperation. This led to the adoption of EU wide recommendations and guidelines against AMR;
    • in animal husbandry, the ban on the use of antimicrobials for growth promotion was introduced in 2006. The Commission has developed legislation on the control of Salmonella at all relevant stages of production, processing and distribution in order to reduce the exposure of humans to potentially resistant Salmonella;
    • in the field of veterinary medicine, the emphasis has been in monitoring zoonotic AMR (i.e. resistance transmissible between animals and humans) and on the use of antimicrobials in animals;
    • the authorisation requirements of human and veterinary medicines and other products, such as food enzymes, probiotics and decontamination agents, with possible effects on development of AMR have also been the focus areas;
    • AMR is the subject of research funded under the Seventh Framework Programme (FP7) and the Innovative Medicines Initiative (IMI). AMR is also the subject of a proposed Joint Programming Initiative (JPI), which aim to coordinate research activities among EU Member States;
    • scientific opinions on AMR by EU Risk Assessment bodies i.e. the European Centre for Disease Prevention and Control (ECDC), the European Food Safety Authority (EFSA), the European Medicines Agency (EMA), the Scientific Committee on Emerging and Newly Identified Health Risks (SCENIHR) have formed the basis for policy planning, for example, development of new antimicrobials and monitoring AMR and antimicrobial usage.

    Based on such holistic approach, the new actions put forward in this Action Plan aim at:

    1. mitigating the risk of developing AMR in humans from the use of antimicrobials both in humans and animals by effectively ensuring across the EU their appropriate use, and promoting microbiological diagnosis as the means to determine, to the extent possible, the need for antimicrobials;
    2. putting in place effective ways to prevent microbial infections and their spread;
    3. developing effective antimicrobials or alternatives for treatment of human and animal infections;
    4. joining forces with international partners to contain the risks of spreading AMR from international trade and travel and via the environment;
    5. reinforcing research to develop the scientific basis and innovative means to combat AMR.

    The Commission proposes to put in place a 5-year Action Plan to fight against AMR based on 12 key actions:

    • Action n° 1: Strengthen the promotion of the appropriate use of antimicrobials in all Member States.
    • Action n° 2: Strengthen the regulatory framework on veterinary medicines and on medicated feed.
    • Action n° 3: Introduce recommendations for prudent use in veterinary medicine, including follow-up reports.
    • Action n° 4: Strengthen infection prevention and control in healthcare settings.
    • Action n° 5: Introduce of a legal tool to enhance prevention and control of infections in animals in the new Animal Health Law.
    • Action n° 6: Promote, in a staged approach, unprecedented collaborative research and development efforts to bring new antimicrobials to patients.
    • Action n° 7: Promote efforts to analyse the need for new antibiotics into veterinary medicine.
    • Action n° 8: Develop and/or strengthen multilateral and bilateral commitments for the prevention and control of AMR in all sectors.
    • Action n° 9: Strengthen surveillance systems on AMR and antimicrobial consumption in human medicine.
    • Action n° 10: Strengthen surveillance systems on AMR and antimicrobial consumption in animal medicine.
    • Action n° 11: Reinforce and co-ordinate research efforts.
    • Action n° 12: Survey and comparative effectiveness research.

    Several Member States have been pro-active in carrying out actions related to those considered at EU level. These actions at national level and the experience gained from it should be the basis of the practical development and implementation of this Action Plan.

activities/6
date
2012-12-10T00:00:00
body
EP
type
Indicative plenary sitting date, 1st reading/single reading
activities/1/docs/0/url
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
activities/1/docs/0/url
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
activities/1/docs/0/url
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
activities/4
body
EP
date
2012-09-11T00:00:00
type
Deadline Amendments
activities/3/committees/1/date
2012-03-23T00:00:00
activities/3/committees/1/rapporteur
  • group: ECR name: ROSBACH Anna
activities/4
date
2012-11-06T00:00:00
body
EP
type
Vote scheduled in committee, 1st reading/single reading
committees/1/date
2012-03-23T00:00:00
committees/1/rapporteur
  • group: ECR name: ROSBACH Anna
activities/1/docs/0/url
http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi!celexplus!prod!DocNumber&lg=EN&type_doc=COMfinal&an_doc=2011&nu_doc=748
activities
  • body: EP date: 2011-11-15T00:00:00 type: Date
  • date: 2011-11-15T00:00:00 docs: celexid: CELEX:52011DC0748:EN type: Non-legislative basic document published title: COM(2011)0748 body: EC type: Non-legislative basic document commission: DG: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers Commissioner: DALLI John
  • body: EP date: 2012-03-08T00:00:00 type: EP officialisation
  • date: 2012-03-15T00:00:00 body: EP type: Committee referral announced in Parliament, 1st reading/single reading committees: body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin body: EP shadows: group: EPP name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin responsible: True committee_full: Environment, Public Health and Food Safety committee: ENVI body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
committees
  • body: EP responsible: False committee: AGRI date: 2012-02-29T00:00:00 committee_full: Agriculture and Rural Development rapporteur: group: Verts/ALE name: HÄUSLING Martin
  • body: EP shadows: group: EPP name: MAZEJ KUKOVIČ Zofija group: S&D name: KADENBACH Karin responsible: True committee_full: Environment, Public Health and Food Safety committee: ENVI
  • body: EP responsible: False committee_full: Industry, Research and Energy committee: ITRE
links
other
  • body: EC dg: url: http://ec.europa.eu/dgs/health_consumer/index_en.htm title: Health and Consumers commissioner: DALLI John
procedure
dossier_of_the_committee
ENVI/7/08364
reference
2012/2041(INI)
title
Microbial challenge - rising threats from antimicrobial resistance
legal_basis
Rules of Procedure of the European Parliament EP 048
stage_reached
Awaiting Parliament 1st reading / single reading / budget 1st stage
subtype
Initiative
type
INI - Own-initiative procedure
subject