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National Adverse Drug Reaction Directory

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National Adverse Drug Reaction Directory

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Author : United States. Food and Drug Administration
language : en
Publisher:
Release Date : 1970

National Adverse Drug Reaction Directory written by United States. Food and Drug Administration and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1970 with Drugs categories.

National Adverse Drug Reaction Directory

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Author : United States. Food and Drug Administration
language : en
Publisher:
Release Date : 1970

Listing of coding symbols accepted as controlled vocabulary applicable to reports of adverse reactions associated with drugs. Purpose of such vocabulary is to aid storage and retrieval by computer of such adverse reactions. Arrangement: categories and subcategories, coding symbols, and index of adverse reaction terms.

National Adverse Drug Reaction Directory

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Author : United States. Food and Drug Administration
language : en
Publisher:
Release Date : 1970

Adverse Drug Event Reporting

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Author : Board on Health Sciences Policy
language : en
Publisher: National Academies Press
Release Date : 2007-04-12

Adverse Drug Event Reporting written by Board on Health Sciences Policy and has been published by National Academies Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2007-04-12 with Medical categories.

Recent concerns about the unexpected adverse effects of marketed drugs, such as COX-2 (cyclooxygenase-2) inhibitors or specific statins, raise concerns not only about reporting these events during premarket studies, but also about the responsibility for ongoing surveillance of drugs once they are on the market. Sometimes serious adverse drug reactions are fully appreciated only after a drug has been on the market for years. Therefore, when a drug is approved and released to the market, large numbers of patients will be exposed before all the potential adverse effects have been identified and thoroughly studied. Currently, there is no clearly defined process for addressing safety questions about drugs after premarketing research has occurred. In November 2005, the Institute of Medicine's Forum on Drug Discovery, Development, and Translation convened a workshop to explore issues associated with the reporting of ADEs. The workshop addressed the following questions: How can ADEs be effectively identified, particularly when the adverse effects are rare? How can the direct, causal effects of drugs be distinguished from simple associations? How can health-care professionals and their patients' aid in the identification of drug-related adverse events? How can knowledge of ADEs be more effectively used in clinical practice? Adverse Drug Event Reporting reviews current sources of information on adverse drug events, including the FDA's MedWatch program and the AERS, institutional review boards, and the CMS. This report considers the ways that consumers and advocacy groups can be involved in reporting adverse events, and discusses drug interactions, problems with current databases for capturing and evaluating interactions, and difficulties in communicating information about adverse drug interactions. This report also describes new requirements for information contained on drug labels and how labels can be used to communicate information about risks and drug interactions to consumers and practitioners.

Adverse Effects Of Vaccines

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Author : Institute of Medicine
language : en
Publisher: National Academies Press
Release Date : 2012-04-26

Adverse Effects Of Vaccines written by Institute of Medicine and has been published by National Academies Press this book supported file pdf, txt, epub, kindle and other format this book has been release on 2012-04-26 with Medical categories.

In 1900, for every 1,000 babies born in the United States, 100 would die before their first birthday, often due to infectious diseases. Today, vaccines exist for many viral and bacterial diseases. The National Childhood Vaccine Injury Act, passed in 1986, was intended to bolster vaccine research and development through the federal coordination of vaccine initiatives and to provide relief to vaccine manufacturers facing financial burdens. The legislation also intended to address concerns about the safety of vaccines by instituting a compensation program, setting up a passive surveillance system for vaccine adverse events, and by providing information to consumers. A key component of the legislation required the U.S. Department of Health and Human Services to collaborate with the Institute of Medicine to assess concerns about the safety of vaccines and potential adverse events, especially in children. Adverse Effects of Vaccines reviews the epidemiological, clinical, and biological evidence regarding adverse health events associated with specific vaccines covered by the National Vaccine Injury Compensation Program (VICP), including the varicella zoster vaccine, influenza vaccines, the hepatitis B vaccine, and the human papillomavirus vaccine, among others. For each possible adverse event, the report reviews peer-reviewed primary studies, summarizes their findings, and evaluates the epidemiological, clinical, and biological evidence. It finds that while no vaccine is 100 percent safe, very few adverse events are shown to be caused by vaccines. In addition, the evidence shows that vaccines do not cause several conditions. For example, the MMR vaccine is not associated with autism or childhood diabetes. Also, the DTaP vaccine is not associated with diabetes and the influenza vaccine given as a shot does not exacerbate asthma. Adverse Effects of Vaccines will be of special interest to the National Vaccine Program Office, the VICP, the Centers for Disease Control and Prevention, vaccine safety researchers and manufacturers, parents, caregivers, and health professionals in the private and public sectors.

Guidelines For The Programmatic Management Of Drug Resistant Tuberculosis

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Author : World Health Organization
language : en
Publisher:
Release Date : 2015-04-20

Guidelines For The Programmatic Management Of Drug Resistant Tuberculosis written by World Health Organization and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2015-04-20 with Medical categories.

This 2011 update of Guidelines for the programmatic management of drug-resistant tuberculosis is intended as a tool for use by public health professionals working in response to the Sixty-second World Health Assembly's resolution on prevention and control of multidrug-resistant tuberculosis and extensively drug-resistant tuberculosis. Resolution WHA62.15, adopted in 2009, calls on Member States to develop a comprehensive framework for the management and care of patients with drug-resistant TB. The recommendations contained in these guidelines address the most topical questions concerning the programmatic management of drug-resistant TB: case-finding, multidrug resistance, treatment regimens, monitoring the response to treatment, and selecting models of care. The guidelines primarily target staff and medical practitioners working in TB treatment and control, and partners and organizations providing technical and financial support for care of drug-resistant TB in settings where resources are limited.

The Detection Of New Adverse Drug Reactions

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Author : M. D. B. Stephens
language : en
Publisher: Springer
Release Date : 1985-06-18

The Detection Of New Adverse Drug Reactions written by M. D. B. Stephens and has been published by Springer this book supported file pdf, txt, epub, kindle and other format this book has been release on 1985-06-18 with Medical categories.

Advances In Patient Safety

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Author : Kerm Henriksen
language : en
Publisher:
Release Date : 2005

Advances In Patient Safety written by Kerm Henriksen and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2005 with Medical categories.

v. 1. Research findings -- v. 2. Concepts and methodology -- v. 3. Implementation issues -- v. 4. Programs, tools and products.

National Library Of Medicine Current Catalog

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Author : National Library of Medicine (U.S.)
language : en
Publisher:
Release Date : 1971

National Library Of Medicine Current Catalog written by National Library of Medicine (U.S.) and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 1971 with Medicine categories.

First multi-year cumulation covers six years: 1965-70.

The Importance Of Pharmacovigilance

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Author : World Health Organization
language : en
Publisher:
Release Date : 2002-01-01

The Importance Of Pharmacovigilance written by World Health Organization and has been published by this book supported file pdf, txt, epub, kindle and other format this book has been release on 2002-01-01 with Drug monitoring categories.

The purpose of this document is to present the case for the importance of pharmacovigilance, to record its growth and potential as a significant discipline within medical science, and to describe its impact on patient welfare and public health.

National Adverse Drug Reaction Directory

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