Postmarketing Surveillance: Viewpoint from a Regulatory Authority-Reference-Cited by-同舟云学术

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Postmarketing Surveillance: Viewpoint from a Regulatory Authority

Published:1991-04 Issue:2 Volume:25 Page:191-195
ISSN:0092-8615
Container-title:Drug Information Journal
language:en
Short-container-title:Drug Information Journal

Author:

Wood Susan M.¹

Affiliation:

1. Adverse Drug Reactions Unit, Medicines Control Agency, Department of Health, London, United Kingdom

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Drug Guides,Pharmacology (nursing)

Link

http://journals.sagepub.com/doi/pdf/10.1177/009286159102500207

Reference10 articles.

1. Spontaneous reporting of adverse drug reactions. I: the data.

2. Spontaneous reporting of adverse drug reactions. II: Uses.

3. NATIONAL ADVERSE DRUG REACTION REPORTING???A SILVER JUBILEE

4. Adenocarcinoma of the Vagina

5. Cutaneous and Ocular Reactions to Practolol

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Strategy support for the Post‐Market Monitoring (PMM) of GM plants: Review of existing PMM strategies developed for the safety assessment of human and animal health;EFSA Supporting Publications;2015-01

2. Post-market surveillance model for potential human health effects of novel foods;Food Policy;2004-12

3. Pharmacovigilance: a science or fielding emergencies?;Statistics in Medicine;2000

4. EPOS: Increasing our understanding of the treatment of schizophrenia; Start of a prospective referenced cohort study of sertindole in clinical practice;International Journal of Psychiatry in Clinical Practice;1997-01

5. Worldwide Regulations for Manufacturers on Clinical Safety Surveillance of Drugs;Drug Information Journal;1992-01

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