A Statewide Program to Stimulate Reporting of Adverse Drug Reactions-Reference-Cited by-同舟云学术

A Statewide Program to Stimulate Reporting of Adverse Drug Reactions

Published:1989-08 Issue:4 Volume:2 Page:239-244
ISSN:0897-1900
Container-title:Journal of Pharmacy Practice
language:en
Short-container-title:Journal of Pharmacy Practice

Author:

Fincham Jack¹

Affiliation:

1. Department of Health Care Administration, School of Pharmacy, University of Mississippi, 217-B Faser Hall, University, MS 38677

Abstract

The purpose of a 26-month Food and Drug Administration sponsored study conducted in Mississippi was to determine how the reporting of adverse drug reactions (ADRs) might be stimulated. The program included both institutional and community based health care facilities located in urban as well as rural settings. Methods used in the study increased the monthly average of reported ADRs from 3.94 to 16.5. Pharmacists have the expertise and responsibility to assume a more active role in the reporting of ADRs.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

Link

http://journals.sagepub.com/doi/pdf/10.1177/089719008900200407

Reference10 articles.

1. PILOT PROJECTS TO STIMULATE ADVERSE DRUG REACTION REPORTING

2. Drug Evaluation After Marketing

3. Discovery of Adverse Drug Reactions

4. National Adverse Drug Reaction Surveillance: 1985

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