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Retricted access

Research article

First published 2006-2

Analysis of Severe Adverse Events Related to the Use of Mifepristone as an Abortifacient

Margaret M Gary, Donna J Harrison

Annals of Pharmacotherapy

Retricted access

Research article

First published 2004-11

FDA Adverse Event Reports on Use of Sibutramine: An Exploratory Analysis

Marcus M Stavchansky, James P Wilson

Journal of Pharmacy Technology

Open access

Research article

First published 2021

Mifepristone Adverse Events Identified by Planned Parenthood in 2009 and 2010 Compared to Those in the FDA Adverse Event Reporting System and Those Obtained Through the Freedom of Information Act

Christina A. Cirucci, Kathi A. Aultman, Donna J. Harrison

Health Services Research and Managerial Epidemiology

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Research article

First published 2008-11

Intracranial Hemorrhage and Liver-Associated Deaths Associated with Tipranavir/Ritonavir: Review of Cases from the FDA's Adverse Event Reporting System

Kirk M. Chan-Tack, Kimberly A. Struble, Debra B. Birnkrant

AIDS Patient Care and STDs

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Case report

First published 2018-12

Hemorrhagic Infarction of Cerebellum and Brainstem Due to Cervical Epidural Steroid Injection – Case Report and Review of the Literature

Connie Bao, Shiping Bao

Academic Forensic Pathology

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Research article

First published 2017-7

Dipeptidyl Peptidase-4 Inhibitor–Associated Risk of Bleeding: An Evaluation of Reported Adverse Events

Md Motiur Rahman, Michael J. Scalese, Richard A. Hansen

Annals of Pharmacotherapy

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Research article

First published 2006-03

Postmarketing Surveillance of Suicidal Adverse Events with Pediatric Use of Antidepressants

Andrew D. Mosholder, Carol A. Pamer

Journal of Child and Adolescent Psychopharmacology

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Research article

First published 2026

Adverse Drug Event Profile of Radiocontrast Iodine in Elderly: A Retrospective Focused Pharmacovigilance-Based Disproportionality Analysis Study

Kannan Sridharan, Gowri Sivaramakrishnan

Hospital Pharmacy

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Other

First published 1999-10

Electronic Reporting of Adverse Event Data to the Food and Drug Administration: The Experiences of Glaxo Wellcome and Zeneca as Participants in the Adverse Event Reporting System Pilot Project

Mark Blake, Vlasta Pinkston

Therapeutic Innovation & Regulatory Science

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Research article

First published 1999-05

Unusual Distributions of Body Fat in AIDS Patients: A Review of Adverse Events Reported to the Food and Drug Administration

Marianne Mann, Toni Piazza-Hepp, Elizabeth Koller [...]

AIDS Patient Care and STDs

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