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Adverse Drug Reaction Reporting Systems
Drug safety assessment in clinical trials: methodological challenges and opportunities.
Systematic review evaluating cardiovascular events of the 5-alpha reductase inhibitor - Dutasteride.
Secondary hypertension due to drugs and toxins--a challenge for research on harm.
Spontaneous reports as evidence of adverse drug reactions.
An Algorithm to Identify Generic Drugs in the FDA Adverse Event Reporting System.
Patient-relevant outcomes associated with generic tamsulosin, levothyroxine and amphetamine in the FDA Adverse Event Reporting System: a pilot study.
Comparison of Data on Serious Adverse Events and Mortality in ClinicalTrials.gov, Corresponding Journal Articles, and FDA Medical Reviews: Cross-Sectional Analysis.
Drug-Related Side Effects and Adverse Reactions
Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies.
Drug Related Side Effects and Adverse Reactions