The Pharmacovigilance Programme of India (“PvPI”) is the primary, drug safety monitoring programme in India which collects, ...

Adverse drug reactions (ADRs) remain a common clinical problem since they can mimic many diseases and cause significant morbidity and mortality. Judicious prescribing is important to minimize ...

When reporting serious adverse reactions from studies, the following information should be included ... Concomitant health products (exclude treatment of action): other health products that were used ...

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In addition, when manufacturers are made aware of adverse reactions to a drug or vaccine, they must report to Health Canada: serious adverse reactions in Canada unexpected serious adverse reactions in ...

Researchers associated with The Ohio State University found that number of severe adverse events linked to generic drugs made ...

A new study reveals that generic drugs made in India are linked to a significantly higher number of severe adverse events, ...

Ensuring 100% Implementation of Companys strategies Pharmacovigilance (Adverse Event Reporting) To collect adverse drugs reaction (ADR) incidences including lack of efficacy related to medicinal ...

Adverse drug reactions from NSAIDs should be considered and treated in children and adolescents, especially those with complex needs. This article is part of the Coroners’ Concerns to Prevent Harms ...