The Pharmacovigilance Programme of India (“PvPI”) is the primary, drug safety monitoring programme in India which collects, collates and analyses drug-related adverse events received through various ...

Generic drugs manufactured in India are linked to significantly more "severe adverse events" for patients who use them than equivalent drugs produced in the United States, a new study finds. These ...

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 ...

A new study reveals that generic drugs made in India are associated with 54 percent more severe adverse events, including hospitalisation and death, compared to those made in the US. The findings ...

A new study reveals that generic drugs manufactured in India have a higher association with severe adverse events such as hospitalization, disability, and death compared to those made in the U.S ...

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Concomitant health products (exclude treatment of action): other health products that were used at the same time as the adverse reaction describe if any drugs or health products are also suspected in ...

Generic drugs manufactured in India are linked to significantly more “severe adverse events” for patients who use them than equivalent drugs produced in the United States, a new study finds. These ...

A new study has found that generic drugs manufactured in India are linked to significantly more severe adverse events — including hospitalization, disability and in some cases death — compared ...

A groundbreaking study has revealed that generic drugs manufactured in India are associated with a 54% increase in severe adverse events, including hospitalization, disability, and death, compared to ...

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