MvPI releases draft IVD-MD adverse event reporting form, invites stakeholders' comments till March 5: Our Bureau, New Delhi Thursday, February 20, 2025, 08:00 Hrs [IST] The Materi ...

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

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

Generic drugs manufactured in India are linked to significantly ... in the United States. These adverse event reports are available in the FDA Adverse Event Reporting System (FAERS).

The drugs had the same active ingredients, the same dosage form and ... in India were linked to adverse event reports compared to their U.S.-made counterparts. The reports of adverse events are ...

A study reveals safety differences in generic drugs based on where they're made, urging stronger regulatory oversight.

Generic drugs manufactured in India are ... associated with adverse event reports for generic drugs made in India versus the matched drugs made in the United States. These adverse event reports are ...