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, ...

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 the same route of administration ... with adverse event reports for generic drugs made in India versus the matched drugs made in the ...

The drugs had the same active ingredients, the same dosage form and the same route of administration ... They analyzed how often generic drugs manufactured in India were linked to adverse event ...