Investigators are required to report to the HSRO any of the following circumstances promptly and within ... places subjects at an increased risk of harm (i.e., a serious adverse event); and Whether ...

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The COVID-19 vaccine has prompted more than 10 times as many reports of adverse symptoms than the measles vaccine.

Note: Investigators serving as sponsors of FDA-regulated research have additional reporting responsibilities (see FDA-Regulated Research). This section defines these terms in relation to UAB IRB ...

The Iowa Senate bill alters a proposal that would have penalized administering gene-based vaccines including the COVID-19 ...

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 ...

Are Your Patients Microdosing? People you wouldn’t normally associate with drug use are self-treating by microdosing with psychedelics. Doctors need to be kept in the loop. Medscape Medical News ...

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

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