How credible are the adverse drug events manufacturers receive?

Collecting adverse drug events from healthcare professionals and the public is mandatory for manufacturers. Minimum criteria apply to make such a case report valid. A valid case report must involve a suspect drug and a suspected adverse drug event, an identifiable patient, and an identifiable reporter. The ability to identify a reporter is essential to enable follow-up and avoid duplication of reports and fraud. The verification of the existence of the patient and a reporter is tricky for a variety

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