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WebMEDWATCH (additional info) In addition to the FDA and the manufacturer reporting problems about the medication, the consumer(patient) may also report problems with … Web10 aug. 2024 · Post marketing surveillance (PMS) of medications is the process by which marketed medicines are monitored for adverse drug reactions (ADRs) post clinical trials. 1 Since most drugs may not reach the market without passing phase III clinical trials, 2 PMS studies are considered to be phase IV studies. 3 The safety and efficacy evaluations of … isis flores
MedWatch Coursework: How It Fits Within the FDA Mission
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