Beyond The REMS: Clozapine Adcomm Shows Why In-Program Assessments Are Not Always Enough

The FDA and sponsors should have surveyed providers and patients who do not prescribe or use the antipsychotic clozapine to find whether the REMS restrictions were hindering access and causing harm, advisory committee members and patient advocates said.

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Schizophrenics are suffering because of the FDA's "myopic" focus on absolute neutrophil counts with clozapine, patient advocates said. (Shutterstock)
Key Takeaways
  • The FDA and clozapine manufacturers presented data on the experience and knowledge of providers who prescribe the antipsychotic under the REMS.

Sometimes you have to look outside a drug’s Risk Evaluation and Mitigation Strategy to evaluate the program, advisory committee members...

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