Advocates urge FDA to end REMS requirements for clozapine

The Treatment Advocacy Center (TAC) and other advocates are trying to convince the Food and Drug Administration (FDA) to end the Risk Evaluation and Mitigation Strategy (REMS) requirements for clozapine. The requirements, they said, reduce the number of providers who will prescribe this “gold standard medication” that works for many people with serious mental illness.

Authors

Publication Details

Journal
Mental Health Weekly
Published
2024-10-18
DOI
https://doi.org/10.1002/mhw.34216
Citations
1
Primary Topic
Science, Research, and Medicine
Type
article
Field-Weighted Citation Impact
0.54
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article

Advocates urge FDA to end REMS requirements for clozapine

Valerie A. Canady
1 citations
Mental Health Weekly
Science, Research, and Medicine
0.54
article

Advocates urge FDA to end REMS requirements for clozapine

Valerie A. Canady
article en
1 citations

Abstract

The Treatment Advocacy Center (TAC) and other advocates are trying to convince the Food and Drug Administration (FDA) to end the Risk Evaluation and Mitigation Strategy (REMS) requirements for clozapine. The requirements, they said, reduce the number of providers who will prescribe this “gold standard medication” that works for many people with serious mental illness.

Mental Health WeeklyVol. 34(40)
Openalex Percentile: Top 26%
Science, Research, and Medicine
0.54
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Advocates urge FDA to end REMS requirements for clozapine — Valerie A. Canady · Mental Health Weekly (2024) | TGRS Research Map | TGRS