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Shutterstock Recently, the European Medicines Agency (EMA)s drug safety committee, PRAC, evaluated and analysed the potential risk of side effects in individuals who have used the GLP-1 class of drugs

In January 2024, the US Food and Drug Administration (FDA) said in a statement that it was evaluating the need for regulatory action on GLP-1 RAs, following reports of suicidal ideation linked to the drugs in the United States

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