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FDA removes suicide risk warnings from weight-loss drugs due to insufficient evidence.
The U.S. Food and Drug Administration has asked manufacturers of popular weight-loss medications to remove suicide risk warnings from their labels, citing insufficient evidence to support the link.
The move follows a review of clinical trial data and safety reports, though the agency emphasized that patient safety remains a priority.
The decision may affect drugs like semaglutide and tirzepatide, widely used for weight management.
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La FDA elimina las advertencias de riesgo de suicidio de los medicamentos para bajar de peso debido a evidencia insuficiente.