
handle: 20.500.12008/41256
La Agencia Española de Medicamentos y Productos Sanitarios (AEMPS) ha publicado una notificación de seguridad el 17 de abril del corriente año, donde se comunica la presencia de reacciones adversas con escopolamina por error de administración en lugar de butilescopolamina. Se han recibido 5 notificaciones donde los pacientes afectados requirieron asistencia médica y los errores detectados indicaron que la confusión pudo presentar en la prescripción, dispensación y administración del medicamento.
FARMACOVIGILANCIA, ESCOPOLAMINA, BROMURO DE BUTILESCOPOLAMONIO
FARMACOVIGILANCIA, ESCOPOLAMINA, BROMURO DE BUTILESCOPOLAMONIO
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