EMA Agrees to Recall of Vimpat Syrup
The EMA has agreed to a recall of Vimpat 15 mg/ml syrup because of a quality defect in some batches.
The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has agreed to a recall of Vimpat 15 mg/ml syrup because of a quality defect in some batches leading to uneven distribution of the active substance lacosamide in the syrup.
Vimpat is used to treat partial-onset seizures (epileptic fits starting from one specific part of the brain) as an add-on to other antiepileptic medicines in patients with epilepsy aged 16 years and older.
Doctors are advised to contact their patients to switch them to Vimpat film coated tablets whenever possible. Patients are advised not to stop their medication or change the dose without speaking to their doctor.
The marketing authorisation holder for V
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