EMA Recommends Discontinuation of Vimpat Syrup
The recommendation follows the voluntary recall of Vimpat 15mg/ml syrup on 15 September 2011. The recall was initiated because of a quality defect in some batches leading to uneven distribution of the active substance lacosamide in the syrup.
The European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) has recommended that Vimpat 15mg/ml syrup should no longer be marketed.
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.
The CHMP’s recommendation follows the voluntary recall of Vimpat 15mg/ml syrup on 15 September 2011. The recall was initiated because of a quality defect in some batches leading to uneven distribution of the active substance lacosamide in the syrup.
As this defect could not be remediated, e.g. by changing storage cond
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