The marketing authorization holder informed its supplied customers by letter dated April 28, 2014, that due to the implementing decision C (2013)9846 in the context of the European risk assessment procedure according to Article 31 of Directive…

The marketing authorization holder informed its supplied customers by letter dated April 28, 2014, that due to the implementing decision C(2013)9846 in the context of the European risk assessment procedure according to Article 31 Directive…

Questions and answers about the stolen vials of Herceptin and other affected products

The distribution company informed its supplied customers on April 18, 2014 and asked for a stock check of the affected batches.

The parallel distributor has informed its supplied customers in a letter dated 18.04.2014 that Herceptin in Italian presentation has been adulterated and introduced into the legal distribution chain. Therefore, a recall of the above mentioned Italian…

Update from the European Medicines Agency on stolen vials of Herceptin and other affected products

The distribution company informed its supplied customers on17.04.2014 and asked for a stock check of the affected batch.

The parallel distributor informed its supplied customers on 04/17/2014 and asked for a stock check of the affected batches.

The parallel distributor informed its supplied customers in a letter dated April 17, 2014, that Alimta in Italian presentation is being recalled as a precautionary measure, as it cannot be ensured that the regular distribution chain has been adhered…

The European Medicines Agency received information that vials of Herceptin, a drug used to treat cancer, were adulterated and introduced into the legal distribution chain.