Prescribing information for Actilyse
IMPORTANT: Please be advised, that the Summary of Product Characteristics (SmPCs) for Actilyse® provided here is the English Master version as approved by the German Health Authority (BfArM), acting as reference member state for the EU countries under mutual recognition. In other EU countries with national registrations or in other regions the wording and language of the Actilyse® prescribing information may differ. Always refer to the current prescribing information as approved in your country.
