DHPC – Zemplar (paricalcitolum)

Translation error in the French text of the package leaflet

26.08.2024
Preparation Zemplar, solution for injection
Marketing authorisation number 56312
Active substance

paricalcitolum

Authorization holder AbbVie AG

The package leaflets enclosed with all batches of Zemplar 5 µg/ml, solution for injection currently on the Swiss market contain a translation error in the French text under ‘Dosage/Administration’.

AbbVie is working on correcting the package leaflet. Until the corrected version is available, the letter will be included with all shipments of Zemplar 5 µg/ml, solution for injection.

For further information, please refer to the company's information letter.