Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01XH03

Farydak(panobinostat lactate anhydrous)

Multiple Myeloma

Marketing Authorisation Holder: pharmaand GmbH

EMA Authorisation: 28/08/2015

INN: panobinostat

Indication

Farydak, in combination with bortezomib and dexamethasone, is indicated for the treatment of adult patients with relapsed and/or refractory multiple myeloma who have received at least two prior regimens including bortezomib and an immunomodulatory agent. Farydak, in combination with bortezomib and dexamethasone, is indicated for the treatment of adult patients with relapsed and/or refractory multiple myeloma who have received at least two prior regimens including bortezomib and an immunomodulatory agent.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.