Aliqopa Bayer AG · Application withdrawn
Therapeutic indication (EMA)
Treatment of adult patients with relapsed marginal zone lymphoma
Active substance
Copanlisib
- US FDA 1
- EMA 1
- Safety 1
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| ALIQOPA | 60MG/VIAL | powder · intravenous | BAYER HEALTHCARE | Discontinued | 14 Sep 2017 |
EMA European Union — centrally authorised medicines
Safety signals and safety-related labeling changes
- US FDA 7 Sep 2023 ALIQOPA — safety-related labeling change
Labeling sections changed: Warnings and Precautions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.