Tecentriq
The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.
| Name | Tecentriq |
|---|---|
| Active Substance | atezolizumab |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | ograničeni recept |
| Distribution | Supply through pharmacies (community) |
| ATC Code | L01FF05 |
| Marketing status | stavljeno u promet |
| Shortage status | nema nestašice |
| Summary of product characteristics (SmPC), labelling and package leaflet (PL) | download |
| Link to the European Medicines Agency's (EMA) product information | download |
| Link to the European Commission's (EC) decisions | download |
| Educational materials for patients / caregivers |
Kartica za bolesnika, verzija 7 |
Packaging
Direct Healthcare Professional Communication
| Name | Date | Download |
|---|---|---|
| Pismo zdravstvenim radnicima o riziku od teških kožnih reakcija uz primjenu lijeka Tecentriq (atezolizumab) | 25.03.2021 | Roche Registration GmbH |
| Pismo zdravstvenim radnicima o ograničenju indikacije lijeka Tecentriq (atezolizumab) | 10.07.2018 | Roche Registration GmbH |
