Human medicines European public assessment report (EPAR): Tacforius, tacrolimus, Date of authorisation: 08/12/2017, Revision: 10, Status: Authorised

Human medicines European public assessment report (EPAR): Tacforius, tacrolimus, Date of authorisation: 08/12/2017, Revision: 10, Status: Authorised

Pharmacovigilance Risk Assessment Committee (PRAC): 10 - 13 March 2025, European Medicines Agency, Amsterdam, the Netherlands, from 10 March 2025 to 13 March 2025

Pharmacovigilance Risk Assessment Committee (PRAC): 10 - 13 March 2025, European Medicines Agency, Amsterdam, the Netherlands, from 10 March 2025 to 13 March 2025

Human medicines European public assessment report (EPAR): Ongentys, opicapone, Date of authorisation: 24/06/2016, Revision: 10, Status: Authorised

Human medicines European public assessment report (EPAR): Ongentys, opicapone, Date of authorisation: 24/06/2016, Revision: 10, Status: Authorised

Human medicines European public assessment report (EPAR): Evenity, romosozumab, Date of authorisation: 09/12/2019, Revision: 8, Status: Authorised

Human medicines European public assessment report (EPAR): Evenity, romosozumab, Date of authorisation: 09/12/2019, Revision: 8, Status: Authorised

Human medicines European public assessment report (EPAR): Vectibix, panitumumab, Date of authorisation: 03/12/2007, Revision: 35, Status: Authorised

Human medicines European public assessment report (EPAR): Vectibix, panitumumab, Date of authorisation: 03/12/2007, Revision: 35, Status: Authorised

Human medicines European public assessment report (EPAR): Daurismo, glasdegib, Date of authorisation: 26/06/2020, Revision: 6, Status: Authorised

Human medicines European public assessment report (EPAR): Daurismo, glasdegib, Date of authorisation: 26/06/2020, Revision: 6, Status: Authorised

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