EMA Medicine safety communications
Gavreto: adverse event;post-authorisation measure
Published by European Medicines Agency: · Ref. EMEA/H/C/005413
Summary
Adverse event;Post-authorisation measure
Medicine
Gavreto
- Category
- Medicine safety communications
- Product type
- Human medicine
- Active substance(s): pralsetinib
- Therapeutic area: Carcinoma, Non-Small-Cell Lung
- ATC code: L01XE
Measures and alternatives
- Regulatory outcome: Variation
Source: EMA — medicine safety communications — European Medicines Agency
Source: European Medicines Agency (EMA). Reproduced with acknowledgement of the source, in line with the EMA legal notice. EU Safety Radar is an independent information service; the text above presents the official data in the original language — the notice published by the authority is authoritative.
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