EMA Medicine safety communications
Desogestrel / etonogestrel: adverse event;post-authorisation measure
Published by European Medicines Agency:
Summary
Adverse event;Post-authorisation measure
Medicine
Desogestrel / etonogestrel
- Category
- Medicine safety communications
- Product type
- Human medicine
- Active substance(s): desogestrel;etonogestrel
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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