Afamelanotide SCENESSE implant label
Administration reported for this specific study or labeled indication.
Context: Adults with erythropoietic protoporphyria and a history of phototoxic reactions
Approved product label: Amount: 16 mg; Route: Subcutaneous implant; Frequency: Every two months; Species: Human; Population: Adults with erythropoietic protoporphyria and a history of phototoxic reactions
Limitations: The pharmaceutical implant increases pain-free light exposure under its labeled indication.
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