- TRADE NAME: Lutathera
- INDICATIONS: Treatment of somatostatin receptor-positive gastroenteropancreatic neuroendocrine tumors (with octreotide)
- CLASS: Radiopharmaceutical, Somatostatin analog
- HALF-LIFE: 7 days
- FDA APPROVAL DATE: 01/26/2018
- CLINICALLY IMPORTANT, POTENTIALLY HAZARDOUS INTERACTIONS WITH:
None known - PREGNANCY: Can cause fetal harm
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Page last updated 07/31/2023