FOSAPREPITANT DIMEGLUMINE (fosaprepitant) by Teva is accordingly, its antiemetic effects are attributable to aprepitant. First approved in 2019.
Drug data last refreshed 10m ago · AI intelligence enriched 4d ago
Fosaprepitant dimeglumine is an intravenous NK1 receptor antagonist prodrug that converts to aprepitant in vivo. It prevents chemotherapy-induced nausea and vomiting (CINV) by crossing the blood-brain barrier and blocking substance P signaling in the central nervous system. It is used as an adjunct to 5-HT3 antagonists and corticosteroids to manage both acute and delayed emesis in cancer patients receiving highly emetogenic chemotherapy.
Product is at peak commercial stage under Teva ownership with moderate competitive pressure (30/100), supporting established brand and medical teams.
accordingly, its antiemetic effects are attributable to aprepitant. Aprepitant is a selective high-affinity antagonist of human substance P/neurokinin 1 (NK 1 ) receptors. Aprepitant has little or no affinity for serotonin (5-HT 3 ), dopamine, and corticosteroid receptors, the targets of existing…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Safety of a Three-Day Fosaprepitant Regimen for the Prevention of Chemotherapy-Induced Nausea and Vomiting in Pediatric Participants (MK-0517-045)
Olanzapine With or Without Fosaprepitant Dimeglumine in Preventing Chemotherapy Induced Nausea and Vomiting in Cancer Patients Receiving Highly Emetogenic Chemotherapy
Efficacy and Safety Study of Fosaprepitant (MK-0517) Plus Ondansetron Versus Ondansetron Alone for the Prevention of Chemotherapy-Induced Nausea and Vomiting in Pediatric Participants (MK-0517-044)
Study Assessing Fosaprepitant in Advanced NSCLC Patients Treated With Carboplatin Based Chemotherapy
Fosaprepitant for N/V With High-dose Interleukin-2 for Metastatic Melanoma and Renal Cell Carcinoma
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