देश: संयुक्त राज्य
भाषा: अंग्रेज़ी
स्रोत: NLM (National Library of Medicine)
PALONOSETRON HYDROCHLORIDE (UNII: 23310D4I19) (PALONOSETRON - UNII:5D06587D6R)
Teva Parenteral Medicines, Inc.
PALONOSETRON HYDROCHLORIDE
PALONOSETRON 0.25 mg in 5 mL
INTRAVENOUS
PRESCRIPTION DRUG
Palonosetron hydrochloride injection is indicated in adults for prevention of: - acute and delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC). - acute nausea and vomiting associated with initial and repeat courses highly emetogenic cancer chemotherapy (HEC). - postoperative nausea and vomiting (PONV) for up to 24 hours following surgery. Efficacy beyond 24 hours has not been demonstrated. As with other antiemetics, routine prophylaxis is not recommended in patients in whom there is little expectation that nausea and/or vomiting will occur postoperatively. In patients where nausea and vomiting must be avoided during the postoperative period, palonosetron hydrochloride injection is recommended even where the incidence of postoperative nausea and/or vomiting is low. Palonosetron hydrochloride injection is indicated in pediatric patients 1 month to less than 17 years of age for prevention of: - acute nausea and vomiting associated with initial
NDC 0703-4094-01, Palonosetron Hydrochloride Injection 0.25 mg/5 mL (free base) single-dose vial individually packaged in a carton. Storage
Abbreviated New Drug Application
PALONOSETRON HYDROCHLORIDE- PALONOSETRON HYDROCHLORIDE INJECTION, SOLUTION TEVA PARENTERAL MEDICINES, INC. ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE PALONOSETRON HYDROCHLORIDE INJECTION SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR PALONOSETRON HYDROCHLORIDE INJECTION. PALONOSETRON HYDROCHLORIDE INJECTION, FOR INTRAVENOUS USE INITIAL U.S. APPROVAL: 2003 INDICATIONS AND USAGE Palonosetron is a serotonin-3 (5-HT ) receptor antagonist indicated in: Adults for prevention of: acute and delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC). (1) acute nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC). (1) postoperative nausea and vomiting (PONV) for up to 24 hours following surgery. Efficacy beyond 24 hours has not been demonstrated (1) Pediatric patients aged 1 month to less than 17 years for prevention of: acute nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including highly emetogenic cancer chemotherapy (HEC). (1) DOSAGE AND ADMINISTRATION Chemotherapy-Induced Nausea and Vomiting (2.1) Age Dose* Infusion Time Adults 0.25 MG as a single dose Infuse over 30 SECONDS beginning approximately 30 minutes before the start of chemotherapy Pediatrics (1 month to less than 17 years) 20 MICROGRAMS PER KILOGRAM (maximum 1.5 mg) as a single dose Infuse over 15 MINUTES beginning approximately 30 minutes before the start of chemotherapy *Note different dosing units in pediatrics Postoperative Nausea and Vomiting (2.1) The recommended adult dosage is 0.075 mg as a single intravenous dose administered over 10 seconds immediately before the induction of anesthesia. DOSAGE FORMS AND STRENGTHS Inje ction: 0.25 mg/5 mL (free base) in a single-dose vial (3) CONTRAINDICATIONS Hypersensitivity to palonosetron or any of its components (4) WAR पूरा दस्तावेज़ पढ़ें