Krajina: Spojené štáty
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
IRINOTECAN HYDROCHLORIDE (UNII: 042LAQ1IIS) (IRINOTECAN - UNII:7673326042)
NorthStar RxLLC
IRINOTECAN HYDROCHLORIDE
IRINOTECAN HYDROCHLORIDE 20 mg in 1 mL
INTRAVENOUS
PRESCRIPTION DRUG
• Irinotecan hydrochloride injection, is indicated as a component of first-line therapy in combination with 5-fluorouracil (5-FU) and leucovorin (LV) for patients with metastatic carcinoma of the colon or rectum. • Irinotecan hydrochloride injection, is indicated for patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. - Irinotecan hydrochloride injection is contraindicated in patients with a known hypersensitivity to the drug or its excipients. Pregnancy Category D [see Warnings and Precautions (5.9)] Irinotecan hydrochloride injection can cause fetal harm when administered to a pregnant woman. Radioactivity related to 14 C-irinotecan crosses the placenta of rats following intravenous administration of 10 mg/kg (which in separate studies produced an irinotecan Cmax and AUC about 3 and 0.5 times, respectively, the corresponding values in patients administered 125 mg/m2 ). Intravenous administration of irinot
Irinotecan hydrochloride injection, USP is available in single-dose amber glass vials in the following package sizes: 40 mg/ 2 mL vial NDC 16714-725-01 100 mg/ 5 mL vial NDC 16714-726-01 Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature]. Protect from light and freezing. Keep the vial in the carton until the time of use. Inspect the vial for damage and visible signs of leaks before removing from the carton. If damaged, incinerate the unopened package.
Abbreviated New Drug Application
IRINOTECAN HYDROCHLORIDE- IRINOTECAN HYDROCHLORIDE INJECTION NORTHSTAR RXLLC ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE IRINOTECAN HYDROCHLORIDE INJECTION SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR IRINOTECAN HYDROCHLORIDE INJECTION. IRINOTECAN HYDROCHLORIDE INJECTION FOR INTRAVENOUS INFUSION INITIAL U.S. APPROVAL: 1996 WARNING: DIARRHEA AND MYELOSUPPRESSION _SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING_. EARLY AND LATE FORMS OF DIARRHEA CAN OCCUR. EARLY DIARRHEA MAY BE ACCOMPANIED BY CHOLINERGIC SYMPTOMS WHICH MAY BE PREVENTED OR AMELIORATED BY ATROPINE. LATE DIARRHEA CAN BE LIFE THREATENING AND SHOULD BE TREATED PROMPTLY WITH LOPERAMIDE. MONITOR PATIENTS WITH DIARRHEA AND GIVE FLUID AND ELECTROLYTES AS NEEDED. INSTITUTE ANTIBIOTIC THERAPY IF PATIENTS DEVELOP ILEUS, FEVER, OR SEVERE NEUTROPENIA. INTERRUPT IRINOTECAN AND REDUCE SUBSEQUENT DOSES IF SEVERE DIARRHEA OCCURS. SEVERE MYELOSUPPRESSION MAY OCCUR. RECENT MAJOR CHANGES Warnings and Precautions, Myelosuppression (5.2) 02/2019 INDICATIONS AND USAGE Irinotecan hydrochloride injection, USP is a topoisomerase inhibitor indicated for: First-line therapy in combination with 5-fluorouracil and leucovorin for patients with metastatic carcinoma of the colon or rectum. (1) Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. (1) DOSAGE AND ADMINISTRATION Colorectal cancer combination regimen 1: Irinotecan 125 mg/m intravenous infusion over 90 minutes on days 1, 8,15, 22 with LV 20 mg/m intravenous bolus infusion on days 1, 8, 15, 22 followed by 5-FU intravenous bolus infusion on days 1, 8, 15, 22 every 6 weeks. (2.1) Colorectal cancer combination regimen 2: Irinotecan 180 mg/m intravenous infusion over 90 minutes on days 1, 15, 29 with LV 200 mg/m intravenous infusion over 2 hours on days 1, 2, 15, 16, 29, 30 followed by 5-FU 400 mg/m intravenous bolus infusion on days 1, 2 Prečítajte si celý dokument