HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use FENTANYL CITRATE INJECTION safely and effectively. See full prescribing information for FENTANYL CITRATE INJECTION. Fentanyl Citrate Injection, for intravenous or intramuscular use, CII Initial U.S. Approval: 1968 WARNING: SERIOUS AND LIFE-THREATENING RISKS FROM USE OF FENTANYL CITRATE INJECTIONSee full prescribing information for complete boxed warning.
RECENT MAJOR CHANGES
INDICATIONS AND USAGEFentanyl Citrate Injection is an opioid agonist indicated for: (1)
DOSAGE AND ADMINISTRATION
DOSAGE FORMS AND STRENGTHSFentanyl Citrate Injection, USP 50 mcg/mL (equivalent to 50 mcg/mL fentanyl base) is available as a 2 mL fill in a 2.5 mL Carpuject™ Single-dose cartridge with Luer Lock for the Carpuject™ Syringe System. (3) CONTRAINDICATIONS
WARNINGS AND PRECAUTIONS
ADVERSE REACTIONSMost common serious adverse reactions were respiratory depression, apnea, rigidity, and bradycardia. (6) To report SUSPECTED ADVERSE REACTIONS, contact Hospira, Inc. at 1-800-441-4100 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. DRUG INTERACTIONS
USE IN SPECIFIC POPULATIONSSee 17 for PATIENT COUNSELING INFORMATION. Revised: 7/2024 |
HIGHLIGHTS OF PRESCRIBING INFORMATIONThese highlights do not include all the information needed to use FENTANYL CITRATE INJECTION safely and effectively. See full prescribing information for FENTANYL CITRATE INJECTION. Fentanyl Citrate Injection, for intravenous or intramuscular use, CII Initial U.S. Approval: 1968 WARNING: SERIOUS AND LIFE-THREATENING RISKS FROM USE OF FENTANYL CITRATE INJECTIONSee full prescribing information for complete boxed warning.
RECENT MAJOR CHANGES
INDICATIONS AND USAGEFentanyl Citrate Injection is an opioid agonist indicated for: (1)
DOSAGE AND ADMINISTRATION
DOSAGE FORMS AND STRENGTHSFentanyl Citrate Injection, USP 50 mcg/mL (equivalent to 50 mcg/mL fentanyl base) is available as a 2 mL fill in a 2.5 mL Carpuject™ Single-dose cartridge with Luer Lock for the Carpuject™ Syringe System. (3) CONTRAINDICATIONS
WARNINGS AND PRECAUTIONS
ADVERSE REACTIONSMost common serious adverse reactions were respiratory depression, apnea, rigidity, and bradycardia. (6) To report SUSPECTED ADVERSE REACTIONS, contact Hospira, Inc. at 1-800-441-4100 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. DRUG INTERACTIONS
USE IN SPECIFIC POPULATIONSSee 17 for PATIENT COUNSELING INFORMATION. Revised: 7/2024 |
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