Does NALMEFENE Cause Off label use? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Off label use have been filed in association with NALMEFENE (Zurnai). This represents 7.1% of all adverse event reports for NALMEFENE.
14
Reports of Off label use with NALMEFENE
7.1%
of all NALMEFENE reports
4
Deaths
12
Hospitalizations
How Dangerous Is Off label use From NALMEFENE?
Of the 14 reports, 4 (28.6%) resulted in death, 12 (85.7%) required hospitalization, and 1 (7.1%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for NALMEFENE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does NALMEFENE Cause?
Drug ineffective (66)
Coma (47)
Toxicity to various agents (43)
Hypotension (30)
Respiratory depression (25)
Depressed level of consciousness (19)
Hepatotoxicity (18)
Acute kidney injury (15)
Drug withdrawal syndrome (15)
Metabolic acidosis (14)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which NALMEFENE Alternatives Have Lower Off label use Risk?
NALMEFENE vs NALOXEGOL OXALATE
NALMEFENE vs NALOXONE
NALMEFENE vs NALOXONE\OXYCODONE
NALMEFENE vs NALOXONE\TILIDINE
NALMEFENE vs NALTREXONE