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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does NALMEFENE Cause Contraindicated product administered? 10 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Contraindicated product administered have been filed in association with NALMEFENE (Zurnai). This represents 5.1% of all adverse event reports for NALMEFENE.

10
Reports of Contraindicated product administered with NALMEFENE
5.1%
of all NALMEFENE reports
0
Deaths
5
Hospitalizations

How Dangerous Is Contraindicated product administered From NALMEFENE?

Of the 10 reports, 5 (50.0%) required hospitalization, and 2 (20.0%) were considered life-threatening.

Is Contraindicated product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for NALMEFENE. However, 10 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 Contraindicated product administered?

ABATACEPT (13,559) METHOTREXATE (13,121) ETANERCEPT (12,062) TOCILIZUMAB (11,547) ADALIMUMAB (11,270) LEFLUNOMIDE (11,206) HYDROXYCHLOROQUINE (10,557) RITUXIMAB (10,479) INFLIXIMAB (9,618) SULFASALAZINE (8,698)

Which NALMEFENE Alternatives Have Lower Contraindicated product administered Risk?

NALMEFENE vs NALOXEGOL OXALATE NALMEFENE vs NALOXONE NALMEFENE vs NALOXONE\OXYCODONE NALMEFENE vs NALOXONE\TILIDINE NALMEFENE vs NALTREXONE

Related Pages

NALMEFENE Full Profile All Contraindicated product administered Reports All Drugs Causing Contraindicated product administered NALMEFENE Demographics