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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 KETAMINE Cause Contraindicated product administered? 36 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Contraindicated product administered have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.5% of all adverse event reports for KETAMINE.

36
Reports of Contraindicated product administered with KETAMINE
0.5%
of all KETAMINE reports
35
Deaths
29
Hospitalizations

How Dangerous Is Contraindicated product administered From KETAMINE?

Of the 36 reports, 35 (97.2%) resulted in death, 29 (80.6%) required hospitalization, and 1 (2.8%) 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 KETAMINE. However, 36 reports have been filed with the FAERS database.

What Other Side Effects Does KETAMINE Cause?

Drug ineffective (1,458) Off label use (992) Drug abuse (748) Anaphylactic shock (568) Hyperhidrosis (496) Hypotension (468) Product use in unapproved indication (457) Toxicity to various agents (420) Sedation (395) Agitation (344)

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 KETAMINE Alternatives Have Lower Contraindicated product administered Risk?

KETAMINE vs KETOCONAZOLE KETAMINE vs KETOPROFEN KETAMINE vs KETOPROFEN LYSINE KETAMINE vs KETOROLAC TROMETHAMINE KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE

Related Pages

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