Does KETAMINE Cause Product use issue? 61 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 61 reports of Product use issue have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.8% of all adverse event reports for KETAMINE.
61
Reports of Product use issue with KETAMINE
0.8%
of all KETAMINE reports
3
Deaths
22
Hospitalizations
How Dangerous Is Product use issue From KETAMINE?
Of the 61 reports, 3 (4.9%) resulted in death, 22 (36.1%) required hospitalization, and 7 (11.5%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 61 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which KETAMINE Alternatives Have Lower Product use issue Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE