Does KETAMINE Cause Multiple organ dysfunction syndrome? 91 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 91 reports of Multiple organ dysfunction syndrome have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 1.1% of all adverse event reports for KETAMINE.
91
Reports of Multiple organ dysfunction syndrome with KETAMINE
1.1%
of all KETAMINE reports
68
Deaths
66
Hospitalizations
How Dangerous Is Multiple organ dysfunction syndrome From KETAMINE?
Of the 91 reports, 68 (74.7%) resulted in death, 66 (72.5%) required hospitalization, and 19 (20.9%) were considered life-threatening.
Is Multiple organ dysfunction syndrome Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 91 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 Multiple organ dysfunction syndrome?
TACROLIMUS (1,847)
CYCLOPHOSPHAMIDE (1,597)
MYCOPHENOLATE MOFETIL (1,566)
PREDNISONE (1,525)
DEXAMETHASONE (1,355)
METHOTREXATE (1,317)
METHYLPREDNISOLONE (1,278)
RITUXIMAB (1,188)
PREDNISOLONE (1,154)
CYCLOSPORINE (933)
Which KETAMINE Alternatives Have Lower Multiple organ dysfunction syndrome Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE