Does KETAMINE Cause Hepatic function abnormal? 33 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 33 reports of Hepatic function abnormal have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.4% of all adverse event reports for KETAMINE.
33
Reports of Hepatic function abnormal with KETAMINE
0.4%
of all KETAMINE reports
3
Deaths
26
Hospitalizations
How Dangerous Is Hepatic function abnormal From KETAMINE?
Of the 33 reports, 3 (9.1%) resulted in death, 26 (78.8%) required hospitalization, and 14 (42.4%) were considered life-threatening.
Is Hepatic function abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 33 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 Hepatic function abnormal?
NIVOLUMAB (1,131)
PEMBROLIZUMAB (1,079)
METHOTREXATE (1,054)
CABOZANTINIB S-MALATE (912)
CYCLOPHOSPHAMIDE (824)
BEVACIZUMAB (769)
PACLITAXEL (603)
LENVATINIB (528)
ATORVASTATIN (520)
CYCLOSPORINE (508)
Which KETAMINE Alternatives Have Lower Hepatic function abnormal Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE