Does KETAMINE Cause Type i hypersensitivity? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Type i hypersensitivity have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.4% of all adverse event reports for KETAMINE.
30
Reports of Type i hypersensitivity with KETAMINE
0.4%
of all KETAMINE reports
0
Deaths
20
Hospitalizations
How Dangerous Is Type i hypersensitivity From KETAMINE?
Of the 30 reports, 20 (66.7%) required hospitalization, and 8 (26.7%) were considered life-threatening.
Is Type i hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 30 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 Type i hypersensitivity?
OXALIPLATIN (266)
AMOXICILLIN (260)
LEVOFLOXACIN (180)
ACETAMINOPHEN (129)
CARBOPLATIN (125)
DICLOFENAC (111)
PANTOPRAZOLE (110)
PACLITAXEL (107)
IBUPROFEN (103)
OMEPRAZOLE (98)
Which KETAMINE Alternatives Have Lower Type i hypersensitivity Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE