Does KETAMINE Cause Condition aggravated? 225 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 225 reports of Condition aggravated have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 2.8% of all adverse event reports for KETAMINE.
225
Reports of Condition aggravated with KETAMINE
2.8%
of all KETAMINE reports
47
Deaths
110
Hospitalizations
How Dangerous Is Condition aggravated From KETAMINE?
Of the 225 reports, 47 (20.9%) resulted in death, 110 (48.9%) required hospitalization, and 32 (14.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 225 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which KETAMINE Alternatives Have Lower Condition aggravated Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE