Does KETAMINE Cause Intentional product use issue? 37 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 37 reports of Intentional product use issue have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.5% of all adverse event reports for KETAMINE.
37
Reports of Intentional product use issue with KETAMINE
0.5%
of all KETAMINE reports
11
Deaths
18
Hospitalizations
How Dangerous Is Intentional product use issue From KETAMINE?
Of the 37 reports, 11 (29.7%) resulted in death, 18 (48.6%) required hospitalization, and 1 (2.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 37 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which KETAMINE Alternatives Have Lower Intentional product use issue Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE