Does KETAMINE Cause Intentional product misuse? 144 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 144 reports of Intentional product misuse have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 1.8% of all adverse event reports for KETAMINE.
144
Reports of Intentional product misuse with KETAMINE
1.8%
of all KETAMINE reports
17
Deaths
102
Hospitalizations
How Dangerous Is Intentional product misuse From KETAMINE?
Of the 144 reports, 17 (11.8%) resulted in death, 102 (70.8%) required hospitalization, and 12 (8.3%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 144 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which KETAMINE Alternatives Have Lower Intentional product misuse Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE