Does KETAMINE Cause Product substitution issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product substitution issue have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.3% of all adverse event reports for KETAMINE.
21
Reports of Product substitution issue with KETAMINE
0.3%
of all KETAMINE reports
21
Deaths
21
Hospitalizations
How Dangerous Is Product substitution issue From KETAMINE?
Of the 21 reports, 21 (100.0%) resulted in death, 21 (100.0%) required hospitalization, and 21 (100.0%) were considered life-threatening.
Is Product substitution issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 21 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 Product substitution issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (2,832)
BUPROPION (1,578)
METHYLPHENIDATE (1,408)
CLONAZEPAM (1,288)
LAMOTRIGINE (979)
ALBUTEROL (864)
LEVOTHYROXINE (803)
DULOXETINE (766)
ESTRADIOL (692)
SERTRALINE (636)
Which KETAMINE Alternatives Have Lower Product substitution issue Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE