Does KETAMINE Cause Wrong technique in product usage process? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Wrong technique in product usage process have been filed in association with KETAMINE (KETAMINE HYDROCHLORIDE). This represents 0.1% of all adverse event reports for KETAMINE.
10
Reports of Wrong technique in product usage process with KETAMINE
0.1%
of all KETAMINE reports
2
Deaths
0
Hospitalizations
How Dangerous Is Wrong technique in product usage process From KETAMINE?
Of the 10 reports, 2 (20.0%) resulted in death, and 2 (20.0%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETAMINE. However, 10 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which KETAMINE Alternatives Have Lower Wrong technique in product usage process Risk?
KETAMINE vs KETOCONAZOLE
KETAMINE vs KETOPROFEN
KETAMINE vs KETOPROFEN LYSINE
KETAMINE vs KETOROLAC TROMETHAMINE
KETAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE