Does KETOROLAC TROMETHAMINE Cause Product administration error? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product administration error have been filed in association with KETOROLAC TROMETHAMINE (ketorolac tromethamine). This represents 0.3% of all adverse event reports for KETOROLAC TROMETHAMINE.
16
Reports of Product administration error with KETOROLAC TROMETHAMINE
0.3%
of all KETOROLAC TROMETHAMINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From KETOROLAC TROMETHAMINE?
Of the 16 reports, 2 (12.5%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOROLAC TROMETHAMINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does KETOROLAC TROMETHAMINE Cause?
Drug ineffective (1,172)
Drug hypersensitivity (838)
Treatment failure (776)
Off label use (593)
Nausea (501)
Hyperhidrosis (353)
Product use in unapproved indication (328)
Nightmare (325)
Sedation (319)
Dyspnoea (244)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which KETOROLAC TROMETHAMINE Alternatives Have Lower Product administration error Risk?
KETOROLAC TROMETHAMINE vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOROLAC TROMETHAMINE vs KETOTIFEN
KETOROLAC TROMETHAMINE vs KLONOPIN
KETOROLAC TROMETHAMINE vs L-ASPARAGINASE
KETOROLAC TROMETHAMINE vs LABETALOL