Does KETOPROFEN Cause Incorrect dose administered? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Incorrect dose administered have been filed in association with KETOPROFEN (Orudis). This represents 0.3% of all adverse event reports for KETOPROFEN.
19
Reports of Incorrect dose administered with KETOPROFEN
0.3%
of all KETOPROFEN reports
0
Deaths
17
Hospitalizations
How Dangerous Is Incorrect dose administered From KETOPROFEN?
Of the 19 reports, 17 (89.5%) required hospitalization, and 5 (26.3%) were considered life-threatening.
Is Incorrect dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 19 reports have been filed with the FAERS database.
What Other Side Effects Does KETOPROFEN Cause?
Pain (595)
Headache (574)
Hypersensitivity (556)
Erythema (546)
Acute kidney injury (517)
Hyperhidrosis (516)
Hepatic enzyme increased (508)
Asthma (507)
Rheumatoid arthritis (493)
Immunodeficiency (492)
What Other Drugs Cause Incorrect dose administered?
TIRZEPATIDE (23,301)
ADALIMUMAB (14,000)
DUPILUMAB (9,907)
RANITIDINE (9,337)
INSULIN LISPRO (8,318)
ACETAMINOPHEN (5,316)
DULAGLUTIDE (5,207)
SECUKINUMAB (4,524)
INSULIN GLARGINE (3,070)
SOMATROPIN (2,772)
Which KETOPROFEN Alternatives Have Lower Incorrect dose administered Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN