Does KETOPROFEN Cause Product use issue? 366 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 366 reports of Product use issue have been filed in association with KETOPROFEN (Orudis). This represents 6.6% of all adverse event reports for KETOPROFEN.
366
Reports of Product use issue with KETOPROFEN
6.6%
of all KETOPROFEN reports
109
Deaths
38
Hospitalizations
How Dangerous Is Product use issue From KETOPROFEN?
Of the 366 reports, 109 (29.8%) resulted in death, 38 (10.4%) required hospitalization, and 11 (3.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 366 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which KETOPROFEN Alternatives Have Lower Product use issue Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN