Does KETOPROFEN Cause Off label use? 456 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 456 reports of Off label use have been filed in association with KETOPROFEN (Orudis). This represents 8.2% of all adverse event reports for KETOPROFEN.
456
Reports of Off label use with KETOPROFEN
8.2%
of all KETOPROFEN reports
112
Deaths
64
Hospitalizations
How Dangerous Is Off label use From KETOPROFEN?
Of the 456 reports, 112 (24.6%) resulted in death, 64 (14.0%) required hospitalization, and 26 (5.7%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 456 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 Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which KETOPROFEN Alternatives Have Lower Off label use Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN