Does KETOPROFEN Cause Treatment failure? 225 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 225 reports of Treatment failure have been filed in association with KETOPROFEN (Orudis). This represents 4.1% of all adverse event reports for KETOPROFEN.
225
Reports of Treatment failure with KETOPROFEN
4.1%
of all KETOPROFEN reports
101
Deaths
9
Hospitalizations
How Dangerous Is Treatment failure From KETOPROFEN?
Of the 225 reports, 101 (44.9%) resulted in death, 9 (4.0%) required hospitalization, and 9 (4.0%) were considered life-threatening.
Is Treatment failure Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 225 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 Treatment failure?
METHOTREXATE (14,672)
ETANERCEPT (11,893)
ADALIMUMAB (9,990)
ABATACEPT (9,301)
RITUXIMAB (9,217)
TOCILIZUMAB (9,097)
HYDROXYCHLOROQUINE (8,786)
LEFLUNOMIDE (8,686)
INFLIXIMAB (8,535)
SULFASALAZINE (7,423)
Which KETOPROFEN Alternatives Have Lower Treatment failure Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN