Does KETOPROFEN Cause Drug hypersensitivity? 478 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 478 reports of Drug hypersensitivity have been filed in association with KETOPROFEN (Orudis). This represents 8.6% of all adverse event reports for KETOPROFEN.
478
Reports of Drug hypersensitivity with KETOPROFEN
8.6%
of all KETOPROFEN reports
104
Deaths
23
Hospitalizations
How Dangerous Is Drug hypersensitivity From KETOPROFEN?
Of the 478 reports, 104 (21.8%) resulted in death, 23 (4.8%) required hospitalization, and 9 (1.9%) were considered life-threatening.
Is Drug hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 478 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 Drug hypersensitivity?
METHOTREXATE (16,677)
ETANERCEPT (12,991)
ADALIMUMAB (11,599)
MORPHINE (11,095)
RITUXIMAB (8,924)
LEFLUNOMIDE (8,148)
INFLIXIMAB (8,119)
TOCILIZUMAB (7,883)
ABATACEPT (7,808)
CODEINE (7,479)
Which KETOPROFEN Alternatives Have Lower Drug hypersensitivity Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN