Does KETOPROFEN Cause Hypersensitivity? 556 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 556 reports of Hypersensitivity have been filed in association with KETOPROFEN (Orudis). This represents 10.0% of all adverse event reports for KETOPROFEN.
556
Reports of Hypersensitivity with KETOPROFEN
10.0%
of all KETOPROFEN reports
108
Deaths
24
Hospitalizations
How Dangerous Is Hypersensitivity From KETOPROFEN?
Of the 556 reports, 108 (19.4%) resulted in death, 24 (4.3%) required hospitalization, and 12 (2.2%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 556 reports have been filed with the FAERS database.
What Other Side Effects Does KETOPROFEN Cause?
Pain (595)
Headache (574)
Erythema (546)
Acute kidney injury (517)
Hyperhidrosis (516)
Hepatic enzyme increased (508)
Asthma (507)
Rheumatoid arthritis (493)
Immunodeficiency (492)
Rash erythematous (485)
What Other Drugs Cause Hypersensitivity?
ETANERCEPT (10,846)
ADALIMUMAB (10,641)
METHOTREXATE (9,799)
TOCILIZUMAB (9,076)
ABATACEPT (8,945)
INFLIXIMAB (8,519)
RITUXIMAB (8,408)
ADAPALENE (8,356)
LEFLUNOMIDE (7,926)
CERTOLIZUMAB PEGOL (7,353)
Which KETOPROFEN Alternatives Have Lower Hypersensitivity Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN