Does KETOPROFEN Cause Adverse event? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Adverse event have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
7
Reports of Adverse event with KETOPROFEN
0.1%
of all KETOPROFEN reports
3
Deaths
4
Hospitalizations
How Dangerous Is Adverse event From KETOPROFEN?
Of the 7 reports, 3 (42.9%) resulted in death, 4 (57.1%) required hospitalization, and 3 (42.9%) were considered life-threatening.
Is Adverse event Listed in the Official Label?
Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for KETOPROFEN.
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 Adverse event?
ABATACEPT (4,028)
APIXABAN (3,871)
ETANERCEPT (3,096)
LENALIDOMIDE (2,426)
INFLIXIMAB (2,269)
ADALIMUMAB (2,121)
METHOTREXATE (1,846)
LEFLUNOMIDE (1,476)
RIVAROXABAN (1,465)
ALENDRONATE (1,462)
Which KETOPROFEN Alternatives Have Lower Adverse event Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN