Does KETOPROFEN Cause Thrombocytopenia? 325 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 325 reports of Thrombocytopenia have been filed in association with KETOPROFEN (Orudis). This represents 5.9% of all adverse event reports for KETOPROFEN.
325
Reports of Thrombocytopenia with KETOPROFEN
5.9%
of all KETOPROFEN reports
107
Deaths
34
Hospitalizations
How Dangerous Is Thrombocytopenia From KETOPROFEN?
Of the 325 reports, 107 (32.9%) resulted in death, 34 (10.5%) required hospitalization, and 21 (6.5%) were considered life-threatening.
Is Thrombocytopenia Listed in the Official Label?
Yes, Thrombocytopenia 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 Thrombocytopenia?
DEXAMETHASONE (5,873)
RITUXIMAB (4,810)
CYCLOPHOSPHAMIDE (4,669)
LENALIDOMIDE (4,584)
CARBOPLATIN (4,483)
METHOTREXATE (3,865)
DOXORUBICIN (3,638)
ETOPOSIDE (3,085)
VINCRISTINE (2,940)
OXALIPLATIN (2,886)
Which KETOPROFEN Alternatives Have Lower Thrombocytopenia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN