Does KETOPROFEN Cause Prothrombin time abnormal? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Prothrombin time abnormal have been filed in association with KETOPROFEN (Orudis). This represents 0.2% of all adverse event reports for KETOPROFEN.
11
Reports of Prothrombin time abnormal with KETOPROFEN
0.2%
of all KETOPROFEN reports
0
Deaths
11
Hospitalizations
How Dangerous Is Prothrombin time abnormal From KETOPROFEN?
Of the 11 reports, 11 (100.0%) required hospitalization, and 2 (18.2%) were considered life-threatening.
Is Prothrombin time abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 11 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 Prothrombin time abnormal?
WARFARIN (53)
ACETAMINOPHEN (25)
IBUPROFEN (19)
RIVAROXABAN (19)
DABIGATRAN ETEXILATE (15)
ENOXAPARIN (14)
PANTOPRAZOLE (14)
DICLOFENAC (13)
APIXABAN (12)
DESLORATADINE (12)
Which KETOPROFEN Alternatives Have Lower Prothrombin time abnormal Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN