Does KETOPROFEN Cause Transaminases increased? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Transaminases increased have been filed in association with KETOPROFEN (Orudis). This represents 0.4% of all adverse event reports for KETOPROFEN.
21
Reports of Transaminases increased with KETOPROFEN
0.4%
of all KETOPROFEN reports
0
Deaths
13
Hospitalizations
How Dangerous Is Transaminases increased From KETOPROFEN?
Of the 21 reports, 13 (61.9%) required hospitalization.
Is Transaminases increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 21 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 Transaminases increased?
METHOTREXATE (1,236)
ACETAMINOPHEN (929)
ATORVASTATIN (472)
RITUXIMAB (448)
CYCLOPHOSPHAMIDE (401)
PREDNISONE (362)
ADALIMUMAB (340)
PACLITAXEL (333)
ROSUVASTATIN (324)
CARBOPLATIN (319)
Which KETOPROFEN Alternatives Have Lower Transaminases increased Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN