Does KETOPROFEN Cause White matter lesion? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of White matter lesion have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
7
Reports of White matter lesion with KETOPROFEN
0.1%
of all KETOPROFEN reports
0
Deaths
0
Hospitalizations
How Dangerous Is White matter lesion From KETOPROFEN?
Of the 7 reports.
Is White matter lesion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 7 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 White matter lesion?
ADALIMUMAB (84)
METHOTREXATE (83)
FINGOLIMOD (71)
CYTARABINE (57)
PREDNISONE (42)
METRONIDAZOLE (41)
LEVETIRACETAM (38)
RITUXIMAB (37)
AMPHOTERICIN B (34)
DAUNORUBICIN (33)
Which KETOPROFEN Alternatives Have Lower White matter lesion Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN