Does KETOPROFEN Cause Fracture displacement? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Fracture displacement have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.
5
Reports of Fracture displacement with KETOPROFEN
0.1%
of all KETOPROFEN reports
0
Deaths
5
Hospitalizations
How Dangerous Is Fracture displacement From KETOPROFEN?
Of the 5 reports, 5 (100.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Fracture displacement Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 5 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 Fracture displacement?
ALENDRONATE (64)
RISEDRONATE (58)
IBANDRONATE (37)
FOSAMAX (18)
ACTONEL (17)
DENOSUMAB (15)
ZOLEDRONIC ACID (14)
ADALIMUMAB (13)
ALENDRONATE\CHOLECALCIFEROL (11)
RAMIPRIL (9)
Which KETOPROFEN Alternatives Have Lower Fracture displacement Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN