Does KETOPROFEN Cause Fluid retention? 423 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 423 reports of Fluid retention have been filed in association with KETOPROFEN (Orudis). This represents 7.6% of all adverse event reports for KETOPROFEN.
423
Reports of Fluid retention with KETOPROFEN
7.6%
of all KETOPROFEN reports
112
Deaths
10
Hospitalizations
How Dangerous Is Fluid retention From KETOPROFEN?
Of the 423 reports, 112 (26.5%) resulted in death, 10 (2.4%) required hospitalization, and 9 (2.1%) were considered life-threatening.
Is Fluid retention Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 423 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 Fluid retention?
AMBRISENTAN (3,927)
TREPROSTINIL (3,804)
MACITENTAN (2,861)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (2,233)
SACUBITRIL\VALSARTAN (2,187)
ADALIMUMAB (1,193)
SELEXIPAG (1,044)
FUROSEMIDE (1,020)
LENALIDOMIDE (1,007)
EPOPROSTENOL (929)
Which KETOPROFEN Alternatives Have Lower Fluid retention Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN