Does KETOPROFEN Cause Dehydration? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Dehydration have been filed in association with KETOPROFEN (Orudis). This represents 0.5% of all adverse event reports for KETOPROFEN.
28
Reports of Dehydration with KETOPROFEN
0.5%
of all KETOPROFEN reports
5
Deaths
28
Hospitalizations
How Dangerous Is Dehydration From KETOPROFEN?
Of the 28 reports, 5 (17.9%) resulted in death, 28 (100.0%) required hospitalization, and 2 (7.1%) were considered life-threatening.
Is Dehydration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 28 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 Dehydration?
LENALIDOMIDE (3,469)
ADALIMUMAB (3,233)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (3,168)
FUROSEMIDE (2,195)
SEMAGLUTIDE (1,816)
METFORMIN (1,754)
CAPECITABINE (1,599)
LENVATINIB (1,526)
TIRZEPATIDE (1,187)
SACUBITRIL\VALSARTAN (1,171)
Which KETOPROFEN Alternatives Have Lower Dehydration Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN