Does KETOPROFEN Cause Hypervolaemia? 9 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Hypervolaemia have been filed in association with KETOPROFEN (Orudis). This represents 0.2% of all adverse event reports for KETOPROFEN.
9
Reports of Hypervolaemia with KETOPROFEN
0.2%
of all KETOPROFEN reports
0
Deaths
9
Hospitalizations
How Dangerous Is Hypervolaemia From KETOPROFEN?
Of the 9 reports, 9 (100.0%) required hospitalization.
Is Hypervolaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 9 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 Hypervolaemia?
TREPROSTINIL (580)
CALCIUM\DEXTROSE\MAGNESIUM\SODIUM\SODIUM (428)
AMBRISENTAN (205)
MACITENTAN (202)
FUROSEMIDE (139)
AMLODIPINE (122)
CYCLOPHOSPHAMIDE (118)
SACUBITRIL\VALSARTAN (115)
TACROLIMUS (100)
PREDNISONE (98)
Which KETOPROFEN Alternatives Have Lower Hypervolaemia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN