Does KETOPROFEN Cause Hyperkalaemia? 89 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 89 reports of Hyperkalaemia have been filed in association with KETOPROFEN (Orudis). This represents 1.6% of all adverse event reports for KETOPROFEN.
89
Reports of Hyperkalaemia with KETOPROFEN
1.6%
of all KETOPROFEN reports
10
Deaths
72
Hospitalizations
How Dangerous Is Hyperkalaemia From KETOPROFEN?
Of the 89 reports, 10 (11.2%) resulted in death, 72 (80.9%) required hospitalization, and 20 (22.5%) were considered life-threatening.
Is Hyperkalaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 89 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 Hyperkalaemia?
METFORMIN (2,565)
SPIRONOLACTONE (2,518)
FUROSEMIDE (2,035)
RAMIPRIL (1,383)
SACUBITRIL\VALSARTAN (1,192)
SULFAMETHOXAZOLE\TRIMETHOPRIM (1,036)
LISINOPRIL (948)
POTASSIUM (944)
BISOPROLOL (850)
TACROLIMUS (713)
Which KETOPROFEN Alternatives Have Lower Hyperkalaemia Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN