Does KETOPROFEN Cause Lactic acidosis? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Lactic acidosis have been filed in association with KETOPROFEN (Orudis). This represents 1.4% of all adverse event reports for KETOPROFEN.
78
Reports of Lactic acidosis with KETOPROFEN
1.4%
of all KETOPROFEN reports
16
Deaths
45
Hospitalizations
How Dangerous Is Lactic acidosis From KETOPROFEN?
Of the 78 reports, 16 (20.5%) resulted in death, 45 (57.7%) required hospitalization, and 22 (28.2%) were considered life-threatening.
Is Lactic acidosis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 78 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 Lactic acidosis?
METFORMIN (16,316)
AMLODIPINE (886)
LINEZOLID (824)
FUROSEMIDE (698)
ACETAMINOPHEN (561)
METFORMIN\SITAGLIPTIN (557)
ALBUTEROL (467)
EMPAGLIFLOZIN (434)
RAMIPRIL (430)
BISOPROLOL (425)
Which KETOPROFEN Alternatives Have Lower Lactic acidosis Risk?
KETOPROFEN vs KETOPROFEN LYSINE
KETOPROFEN vs KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE
KETOPROFEN vs KETOTIFEN
KETOPROFEN vs KLONOPIN