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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does KETOPROFEN Cause Low density lipoprotein increased? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Low density lipoprotein increased have been filed in association with KETOPROFEN (Orudis). This represents 0.1% of all adverse event reports for KETOPROFEN.

5
Reports of Low density lipoprotein increased with KETOPROFEN
0.1%
of all KETOPROFEN reports
0
Deaths
3
Hospitalizations

How Dangerous Is Low density lipoprotein increased From KETOPROFEN?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Low density lipoprotein increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for KETOPROFEN. However, 5 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 Low density lipoprotein increased?

EVOLOCUMAB (1,024) INCLISIRAN (423) ALIROCUMAB (336) ROSUVASTATIN (241) ATORVASTATIN (217) EZETIMIBE (217) LOMITAPIDE (164) TOFACITINIB (135) FINGOLIMOD (132) SOMATROPIN (93)

Which KETOPROFEN Alternatives Have Lower Low density lipoprotein increased Risk?

KETOPROFEN vs KETOPROFEN LYSINE KETOPROFEN vs KETOROLAC TROMETHAMINE KETOPROFEN vs KETOROLAC\KETOROLAC TROMETHAMINE KETOPROFEN vs KETOTIFEN KETOPROFEN vs KLONOPIN

Related Pages

KETOPROFEN Full Profile All Low density lipoprotein increased Reports All Drugs Causing Low density lipoprotein increased KETOPROFEN Demographics