Does GEMFIBROZIL Cause Condition aggravated? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Condition aggravated have been filed in association with GEMFIBROZIL (Gemfibrozil). This represents 1.5% of all adverse event reports for GEMFIBROZIL.
16
Reports of Condition aggravated with GEMFIBROZIL
1.5%
of all GEMFIBROZIL reports
2
Deaths
7
Hospitalizations
How Dangerous Is Condition aggravated From GEMFIBROZIL?
Of the 16 reports, 2 (12.5%) resulted in death, 7 (43.8%) required hospitalization, and 1 (6.3%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for GEMFIBROZIL. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does GEMFIBROZIL Cause?
Drug hypersensitivity (242)
Drug ineffective (77)
Rhabdomyolysis (63)
Fatigue (60)
Drug interaction (59)
Myalgia (58)
Nausea (54)
Acute kidney injury (52)
Diarrhoea (43)
Rash (41)
What Other Drugs Cause Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which GEMFIBROZIL Alternatives Have Lower Condition aggravated Risk?
GEMFIBROZIL vs GEMTUZUMAB OZOGAMICIN
GEMFIBROZIL vs GEMZAR
GEMFIBROZIL vs GENTAMICIN
GEMFIBROZIL vs GEODON
GEMFIBROZIL vs GILENYA