Does FENOFIBRATE Cause Condition aggravated? 125 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 125 reports of Condition aggravated have been filed in association with FENOFIBRATE (Fenofibrate). This represents 2.2% of all adverse event reports for FENOFIBRATE.
125
Reports of Condition aggravated with FENOFIBRATE
2.2%
of all FENOFIBRATE reports
6
Deaths
61
Hospitalizations
How Dangerous Is Condition aggravated From FENOFIBRATE?
Of the 125 reports, 6 (4.8%) resulted in death, 61 (48.8%) required hospitalization, and 1 (0.8%) 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 FENOFIBRATE. However, 125 reports have been filed with the FAERS database.
What Other Side Effects Does FENOFIBRATE Cause?
Myalgia (411)
Dyspnoea (373)
Fatigue (365)
Asthenia (356)
Dizziness (356)
Fall (354)
Drug ineffective (326)
Pruritus (325)
Nausea (311)
Diarrhoea (310)
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 FENOFIBRATE Alternatives Have Lower Condition aggravated Risk?
FENOFIBRATE vs FENOFIBRIC ACID
FENOFIBRATE vs FENOTEROL
FENOFIBRATE vs FENOTEROL HYDROBROMIDE
FENOFIBRATE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM
FENOFIBRATE vs FENTANYL