Does FENOFIBRATE Cause Product prescribing error? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product prescribing error have been filed in association with FENOFIBRATE (Fenofibrate). This represents 0.1% of all adverse event reports for FENOFIBRATE.
7
Reports of Product prescribing error with FENOFIBRATE
0.1%
of all FENOFIBRATE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Product prescribing error From FENOFIBRATE?
Of the 7 reports, 6 (85.7%) required hospitalization.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FENOFIBRATE. However, 7 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which FENOFIBRATE Alternatives Have Lower Product prescribing error Risk?
FENOFIBRATE vs FENOFIBRIC ACID
FENOFIBRATE vs FENOTEROL
FENOFIBRATE vs FENOTEROL HYDROBROMIDE
FENOFIBRATE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM
FENOFIBRATE vs FENTANYL