Does FENOFIBRATE Cause Haematemesis? 206 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 206 reports of Haematemesis have been filed in association with FENOFIBRATE (Fenofibrate). This represents 3.6% of all adverse event reports for FENOFIBRATE.
206
Reports of Haematemesis with FENOFIBRATE
3.6%
of all FENOFIBRATE reports
199
Deaths
2
Hospitalizations
How Dangerous Is Haematemesis From FENOFIBRATE?
Of the 206 reports, 199 (96.6%) resulted in death, 2 (1.0%) required hospitalization, and 3 (1.5%) were considered life-threatening.
Is Haematemesis Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FENOFIBRATE. However, 206 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 Haematemesis?
ASPIRIN (1,538)
RIVAROXABAN (1,085)
CLOPIDOGREL BISULFATE (954)
IBUPROFEN (836)
APIXABAN (650)
ADALIMUMAB (563)
ACETAMINOPHEN (454)
WARFARIN (426)
SERTRALINE (412)
ENOXAPARIN (404)
Which FENOFIBRATE Alternatives Have Lower Haematemesis Risk?
FENOFIBRATE vs FENOFIBRIC ACID
FENOFIBRATE vs FENOTEROL
FENOFIBRATE vs FENOTEROL HYDROBROMIDE
FENOFIBRATE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM
FENOFIBRATE vs FENTANYL