Does FENOFIBRATE Cause International normalised ratio increased? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of International normalised ratio increased have been filed in association with FENOFIBRATE (Fenofibrate). This represents 1.0% of all adverse event reports for FENOFIBRATE.
55
Reports of International normalised ratio increased with FENOFIBRATE
1.0%
of all FENOFIBRATE reports
21
Deaths
33
Hospitalizations
How Dangerous Is International normalised ratio increased From FENOFIBRATE?
Of the 55 reports, 21 (38.2%) resulted in death, 33 (60.0%) required hospitalization, and 3 (5.5%) were considered life-threatening.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FENOFIBRATE. However, 55 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 International normalised ratio increased?
WARFARIN (5,622)
RIVAROXABAN (863)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
Which FENOFIBRATE Alternatives Have Lower International normalised ratio increased Risk?
FENOFIBRATE vs FENOFIBRIC ACID
FENOFIBRATE vs FENOTEROL
FENOFIBRATE vs FENOTEROL HYDROBROMIDE
FENOFIBRATE vs FENOTEROL HYDROBROMIDE\IPRATROPIUM
FENOFIBRATE vs FENTANYL