Does SIMVASTATIN Cause International normalised ratio increased? 80 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of International normalised ratio increased have been filed in association with SIMVASTATIN (Simvastatin). This represents 0.3% of all adverse event reports for SIMVASTATIN.
80
Reports of International normalised ratio increased with SIMVASTATIN
0.3%
of all SIMVASTATIN reports
6
Deaths
74
Hospitalizations
How Dangerous Is International normalised ratio increased From SIMVASTATIN?
Of the 80 reports, 6 (7.5%) resulted in death, 74 (92.5%) required hospitalization, and 10 (12.5%) 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 SIMVASTATIN. However, 80 reports have been filed with the FAERS database.
What Other Side Effects Does SIMVASTATIN Cause?
Myalgia (3,919)
Fatigue (2,066)
Arthralgia (1,775)
Drug interaction (1,744)
Nausea (1,676)
Rhabdomyolysis (1,616)
Dyspnoea (1,542)
Headache (1,470)
Drug hypersensitivity (1,433)
Muscular weakness (1,356)
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 SIMVASTATIN Alternatives Have Lower International normalised ratio increased Risk?
SIMVASTATIN vs SINGULAIR
SIMVASTATIN vs SINTILIMAB
SIMVASTATIN vs SIPONIMOD
SIMVASTATIN vs SIPULEUCEL-T
SIMVASTATIN vs SIROLIMUS