Does TIPIRACIL\TRIFLURIDINE Cause International normalised ratio increased? 6 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of International normalised ratio increased have been filed in association with TIPIRACIL\TRIFLURIDINE. This represents 0.1% of all adverse event reports for TIPIRACIL\TRIFLURIDINE.
6
Reports of International normalised ratio increased with TIPIRACIL\TRIFLURIDINE
0.1%
of all TIPIRACIL\TRIFLURIDINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is International normalised ratio increased From TIPIRACIL\TRIFLURIDINE?
Of the 6 reports, 2 (33.3%) required hospitalization.
Is International normalised ratio increased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TIPIRACIL\TRIFLURIDINE. However, 6 reports have been filed with the FAERS database.
What Other Side Effects Does TIPIRACIL\TRIFLURIDINE Cause?
Death (3,017)
Disease progression (1,774)
Fatigue (1,298)
Nausea (1,135)
Diarrhoea (965)
Decreased appetite (659)
Vomiting (628)
White blood cell count decreased (483)
Asthenia (472)
Anaemia (388)
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 TIPIRACIL\TRIFLURIDINE Alternatives Have Lower International normalised ratio increased Risk?
TIPIRACIL\TRIFLURIDINE vs TIPRANAVIR
TIPIRACIL\TRIFLURIDINE vs TIRAGOLUMAB
TIPIRACIL\TRIFLURIDINE vs TIRBANIBULIN
TIPIRACIL\TRIFLURIDINE vs TIROFIBAN
TIPIRACIL\TRIFLURIDINE vs TIRZEPATIDE