Does RIVAROXABAN Cause International normalised ratio increased? 863 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 863 reports of International normalised ratio increased have been filed in association with RIVAROXABAN (Rivaroxaban). This represents 0.7% of all adverse event reports for RIVAROXABAN.
863
Reports of International normalised ratio increased with RIVAROXABAN
0.7%
of all RIVAROXABAN reports
58
Deaths
438
Hospitalizations
How Dangerous Is International normalised ratio increased From RIVAROXABAN?
Of the 863 reports, 58 (6.7%) resulted in death, 438 (50.8%) required hospitalization, and 68 (7.9%) 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 RIVAROXABAN. However, 863 reports have been filed with the FAERS database.
What Other Side Effects Does RIVAROXABAN Cause?
Gastrointestinal haemorrhage (20,041)
Haemorrhage (6,571)
Epistaxis (5,629)
Rectal haemorrhage (4,501)
Off label use (4,463)
Haematuria (4,387)
Upper gastrointestinal haemorrhage (4,247)
Cerebrovascular accident (4,111)
Anaemia (3,907)
Acute kidney injury (3,735)
What Other Drugs Cause International normalised ratio increased?
WARFARIN (5,622)
ACETAMINOPHEN (533)
ASPIRIN (448)
APIXABAN (317)
CLOPIDOGREL BISULFATE (314)
FLUINDIONE (286)
AMIODARONE (277)
FUROSEMIDE (277)
DABIGATRAN ETEXILATE (223)
ENOXAPARIN (217)
Which RIVAROXABAN Alternatives Have Lower International normalised ratio increased Risk?
RIVAROXABAN vs RIVASTIGMINE
RIVAROXABAN vs RIVOTRIL
RIVAROXABAN vs RIZATRIPTAN
RIVAROXABAN vs ROACTEMRA
RIVAROXABAN vs ROCURONIUM