Does RIVAROXABAN Cause Product administration interrupted? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product administration interrupted have been filed in association with RIVAROXABAN (Rivaroxaban). This represents 0.0% of all adverse event reports for RIVAROXABAN.
5
Reports of Product administration interrupted with RIVAROXABAN
0.0%
of all RIVAROXABAN reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product administration interrupted From RIVAROXABAN?
Of the 5 reports, 3 (60.0%) required hospitalization, and 1 (20.0%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIVAROXABAN. However, 5 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 Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which RIVAROXABAN Alternatives Have Lower Product administration interrupted Risk?
RIVAROXABAN vs RIVASTIGMINE
RIVAROXABAN vs RIVOTRIL
RIVAROXABAN vs RIZATRIPTAN
RIVAROXABAN vs ROACTEMRA
RIVAROXABAN vs ROCURONIUM