Does RIVAROXABAN Cause Product dose omission? 401 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 401 reports of Product dose omission have been filed in association with RIVAROXABAN (Rivaroxaban). This represents 0.3% of all adverse event reports for RIVAROXABAN.
401
Reports of Product dose omission with RIVAROXABAN
0.3%
of all RIVAROXABAN reports
7
Deaths
79
Hospitalizations
How Dangerous Is Product dose omission From RIVAROXABAN?
Of the 401 reports, 7 (1.7%) resulted in death, 79 (19.7%) required hospitalization, and 6 (1.5%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RIVAROXABAN. However, 401 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which RIVAROXABAN Alternatives Have Lower Product dose omission Risk?
RIVAROXABAN vs RIVASTIGMINE
RIVAROXABAN vs RIVOTRIL
RIVAROXABAN vs RIZATRIPTAN
RIVAROXABAN vs ROACTEMRA
RIVAROXABAN vs ROCURONIUM