Does WARFARIN Cause Product dose omission? 29 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 29 reports of Product dose omission have been filed in association with WARFARIN (Warfarin Sodium). This represents 0.1% of all adverse event reports for WARFARIN.
29
Reports of Product dose omission with WARFARIN
0.1%
of all WARFARIN reports
3
Deaths
17
Hospitalizations
How Dangerous Is Product dose omission From WARFARIN?
Of the 29 reports, 3 (10.3%) resulted in death, 17 (58.6%) required hospitalization, and 1 (3.4%) 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 WARFARIN. However, 29 reports have been filed with the FAERS database.
What Other Side Effects Does WARFARIN Cause?
International normalised ratio increased (5,622)
Haemorrhage (2,930)
Gastrointestinal haemorrhage (2,469)
Anaemia (2,409)
Drug interaction (2,056)
Fall (1,702)
Drug ineffective (1,658)
Epistaxis (1,498)
Contusion (1,467)
Dyspnoea (1,374)
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)