Does EDOXABAN Cause Product prescribing error? 56 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 56 reports of Product prescribing error have been filed in association with EDOXABAN (SAVAYSA). This represents 0.7% of all adverse event reports for EDOXABAN.
56
Reports of Product prescribing error with EDOXABAN
0.7%
of all EDOXABAN reports
1
Deaths
53
Hospitalizations
How Dangerous Is Product prescribing error From EDOXABAN?
Of the 56 reports, 1 (1.8%) resulted in death, 53 (94.6%) required hospitalization, and 1 (1.8%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for EDOXABAN. However, 56 reports have been filed with the FAERS database.
What Other Side Effects Does EDOXABAN Cause?
Anaemia (663)
Cerebral infarction (419)
Gastrointestinal haemorrhage (378)
Renal impairment (359)
Cerebrovascular accident (337)
Dyspnoea (331)
General physical health deterioration (315)
Haematuria (312)
Fall (298)
Cardiac failure (272)
What Other Drugs Cause Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which EDOXABAN Alternatives Have Lower Product prescribing error Risk?
EDOXABAN vs EDOXABAN TOSILATE
EDOXABAN vs EFALIZUMAB
EDOXABAN vs EFANESOCTOCOG ALFA
EDOXABAN vs EFAVIRENZ
EDOXABAN vs EFAVIRENZ\EMTRICITABINE\TENOFOVIR DISOPROXIL