Does DOFETILIDE Cause Product prescribing error? 71 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 71 reports of Product prescribing error have been filed in association with DOFETILIDE (Dofetilide). This represents 1.4% of all adverse event reports for DOFETILIDE.
71
Reports of Product prescribing error with DOFETILIDE
1.4%
of all DOFETILIDE reports
2
Deaths
29
Hospitalizations
How Dangerous Is Product prescribing error From DOFETILIDE?
Of the 71 reports, 2 (2.8%) resulted in death, 29 (40.8%) required hospitalization, and 5 (7.0%) 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 DOFETILIDE. However, 71 reports have been filed with the FAERS database.
What Other Side Effects Does DOFETILIDE Cause?
Drug ineffective (654)
Atrial fibrillation (438)
Death (285)
Electrocardiogram qt prolonged (267)
Dyspnoea (230)
Dizziness (228)
Fatigue (180)
Malaise (175)
Headache (154)
Palpitations (128)
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 DOFETILIDE Alternatives Have Lower Product prescribing error Risk?
DOFETILIDE vs DOLUTEGRAVIR
DOFETILIDE vs DOLUTEGRAVIR\LAMIVUDINE
DOFETILIDE vs DOLUTEGRAVIR\LAMIVUDINE\TENOFOVIR DISOPROXIL
DOFETILIDE vs DOLUTEGRAVIR\RILPIVIRINE
DOFETILIDE vs DOMPERIDONE