Does FLECAINIDE Cause Product dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission have been filed in association with FLECAINIDE (Flecainide Acetate). This represents 0.2% of all adverse event reports for FLECAINIDE.
7
Reports of Product dose omission with FLECAINIDE
0.2%
of all FLECAINIDE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission From FLECAINIDE?
Of the 7 reports, 2 (28.6%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLECAINIDE. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does FLECAINIDE Cause?
Toxicity to various agents (676)
Drug ineffective (437)
Bradycardia (327)
Electrocardiogram qrs complex prolonged (324)
Hypotension (299)
Atrial fibrillation (278)
Electrocardiogram qt prolonged (258)
Cardiac arrest (252)
Completed suicide (223)
Ventricular tachycardia (221)
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 FLECAINIDE Alternatives Have Lower Product dose omission Risk?
FLECAINIDE vs FLIBANSERIN
FLECAINIDE vs FLOLAN
FLECAINIDE vs FLUCICLOVINE F-18
FLECAINIDE vs FLUCLOXACILLIN
FLECAINIDE vs FLUCONAZOLE