Does FLECAINIDE Cause Wrong technique in product usage process? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Wrong technique in product usage process have been filed in association with FLECAINIDE (Flecainide Acetate). This represents 0.2% of all adverse event reports for FLECAINIDE.
7
Reports of Wrong technique in product usage process with FLECAINIDE
0.2%
of all FLECAINIDE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FLECAINIDE?
Of the 7 reports, 4 (57.1%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Wrong technique in product usage process 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which FLECAINIDE Alternatives Have Lower Wrong technique in product usage process Risk?
FLECAINIDE vs FLIBANSERIN
FLECAINIDE vs FLOLAN
FLECAINIDE vs FLUCICLOVINE F-18
FLECAINIDE vs FLUCLOXACILLIN
FLECAINIDE vs FLUCONAZOLE