Does SILDENAFIL Cause Product dose omission? 113 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 113 reports of Product dose omission have been filed in association with SILDENAFIL (Sildenafil). This represents 0.3% of all adverse event reports for SILDENAFIL.
113
Reports of Product dose omission with SILDENAFIL
0.3%
of all SILDENAFIL reports
7
Deaths
56
Hospitalizations
How Dangerous Is Product dose omission From SILDENAFIL?
Of the 113 reports, 7 (6.2%) resulted in death, 56 (49.6%) required hospitalization, and 1 (0.9%) 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 SILDENAFIL. However, 113 reports have been filed with the FAERS database.
What Other Side Effects Does SILDENAFIL Cause?
Drug ineffective (6,289)
Death (2,820)
Headache (2,096)
Dyspnoea (2,023)
Erection increased (1,683)
Off label use (1,464)
Malignant melanoma (1,248)
Malaise (1,044)
Product use issue (1,039)
Dizziness (985)
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 SILDENAFIL Alternatives Have Lower Product dose omission Risk?
SILDENAFIL vs SILODOSIN
SILDENAFIL vs SILTUXIMAB
SILDENAFIL vs SILVER SULFADIAZINE
SILDENAFIL vs SIMEPREVIR
SILDENAFIL vs SIMPONI