Does SILDENAFIL Cause Product dose omission in error? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Product dose omission in error have been filed in association with SILDENAFIL (Sildenafil). This represents 0.1% of all adverse event reports for SILDENAFIL.
22
Reports of Product dose omission in error with SILDENAFIL
0.1%
of all SILDENAFIL reports
4
Deaths
12
Hospitalizations
How Dangerous Is Product dose omission in error From SILDENAFIL?
Of the 22 reports, 4 (18.2%) resulted in death, 12 (54.5%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SILDENAFIL. However, 22 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 in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which SILDENAFIL Alternatives Have Lower Product dose omission in error Risk?
SILDENAFIL vs SILODOSIN
SILDENAFIL vs SILTUXIMAB
SILDENAFIL vs SILVER SULFADIAZINE
SILDENAFIL vs SIMEPREVIR
SILDENAFIL vs SIMPONI