Does FINASTERIDE Cause Product administration error? 8 Reports in FDA Database
Prostate Health & Male Vitality — Naturally
ProstaVive: better flow, better sleep, better energy. 180-day guarantee.
According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product administration error have been filed in association with FINASTERIDE (Finasteride). This represents 0.1% of all adverse event reports for FINASTERIDE.
8
Reports of Product administration error with FINASTERIDE
0.1%
of all FINASTERIDE reports
3
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From FINASTERIDE?
Of the 8 reports, 3 (37.5%) resulted in death, 2 (25.0%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FINASTERIDE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does FINASTERIDE Cause?
Erectile dysfunction (3,043)
Depression (2,530)
Anxiety (1,921)
Adverse drug reaction (1,902)
Sexual dysfunction (1,757)
Adverse event (1,399)
Loss of libido (1,353)
Suicidal ideation (1,301)
Insomnia (1,202)
Fatigue (1,184)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which FINASTERIDE Alternatives Have Lower Product administration error Risk?
FINASTERIDE vs FINASTERIDE\TAMSULOSIN
FINASTERIDE vs FINERENONE
FINASTERIDE vs FINGOLIMOD
FINASTERIDE vs FINGOLIMOD LAURYL
FINASTERIDE vs FISH OIL