Does ALPROSTADIL Cause Product administration error? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Product administration error have been filed in association with ALPROSTADIL (Edex). This represents 0.4% of all adverse event reports for ALPROSTADIL.
12
Reports of Product administration error with ALPROSTADIL
0.4%
of all ALPROSTADIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Product administration error From ALPROSTADIL?
Of the 12 reports, and 1 (8.3%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does ALPROSTADIL Cause?
Drug ineffective (1,412)
Wrong technique in product usage process (510)
Product quality issue (227)
Penile pain (164)
Off label use (112)
Penile burning sensation (92)
Erection increased (75)
Penile haemorrhage (62)
No adverse event (60)
Injection site pain (57)
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 ALPROSTADIL Alternatives Have Lower Product administration error Risk?
ALPROSTADIL vs ALTEPLASE
ALPROSTADIL vs ALTERNARIA ALTERNATA
ALPROSTADIL vs ALTHIAZIDE
ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE
ALPROSTADIL vs ALUMINUM