Does ALPROSTADIL Cause Incorrect product storage? 18 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Incorrect product storage have been filed in association with ALPROSTADIL (Edex). This represents 0.6% of all adverse event reports for ALPROSTADIL.
18
Reports of Incorrect product storage with ALPROSTADIL
0.6%
of all ALPROSTADIL reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect product storage From ALPROSTADIL?
Of the 18 reports.
Is Incorrect product storage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 18 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 Incorrect product storage?
ETANERCEPT (2,149)
INSULIN LISPRO (1,114)
ABATACEPT (583)
TERIPARATIDE (573)
ADALIMUMAB (476)
GOLIMUMAB (392)
INSULIN GLARGINE (341)
INSULIN HUMAN (336)
USTEKINUMAB (299)
ERYTHROPOIETIN (268)
Which ALPROSTADIL Alternatives Have Lower Incorrect product storage Risk?
ALPROSTADIL vs ALTEPLASE
ALPROSTADIL vs ALTERNARIA ALTERNATA
ALPROSTADIL vs ALTHIAZIDE
ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE
ALPROSTADIL vs ALUMINUM