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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ALPROSTADIL Cause Device defective? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Device defective have been filed in association with ALPROSTADIL (Edex). This represents 0.3% of all adverse event reports for ALPROSTADIL.

9
Reports of Device defective with ALPROSTADIL
0.3%
of all ALPROSTADIL reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device defective From ALPROSTADIL?

Of the 9 reports.

Is Device defective Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 9 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 Device defective?

SOMATROPIN (1,719) USTEKINUMAB (1,071) SECUKINUMAB (666) GUSELKUMAB (574) GOLIMUMAB (539) ABATACEPT (458) ALBUTEROL (445) TOCILIZUMAB (400) INSULIN GLARGINE (397) EXENATIDE (387)

Which ALPROSTADIL Alternatives Have Lower Device defective Risk?

ALPROSTADIL vs ALTEPLASE ALPROSTADIL vs ALTERNARIA ALTERNATA ALPROSTADIL vs ALTHIAZIDE ALPROSTADIL vs ALTHIAZIDE\SPIRONOLACTONE ALPROSTADIL vs ALUMINUM

Related Pages

ALPROSTADIL Full Profile All Device defective Reports All Drugs Causing Device defective ALPROSTADIL Demographics