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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 Expired product administered? 52 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Expired product administered have been filed in association with ALPROSTADIL (Edex). This represents 1.9% of all adverse event reports for ALPROSTADIL.

52
Reports of Expired product administered with ALPROSTADIL
1.9%
of all ALPROSTADIL reports
0
Deaths
3
Hospitalizations

How Dangerous Is Expired product administered From ALPROSTADIL?

Of the 52 reports, 3 (5.8%) required hospitalization.

Is Expired product administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ALPROSTADIL. However, 52 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 Expired product administered?

POLYETHYLENE GLYCOL 3350 (1,637) NAPROXEN (1,305) ALBUTEROL (1,233) LORATADINE (1,095) MINOXIDIL (982) ACETAMINOPHEN (797) INSULIN LISPRO (770) FLUTICASONE\SALMETEROL (753) CETIRIZINE (714) DICLOFENAC (714)

Which ALPROSTADIL Alternatives Have Lower Expired product administered Risk?

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

Related Pages

ALPROSTADIL Full Profile All Expired product administered Reports All Drugs Causing Expired product administered ALPROSTADIL Demographics