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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 SILODOSIN Cause Wrong patient received product? 11 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Wrong patient received product have been filed in association with SILODOSIN (Silodosin). This represents 0.6% of all adverse event reports for SILODOSIN.

11
Reports of Wrong patient received product with SILODOSIN
0.6%
of all SILODOSIN reports
0
Deaths
10
Hospitalizations

How Dangerous Is Wrong patient received product From SILODOSIN?

Of the 11 reports, 10 (90.9%) required hospitalization.

Is Wrong patient received product Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for SILODOSIN. However, 11 reports have been filed with the FAERS database.

What Other Side Effects Does SILODOSIN Cause?

Dizziness (104) Drug ineffective (104) Off label use (98) Acute kidney injury (93) Erectile dysfunction (80) Dyspnoea (79) Fall (75) Urinary retention (54) Hypotension (52) Reversible airways obstruction (52)

What Other Drugs Cause Wrong patient received product?

INSULIN LISPRO (334) CLOZAPINE (198) RISPERIDONE (176) OXAZEPAM (152) BISOPROLOL (150) LEVETIRACETAM (126) ACETAMINOPHEN (123) METFORMIN (116) INSULIN GLARGINE (114) CLONAZEPAM (112)

Which SILODOSIN Alternatives Have Lower Wrong patient received product Risk?

SILODOSIN vs SILTUXIMAB SILODOSIN vs SILVER SULFADIAZINE SILODOSIN vs SIMEPREVIR SILODOSIN vs SIMPONI SILODOSIN vs SIMVASTATIN

Related Pages

SILODOSIN Full Profile All Wrong patient received product Reports All Drugs Causing Wrong patient received product SILODOSIN Demographics