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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 SOLIFENACIN Cause Wrong patient received product? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Wrong patient received product have been filed in association with SOLIFENACIN (solifenacin succinate). This represents 0.1% of all adverse event reports for SOLIFENACIN.

8
Reports of Wrong patient received product with SOLIFENACIN
0.1%
of all SOLIFENACIN reports
0
Deaths
6
Hospitalizations

How Dangerous Is Wrong patient received product From SOLIFENACIN?

Of the 8 reports, 6 (75.0%) 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 SOLIFENACIN. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does SOLIFENACIN Cause?

Drug ineffective (1,654) Dry mouth (854) Constipation (651) Off label use (522) Dizziness (300) Vision blurred (290) Fall (269) Urinary retention (262) Fatigue (247) Urinary incontinence (246)

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 SOLIFENACIN Alternatives Have Lower Wrong patient received product Risk?

SOLIFENACIN vs SOLIRIS SOLIFENACIN vs SOLOSTAR SOLIFENACIN vs SOLRIAMFETOL SOLIFENACIN vs SOLU-MEDROL SOLIFENACIN vs SOMATREM

Related Pages

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