Does SOLIFENACIN Cause Product dose omission? 28 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 28 reports of Product dose omission have been filed in association with SOLIFENACIN (solifenacin succinate). This represents 0.3% of all adverse event reports for SOLIFENACIN.
28
Reports of Product dose omission with SOLIFENACIN
0.3%
of all SOLIFENACIN reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From SOLIFENACIN?
Of the 28 reports, 1 (3.6%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIFENACIN. However, 28 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 Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which SOLIFENACIN Alternatives Have Lower Product dose omission Risk?
SOLIFENACIN vs SOLIRIS
SOLIFENACIN vs SOLOSTAR
SOLIFENACIN vs SOLRIAMFETOL
SOLIFENACIN vs SOLU-MEDROL
SOLIFENACIN vs SOMATREM