Does SOLIFENACIN Cause Wrong technique in product usage process? 156 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 156 reports of Wrong technique in product usage process have been filed in association with SOLIFENACIN (solifenacin succinate). This represents 1.9% of all adverse event reports for SOLIFENACIN.
156
Reports of Wrong technique in product usage process with SOLIFENACIN
1.9%
of all SOLIFENACIN reports
3
Deaths
6
Hospitalizations
How Dangerous Is Wrong technique in product usage process From SOLIFENACIN?
Of the 156 reports, 3 (1.9%) resulted in death, 6 (3.8%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SOLIFENACIN. However, 156 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 technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which SOLIFENACIN Alternatives Have Lower Wrong technique in product usage process Risk?
SOLIFENACIN vs SOLIRIS
SOLIFENACIN vs SOLOSTAR
SOLIFENACIN vs SOLRIAMFETOL
SOLIFENACIN vs SOLU-MEDROL
SOLIFENACIN vs SOMATREM