Does VIBEGRON Cause Wrong technique in product usage process? 50 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 50 reports of Wrong technique in product usage process have been filed in association with VIBEGRON (GEMTESA). This represents 1.1% of all adverse event reports for VIBEGRON.
50
Reports of Wrong technique in product usage process with VIBEGRON
1.1%
of all VIBEGRON reports
1
Deaths
1
Hospitalizations
How Dangerous Is Wrong technique in product usage process From VIBEGRON?
Of the 50 reports, 1 (2.0%) resulted in death, 1 (2.0%) 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 VIBEGRON. However, 50 reports have been filed with the FAERS database.
What Other Side Effects Does VIBEGRON Cause?
Drug ineffective (732)
Inability to afford medication (267)
Urinary retention (223)
Headache (218)
Diarrhoea (215)
Urinary tract infection (184)
Pollakiuria (171)
Therapeutic product effect incomplete (167)
Urinary incontinence (166)
Product availability issue (164)
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 VIBEGRON Alternatives Have Lower Wrong technique in product usage process Risk?
VIBEGRON vs VICODIN
VIBEGRON vs VICTOZA
VIBEGRON vs VICTRELIS
VIBEGRON vs VIDAZA
VIBEGRON vs VIGABATRIN