Does VIBEGRON Cause Inappropriate schedule of product administration? 111 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 111 reports of Inappropriate schedule of product administration have been filed in association with VIBEGRON (GEMTESA). This represents 2.4% of all adverse event reports for VIBEGRON.
111
Reports of Inappropriate schedule of product administration with VIBEGRON
2.4%
of all VIBEGRON reports
0
Deaths
5
Hospitalizations
How Dangerous Is Inappropriate schedule of product administration From VIBEGRON?
Of the 111 reports, 5 (4.5%) required hospitalization.
Is Inappropriate schedule of product administration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VIBEGRON. However, 111 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 Inappropriate schedule of product administration?
ADAPALENE (16,473)
DUPILUMAB (14,927)
AVOBENZONE\OCTISALATE\OCTOCRYLENE (12,546)
INSULIN GLARGINE (8,982)
INFLIXIMAB (6,847)
INFLIXIMAB-DYYB (5,977)
SECUKINUMAB (4,817)
DULAGLUTIDE (3,606)
VEDOLIZUMAB (3,259)
SACUBITRIL\VALSARTAN (2,870)
Which VIBEGRON Alternatives Have Lower Inappropriate schedule of product administration Risk?
VIBEGRON vs VICODIN
VIBEGRON vs VICTOZA
VIBEGRON vs VICTRELIS
VIBEGRON vs VIDAZA
VIBEGRON vs VIGABATRIN