Does MIRABEGRON Cause Intentional dose omission? 22 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 22 reports of Intentional dose omission have been filed in association with MIRABEGRON (MIRABEGRON). This represents 0.1% of all adverse event reports for MIRABEGRON.
22
Reports of Intentional dose omission with MIRABEGRON
0.1%
of all MIRABEGRON reports
0
Deaths
7
Hospitalizations
How Dangerous Is Intentional dose omission From MIRABEGRON?
Of the 22 reports, 7 (31.8%) required hospitalization.
Is Intentional dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIRABEGRON. However, 22 reports have been filed with the FAERS database.
What Other Side Effects Does MIRABEGRON Cause?
Drug ineffective (4,151)
Off label use (1,704)
Intentional product misuse (1,416)
Dizziness (1,297)
Headache (1,288)
Blood pressure increased (1,100)
Hypertension (1,057)
Dry mouth (1,034)
Diarrhoea (921)
Pain (921)
What Other Drugs Cause Intentional dose omission?
DUPILUMAB (2,269)
CERTOLIZUMAB PEGOL (1,253)
ADALIMUMAB (845)
TOFACITINIB (845)
INFLIXIMAB (815)
ABALOPARATIDE (623)
ETANERCEPT (615)
AMBRISENTAN (595)
SODIUM OXYBATE (580)
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (518)
Which MIRABEGRON Alternatives Have Lower Intentional dose omission Risk?
MIRABEGRON vs MIRALAX
MIRABEGRON vs MIRCERA
MIRABEGRON vs MIRENA
MIRABEGRON vs MIRIKIZUMAB-MRKZ
MIRABEGRON vs MIRTAZAPINE