Does MIRABEGRON Cause Intentional product use issue? 917 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 917 reports of Intentional product use issue have been filed in association with MIRABEGRON (MIRABEGRON). This represents 4.5% of all adverse event reports for MIRABEGRON.
917
Reports of Intentional product use issue with MIRABEGRON
4.5%
of all MIRABEGRON reports
478
Deaths
404
Hospitalizations
How Dangerous Is Intentional product use issue From MIRABEGRON?
Of the 917 reports, 478 (52.1%) resulted in death, 404 (44.1%) required hospitalization, and 403 (43.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIRABEGRON. However, 917 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 product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which MIRABEGRON Alternatives Have Lower Intentional product use issue Risk?
MIRABEGRON vs MIRALAX
MIRABEGRON vs MIRCERA
MIRABEGRON vs MIRENA
MIRABEGRON vs MIRIKIZUMAB-MRKZ
MIRABEGRON vs MIRTAZAPINE