Does MIRABEGRON Cause Maternal exposure timing unspecified? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Maternal exposure timing unspecified have been filed in association with MIRABEGRON (MIRABEGRON). This represents 0.1% of all adverse event reports for MIRABEGRON.
16
Reports of Maternal exposure timing unspecified with MIRABEGRON
0.1%
of all MIRABEGRON reports
16
Deaths
16
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From MIRABEGRON?
Of the 16 reports, 16 (100.0%) resulted in death, 16 (100.0%) required hospitalization, and 16 (100.0%) were considered life-threatening.
Is Maternal exposure timing unspecified Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIRABEGRON. However, 16 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 Maternal exposure timing unspecified?
RITUXIMAB (402)
METHOTREXATE (350)
ADALIMUMAB (343)
DICLOFENAC (331)
TOCILIZUMAB (327)
HYDROXYCHLOROQUINE (309)
FOLIC ACID (304)
INFLIXIMAB (303)
LEFLUNOMIDE (302)
SECUKINUMAB (301)
Which MIRABEGRON Alternatives Have Lower Maternal exposure timing unspecified Risk?
MIRABEGRON vs MIRALAX
MIRABEGRON vs MIRCERA
MIRABEGRON vs MIRENA
MIRABEGRON vs MIRIKIZUMAB-MRKZ
MIRABEGRON vs MIRTAZAPINE