Does MIRABEGRON Cause Incorrect product administration duration? 55 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 55 reports of Incorrect product administration duration have been filed in association with MIRABEGRON (MIRABEGRON). This represents 0.3% of all adverse event reports for MIRABEGRON.
55
Reports of Incorrect product administration duration with MIRABEGRON
0.3%
of all MIRABEGRON reports
55
Deaths
54
Hospitalizations
How Dangerous Is Incorrect product administration duration From MIRABEGRON?
Of the 55 reports, 55 (100.0%) resulted in death, 54 (98.2%) required hospitalization, and 54 (98.2%) were considered life-threatening.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIRABEGRON. However, 55 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which MIRABEGRON Alternatives Have Lower Incorrect product administration duration Risk?
MIRABEGRON vs MIRALAX
MIRABEGRON vs MIRCERA
MIRABEGRON vs MIRENA
MIRABEGRON vs MIRIKIZUMAB-MRKZ
MIRABEGRON vs MIRTAZAPINE