Does MIFEPRISTONE Cause Product dose omission? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product dose omission have been filed in association with MIFEPRISTONE (Mifepristone). This represents 0.2% of all adverse event reports for MIFEPRISTONE.
8
Reports of Product dose omission with MIFEPRISTONE
0.2%
of all MIFEPRISTONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From MIFEPRISTONE?
Of the 8 reports, 3 (37.5%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIFEPRISTONE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does MIFEPRISTONE Cause?
Nausea (709)
Fatigue (627)
Abortion incomplete (533)
Haemorrhage (527)
Blood potassium decreased (411)
Vomiting (376)
Dizziness (375)
Headache (365)
Pain (314)
Blood pressure increased (311)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which MIFEPRISTONE Alternatives Have Lower Product dose omission Risk?
MIFEPRISTONE vs MIGALASTAT
MIFEPRISTONE vs MIGLITOL
MIFEPRISTONE vs MIGLUSTAT
MIFEPRISTONE vs MILNACIPRAN
MIFEPRISTONE vs MILRINONE