Does MIFEPRISTONE Cause Maternal exposure timing unspecified? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Maternal exposure timing unspecified have been filed in association with MIFEPRISTONE (Mifepristone). This represents 0.2% of all adverse event reports for MIFEPRISTONE.
10
Reports of Maternal exposure timing unspecified with MIFEPRISTONE
0.2%
of all MIFEPRISTONE reports
6
Deaths
5
Hospitalizations
How Dangerous Is Maternal exposure timing unspecified From MIFEPRISTONE?
Of the 10 reports, 6 (60.0%) resulted in death, 5 (50.0%) required hospitalization, and 1 (10.0%) 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 MIFEPRISTONE. However, 10 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 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 MIFEPRISTONE Alternatives Have Lower Maternal exposure timing unspecified Risk?
MIFEPRISTONE vs MIGALASTAT
MIFEPRISTONE vs MIGLITOL
MIFEPRISTONE vs MIGLUSTAT
MIFEPRISTONE vs MILNACIPRAN
MIFEPRISTONE vs MILRINONE