Does MIFEPRISTONE Cause Wrong technique in product usage process? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Wrong technique in product usage process have been filed in association with MIFEPRISTONE (Mifepristone). This represents 0.2% of all adverse event reports for MIFEPRISTONE.
11
Reports of Wrong technique in product usage process with MIFEPRISTONE
0.2%
of all MIFEPRISTONE reports
2
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in product usage process From MIFEPRISTONE?
Of the 11 reports, 2 (18.2%) resulted in death, 3 (27.3%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MIFEPRISTONE. However, 11 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which MIFEPRISTONE Alternatives Have Lower Wrong technique in product usage process Risk?
MIFEPRISTONE vs MIGALASTAT
MIFEPRISTONE vs MIGLITOL
MIFEPRISTONE vs MIGLUSTAT
MIFEPRISTONE vs MILNACIPRAN
MIFEPRISTONE vs MILRINONE