Does MEDROXYPROGESTERONE Cause Product administration error? 187 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 187 reports of Product administration error have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 2.2% of all adverse event reports for MEDROXYPROGESTERONE.
187
Reports of Product administration error with MEDROXYPROGESTERONE
2.2%
of all MEDROXYPROGESTERONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From MEDROXYPROGESTERONE?
Of the 187 reports, 2 (1.1%) required hospitalization, and 1 (0.5%) were considered life-threatening.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 187 reports have been filed with the FAERS database.
What Other Side Effects Does MEDROXYPROGESTERONE Cause?
Meningioma (1,364)
Drug dose omission by device (510)
Device leakage (500)
Incorrect dose administered by device (410)
Drug ineffective (403)
Off label use (390)
Syringe issue (354)
Needle issue (346)
Headache (288)
Device occlusion (284)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which MEDROXYPROGESTERONE Alternatives Have Lower Product administration error Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE