Does MEDROXYPROGESTERONE Cause Incorrect product administration duration? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Incorrect product administration duration have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.1% of all adverse event reports for MEDROXYPROGESTERONE.
8
Reports of Incorrect product administration duration with MEDROXYPROGESTERONE
0.1%
of all MEDROXYPROGESTERONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect product administration duration From MEDROXYPROGESTERONE?
Of the 8 reports, 2 (25.0%) required hospitalization, and 2 (25.0%) 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 MEDROXYPROGESTERONE. However, 8 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 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 MEDROXYPROGESTERONE Alternatives Have Lower Incorrect product administration duration Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE