Does MEDROXYPROGESTERONE Cause Product use issue? 151 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 151 reports of Product use issue have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 1.8% of all adverse event reports for MEDROXYPROGESTERONE.
151
Reports of Product use issue with MEDROXYPROGESTERONE
1.8%
of all MEDROXYPROGESTERONE reports
2
Deaths
18
Hospitalizations
How Dangerous Is Product use issue From MEDROXYPROGESTERONE?
Of the 151 reports, 2 (1.3%) resulted in death, 18 (11.9%) required hospitalization, and 6 (4.0%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 151 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which MEDROXYPROGESTERONE Alternatives Have Lower Product use issue Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE