Does MEDROXYPROGESTERONE Cause Device defective? 78 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 78 reports of Device defective have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.9% of all adverse event reports for MEDROXYPROGESTERONE.
78
Reports of Device defective with MEDROXYPROGESTERONE
0.9%
of all MEDROXYPROGESTERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device defective From MEDROXYPROGESTERONE?
Of the 78 reports.
Is Device defective Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 78 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 Device defective?
SOMATROPIN (1,719)
USTEKINUMAB (1,071)
SECUKINUMAB (666)
GUSELKUMAB (574)
GOLIMUMAB (539)
ABATACEPT (458)
ALBUTEROL (445)
TOCILIZUMAB (400)
INSULIN GLARGINE (397)
EXENATIDE (387)
Which MEDROXYPROGESTERONE Alternatives Have Lower Device defective Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE