Does MEDROXYPROGESTERONE Cause Device issue? 243 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 243 reports of Device issue have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 2.9% of all adverse event reports for MEDROXYPROGESTERONE.
243
Reports of Device issue with MEDROXYPROGESTERONE
2.9%
of all MEDROXYPROGESTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Device issue From MEDROXYPROGESTERONE?
Of the 243 reports, 1 (0.4%) required hospitalization.
Is Device issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 243 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 issue?
ADALIMUMAB (17,630)
SOMATROPIN (5,131)
PEGFILGRASTIM (5,071)
ETANERCEPT (4,143)
INSULIN GLARGINE (3,175)
EXENATIDE (2,862)
LEVONORGESTREL (2,623)
CARBIDOPA\LEVODOPA (2,574)
GOLIMUMAB (1,827)
USTEKINUMAB (1,716)
Which MEDROXYPROGESTERONE Alternatives Have Lower Device issue Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE