Does MEDROXYPROGESTERONE Cause Device occlusion? 284 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 284 reports of Device occlusion have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 3.4% of all adverse event reports for MEDROXYPROGESTERONE.
284
Reports of Device occlusion with MEDROXYPROGESTERONE
3.4%
of all MEDROXYPROGESTERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Device occlusion From MEDROXYPROGESTERONE?
Of the 284 reports.
Is Device occlusion Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 284 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 issue (243)
What Other Drugs Cause Device occlusion?
PEGFILGRASTIM (3,239)
CARBIDOPA\LEVODOPA (1,464)
SOMATROPIN (823)
LEUPROLIDE (786)
EPOPROSTENOL (580)
TREPROSTINIL (458)
ALBUTEROL (431)
BACLOFEN (254)
LEVODOPA (224)
RISPERIDONE (182)
Which MEDROXYPROGESTERONE Alternatives Have Lower Device occlusion Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE