Does MEDROXYPROGESTERONE Cause Condition aggravated? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Condition aggravated have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 1.1% of all adverse event reports for MEDROXYPROGESTERONE.
90
Reports of Condition aggravated with MEDROXYPROGESTERONE
1.1%
of all MEDROXYPROGESTERONE reports
0
Deaths
24
Hospitalizations
How Dangerous Is Condition aggravated From MEDROXYPROGESTERONE?
Of the 90 reports, 24 (26.7%) required hospitalization, and 2 (2.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 90 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which MEDROXYPROGESTERONE Alternatives Have Lower Condition aggravated Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE