Does MEDROXYPROGESTERONE Cause Intentional product misuse? 32 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 32 reports of Intentional product misuse have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.4% of all adverse event reports for MEDROXYPROGESTERONE.
32
Reports of Intentional product misuse with MEDROXYPROGESTERONE
0.4%
of all MEDROXYPROGESTERONE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Intentional product misuse From MEDROXYPROGESTERONE?
Of the 32 reports, 13 (40.6%) required hospitalization, and 1 (3.1%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 32 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which MEDROXYPROGESTERONE Alternatives Have Lower Intentional product misuse Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE