Does MEDROXYPROGESTERONE Cause Product complaint? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product complaint have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.2% of all adverse event reports for MEDROXYPROGESTERONE.
20
Reports of Product complaint with MEDROXYPROGESTERONE
0.2%
of all MEDROXYPROGESTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product complaint From MEDROXYPROGESTERONE?
Of the 20 reports, 1 (5.0%) required hospitalization, and 1 (5.0%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 20 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which MEDROXYPROGESTERONE Alternatives Have Lower Product complaint Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE