Does MEDROXYPROGESTERONE Cause Incorrect dose administered by device? 410 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 410 reports of Incorrect dose administered by device have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 4.9% of all adverse event reports for MEDROXYPROGESTERONE.
410
Reports of Incorrect dose administered by device with MEDROXYPROGESTERONE
4.9%
of all MEDROXYPROGESTERONE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Incorrect dose administered by device From MEDROXYPROGESTERONE?
Of the 410 reports.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 410 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)
Drug ineffective (403)
Off label use (390)
Syringe issue (354)
Needle issue (346)
Headache (288)
Device occlusion (284)
Device issue (243)
What Other Drugs Cause Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which MEDROXYPROGESTERONE Alternatives Have Lower Incorrect dose administered by device Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE