Does MEDROXYPROGESTERONE Cause Drug dose omission by device? 510 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 510 reports of Drug dose omission by device have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 6.1% of all adverse event reports for MEDROXYPROGESTERONE.
510
Reports of Drug dose omission by device with MEDROXYPROGESTERONE
6.1%
of all MEDROXYPROGESTERONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Drug dose omission by device From MEDROXYPROGESTERONE?
Of the 510 reports, 1 (0.2%) required hospitalization.
Is Drug dose omission by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 510 reports have been filed with the FAERS database.
What Other Side Effects Does MEDROXYPROGESTERONE Cause?
Meningioma (1,364)
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)
Device issue (243)
What Other Drugs Cause Drug dose omission by device?
EVOLOCUMAB (23,957)
SOMATROPIN (15,921)
ALBUTEROL (8,162)
ERENUMAB-AOOE (6,340)
ETANERCEPT (2,420)
PEGFILGRASTIM (2,051)
EXENATIDE (983)
SECUKINUMAB (621)
BUDESONIDE\FORMOTEROL (521)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (427)
Which MEDROXYPROGESTERONE Alternatives Have Lower Drug dose omission by device Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE