Does MEDROXYPROGESTERONE Cause Wrong technique in product usage process? 39 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 39 reports of Wrong technique in product usage process have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.5% of all adverse event reports for MEDROXYPROGESTERONE.
39
Reports of Wrong technique in product usage process with MEDROXYPROGESTERONE
0.5%
of all MEDROXYPROGESTERONE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Wrong technique in product usage process From MEDROXYPROGESTERONE?
Of the 39 reports, 3 (7.7%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 39 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which MEDROXYPROGESTERONE Alternatives Have Lower Wrong technique in product usage process Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE