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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does MEDROXYPROGESTERONE Cause Device breakage? 81 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 81 reports of Device breakage have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 1.0% of all adverse event reports for MEDROXYPROGESTERONE.

81
Reports of Device breakage with MEDROXYPROGESTERONE
1.0%
of all MEDROXYPROGESTERONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Device breakage From MEDROXYPROGESTERONE?

Of the 81 reports.

Is Device breakage Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 81 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 Device breakage?

COPPER (9,201) SOMATROPIN (7,761) ETONOGESTREL (4,140) LEVONORGESTREL (2,726) ETHINYL ESTRADIOL\ETONOGESTREL (741) CARBIDOPA\LEVODOPA (634) TREPROSTINIL (396) ADALIMUMAB (375) ALBUTEROL (256) EPOPROSTENOL (240)

Which MEDROXYPROGESTERONE Alternatives Have Lower Device breakage Risk?

MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE MEDROXYPROGESTERONE vs MEFENAMIC ACID MEDROXYPROGESTERONE vs MEFLOQUINE MEDROXYPROGESTERONE vs MEGESTROL MEDROXYPROGESTERONE vs MEGLUMINE

Related Pages

MEDROXYPROGESTERONE Full Profile All Device breakage Reports All Drugs Causing Device breakage MEDROXYPROGESTERONE Demographics