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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 Poor quality device used? 80 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 80 reports of Poor quality device used have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 1.0% of all adverse event reports for MEDROXYPROGESTERONE.

80
Reports of Poor quality device used with MEDROXYPROGESTERONE
1.0%
of all MEDROXYPROGESTERONE reports
0
Deaths
0
Hospitalizations

How Dangerous Is Poor quality device used From MEDROXYPROGESTERONE?

Of the 80 reports.

Is Poor quality device used Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 80 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 Poor quality device used?

SOMATROPIN (3,162) MOMETASONE FUROATE (2,159) ALBUTEROL (1,251) FORMOTEROL\MOMETASONE FUROATE (1,091) ETHINYL ESTRADIOL\ETONOGESTREL (77) FOLLITROPIN (58) ETONOGESTREL (55) ETANERCEPT (46) ESTRADIOL (41) PEGFILGRASTIM (38)

Which MEDROXYPROGESTERONE Alternatives Have Lower Poor quality device used Risk?

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

Related Pages

MEDROXYPROGESTERONE Full Profile All Poor quality device used Reports All Drugs Causing Poor quality device used MEDROXYPROGESTERONE Demographics