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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 Product quality issue? 102 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 102 reports of Product quality issue have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 1.2% of all adverse event reports for MEDROXYPROGESTERONE.

102
Reports of Product quality issue with MEDROXYPROGESTERONE
1.2%
of all MEDROXYPROGESTERONE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product quality issue From MEDROXYPROGESTERONE?

Of the 102 reports, 3 (2.9%) required hospitalization, and 2 (2.0%) were considered life-threatening.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 102 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 Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Which MEDROXYPROGESTERONE Alternatives Have Lower Product quality issue Risk?

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

Related Pages

MEDROXYPROGESTERONE Full Profile All Product quality issue Reports All Drugs Causing Product quality issue MEDROXYPROGESTERONE Demographics