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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 Hypersensitivity? 80 Reports in FDA Database

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

80
Reports of Hypersensitivity with MEDROXYPROGESTERONE
1.0%
of all MEDROXYPROGESTERONE reports
0
Deaths
22
Hospitalizations

How Dangerous Is Hypersensitivity From MEDROXYPROGESTERONE?

Of the 80 reports, 22 (27.5%) required hospitalization, and 13 (16.3%) were considered life-threatening.

Is Hypersensitivity Listed in the Official Label?

Yes, Hypersensitivity is listed as a known adverse reaction in the official FDA drug label for MEDROXYPROGESTERONE.

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 Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which MEDROXYPROGESTERONE Alternatives Have Lower Hypersensitivity Risk?

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

Related Pages

MEDROXYPROGESTERONE Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity MEDROXYPROGESTERONE Demographics