Does MEDROXYPROGESTERONE Cause Haemoglobin decreased? 48 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 48 reports of Haemoglobin decreased have been filed in association with MEDROXYPROGESTERONE (Provera). This represents 0.6% of all adverse event reports for MEDROXYPROGESTERONE.
48
Reports of Haemoglobin decreased with MEDROXYPROGESTERONE
0.6%
of all MEDROXYPROGESTERONE reports
0
Deaths
23
Hospitalizations
How Dangerous Is Haemoglobin decreased From MEDROXYPROGESTERONE?
Of the 48 reports, 23 (47.9%) required hospitalization, and 11 (22.9%) were considered life-threatening.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MEDROXYPROGESTERONE. However, 48 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 Haemoglobin decreased?
LENALIDOMIDE (4,031)
RUXOLITINIB (3,297)
ECULIZUMAB (3,028)
ADALIMUMAB (2,459)
CLOZAPINE (2,396)
RITUXIMAB (1,803)
APIXABAN (1,779)
NIRAPARIB (1,759)
METHOTREXATE (1,754)
RIBAVIRIN (1,753)
Which MEDROXYPROGESTERONE Alternatives Have Lower Haemoglobin decreased Risk?
MEDROXYPROGESTERONE vs MEDROXYPROGESTERONE\MEDROXYPROGESTERONE
MEDROXYPROGESTERONE vs MEFENAMIC ACID
MEDROXYPROGESTERONE vs MEFLOQUINE
MEDROXYPROGESTERONE vs MEGESTROL
MEDROXYPROGESTERONE vs MEGLUMINE