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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 EDETATE Cause Haemoglobin decreased? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Haemoglobin decreased have been filed in association with EDETATE (Edetate Calcium Disodium). This represents 6.2% of all adverse event reports for EDETATE.

9
Reports of Haemoglobin decreased with EDETATE
6.2%
of all EDETATE reports
6
Deaths
9
Hospitalizations

How Dangerous Is Haemoglobin decreased From EDETATE?

Of the 9 reports, 6 (66.7%) resulted in death, 9 (100.0%) required hospitalization, and 6 (66.7%) 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 EDETATE. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does EDETATE Cause?

Condition aggravated (122) Drug ineffective (93) Musculoskeletal stiffness (91) Pain in extremity (91) Arthralgia (90) Gastrointestinal toxicity (90) Hepatotoxicity (90) Joint injury (90) Musculoskeletal pain (90) Neoplasm malignant (90)

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 EDETATE Alternatives Have Lower Haemoglobin decreased Risk?

EDETATE vs EDOXABAN EDETATE vs EDOXABAN TOSILATE EDETATE vs EFALIZUMAB EDETATE vs EFANESOCTOCOG ALFA EDETATE vs EFAVIRENZ

Related Pages

EDETATE Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased EDETATE Demographics