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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 CEFUROXIME Cause Haemoglobin decreased? 54 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 54 reports of Haemoglobin decreased have been filed in association with CEFUROXIME (Cefuroxime sodium). This represents 1.0% of all adverse event reports for CEFUROXIME.

54
Reports of Haemoglobin decreased with CEFUROXIME
1.0%
of all CEFUROXIME reports
3
Deaths
31
Hospitalizations

How Dangerous Is Haemoglobin decreased From CEFUROXIME?

Of the 54 reports, 3 (5.6%) resulted in death, 31 (57.4%) required hospitalization, and 1 (1.9%) 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 CEFUROXIME. However, 54 reports have been filed with the FAERS database.

What Other Side Effects Does CEFUROXIME Cause?

Dyspnoea (476) Drug ineffective (386) Condition aggravated (326) Anaphylactic reaction (319) Off label use (319) Rash (303) Drug hypersensitivity (287) Pyrexia (287) Diarrhoea (259) Anaphylactic shock (234)

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 CEFUROXIME Alternatives Have Lower Haemoglobin decreased Risk?

CEFUROXIME vs CEFUROXIME AXETIL CEFUROXIME vs CELEBREX CEFUROXIME vs CELECOXIB CEFUROXIME vs CELIPROLOL CEFUROXIME vs CELLCEPT

Related Pages

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