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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 SUTENT Cause Haemoglobin decreased? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Haemoglobin decreased have been filed in association with SUTENT. This represents 1.0% of all adverse event reports for SUTENT.

12
Reports of Haemoglobin decreased with SUTENT
1.0%
of all SUTENT reports
3
Deaths
7
Hospitalizations

How Dangerous Is Haemoglobin decreased From SUTENT?

Of the 12 reports, 3 (25.0%) resulted in death, 7 (58.3%) required hospitalization, and 2 (16.7%) 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 SUTENT. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does SUTENT Cause?

Disease progression (226) Death (225) Diarrhoea (164) Fatigue (140) Nausea (119) Decreased appetite (78) Vomiting (73) Asthenia (67) Oral pain (66) Dysgeusia (63)

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 SUTENT Alternatives Have Lower Haemoglobin decreased Risk?

SUTENT vs SUTIMLIMAB-JOME SUTENT vs SUVOREXANT SUTENT vs SUZETRIGINE SUTENT vs SYMBICORT SUTENT vs SYNAGIS

Related Pages

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