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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 DACOMITINIB Cause Haemoglobin decreased? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Haemoglobin decreased have been filed in association with DACOMITINIB (Vizimpro). This represents 3.4% of all adverse event reports for DACOMITINIB.

23
Reports of Haemoglobin decreased with DACOMITINIB
3.4%
of all DACOMITINIB reports
5
Deaths
6
Hospitalizations

How Dangerous Is Haemoglobin decreased From DACOMITINIB?

Of the 23 reports, 5 (21.7%) resulted in death, 6 (26.1%) required hospitalization, and 2 (8.7%) 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 DACOMITINIB. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does DACOMITINIB Cause?

Death (253) Diarrhoea (114) Rash (108) Neoplasm progression (78) Paronychia (55) Blood pressure increased (47) Off label use (35) Pruritus (34) Dyspnoea (30) Carcinoembryonic antigen increased (28)

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 DACOMITINIB Alternatives Have Lower Haemoglobin decreased Risk?

DACOMITINIB vs DACTINOMYCIN DACOMITINIB vs DALBAVANCIN DACOMITINIB vs DALFAMPRIDINE DACOMITINIB vs DALTEPARIN DACOMITINIB vs DAMOCTOCOG ALFA PEGOL

Related Pages

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