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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 ENTRECTINIB Cause Haemoglobin decreased? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Haemoglobin decreased have been filed in association with ENTRECTINIB (Rozlytrek). This represents 0.3% of all adverse event reports for ENTRECTINIB.

5
Reports of Haemoglobin decreased with ENTRECTINIB
0.3%
of all ENTRECTINIB reports
1
Deaths
2
Hospitalizations

How Dangerous Is Haemoglobin decreased From ENTRECTINIB?

Of the 5 reports, 1 (20.0%) resulted in death, 2 (40.0%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ENTRECTINIB. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does ENTRECTINIB Cause?

Dizziness (143) Off label use (137) Death (126) Disease progression (105) Taste disorder (68) No adverse event (65) Constipation (60) Fatigue (60) Drug ineffective (58) Blood creatinine increased (57)

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 ENTRECTINIB Alternatives Have Lower Haemoglobin decreased Risk?

ENTRECTINIB vs ENZALUTAMIDE ENTRECTINIB vs EPCORITAMAB ENTRECTINIB vs EPCORITAMAB-BYSP ENTRECTINIB vs EPERISONE ENTRECTINIB vs EPHEDRINE

Related Pages

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