Does TUCATINIB Cause Haemoglobin decreased? 51 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 51 reports of Haemoglobin decreased have been filed in association with TUCATINIB (TUKYSA). This represents 0.8% of all adverse event reports for TUCATINIB.
51
Reports of Haemoglobin decreased with TUCATINIB
0.8%
of all TUCATINIB reports
3
Deaths
19
Hospitalizations
How Dangerous Is Haemoglobin decreased From TUCATINIB?
Of the 51 reports, 3 (5.9%) resulted in death, 19 (37.3%) required hospitalization.
Is Haemoglobin decreased Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for TUCATINIB. However, 51 reports have been filed with the FAERS database.
What Other Side Effects Does TUCATINIB Cause?
Diarrhoea (1,587)
Nausea (862)
Fatigue (843)
Vomiting (483)
Death (400)
Off label use (392)
Malignant neoplasm progression (361)
Palmar-plantar erythrodysaesthesia syndrome (355)
Product dose omission issue (332)
Asthenia (322)
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 TUCATINIB Alternatives Have Lower Haemoglobin decreased Risk?
TUCATINIB vs TUCIDINOSTAT
TUCATINIB vs TYKERB
TUCATINIB vs TYLENOL
TUCATINIB vs TYROTHRICIN
TUCATINIB vs TYSABRI