Does TOPOTECAN Cause Haemoglobin decreased? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Haemoglobin decreased have been filed in association with TOPOTECAN (HYCAMTIN). This represents 1.2% of all adverse event reports for TOPOTECAN.
43
Reports of Haemoglobin decreased with TOPOTECAN
1.2%
of all TOPOTECAN reports
4
Deaths
32
Hospitalizations
How Dangerous Is Haemoglobin decreased From TOPOTECAN?
Of the 43 reports, 4 (9.3%) resulted in death, 32 (74.4%) required hospitalization, and 6 (14.0%) 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 TOPOTECAN. However, 43 reports have been filed with the FAERS database.
What Other Side Effects Does TOPOTECAN Cause?
Febrile neutropenia (425)
Off label use (390)
Death (332)
Product use in unapproved indication (323)
Neutropenia (255)
Pyrexia (252)
Anaemia (242)
Malignant neoplasm progression (238)
Drug ineffective (216)
Disease progression (207)
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 TOPOTECAN Alternatives Have Lower Haemoglobin decreased Risk?
TOPOTECAN vs TOPOTECAN\TOPOTECAN
TOPOTECAN vs TOPROL
TOPOTECAN vs TOREMIFENE
TOPOTECAN vs TORIPALIMAB
TOPOTECAN vs TORSEMIDE