Does REPOTRECTINIB Cause Anaemia? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Anaemia have been filed in association with REPOTRECTINIB (Augtyro). This represents 3.7% of all adverse event reports for REPOTRECTINIB.
7
Reports of Anaemia with REPOTRECTINIB
3.7%
of all REPOTRECTINIB reports
0
Deaths
5
Hospitalizations
How Dangerous Is Anaemia From REPOTRECTINIB?
Of the 7 reports, 5 (71.4%) required hospitalization, and 1 (14.3%) were considered life-threatening.
Is Anaemia Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for REPOTRECTINIB. However, 7 reports have been filed with the FAERS database.
What Other Side Effects Does REPOTRECTINIB Cause?
Dizziness (32)
Death (21)
Nausea (12)
Adverse event (11)
Neuropathy peripheral (11)
Off label use (10)
Paraesthesia (10)
Balance disorder (9)
Pain (9)
Hospitalisation (8)
What Other Drugs Cause Anaemia?
LENALIDOMIDE (5,322)
CARBOPLATIN (5,312)
RIBAVIRIN (5,130)
ASPIRIN (4,568)
CYCLOPHOSPHAMIDE (4,486)
RITUXIMAB (4,399)
DEXAMETHASONE (4,352)
ADALIMUMAB (3,994)
PACLITAXEL (3,949)
METHOTREXATE (3,913)
Which REPOTRECTINIB Alternatives Have Lower Anaemia Risk?
REPOTRECTINIB vs REQUIP
REPOTRECTINIB vs RESLIZUMAB
REPOTRECTINIB vs RESMETIROM
REPOTRECTINIB vs RESTASIS
REPOTRECTINIB vs RETINOL