Zykadia (ceritinib) - Novartis
Augtyro (repotrectinib) - BMS
Rozlytrek (entrectinib) - Roche
Xalkori (crizotinib) - Pfizer
Lorbrena (lorlatinib) - Pfizer
Cabometyx (cabozantinib tablet) - Exelixis
Alunbrig (brigatinib) - Takeda
Age-stratified adverse-event reporting signals of seven ALK/ROS1 tyrosine kinase inhibitors in FAERS: a disproportionality and time to onset study. (PubMed, Front Pharmacol) - Sep 23, 2026 - "The study included 38,479 primary-suspect reports with known age for crizotinib, entrectinib, brigatinib, lorlatinib, repotrectinib, cabozantinib, or ceritinib...The early reporting pattern favors close assessment soon after treatment initiation. FAERS signals remain hypothesis-generating and require confirmation in longitudinal patient-level data." 
Adverse events • Journal • Oncology • Pediatrics • ALK • ROS1
http://www.ncbi.nlm.nih.gov/pubmed/42769117
 
Hao Zhong; Xingjun Huang; Yige Yu; Yingyu Yu; Yongjian Liu
 
Sep 23, 2026
 
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