These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
467 related articles for article (PubMed ID: 37610085)
1. Post-marketing safety of anti-IL-5 monoclonal antibodies (mAbs): an analysis of the FDA Adverse Event Reporting System (FAERS). Zou SP; Yang HY; Ouyang M; Cheng Q; Shi X; Sun MH Expert Opin Drug Saf; 2024 Mar; 23(3):353-362. PubMed ID: 37610085 [TBL] [Abstract][Full Text] [Related]
2. A disproportionality analysis of adverse events associated to pertuzumab in the FDA Adverse Event Reporting System (FAERS). Zou SP; Yang HY; Ouyang ML; Cheng Q; Shi X; Sun MH BMC Pharmacol Toxicol; 2023 Nov; 24(1):62. PubMed ID: 37957717 [TBL] [Abstract][Full Text] [Related]
3. A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) events for osimertinib. Yin Y; Shu Y; Zhu J; Li F; Li J Sci Rep; 2022 Nov; 12(1):19555. PubMed ID: 36380085 [TBL] [Abstract][Full Text] [Related]
4. A real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events for niraparib. Guo M; Shu Y; Chen G; Li J; Li F Sci Rep; 2022 Nov; 12(1):20601. PubMed ID: 36446798 [TBL] [Abstract][Full Text] [Related]
5. Post-marketing drug safety surveillance of enfortumab vedotin: an observational pharmacovigilance study based on a real-world database. Yu M; Zhou L; Cao M; Ji C; Zheng Y Front Immunol; 2024; 15():1397692. PubMed ID: 39234238 [TBL] [Abstract][Full Text] [Related]
6. Parasitic infections related to anti-type 2 immunity monoclonal antibodies: a disproportionality analysis in the food and drug administration's adverse event reporting system (FAERS). Pera V; Brusselle GG; Riemann S; Kors JA; Van Mulligen EM; Parry R; de Wilde M; Rijnbeek PR; Verhamme KMC Front Pharmacol; 2023; 14():1276340. PubMed ID: 38035014 [No Abstract] [Full Text] [Related]
7. Post-Marketing Safety Concerns with Upadacitinib: A Disproportionality Analysis of the FDA Adverse Event Reporting system. Wu XP; Lu XK; Wang ZT; Huang L; Cai RW; Yu HM; Li JY; Xiao J Expert Opin Drug Saf; 2023; 22(10):975-984. PubMed ID: 37310063 [TBL] [Abstract][Full Text] [Related]
8. Adverse events with risankizumab in the real world: postmarketing pharmacovigilance assessment of the FDA adverse event reporting system. Shu Y; Chen J; Ding Y; Zhang Q Front Immunol; 2023; 14():1169735. PubMed ID: 37256136 [TBL] [Abstract][Full Text] [Related]
9. Disproportionality analysis of reslizumab based on the FDA Adverse Event Reporting System. Li H; Guo C; Wang C Ther Adv Drug Saf; 2024; 15():20420986241284112. PubMed ID: 39381062 [TBL] [Abstract][Full Text] [Related]
10. Safety of Biological Therapies for Severe Asthma: An Analysis of Suspected Adverse Reactions Reported in the WHO Pharmacovigilance Database. Cutroneo PM; Arzenton E; Furci F; Scapini F; Bulzomì M; Luxi N; Caminati M; Senna G; Moretti U; Trifirò G BioDrugs; 2024 May; 38(3):425-448. PubMed ID: 38489062 [TBL] [Abstract][Full Text] [Related]
11. A real-world pharmacovigilance study of axitinib: data mining of the public version of FDA adverse event reporting system. Shu Y; Ding Y; Dai B; Zhang Q Expert Opin Drug Saf; 2022 Apr; 21(4):563-572. PubMed ID: 34918584 [TBL] [Abstract][Full Text] [Related]
12. Adverse Event Profiles of Anti-CTLA-4 and Anti-PD-1 Monoclonal Antibodies Alone or in Combination: Analysis of Spontaneous Reports Submitted to FAERS. Ji HH; Tang XW; Dong Z; Song L; Jia YT Clin Drug Investig; 2019 Mar; 39(3):319-330. PubMed ID: 30674039 [TBL] [Abstract][Full Text] [Related]
13. Adverse events of guselkumab in the real world: emerging signals to target preventive strategies from the FDA adverse event reporting system. Xiang DC; Chen W; Fu ZW; Wu XH; Gao P; Wu Y Expert Opin Drug Saf; 2023; 22(10):943-955. PubMed ID: 37294594 [TBL] [Abstract][Full Text] [Related]
14. Anti-IL5 therapies for asthma. Farne HA; Wilson A; Powell C; Bax L; Milan SJ Cochrane Database Syst Rev; 2017 Sep; 9(9):CD010834. PubMed ID: 28933516 [TBL] [Abstract][Full Text] [Related]
15. Anti-IL-5 therapies for asthma. Farne HA; Wilson A; Milan S; Banchoff E; Yang F; Powell CV Cochrane Database Syst Rev; 2022 Jul; 7(7):CD010834. PubMed ID: 35838542 [TBL] [Abstract][Full Text] [Related]
16. Safety assessment of Tafamidis: a real-world pharmacovigilance study of FDA adverse event reporting system (FAERS) events. Li Y; Sun S; Wu H; Zhao L; Peng W BMC Pharmacol Toxicol; 2024 Sep; 25(1):71. PubMed ID: 39334280 [TBL] [Abstract][Full Text] [Related]
17. A real‑world pharmacovigilance study of FDA adverse event reporting system events for daratumumab. Yun X; Zhou Y; Wu D; Liu Y; Wu Q Expert Opin Drug Saf; 2024 May; 23(5):581-591. PubMed ID: 38600747 [TBL] [Abstract][Full Text] [Related]
18. A real-world pharmacovigilance study of mepolizumab in the FDA adverse event reporting system (FAERS) database. Zou F; Zhu C; Lou S; Cui Z; Wang D; Ou Y; Wang L; Chen J; Lan Y Front Pharmacol; 2023; 14():1320458. PubMed ID: 38186645 [TBL] [Abstract][Full Text] [Related]
19. A real-world disproportionality analysis of FDA Adverse Event Reporting System (FAERS) events for baricitinib. Peng L; Xiao K; Ottaviani S; Stebbing J; Wang YJ Expert Opin Drug Saf; 2020 Nov; 19(11):1505-1511. PubMed ID: 32693646 [TBL] [Abstract][Full Text] [Related]
20. A real-world disproportionality analysis of mepolizumab based on the FDA adverse event reporting system. Li H; Wang C; Deng A; Guo C Front Pharmacol; 2023; 14():1280490. PubMed ID: 38143494 [No Abstract] [Full Text] [Related] [Next] [New Search]