BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

289 related articles for article (PubMed ID: 36446798)

  • 21. Adverse Event Profiles of PARP Inhibitors: Analysis of Spontaneous Reports Submitted to FAERS.
    Tian X; Chen L; Gai D; He S; Jiang X; Zhang N
    Front Pharmacol; 2022; 13():851246. PubMed ID: 35401230
    [No Abstract]   [Full Text] [Related]  

  • 22. Post-marketing safety concerns with abrocitinib: a real-world pharmacovigilance analysis of the FDA adverse event reporting system.
    Zhu Z; Liu M; Zhang H; Zheng H; Li J
    Expert Opin Drug Saf; 2024 May; ():1-8. PubMed ID: 38743462
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A real-world pharmacovigilance study of FDA Adverse Event Reporting System (FAERS) events for venetoclax.
    Yang Y; Shu Y; Chen G; Yin Y; Li F; Li J
    PLoS One; 2022; 17(12):e0278725. PubMed ID: 36477747
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Post-marketing safety concerns with palbociclib: a disproportionality analysis of the FDA adverse event reporting system.
    Cheng Q; Shi X; Zhao Y; Zou S; Sun M
    Expert Opin Drug Saf; 2024 May; 23(5):637-648. PubMed ID: 38564277
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A pharmacovigilance study of etoposide in the FDA adverse event reporting system (FAERS) database, what does the real world say?
    Cui Z; Cheng F; Wang L; Zou F; Pan R; Tian Y; Zhang X; She J; Zhang Y; Yang X
    Front Pharmacol; 2023; 14():1259908. PubMed ID: 37954852
    [No Abstract]   [Full Text] [Related]  

  • 26. Post-Marketing Safety Concerns With Secukinumab: A Disproportionality Analysis of the FDA Adverse Event Reporting System.
    Shu Y; Ding Y; Liu Y; Wu P; He X; Zhang Q
    Front Pharmacol; 2022; 13():862508. PubMed ID: 35754494
    [No Abstract]   [Full Text] [Related]  

  • 27. Psychiatric adverse events associated with GLP-1 receptor agonists: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database.
    Chen W; Cai P; Zou W; Fu Z
    Front Endocrinol (Lausanne); 2024; 15():1330936. PubMed ID: 38390214
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Metformin adverse event profile: a pharmacovigilance study based on the FDA Adverse Event Reporting System (FAERS) from 2004 to 2022.
    Du Y; Zhu J; Guo Z; Wang Z; Wang Y; Hu M; Zhang L; Yang Y; Wang J; Huang Y; Huang P; Chen M; Chen B; Yang C
    Expert Rev Clin Pharmacol; 2024; 17(2):189-201. PubMed ID: 38269492
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Drug-induced interstitial lung disease: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System from 2004 to 2021.
    Jiang T; Su H; Xu J; Li C; Zhang N; Li Y; Wu Y; Ni R; Ming Y; Li Z; Li L; Liu Y
    Ther Adv Drug Saf; 2024; 15():20420986231224227. PubMed ID: 38293566
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Exploring the safety profile of tremelimumab: an analysis of the FDA adverse event reporting system.
    Zhao Y; Jiang H; Xue L; Zhou M; Zhao X; Liu F; Jiang S; Huang J; Meng L
    Int J Clin Pharm; 2024 Apr; 46(2):480-487. PubMed ID: 38245663
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cardiac adverse events associated with quetiapine: Disproportionality analysis of FDA adverse event reporting system.
    Shu Y; Ding Y; Liu L; Zhang Q
    CNS Neurosci Ther; 2023 Sep; 29(9):2705-2716. PubMed ID: 37032639
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A pharmacovigilance analysis of FDA adverse event reporting system events for romosozumab.
    Chen Z; Li M; Li S; Li Y; Wu J; Qiu K; Yu X; Huang L; Chen G
    Expert Opin Drug Saf; 2023 Apr; 22(4):339-342. PubMed ID: 36178002
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Adverse events in patients with advanced urothelial carcinoma treated with erdafitinib: a retrospective pharmacovigilance study.
    Yuan T; Li F; Hou Y; Guo H
    Front Pharmacol; 2023; 14():1266890. PubMed ID: 38074150
    [No Abstract]   [Full Text] [Related]  

  • 34. Post-marketing safety evaluation of lurbinectedin: a pharmacovigilance analysis based on the FAERS database.
    Li Z; Guo C; Liu X; Qiu Z; Zhang R
    Front Pharmacol; 2024; 15():1368763. PubMed ID: 38549677
    [No Abstract]   [Full Text] [Related]  

  • 35. Post-marketing safety surveillance of sacituzumab govitecan: an observational, pharmacovigilance study leveraging FAERS database.
    Liu W; Du Q; Guo Z; Ye X; Liu J
    Front Pharmacol; 2023; 14():1283247. PubMed ID: 38027003
    [No Abstract]   [Full Text] [Related]  

  • 36. A real-world pharmacovigilance study of FDA adverse event reporting system events for diazepam.
    He W; Wang Y; Chen K
    Front Pharmacol; 2024; 15():1278442. PubMed ID: 38327980
    [No Abstract]   [Full Text] [Related]  

  • 37. A real-world disproportionality analysis of the FDA adverse event reporting system events for ibuprofen.
    Du Y; Guo Z; Xu B; Yang Y; Hu M; Hu Y; Yang Y; Zhang M; Wang Z; Guo X; Huang Y; Zhu J; Zhang W; Yang C
    Expert Opin Drug Saf; 2024 May; ():1-11. PubMed ID: 38686498
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Characteristics of adverse drug reactions induced by flutamide and bicalutamide: a real-world pharmacovigilance study using FAERS.
    Sun Y; Xu T; Zhu S; Xu H
    Expert Opin Drug Saf; 2024 Mar; 23(3):305-311. PubMed ID: 37795911
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Safety analysis of pemigatinib leveraging the US Food and Drug administration adverse event reporting system.
    Zhang Y; Ran L; Liang Y; Zhang Y; An Z
    Front Pharmacol; 2023; 14():1194545. PubMed ID: 37554985
    [No Abstract]   [Full Text] [Related]  

  • 40. A Real-World Pharmacovigilance Study of Ceftazidime/Avibactam: Data Mining of the Food and Drug Administration Adverse Event Reporting System Database.
    Yao H; Wang Y; Peng Y; Huang Z; Gan G; Wang Z
    J Clin Pharmacol; 2024 Feb; ():. PubMed ID: 38375685
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.