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.
265 related articles for article (PubMed ID: 36829251)
1. Pharmacovigilance-based drug repurposing: searching for putative drugs with hypohidrosis or anhidrosis adverse events for use against hyperhidrosis. Liu Y; Liu Y; Fan R; Kehriman N; Zhang X; Zhao B; Huang L Eur J Med Res; 2023 Feb; 28(1):95. PubMed ID: 36829251 [TBL] [Abstract][Full Text] [Related]
2. Opportunities for Web-based Drug Repositioning: Searching for Potential Antihypertensive Agents with Hypotension Adverse Events. Wang K; Wan M; Wang RS; Weng Z J Med Internet Res; 2016 Apr; 18(4):e76. PubMed ID: 27036325 [TBL] [Abstract][Full Text] [Related]
3. Drug-Associated Acute Kidney Injury Identified in the United States Food and Drug Administration Adverse Event Reporting System Database. Welch HK; Kellum JA; Kane-Gill SL Pharmacotherapy; 2018 Aug; 38(8):785-793. PubMed ID: 29883524 [TBL] [Abstract][Full Text] [Related]
4. 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]
6. Are finasteride-related penile curvature/Peyronie's disease Adverse Event Reports worthy of further clinical investigation? Disproportionality analysis based on both the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) pharmacovigilance databases. Schifano N; Capogrosso P; Boeri L; Fallara G; Chiappini S; Rewhorn M; Cakir OO; Harvey H; Castiglione F; Alnajjar HM; Muneer A; Deho' F; Schifano F; Montorsi F; Salonia A Int J Impot Res; 2023 Aug; 35(5):465-471. PubMed ID: 35513712 [TBL] [Abstract][Full Text] [Related]
7. Use of Disproportionality Analysis to Identify Previously Unknown Drug-Associated Causes of Cardiac Arrhythmias Using the Food and Drug Administration Adverse Event Reporting System (FAERS) Database. Moreland-Head LN; Coons JC; Seybert AL; Gray MP; Kane-Gill SL J Cardiovasc Pharmacol Ther; 2021 Jul; 26(4):341-348. PubMed ID: 33403858 [TBL] [Abstract][Full Text] [Related]
8. Disproportionality analysis in VigiBase as a drug repositioning method for the discovery of potentially useful drugs in Alzheimer's disease. Chrétien B; Jourdan JP; Davis A; Fedrizzi S; Bureau R; Sassier M; Rochais C; Alexandre J; Lelong-Boulouard V; Dolladille C; Dallemagne P Br J Clin Pharmacol; 2021 Jul; 87(7):2830-2837. PubMed ID: 33274491 [TBL] [Abstract][Full Text] [Related]
9. An Updated Comprehensive Pharmacovigilance Study of Drug-Induced Thrombocytopenia Based on FDA Adverse Event Reporting System Data. Kunyu L; Shuping S; Chang S; Yiyue C; Qinyu X; Ting Z; Bin W J Clin Pharmacol; 2024 Apr; 64(4):478-489. PubMed ID: 38041205 [TBL] [Abstract][Full Text] [Related]
10. Analysis of the nervous system and gastrointestinal adverse events associated with solifenacin in older adults using the US FDA adverse event reporting system. Nicholls C; Chyou TY; Nishtala PS Int J Risk Saf Med; 2023; 34(1):63-73. PubMed ID: 35491805 [TBL] [Abstract][Full Text] [Related]
12. A Pharmacovigilance Study of Adverse Drug Reactions Reported for Cardiovascular Disease Medications Approved Between 2012 and 2017 in the United States Food and Drug Administration Adverse Event Reporting System (FAERS) Database. Patel NM; Stottlemyer BA; Gray MP; Boyce RD; Kane-Gill SL Cardiovasc Drugs Ther; 2022 Apr; 36(2):309-322. PubMed ID: 33599896 [TBL] [Abstract][Full Text] [Related]
13. Data mining for adverse drug reaction signals of daptomycin based on real-world data: a disproportionality analysis of the US Food and Drug Administration adverse event reporting system. Chen JJ; Huo XC; Wang SX; Wang F; Zhao Q Int J Clin Pharm; 2022 Dec; 44(6):1351-1360. PubMed ID: 36178607 [TBL] [Abstract][Full Text] [Related]
14. Association of Hyponatraemia and Antidepressant Drugs: A Pharmacovigilance-Pharmacodynamic Assessment Through an Analysis of the US Food and Drug Administration Adverse Event Reporting System (FAERS) Database. Mazhar F; Pozzi M; Gentili M; Scatigna M; Clementi E; Radice S; Carnovale C CNS Drugs; 2019 Jun; 33(6):581-592. PubMed ID: 30977109 [TBL] [Abstract][Full Text] [Related]
15. Drug-induced hyperhidrosis and hypohidrosis: incidence, prevention and management. Cheshire WP; Fealey RD Drug Saf; 2008; 31(2):109-26. PubMed ID: 18217788 [TBL] [Abstract][Full Text] [Related]
16. Endocrine toxicity of immune checkpoint inhibitors: a real-world study leveraging US Food and Drug Administration adverse events reporting system. Zhai Y; Ye X; Hu F; Xu J; Guo X; Zhuang Y; He J J Immunother Cancer; 2019 Nov; 7(1):286. PubMed ID: 31694698 [TBL] [Abstract][Full Text] [Related]
17. Exploring the association between weight loss-inducing medications and multiple sclerosis: insights from the FDA adverse event reporting system database. Shirani A; Cross AH; Stuve O Ther Adv Neurol Disord; 2024; 17():17562864241241383. PubMed ID: 38566910 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Drug Repurposing Using FDA Adverse Event Reporting System (FAERS) Database. Morris R; Ali R; Cheng F Curr Drug Targets; 2024; 25(7):454-464. PubMed ID: 38566381 [TBL] [Abstract][Full Text] [Related]
20. Renal toxicities in immune checkpoint inhibitors with or without chemotherapy: An observational, retrospective, pharmacovigilance study leveraging US FARES database. Hu F; Zhai Y; Yuan L; Liang J; Xu J; Guo X; Zhou X; Lin Z; Sun J; Ye X; He J Cancer Med; 2021 Dec; 10(24):8754-8762. PubMed ID: 34845857 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]