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.
3. Safety of Biologics, Including Biosimilars: Perspectives on Current Status and Future Direction. Ingrasciotta Y; Cutroneo PM; Marcianò I; Giezen T; Atzeni F; Trifirò G Drug Saf; 2018 Nov; 41(11):1013-1022. PubMed ID: 29796832 [TBL] [Abstract][Full Text] [Related]
5. Current state of biologic pharmacovigilance in the European Union: improvements are needed. Felix T; Jordan JB; Akers C; Patel B; Drago D Expert Opin Drug Saf; 2019 Mar; 18(3):231-240. PubMed ID: 30714424 [TBL] [Abstract][Full Text] [Related]
6. [Biologicals and Biosimilars: Gaps in the Pharmacovigilance System in Portugal]. Portela MC; Sinogas C; Almeida FA; Baptista-Leite R; Castro-Caldas A Acta Med Port; 2017 Mar; 30(3):205-212. PubMed ID: 28550830 [TBL] [Abstract][Full Text] [Related]
7. Biosimilars: A consideration of the regulations in the United States and European union. Daller J Regul Toxicol Pharmacol; 2016 Apr; 76():199-208. PubMed ID: 26732800 [TBL] [Abstract][Full Text] [Related]
8. [Evolution of biologicals in inflammation medicine--biosimilars in gastroenterology, rheumatology and dermatology]. Schreiber S; Luger T; Mittendorf T; Mrowietz U; Müller-Ladner U; Schröder J; Stallmach A; Bokemeyer B Dtsch Med Wochenschr; 2014 Nov; 139(47):2399-404. PubMed ID: 25390629 [TBL] [Abstract][Full Text] [Related]
9. Identifiability of Biologicals in Adverse Drug Reaction Reports Received From European Clinical Practice. Vermeer NS; Giezen TJ; Zastavnik S; Wolff-Holz E; Hidalgo-Simon A Clin Pharmacol Ther; 2019 Apr; 105(4):962-969. PubMed ID: 30460997 [TBL] [Abstract][Full Text] [Related]
10. [The Polish Task Force position statement on safety of biologic treatment with monoclonal antibodies and soluble receptors]. Jahnz-Rozyk K; Wiesik-Szewczyk E; Pol Merkur Lekarski; 2014 Jul; 37(217):5-9. PubMed ID: 25154192 [TBL] [Abstract][Full Text] [Related]
11. EU pharmacovigilance regulatory requirements of anticancer biosimilar monoclonal antibodies. Francescon S; Fornasier G; Baldo P Int J Clin Pharm; 2018 Aug; 40(4):778-782. PubMed ID: 30094558 [TBL] [Abstract][Full Text] [Related]
12. Biosimilars: Implications for health-system pharmacists. Lucio SD; Stevenson JG; Hoffman JM Am J Health Syst Pharm; 2013 Nov; 70(22):2004-17. PubMed ID: 24173009 [TBL] [Abstract][Full Text] [Related]
13. The similarity question for biologicals and non-biological complex drugs. Crommelin DJ; Shah VP; Klebovich I; McNeil SE; Weinstein V; Flühmann B; Mühlebach S; de Vlieger JS Eur J Pharm Sci; 2015 Aug; 76():10-7. PubMed ID: 25912826 [TBL] [Abstract][Full Text] [Related]
14. The global landscape on interchangeability of biosimilars. Rathore AS; Stevenson JG; Chhabra H; Maharana C Expert Opin Biol Ther; 2022 Feb; 22(2):133-148. PubMed ID: 33567923 [TBL] [Abstract][Full Text] [Related]