Dulaglutide/ja: Difference between revisions

米国[[Food and Drug Administration/ja|食品医薬品局]]（FDA）はデュラグルチドを[[Risk Evaluation and Mitigation Strategies/ja|リスク評価と軽減戦略]]（REMS）付きで承認し、[[Eli Lilly and Company|イーライリリー・アンド・カンパニー]]にトルリシティの承認を認めた。REMSは、膵炎のリスクと薬物に関連する[[medullary thyroid carcinoma/ja|甲状腺髄様癌]]の潜在的なリスクを医師に認識させるためにイーライリリーがとるいくつかのステップから構成されている。

== Further reading ==

* {{cite journal | vauthors = Scott LJ | title = Dulaglutide: A Review in Type 2 Diabetes | journal = Drugs | volume = 80 | issue = 2 | pages = 197–208 | date = February 2020 | pmid = 32002850 | doi = 10.1007/s40265-020-01260-9 | s2cid = 210954338 }}

* {{cite journal | vauthors = Edwards KL, Minze MG | title = Dulaglutide: an evidence-based review of its potential in the treatment of type 2 diabetes | journal = Core Evidence | volume = 10 | pages = 11–21 | date = 2015 | pmid = 25657615 | pmc = 4295897 | doi = 10.2147/CE.S55944 | doi-access = free }}

* {{cite journal | vauthors = Romera I, Cebrián-Cuenca A, Álvarez-Guisasola F, Gomez-Peralta F, Reviriego J | title = A Review of Practical Issues on the Use of Glucagon-Like Peptide-1 Receptor Agonists for the Management of Type 2 Diabetes | journal = Diabetes Therapy | volume = 10 | issue = 1 | pages = 5–19 | date = February 2019 | pmid = 30506340 | pmc = 6349277 | doi = 10.1007/s13300-018-0535-9 }}

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[[Category:Drugs developed by Eli Lilly and Company]]

[[Category:GLP-1 receptor agonists]]

[[Category:Peptide therapeutics]]