Back to Search Start Over

Transition to lanadelumab‐flyo from three medications for a hereditary angioedema patient with a variant in the SYTL2 gene: A case report

Authors :
Stephanie Burns
Elena Lewis
Source :
Clinical Case Reports, Vol 9, Iss 4, Pp 2438-2441 (2021)
Publication Year :
2021
Publisher :
Wiley, 2021.

Abstract

Abstract Non‐SERPING1 gene variant hereditary angioedema patients often need to take progesterone, attenuated androgens, and antifibrinolytics to control symptoms. These drugs may need to be tapered to extinction or reduced as lanadelumab‐flyo reaches maximum concentration.

Details

Language :
English
ISSN :
20500904
Volume :
9
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Clinical Case Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.653d724c0420ea43f30c060327275
Document Type :
article
Full Text :
https://doi.org/10.1002/ccr3.4060