Myocardial infarction associated with erenumab: A case report

被引:13
|
作者
Perino, Justine [1 ,2 ]
Corand, Virginie [3 ]
Laurent, Elise [1 ]
Theophile, Helene [1 ]
Miremont-Salame, Ghada [1 ]
Pariente, Antoine [1 ,2 ]
Colas, Jean-Laurent [4 ]
Couffinhal, Thierry [5 ]
Salvo, Francesco [1 ,2 ]
机构
[1] Univ Hosp Bordeaux, Pharmacovigilance Ctr Bordeaux, Dept Med Pharmacol, Bordeaux, France
[2] Univ Bordeaux, U1219, BPH, INSERM, Bordeaux, France
[3] Univ Hosp Bordeaux, Pain Ctr Bordeaux, Dept Clin Neurosci, Bordeaux, France
[4] Polyclin Bordeaux Nord Aquitaine, Dept Cardiol, Bordeaux, France
[5] Univ Bordeaux, CHU Bordeaux, U1034, INSERM,Biol Cardiovasc Dis, Bordeaux, France
来源
PHARMACOTHERAPY | 2022年 / 42卷 / 07期
关键词
adverse event; calcitonin gene-related peptide; case report; drug safety; migraine disorder; pharmacovigilance; GENE-RELATED PEPTIDE; SAFETY; CGRP;
D O I
10.1002/phar.2706
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background Monoclonal antibodies acting on the calcitonin gene-related peptide or its receptor (CGRP-mabs) are novel drugs for resistant migraine prophylaxis. As CGRP-mabs cause inhibition of vasodilatation, their use is reserved to patients with no recent history of cardiovascular diseases. We report a case of myocardial infarction associated with erenumab. Case A 57-year-old woman with a familial history of coronaropathy was first treated with erenumab 70 mg for 6 months and then increased to 140 mg. Almost 5 months after, the patient presented chest pain, increased troponin, and abnormal electrocardiogram. A myocardial infarction without coronarography abnormality was diagnosed through MRI. Conclusion Further evidence is needed to assess the risk of myocardial infarction in patients treated with a CGRP-mab. In patients over 40 years of age, the risk of coronary or cardiovascular events should be assessed using risk tables or algorithms to take into account cardiovascular risk factors. This may be complemented by appropriate examinations to measure the burden of coronary atherosclerosis, if necessary.
引用
收藏
页码:585 / 589
页数:5
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