Eletriptan in the management of acute migraine: an update on the evidence for efficacy, safety, and consistent response

Author:

Capi Matilde1,Curto Martina2,Lionetto Luana3,de Andrés Fernando4,Gentile Giovanna5,Negro Andrea6,Martelletti Paolo6

Affiliation:

1. NESMOS Department, Sapienza University of Rome, Italy

2. Sapienza University of Rome, Azienda Ospedaliera Sant’Andrea Via di Grottarossa 1035-1039, Rome 00189, Italy

3. Advanced Molecular Diagnostics, IDI-IRCCS, Rome, Italy

4. CICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain

5. NESMOS Department, Sapienza University of Rome, Italy Psychiatry and Neurology Department, Sapienza University of Rome, Italy Department of Psychiatry, Harvard Medical School, Boston, MA, USA Department of Molecular Medicine, Sant’Andrea Medical Center, Sapienza University of Rome, Italy Regional Referral Headache Center, Sant’Andrea Hospital, Rome, Italy Advanced Molecular Diagnostics, IDI-IRCCS, Rome, Italy

6. Department of Molecular Medicine, Sant’Andrea Medical Center, Sapienza University of Rome, Italy Regional Referral Headache Center, Sant’Andrea Hospital, Rome, Italy

Abstract

Migraine is a multifactorial, neurological and disabling disorder, also characterized by several autonomic symptoms. Triptans, selective serotonin 5-HT1B/1D agonists, are the first-line treatment option for moderate-to-severe headache attacks. In this paper, we review the recent data on eletriptan clinical efficacy, safety, and tolerability, and potential clinically relevant interactions with other drugs. Among triptans, eletriptan shows a consistent and significant clinical efficacy and a good tolerability profile in the treatment of migraine, especially for patients with cardiovascular risk factors without coronary artery disease. It shows the most favorable clinical response, together with sumatriptan injections, zolmitriptan and rizatriptan. Additionally, eletriptan shows the most complex pharmacokinetic/dynamic profile compared with the other triptans. It is metabolized primarily by the CYP3A4 hepatic enzyme and therefore the concomitant administration of CYP3A4-potent inhibitors should be carefully evaluated. A relatively low risk of serotonin syndrome is given by the co-administration with serotoninergic drugs. No clinically relevant interaction has been found with drugs used for migraine prophylactic treatment or other acute drugs, with the exception of ergot derivatives that should not be co-administered with eletriptan.

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology,Pharmacology

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