Methysergide-containing medicines

  • Email
  • Help

Restrictions on the use of methysergide-containing medicines

On 20 February 2014, the European Medicines Agency recommended restricting the use of methysergide due to concerns that it could cause fibrosis, a condition in which fibrous (scar) tissue accumulates in the body’s organs potentially damaging them. Methysergide medicines are now only to be used for preventing severe intractable migraines and cluster headaches (a type of severe, recurring headache on one side of the head, usually around the eye) when standard medicines have failed.

In addition, treatment should only be started and supervised by a specialist doctor with experience in treating migraine and cluster headaches. Patients should also be screened for fibrosis at the start of treatment and should have additional screenings every 6 months. Treatment must be discontinued if symptoms of fibrosis occur.

The Agency’s Committee for Medicinal Products for Human Use (CHMP), which conducted the review, noted that these recommendations were necessary due to the reports of fibrosis seen with methysergide and other medicines of the same class (ergot derivatives). The symptoms of fibrosis often take some time to appear and without screening the diagnosis may come too late to prevent severe (and potentially life-threatening) damage to organs .

Regarding the benefits, the Committee noted that there is some evidence of a clinically relevant effect of methysergide when used for prevention in patients who regularly get migraines and cluster headaches and for whom treatment options are limited. Methysergide has also been used for treating diarrhoea caused by carcinoid disease (a slow-growing tumour that commonly affects the gut). However, there were no data to support this use and Methysergide should therefore no longer be used in carcinoid disease.

The prescribing information for physicians and information in the patients’ information leaflet has been updated. The CHMP recommendations were sent to the European Commission, which has endorsed them and issued a final legally-binding decision that is valid throughout the EU.

Information to patients
  • Methysergide-containing medicines may cause a potentially serious condition known as fibrosis, in which scar tissue accumulates in some of the body’s organs. As a result of this, the use of these medicines is being restricted to the prevention of severe intractable migraines and cluster headaches when standard medicines have failed.
  • Methysergide should no longer be used for treating diarrhoea caused by carcinoid disease (a type of slow-growing tumour). If you are being treated for this purpose, please contact your doctor to discuss alternative treatment.
  • If you are using methysergide to prevent migraines and cluster headaches, your doctor will check on a regular basis whether you are developing any signs or symptoms of fibrosis. Your doctor will stop your treatment if fibrosis is suspected.
  • Your doctor will also regularly re-assess the need for you to continue treatment with methysergide by seeing if your symptoms return after periodic breaks in treatment.
  • Patients who have any questions should speak to their doctor or pharmacist.
Information to healthcare professionals
  • Methysergide should no longer be used for treating diarrhoea caused by carcinoid disease.
  • Following the review of methysergide-containing medicines, methysergide should now only be used for:
    • Prophylactic treatment of severe intractable migraine (with or without aura) with functional disability in adults, when treatment with standard medicines has failed. Previous treatment must have included treatment with medicines of other classes for at least 4 months at the maximum tolerated dose;
    • Prophylactic treatment of episodic and chronic cluster headache in adults when treatment with standard medicines has failed. Previous treatment must have included treatment with medicines of at least 2 classes for a minimum of 2 months.
  • Treatment with methysergide should only be started and supervised by specialised physicians with experience in treating migraine and cluster headaches.
  • Patients should be screened for fibrosis at baseline and at least every 6 months thereafter. Screening investigations may include heart ultrasound, abdominal MRI and lung function tests. Treatment must be stopped if a patient develops symptoms suggestive of fibrosis unless an alternative cause is confirmed.
  • Treatment must not begin until after the patient has been examined for any pre-existing fibrotic conditions. Once treatment is started the patient must be examined for occurrence of fibrosis at 6-monthly intervals. This examination should include a re-assessment of the benefit-risk balance in the individual patient.
  • During treatment with methysergide, a treatment-free period of at least 4 weeks must be allowed between treatment courses at least every 6 months.

The Agency’s recommendations are based on available data on the benefits and risks of methysergide, from clinical studies, post-marketing safety reports and the scientific literature. Based on these data a potential causal association between methysergide and fibrosis seems likely. The mechanism by which methysergide could cause fibrosis through serotoninergic-receptor activation is widely described in the literature.

More about the medicine

Methysergide is a medicine that belongs to the class ‘ergot alkaloids’ that has been used in the EU for preventing migraines (with or without aura) and other types of throbbing headaches. It was also used to treat diarrhoea caused by carcinoid disease.

In the EU, medicines containing methysergide have been authorised by national procedures and have been marketed under various trade names. The pharmaceutical forms and the approved indications, strengths and doses vary in different EU countries.

More about the procedure

The review of methysergide was initiated on 24 May 2012 at the request of the French medicines agency ANSM under Article 31 of Directive 2001/83/EC following concerns about serious cases of fibrosis identified by the French agency.

The CHMP opinion was sent to the European Commission, which endorsed it and issued a final legally binding decision on 28 April 2014.

Name Language First published Last updated
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines BG = bălgarski 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines ES = español 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines CS = čeština 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines DA = dansk 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines DE = Deutsch 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines ET = eesti keel 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines EL = elliniká 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines EN = English 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines FR = français 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines IT = italiano 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines LV = latviešu valoda 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines LT = lietuvių kalba 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines HU = magyar 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines MT = Malti 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines NL = Nederlands 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines PL = polski 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines PT = português 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines RO = română 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SK = slovenčina 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SL = slovenščina 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines FI = suomi 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SV = svenska 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines HR = Hrvatski 27/05/2014  

Key facts

Approved nameMethysergide-containing medicines
International non-proprietary name (INN) or common name

methysergide

Associated namesDeseril, Desernil
ClassErgot alkaloids
Reference numberEMEA/H/A-31/1335
TypeArticle 31 referrals

This type of referral is triggered when the interest of the Community is involved, following concerns relating to the quality, safety or efficacy of a medicine or a class of medicines.

StatusOpinion provided by Committee for Medicinal Products for Human Use
Opinion date20/02/2014

All documents

Name Language First published Last updated
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines BG = bălgarski 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines ES = español 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines CS = čeština 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines DA = dansk 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines DE = Deutsch 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines ET = eesti keel 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines EL = elliniká 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines EN = English 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines FR = français 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines IT = italiano 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines LV = latviešu valoda 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines LT = lietuvių kalba 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines HU = magyar 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines MT = Malti 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines NL = Nederlands 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines PL = polski 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines PT = português 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines RO = română 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SK = slovenčina 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SL = slovenščina 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines FI = suomi 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines SV = svenska 27/05/2014  
Methysergide Article-31 referral - Restrictions on the use of methysergide-containing medicines HR = Hrvatski 27/05/2014  
Methysergide Article-31 referral - European Medicines Agency recommends restricting the use of methysergide-containing medicines (English only) 21/02/2014  
Methysergide Article-31 referral - Assessment report (English only) 27/05/2014  
Methysergide Article-31 referral - Annex I BG = bălgarski 27/05/2014  
Methysergide Article-31 referral - Annex I ES = español 27/05/2014  
Methysergide Article-31 referral - Annex I CS = čeština 27/05/2014  
Methysergide Article-31 referral - Annex I DA = dansk 27/05/2014  
Methysergide Article-31 referral - Annex I DE = Deutsch 27/05/2014  
Methysergide Article-31 referral - Annex I ET = eesti keel 27/05/2014  
Methysergide Article-31 referral - Annex I EL = elliniká 27/05/2014  
Methysergide Article-31 referral - Annex I EN = English 27/05/2014  
Methysergide Article-31 referral - Annex I FR = français 27/05/2014  
Methysergide Article-31 referral - Annex I IT = italiano 27/05/2014  
Methysergide Article-31 referral - Annex I LV = latviešu valoda 27/05/2014  
Methysergide Article-31 referral - Annex I LT = lietuvių kalba 27/05/2014  
Methysergide Article-31 referral - Annex I HU = magyar 27/05/2014  
Methysergide Article-31 referral - Annex I MT = Malti 27/05/2014  
Methysergide Article-31 referral - Annex I NL = Nederlands 27/05/2014  
Methysergide Article-31 referral - Annex I PL = polski 27/05/2014  
Methysergide Article-31 referral - Annex I PT = português 27/05/2014  
Methysergide Article-31 referral - Annex I RO = română 27/05/2014  
Methysergide Article-31 referral - Annex I SK = slovenčina 27/05/2014  
Methysergide Article-31 referral - Annex I SL = slovenščina 27/05/2014  
Methysergide Article-31 referral - Annex I FI = suomi 27/05/2014  
Methysergide Article-31 referral - Annex I SV = svenska 27/05/2014  
Methysergide Article-31 referral - Annex I HR = Hrvatski 27/05/2014  
Methysergide Article-31 referral - Annex I NO = Norsk 27/05/2014  
Methysergide Article-31 referral - Annex II BG = bălgarski 27/05/2014  
Methysergide Article-31 referral - Annex II ES = español 27/05/2014  
Methysergide Article-31 referral - Annex II CS = čeština 27/05/2014  
Methysergide Article-31 referral - Annex II DA = dansk 27/05/2014  
Methysergide Article-31 referral - Annex II DE = Deutsch 27/05/2014  
Methysergide Article-31 referral - Annex II ET = eesti keel 27/05/2014  
Methysergide Article-31 referral - Annex II EL = elliniká 27/05/2014  
Methysergide Article-31 referral - Annex II EN = English 27/05/2014  
Methysergide Article-31 referral - Annex II FR = français 27/05/2014  
Methysergide Article-31 referral - Annex II IT = italiano 27/05/2014  
Methysergide Article-31 referral - Annex II LV = latviešu valoda 27/05/2014  
Methysergide Article-31 referral - Annex II LT = lietuvių kalba 27/05/2014  
Methysergide Article-31 referral - Annex II HU = magyar 27/05/2014  
Methysergide Article-31 referral - Annex II MT = Malti 27/05/2014  
Methysergide Article-31 referral - Annex II NL = Nederlands 27/05/2014  
Methysergide Article-31 referral - Annex II PL = polski 27/05/2014  
Methysergide Article-31 referral - Annex II PT = português 27/05/2014  
Methysergide Article-31 referral - Annex II RO = română 27/05/2014  
Methysergide Article-31 referral - Annex II SK = slovenčina 27/05/2014  
Methysergide Article-31 referral - Annex II SL = slovenščina 27/05/2014  
Methysergide Article-31 referral - Annex II FI = suomi 27/05/2014  
Methysergide Article-31 referral - Annex II SV = svenska 27/05/2014  
Methysergide Article-31 referral - Annex II HR = Hrvatski 27/05/2014  
Methysergide Article-31 referral - Annex III BG = bălgarski 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III ES = español 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III CS = čeština 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III DA = dansk 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III DE = Deutsch 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III ET = eesti keel 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III EL = elliniká 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III EN = English 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III FR = français 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III IT = italiano 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III LV = latviešu valoda 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III LT = lietuvių kalba 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III HU = magyar 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III MT = Malti 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III NL = Nederlands 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III PL = polski 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III PT = português 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III RO = română 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III SK = slovenčina 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III SL = slovenščina 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III FI = suomi 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III SV = svenska 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III HR = Hrvatski 21/02/2014 27/05/2014
Methysergide Article-31 referral - Annex III NO = Norsk 21/02/2014 27/05/2014

Document description

  • Questions and answers (Q&A) - easy-to-understand summary of key issues and Committee conclusions
  • Summary of Opinion - contains the CHMP opinion of the referred medicine(s)
  • List of the medicines affected by the referral (Annex I)
  • Scientific conclusions of the Committee (Annex II)

The following two documents are sometimes available:

  • Changes to the summary of product characteristics, labeling or package leaflet (also known as Annex III) - available when changes have been recommended by the Committee
  • Conditions of the marketing authorisation (also known as Annex IV) - available when the Committee recommends measures to be taken for the marketing authorisation(s) such as safety measures or extra studies

Current status:
Opinion provided by Committee for Medicinal Products for Human Use

Related information