Treatment: leflunomide, sulfasalazine, azathioprine, mycophenolate (tests before treatment and monitoring)
BioMG follows French guidelines. Adapt it to the guidelines and the tests available where you practise.
Before starting
Laboratory tests
- FBC with platelets
- Serum creatinine with eGFR
- AST
- ALT
- Serum albumin
- Hepatitis B serology (HBsAg, anti-HBc, anti-HBs)
- Hepatitis C serology
- TPMT phenotyping or genotyping (azathioprine)if neededBefore any azathioprine: recommended by the SmPC [2] and by the BSR [3]. Outside the French fee schedule (no NABM code) [4].
- EBV serology (azathioprine, especially in inflammatory bowel disease)if needednon-French guidelineBefore a thiopurine: ECCO suggests looking for past EBV infection; in a seronegative patient, consider avoiding the thiopurine (risk of severe primary infection and lymphoproliferation); no comparative data prove the benefit of this screening [5].
- G6PD (sulfasalazine)if neededBefore sulfasalazine: G6PD deficiency is a contraindication (risk of haemolysis) [6]. None of the sources cited requires routine testing: to be done at least if origin or history is suggestive.
- Proteinuria: urine dipstick (sulfasalazine)if neededOn sulfasalazine, renal function is monitored by creatinine and proteinuria [6]: a baseline value is useful.
- Serum β-hCG (leflunomide; woman of childbearing potential)if neededLeflunomide: pregnancy must be excluded before treatment [7].
- Serum β-hCG, two tests 8-10 days apart (mycophenolate; woman of childbearing potential)if neededMycophenolate: two negative pregnancy tests (sensitivity ≥ 25 mIU/mL), the second 8 to 10 days after the first [8].
- HIV serology (with the patient's consent)if needednon-French guidelineThe BSR (2025) screens for HIV in every adult starting a disease-modifying treatment, except on hydroxychloroquine [3]. EULAR suggests considering this screening before conventional disease-modifying treatments and immunosuppressants [9].
- IGRA (QuantiFERON), or tuberculin skin testif neededLeflunomide: the SmPC requires a search for latent tuberculosis in all patients [7]. For other conventional disease-modifying treatments, the BSR looks for it if the risk is increased [3] and EULAR suggests considering it [9]. Not reimbursed in France for this indication [4].
- Varicella serology (anti-VZV IgG), if no history of varicellaif neededNo history of chickenpox or doubtful history: vaccinate if serology is negative, at least 6 weeks before treatment [10]. Reimbursed in France before long-term immunosuppressive treatment [4].
- Leflunomide: blood pressure (and weight) before treatment.
Also consider
- Biologic therapy or JAK inhibitor? For a biologic therapy or JAK inhibitor, see the page "Biothérapie ou inhibiteur de JAK" (tests before and monitoring).
Monitoring: azathioprine
Every week for the first 8 weeks
- FBC with platelets
Every month for 3 months
- AST
- ALT
- Serum creatinine with eGFRif neededThe BSR includes creatinine in the monitoring of all disease-modifying treatments [3]; the SmPC does not ask for it routinely [2].
Then every 1 to 3 months
- FBC with platelets
- AST
- ALT
- Serum creatinine with eGFRif needednon-French guidelineBSR “standard” monitoring, every 3 months after initiation [3].
Monitoring: leflunomide
Every 2 weeks for 6 months
- FBC (with platelets and differential)
- ALT
Then every 8 weeks
- FBC (with platelets and differential)
- ALT
- Serum creatinine with eGFRif neededBSR “standard” monitoring (FBC, GFR, transaminases, albumin) [3]; the SmPC asks only for FBC and ALT [7].
- Serum albuminif neededBSR “standard” monitoring (FBC, GFR, transaminases, albumin) [3]; the SmPC asks only for FBC and ALT [7].
- Blood pressure and weight at every check.
Monitoring: sulfasalazine
Every 2 weeks for 3 months
- FBC with platelets
- AST
- ALT
Every month from the 4th to the 6th month
- FBC with platelets
- AST
- ALT
Then every 3 months
- FBC with platelets
- AST
- ALT
- Serum creatinine with eGFR
- Proteinuria: urine dipstick
Monitoring: mycophenolate
Every week in the 1st month
- FBC with platelets
Twice a month in the 2nd and 3rd months
- FBC with platelets
Then every month until 1 year
- FBC with platelets
- Serum creatinine with eGFRif neededBSR “standard” monitoring for all disease-modifying treatments [3]; the SmPC details only FBC [8].
- ASTif neededBSR “standard” monitoring for all disease-modifying treatments [3]; the SmPC details only FBC [8].
- ALTif neededBSR “standard” monitoring for all disease-modifying treatments [3]; the SmPC details only FBC [8].
- Serum albuminif neededBSR “standard” monitoring for all disease-modifying treatments [3]; the SmPC details only FBC [8].
- Serum immunoglobulins (if recurrent infections)if neededRecurrent infections on mycophenolate: immunoglobulin measurement recommended (hypogammaglobulinaemia reported) [8].
Sources (17)
- Assurance maladie. Open Medic 2025 : nombre de consommants par substance active (ATC5), médicaments remboursés délivrés en officine de ville (fichier NB_2025_atc5). open-data-assurance-maladie.ameli.fr.
- ANSM. Résumé des caractéristiques du produit IMUREL 50 mg, comprimé pelliculé (azathioprine), rubriques 4.2, 4.3, 4.4, 4.5 et 4.6. Base de données publique des médicaments (CIS 64204250), base mise à jour le 29/09/2026, consultée le 11/10/2026 ; date de révision du RCP non renseignée (« A compléter ultérieurement par le titulaire »).
- Bechman K, Song K, Abhishek A, et al. The 2025 British Society for Rheumatology guideline for the prescription and monitoring of conventional synthetic disease-modifying anti-rheumatic drugs. Rheumatology (Oxford). 2025 (publication en ligne), keaf522. Licence CC BY-NC. Remplace la recommandation BSR-BHPR de 2017.
- Assurance maladie. Nomenclature des actes de biologie médicale (NABM), version 105 : actes 4103 (test IGRA), 1779 (anticorps anti-VZV) et 1518 (G6PD) ; absence d'acte pour la TPMT.
- Kucharzik T, Ellul P, Greuter T, et al. ECCO Guidelines on the Prevention, Diagnosis, and Management of Infections in Inflammatory Bowel Disease. J Crohns Colitis. 2021;15(6):879-913.
- ANSM. Résumé des caractéristiques du produit SALAZOPYRINE 500 mg, comprimé enrobé gastro-résistant (sulfasalazine), rubriques 4.3 et 4.4. Base de données publique des médicaments (CIS 67124724), consultée le 11/10/2026 ; date de révision du RCP non renseignée.
- Agence européenne des médicaments. Arava (léflunomide) : résumé des caractéristiques du produit (information produit EPAR, version française), rubriques 4.2, 4.3, 4.4 et 4.6, consulté le 11/10/2026.
- Agence européenne des médicaments. CellCept (mycophénolate mofétil) : résumé des caractéristiques du produit (information produit EPAR, version française), rubriques 4.4 et 4.6, consulté le 11/10/2026.
- Fragoulis GE, Nikiphorou E, Dey M, et al. 2022 EULAR recommendations for screening and prophylaxis of chronic and opportunistic infections in adults with autoimmune inflammatory rheumatic diseases. Ann Rheum Dis. 2023;82(6):742-753.
- Haut Conseil de la santé publique. Vaccination des personnes immunodéprimées ou aspléniques. Recommandations. Rapport, 2e édition, novembre 2014 ; chapitre 5.
- National Institute for Health and Care Excellence. Crohn’s disease: management. NICE guideline NG129, mai 2019 (recommandation 1.2.8).
- NHS Specialist Pharmacy Service (Royaume-Uni). Medicines monitoring : azathioprine, léflunomide, sulfasalazine et mycophénolate mofétil. Pages mises à jour le 7 janvier 2026, avant leur alignement sur la recommandation BSR de 2025.
- Zorginstituut Nederland. Farmacotherapeutisch Kompas : azathioprine, léflunomide, sulfasalazine et mycophénolate mofétil (Pays-Bas). Consulté le 30 octobre 2026.
- U.S. Food and Drug Administration. Étiquetages américains (base openFDA) : azathioprine (19/05/2025), léflunomide (17/12/2025), mycophénolate mofétil (14/05/2026), sulfasalazine (12/12/2022).
- Relling MV, Schwab M, Whirl-Carrillo M, et al. Clinical Pharmacogenetics Implementation Consortium Guideline for Thiopurine Dosing Based on TPMT and NUDT15 Genotypes: 2018 Update. Clin Pharmacol Ther. 2019;105(5):1095-1105.
- Lamb CA, Kennedy NA, Raine T, et al. British Society of Gastroenterology consensus guidelines on the management of inflammatory bowel disease in adults. Gut. 2019;68(Suppl 3):s1-s106.
- British Society for Rheumatology. The 2025 BSR guideline for the prescription and monitoring of conventional synthetic disease-modifying anti-rheumatic drugs : Frequently Asked Questions, version 2.0, mai 2026 (Bechman K, Kavirayani A, Galloway J, Mercer L ; recommandation : Bechman K, et al. Rheumatology (Oxford). 2026;65(2):keaf522).