10.1 Arthritis
First line drugs | Second line drugs | Specialist drugs | Secondary care drugs |
Traffic light status (TLS) explained:
- Green: Routine prescribing within licensed indication
- Amber 1: specialist recommendation followed by GP initiation and continuation
- Amber 2: specialist or GP initiation in line with local guideline after 1st line failure followed by GP continuation
- Amber 3: specialist initiation and stabilisation followed by GP continuation
- Amber SCG: specialist initiation and stabilisation followed by GP continuation in line with an agreed shared care guideline
- Red: Hospital or specialist prescribing only
- Double Red: These medicines have been evaluated and rejected by MKPAG and are NOT approved for use within MK. They are not recommended for use because of lack of clinical effectiveness, cost effectiveness or safety.
Disease-Modifying Rheumatic Drugs (DMARDS)
Shared Care Guideline
DMARD Shared Care Guideline can be found by clicking on the following link: https://www.formularymk.nhs.uk/includes/documents/Shared-Care-Guideline-for-the-use-of-DMARDs-Final-Jan-2019.pdf
Azathioprine (Amber SCG, DMARD SCG)
- Tablets 25mg, 50mg
Chloroquine (Amber 2)
- Tablets 250mg
- Syrup 68mg in 5ml (Hospital only)
Ciclosporin (Amber SCG, DMARD SCG)
- Capsules 10mg, 25mg, 50mg, 100mg
- Oral solution 100mg/ml
Notes:
- Ciclosporin (Neoral®) is licensed for severe active RA when conventional second-line therapy is inappropriate or ineffective.
- It is contraindicated in abnormal renal function, uncontrolled hypertension, uncontrolled infections and malignancy.
- Monitor hepatic function if concomitant NSAIDs given.
- As there are differences in bioavailability, the brand of ciclosporin to be dispensed should be specified by the prescriber.
Hydroxychloroquine sulfate (Amber SCG, DMARD SCG)
- Tablets 200mg
Leflunomide (Amber SCG, DMARD SCG)
- Tablets 10mg,20mg
Methotrexate (Amber SCG, DMARD SCG)
- Tablets 2.5mg
- Metoject® Injection prefilled syringe 10mg, 15mg, 20mg, 25mg
Notes:
- CSM Warning – Methotrexate: In view of reports of blood dyscrasias (including fatalities) and liver cirrhosis with low-dose methotrexate, the CSM has advised:
- specific monitoring guidance (superseded by NPSA alerts and nGMS);
- that patients should be advised to report all symptoms and signs suggestive of infection, especially sore throat.
- Treatment with folinic acid (as calcium folinate) may be required in acute toxicity.
- The CSM has received reports of prescription and dispensing errors with methotrexate, including fatalities. Attention should be paid to the strength of methotrexate tablets prescribed and the frequency of dosing.
- The label on prescribed/dispensed methotrexate should state the instructions clearly, for example: ‘methotrexate 2.5mg tablets: (number of tablets) to be taken as a single dose ONCE A WEEK on XXXDAY’.
- Keep repeat prescriptions for methotrexate separate from others
- In the treatment of non-cancer conditions (eg. rheumatology and dermatology), methotrexate must be given once a week or once a month. Staff that encounter methotrexate prescriptions must ensure the correct dosing interval is given.
- In patients who experience mucosal or gastrointestinal side effects with methotrexate, folic acid 5mg each week (taken 48 hours after the methotrexate dose) may be given. It may be given routinely to help reduce the frequency of such side effects.
Methotrexate-induced mucositis or myelosuppression: folinic acid (given as calcium folinate) is used to counteract the folate-antagonist action of methotrexate and so facilitate recovery from methotrexate-induced mucositis or myelosuppression. - Methotrexate and NSAIDs: if aspirin or other NSAIDs are given concurrently the dose of methotrexate should be carefully monitored. Patients should be advised to avoid self-medication with over-the-counter aspirin or ibuprofen.
Penicillamine (Amber SCG, DMARD SCG)
- Tablets 125mg,250mg
Sodium aurothiomalate (Amber SCG, DMARD SCG)
- Injection 10mg in 0.5mL, 50mg in 0.5mL
Sulfasalazine (Amber SCG, DMARD SCG)
- Tablets e/c 500mg
Interleukin inhibitors
Sarilumab
- Kevzara® Solution for injection 150mg, 200mg pre-filled syringe or pen
Note:
- Use as per NICE TA485: Sarilumab for moderate to severe rheumatoid arthritis (November 2017)
Secukinumab
- Cosentyx® Solution for injection, 150mg in pre-filled pen or syringe
Notes:
- Use by per NICE TA445:Certolizumab pegol and secukinumab for treating active psoriatic arthritis after inadequate response to DMARD (May 2017)
- Use by per NICE TA407:Secukinumab for active ankylosing spondylitis after treatment with non-steroidal anti-inflammatory drugs or TNF-alpha inhibitors (September 2016)
Tocilizumab
- RoActemra® 162mg solution for injection in pre-filled pen or pre-filled syringe.
- RoActemra® Intravenous infusion 20mg in 1mL
Notes:
- Use as per NICE TA518: Tocilizumab for treating giant cell arteritis(April 2018)
- Use as per NICE TA375:Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed (January 2016)
- Use as per NICE TA247: Tocilizumab for the treatment of rheumatoid arthritis (Feb 2012)
- Use as per NICE TA238:Tocilizumab for the treatment of systemic juvenile idiopathic arthritis (December 2011)
Ustekinumab
- Stelara® Injection, 45mg, 90mg solution in pre-filled syringe or vial
Notes:
- Use as per NICE TA445: Certolizumab pegol and secukinumab for treating active psoriatic arthritis after inadequate response to DMARDs (May 2017)
- Use as per NICE TA340:Ustekinumab for treating active psoriatic arthritis (March 2017)
- Use as per NICE TA180:Ustekinumab for the treatment of adults with moderate to severe psoriasis(March 2017)
Protein Kinase Inhibitors
Baricitinib
- Olumiant® Tablets film-coated 2mg, 4mg
Note:
- Use as per NICE TA466: Baricitinib for moderate to severe rheumatoid arthritis (August 2017)
Tofacitinib citrate
- Xeljanz® Tablets film-coated 5mg
Notes:
- Use as per NICE TA543: Tofacitinib for treating active psoriatic arthritis after inadequate response to DMARDs (October 2018)
- Use as per NICE TA480: Tofacitinib for moderate to severe rheumatoid arthritis (October 2017)
T-Cell Activation Inhibitors
Abatacept
- Orencia® Intravenous infusion 250mg
Notes:
- Use as per NICE TA375 Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed (January 2016)
- Use as per NICE TA280: Abatacept for treating rheuma
- toid arthritis after the failure of conventional disease-modifying anti-rheumatic drugs (April 2013)
- Use as per NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor (August 2010)
Tumour Necrosis Factor Alpha (TNF-alpha) Inhibitors
Adalimumab
- Imraldi, Injection, 40mg/0.8mL prefilled pen or prefilled syringe
- Amgevita, Injection, 20mg/0.4mL; 40mg/0.8mL prefilled pen or prefilled syringe
- Humira, Injection, 40mg/0.4mL; 80mg/0.8mL prefilled pen or prefilled syringe
- Humira, Injection, 20mg/0.2mL pre-filled syringe, 40mg/0.8mL solution in vial for first line use in paediatrics
Notes:
- To be prescribed by brand.
- First line brand in adults = Imraldi®
- Second line brand in adults = Amgevita®
- Third line brand in adults = Humira®
- Hulio and Hyrimoz are non-formulary within Milton Keynes Healthcare
- Use as per NICE TA383:TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis (February 2016)
- Use as per NICE TA375:Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed(January 2016)
- Use as per NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor (August 2010)
- Use as per NICE TA199: Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis(August 2010)
Certolizumab Pegol
- Cimzia® Solution for injection, 200mg in pre-filled pen or in pre-filled syringe
Notes:
- Use as per NICE TA574: Certolizumab pegol for treating moderate to severe plaque psoriasis (April 2019)
- Use as per NICE TA445:Certolizumab pegol and secukinumab for treating active psoriatic arthritis after inadequate response to DMARDs (May 2017)
- Use as per NICE TA415: Certolizumab pegol for treating rheumatoid arthritis after inadequate response to a TNF-alpha inhibitor(October 2016)
- Use as per NICE TA375:Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed (January 2016)
Etanercept
- Enbrel® 25mg in 0.5mL pre filled syringe, 25mg injection.
Notes:
- Use as per NICE TA375:Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed (January 2016)
- Use as per NICE TA199: Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis(August 2010)
- Use as per NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor (August 2010)
- Use as per NICE TA383:TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis (February 2016)
Golimumab
- Simponi®
- 50mg in 0.5mL solution in pre-filled pen, 100mg in1mL solution in pre-filled pen
- Notes:
- Use as per NICE TA497: Golimumab for treating non-radiographic axial spondyloarthritis (January 2018)
Infliximab
- Remicade® 100mg vial powder for reconstition.
Notes:
- Use as per NICE TA383: TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis (Feb 2016)
-
Use as per NICE TA199:Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis(August 2010)
Rituximab
- MabThera®Concentrate for IV infusion 100mg in 10mL, 500mg in 50mL
Notes:
- Use as per NICE TA195: Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor (August 2010)
Phosphodiesterase type-4 inhibitors
Apremilast
- Tablet 10mg,20mg,30mg
Notes:
- Use as per NICE TA433:Apremilast for treating active psoriatic arthritis (February 2017)
Traffic light status (TLS) explained:
- Green: Routine prescribing within licensed indication
- Amber 1: specialist recommendation followed by GP initiation and continuation
- Amber 2: specialist or GP initiation in line with local guideline after 1st line failure followed by GP continuation
- Amber 3: specialist initiation and stabilisation followed by GP continuation
- Amber SCG: specialist initiation and stabilisation followed by GP continuation in line with an agreed shared care guideline
- Red: Hospital or specialist prescribing only
- Double Red: These medicines have been evaluated and rejected by MKPAG and are NOT approved for use within MK. They are not recommended for use because of lack of clinical effectiveness, cost
- effectiveness or safety
Return to Chapter: 10. Musculoskeletal and Joint Diseases
Last updated by: Sheila Wood on 05-06-2019 13:39