| Formulary Chapter 10: Musculoskeletal and joint diseases - Full Chapter
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| Notes: |
This chapter of the formulary is under continual development, please let the team know if you have any comments about the contents: mlcsu.lscformulary@nhs.net.
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| Chapter Links... |
 LSCMMG: Gout Management Summary Guidelines |
| LSCMMG: Psoriatic Arthritis Pathway |
| LSCMMG: Radiographic (Ankylosing Spondylitis) and Non-radiographic Axial Spondyloarthritis (ASp) Pathway |
| LSCMMG: Rheumatoid Arthritis Pathway |
| Details... |
| 10.01.03 |
Drugs which suppress the rheumatic disease process |
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Gold |
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| 10.01.03 |
Penicillamine |
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Antimalarials |
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| 10.01.03 |
Drugs affecting the immune response |
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Abatacept (Orencia®)
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Formulary
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Intravenous infusion 250mg
S/C injection 125mg prefilled syringe pre-filled pen
Usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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 NICE TA373: Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis
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
NICE TA715: Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed
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Adalimumab (Biosimilars avaliable)
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Formulary
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S/C injection 40mg prefilled syringe and pen
Usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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MHRA: Tumour necrosis factor alpha inhibitors
NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor
NICE TA199: Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis
NICE TA373: Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis
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
NICE TA383: TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis
NICE TA715: Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed
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Anakinra (Kineret®)
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Formulary
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Solution for injection pre-filled syringes 100mg/0.67mL
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NICE TA685: Anakinra for treating Still’s disease
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Apremilast
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Formulary
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Tablets 10mg, 20mg, 30mg
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MHRA: Apremilast (Otezla ▼): risk of suicidal thoughts and behaviour
NICE TA433: Apremilast for treating active psoriatic arthritis
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Azathioprine
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Formulary
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Tablets 25mg, 50mg
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LSCMMG: Shared care guideline - Azathioprine
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Certolizumab Pegol (Cimzia®)
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Formulary
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S/C injection 200mg prefilled syringe pre-filled pen
Usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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MHRA: Tumour necrosis factor alpha inhibitors
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
NICE TA415: Certolizumab pegol for treating rheumatoid arthritis after inadequate response to a TNF-alpha inhibitor
NICE TA445: Certolizumab pegol and secukinumab for treating active psoriatic arthritis after inadequate response to DMARDs
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Ciclosporin
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Formulary
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Capsules 25mg, 50mg, 100mg
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LSCMMG: Shared care guideline - Ciclosporin
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Cyclophosphamide
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Formulary
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Tablets 50mg
Injection 200mg, 500mg, 1g
 unlicensed use
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Etanercept (Biosimilars avaliable)
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Formulary
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S/C injection 25mg, 50mg vial with diluent and prefilled syringe pre-filled pen
usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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MHRA: Tumour necrosis factor alpha inhibitors
NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor
NICE TA199: Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis
NICE TA373: Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis
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
NICE TA383: TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis
NICE TA715: Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed
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Golimumab (Simponi®)
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Formulary
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S/C injection 50mg, 100mg, prefilled syringe pre-filled pen
Usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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MHRA: Tumour necrosis factor alpha inhibitors
NICE TA220: Golimumab for the treatment of psoriatic arthritis
NICE TA225: Golimumab for the treatment of rheumatoid arthritis after the failure of previous disease-modifying anti-rheumatic drugs
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
NICE TA383: TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis
NICE TA497: Golimumab for treating non-radiographic axial spondyloarthritis
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Guselkumab (Tremfya®)
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Formulary
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Solution for injection in pre-filled pen 100mg/1ml
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NICE TA815: Guselkumab for treating active psoriatic arthritis after inadequate response to DMARDs
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Infliximab (Biosimilars avaliable)
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Formulary
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Intravenous infusion 100mg, 120mg/ml pre-filled pen
REQUIRES BLUETEQ APPROVAL
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MHRA: Tumour necrosis factor alpha inhibitors
NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor
NICE TA199: Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis
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
NICE TA383: TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis
NICE TA715: Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed
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Ixekizumab
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Formulary
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80mg solution for injection prefilled syringe; prefilled pen
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NICE TA537: Ixekizumab for treating active psoriatic arthritis after inadequate response to DMARDs
NICE TA718: Ixekizumab for treating axial spondyloarthritis
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Leflunomide
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Formulary
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Tablets 10mg, 20mg
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LSCMMG: Shared care guideline - Leflunomide
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Methotrexate (check local policy - branded generic available )
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Formulary
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Tablets 2.5mg
S/C 5mg, 7.5mg, 10mg, 12.5mg, 15mg, 17.5mg, 20mg, 22.5mg, 25mg and 30mg
Methotrexate should be prescribed once weekly as a single dose on the same day each week.
If oral methotrexate is prescribed only use the 2.5 mg strength.
See hospital policy for prescribing and supply of oral methotrexate
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LSCMMG: Shared care guideline - Methotrexate
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Risankizumab (Skyrizi®)
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Formulary
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solution for injection pre-filled syringes, solution for injection pre-filled pen 150mg/mL
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NICE TA803: Risankizumab for treating active psoriatic arthritis after inadequate response to DMARDs
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Rituximab (rheumatology) (Biosimilars avaliable)
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Formulary
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Concentrate for intravenous infusion 500mg/50mL
REQUIRES BLUETEQ APPROVAL
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NICE TA195:Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor
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Secukinumab
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Formulary
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150mg/ml pre-filled pens/syringes
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NICE TA407: Secukinumab for active ankylosing spondylitis after treatment with non-steroidal anti-inflammatory drugs or TNF-alpha inhibitors
NICE TA445: Certolizumab pegol and secukinumab for treating active psoriatic arthritis after inadequate response to DMARDs
NICE TA719: Secukinumab for treating non-radiographic axial spondyloarthritis
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Tocilizumab (Biosimilars avaliable)
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Formulary
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Concentrate for intravenous infusion (20mg/mL) 80mg, 200mg, 400mg vials
Soution for injection in pre-filled syringe 162mg
Solution for injection in pre-filled pen 162mg
Usually supplied to patients by a home delivery company
REQUIRES BLUETEQ APPROVAL
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MHRA: Tocilizumab (RoActemra): rare risk of serious liver injury including cases requiring transplantation
NICE TA373: Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis
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
NICE TA518: Tocilizumab for treating giant cell arteritis
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Ustekinumab
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Formulary
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Subcutaneous injection 45mg, 90mg prefilled syringes and 45mg/0.5ml vials
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NICE TA340: Ustekinumab for treating active psoriatic arthritis
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Cytokine modulators |
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Sulfasalazine |
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| Non Formulary Items |
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Key |
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Cytotoxic Drug
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Controlled Drug
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High Cost Medicine
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Cancer Drugs Fund
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NHS England |
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Homecare |
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CCG |
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Low carbon footprint |
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Medium carbon footprint |
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High carbon footprint |
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Traffic Light Status Information
| Status |
Description |
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Green:
Appropriate for initiation and ongoing prescribing in both primary and secondary care.
Generally, little or no routine drug monitoring is required. |
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Green (Restricted):
Appropriate for initiation and ongoing prescribing in both primary and secondary care provided:
Additional criteria specific to the medicine or device are met, or
The medicine or device is used following the failure of other therapies as defined by the relevant LSCMMG pathway.
Generally, little or no routine drug monitoring is required.
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Red medicines:
Medicine is supplied by the hospital for the duration of the treatment course.
Primary care initiation or continuation of treatment is not recommended unless exceptional circumstances such as specialist GP.
Red medicines are those where primary care prescribing is not recommended. These treatments should be initiated by specialists only and prescribing retained within secondary care. They require specialist knowledge, intensive monitoring, specific dose adjustments or further evaluation in use. If however, a primary care prescriber has particular specialist knowledge or experience of prescribing a particular drug for a particular patient it would not always be appropriate for them to expect to transfer that prescribing responsibility back to secondary care. There should be a specific reason and a specific risk agreement, protocol and service set up to support this.
Primary care prescribers may prescribe RED medicines in exceptional circumstances to patients to ensure continuity of supply while arrangements are made to obtain ongoing supplies from secondary care. |
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Amber level 0:
Suitable for prescribing in primary care following recommendation or initiation by a specialist.
Little or no specific monitoring required.
Patient may need a regular review, but this would not exceed that required for other medicines routinely prescribed in primary care.
Brief prescribing document or information sheet may be required.
Primary care prescribers must be familiar with the drug to take on prescribing responsibility or must get the required information.
When recommending or handing over care, specialists should ask primary care prescribers to take over prescribing responsibility, and should give enough information about the indication, dose, monitoring requirements, use outside product licence and any necessary dose adjustments to allow them to confidently prescribe. |
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Amber level 1 (with shared care):
Suitable for prescribing in primary care following recommendation or initiation by a specialist.
Minimal monitoring required.
Patient may need a regular review, but this would not exceed that required for other medicines routinely prescribed in primary care.
Full prior agreement about patient’s on-going care must be reached under the shared care agreement.
Primary care prescribers are advised not to take on prescribing of these medicines unless they have been adequately informed by letter of their responsibilities with regards monitoring, side effects and interactions and are happy to take on the prescribing responsibility. A copy of locally approved shared care guidelines should accompany this letter which outlines these responsibilities. Primary care prescribers should then tell secondary care of their intentions as soon as possible by letter so that arrangements can be made for the transfer of care. |
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Amber level 2 (with shared care and enhanced service):
Initiated by specialist and transferred to primary care following a successful initiation period.
Significant monitoring required on an on-going basis.
Full prior agreement about patient’s on-going care must be reached under the shared care agreement.
Suitable for enhanced service.
These medicines are considered suitable for GP prescribing following specialist initiation of therapy, as per shared care document which will be sent out with the request to prescribe, with on-going communication between the primary care prescriber and specialist. Amber Level 2 medicines require significant monitoring for which an enhanced service may be suitable. (Subject to local commissioning agreements). |
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Do not prescribe: NOT recommended for use by the NHS in Lancashire and South Cumbria.
Includes medicines that NICE has not recommended for use and terminated technology appraisals, unless there is a local need. |
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Grey medicines:
Medicines which have not yet been reviewed or are under the review process.
GPs and specialists are recommended not to prescribe these drugs.
This category includes drugs where funding has not yet been agreed.
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Refer to local guidance. |
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