BNF Section/s |
Title |
Issuing Body |
Date of Issue |
Update Due |
10.1.3 |
Anakinra (Kineret®) |
High-Cost Drugs |
|
|
10.1.3 |
Anakinra (Kineret®) for Haemophagocytic Lymphohistiocytosis (HLH) for adults and children in all ages [210701P] (1924) |
NHS England |
Nov 2021 |
|
10.1 |
Apremilast |
High-Cost Drugs |
|
|
10.1.3 |
Bimekizumab
|
High-Cost Drugs |
|
|
10.1.3 |
Bimekizumab - Bimekizumab for treating axial spondyloarthritis TA918 |
NICE |
Oct 2023 |
|
10.1.3 |
Bimekizumab - Bimekizumab for treating active psoriatic arthritis TA916 |
NICE |
Oct 2023 |
|
10.2.2 |
Febuxostat - Febuxostat: updated advice for the treatment of patients with a history of major cardiovascular disease |
MHRA Drug Safety Update |
May 2023 |
- |
10.1.3 |
Filgotinib |
High-Cost Drugs |
|
|
10.1.3 |
Filgotinib - Filgotinib for treating moderate to severe rheumatoid arthritis TA676 |
NICE |
Feb 2021 |
2024 |
10.2.2 |
Gout: diagnosis and management NICE guideline NG219 |
NICE |
Jun 2022 |
- |
10.1.3 |
Guselkumab |
High-Cost Drugs |
- |
- |
10.1.3 |
Guselkumab - Guselkumab for treating active psoriatic arthritis after inadequate response to DMARDs TA815 |
NICE |
Aug 2022 |
- |
10.1.1 |
Hydroxychloroquine, chloroquine - increased risk of cardiovascular events when used with macrolide antibiotics; reminder of psychiatric reactions
|
MHRA Drug Safety Update |
Feb 2022 |
- |
10.1.3 |
Infliximab biosimilar (Flixabi®) |
High-Cost Drugs |
|
|
10.1.3 |
Infliximab biosimilar - Flixabi® Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed TA375 ICB commissioned - approval via Blueteq |
NICE |
Dec 2015 |
|
10.1.3 |
Infliximab biosimilar - Flixabi® Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor TA195 ICB commissioned - approval via Blueteq
|
NICE |
Aug 2010 |
|
10.1.3 |
Infliximab biosimilar - Flixabi® Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed TA715 ICB commissioned - approval via Blueteq |
NICE |
Jul 2021 |
|
10.1.3 |
Infliximab biosimilar - Flixabi® Etanercept, infliximab and adalimumab for the treatment of psoriatic arthritis TA199 ICB commissioned - approval via Blueteq |
NICE |
Aug 2010 |
|
10.1.3 |
Infliximab biosimilar - Flixabi® TNF-alpha inhibitors for ankylosing spondylitis and non-radiographic axial spondyloarthritis TA383 ICB commissioned - approval via Blueteq |
NICE |
Feb 2016 |
|
10.4 |
NSAIDS - Non-steroidal anti-inflammatory drugs (NSAIDs): potential risks following prolonged use after 20 weeks of pregnancy
|
MHRA Drug Safety Update |
Jun 2023 |
- |
10.3.3 |
Quinine - Safety Alert - Quinine not to be used routinely for nocturnal leg cramps |
MHRA Drug Safety Update |
Dec 2014 |
- |
10.3.3 |
Quinine - Safety Alert - Quinine reminder of dose-dependent QT-prolonging effects; updated medicine interactions |
MHRA Drug Safety Update |
Nov 2017 |
- |
10.1.3 |
Risankizumab |
High-Cost Drugs |
- |
- |
10.1.3 |
Risankizumab - Risankizumab for treating active psoriatic arthritis after inadequate response to DMARDs TA803 |
NICE |
Jul 2022 |
2025 |
10.1.3 |
Rituximab see High Cost Drugs Manual for all commissioning indications
|
High-Cost Drugs |
|
|
10.1.3 |
Tocilizumab biosimilar Tyenne® |
High-Cost Drugs |
|
|
10.1.3 |
Tocilizumab biosimilar Tyenne® - Tocilizumab for the treatment of systemic juvenile idiopathic arthritis NICE Guidance TA238 ICB commissioned - approval via Blueteq |
NICE |
Dec 2011 |
|
10.1.3 |
Tocilizumab biosimilar Tyenne® - Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis NICE Guidance TA373 NHSE commissioned - Prior approval proforma required via Blueteq
|
NICE |
Dec 2015 |
|
10.1.3 |
Tocilizumab biosimilar Tyenne® - 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 GuidanceTA375 ICB commissioned - approval via Blueteq |
NICE |
Jan 2016 |
|
10.1.3 |
Tofacitnib (Xeljanz®) |
High-Cost Drugs |
- |
- |
10.1.3 |
Tofacitnib - Tofacitinib for treating active ankylosing spondylitis TA920 |
NICE |
Oct 2023 |
- |
10.1.3 |
Upadacitinib |
High-Cost Drugs |
- |
- |
10.1.3 |
Upadacitinib - Upadacitinib for treating moderate rheumatoid arthritis TA744 |
NICE |
Nov 2021 |
2024 |
10.1.3 |
Upadacitinib - Upadacitinib for treating active ankylosing spondylitis TA829 |
NICE |
Sep 2022 |
- |
10.1.3 |
Upadacitinib - Upadacitinib for treating active non-radiographic axial spondyloarthritis TA861 |
NICE |
Feb 2023 |
|