Formulary Chapter 1: Gastro-intestinal system - Full Chapter
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Chapter Links... |
County Durham and Tees Valley Guidance for Prescribing and Monitoring in Post Bariatric Surgery in Primary Care |
Guidelines for the Management of Adults with Asymptomatic Liver Blood Test Abnormalities |
North of Tyne, Gateshead and North Cumbria - Management of patients, post-bariatric surgery in primary care |
NTAG: Transanal irrigation (TAI) systems (Peristeen Plus®, Aquaflush®, and QuFora®) for neurogenic bowel dysfunction, chronic constipation and chronic faecal incontinence |
Details... |
01.01 |
Dyspepsia and gastro-oesophageal reflux disease |
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01.01 |
Gastro-oesophageal reflux disease |
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01.01.01 |
Antacids and simeticone |
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01.01.01 |
Aluminium and magnesium containing antacids |
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Co-magaldrox (Mucogel®)
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First Choice
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- First choice in the community due to cost.
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Co-magaldrox (Maalox®)
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Formulary
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- Mucogel is first choice in the community due to cost.
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01.01.01 |
Aluminium-magnesium complexes |
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01.01.01 |
Antacid preparations containing simeticone |
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Co-simalcite (Altacite plus®)
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Formulary
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01.01.01 |
Simeticine alone |
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Simeticone (Infacol® Dentinox®)
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Formulary
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01.01.01 |
Antacid preparations containing dimeticone or local anaesthetics |
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01.01.02 |
Compound alginates and proprietary indigestion preparations |
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01.01.02 |
Compound alginate preparations |
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Peptac
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First Choice
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- Preferred antacid for treating reflux. Use instead of Gaviscon®.
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Gaviscon Infant
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Formulary
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- Note: each half of the dual-sachet is identified as ‘one dose'.
To avoid errors prescribe as ‘dual-sachet' with directions in terms of ‘dose'
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Antacid with oxetacaine
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Unlicensed
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- Used to relieve symptoms in patients who have had radiotherapy and may be of value in some patients with acute oesophagitis. Not for routine use as an antacid.
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01.02 |
Antispasmodics and other drugs altering gut motility |
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Hyoscine Butylbromide (Buscopan®)
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First Choice
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- First choice for respiratory secretions
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MHRA Drug Safety Update (Feb 2017): Hyoscine butylbromide (Buscopan) injection: risk of serious adverse effects in patients with underlying cardiac disease
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Propantheline
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Formulary
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Dicycloverine
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Formulary
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Glycopyrronium bromide
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Restricted
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- 1mg/5mL oral solution sugar free
- Approved for the first line treatment of uncontrolled oral/respiratory secretions/sialorrhoea in Motor Neurone Disease/Home Ventilation patients who have cognitive impairment.
- Approved for second line treatment of uncontrolled oral/respiratory secretions/sialorrhoea in Motor Neurone Disease/Home Ventilation patients who have failed other treatment options such as hyoscine patches or who have intolerance to other agents.
- 2mg/5ml oral solution (Sialanar®)
- approved for the treatment of severe sialorrhoea in children and adolescents with chronic neurological disorders.
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01.02 |
Other antispasmodics |
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Mebeverine
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Formulary
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Peppermint Oil (Colpermin®)
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Formulary
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Peppermint water
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Formulary
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01.02 |
Motility stimulants |
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Domperidone
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Formulary
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Tablets - 10mg Suspension - 5mg/5ml
MHRA Drug Safety Alert (May 2014): Domperidone: risk of cardiac side effects MHRA Drug Safety Update (Dec 2019): Domperidone for nausea and vomiting: lack of efficacy in children; reminder of contraindications in adults and adolescents
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Metoclopramide
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Formulary
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Tablets - 10mg Oral Solution - 5mg/5ml Caution in elderly, young adults and children Do not use in people under 20 years
MHRA Drug Safety Update Alert (Aug 2013): Metoclopramide: risk of neurological adverse effects
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01.03 |
Antisecretory drugs and mucosal protectants |
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01.03 |
Helicobacter pylori infection |
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First choice regimen - eradication (H.Pylori)
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Formulary
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- The most current H.Pylori guidance and treatment regimens can be found here
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01.03 |
NSAID-associated ulcers |
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01.03.01 |
H2-receptor antagonists |
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Cimetidine
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Formulary
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Famotidine
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Formulary
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Nizatidine
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Formulary
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01.03.02 |
Selective antimuscarinics |
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01.03.03 |
Chelates and complexes |
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Sucralfate 1g/5ml oral suspension
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Restricted
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- Approved for bile reflux and stomal ulceration.
- Approved for short term use post Radio Frequency Ablation (RFA) for Barret's Oesophagus and Endoscopic Mucosal Resection (EMR).
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01.03.04 |
Prostaglandin analogues |
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Misoprostol
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Formulary
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- Note: 100 microgram tablets (unlicensed) are also on formulary - mainly for use in paediatric nephrology at the RVI.
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01.03.05 |
Proton pump inhibitors (PPIs) |
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Lansoprazole
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Formulary
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- 15mg and 30mg capsules
- Orodispersible tablets should only be used in patients who cannot swallow capsules or tablets and for NG/PEG/PEJ use. Omeprazole capsules are currently cheaper than lansoprazole capsules in primary care.
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Omeprazole
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Formulary
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- 10mg, 20mg & 40m capsules
- Dispersible tablets (Losec® MUPS) should only be used in patients who cannot swallow capsules or tablets and where lansoprazole orodispersible tablets are unsuitable.
- 10mg in 5ml oral suspension can be obtained for use in very small children and where a suspension has to be given down a very fine NG tube (below French Size 8) . Green plus
- For acute Gastrointestinal bleeding see local guidelines
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Esomeprazole
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Formulary
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Omeprazole IV
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Formulary
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- 40mg IV Infusion
- 40mg Injection (powder for reconstitution)
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Pantoprazole IV
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Formulary
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01.03.06 |
Other ulcer-healing drugs |
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01.04 |
Acute diarrhoea |
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01.04.01 |
Adsorbents and bulk-forming drugs |
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01.04.02 |
Antimotility drugs |
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Loperamide
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First Choice
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- 2mg tablets and capsules
- 2mg orodispersible tablets: approved for use in patients with high output stoma only when crushing tablets or opening capsules has failed. Also apporved for oral cancer patients struggling to take capsules
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MHRA Drug Safety Alert Sept 2017: Loperamide (Imodium): Reports of serious cardiac adverse reactions with high doses of loperamide associated with abuse or misuse
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Teduglutide (Revestive®)
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Formulary
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- Approved for treating short bowel syndrome in people 1 year and above in line with NICE
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NICE TA804: Teduglutide for treating short bowel syndrome
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Codeine
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Alternatives
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MHRA Drug Safety Update (Dec 2014): Codeine for analgesia: restricted use in children because of reports of morphine toxicity
MHRA Drug Safety Update (Dec 2014): Codeine: very rare risk of side-effects in breastfed babies
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01.04.03 |
Enkephalinase Inhibitors |
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01.05 |
Chronic bowel disorders |
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01.05 |
Irritable bowel syndrome |
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01.05 |
Malabsorption syndromes |
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01.05 |
Inflammatory bowel disease |
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01.05 |
Antibiotic-associated colitis |
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01.05 |
Diverticular disease |
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01.05 |
Aminosalicylates |
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01.05 |
Cytokine inhibitors |
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01.05.01 |
Aminosalicylates |
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Mesalazine (Oral preparations)
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Formulary
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First Choice
- Octasa MR® (400mg e/c m/r tablets): approved as first choice 400mg e/c m/r preparation for all new patients. Patients receiving Asacol® and Mesren® should be switched to Octasa® when appropriate. 800mg & 1600mg e/c m/r tablets also approved for suitable patients - to reduce tablet burden.
- Pentasa® (500mg & 1000mg m/r tablets).
- Mezavant® XL (1.2g e/c m/r tablets).
- Salofalk® (500mg, 1000mg, 1500mg & 3000mg m/r granules/sachet) - only to be used in patients with difficulty in swallowing.
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MSN/2024/028: Discontinuation of Asacol 400mg MR gastro-resistant tablets
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Balsalazide Sodium (Oral Preparations)
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Formulary
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Alternatives
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Mesalazine (Rectal Preparations)
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Formulary
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- 1g in 100ml retention enema, 2g in 59ml enema
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Sulfasalazine (Oral Preparations)
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Alternatives
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County Durham and Darlington - Sulfasalazine shared care guideline
North of Tyne, Gateshead and North Cumbria - Monitoring of Immune Modifying Drugs (IMDs) in Stable Adult Patients (excluding post transplantation) in Primary and Secondary Care shared care guideline
South Tyneside and Sunderland APC Shared Care Guideline - sulfasalazine
Tees Valley Shared Care Guideline - sulfasalazine
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Prednisolone (Oral Preparations)
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Formulary
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First Choice
See BNF 06:03:02 for formulations
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Budesonide (Oral Preparations)
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Formulary
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- Alternative
- Budenofalk® (3mg capsules enclosing e/c pellets)
- Entocort® (3mg capsules enclosing e/c m/r pellets)
- For use on consultant gastroenterologist advice only
- Oral Viscous Budesonide unlicensed
- For the treatment of eosinophilic oesophagitis.
- 0.5mg or 1mg nebule is added to 13ml of syrup and this is then mixed and swallowed.
- Orodispersible tablet (Jorveza®)
- For the treatment of eosinophilic oesophagitis in adults in line with NICE
- Approved for the maintenance of eosinophilic oesophagitis in line with NTAG
- 9mg MR tablet (Cortiment®)
- For induction of remission in patients with mild to moderate active ulcerative colitis (UC) where 5-ASA treatment is not sufficient.
- 8 week course to be provided by secondary care.
- 4mg modified-release capsules (Kinpeygo®)
- Approved for treating primary IgA nephropathy in line with NICE
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NICE TA708 - Budesonide orodispersible tablet for inducing remission of eosinophilic oesophagitis
NICE TA937: Targeted-release budesonide for treating primary IgA nephropathy
NTAG Treatment Appraisal: Budesonide orodispersible (Jorveza®) for maintenance treatment of eosinophilic oesophagitis
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Prednisolone (Rectal Preparations)
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Formulary
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Budesonide (Rectal Preparations)
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Formulary
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- 2mg foam enema
- Equal first choice with hydrocortisone foam enema
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01.05.03 |
Drugs affecting the immune response |
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Azathioprine
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Formulary
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North Cumbria SCG - Azathioprine & Mercaptopurine
South Tyneside & Sunderland APC Shared Care Guideline - Azathioprine and Mercaptopurine in Gastroenterology
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Ciclosporin
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Formulary
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- Capsules: 10mg, 25mg, 50mg, 100mg
- Oral solution: 100mg/ml
- Must be prescribed by brand name
- Brands include Capimune, Capsorin, Deximune, Neoral, Sandimmun, Vanquoral
- 50mg/1ml continuous infusion
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County Durham and Darlington Shared Care Guideline: Ciclosporin
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Etrasimod (Velsipity®)
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Formulary
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- 2mg tablet
- Approved for treating moderately to severely active ulcerative colitis in people aged 16 and over in line with NICE
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NICE TA956: Etrasimod for treating moderately to severely active ulcerative colitis in people aged 16 and over
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Filgotinib (Jyseleca®)
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Formulary
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- 100mg and 200mg tablets
- Approved for the treatment of moderate to severe active ulcerative colitis in line with NICE
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MHRA Drug Safety Update April 2023: Janus kinase (JAK) inhibitors: new measures to reduce risks of major cardiovascular events, malignancy, venous thromboembolism, serious infections and increased mortality
NICE TA792: Filgotinib for treating moderately to severely active ulcerative colitis
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Mercaptopurine
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Formulary
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County Durham and Darlington Shared Care Guideline: 6-Mercaptopurine
North Cumbria SCG - Azathioprine & Mercaptopurine
South Tyneside & Sunderland APC Shared Care Guideline - Azathioprine and Mercaptopurine in Gastroenterology
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Tofacitinib (Xeljanz®) (See 10.01.03 Drugs which suppress the rheumatic disease process)
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Formulary
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- 5mg and 10mg tablets.
- Approved for the treatment of moderate to severe active ulcerative colitis in line with NICE
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MHRA Drug Safety Alert Oct 2021: Tofacitinib (Xeljanz▼): new measures to minimise risk of major adverse cardiovascular events and malignancies
MHRA Drug Safety Alert March 2020: Tofacitinib (Xeljanz▼): new measures to minimise risk of venous thromboembolism and of serious and fatal infections
MHRA Drug Safety Update (April 2023): Janus kinase (JAK) inhibitors: new measures to reduce risks of major cardiovascular events, malignancy, venous thromboembolism, serious infections and increased mortality
MHRA Drug Safety Update May 2019: Tofacitinib (Xeljanz▼): restriction of 10 mg twice-daily dose in patients at high risk of pulmonary embolism while safety review is ongoing
NICE TA547: Tofacitinib for moderately to severely active ulcerative colitis
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Upadacitinib (Rinvoq®)
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Formulary
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- 15 and 30mg tablets
- Approved for the treatment of moderate to severe active ulcerative colitis in line with NICE
- Approved for previously treated moderately to severely active Crohn's disease in line with NICE
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MHRA Drug Safety Update April 2023: Janus kinase (JAK) inhibitors: new measures to reduce risks of major cardiovascular events, malignancy, venous thromboembolism, serious infections and increased mortality
NICE TA856: Upadacitinib for treating moderately to severely active ulcerative colitis
NICE TA905: Upadacitinib for previously treated moderately to severely active Crohn’s disease
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Methotrexate
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Formulary
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- See section 8.1.3
- NOTE: Subcutaneous injection for chronic inflammatory conditions in Tees SICBL
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County Durham and Darlington Shared Care Guideline: Methotrexate
MHRA Drug Safety Update (August 2023): Methotrexate: advise patients to take precautions in the sun to avoid photosensitivity reactions
MHRA Drug Safety Update (Sept 2020): Methotrexate once weekly for autoimmune diseases: new measures to reduce risk of fatal overdose due to inadvertent daily instead of weekly dosing
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Vedolizumab
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Formulary
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- Only approved for use in accordance with NICE guidance.
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NICE TA352: Vedolizumab for treating moderately to severely active Crohn’s disease after prior therapy
NICE TA342: Vedolizumab for treating moderately to severely active ulcerative colitis
NICE TA826: Vedolizumab for treating chronic refractory pouchitis after surgery for ulcerative colitis (terminated appraisal)
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01.05.03 |
Cytokine inhibitors |
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Adalimumab
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Formulary
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- Only approved for use in accordance with NICE guidance.
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NICE TA187: Crohn’s disease - infliximab and adalimumab
NICE TA329: Infliximab, adalimumab and golimumab for moderately to severely active ulcerative colitis
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Golimumab
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Formulary
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- Only approved for use in accordance with NICE guidance.
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NICE TA329: Infliximab, adalimumab and golimumab for moderately to severely active ulcerative colitis
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Infliximab (Remicade®, Inflectra®, Remsima®)
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Formulary
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- Only approved for use in accordance with NICE guidance.
- Prescribe by brand only.
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NICE TA163: Ulcerative colitis (acute manifestations) Infliximab
NICE TA187: Crohns disease - infliximab & adalimumab
NICE TA329: Infliximab, adalimumab and golimumab for moderately to severely active ulcerative colitis
NTAG recommends the use of infliximab biosimilars as an option where the originator product (Remicade®) would normally be prescribed
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Mirikizumab (Omvoh®)
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Formulary
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- 100mg/1ml solution for injection pre-filled pens & 300mg/15ml concentrate for solution for infusion
- Approved for treating moderately to severely active ulcerative colitis in adults in line with NICE
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NICE TA925: Mirikizumab for treating moderately to severely active ulcerative colitis
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Risankizumab (Skyrizi®)
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Formulary
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- 150mg/1ml solution for injection (pre-filled devices)
- Approved for previously treated moderately to severely active Crohn's disease in people 16 years and over in line with NICE
- Approved for treating moderately to severely active ulcerative colitis in adults in line with NICE
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NICE TA888: Risankizumab for previously treated moderately to severely active Crohn’s disease
NICE TA998: Risankizumab for treating moderately to severely active ulcerative colitis
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Ustekinumab (Stelara® )
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Formulary
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- 130 mg concentrate for solution for infusion
- Approved for previously treated moderately to severely active Crohn’s disease in adults in line with NICE
- Approved for treating moderately to severely active ulcerative colitis in line with NICE
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MHRA Drug Safety Update (Jan 2015): Ustekinumab (Stelara): risk of exfoliative dermatitis
NICE TA456 Ustekinumab for moderately to severely active Crohn’s disease after previous treatment
NICE TA633: Ustekinumab for treating moderately to severely active ulcerative colitis
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Ozanimod (Zeposia®)
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Formulary
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- Approved for moderately to severely active ulcerative colitis in adults in line with NICE.
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NICE TA 828: Ozanimod for treating moderately to severely active ulcerative colitis
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01.06.01 |
Bulk-forming laxatives |
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Ispaghula Husk
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First Choice
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01.06.02 |
Stimulant laxatives |
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Senna
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First Choice
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- Avoid 15mg strength, this is an OTC product.
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Sodium hydrogen carbonate / sodium dihydrogen phosphate (Lecicarbon A® Suppository)
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Formulary
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Sodium hydrogen carbonate 500mg, sodium dihydrogen phosphate 680mg - Lecicarbon A® Suppository
- Pre-operative use for patients undergoing rectal surgery or diagnostic procedure
- 2nd/3rd line in spinal injuries after bisacodyl and glycerol rectal have been tried.
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Bisacodyl
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Alternatives
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Docusate sodium
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Alternatives
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Glycerol (Glycerin)
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Alternatives
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Sodium Picosulfate (Elixir)
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Alternatives
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- For use as a second line agent in paediatric patients with constipation when Movicol, lactulose and senna are ineffective as single agent therapy.
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Co-danthramer
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Restricted
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- Note: Co-danthramer and Co-danthrusate are generally restricted to use in the treatment of constipation in terminally ill patients. A combination of Senna and Docusate is normally preferred.
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Co-danthrusate
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Restricted
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- Note: Co-danthramer and Co-danthrusate are generally restricted to use in the treatment of constipation in terminally ill patients. A combination of Senna and Docusate is normally preferred.
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01.06.02 |
Other Stimulant laxatives |
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01.06.03 |
Faecal softeners |
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Arachis Oil (Enema)
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Formulary
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01.06.04 |
Osmotic laxatives |
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Lactulose
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Formulary
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- Oral solution only
- Not for PRN use - not effective.
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Macrogol oral powder
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Formulary
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Macrogol oral powder, Compound
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Formulary
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- Macrogol Compound oral powder
- Macrogol Compound oral powder, Half-Strength
- Macrogol Compound oral powder, Paediatric
Use the product with the lowest acquisition cost.
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MHRA Drug Safety Update (April 2021): Polyethylene glycol (PEG) laxatives and starch-based thickeners: potential interactive effect when mixed, leading to an increased risk of aspiration
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Phosphates (Rectal Preparations)
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Formulary
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Sodium Citrate (Rectal Preparations)
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Formulary
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Macrogol (Movicol liquid®)
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Restricted
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Approved as a second line macrogol laxative for care home residents only.
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01.06.05 |
Bowel cleansing preparations |
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Sodium Picosulfate with Magnesium Citrate (Citrafleet® Picolax®)
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First Choice
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Macrogols (Klean-Prep®)
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Alternatives
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Macrogols (Moviprep®)
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Alternatives
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Plenvu ®
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Alternatives
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- Approved as a second line option to Moviprep for bowel cleansing prior to colonoscopy where large fluid volumes are a problem.
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01.06.06 |
Peripheral opioid-receptor antagonist |
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Naldemedine (Rizmoic®)
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Formulary
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- 200microgram tablet
- Approved for the treatment of opioid-induced constipation in line with NICE
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NICE TA651 - Naldemedine for treating opioid-induced constipation
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Naloxegol
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Formulary
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- 12.5mg and 25mg tablets
- Approved for the treatment of opioid-induced constipation in line with NICE
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NICE TA345: Naloxegol for treating opioid‑induced constipation
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01.06.07 |
Other drugs used in constipation |
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Prucalopride
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Formulary
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- Approved for chronic constipation in women in line with NICE guidance.
- Also approved for use in men with chronic constipation according to the NICE criteria for women.
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NICE TA211: Constipation (women) - prucalopride
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Linaclotide
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Formulary
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- Approved for specialist initiation for the symptomatic treatment of moderate-to-severe irritable bowel syndrome with constipation (IBS-C).
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01.06.08 |
Other preparations for bowel obstruction |
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01.07 |
Local preparations for anal and rectal disorders |
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Sucralfate 2g/50ml enema
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Unlicensed
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- Unlicensed
- For radiation proctitis; bowel inflammation following radiotherapy
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01.07.01 |
Soothing haemorrhoidal preparations |
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Anusol ®
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Formulary
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- Cream and Suppositories
- Self Care Medicine: Advise that a prescription for treatment of haemorrhoids should not routinely be offered in primary care as the condition is self-limiting and will clear up on its own without the need for treatment.
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Haemorrhoid relief ointment
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Formulary
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- Self Care Medicine: Advise that a prescription for treatment of haemorrhoids should not routinely be offered in primary care as the condition is self-limiting and will clear up on its own without the need for treatment.
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Lidocaine 5% ointment
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Formulary
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- Topical preparations containing local anaesthetics should only be used for a few days as they may cause sensitisation of the anal skin.
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01.07.02 |
Compound haemorrhoidal preparations with corticosteroids |
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Anusol®HC (Ointment / Suppositories)
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Formulary
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- Self Care Medicine: Advise CCGs that a prescription for treatment of haemorrhoids should not routinely be offered in primary care as the condition is self-limiting and will clear up on its own without the need for treatment.
- Topical corticosteroids are suitable for occasional short-term use (no more than 7 days) after exclusion of infections
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Proctosedyl®
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Formulary
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- Cinchocaine 0.5% / Hydrocortisone 0.5% ointment
- Self Care Medicine: Advise CCGs that a prescription for treatment of haemorrhoids should not routinely be offered in primary care as the condition is self-limiting and will clear up on its own without the need for treatment.
- Topical corticosteroids are suitable for occasional short-term use (no more than 7 days) after exclusion of infections
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Scheriproct® (Ointment / Suppositories)
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Formulary
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01.07.03 |
Rectal sclerosants |
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Oily phenol injection BP
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Formulary
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01.07.04 |
Management of anal fissures |
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Glyceryl Trinitrate 0.4% ointment (Rectogesic®)
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First Choice
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- 0.2% also available unlicensed.
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Botulinum toxin type A
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Formulary
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- Approved for use by specialists as an alternative to surgery in patients failing other treatments. Also approved for use in paediatrics but there must be documented informed consent from patients/carers.
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Diltiazem 2% (Cream and ointment)
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Unlicensed
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- The most effective formulation is to be prescribed
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01.09 |
Drugs affecting intestinal secretions |
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01.09.01 |
Drugs affecting biliary composition and flow |
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Cholic acid
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Formulary
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- Approved for the treatment of inborn errors of bile acid synthesis (all ages) in line with NHS England Commissioning Policy
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Ursodeoxycholic acid
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Formulary
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01.09.01 |
Other prepatations for biliary disorders |
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Obeticholic acid
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Formulary
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- 5mg & 10mg tablets
- Approved for the treatment of primary biliary cholangitis in line with NICE and NHS England Commissioning Policy.
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MHRA Drug Safety Update (April 2018): Obeticholic acid (Ocaliva▼): risk of serious liver injury in patients with pre-existing moderate or severe hepatic impairment; reminder to adjust dosing according to liver function monitoring
NICE TA443 Obeticholic acid for treating primary biliary cholangitis
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Odevixibat (Bylvay®)
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Formulary
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- Approved for the treatment of progressive familial intrahepatic cholestasis in line with NICE
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NICE HST17: Odevixibat for treating progressive familial intrahepatic cholestasis
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01.09.02 |
Bile acid sequestrants |
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Colestyramine
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First Choice
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- Also approved for the treatment for leflunomide toxicity
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Colesevelam
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Second Choice
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- Approved for second line use (after Colestyramine) for the treatment of bile malabsorption that results in diarrhoea.
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Pancreatin (Creon® Micro)
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Formulary
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Pancreatin (Creon® )
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Formulary
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Pancreatin (Pancrex® V)
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Formulary
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01.10 |
Other preparations |
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Botulinum A toxin
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Formulary
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- Approved for use in the repair of complex hernia
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.... |
Non Formulary Items |
Dupilumab (Dupixent®)
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Non Formulary
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- 200mg/1.14ml & 300mg/2ml solution for injection
- Not recommended for treating eosinophilic oesophagitis in people 12 years and over (terminated appraisal).
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NICE TA938: Dupilumab for treating eosinophilic oesophagitis in people 12 years and over (terminated appraisal)
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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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NHS England |
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Homecare |
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CCG |
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Traffic Light Status Information
Status |
Description |
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Drugs for hospital use only. The responsibility for initiation and monitoring treatment should rest with an appropriate hospital clinician and the drug should be supplied through the hospital throughout the duration of treatment.
In some very exceptional circumstances (e.g. due to distance from the hospital, storage, supply or mobility/transport problems) it may be appropriate for the GP to be asked to prescribe a Red drug. This should be negotiated on an individual patient basis and should only be done with the GP’s prior informed agreement where the roles of the GP and hospital services are clearly defined and agreed. The GP should not feel under pressure to prescribe in these circumstances.
For all RED drugs automatically added to the formulary in response to a positive NICE TA: Prescribers need to ensure that local Trust new drug governance procedures and pharmacy processes are followed before any prescribing. |
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Drugs initiated by hospital specialist, but where continuing treatment by GPs may be appropriate under a shared care arrangement.
The specialist should send the GP a copy of the shared care agreement to sign. The GP should sign the shared care agreement, or indicate they do not want to be part of such an agreement, and return a copy back to the specialist. Shared care guidelines are available or are being developed for most of the drugs listed as Amber.
If no shared care guideline is available, the hospital specialist should provide the patient’s GP with sufficient information and support to allow treatment to be continued and managed safely in primary care. |
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Drugs normally recommended or initiated by a specialist (hospital or GP with an extended role https://www.rcgp.org.uk/gpwer), but can be safely maintained in primary care with very little or no monitoring required. In some cases there may be a further restriction for use outlined - these will be defined in each case. Provision of additional information, or an information leaflet, may be appropriate in some cases to facilitate continuing treatment by GPs. |
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Drugs where prescribing by GPs is appropriate. Can be initiated and prescribed in all care settings, and if appropriate, discontinued without recourse to secondary care. |
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NOT APPROVED: Drugs that have been considered by NTAG or the NENC ICB Medicines Subcommittee (or other approved body) and are not approved for prescribing within the North East and North Cumbria. |
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UNDER REVIEW: drugs whose current formulary status or RAG status is currently under review. |
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NOT REVIEWED: Drugs that haven not been reviewed yet. This usually means that an application is in progress. These drugs are not normally considered appropriate for prescribing in the North East and North Cumbria until such time that a decision is taken on their formulary status. |
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