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- Tablets
- Not Specified
- Not Specified
- Tablets
Off-label use. Specialist initiation and prescribing for at least 1 month before any request is made for primary care prescribing.
- Tablets
Only recommended as an option in secondary prevention where other options have been exhausted.
- Tablets
For post-exposure prophylaxis (e.g. needlestick injuries), follow your organisation's protocols for referral and access. Use as recommended by BHIVA/BASHH guidelines.
- Capsules
- Capsules
- Intravitreal injection
- Intravitreal injection
- Intravitreal injection
- Intravitreal injection
- Not Specified
- Modified release tablets
- Not Specified
- Tablets
- Intravenous infusion
- Not Specified
- Tablets
Specialist to prescribe at least 1 month treatment, prior to transfer of care
- Tablets
Not assessed for formulary status. An application to APC is required.
- Tablets
Specialist team initiation and at least 3 months of treatment prior to any request for primary care prescribing.
A DXA scan is recommended after the first 52 weeks of treatment
- Intravenous infusion
- Powder
Prescribe on advice from specialist e.g. dietitian
- Powder
Prescribe on advice from specialist e.g. dietitian
- Liquid
Prescribe on advice from specialist e.g. dietitian
- Powder
Prescribe on advice from specialist e.g. dietitian
- Tablets
On advice from specialist.
NHSE do not recommend the routine prescription of vitamins and mineral preparations, with the exceptions of patients with medically diagnosed deficiency, including those with lifelong or chronic conditions, or post surgery resulting in malabsorption (e.g. Whipple’s procedure and some other GI surgeries), calcium and vitamin D for osteoporosis, prescription-only vitamin D analogues or malnutrition. Continuing need should be reviewed on a regular basis. Not for use for prevention of deficiency
- Liquid
Prescribe on advice from specialist e.g. dietitian
- Tablets
- Not Specified
- Liquid
- Liquid
Altraplen Energy is the preferred second line 1.5kcal/ml supplement when required in primary care. Ready to drink supplements should only be prescribed if individual cannot prepare milkshake from powder.
- Powder
- Capsules
- Injection
- Oral solution
- Tablets
- Not Specified
- Capsules
- Not Specified
- Tablets
- Tablets
- Tablets
- Not Specified
- Tablets
- Oral suspension
- Orodispersible films
- Tablets
- Oral lyophilisates
- Oral lyophilisates
- Not Specified
NHSE commissioned services only. No Surrey Heartlands Trusts are commissioned to provide this.
- Intravenous infusion
- Subcutaneous injection (sc)
- Not Specified
- Subcutaneous injection (sc)
- Tablets
Weekly tablets are 35mg. Daily tablets are 5mg.
NOTE - 30mg tablets are licensed for Paget's disease only
- Tablets
30mg tablets are licensed for Paget's disease.
- Oral solution
- Tablets
Licensed for up to 6 weeks in Alzheimer's dementia. On initiation, patients need a referal to SABP so that an assessment can be made at 6 weeks to weigh up response to treatment and benefit of treatment v risk of harm.
- Oro-dispersible tablets
Licensed for up to 6 weeks in Alzheimer's dementia. On initiation, patients need a referal to SABP so that an assessment can be made at 6 weeks to weigh up response to treatment and benefit of treatment v risk of harm.
Only for use where the liquid formulation is unsuitable e.g. for supervised administration to ensure compliance.
- Tablets
Primary Care prescribing on advice from palliative care specialist team
- Oral solution
- Tablets
Initiation by a SABP specialist and stabilisation for a minimum of 3 months before any request to transfer prescribing responsibility.
- Oro-dispersible tablets
Initiation by a SABP specialist and stabilisation for a minimum of 3 months before any request to transfer prescribing responsibility.
Only for use where the liquid formulation is unsuitable e.g. for supervised administration to ensure compliance.
- Oral solution
- Tablets
Initiation by a SABP specialist and stabilisation for a minimum of 3 months before any request to transfer prescribing responsibility.
- Oro-dispersible tablets
Initiation by a SABP specialist and stabilisation for a minimum of 3 months before any request to transfer prescribing responsibility.
Only for use where the liquid formulation is unsuitable e.g. for supervised administration to ensure compliance.
- Capsules
- Tablets
- Not Specified
- Not Specified
- Not Specified
- Not Specified
- Not Specified
- Injection
- Not Specified
- Not Specified
- Not Specified
- Intravenous infusion
- Not Specified
- Not Specified
- Tablets
- Tablets
- Tablets
- Tablets
- Tablets
- Capsules
- Patches
Rivastigmine is BLUE (with information sheet) for those patients who are stable and suitable for discharge from specialist care.
This entry has not yet been reviewed for inclusion on the joint formulary. However, this information has been published due to the ongoing requirement for prescribers to access the shared care agreement and other resources that were in place prior to the launch of the joint formulary.
- Capsules
- Patches
AMBER shared care applies for patients that are not suitable for discharge and who will continue to receive follow up by SABP.
This entry has not yet been reviewed for inclusion on the joint formulary. However, this information has been published due to the ongoing requirement for prescribers to access the shared care agreement and other resources that were in place prior to the launch of the joint formulary.
- Not Specified
- Tablets
- Oro-dispersible tablets
- Oral lyophilisates
- Tablets
- Subcutaneous injection (sc)
Haematology use only - treating chronic immune thrombocytopenia as per NICE TA221.
- Injection
- Immediate release tablets
- Tablets
- Modified release tablets
- Not Specified
- Tablets
- Patches
- Patches
- Tablets
Renal specialist teams only.
- Tablets
- Oral suspension
- Not Specified