Formulary Chapter 8: Malignant disease and immunosuppression - Full Chapter
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08.01 |
Side-effects of cytotoxic drugs |
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08.01 |
Drugs for cytotoxic-induced side-effects |
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Calcium Folinate (Folinic acid)
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Formulary
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Tablets: 15mg Injection: 3mg, 15mg, 30mg and 300mg An unlicensed 1mg per 1ml mouthwash can be prepared if needed unlicensed
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08.01.01 |
Alkylating drugs |
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08.01.02 |
Anthracyclines and other cytotoxic antibiotics |
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08.01.04 |
Vinca alkaloids and etoposide |
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08.01.05 |
Other antineoplastic drugs |
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08.01.05 |
Arsenic trioxide |
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08.01.05 |
Brentuximab vedotin |
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08.01.05 |
Dacarbazine and Temozolomide |
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08.01.05 |
Hydroxycarbamide |
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08.01.05 |
Platinum compounds |
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08.01.05 |
Porfimer sodium and temoporfin |
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08.01.05 |
Protein kinase inhibitors |
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08.01.05 |
Topoisomerase I inhibitors |
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Calcium Leofolinate (Isovorin®)

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Non Formulary
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Disodium Folinate (Sodiofolin®)

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Non Formulary
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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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Traffic Light Status Information
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Description |

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Drugs for hospital use or use by a specialist within specialist centre only. Initiation and monitoring of treatment should remain under the total responsibility of the appropriate hospital clinician or specialist.
These drugs should only be prescribed under the direct supervision of that clinician or specialist and are not suitable for shared care arrangements. The drug should be supplied via the hospital or specialist centre for the duration of treatment.
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These are specialist drugs which must be initiated by secondary care specialist prescribers, but with the potential to transfer prescribing to primary care within written and agreed shared care protocols and according to the agreed process for transfer of care.
For these drugs, in order to ensure patient safety, some aspects of care must remain with the specialist due to their complexity e.g. monitoring of disease or drug response. Other more routine aspects can be transferred to the GP e.g. monitoring of adverse effects and supply of the medicine. The specific responsibilities of the specialist and GP are defined in the shared care agreement for each drug.
Shared care agreements are still under development for some amber drugs. Until these are available, it would be expected that any shared care request from secondary care to a GP would be accompanied by written information which defines prescribing and monitoring responsibilities. The hospital specialist should also provide the GP with enough information and support to allow the safe transfer and ongoing management of prescribing into primary care.
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Drugs which should usually be initiated in secondary care, or by a specialist clinician, 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. |

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These are defined as new and established drugs, which may be prescribed, initiated, changed or maintained on FP10 by the GP and, if appropriate, discontinued without recourse to secondary care.
N.B. DRUGS NOT IDENTIFIED IN THE FORMULARY BY A RED, AMBER OR GREEN+ SYMBOL ARE CLASSIFIED AS GREEN. |
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