Phenobarbital sodium 200mg/ml injection: 1ml ampoules. Excipients include propylene glycol 90%.
This formulation is classified as Controlled Drug Schedule 3.
We are pleased to advise that deep linking capability, enabling users to directly download individual mobile toolkits, has now been released on the RDS mobile app. When you install the update, you will see that each toolkit has a small QR code icon the header area beside the search icon – see screenshot below. Clicking on this icon will open up a window with a full-size QR code and the alternative of a short URL for sharing with users. Instructions are provided.
You may need to actively install the update to install RDS app version 4.7.1 to see this improvement. Installing this update is also strongly recommended to get the full benefits of the new contingency arrangements – specifically, that if the RDS website should fail, you will still be able to download new mobile app toolkits.
To check your current RDS version, click on the three dots bottom right of the RDS app screen. This takes you to a “More” page where you will see the version number. To install latest updates:
On iPhones – go to the Apple store, click on your profile icon top right, scroll down to see the apps waiting to be updated and update the RDS app.
On Android phones – these can vary, but try going to the Google Play store, click on your profile icon top right, click on “Manage apps and device”, select and update the RDS app.
Please get in touch with ann.wales3@nhs.scot with any questions.
Specialist palliative care involvement essential.
Description:
Phenobarbital is classed as a sedative anti-epileptic that has an overall effect of depressing the central nervous system. This is achieved by a dual action of prolonging the opening of chloride channels on GABA receptor complex and inhibiting glutamate transmission at non-NMDA receptor channels.
High doses of Phenobarbital can result in general anaesthesia.
Phenobarbital sodium 200mg/ml injection: 1ml ampoules. Excipients include propylene glycol 90%.
This formulation is classified as Controlled Drug Schedule 3.
Licensed indications - all forms of epilepsy except typical absence seizures and status epilepticus.
In palliative care phenobarbital may be considered by specialist palliative care practitioners for the following:
These are not absolute contra-indications if the patient is in the last days of life. Careful titration is however necessary.
Phenobarbital is metabolised by CYP2C19. CYP2C19 Inhibitors may enhance the effect of phenobarbital.
Examples of CYP2C19 inhibitors:
Phenobarbital induces various cytochrome P450 enzymes (CYP1A2, CYP2B6, CYP2C8/9, CYP2C19 and CYP3A4) that can cause many clinically significant drug interactions. As enzyme induction may take up to two weeks to develop, dose adjustments of concurrently administered drugs, that are predominantly metabolised by the cytochrome pathway or undergo glucuronidation, may be necessary.
Phenobarbital may decrease the effect of the following (the list is not exhaustive):
Corticosteroids - (dexamethasone, methylprednisolone, prednisolone):
Be aware of the potential for interactions: doses may need to be adjusted
Terminal refractory agitation: generally third line with specialist palliative care input.
Epilepsy: Refer to guideline for treating seizures.
Status epilepticus: Refer to local guidance.
Patient and carer advice point
Report any signs of skin reactions.
Dickman A, Schneider J. The Syringe Driver. 4th ed: Oxford University Press; 2016.
Twycross R, Wilcock A, Howard P. Palliative Care Formulary PCF6. 6th ed. England: Pharmaceutical Press; 2017.