Dose Table
See Sialanar®’s dosing table in full.
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Care should be taken when moving from another type of anticholinergic drug due to the potential for increased risk of anticholinergic adverse effects. There is no available data to support a direct dose conversion for patients changing from hyoscine/scopolamine or atropine to Sialanar®.1,2
A washout period from the first drug should be considered. Sialanar® should be prescribed following the dose table (please click this link to view the table), starting from dose level 1 and titrating in accordance with the SmPC to balance efficacy with undesirable effects.1
Please see the Dosing and Titration Page for further information on initiating Sialanar®
The half-life of free scopolamine is approximately 10 hours so the drug should be cleared within about 3 days. However, it is the clinicians responsibility to decide when the new medicine should be started following the withdrawal of the previous medicine.2
Glycopyrronium bromide (GB) tablets and oral solutions are not interchangeable on a microgram-for-microgram basis due to differences in bioavailability. Sialanar® oral solution has approximately 25% higher bioavailability and therefore equivalent doses will be lower than for tablets and generic oral solutions.3
Care should be taken if switching between oral preparations and dosing adjusted accordingly.
Please click on the the button below to see the dose conversion guidance to Sialanar, from either the generic 1mg/5ml GB products or the 2mg/5ml GB generic product1,4-7
See Sialanar®’s dosing table in full.
Head to this section for guidance on side effects and titration.
The first and only double-blind, randomised, placebo-controlled study of oral anticholinergics in sialorrhoea that has investigated efficacy, safety and impact on quality of life,8,9 continued as an open-label study extension (OLSE)9 . Find out more
All references last accessed August 2026
UK-SIA-26-0023 | August 2026
Adverse Event Reporting Information
UK: Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard.
Adverse events should also be reported to Proveca Limited. Phone: +44 333 200 1866 E-Mail: medinfo@proveca.com