Switching Patients to Sialanar®
Guidance on switching patients from hyoscine or glycopyrronium bromide oral solutions to Sialanar®
Switching Patients to Sialanar®
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Click on the patient's weight below to find the recommended dose
0.6ml
1.2ml
1.8ml
2.4ml
3ml*
* Maximum individual dose in this weight range.
Click on the patient's weight below to find the recommended dose
0.4ml
0.8ml
1.2ml
1.7ml
2.1ml*
* Maximum individual dose in this weight range.
Please refer to the SmPC for full dosing information
Submit this form to request a printed dosing wheel to support you or your team:
Guidance on switching patients from hyoscine or glycopyrronium bromide oral solutions to Sialanar®
Switching Patients to Sialanar®
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 life2,3 continued as an open-label study extension (OLSE)3
UK-SIA-26-0022 | September 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