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From non-glycopyyronium bromide anticholinergics

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.

From generic glycopyrronium bromide oral solutions:

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

 

Safety

Head to this section for guidance on side effects and titration.

Clinical Evidence

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

References

  1. Sialanar® SmPC (August 2026) https://www.medicines.org.uk/emc/product/2301  
  2. Scopoderm (hyoscine) SmPC (September 2024).https://www.medicines.org.uk/emc/product/13379/smpc 
  3. BNFC Glycopyrronium Bromide https://bnfc.nice.org.uk/drugs/glycopyrronium-bromide/ 
  4. Glycopyrronium Bromide 1 mg/5 ml Oral Solution (Colonis Pharma) SmPC (November 2025) https://www.medicines.org.uk/emc/product/7344/smpc 
  5. Glycopyrronium Bromide 1 mg/5 ml Oral Solution (Rosemont Pharmaceuticals Limited) SmPC (August 2026) 2022) https://www.medicines.org.uk/emc/product/13136/smpc 
  6. Glycopyrronium Bromide 1 mg/5 ml Oral Solution (Strandhaven Limited t/a Somex Pharma UK Limited) SmPC (June 2026)  https://www.medicines.org.uk/emc/product/14104/smpc – 
  7. Glycopyrronium Bromide 2 mg/5 ml Oral Solution (Colonis Pharma) SmPC (January 2026). https://www.medicines.org.uk/emc/product/100528/smpc#gref  
  8. Fayoux P et al., Glycopyrronium 320 μg/mL in children and adolescents with severe sialorrhoea and neurodisabilities: A randomized, double-blind, placebo-controlled trial. Developmental Medicine & Child Neurology 2024; 00: 1–9. DOI:10.1111/dmcn.15841. https://onlinelibrary.wiley.com/doi/10.1111/dmcn.15841 
  9. Fayoux P, et al. Glycopyrronium 320 μg/mL in children and adolescents with severe sialorrhoea and neurodisabilities: An open-label study extension of the SALIVA trial. Dev Med Child Neurol. 2025; 00:1–10.DOI: 10.1111/dmcn.16251  

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

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