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Amoxil - European Harmonisation process

On 25 June 2015, the European Medicines Agency completed a review of Amoxil. The Agency’s Committee for Medicinal Products for Human Use (CHMP) concluded that there was a need to harmonise the prescribing information for Amoxil in the European Union (EU).

Please note that the Amoxil SPCs and PILs were updated on 22nd April Marc 2016 in line with this European Harmonisation process. Please follow the links below for further information.

Summaries of product characteristics (SPCs)

This link will take you to the electronic Medicines Compendium (eMC) website which is a non-GSK website.

View SPCs

Patient information leaflets (PILs)

This link will take you to the electronic Medicines Compendium (eMC) website which is a non-GSK website.

View PILs

 

NHS Choices

This link will take you to the NHS Choices (England and Wales) website where you can find information on symptoms, conditions, medicines and treatments.

Go to NHS Choices

NHS Inform

This link will take you to the NHS Inform (Scotland) website where you can find information on symptoms, conditions, medicines and treatments.

Go to NHS Inform

If you experience any side effects, talk to your doctor, pharmacist or nurse. This includes any side effects not listed in the package leaflet.
You can also report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.
By reporting side effects you can help provide more information on the safety of this medicine.

Amoxil is a registered trademark of the GlaxoSmithKline Group of Companies