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This information is intended solely for patients who have been prescribed a Chiesi product by a UK healthcare professional, and their carers. Please confirm below, or go back to the home page.

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Our medicines. Your treatment.

This website has been provided by Chiesi Limited to support patients, and carers of patients, who have been prescribed Chiesi respiratory products to help manage their asthma or chronic obstructive pulmonary disease (COPD).

To access the appropriate information, please select the treatment prescribed from those shown below:

Trimbow® pMDI (beclometasone/formoterol/glycopyrronium) - Device Image
Fostair® NEXThaler® (beclometasone/formoterol) - Device Image
Fostair® pMDI (beclometasone/formoterol) - Device Image
Atimos® Modulite® pMDI (formoterol) - Device Image
Clenil® Modulite® pMDI (beclometasone) - Device Image
Find out more about Chiesi Limited
Trimbow® pMDI (beclometasone/formoterol/glycopyrronium) - Device Image
Fostair® NEXThaler® (beclometasone/formoterol)
Fostair® pMDI (beclometasone/formoterol)
Atimos® Modulite® pMDI (formoterol)
Clenil® Modulite® pMDI (beclometasone)
Find out more about Chiesi Limited

If you are not a patient, or a carer of a patient, who has been prescribed a Chiesi respiratory product shown above and would like to find out more about Chiesi please visit www.chiesi.uk.com

If you need advice, or have any questions about your condition or the treatment you have been prescribed, please speak to a healthcare professional.

Reporting of side effects: If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible 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.

Privacy & Cookie Policy  |  Terms of Use  |  Contact Us  | Adverse Event Reporting  | About Chiesi

UK-RES-1901935 Nov 2019

Privacy & Cookie Policy  |  Terms of Use  |  Contact Us  | Adverse Event Reporting  | About Chiesi

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UK-RES-1901935 Nov 2019