Our Products
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Fingolimod 0.5mg hard capsules (fingolimod hydrochloride)
UK ADVERSE EVENT REPORTING
Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/. Adverse events should also be reported to Flynn Pharma Ltd. Medical Information: Tel 01438 727822,
E-mail medinfo@flynnpharma.com
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It hosts a wealth of education, training, resources, events and product information for healthcare professionals working with neurodevelopmental disorders (NDD) and women’s health. VISIT FLYNN FORUM ➜
REPUBLIC OF IRELAND ADVERSE EVENT REPORTING
Adverse events should be reported. Reporting forms and information can be found at www.hpra.ie. Adverse events should also be reported to Flynn Pharma Ltd. Medical Information: Tel 01438 727822,
E-mail medinfo@flynnpharma.com
Reporting Side Effects
Adverse events should be reported to Flynn Pharma Ltd, Hertlands House, Primett Road, Stevenage, Hertfordshire, SG1 3EE, +44 (0) 1438 727 822, medinfo@flynnpharma.com. Information on adverse event reporting can also be obtained from www.yellowcard.mhra.gov.uk.
Information about our products, including adverse reactions, precautions, contraindications and method of use can be found at www.medicines.org.uk/emc.
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Fingolimod - Patient Information Booklet - for patients
This patient booklet contains important things to remember about fingolimod treatment for patients, parents and caregivers
Fingolimod - Pregnancy-Specific Patient Reminder Card - for patients
This reminder card contains pregnancy-specific safety information about fingolimod treatment
Fingolimod - Prescribers checklist - for Healthcare Professionals
This checklist outlines important points to remember before, during and after treatment
June 2023