Report Adverse Events

Thank you for choosing to report an adverse event. Information about adverse event reporting can be found at MHRA Yellowcard website.

GSK routinely monitors the safety of all its medicines. This includes review of safety data from clinical studies, and collection of reports and cases of adverse events for marketed products.

This information contributes to the continuing safety surveillance of our products. If you become aware of a patient who has experienced an adverse event, pregnancy, overdose or unexpected benefits with one of our products, we would be grateful if you would contact GlaxoSmithKline on 0800 221 441 or complete the form below. GSK will only use your details to contact you about your adverse event report.

GSK does not recommend, endorse or accept liability for sites controlled by third-parties.

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M.C: Last updated 22 October 2014: UK/COM/0032ae/10(1)