Reporting to the MHRA
How to report a side effect, adverse effect, product fault or other issue...
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We are very sorry if you're experiencing an issue with the medication. Sometimes the medication simply does not agree with us or other times, it can cause a side effect that is not noted in the Patient Information Leaflet or fully explored during the clinical trials during the medication's inception.
We recommend all issues, no matter how big or small, be reported to the Medicines and Healthcare products Regulatory Agency (the MHRA). This will allow them to collate evidence to submit to the relevant manufacturer of the medication. This will allow the manufacturer to keep their guidance and Patient Information Leaflets as up-to-date as possible.
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If you have any questions, please do not hesitate to contact us via our Contact page.
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