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Any suspected adverse reactions can be reported via the MHRA Yellow Card scheme (yellowcard.mhra.gov.uk)

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Subgroup analysis on the addition of different drugs to monotherapy demonstrated that the incidence of several adverse events was generally similar, except that the incidences of adverse events leading to discontinuation, hypoglycaemia, diarrhoea, nausea, injection-site-related events and vomiting were mildly increased in the combination treatment when compared with SLGT-2i monotherapy, and the incidence of genital infection was mildly increased when compared with GLP-1RA monotherapy