This page is only intended for UK healthcare professionals. Adverse event reporting can be found near the bottom of the page.
Tillotts Products may be discussed in the content of these modules where prescribing information will be available.

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CDI Testing and Diagnosis Algorithm

Updated guidance adapted from the UKHSA algorithm for management of a patient with unexplained diarrhoea – suspected Clostridioides difficile infection

Report a side effect

Adverse events should be reported. Reporting forms and information can be found at:

www.mhra.gov.uk/yellowcard

Adverse events should also be reported to Tillotts Pharma UK Ltd on:

T. 01522 813500

E. uksafety@tillotts.com

PU-03395 | July 2026