Prescribing Entyvio

Prescribing Entyvio

Entyvio is given by intravenous infusion every 8 weeks after an initial induction phase. Treatment should be initiated and supervised by specialist healthcare professionals experienced in the diagnosis and treatment of ulcerative colitis or Crohn’s disease.1

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Why prescribe Entyvio?

Why prescribe Entyvio?

The safety and efficacy of Entyvio are supported by the results of the Phase III GEMINI studies2-4 involving 2,400 individuals with UC or CD who were recruited from nearly 40 countries. GEMINI is the largest Phase III clinical trial programme to date that evaluated a new treatment for UC or CD concurrently. In an interim analysis5 of the GEMINI-LTS study, a favourable safety profile was demonstrated in more than 2,800 patients receiving Entyvio for UC or CD for up to 5 years.

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About Takeda

Takeda

Takeda Pharmaceutical Company Limited has a long history in the research and development, manufacturing, sales and marketing, and import/export of pharmaceutical products. The corporate mission to “strive towards better health for people worldwide through leading innovation in medicine” has led to the development of several state-of-the-art medicines, including Entyvio for UC and CD.

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Adverse events should be reported. In the United Kingdom, reporting forms and information can be found at www.mhra.gov.uk/yellowcard.

Adverse events should also be reported to Takeda on 01628 537900 or e-mail DSO-UK@takeda.com