Neuroscience Focus Areas:
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      • This website is for UK Healthcare Professionals only

      Contact us

      Please complete the form below and a member of the BOTOX® team will get back to you.

      Please fill in your details below only if you are a UK registered healthcare professional and would like to be contacted by an AbbVie representative.

      BOTOX® is indicated for the management of bladder dysfunctions in adult patients who are not adequately managed with anticholinergics: overactive bladder with symptoms of urinary incontinence, urgency and frequency; neurogenic detrusor overactivity with urinary incontinence due to subcervical spinal cord injury (traumatic or non-traumatic), or multiple sclerosis.1

      The BOTOX® (botunlinum toxin type A) prescribing information and adverse event reporting information can be found at the bottom of the page. 

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      Please note that there may be certain circumstances where we contact you in relation to important AbbVie product information which we are required to provide to you or your patients as a matter of law, or in order to comply with the obligations we owe to you or them. This type of communication does not constitute promotional communication.

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      References

      1. BOTOX® Summary of Product Characteristics. Available at: www.medicines.org.uk. Accessed December 2022

       

      Please refer to the BOTOX® Summary of Product Characteristics for further information on adverse events, contraindications and special warnings and precautions for use.

       

      BOTOX® PRESCRIBING INFORMATION

       

      Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/

      Adverse events should also be reported to AbbVie on [email protected] 

       

      Date of preparation: December 2022. UK-BUO-220113.