This website is for UK Healthcare Professionals only

This promotional material is intended for UK Healthcare Professionals experienced in the diagnosis and treatment of Chronic Migraine. BOTOX® (botulinum toxin type A) Prescribing Information and adverse event reporting information can be found below.

 

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Please complete the form below and a member of the BOTOX® (botulinum toxin type A) 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® (botulinum toxin type A) is indicated for the prophylaxis of headaches in adults with chronic migraine (headaches on at least 15 days per month of which at least 8 days are with migraine).1

The BOTOX® (botulinum 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 or 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 communications does not constitute as promotional communication.

You can withdraw your consent at any time by using the unsubscribe option in the email or contacting privacyoffice@abbvie.com. For further information about AbbVie’s privacy practices, please refer to the AbbVie Privacy notice.

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References

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

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

By clicking the link above you will leave the AbbVie Pro website and be taken to the eMC PI portal website.

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 GBPV@abbvie.com

 

Date of preparation: March 2025. UK-BCM-240112.