Copyrights, linking and use of our website

Requests concerning use of information

  1. Kowa Pharmaceutical Europe Co. Ltd. and its associated companies (hereinafter called the “Company” ) were designed to disclose information.
  2. The content or URL address on this server is subject to change or withdrawal without notice.
  3. All rights are reserved by the Company concerning content on this server (information, materials, images, sounds, etc.). It is strictly prohibited to make use of this content in a secondary manner without notification and permission in any form of reproduction, transfer and sales. It is also prohibited to change or modify the content/descriptions.
  4. The Company shall not be responsible for the validity and correctness of the content and descriptions.
  5. You can freely link your site to the website of the Company, provided that the URL address you link to is as follows:
  6. You do not need to inform the Company of your linking.
  7. The Company absolutely refuses a link that applies any of the following conditions:
    1. Links from sites that contain content that may abuse or slander the Company or its products and services or damage credibility.
    2. Links where by use of the frames or any other means it becomes difficult to determine that the content belongs to the Company.
    3. Links from sites that contain sexually explicit content.
    4. Links from sites that contain illegal content (including potentially illegal site) or are involved (or may be involved) in such activities.

Requests concerning linking and reprinting/reproduction of our website

  1. We cannot assure the validity and correctness of all information contained on our website.
  2. Use information at your own discretion. We shall not be responsible for any inconveniences and disadvantages that may arise as a result of using the information.

Report adverse event

Kowa routinely monitors the safety of all its medicines. This includes review of safety data from clinical studies, and collection of reports and cases of adverse events for marketed products.

Patients and Volunteers in clinical trials reporting an adverse event must contact the investigator.

For specific medical information requests please visit the relevant product page to get in touch.

For the reporting of Livazo adverse events within Europe Union please contact local distributor or Recordati

For the reporting of Livazo adverse events within Middle East and North Africa (MENA) please contact...

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