The following situations constitute examples of safety information which are important to the ongoing safety monitoring of Lundbeck medications:

• Suspected side effects
• Pregnancy while taking Lundbeck medication (this also applies for pregnancies without any associated complications and if the father was the person treated with Lundbeck medication)
• Suspected side effects in nursing children if the mother is treated with Lundbeck medication
• Overdoses, misuse, or abuse of Lundbeck medication
• Lack of efficacy
• Medication errors or intentional deviations from the intended treatment schedule or method

In the side effect reporting form, you will be provided with the opportunity to fill in information on who is reporting the side effect, the patient and type of Lundbeck medication involved, as well as details on the side effect. Information on other medical conditions and/or additional medications taken can also be provided.

Please do not provide personal information such as full name, address or social security/personal identity number when filling out the form. 

Any information shared with Lundbeck will be treated confidentially in line with Lundbeck’s data handling procedures and in accordance with current data protection legislation. Data reported on side effects will be entered into the Lundbeck global safety database and retained for the time frame required by current legislation. Lundbeck is obligated by law to report information on side effects to Health Authorities.

To find out more about how we process personal data and what your rights are please visit Privacy Notification or contact the Lundbeck Data Protection Officer at dataprivacy@lundbeck.com.

Questions about Lundbeck products: info@lundbeck.com

Questions about reporting side effects: safety@lundbeck.com

Questions about the reporting form: info@lundbeck.com