If you are reporting a side effect from Canada or the United States, please use the following link: Canada & US reporting

If you wish to report a side effect or product complaint which you suspect is related to a Novo Nordisk product, you can contact us by phone or email: IO-BALAT-SAS-Safety@novonordisk.com. If you use email, please write “Reporting of adverse reaction” for side effect complaints and “Reporting of product complaint” for product complaints in subject line.

By reporting side effects/product complaints, you provide Novo Nordisk with important feedback about our products.

 

Disclaimer:
We treat all your “personal data” in accordance with local data protection rule. Any personal data provided here related to adverse events or other activities related to pharmacovigilance will be used solely for these purposes. Read our notice of personal data processing

A side effect (also known as adverse reaction) is a harmful and unintended response to a pharmaceutical product. This includes any undesirable patient effect suspected to be associated with pharmaceutical product use. An unintended effect, pharmaceutical product abuse, overdose, interaction (including drug-drug and drug-food interactions) and unusual lack of therapeutic efficacy are also considered reportable side effects.

Although our products are tested extensively in clinical trials before they are authorized, not everything is known about their side effects until they have been used by many people over time. Novo Nordisk routinely monitors the safety of all our products. By reporting complaints and side effects, you are giving us important feedback which will ultimately help us take appropriate actions and to provide better instructions for how to use our products.

When reporting side effects please provide the following information, if possible:

 

Product details

  • Name of product (brand name)?
  • What disease is the product used for?
  • How do you take the product (dose, how often)?
  • What is the product batch number?
  • If it concerns a product fault: Which product part and product function is affected? How did the fault occur? Is a sample available?
  • What were the actions taken to the product? Has the product been discontinued? Any changes in product dose? Were the actions taken to suspected product advised by your HCP?

 

Side effect details

  • Description of the suspected side effect including whether you have recovered from the event
  • When did the side effect occur?
  • Are you experiencing other medical conditions?

 

Patient details

  • Gender
  • Age, date of birth or age group (e.g. child, adolescent, adult, elderly)
  • Country of residence

 

Reporter details

  • Name
  • Contact details

Email: IO-BALAT-SAS-Safety@novonordisk.com

Quality complaint report
If you have a quality complaint about a Novo Nordisk product, for example:

  • Bad device function
  • Color change, clumping, etc

We request that you contact us at the email: IO-BALAT-SAS-Safety@novonordisk.com