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Do you have to report an adverse reaction related to a Bracco product? We recommend you submitting your report through the Pharmacovigilance Service.
Pharmacovigilance guarantees, monitors and ensures the safety of drugs by collecting and evaluating information about potential adverse reactions. To find the appropriate contact details and reporting procedures specific to your country, please select your country from the dropdown menu below.
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To explore open positions and submit your application, we invite you to visit our Career Portal.
For further information not connected to Human Resources or recruitment, you may use the Careers Information section in the dropdown menu below, choosing your country of reference.
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Medical Services
If you wish to report adverse reactions related to the use of Bracco drugs, we kindly ask you to contact us through E-mail or telephone.
E-mail: [email protected]
Telephone: +46 31 760 18 80
The following information is kindly requested:
- An identifiable patient (with at least any of the following information: Gender, Age, Date of Birth or Initials)
- An identifiable reporting source (reporter)
- An event (an undesirable effect)
- The name of the suspected Bracco product and batch number
If you wish to report a complaint related to a Bracco product, we kindly ask you to contact us through E-mail or telephone. All complaints received are investigated and a reply provided.
E-mail: [email protected]
Telephone: +46 31 760 18 80
The following information is kindly requested:
- The name of the product and batch number, if available.
- A description of the complaint
- The reporting source (medical doctor, hospital etc.)
If you wish to report an unwanted incident related to the use of Bracco medical devices, we kindly ask you to contact us through E-mail or telephone.
E-post: [email protected]
Tel: +46 31 760 18 80
The following information is kindly requested:
- Date when the incident occurred
- Information about the hospital/healthcare facility where the incident occured
- Information about the reporter
- Information about the patient
- A description of the event
- Indication/use of the medical device
- Outcome
- Product information including batch number