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Adverse Event Reporting

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  • Current Preliminary information
  • Reporter/enquirer details
  • Product information
  • Adverse event information

Preliminary information

 

 

CSL Vifor takes the safety of patients very seriously. Reporting an adverse event allows us to continuously monitor the safety of our products.   

To help us process your report quickly and effectively, fill out the form below with as much relevant information as possible to report an adverse event for a CSL Vifor product.

 

Data privacy

In order to respond to your enquiry it is necessary to collect some personal information such as your name and contact details. If you have queries concerning personal data or data privacy, please see our data privacy policy.

 

Fields marked with * are mandatory

Personal information

Reporter/enquirer details

 

Fields marked with * are mandatory

 

Contact information

Address

Product information

Fields marked with * are mandatory

Adverse event information

 

Fields marked with * are mandatory
 

 

Adverse event or special situation

Please provide the adverse event term in your local language. You may report up to six adverse events. Please include one term per field.

Adverse event terms

Narrative

 

Describe the event and provide any relevant additional information that you wish to include in your local language.

Case seriousness

Assessment should always be done by a health care professional.

Patient details

If known, please provide the patient's date of birth only, if unknown, you may provide either the patient's age or age group.

Additional comments

Data privacy

In order to respond to your enquiry it is necessary to collect some personal information such as your name and contact details. If you have queries concerning personal data or data privacy, please see our data privacy policy

Have you informed the reporter/enquirer about Data Privacy Notice?
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BR-AVA-2500003 | Data de preparação: maio de 2025