Adverse reactions - Pharmacovigilance

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse reactions and other medicine-related problems. Medicines may affect the body in unintended, harmful ways. These effects, called side effects or adverse reactions, represent risks of medicines. It is therefore important to identify any new or changing risk of a medicine as quickly as possible, and to take measures to minimize risk and promote safe and effective use.

Please fulfill the following form in case you think you could have presented any side effect or adverse reaction after receiving treatment with a Grifols product.

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* Patient identification

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DATA PROTECTION INFORMATION
Data controller Instituto Grifols, S.A.
Purpose To detect, evaluate, assess and prevent the adverse events or any other safety issue related to the pharmaceutical products of the Grifols group.
Legal basis To guarantee the quality and security of any medicine based on the applicable legislation on pharmacovigilance.
Recipients Companies within the Grifols group, healthcare professionals, companies that have entered into licence and/or commercial agreements with the Grifols group, and national and international competent authorities.
Rights To access, rectify and erase personal data, as well as any other right as specified in the additional information layer.
Additional information You may access the additional and detailed information on data protection here.