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Pharmacovigilance

Laboratorios Cinfa has a Pharmacovigilance System for collecting and assessing adverse reactions suspected to be related to their marketed medicinal products. If you wish to report a possible adverse reaction related to any of our products, please fill in and submit the following form.

I’m a patient
I’m a healthcare professional

Pharmacovigilance email
farmacovigilancia@cinfa.com

For events occurred in Saudi Arabia you can also contact

+96612 614 8000
drug-safety@cigalah.com.sa

    Notifying person

    Patient identification

    Prescribing doctor

    Suspect medicinal products

    Start date

    End daten

    (Format dd/mm/yyyy)

    Adverse reaction

    Start date

    (Format dd/mm/yyyy)

    End date

    (Format dd/mm/yyyy)

    Comments

    Annex

    If you wish, you may attach an image or file below:

    Max. 2 Mb

    The personal data you provide by completing this form will be processed by Laboratorios Cinfa S.A., as the data controller of this website. This information will be used exclusively to manage and assess reports of potential adverse drug reactions, in compliance with legal pharmacovigilance obligations established by applicable national and European regulations. You are hereby informed that, if necessary, additional information may be obtained from healthcare professionals involved in the patient's care, in accordance with current pharmacovigilance legislation. The data may be communicated to the competent health authorities, such as the Spanish Agency of Medicines and Medical Devices (AEMPS), and, where applicable, to the European Medicines Agency (EMA), in accordance with current pharmacovigilance regulations. You may exercise your rights of access, rectification, erasure, restriction of processing, objection, and, where applicable, data portability by contacting lopd@cinfa.com.
    Further information can be found in our Privacy Policy.

      Patient identification

      Está embarazada:

      Professional notifying

      Suspect medicinal products

      Start date

      End daten

      (Format dd/mm/yyyy)

      Adverse reaction

      Start date

      (Format dd/mm/yyyy)

      End date

      (Format dd/mm/yyyy)

      Comments

      Annex

      If you wish, you may attach an image or file below:

      Max. 2 Mb

      The personal data you provide by completing this form will be processed by Laboratorios Cinfa S.A., as the data controller of this website. This information will be used exclusively to manage and assess reports of potential adverse drug reactions, in compliance with legal pharmacovigilance obligations established by applicable national and European regulations. You are hereby informed that, if necessary, additional information may be obtained from healthcare professionals involved in the patient's care, in accordance with current pharmacovigilance legislation. The data may be communicated to the competent health authorities, such as the Spanish Agency of Medicines and Medical Devices (AEMPS), and, where applicable, to the European Medicines Agency (EMA), in accordance with current pharmacovigilance regulations. You may exercise your rights of access, rectification, erasure, restriction of processing, objection, and, where applicable, data portability by contacting lopd@cinfa.com.
      Further information can be found in our Privacy Policy.