Do you have questions about possible side effects of a Pannoc product? You can always contact us directly. It is also possible to report to the FAMHP for medication or medical devices via www.famhp.be/en/side_effect
Reporting a possible side effect
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Medicines and medical products can sometimes cause unwanted effects. That is why every package is required to include a leaflet with information about known risks.
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An adverse reaction is an unexpected or unwanted health problem that occurs in someone taking a medicine or medical preparation. This does not always mean that the complaint is directly caused by the treatment. Many side effects are already being identified during clinical trials, but some only come to light when the medicine is used by a large group of people. There are also side effects that only become visible after prolonged use, or that occur due to interaction with other medicines. In addition, medical devices and cosmetic products can also cause side effects.
Why reporting is important
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At Pannoc, we take the safety of our products very seriously. That's why we collect and review all reports submitted by healthcare providers or users. These reports are stored anonymously and added to an international database, where countries around the world exchange data on possible side effects.
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The Federal Agency for Medicines and Health Products (FAMHP) monitors this obligation and carries out regular checks at pharmaceutical companies, including Pannoc. For that reason, it is essential that you report any possible side effects.
Therefore, please fill out the notification form below.
What happens next?
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Our Pharmacovigilance department - via Infarama - registers and investigates each report individually. An adverse reaction to a Pannoc medicinal product or medical device must be reported to Infarama within 24 hours via email phvig@infarama.be or. For more information, contact Infarama via the 24/7 Vigilance Call Service: +32 479 423297.
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When processing reports, limited personal data can be collected. More information can be found in our privacy policy.
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All reports are anonymized and stored in our internal database. If the available information is complete enough, we will also add the data to the international database. Competent authorities and experts analyse this data and can take measures if necessary, for example by updating the package insert or informing healthcare professionals.
