Dear Sir or Madam,<\/p>\n\n\n\n
In the interest of patient safety, Panaceum Ltd performs monitoring of adverse events.<\/p>\n\n\n\n
What is an adverse event.<\/strong><\/p>\n\n\n\n Definition from the Act on Quality in Healthcare and Patient Safety (Journal of Laws 2023, item 1692):<\/p>\n\n\n\n Adverse event \u2013 an event occurring during or as a result of the provision or omission of healthcare, which causes or may cause a negative effect on the patient's health or life, in particular death, physical injury or mental disorder, illness, life threat, need for hospitalisation or its extension, as well as damage to the body or mental disorder of the foetus.<\/p>\n\n\n\n An event whose outcome is a predictable result of the correct provision of healthcare is not an adverse event.<\/p>\n\n\n\n Adverse events should not be confused with the natural progression of the disease or predictable complications of therapy.<\/p>\n\n\n\n Events can be reported by employees, patients, and their relatives or witnesses to such events.<\/p>\n\n\n\n Adverse events include:<\/p>\n\n\n\n The purposes of reporting adverse events:<\/strong><\/p>\n\n\n\n Method of reporting:<\/strong><\/p>\n\n\n\n Caution:<\/strong><\/p>\n\n\n\n Every patient has the right to report adverse reactions to medicinal products. This includes both serious reactions and those that cause discomfort or concern. More information:<\/p>\n\n\n\n\n
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