Suspected adverse drug reaction reporting for patients Patient information leaflet: 1Fluart 3Fluart You can directly report any suspected adverse drug reaction related to our products to the national competent authority here:On-line reporting directly to the national competent authority, or by using our website here: Please enable JavaScript in your browser to complete this form.Name of product: *FLUVAL AB suspension for injection1Fluart suspension for injection3Fluart suspension for injectionBatch / Manufacturing Number (if you can identify it)Do you take any other medication? *yesnoPatient’s date of birth, age, gender: *Contact details: *Description of the side effect, remarks, or complaints: *Information on data protection <<< Click here to openSingle Checkbox Field *I have read and accept the information on data protection. I give consent to managing my personal data provided herein.Send
