Step 1 Reporter information Step 2 Patient information Step 3 product information Step 4 Adverse event Step 5 Additional Information Your Name* Your profession* Please choose Your unit (if you are a medical staff) Your phone number* Do you accept follow -up ...
In case you have experienced any adverse event related to the use of the Linde Healthcare products and/or services, please fill out the form below with as much detail as possible. Our top priority is to ensure the safety and satisfaction of our customers, users and patients. Thank you for...
In case you have experienced any adverse event related to the use of the Linde Healthcare products and/or services, please fill out the form below with as much detail as possible. Our top priority is to ensure the safety and satisfaction of our customers, users and patients. Thank you for...
The FDA Adverse Event Reporting System is a publicly available database containing information on adverse events and medication error reports submitted to FDA.
Healthcare professionals and patients may report information on adverse events by submitting the adverse event reporting form or contacting us by fax (+1 (415) 532-3144) or email (drugsafety@bmrn.com). BioMarin recommends the use of its marketed products in accordance with approved prescribing ...
To report an adverse event or adverse drug reaction, please download and complete the reporting form below. Please return the form to us by fax or e-mail as indicated at the top of the form. Are you a patient? If you are a patient, you should always ask your doctor for medical advice...
NumberofPages(includingSAEFormSupplementalpageCTT21Aifrequired)___ Thisreportis:Initial FollowUp ThisSAEisaSUSAR:Yes No ThisSAErequiresun-blinding?Yes No (R&Dnumber/PatientID/SAEnumber) Page1of4 SAEReportCTT21V5.0131021 SeriousAdverseEvent(SAE)Report PatientinitialsPatientID CentreNumberTrialNumber EudraCT...
Notification ofnearlyadverse events form Report date:Reportnumber: Reporter:ManufacturerDistributorUserReporter name: Address: Post code:Telephone: A.Patient Information 1.Name: 2.Age: 3.Sexual MaleFemale 4.Intend to treat diseases or functions: B.Adverse events 5.Content: 6.Event happened date: 7...
If the information you provide relates to a adverse event involving Akeso’s products, the relevant patient information and data will be disclosed to Akeso’s pharmacovigilance department in accordance with the applicable laws and regulations, and the relevant personnel may follow up with you on the...
You can use this website to report Adverse Events on our COVID-19 mRNA vaccine (COMIRNATY®). You may report an Adverse Event by completing the following web-form:Reporter's Personal Information Suspect Drug Information Name of the Suspect Product* Batch/Lot no. Expiry date Indication Adm...