PDF file: 441-1482_changes_in_the_AEFI_program_of_self_reporting.pdf OPQ ID: 441-1482 Session: 441 Question number: Q-1482 Sessional paper: Q-1482 Title: changes in the AEFI program of self reporting Short description: Topic: vaccines Identified concern: Keywords: Agencies: HC, PHAC Date asked: 2023-05-01 Date tabled: Submitted by: Mr. Carrie (Oshawa) Reply by: Minister of Health Responded by: Mr. van Koeverden Pages: 9 Status: not processed Alert: yellow Questions asked: 9 Questions answered: 7 Percent responded: 78% Referenced sources: (none extracted) Referenced links: (none extracted) Official link: https://www.google.com/search?q=Q-1482+ourcommons.ca PDF URL: https://ivim.ca/foi/opq/r/441-1482_changes_in_the_AEFI_program_of_self_reporting.pdf TXT URL: https://ivim.ca/foi/opq/r/441-1482.txt Original filename: Q-1482 (ORDER) ABOUT changes in the AEFI program of self reporting.pdf Local source path: C:\Users\Dmitry\Documents\CODES\OPQ-App\data-raw\OPQ\ALL OPQ TO DATE\2022\Q-1482 (ORDER) ABOUT changes in the AEFI program of self reporting.pdf Machine extracted at: 2026-06-30 12:58:13 References / links: (none extracted) Machine notes: (none) Question text preview: With regard to Health Canada’s website currently titled “Report a side effect to a vaccine: Consumers”: (a) why was the website changed in December 2020 to prevent consumers from reporting vaccine injuries directly to Health Canada; (b) why did the website change back on February 28, 2023 to allow consumers to resume reporting vaccine injuries to Health Canada; (c) who authorized the changes in (a) and (b); (d) how and on what dates were (i) health care providers, (ii) the general public, (iii) provincial and territorial health ministers, (iv) provincial and territorial immunization authorities, (v) regulatory bodies, (vi) local health authorities notified of each of these changes; (e) for each notification in (d) did it mention a legal obligation to report adverse reactions; (f) what efforts did Health Canada take to inform vaccine recipients of their ability to report adverse reactions through the website; and (g) what were the expenditures incurred by the government promoting the efforts in (f), broken down by type of expense?