Completed Access to Information Requests

About this information

Search the summaries of completed Access to Information (ATI) requests to find information about ATI requests made to the Government of Canada after January 2020. If you find a summary of interest, you can request a copy of the records at no cost using the form below each summary. Requests made through this form are considered informal requests and are not subject to the same requirements as requests under the Access to Information Act (ATIA).

If you don’t find what you are looking for you can request additional government records under an institution’s control by contacting the institution’s Access to Information and Privacy Coordinator or by submitting a formal access to information request.

*All information provided will incorporate the necessary exemptions and exclusions as per the Access to Information Act and the Privacy Act.

Download datasets of the summaries of completed access to information requests.

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Year

Month

Found 116 record(s)

Req # A-2021-001927

Adverse Drug Reaction (ADR) for Prevmyis. Report number: 000719418. ADRs for Primaxin. Report numbers: 000723189, E2B_02530829. ADR for PROGLYCEM. Report number: E2B_02274473. ADR for ProQuad. Report number: 000715486. ADRs for RECOMBIVAX HB. Report numbers: E2B_01820654, E2B_01843946, E2B_01843954, E2B_01843958, E2B_02025546, E2B_02069932.

Organization: Health Canada

70 page(s)
August 2022

Req # A-2021-002051

Adverse Drug Reactions (ADRs) for VAQTA. Report numbers: 000607875, E2B_02020690, E2B_02022693. Adverse Drug Reactions (ADRs) for VARIVAX III. Report numbers: 000716219, 000720076, E2B_02314825, E2B_02316910, E2B_02513081, E2B_02510059, E2B_02162521.

Organization: Health Canada

162 page(s)
August 2022

Req # A-2021-002082

Adverse Drug Reactions (ADRs) for [NAME] (). Report numbers: E2B_03738275, E2B_03738565, 000965621, E2B_04804253.

Organization: Health Canada

89 page(s)
August 2022

Req # A-2021-002083

Adverse Drug Reactions (ADRs) for ANTI-THYMOCYTE GLOBULIN (RABBIT), DUPILUMAB, ALEMTUZUMAB. Report numbers: E2B_04926642, E2B_04731617, E2B_04876141, E2B_04937460, E2B_04703758, E2B_04713387, E2B_02395265, E2B_04702989, E2B_04685799, 973025.

Organization: Health Canada

155 page(s)
August 2022

Req # A-2021-002094

Adverse Drug Reactions (ADRs) for ALEMTUZUMAB, METOLAZONE, METFORMIN HYDROCHLORIDE. Report numbers: E2B_04943076, E2B_04768754, E2B_04812820, E2B_04715183, E2B_04674084, E2B_04771838.

Organization: Health Canada

231 page(s)
August 2022

Req # A-2021-002095

Adverse Drug Reactions (ADRs) for Furosemide, Zopiclone, Leflunomide. Report numbers: E2B_04913154, E2B_04909974, E2B_04643237, E2B_04934504.

Organization: Health Canada

143 page(s)
August 2022

Req # A-2021-002117

Adverse Drug Reactions (ADRs) for ZOSTAVAX II. Report numbers: 000711590, 000713968, 000715122, 000715726, 000715907, E2B_01863278, E2B_01873223, E2B_01889662, E2B_01892634, E2B_02096585.

Organization: Health Canada

133 page(s)
August 2022

Req # A-2021-002118

Adverse Drug Reaction (ADR) for FUROSEMIDE. Report number: E2B_04801670.

Organization: Health Canada

68 page(s)
August 2022

Req # A-2021-002141

Adverse Drug Reactions (ADRs) for ARIPIPRAZOLE. Report numbers: E2B_04897492, E2B_04938534, E2B_04952767. ADRs for PATIROMER. Report numbers: E2B_04852751, E2B_04852752, E2B_04852753, E2B_04894325, E2B_04916570, E2B_04943652.

Organization: Health Canada

128 page(s)
August 2022

Req # A-2021-002145

Adverse Drug Reactions (ADRs) for ARIPIPRAZOLE. Report numbers: E2B_04897492, E2B_04938534, E2B_04952767. ADRs for PATIROMER. Report numbers: E2B_04852751, E2B_04852752, E2B_04852753, E2B_04894325, E2B_04916570, E2B_04943652.

Organization: Health Canada

133 page(s)
August 2022
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