From December 2020 to November 2, 2024 1,407 reportable AEFI reports have been received following 3,218,033 doses of COVID-19 vaccines administered in SK with a reporting rate of 0.44 AEFIs per 1000 doses administered (0.044% of all doses administered). Refer to Tables 1 and 2 for more details.
AEFI Reports are updated every four weeks.
Table 1: Summary of COVID-19 Vaccine AEFI Reports Received in Saskatchewan, as of November 2, 2024
|
Pfizer 2024-25 12+
|
Pfizer
XBB.1.5
12y+ |
Pfizer
XBB.1.5
5-11y |
Pfizer
XBB.1.5
6m-4y |
Pfizer
BA.1 |
Pfizer
BA.4/5
12y+ |
Pfizer
BA.4/5
5-11y |
Pfizer
Original
12y+ |
Pfizer
Original
5-11y |
Pfizer
Original
6m-4y |
Moderna 2024-25 6+mo |
Moderna
XBB.1.5
6m+ |
Moderna
BA.1
18y+ |
Moderna
BA.4/5
18y+< |
Moderna
Original
6y+ |
Moderna
Original
6m-5y |
Novavax XBB |
Novavax 12+ |
Astra
Zeneca 18+ |
COVI-
SHIELD
18+ |
Janssen
18+ |
Totals |
Total number of doses administered |
89,595 |
97,005 |
2,360 |
1,394 |
82 |
138,011 |
2,108 |
1,844,218 |
124,840 |
7,038 |
21,970 |
144,400 |
98,711 |
8,716 |
529,436 |
12,867 |
54 |
531 |
75,422 |
17,203 |
2,072 |
3,218,033 |
Total number of AEFI reports received |
0 |
8 |
0 |
1 |
0 |
19 |
0 |
863 |
15 |
5 |
0 |
8 |
9 |
0 |
330 |
6 |
0 |
1 |
113 |
25 |
4 |
1,407 |
Number of non-serious reports |
0 |
8 |
0 |
1 |
0 |
17 |
0 |
798 |
14 |
5 |
0 |
8 |
8 |
0 |
316 |
6 |
0 |
1 |
95 |
24 |
3 |
1,304 |
Number of serious reports1 |
0 |
0 |
0 |
0 |
0 |
2 |
0 |
65 |
1 |
0 |
|
0 |
1 |
0 |
14 |
0 |
0 |
0 |
18 |
1 |
1 |
103 |
Proportion of serious AEFI reports |
0 |
0% |
0% |
0% |
0% |
10.5% |
0% |
7.5% |
6.7% |
0% |
0% |
0% |
11.1% |
0% |
4.2% |
0% |
0% |
0% |
15.9% |
4% |
25% |
7.3% |
Total AEFI reporting rate per 1,000 doses administered |
0 |
0.08 |
0 |
0.72 |
0 |
0.14 |
0 |
0.47 |
0.12 |
0.71 |
0 |
0.06 |
0.09 |
0 |
0.62 |
0.47 |
0 |
1.88 |
1.5 |
1.45 |
1.93 |
0.44 |
Serious AEFI reporting rate per 1,000 doses administered |
0 |
0 |
0 |
0 |
0 |
0.01 |
0 |
0.04 |
0.01 |
0 |
0 |
0 |
0.01 |
0 |
0.03 |
0 |
0 |
0 |
0.24 |
0.06 |
0.48 |
0.03 |
Serious criteria include an adverse event that is life threatening or results in death, requires hospitalization or prolongation of an existing hospitalization, results in residual disability or causes congenital malformation.
Table 2: Cumulative Frequency of AEFIs Reported
Adverse event type |
# of events |
Edema (allergic, not injection site) |
313 |
Rashes (all) |
271 |
Anesthesia/paresthesia |
228 |
Injection site reactions |
203 |
Gastrointestinal |
151 |
Anaphylaxis |
84 |
Chest tightness |
73 |
Headache |
69 |
Arthralgia/arthritis/joint pain |
51 |
Malaise/lethargy |
48 |
Fever |
42 |
Not inclusive of all AEFIs that can be reported
There are safety signals identified by the Public Health Agency of Canada (PHAC) for vaccine-induced immune thrombotic thrombocytopenia (VITT)/thrombosis with thrombocytopenia syndrome (TTS), myocarditis/pericarditis, Guillain-Barre Syndrome (GBS) and capillary leak syndrome (CLS) requiring provinces and territories to report these events as adverse events of special interest to the PHAC. As of November 4, 2024, 3 TTS, 36 myocarditis/pericarditis, 4 GBS and 0 CLS following COVID-19 immunizations have been reported in Saskatchewan.
Information on reported adverse events following COVID-19 vaccination in Canada can be found at the PHAC AEFI reporting site at COVID-19 vaccine safety: Weekly report on side effects following immunization on Canada.ca.