Adverse Events Following Immunization Associated with the First and Second Doses of the ChAdOx1 nCoV-19 Vaccine among Healthcare Workers in Korea
1
Division of Infectious Diseases, Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan 49267, Korea
2
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan 49267, Korea
3
Department of Pediatrics, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan 49267, Korea
*
Author to whom correspondence should be addressed.
Vaccines 2021, 9(10), 1096; https://doi.org/10.3390/vaccines9101096
Submission received: 8 July 2021
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Revised: 28 August 2021
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Accepted: 24 September 2021
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Published: 28 September 2021
(This article belongs to the Special Issue Safety Concerns, Sources of Liability, Compensation Strategies and the Right to Be Informed: Ethical and Legal Issues of COVID-19 Vaccination)
Abstract
:As worldwide large-scale inoculation of novel vaccines is on the way, the importance of real-world data on safety cannot be overemphasized. We aimed to investigate the adverse events following immunization (AEFIs) associated with the ChAdOx1 nCoV-19 vaccine among healthcare workers (HCWs). We investigated the systemic and local adverse events reported within seven days following the first and second doses of vaccination, using the mobile vaccine adverse events reporting system (MVAERS) developed by our hospital. The response rates were 71.8% (994/1384) and 52.9% (727/1375) after the first and second doses, respectively. The most commonly reported AEFIs were tenderness and pain at the injection site and fatigue after the first and second doses. In comparison to the first dose, the incidence and severity of AEFIs were lower following the second dose. Since the Korean government does not recommend the ChAdOx1 nCoV-19 vaccination for those under 30 years of age, with greater risk than benefit, we additionally compared the AEFIs of age groups under and above 30 years of age. The overall incidence of AEFIs was similar in both the under and over 30 age groups. In conclusion, AEFIs associated with the ChAdOx1 nCoV-19 vaccine were found to be tolerable, and AEFIs associated with the second dose were less common and severe compared to the first dose. Further safety surveillance studies on COVID-19 vaccines are required to validate our findings.
1. Introduction
Globally, the coronavirus disease 2019 (COVID-19) has been reported have a morbidity of more than 170 million patients and a mortality of more than 3 million as of June 2021 [1]. Antiviral drugs (e.g., remdesivir) and immune modulators (e.g., tocilizumab and baricitinib) are being tried as therapeutic agents; however, the most important way to overcome the current pandemic is large-scale vaccination worldwide. Vaccination policies differ from country to country, but in some countries, vaccination is still not available or is preferentially administered.
In the Republic of Korea, COVID-19 vaccination has been initiated in February 2021, with a total of 15,279,057 people having received either one or more vaccine doses as of 26 June 2021 [2]. Notably, frontline healthcare workers (HCWs) were given vaccination priority, with the allocation of BNT162b2 mRNA vaccines (Pfizer/BioNTech) or the ChAdOx1 nCoV-19 vaccines (AstraZeneca). Although randomized controlled trials have demonstrated the efficacy and safety of the ChAdOx1 nCoV-19 vaccine [3,4], several cases of severe adverse events associated with this vaccine have also been reported [5,6]. Poor dissemination of medical information and concerns regarding the safety and efficacy of rapidly developed novel vaccines are the factors that lead to vaccine hesitancy [7]. Moreover, since many people are easily exposed to disinformation about vaccination and treatment of COVID-19 when using the internet or social media, evidence-based accurate information should be shared seamlessly worldwide.
To consistently achieve large-scale inoculation and provide precise information on novel vaccines against COVID-19, research on the incidence and severity of adverse events in real-world settings is needed. Therefore, we aimed to evaluate the incidence and severity of adverse events following immunization (AEFIs) associated with the ChAdOx1 nCoV-19 vaccine and to investigate the differences in AEFIs between the first and second vaccine doses among HCWs at a single university hospital. Specifically, we used the medical records of AEFIs among HCWs, which were voluntarily reported in the mobile vaccine adverse events reporting system (MVAERS) developed by our hospital.
2. Materials and Methods
2.1. Study Design and Population
This was a retrospective, single-center cohort study conducted at a teaching hospital in the Republic of Korea, and the study subjects were HCWs who had received at least one dose of the ChAdOx1 nCoV-19 vaccine. Since the Korean government recommended the ChAdOx1 nCoV-19 vaccine for those under 65 years of age initially, only HCWs under the age of 65 years were included in this study. Subsequently, following the reports of serious adverse events associated with the ChAdOx1 nCoV-19 vaccine [5,6,8], the Korean government has also banned its vaccination for those under 30 years of age; however, it was possible to voluntarily proceed with the second dose for HCWs under the age of 30, if they had already received the first dose and did not have any serious adverse events at that time [9]. For those who consented to undergo vaccination with the second dose, the vaccine was administered at an interval of 11 weeks. Among those who received the vaccine, HCWs who did not report to the MVAERS or had retired from our hospital before the end of the monitoring period after the second dose were excluded.
2.2. Adverse Events Reporting System
We developed a mobile web page, named “MVAERS,” to systematically capture spontaneous reporting of AEFIs for their monitoring and management, which was used to collect the data that were analyzed in this study. In brief, all vaccinated HCWs received webpage hyperlinks by a short message system twice a day for seven days from the day of vaccination, in which AEFIs were voluntarily reported using a questionnaire inquiring about the 12 adverse events of local and systemic AEFIs. Solicited local AEFIs included tenderness, pain at rest, redness, and swelling at the injection site, whereas solicited systemic AEFIs included fatigue, headache, malaise, arthralgia, chills, fever, nausea or vomiting, and diarrhea. Additionally, the severity of the local and systemic AEFIs was graded on a scale of 1 to 4 based on the guidelines of the Korean Ministry of Food and Drug Safety and the U.S. Food and Drug Administration (Supplementary Table S1) [10].
2.3. Statistical Analysis
Categorical variables were compared using Pearson’s χ2 test, continuous variables were compared using the Student’s t-test or the Mann-Whitney test, and the severity of AEFIs between the first and second doses were compared using the Wilcoxon signed-rank test. Data of the AEFIs after the first dose from our previous study were used in the current study [11]. Statistical significance was set at p < 0.05, and statistical analyses were performed using the SPSS software (version 25.0; IBM Corp., Armonk, NY, USA).
3. Results
A total of 1954 HCWs were employed at the end of monitoring after second dose administration. Among them, a total of 1384 HCWs were administered the first vaccine dose, wherein 994 of them (71.8%) were reported in the MVAERS. The mean age of the respondents was 35.7 years (range: 19–63 years), and 76.7% were female. Meanwhile, a total of 1375 HCWs received the second vaccine dose, wherein the data of 727 of them (52.9%) were reported in the MVAERS. The mean age of the respondents for this group was 36.7 years (range: 20–63 years), and 76.9% were female. When the confidence level was 95%, the sample distribution had a 2.2% and 2.8% margin of error after the first and second dose vaccination, respectively.
The incidence and severity of AEFIs associated with the first and second doses of the ChAdOx1 nCoV-19 vaccine are shown in Table 1. After first dose administration, 975 (98.1%) reported more than one AEFI, and the incidence of local AEFIs was similar to that of systemic AEFIs (95.4% vs. 95.1%, respectively). The most commonly reported systemic AEFIs were fatigue (923, 92.9%) and malaise (833, 83.8%), whereas the most commonly reported local AEFIs were resting pain (871, 87.6%) and tenderness (608, 61.2%) at the injection site. On the other hand, after second dose administration, 661 (90.9%) reported more than one AEFI, and the incidence of local AEFIs was higher than that of systemic AEFIs (84.2% vs. 75.5%, respectively). The most commonly reported AEFIs for this group were tenderness at the injection site (602, 82.8%), fatigue (505, 69.5%), and resting pain at the injection site (481, 66.2%).
The incidence of AEFIs after the administration of the first and second doses of ChAdOx1 nCoV-19 vaccine is shown in Figure 1. As compared to the first dose, the incidence of any AEFIs was lower after the second dose (98.1% vs. 90.9%, p < 0.001). In particular, systemic AEFIs were significantly fewer after the second dose than after the first dose. The distribution of the types of AEFIs after administration of the first and second ChAdOx1 nCoV-19 vaccine doses is illustrated in Figure 2. It was found that local AEFIs accounted for approximately 40% of the reported AEFIs within seven days after the first dose administration. In contrast, as time passed after the second dose administration, the proportion of local AEFIs decreased, while the proportion of fatigue and headache increased.
The incidence of AEFIs by age group is summarized in Table 2 and Figure 3. After first dose administration, AEFIs showed a significant decreasing trend with age, with the exception of redness at the injection site and arthralgia. Moreover, all AEFIs were reported to be more severe in younger HCWs than in older HCWs (Supplementary Table S2). However, after second dose administration, there were no significant differences in the incidence of AEFIs according to age groups, with the exception of arthralgia (p for trend = 0.020).
Additionally, we analyzed the paired data of the 652 HCWs who reported AEFIs after the first and second doses (652/1375, 47.4%), showing that the incidence and severity of all AEFIs after the second dose were significantly lower than those after the first dose (Table 3). Similar to the overall cohort, there was also no correlation in the incidence of AEFIs according to age group, with the exception of arthralgia (data not shown).
In accordance with the government’s policy not to recommend ChAdOx1 nCoV-19 vaccination for those under 30 years of age, who were evaluated as having a greater risk than benefit, only HCWs under 30 years of age who did not have severe AEFIs after the first dose voluntarily received a second dose. In our hospital, 480 HCWs under 30 years of age were administered the first dose, while only 459 HCWs received the second dose. Among them, 217 HCWs reported at least one AEFI after receiving both the first and second doses (response rate: 217/459, 47.3%), with no serious events requiring hospitalization observed among HCWs under 30 years of age. In paired data analysis from the 217 HCWs under 30 years of age, the incidence and severity of AEFIs after the second dose were found to be significantly lower than those after the first dose (Table 4, p < 0.001 for all).
On comparison between the two age groups, both the incidence of overall AEFIs after the first and second doses was similar between those under 30 years of age and those over 30 years of age (Supplementary Table S3). However, in terms of individual categories, local AEFIs, including tenderness and swelling at the injection site, and systemic AEFIs, including headache, malaise, fever, nausea or vomiting, and diarrhea, were more frequent in HCWs under 30 years of age after first dose administration. Meanwhile, after second dose administration, only redness at the injection site was more frequently reported in HCWs over 30 years of age than in those under 30 years of age (28.8% vs. 20.9%, p = 0.028).
We summarized the information and chief complaints of HCWs who visited the emergency room (ER) or outpatient clinic at the Infectious Diseases Department (ID) in Supplementary Table S4. After first dose administration, 13 HCWs visited the ER or outpatient clinic at the ID, presenting with chief complaints of urticaria, pain at the injection site, fever, chills, malaise, headache, dizziness, diarrhea, tingling sensation, and weakness of the lower extremities. One HCW, in particular, was immediately referred to the ER due to dyspnea, nausea, and hypotension within 10 min after vaccination, but the HCW rapidly recovered and was discharged after supportive treatment. On the other hand, after second dose administration, 5 HCWs visited the outpatient clinic at the ID, presenting with chief complaints of arthralgia and a tingling sensation in both legs, throat pain, and fatigue, all of which improved spontaneously within a few days. In particular, only one HCW, who did not report any AEFIs to MVAERS, complained of multiple bruises in both arms, and visited the outpatient clinic seven days after receiving the second dose. On initial consultation, the HCW refused any further evaluation despite being warned. Five days later, he revisited the outpatient clinic and underwent laboratory tests, showing a platelet count of 149 × 103/µL and the d-dimer level of 0.26 µg/mL. He then refused brain imaging, since his symptoms improved spontaneously without any intervention, and is currently under close follow-up.
4. Discussion
In this study, we found that at least one AEFI was reported in more than 90% of HCWs who received the ChAdOx1 nCoV-19 vaccine. As compared to the first dose administration, the incidence and severity of AEFIs after the second dose were reported to be lower. Moreover, after first dose vaccination, the incidence of most AEFIs showed a decreasing trend with age; however, there was no significant trend between incidence and age following second dose vaccination. Furthermore, no serious AEFIs requiring hospitalization or death were reported during the monitoring period after the first and second dose vaccinations.
With the implementation of large-scale vaccinations worldwide, AEFIs associated with the ChAdOx1 nCoV-19 vaccine have been reported in several countries, with varying incidences between recent studies [12,13,14,15,16]. However, similar to our findings, fatigue, malaise, tenderness, and pain at the injection site were the commonly reported AEFIs after the first dose of vaccination in several studies [12,13,14,15,16]. As compared to previous studies of AEFIs associated with the first dose of the ChAdOx1 nCoV-19 vaccine in Korea [12,16], the incidence of local and systemic AEFIs after the first vaccination was higher in our study. Particularly, a study by Kim et al., which performed a multicenter survey in referral teaching hospitals, reported that injection site tenderness (69.6%) and malaise (74.6%) were the most commonly reported AEFIs [12]. Similarly, in another study by Kim et al. performed in a tertiary hospital, they reported that injection site pain (77.8%) and malaise (60.5%) were the most commonly reported AEFIs [16]. Since the demographics of the study population were similar, this may have been influenced by the subjectivity of self-reported symptoms caused by the nature of the survey.
We reported that the incidence and severity of AEFIs after the second dose were lower than those after the first dose, which were consistent with the results of the ChAdOx1 nCoV-19 vaccine clinical trials [4,17], reporting that the reactogenicity profile after the second dose appeared to be less severe. As of 8 August 2021, a total of 11,563,991 ChAdOx1 nCoV-19 vaccine doses were inoculated in Korea, and the total number of reported AEFIs was 78,058. Among them, the incidence of AEFIs after the second dose was reported to be lower than that after the first dose (0.72% vs. 0.22%, respectively) [18]. These findings may lead to improved vaccination rates for those who are reluctant to receive the second dose due to experiencing adverse events after the first ChAdOx1 nCoV-19 vaccine dose. In our study, unlike the first dose vaccination, there was no significant trend between incidence and age following the second dose vaccination. Previous studies on AEFIs showed that the incidence of AEFIs tended to decrease with increasing age after first dose administration [12,13,16]. However, since these studies do not deal with AEFIs after the second dose, additional research is needed on the correlation between the AEFIs after the second dose and age in real-world settings.
As of 11 April 2021, the Korean government has not allowed the administration of the ChAdOx1 nCoV-19 vaccine for those under 30 years of age who were evaluated as having a greater risk than benefit [9]. Therefore, we additionally analyzed the differences in the incidence and severity of AEFIs between HCWs under 30 years of age and those over 30 years of age. On comparison, we found that the incidence of overall AEFIs was similar between the two groups after the first and second doses. However, tenderness and swelling at the injection site, headache, malaise, fever, nausea or vomiting, and diarrhea were frequently reported to occur after the first dose in the under 30 years of age group. Meanwhile, after second dose administration, only redness at the injection site was more frequently reported in the over 30 years age group. These findings support the Korean vaccination policy for the allowance of select individuals under the age of 30 who have already received the first ChAdOx1 nCoV-19 vaccine dose to receive the second dose.
In our study, there were no reports of serious adverse events, except for one case of thrombocytopenia, which spontaneously recovered within a few days. By 8 August 2021, 11.56 million doses of the ChAdOx1 nCoV-19 vaccine were administered in Korea, and 78,058 adverse events were reported. The incidence of severe adverse events was 0.03% (3109/11,563,991): encephalopathy, 223 (19.3 per million); Guillain Barre Syndrome, 104 (9.0 per million); thrombocytopenic purpura, 787 (68.1 per million); and anaphylaxis, 78 (6.7 per million) [18]. In particular, only two cases of thrombosis with thrombocytopenia syndrome (TTS) were reported (0.2 per million) [18]. In particular, only two cases of thrombosis with thrombocytopenia syndrome (TTS) were reported (0.2 per million). As a result, to reflect the risk of this fatal adverse event, the ChAdOx1 nCoV-19 vaccination policy was revised to be recommended for those aged 50 and over as of July 2021 [19]. On the other hand, 803 cases of anaphylaxis and 412 cases of TTS were reported in the United Kingdom (administration: 38.5 million doses as at 4 August 2021) and 55 cases of anaphylaxis and 157 cases of TTS were reported in the Germany (administration: 11.5 million doses until 30 June 2021) [20,21]. This is significantly higher than the results of an interim analysis of four clinical trials on the ChAdOx1 nCoV-19 vaccine, which reported that the incidence of thromboembolic events, including coronary artery occlusion, ischemic stroke, pulmonary embolism, and thrombosis, was less than 0.1% [17]. The difference in the incidence of severe adverse events across countries may be attributed to differences in the total number of vaccinations or racial differences. In terms of vaccine hesitancy, medical education or contents of mass media that reinforce confidence in the safety of novel vaccines may have led to a shift toward vaccine acceptance [22,23]. Therefore, we considered our findings to be quite important, because they support the fact that the incidence of severe adverse events is not very high. Our findings will contribute to improving vaccination rates globally.
Notably, Cheng et al.’s meta-analysis reported that all of the COVID-19 vaccines that have published their phase III clinical trials data did not increase the risk of serious adverse events [24]. Despite this, a number of important adverse events reported in real-world settings require careful evaluation and monitoring. Although several previous studies on adverse events associated with the ChAdOx1 nCoV-19 vaccine have been published, these studies included populations only after the first dose or a lower proportion of second dose recipients. In contrast, to date and to the best of our knowledge, this is the first study to compare the incidence and severity of AEFIs after the first and second ChAdOx1 nCoV-19 vaccine doses using paired data analysis. Thus, we believe that our study results provided more information on the adverse events associated with the ChAdOx1 nCoV-19 vaccine, especially after second dose administration.
Despite these findings, our study has several limitations. First, the AEFIs were not objectively reported due to the design of the voluntary reporting system. Additionally, AEFIs that were not included in the questionnaire were not routinely monitored. Second, the results might not be generalizable since this study was conducted at a single center, comprising subjects younger than 65 years of age. And the sample size was relatively small, and there were unresponded data that could cause bias. Large-scale, long-term safety monitoring research is required in the future. Third, the response rate after the second dose vaccination was lower than that after the first dose vaccination, thus the possibility of underestimation cannot be excluded. Fourth, we cannot rule out the possibility of unobserved bias caused by the occupational status of the participants. Medical professionals might do a better job of self-reporting on their symptoms; however, the reported AEFIs could be underestimated or overestimated. Finally, further studies are required to compare the AEFIs of other novel vaccines. During the study period, the vaccine that was first supplied to healthcare workers in our hospital was limited to the ChAdOx1 nCoV-19 vaccine. Reviewing other vaccines can provide reasonable safety results.
In conclusion, fatigue, pain, and tenderness at the injection site were frequently reported after ChAdOx1 nCoV-19 vaccination. On comparison, the incidence and severity of AEFIs after the second dose were lower than those after the first dose. Moreover, following second dose administration, there was no difference in the incidence of AEFIs according to age, unlike after the first dose. The overall incidence of AEFIs in patients under 30 years of age, who were evaluated as having a greater risk than benefit for vaccination, was similar to the incidence for those over 30 years of age. Given the limitations of this study, further safety surveillance studies of COVID-19 vaccines are required. Safe vaccination can be promoted through active monitoring of adverse events through various methods such as MVAERS and further investigation of safety.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/vaccines9101096/s1, Table S1: Solicited adverse events and grades, Table S2: Severity of adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses by age group, Table S3: Incidence of the adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses by healthcare workers under 30 years of age and over 30 years of age, Table S4: Patients who visited the outpatient clinic or emergency room due to adverse events following immunization.
Author Contributions
Conceptualization: C.E.O. Data curation: J.K., M.J. Formal analysis: J.K., M.J. Investigation: M.J., J.K., C.E.O., J.-Y.L. Methodology: J.K. Validation: J.-Y.L. Writing—original draft: M.J. Writing—review & editing: J.-Y.L. All authors have read and agreed to the published version of the manuscript.
Funding
This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (grant No. 2021R1F1A1062638).
Institutional Review Board Statement
This study was reviewed and approved by the Institutional Review Board of Kosin University College of Medicine (approval No. 2021-03-029).
Informed Consent Statement
Informed consent was waived because of the retrospective nature of the study.
Data Availability Statement
The data presented in this study are available from the corresponding author upon reasonable request. The data are not publicly available due to restricted consent.
Acknowledgments
We are grateful to all healthcare workers at the Kosin University Gospel Hospital for their dedication and cooperation in doing this survey during the COVID-19 pandemic. We are also grateful to Sung-Lim Song, the director of the Kosin University Gospel Hospital’s computer system, for his technical assistance in developing an exclusive mobile vaccine adverse event reporting system.
Conflicts of Interest
The authors declare no conflict of interest.
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Figure 1.
Incidence of adverse events following the administration of the first and second ChAdOx1 nCoV-19 vaccine doses. The numbers are presented as rate (%). (p < 0.001 for all variables).
Figure 1.
Incidence of adverse events following the administration of the first and second ChAdOx1 nCoV-19 vaccine doses. The numbers are presented as rate (%). (p < 0.001 for all variables).
Figure 2.
Distribution of the types of adverse events after administering the first dose (A) and second dose (B) of the ChAdOx1 nCoV-19 vaccine.
Figure 2.
Distribution of the types of adverse events after administering the first dose (A) and second dose (B) of the ChAdOx1 nCoV-19 vaccine.
Figure 3.
Incidence of adverse events after administering the first dose (A) and second dose (B) of the ChAdOx1 nCoV-19 vaccine stratified by age. (* p < 0.05, ** p < 0.01, *** p < 0.001).
Figure 3.
Incidence of adverse events after administering the first dose (A) and second dose (B) of the ChAdOx1 nCoV-19 vaccine stratified by age. (* p < 0.05, ** p < 0.01, *** p < 0.001).
Table 1.
Incidence and severity of adverse events following the first and second doses of the ChAdOx1n CoV-19 vaccine.
Table 1.
Incidence and severity of adverse events following the first and second doses of the ChAdOx1n CoV-19 vaccine.
| Adverse Events | 1st Dose (n = 994) | 2nd Dose (n = 727) | p Value | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Any | None | G1 | G2 | G3 | G4 a | Any | None | G1 | G2 | G3 | G4 a | ||
| Age, mean ± SD | 35.66 ± 10.46 (range, 19–63) | 36.75 ± 10.45 (range, 20–63) | 0.034 | ||||||||||
| Female sex | 762 (76.7) | 559 (76.9%) | 0.911 | ||||||||||
| Any AEFIs | 975 (98.1) | 19 (1.9) | 108 (10.9) | 422 (42.5) | 428 (43.1) | 17 (1.7) | 661 (90.9) | 66 (9.1) | 221 (30.4) | 303 (41.7) | 134 (18.4) | 3 (0.4) | <0.001 |
| Local AEFIs | 948 (95.4) | 46 (4.6) | 189 (19.0) | 547 (55.0) | 207 (20.8) | 5 0.5) | 612 (84.2) | 115 (15.8) | 242 (33.3) | 252 (34.7) | 115 (15.8) | 3 (0.4) | <0.001 |
| Tenderness | 939 (94.5) | 55 (5.5) | 208 (20.9) | 400 (40.2) | 331 (33.3) | 602 (82.8) | 125 (17.2) | 240 (33.0) | 250 (34.4) | 112 (15.4) | <0.001 | ||
| Resting pain | 875 (88.0) | 119 (12.0) | 543 (54.6) | 328 (33.0) | 4 (0.4) | 481 (66.2) | 246 (33.8) | 413 (56.8) | 68 (9.4) | 0 (0.0) | <0.001 | ||
| Redness | 339 (34.1) | 655 (65.9) | 251 (25.3) | 49 (4.9) | 31 (3.1) | 8 (0.8) | 190 (26.1) | 537 (73.9) | 172 (23.7) | 12 (1.7) | 5 (0.7) | 1 (0.1) | <0.001 |
| Swelling | 484 (48.7) | 510 (51.3) | 326 (32.8) | 108 (10.9) | 40 (4.0) | 10 (1.0) | 239 (32.9) | 488 (67.1) | 186 (25.6) | 42 (5.8) | 8 (1.1) | 3 (0.4) | <0.001 |
| Systemic AEFIs | 945 (95.1) | 49 (4.9) | 191 (19.2) | 405 (40.7) | 337 (33.9) | 12 (1.2) | 549 (75.5) | 178 (24.5) | 294 (40.4) | 223 (30.7) | 32 (4.4) | 0 (0.0) | <0.001 |
| Fatigue | 923 (92.9) | 71 (7.1) | 276 (27.8) | 454 (45.7) | 193 (19.4) | 505 (69.5) | 222 (30.5) | 310 (42.6) | 165 (22.7) | 30 (4.1) | <0.001 | ||
| Headache | 772 (77.7) | 222 (22.3) | 262 (26.4) | 502 (50.5) | 8 (0.8) | 294 (40.4) | 433 (59.6) | 175 (24.1) | 118 (16.2) | 1 (0.1) | <0.001 | ||
| Malaise | 833 (83.8) | 161 (16.2) | 236 (23.7) | 580 (58.4) | 17 (1.7) | 292 (40.2) | 435 (59.8) | 196 (27.0) | 94 (12.9) | 2 (0.3) | <0.001 | ||
| Arthralgia | 611 (61.5) | 383 (38.5) | 227 (22.8) | 377 (37.9) | 7 (0.7) | 165 (22.7) | 562 (77.3) | 114 (15.7) | 51 (7.0) | 0 (0.0) | <0.001 | ||
| Chills | 668 (67.2) | 326 (32.8) | 232 (23.3) | 421 (42.4) | 15 (1.5) | 124 (17.1) | 603 (82.9) | 86 (11.8) | 35 (4.8) | 3(0.4) | <0.001 | ||
| Fever | 274 27.6) | 720 (72.4) | 181 (18.2) | 74 (7.4) | 17 (1.7) | 2 (0.2) | 14 (1.9) | 713 (98.1) | 11 (1.5) | 2 (0.3) | 1 (0.1) | 0 (0.0) | <0.001 |
| Nausea/ vomiting | 362 (36.4) | 632 (63.6) | 288 (29.0) | 67 (6.7) | 7 (0.7) | 92 (12.7) | 635 (87.3) | 84 (11.6) | 6 (0.8) | 2 (0.3) | <0.001 | ||
| Diarrhea | 198 19.9) | 796 (80.1) | 119 (12.0) | 66 (6.6) | 10 (1.0) | 3 (0.3) | 76 (10.5) | 651 (89.5) | 43 (5.9) | 29 (4.0) | 4 (0.6) | 0 (0.0) | <0.001 |
Data are shown as number (%). AEFI = adverse event following immunization; G = Grade. a Fever, diarrhea, redness, and swelling at the injection site were included in Grade 4 severity.
Table 2.
Incidence of adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses by age group.
Table 2.
Incidence of adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses by age group.
| 1st Dose | 2nd Dose | |||||||
|---|---|---|---|---|---|---|---|---|
| Adverse Events | <30 Years (n = 394) | 30–50 Years (n = 471) | >50 Years (n = 129) | p Value for Trend | <30 Years (n = 244) | 30–50 Years (n = 378) | >50 Years (n = 105) | p Value for Trend |
| Any AEFIs | 389 (98.7) | 464 (98.5) | 122 (94.6) | 0.017 | 223 (91.4) | 346 (91.5) | 92 (87.6) | 0.384 |
| Local AEFIs | 382 (97.0) | 450 (95.5) | 113 (87.6) | <0.001 | 205 (84.0) | 326 (86.2) | 81 (77.1) | 0.321 |
| Tenderness | 382 (97.0) | 448 (95.1) | 109 (84.5) | <0.001 | 198 (81.1) | 324 (85.7) | 80 (76.2) | 0.712 |
| Resting pain | 355 (90.1) | 424 (90.0) | 96 (74.4) | <0.001 | 157 (64.3) | 259 (68.5) | 65 (61.9) | >0.999 |
| Redness | 145 (36.8) | 159 (33.8) | 35 (27.1) | 0.053 | 51 (20.9) | 110 (29.1) | 29 (27.6) | 0.076 |
| Swelling | 209 (53.0) | 221 (46.9) | 54 (41.9) | 0.016 | 72 (29.5) | 129 (34.1) | 38 (36.2) | 0.173 |
| Systemic AEFIs | 383 (97.2) | 452 (96.0) | 113 (87.6) | <0.001 | 182 (74.6) | 290 (76.7) | 77 (73.3) | >0.999 |
| Fatigue | 374 (94.9) | 440 (93.4) | 109(84.5) | 0.001 | 163 (66.8) | 274 (72.5) | 68 (64.8) | 0.856 |
| Headache | 334 (84.8) | 356 (75.6) | 82 (63.6) | <0.001 | 104 (42.6) | 149 (39.4) | 41 (39.0) | 0.461 |
| Malaise | 343 (87.1) | 397 (84.3) | 93 (72.1) | <0.001 | 88 (36.1) | 160 (42.3) | 44 (41.9) | 0.192 |
| Arthralgia | 240 (60.9) | 302 (64.1) | 69 (53.5) | 0.440 | 47 (19.3) | 85 (22.5) | 33 (31.4) | 0.020 |
| Chills | 277 (70.3) | 322 (68.4) | 69 (53.5) | 0.003 | 38 (15.6) | 70 (18.5) | 16 (15.2) | 0.825 |
| Fever | 130 (33.0) | 134 (28.5) | 10 (7.8) | <0.001 | 1 (0.4) | 11 (2.9) | 2 (1.9) | 0.158 |
| Nausea/vomiting | 177 (44.9) | 160 (34.0) | 25 (19.4) | <0.001 | 36 (14.8) | 45 (11.9) | 11 (10.5) | 0.241 |
| Diarrhea | 92 (23.4) | 85 (18.0) | 21 (16.3) | 0.034 | 25 (10.2) | 45 (11.9) | 6 (5.7) | 0.467 |
Values are presented as number (%). AEFI = adverse event following immunization.
Table 3.
Incidence and severity of the adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses in paired data.
Table 3.
Incidence and severity of the adverse events following the first and second ChAdOx1 nCoV-19 vaccine doses in paired data.
| Adverse Events | 1st Dose (n = 652) | 2nd Dose (n = 652) | p Value b | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Any | None | G1 | G2 | G3 | G4 a | Any | None | G1 | G2 | G3 | G4 a | ||
| Age, mean ± SD | 36.75 ± 10.41 (range, 20–63) | ||||||||||||
| Female sex | 513 (78.7) | ||||||||||||
| Any AEFIs | 642 (98.5) | 10 (1.5) | 82 (12.6) | 256 (39.3) | 293 (44.9) | 11 (1.7) | 598 (91.7) | 54 (8.3) | 194 (29.8) | 275 (42.2) | 127 (19.5) | 2 (0.3) | <0.001 |
| Local AEFIs | 626 (96.0) | 26 (4.0) | 132 (20.2) | 252 (38.7) | 234 (35.9) | 8 (1.2) | 557 (85.4) | 95 (14.6) | 213 (32.7) | 232 (35.6) | 110 (16.9) | 2 (0.3) | <0.001 |
| Tenderness | 622 (95.4) | 30 (4.6) | 144 (22.1) | 251 (38.5) | 227 (34.8) | 548 (84.0) | 104 (16.0) | 212 (32.5) | 229 (35.1) | 107 (16.4) | <0.001 | ||
| Resting pain | 583 (89.4) | 69 (10.6) | 355 (54.4) | 226 (34.7) | 2 (0.3) | 445 (68.3) | 207 (31.7) | 380 (58.3) | 65 (10.0) | 0 (0.0) | <0.001 | ||
| Redness | 222 (34.0) | 430 (66.0) | 159 (24.4) | 35 (5.4) | 23 (3.5) | 5 (0.8) | 177 (27.1) | 475 (72.9) | 161 (24.7) | 12 (1.8) | 4 (0.6) | 0 (0.0) | <0.001 |
| Swelling | 327 (50.2) | 325 (49.8) | 216 (33.1) | 73 (11.2) | 31 (4.8) | 7 (1.1) | 223 (34.2) | 429 (65.8) | 173 (26.5) | 42 (6.4) | 6 (0.9) | 2 (0.3) | <0.001 |
| Systemic AEFIs | 621 (95.2) | 31 (4.8) | 130 (19.9) | 354 (54.3) | 134 (20.6) | 3 (0.5) | 497 (76.2) | 155 (23.8) | 265 (40.6) | 202 (31.0) | 30 (4.6) | 0 (0.0) | <0.001 |
| Fatigue | 604 (92.6) | 48 (7.4) | 178 (27.3) | 301 (46.2) | 125 (19.2) | 458 (70.2) | 194 (29.8) | 282 (43.3) | 148 (22.7) | 28 (4.3) | <0.001 | ||
| Headache | 504 (77.3) | 148 (22.7) | 175 (26.8) | 323 (49.5) | 6 (0.9) | 271 (41.6) | 381 (58.4) | 161 (24.7) | 109 (16.7) | 1 (0.2) | <0.001 | ||
| Malaise | 542 (83.1) | 110 (16.9) | 156 (23.9) | 373 (57.2) | 13 (2.0) | 262 (40.2) | 390 (59.8) | 177 (27.1) | 83 (12.7) | 2 (0.3) | <0.001 | ||
| Arthralgia | 395 (60.6) | 257 (39.4) | 151 (23.2) | 240 (36.8) | 4 (0.6) | 150 (23.0) | 502 (77.0) | 103 (15.8) | 47 (7.2) | 0 (0.0) | <0.001 | ||
| Chills | 418 (64.1) | 243 (35.9) | 138 (21.2) | 271 (41.6) | 9 (1.4) | 112 (17.2) | 540 (82.8) | 75 (11.5) | 34 (5.2) | 3 (0.5) | <0.001 | ||
| Fever | 171 (26.2) | 481 (73.8) | 116 (17.8) | 41 (6.3) | 12 (1.8) | 2 (0.3) | 12 (1.8) | 640 (98.2) | 10 (1.5) | 1 (0.2) | 1 (0.2) | 0 (0.0) | <0.001 |
| Nausea/vomiting | 226 (34.7) | 426 (65.3) | 185 (28.4) | 36 (5.5) | 5 (0.8) | 86 (13.2) | 566 (86.8) | 79 (12.1) | 5 (0.8) | 2 (0.3) | <0.001 | ||
| Diarrhea | 127 (19.5) | 525 (80.5) | 82 (12.6) | 39 (6.0) | 5 (0.8) | 1 (0.2) | 70 (10.7) | 582 (89.3) | 41 (6.3) | 27 (4.1) | 2 (0.3) | 0 (0.0) | <0.001 |
Data are presented as number (%). AEFI = adverse event following immunization; G = Grade. a Fever, diarrhea, redness, and swelling at the injection site were included in Grade 4 severity. b p value analyzed by Wilcoxon signed rank test.
Table 4.
Incidence and peak grade of adverse events following the first and the second ChAdOx1 nCoV-19 vaccine doses of healthcare workers under 30 years of age in paired data.
Table 4.
Incidence and peak grade of adverse events following the first and the second ChAdOx1 nCoV-19 vaccine doses of healthcare workers under 30 years of age in paired data.
| Adverse Events | 1st Dose (n = 217) | 2nd Dose (n = 217) | p Value a | ||
|---|---|---|---|---|---|
| Age, Mean ± SD | 26.1 ± 2.1 (Range, 20–29) | ||||
| Female sex | 192 (88.5) | ||||
| Incidence | Peak grade | Incidence | Peak grade | ||
| Any AEFIs | 215 (99.1) | 3.5 ± 0.7 | 202 (93.1) | 2.8 ± 0.8 | <0.001 |
| Local AEFIs | 212 (97.7) | 3.3 ± 0.8 | 185 (85.3) | 2.5 ± 0.9 | <0.001 |
| Tenderness | 212 (97.7) | 3.2 ± 0.8 | 179 (82.5) | 2.5 ± 0.9 | <0.001 |
| Resting pain | 196 (90.3) | 2.3 ± 0.6 | 143 (65.9) | 1.7 ± 0.6 | <0.001 |
| Redness | 80 (36.9) | 1.5 ± 0.9 | 48 (22.1) | 1.2 ± 0.5 | <0.001 |
| Swelling | 117 (53.9) | 1.8 ± 1.0 | 69 (31.8) | 1.4 ± 0.7 | <0.001 |
| Systemic AEFIs | 212 (97.7) | 3.1 ± 0.7 | 165 (76.0) | 2.2 ± 0.8 | <0.001 |
| Fatigue | 206 (94.9) | 2.9 ± 0.8 | 148 (68.2) | 2.0 ± 0.8 | <0.001 |
| Headache | 186 (85.7) | 2.5 ± 0.7 | 94 (43.3) | 1.6 ± 0.8 | <0.001 |
| Malaise | 190 (87.6) | 2.5 ± 0.7 | 80 (36.9) | 1.5 ± 0.7 | <0.001 |
| Arthralgia | 126 (58.1) | 2.0 ± 0.9 | 42 (19.4) | 1.3 ± 0.6 | <0.001 |
| Chills | 146 (67.3) | 2.2 ± 0.9 | 34 (15.7) | 1.2 ± 0.6 | <0.001 |
| Fever | 73 (33.6) | 1.5 ± 0.7 | 1 (0.5) | 1.0 ± 0.1 | <0.001 |
| Nausea/vomiting | 95 (43.8) | 1.5 ± 0.7 | 33 (15.2) | 1.2 ± 0.4 | <0.001 |
| Diarrhea | 49 (22.6) | 1.3 ± 0.6 | 24 (11.1) | 1.2 ± 0.6 | <0.001 |
Data are presented as number (%) and mean ± SD. AEFI = adverse event following immunization; SD = standard deviation. a p value analyzed by Wilcoxon signed rank test.
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Jeon, M.; Kim, J.; Oh, C.E.; Lee, J.-Y. Adverse Events Following Immunization Associated with the First and Second Doses of the ChAdOx1 nCoV-19 Vaccine among Healthcare Workers in Korea. Vaccines 2021, 9, 1096. https://doi.org/10.3390/vaccines9101096
AMA Style
Jeon M, Kim J, Oh CE, Lee J-Y. Adverse Events Following Immunization Associated with the First and Second Doses of the ChAdOx1 nCoV-19 Vaccine among Healthcare Workers in Korea. Vaccines. 2021; 9(10):1096. https://doi.org/10.3390/vaccines9101096
Chicago/Turabian StyleJeon, Minji, Jehun Kim, Chi Eun Oh, and Jin-Young Lee. 2021. "Adverse Events Following Immunization Associated with the First and Second Doses of the ChAdOx1 nCoV-19 Vaccine among Healthcare Workers in Korea" Vaccines 9, no. 10: 1096. https://doi.org/10.3390/vaccines9101096
APA StyleJeon, M., Kim, J., Oh, C. E., & Lee, J. -Y. (2021). Adverse Events Following Immunization Associated with the First and Second Doses of the ChAdOx1 nCoV-19 Vaccine among Healthcare Workers in Korea. Vaccines, 9(10), 1096. https://doi.org/10.3390/vaccines9101096
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