Participants could report more than 1 adverse effect. Denominators include all participants who provided an answer to the question.
eTable 1. Characteristics of COVID-19 Citizen Science Study Participants
eTable 2. Adverse Effects in Participants With Asthma by Inhaled Corticosteroid Use
eFigure. Free-Text Entries for Other Vaccine Adverse Effects
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Beatty AL, Peyser ND, Butcher XE, et al. Analysis of COVID-19 Vaccine Type and Adverse Effects Following Vaccination. JAMA Netw Open. 2021;4(12):e2140364. doi:10.1001/jamanetworkopen.2021.40364
What factors are associated with adverse effects after COVID-19 vaccination?
In an online cohort study including 19 586 adults who received a COVID-19 vaccination, the factors most strongly associated with adverse effects were full vaccination dose, brand of vaccine, younger age, female sex, and having had COVID-19 before vaccination. Allergic reaction or anaphylaxis was reported in 0.3% of participants after partial vaccination and 0.2% of participants after full vaccination.
These findings suggest that some individuals experience more adverse effects after COVID-19 vaccination, but serious adverse effects are rare.
Little is known about the factors associated with COVID-19 vaccine adverse effects in a real-world population.
To evaluate factors potentially associated with participant-reported adverse effects after COVID-19 vaccination.
Design, Setting, and Participants
The COVID-19 Citizen Science Study, an online cohort study, includes adults aged 18 years and older with a smartphone or internet access. Participants complete daily, weekly, and monthly surveys on health and COVID-19–related events. This analysis includes participants who provided consent between March 26, 2020, and May 19, 2021, and received at least 1 COVID-19 vaccine dose.
Participant-reported COVID-19 vaccination.
Main Outcomes and Measures
Participant-reported adverse effects and adverse effect severity. Candidate factors in multivariable logistic regression models included age, sex, race, ethnicity, subjective social status, prior COVID-19 infection, medical conditions, substance use, vaccine dose, and vaccine brand.
The 19 586 participants had a median (IQR) age of 54 (38-66) years, and 13 420 (68.8%) were women. Allergic reaction or anaphylaxis was reported in 26 of 8680 participants (0.3%) after 1 dose of the BNT162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) vaccine, 27 of 11 141 (0.2%) after 2 doses of the BNT162b2 or mRNA-1273 vaccine or 1 dose of the JNJ-78436735 (Johnson & Johnson) vaccine. The strongest factors associated with adverse effects were vaccine dose (2 doses of BNT162b2 or mRNA-1273 or 1 dose of JNJ-78436735 vs 1 dose of BNT162b2 or mRNA-1273; odds ratio [OR], 3.10; 95% CI, 2.89-3.34; P < .001), vaccine brand (mRNA-1273 vs BNT162b2, OR, 2.00; 95% CI, 1.86-2.15; P < .001; JNJ-78436735 vs BNT162b2: OR, 0.64; 95% CI, 0.52-0.79; P < .001), age (per 10 years: OR, 0.74; 95% CI, 0.72-0.76; P < .001), female sex (OR, 1.65; 95% CI, 1.53-1.78; P < .001), and having had COVID-19 before vaccination (OR, 2.17; 95% CI, 1.77-2.66; P < .001).
Conclusions and Relevance
In this real-world cohort, serious COVID-19 vaccine adverse effects were rare and comparisons across brands could be made, revealing that full vaccination dose, vaccine brand, younger age, female sex, and having had COVID-19 before vaccination were associated with greater odds of adverse effects. Large digital cohort studies may provide a mechanism for independent postmarket surveillance of drugs and devices.
In December 2020, the first COVID-19 vaccines received emergency use authorization in the United States.1,2 Billions of doses of vaccine have been administered worldwide.3 However, some individuals have concerns about receiving COVID-19 vaccination related to vaccine safety and adverse effects.4
In randomized clinical trials of COVID-19 vaccines, reported adverse effects included injection site events (eg, pain, redness, swelling) and systemic effects (eg, fatigue, headache, muscle or joint pain), with rare serious adverse events.5-8 Most adverse effects were mild, but studies reported approximately 50% to 90% of participants experiencing some adverse effects.5,6,8 Although data have begun to emerge on adverse effects reported through government-sponsored reporting systems,9-13 there is little real-world, patient-reported data on adverse effects after receiving COVID-19 vaccination and in whom adverse effects may be more common.
The objectives of this study were to describe adverse effects and identify factors associated with adverse effects after COVID-19 vaccination in participants in an online cohort study. In addition, the study sought to identify factors associated with more severe adverse effects. These results may help the public gain a greater understanding of the real-world experience of adverse effects after COVID-19 vaccination.
The COVID-19 Citizen Science (CCS) study is an online cohort study that began enrolling participants on March 26, 2020.14 CCS is hosted on the Eureka Research Platform (University of California, San Francisco), a digital platform for clinical research studies including a mobile application (app) and web-based software. Participants are recruited to the study through email invitations to participants in other Eureka Research Platform studies, press releases, word-of-mouth, and recruitment through partner organizations. Participants must be 18 years or older, register for a Eureka Research Platform account, have an iOS or Android smartphone with a cellular phone number (or enroll in the web-based study launched January 21, 2021), agree to participate in English, and be able to provide consent to participate in the study. After providing electronic consent, participants complete baseline, daily, weekly, and monthly surveys. CCS methods have been previously described.14-17 For this analysis, we included data collected between March 26, 2020, and May 19, 2021. The study was reviewed and approved by the University of California, San Francisco, institutional review board. Results are reported in accordance with Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline.18
On January 14, 2021, participants began receiving baseline and monthly surveys asking, “Have you ever received a COVID-19 (SARS-CoV-2) vaccine?” Follow-up questions immediately after a participant reported receiving a vaccine asked participants how many doses they received, the dates of vaccine doses, vaccine brand, and where they received the vaccine. Participants received a monthly follow-up survey asking about receiving additional doses of vaccine. Monthly surveys were chosen to limit participant survey burden and because the administration schedules for vaccines with multiple doses separated doses by 3 to 4 weeks. Partial vaccination was defined as receiving 1 dose of any vaccine other than JNJ-78436735 (Johnson & Johnson). Full vaccination was defined as receiving 1 dose of JNJ-78436735 or 2 doses of any other vaccine. At the time these data were collected, third or booster doses were not yet recommended, so data on additional doses were not collected. Final analyses included only participants who reported receiving BNT162b2 (Pfizer/BioNTech), mRNA-1273 (Moderna), or JNJ-78436735 vaccines because of small numbers of receipt of other vaccines in this study.
After reporting vaccination, participants were asked to report vaccine adverse effects, with response options including fever, chills, fatigue, sore/scratchy throat, muscle pain, joint pain, headache, other pain, redness/swelling at the injection site, rash other than at the injection site, allergic reaction/anaphylaxis, other, and none of the above. These response options were chosen because these adverse effects had been reported in vaccine clinical trials. Participants could provide free-text responses to the option of other. Following branching logic, participants reporting adverse effects were also asked the duration of adverse effects and self-rated adverse effect severity (very mild, mild, moderate, severe, and very severe). If participants reported receiving 2 doses of vaccine on the same survey, they were not asked to report adverse effects by dose separately.
At baseline, participants reported characteristics, including age, sex, gender, race (American Indian or Alaska Native, Asian, Black or African American, Native Hawaiian or Pacific Islander, White, and other or do not know), ethnicity, zip code, Macarthur subjective social status (rated 0-10, with 10 being the highest),19 highest educational attainment, primary employment, working from home, regular contact with people 65 years and older, receipt of influenza shot in the past year, medical conditions, and current tobacco and marijuana use. Rural and urban status was determined using 2010 zip code and rural-urban commuting area codes from the US Department of Agriculture.20 Median income by zip code was determined using American Community Survey 5-year estimates from 2019.21 Participants provide current medication lists, which are indexed to RxNorm.
Participants reported results of COVID-19 testing and date of testing at baseline and on weekly surveys. In this study, we defined COVID-19 as a participant-reported positive test for active infection (polymerase chain reaction or antigen testing).
Descriptive statistics including mean, SD, median, and IQR are used to describe baseline characteristics and questionnaire responses. For baseline characteristics and survey responses, differences in characteristics were examined with a t test or Kruskal-Wallis test for continuous variables and χ2 test for categorical variables. A multivariable logistic regression model was constructed to identify factors associated with any adverse effects (vs no adverse effects). Given that vaccination and adverse effects were queried monthly, participants could report 2 doses of vaccine in 1 survey. When participants reported 2 doses of vaccine in a monthly survey, the reported adverse effects were associated with the second vaccine dose. Candidate factors in the multivariable models (with all factors entered into the model simultaneously) included age (as a continuous variable, per 10 years), sex assigned at birth (female or all others), race (Asian, Black or African American, multiracial, White, or other), Hispanic ethnicity, subjective social status, medical conditions (hypertension, diabetes, myocardial infarction, coronary heart disease, heart failure, stroke or transient ischemic attack, atrial fibrillation, obstructive sleep apnea, chronic obstructive pulmonary disease, asthma, immunodeficiency, HIV, anemia, and pregnancy), influenza shot in the past year, current tobacco use, current marijuana use, COVID-19 prior to vaccination, vaccine dose, and vaccine brand (BNT162b2, mRNA-1273, or JNJ-78436735). A separate multivariable logistic regression model was constructed to identify factors associated with severe or very severe adverse effects (vs no, very mild, mild, or moderate adverse effects) using the same candidate factors. We conducted an exploratory analysis of adverse effects in participants with asthma with and without use of inhaled corticosteroids. Statistical significance was considered to be P < .05, and all tests were 2-tailed. All analyses were conducted with SAS version 9.4 (SAS Institute).
As of May 19, 2021, 19 586 participants reported receiving at least 1 dose of vaccine, with a median (IQR) age of 54 (38-66) years and 13 492 (68.8%) female participants (Table 1). In the overall cohort, 65 921 participants had enrolled, and 46 204 (70%) remained active in the study (ie, completed at least 1 survey in 2021) (eTable 1 in the Supplement). Among 12 215 participants who reported where they were vaccinated (62.3%), the most common sites were at a doctor’s office, clinic, or hospital (5307 [43.4%]), workplace (1834 [15.0%]), public health department (1685 [13.8%]), pharmacy (1217 [10.0%]), and health fair or other public event (1025 [8.4%]).
After 1 dose of BNT162b2 or mRNA-1273, 8680 or 8682 participants completed the adverse effects survey and 5629 of 8682 (64.9%) reported adverse effects. After 2 doses of BNT162b2 or mRNA-1273 or 1 dose of JNJ-78436735, 11 140 of 11 141 participants completed the adverse effects survey and 8947 (80.3%) reported adverse effects. The most common vaccine adverse effects were fatigue, muscle pain, headache, chills, redness/swelling at the injection site, joint pain, and fever (Figure 1 and Figure 2). Allergic reaction or anaphylaxis was reported in 26 of 8680 participants (0.3%) after 1 dose of BNT162b2 or mRNA-1273 and 27 of 11 140 participants (0.2%) after 2 doses of BNT162b2 or mRNA-1273 or 1 dose of JNJ-78436735. Other write-in adverse effects included nausea, vomiting, diarrhea, dizziness, brain fog, swollen lymph nodes, and pain/soreness at injection site (eFigure in the Supplement). Two participants reported thrombocytopenia.
In a multivariable logistic regression model examining the association of multiple factors entered into the model simultaneously (age, sex, race, Hispanic ethnicity, subjective social status, medical conditions, influenza shot in the past year, current tobacco use, current marijuana use, COVID-19 prior to vaccination, vaccine dose, and vaccine brand), the factor most strongly associated with the outcome of any adverse effects (compared with no adverse effects) was vaccine dose (2 doses of BNT162b2 or mRNA-1273 or 1 dose of JNJ-78436735 vs 1 dose of BNT162b2 or mRNA-1273: odds ratio [OR], 3.10; 95% CI, 2.89 to 3.34; P < .001) (Table 2). Older age (per 10 years: OR, 0.74; 95% CI, 0.72-0.76; P < .001), receipt of JNJ-78436735 vaccine (vs BNT162b2), Black or African American race, higher subjective social status, asthma, and anemia were associated with lower odds of reporting adverse effects. Receipt of mRNA-1273 vaccine (vs BNT162b2), female sex (OR, 1.65; 95% CI, 1.53-1.78; P < .001), prior COVID-19 (OR, 2.17; 95% CI, 1.77-2.66; P < .001), Asian race, pregnancy at baseline, and marijuana use were associated with higher odds of reporting adverse effects. Use of inhaled corticosteroids did not appear to be associated with fewer adverse effects in participants with asthma (eTable 2 in the Supplement).
In a multivariable logistic regression model for the outcome of severe or very severe adverse effects (compared with no adverse effects, very mild, mild, or moderate), the strongest factor associated with severe or very severe adverse effects was vaccine dose (Table 3). Older age, receiving a influenza shot last year, asthma, obstructive sleep apnea, and higher subjective social status were associated with lower odds of reporting severe or very severe adverse effects. Receipt of mRNA-1273 vaccine (vs BNT162b2), female sex, and prior COVID-19 were associated with higher odds of reporting severe or very severe adverse effects.
Adverse effects and adverse effect severity varied across vaccine brands. Compared with participants receiving BNT162b2 vaccine, participants receiving mRNA-1273 had double the odds of reporting adverse effects (odds ratio, 2.00; 95% CI, 1.86 to 2.15; P < .001). Participants receiving JNJ-78436735 had lower odds of adverse effects compared with BNT162b2 (OR, 0.64; 95% CI, 0.52-0.79; P < .001). Compared with participants receiving BNT162b2 vaccine, participants receiving mRNA-1273 had 1.88 times (95% CI, 1.63-2.17) the odds of reporting severe or very severe adverse effects (P < .001). There was not a statistically significant difference in odds of severe or very severe adverse effects reported by participants receiving the JNJ-78436735 vaccine compared with the BNT162b2 vaccine (OR, 1.03; 95% CI, 0.67-1.58; P = .89).
In this real-world digital cohort of 19 586 people who reported receiving COVID-19 vaccination, serious adverse effects, such as anaphylaxis or allergy, were rare. Adverse effects were more common after the full vaccination dose, the mRNA-1273 vaccine, and in participants with younger age, female sex, prior COVID-19, Asian race, pregnancy at baseline, and marijuana use. Older age, Black or African American race, higher subjective social status, asthma, and anemia were associated with lower odds of reporting adverse effects.
The finding of low rates of serious adverse effects is consistent with data from randomized clinical trials and government-sponsored surveillance of vaccine safety.5-12 US government-sponsored surveillance has reported incidence of anaphylaxis of 4.5 to 5.1 cases per million doses administered, although this may be underreported if individuals did not seek care or received care at another facility.10,13 Other reports suggest patient-reported anaphylaxis or severe allergy may be more common, at 2%.22 Our study finding of participant-reported anaphylaxis or allergy in 0.3% is higher than surveillance reports but lower than reports of patient-reported adverse effects. Similarly, the array of adverse effects and finding of more adverse effects in younger participants in our study are consistent with adverse effects that were observed in randomized clinical trials and government-sponsored surveillance and that are listed on government-sponsored websites.5-12,23 Additionally, the array of adverse effects is similar to those identified through systematic reviews and meta-analysis of randomized trials and US-government-sponsored reporting.24,25
Because randomized clinical trials of vaccine safety and efficacy were conducted with single brands of vaccines, it is difficult to make comparisons regarding rates of adverse effects from different brands of vaccines and different studies. US government–sponsored surveillance reported rates of adverse effects with BNT162b2 and mRNA-1273 vaccines.10 Although it appeared that there were more adverse effects with mRNA-1273 than BNT162b2, the reports did not make formal comparisons between vaccine brands.10 This study enables comparisons across vaccine brands because it included participants who received any brand of vaccine, comes from a nongovernment source, and administered the same survey to all participants.
In this study, people with prior COVID-19 had greater odds of adverse effects and more severe adverse effects after COVID-19 vaccination. Data from randomized clinical trials were not conclusive with regard to the association between prior COVID-19 and adverse effects after vaccination.5 Other smaller real-world reports have also reported increased adverse effects in people with prior COVID-19.22 In this study, which included 895 participants with prior COVID-19, there was a strong association between prior COVID-19 and vaccine adverse effects.
To our knowledge, this is the first report of lower risk of vaccine adverse effects or severe adverse effects in individuals with asthma. A meta-analysis found that people with asthma may appear to have lower risk of COVID-19 than the general population.26 It is possible that the airway effects of asthma or immune effects of inhaled corticosteroids may affect the response to COVID-19 or COVID-19 vaccine. Rare adverse effects, such as thrombocytopenia, were reported by participants; rare reports of thrombocytopenia have also emerged in the literature.27
Racial differences in the risk of adverse effects were observed in our study, with people identifying as Asian more likely to report adverse effects and people identifying as Black or African American less likely to report adverse effects. However, we are unable to determine whether these differences are present because of differential reporting, different experience of receiving the vaccine, differences in other social determinants of health or experiences of health, differences in immune system reaction to vaccines, or other incompletely measured confounders.
This study provides important data for the public about adverse effects and vaccine safety that confirm data from randomized clinical trials and government-sponsored surveillance. Indeed, large digital cohort studies may provide a mechanism for simple, inexpensive, and independent postmarket surveillance for adverse effects of new drugs and devices. Additionally, this study found that groups including older individuals, males, people who identify as Black or African American, and people with asthma were less likely to experience adverse effects or severe adverse effects. The overall low rates of serious adverse effects and greater knowledge about patterns and factors associated with adverse effects may enhance public vaccine confidence and promote greater adoption of vaccination to enable global recovery from the pandemic. However, given the limited representativeness of this study, future studies should conduct targeted efforts to recruit representative populations. Previously, we have shown that recruiting through community organizations can promote participation in digital clinical studies.28
This study has limitations. Although the digital cohort study did include people from diverse groups, some groups, such as men, older adults, people belonging to minoritized racial and ethnic groups, rural residents, people reporting lower subjective social status, and non-US residents, are underrepresented, which may limit generalizability to all groups or populations outside of the United States. Given the online nature of the study, not all participants responded to all surveys. This may contribute to both measurement bias through undermeasurement of vaccine receipt or COVID-19 diagnosis and selection bias if participants from different groups or participants with adverse effects responded differentially to surveys. In previous studies, we found that self-reported COVID-19 test results appeared to accurately reflect COVID-19 diagnosis.16 Additionally, administration of surveys on a monthly basis could lead to measurement bias through inaccurate reporting of vaccine-related adverse effects. Because this study included data until May 19, 2021, this reflects the early experience with vaccination, and results could differ in later time periods or with other vaccines.
In this real-world cohort, serious COVID-19 vaccine adverse effects were rare, and overall adverse effects were similar to industry and government reports. This independent evaluation enabled the comparison of adverse effects between vaccine manufacturers, noting that adverse effects were more common with mRNA-1273 compared with BNT162b2. Large digital cohort studies may provide a mechanism for independent postmarket surveillance of drugs and devices.
Accepted for Publication: October 29, 2021.
Published: December 22, 2021. doi:10.1001/jamanetworkopen.2021.40364
Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2021 Beatty AL et al. JAMA Network Open.
Corresponding Author: Alexis L. Beatty, MD, MAS, Division of Cardiology, Department of Epidemiology and Biostatistics, Department of Medicine, University of California, San Francisco, 550 16th St, PO Box 0560, San Francisco, CA 94143 (email@example.com).
Author Contributions: Dr Beatty had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Concept and design: Beatty, Peyser, Butcher, Cocohoba, Olgin, Pletcher, Marcus.
Acquisition, analysis, or interpretation of data: Beatty, Peyser, Cocohoba, Lin, Olgin, Pletcher, Marcus.
Drafting of the manuscript: Beatty.
Critical revision of the manuscript for important intellectual content: All authors.
Statistical analysis: Beatty, Lin.
Obtained funding: Peyser, Olgin, Pletcher.
Administrative, technical, or material support: Peyser, Butcher, Cocohoba, Olgin, Marcus.
Supervision: Peyser, Olgin, Pletcher, Marcus.
Conflict of Interest Disclosures: Dr Beatty reported being formerly employed by and holding stock in Apple, Inc, outside the submitted work. Dr Olgin reported receiving personal fees from Vivalnk and grants from Samsung outside the submitted work. Dr Pletcher reported receiving grants from the Patient-Centered Outcomes Research Institute, the National Institutes of Health (NIH), and the Bill and Melinda Gates Foundation during the conduct of the study. No other disclosures were reported.
Funding/Support: The Eureka Research Platform is supported by grant 3U2CEB021881-05S1 from NIH/National Institute of Biomedical Imaging and Bioengineering to Drs Marcus, Olgin, and Pletcher. The COVID-19 Citizen Science Study is supported by Patient-Centered Outcomes Research Institute contract COVID-2020C2-10761 to Drs Pletcher, Marcus, and Olgin; the Bill and Melinda Gates Foundation contract INV-017206 to Drs Pletcher, Marcus, and Olgin, and grant 75N91020C00039 from NIH/National Cancer Institute to Drs Marcus, Hswen, Pletcher, and Olgin.
Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.