Category: Covid-19 Vaccine

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COVID-19: Vaccine – NYC Health – New York City

October 15, 2022

Main Page Workplace Requirement Vaccine Equity Data

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Updated COVID-19 vaccine boosters are now available for everyone 5 and older who received their most recent vaccine dose at least two months ago. The updated Pfizer booster is recommended for everyone 5 and older, and the updated Moderna booster for everyone 6 and older. You can choose which booster to get.

The updated boosters are specifically designed to protect you against the omicron subvariants that account for nearly all recent infections in NYC.

You can get this updated booster at the same time as other vaccines, so schedule both your booster and your flu shot today.

Learn more about getting the updated booster.

To find a vaccination site, use the City's Vaccine Finder. You can search for specific types of vaccines, including boosters and age-specific doses.

Call 877-VAX-4NYC (877-829-4692) to schedule an appointment at certain sites, as well as to get other vaccination assistance.

If you are a New York resident who is homebound or at least 65 years old, you can sign up online for an in-home vaccination or by calling 877-VAX-4NYC (877-829-4692).

Vaccines can protect you and your community from severe COVID-19 illness, hospitalization and death. Vaccines are available at no cost to you and regardless of immigration status.

Vaccination is safer than risking illness and long-term health effects from COVID-19. Even people who have had COVID-19 should get vaccinated.

COVID-19 vaccines are available for children ages 6 months and older.

The vaccines will help your child develop immunity and provide them with protection against severe illness and death from COVID-19. Children may experience similar side effects of vaccination as adults, with usually mild effects lasting one to two days.

The more contagious variants of COVID-19 that have been spreading have caused some children to get sick, be hospitalized and die. The best way to protect your child is to get them vaccinated as soon as possible.

Children younger than 5 years should get the same vaccine for their second (and third) doses of their primary series as they received for their first dose. They will be considered fully vaccinated two weeks after either their third Pfizer dose or second Moderna dose.

Ask your childs pediatrician if they will be offering the vaccine. Some pharmacies may offer vaccine to children 3 years and older.

A parent or guardian must provide consent for their child to be vaccinated in person, by phone or in writing, depending on the vaccination site. They will not need to provide proof they are the child's parent or guardian.

Children ages 15 and younger should be accompanied to the vaccination site by a parent or guardian, or another adult caregiver designated by the parent or guardian.

Updated Pfizer and Moderna COVID-19 vaccine boosters are now available. Updated boosters are recommended for everyone 5 and older, even if they have already received a booster dose. They are called "bivalent" booster vaccines because half of the dose is specifically targeting the omicron subvariants that account for nearly all recent infections in NYC. These boosters increase your immunity from your prior doses.

You can get your updated bivalent booster if it has been at least two months since your most recent COVID-19 vaccine dose.

People ages 6 and older can get either the Pfizer or Moderna booster, regardless of which brand of vaccine they previously received. Children age 5 can get only the Pfizer booster.

If you recently had COVID-19, you can wait to get a booster until three months after you first felt symptoms, or, if you had no symptoms, three months after your test date. You may want to get a booster sooner than three months after you had COVID-19 if you are at higher risk of severe disease or getting COVID-19 again.

Talk to your provider about when you should get your next vaccine.

Children younger than 5 are currently not eligible for a booster dose.

Separate from boosters, people who are moderately to severely immunocompromised (meaning they have a weakened immune system) should get an additional vaccine dose, as part of their primary vaccine series.

This dose is intended to help people who may not have had a strong response to the first two doses due to a medical condition or treatment. People ages 5 and older who receive this dose should also get a booster dose when eligible.

The Health Department is ensuring there is fair and equitable access to COVID-19 vaccines. We are ensuring the communities hit hardest by the pandemic have access to the vaccine.

People with disabilities can get help making a vaccination appointment at an accessible site, traveling to their appointment and getting their vaccine. This kind of help is called a reasonable accommodation.

You can get a reasonable accommodation if you have difficulty with:

Though not a complete list, some common examples of a reasonable accommodation are: a wheelchair provided on arrival; ASL interpretation or tactile interpretation; a quiet space if loud spaces are overwhelming; and verbal or physical guidance to navigate the vaccination site.

You can request a reasonable accommodation when you schedule your vaccination, either through the City's online appointment scheduler or by calling 855-491-2667. You can also ask for a reasonable accommodation from staff at a City-run vaccination site, or email hubaccess@health.nyc.gov for more information.

You can also sign up for an in-home vaccination online or by calling 877-VAX-4NYC (877-829-4692).

For more information, see:

Other City, State and Federal Government Websites

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COVID-19: Vaccine - NYC Health - New York City

Know the COVID-19 Vaccine, Treatment Options – Pharmacy Times

October 15, 2022

Latest Information is key to helping patients stay healthy amid continuously changing landscape.

With fall having arrived, it is important for pharmacists to be sure they are up-to-date with information on COVID-19 vaccines and options for treatment. Because of their role as a resource in keeping patients healthy, pharmacists have a special responsibility in shar-ing the latest information and statistics surrounding the pandemic.

Approximately 96 million individuals in the United States have had some version of the COVID-19 virus; of that number, 1.05 million have died, according to the CDC.1 Most individuals who experience severe illness from COVID-19 are older than 50 years (though not always) and have underlying medical conditions such as chronic kidney disease, chronic obstructive pulmonary disease, diabetes, heart disease, or obesity.1

Control Efforts

Due to the rising number of COVID-19 cases and lack of knowledge about the disease at the beginning of 2020, efforts to prevent spread of the virus were extreme. These included banning large gatherings, closing public places and schools, and encouraging work from home. Many individuals were required to wear masks outside their homes.

These measures slowed the spread of COVID-19 but also hurt the economy, forcing many small businesses to close. Many individuals were scared, creating a defensive, tense environment. Children forced to stay home from school often fell behind in their studies and developed anxiety disorders.

In hindsight, perhaps these efforts were too extreme for individuals not at high risk for developing severe disease, but because little was known about COVID-19 at the time, it was a decision based on protecting the population.

Vaccination

Operation Warp Speed (OWS), a partnership between the US Departments of Defense and Health & Human Services, was designed to speed development of a COVID-19 vaccine. The US Government Accountability Office determined that vac-cine makers and OWS adopted strategies for quickly developing vaccines while mitigating risk.2

The 3 vaccines resulting from OWS were from Johnson & Johnson, Moderna, and Pfizer/BioNTech. These fast-tracked vaccines started to be available in January 2021. Since then, more than 262 million individuals or 79% of the US population have received at least 1 dose. Overall, more than 224 million individuals or 68% of the population are considered fully vaccinated. Additionally, more than 108 million individuals or 33% of the population have received a booster dose.3

On August 31, 2022, the FDA authorized using bivalent formulations of the vaccines as single booster doses at least 2 months after primary or booster vaccination. These bivalent vaccines consist of 2 messenger RNA (mRNA) com-ponents of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), according to an FDA news release. The first component is from the original strain of SARS-CoV-2, for broad protection against COVID-19. The other is a com-ponent in common between the Omicron variants BA.4 and BA.5. lineages, which are causing most US cases of COVID-19 and are expected to circulate from now through the winter, according to the FDA release.4 In June 2022, the FDAs Vaccines and Related Biological Products Advisory Committee voted to include an Omicron component in COVID-19 booster vaccines.4

For each bivalent COVID-19 vaccine, the FDA considered available evidence. According to the FDA news release, this included effectiveness and safety data for each monovalent mRNA COVID-19 vaccine; immunogenicity and safety data from a study of a bivalent COVID-19 vaccine containing mRNA from Omicron variant BA.1 lineage that is similar to each vaccine being authorized; and nonclinical data obtained using a bivalent COVID-19 vaccine with mRNA of the original strain and mRNA in common between Omicrons BA.4 and BA.5 lineages.4 Based on data supporting these authorizations, the bivalent COVID-1 vaccines should provide increased protec-tion against Omicron, accor ing to the FDA news release. Individuals getting a bivalent COVID-19 vaccine may experience adverse effects (AEs) common among those getting monovalent mRNA COVID-19 vaccines.4 The monovalent mRNA COVID-19 vaccines are no longer authorized as booster doses for individuals 12 years and older, according to the FDA, which said it will evaluate data and submissions to support authorization of bivalent COVID-19 boosters for more age groups.3 The bivalent Moderna COVID-19 vaccine is authorized for use as a single booster dose in individuals 18 years and older, provided it has been at least 2 months since they completed primary vaccination or got their most recent booster dose of any authorized monovalent COVID-19 vaccine. Similarly, the bivalent Pfizer-BioNTech COVID-19 vaccine is authorized for use as a single booster dose in individuals 12 years and older, according to the FDA release.4

COVID-19 Treatment

The FDA has authorized certain antiviral medications and monoclonal antibodies to treat mild to moderate COVID-19 in individuals more likely to experience severe illness, according to the CDC. Antiviral treatments target specific parts of the virus to stop it from multiplying in the body, helping prevent severe illness and death. Monoclonal antibodies help the immune system recognize the virus and do a better job of fighting it. According to the CDC, these treatments include the following5:

Bebtelovimab. This monoclonal antibody is indicated in adults and children 12 years and older. Given as a single intravenous (IV) injection, it should be started within 7 days of symptom onset.

Nirmatrelvir with ritonavir (Paxlovid; Pfizer).This antiviral treatment is indicated in adults and children 12 years and older. This is an oral dosage taken at home that should be started within 5 days of symptom onset.5

Remdesivir (Veklury; Gilead). This antiviral treatment is indicated in children and adults. This is an IV infusion given at a health care facility for 3 consecutive days and should begin within 7 days of symptom onset.5

Patient Pearls

Some treatments might have AEs or interact with other medications, according to the CDC. Patients should ask physicians about the medications; those without health care providers can visit Test to Treat locations or contact a local community health center or health department.5

Hospitalized patients might receive other types of treatments, depending on the extent of illness. These could include medications to treat the virus, reduce an overactive immune response, or treat COVID-19 complications, according to the CDC.5 Many individuals with COVID-19 experience mild illness and can recover at home by using OTC medicines such as acetaminophen or ibuprofen, the CDC said.

Pharmacists who counsel patients this fall and winter should understand that COVID-19 presents a constantly changing landscape. Patients may look to pharmacists as an important community resource and as a way of keeping informed about the latest developments regarding the coronavirus. It is crucial that pharmacists stay informed about COVID-19.

References

1. COVID data tracker. CDC. Updated September 22, 2022. Accessed September 14, 2022. https://covid.cdc.gov/covid-da-ta-tracker/#datatracker-home

2. Operation Warp Speed. US Government Accountability Office. February 11, 2021. Accessed September 14, 2022. https://www.gao.gov/products/gao-21-319

3. US coronavirus vaccine tracker. USA Facts. Updated August 31, 2022. Accessed September 14, 2022. https://usafacts.org/visualizations/covid-vaccine-tracker-states/

4. Coronavirus (COVID-19) update: FDA authorizes Moderna, Pfizer-BioNTech bivalent COVID-19 vaccines for use as a booster dose. News release. FDA. August 31, 2022. Accessed September 14, 2022. https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-au-thorizes-moderna-pfizer-biontech-bivalent-covid-19-vac-cines-use

5. COVID-19 treatments and medications. CDC. Updated August 5, 2022. Accessed September 14, 2022. https://www.cdc.gov/coronavirus/2019-ncov/your-health/treatments-for-se-vere-illness.html

About the Author

Kathleen Kenny, PharmD, Rph,has more than 25 years experience as a community pharmacist. She is a freelance clinical medical writer based in Homosassa, Florida.

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Know the COVID-19 Vaccine, Treatment Options - Pharmacy Times

Time to Get Your Flu Shot and Your COVID-19 Booster Too – Health.mil

October 15, 2022

COVID-19 vaccinations used to be given separately due to concerns about possible immediate side effects, said Dr. David Hrncir, regional medical director of the Central Vaccine Safety Hub, DHA-Immunization Healthcare Division.

However, with the very large number of immunizations, immediate side effects following receipt of the COVID-19 vaccine have proven to be extremely rare, he said.

The bivalent boosters protect against the original form of the infectious respiratory disease as well as against the dominant omicron variant and its subvariants, which continue to mutate to become more easily transmissible.

Ideally, everyone 6 months and older should be vaccinated for flu by the end of October, said U.S. Army Lt. Col. Katie Martinez, deputy director of operations at IHD.Nevertheless, getting the flu vaccine later can still offer protection, even if you get it in the fall or early winter.

All flu vaccines in the United States for the 2022-2023 season protect against four different circulating flu viruses.

There should be no shortage of vaccine. The Department of Defense has received 100% of ordered flu vaccine, and 2 million doses have shipped to military medical treatment facility locations both CONUS and OCONUS for administration, Martinez said.

Shipments continue every week, and we recommend that beneficiaries check with their local military medical treatment facility for availability, she noted.

All active-duty service members are required to get an annual flu shot. Vaccines are available to all MHS beneficiaries at military hospitals and clinics, at installation vaccination events, and through TRICARE participating network pharmacies.

If you use a TRICARE-authorized provider, the flu shot itself comes at no cost, but when you get the vaccine from your provider, you may have a copay or cost-share for the office visit or for other services received during the office visit.

Its particularly important to get vaccinated against the flu and its potentially serious complications if you are at higher risk.

CDC has a full list of age and health factors that mean an increased risk, but some of those populations are:

Influenza can cause significant illness, especially in children under 5. Getting the vaccine helps children protect themselves and more at-risk people they come in regular contact with, such as their grandparents or siblings under 6 months old.

Some children may need two doses of flu vaccine, CDC noted. Those children should get the first dose as soon as vaccine is available, because the second dose needs to be given at least four weeks after the first.

For those 65 and older, the CDC recommends one of three flu vaccines because they have shown in studies of older individuals to create a stronger immune response. These vaccines are:

If you have questions, consult with your provider about which vaccine is right for you, Martinez said.

The CDC recommends treatment with antivirals for people who have flu or suspected symptoms and who are at higher risk of serious flu complications, such as people with asthma, diabetes, including gestational diabetes, or heart disease.

The antivirals work best when treatment is started within two days of becoming sick with flu symptoms and can lessen fever and flu symptoms and shorten the time you are sick by about one day, Martinez said.

Flu season usually runs from October through May, peaking in December through February, but it can continue through June.

Global health organizations, including DHA, monitor influenza activity around the world so health agencies can work with industry to develop the best vaccines suited to the particular strains that are circulating.

One region they base their formulations on is the Southern Hemisphere. Thats because peak flu season is the fall and winter, and those seasons are reversed in the Southern Hemisphere.

Hrncir said there was an early influenza season in the Southern Hemisphere, so it is reasonable to expect an early influenza season this fall and winter in the Northern Hemisphere.

The number of cases in Australia, for example, surpassed pre-COVID pandemic levels. However, since the start of the COVID pandemic in early 2020, the timing and duration of flu activity has been less predictable.

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Time to Get Your Flu Shot and Your COVID-19 Booster Too - Health.mil

Chinese study determines the real-world effectiveness of COVID-19 vaccines – News-Medical.Net

October 15, 2022

The outbreak of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was first reported in 2019 in Wuhan, China. The subsequent global transmission of SARS-CoV-2 ultimately led to the coronavirus disease 2019 (COVID-19) pandemic.

Implementing strict prevention measures and quarantine policies rapidly decreased COVID-19 cases in China. Despite these efforts, several localized COVID-19 outbreaks have still been reported.

Study:Real-world effectiveness and protection of SARS-CoV-2 vaccine among patients hospitalized for COVID-19 in Xi'an, China, December 8, 2021, to January 20, 2022: A retrospective study. Image Credit: Take Photo / Shutterstock.com

The first local confirmed COVID-19 case in Xian was reported on December 8, 2021. Soon after, whole genomic sequencing was conducted on nasal samples collected from patients in this region. This analysis revealed that all patients were infected with the SARS-CoV-2 Delta variant.

The enforcement of widespread prevention measures temporarily reduced new COVID-19 cases in Xian to zero until January 20, 2022. Thereafter, a total of 2,050 confirmed COVID-19 cases were reported, thus making it one of the most severe outbreaks since Wuhan, China.

A large number of cases not only increases the transmission rate but also enhances the potential for SARS-CoV-2 to mutate. These mutations lead to the emergence of more virulent variants, which might have the potential to cause epidemics on a larger scale.

The SARS-CoV-2 Delta variant, which was first reported in India, contained nine amino acid site mutations in the spike protein. This enhanced the infectivity, pathogenicity, and immune escape capacity of this variant. As compared to the ancestral SARS-CoV-2 strain, the reproductive number of the Delta variant was also much higher.

Several vaccines, such as the Pfizer messenger ribonucleic acid (mRNA) vaccine and Sinovac inactivated vaccine, have received approval from global regulatory bodies. Previous studies have shown that complete vaccination against COVID-19 can induce substantial immunity against SARS-CoV-2 in most individuals.

Certain SARS-CoV-2 variants, such as Delta, are associated with reduced efficacy against available vaccines. Nevertheless, most COVID-19 vaccines are still effective in protecting immunized people against mortality, hospitalization, and severe infection.

Notably, the majority of Xian residents were vaccinated with two or three doses of COVID-19 vaccines during the aforementioned epidemic period. Only a few unvaccinated people were present in this region.

A recentFrontiers in Immunologystudy aimed to determine the real-world effectiveness of COVID-19 vaccines against SARS-CoV-2 infection based on the Xian population.

The current retrospective study included 231 COVID-19 patients who were hospitalized in Xian Chest Hospital between December 8, 2021, and January 20, 2022. The median age of the cohort was 37 years.

All participants were classified as mild, moderate, and severely infected and were also grouped based on vaccination doses. All relevant laboratory data, including coagulative function tests, lymphocyte subtypes, antigen-specific immunoglobulin G (IgG) and IgM levels, as well as demographic information, were obtained.

Many of the participants reported comorbidities such as hypertension, cardiovascular disease, diabetes, cerebrovascular disease, chronic liver disease, and chronic obstructive pulmonary disease.

The study participants received different types of vaccines, including those produced by China National Biotec Group Company Limited (CNBG) and Sinovac Biotech Ltd, as well as recombinant antigen protein vaccines manufactured by Anhui Zhifei Longcom Biopharmaceutical.

Over 9% of the study cohort was unvaccinated, whereas 68.4% received two vaccine doses and 22.5% received three vaccine doses. Two and three vaccine doses significantly elevated IgG levels in the serum of COVID-19 patients. As compared to the unvaccinated group, the two- and three-dose vaccinated groups exhibited higher IgG levels against SARS-CoV-2.

Importantly, vaccination significantly reduced activated partial thromboplastin time (APTT) and thrombin time (TT). However, no change in the prothrombin time (PT) value was found.

Thromboembolism has been previously determined as a key factor that influences poor prognosis and death related to SARS-CoV-2 infection. In the current study cohort, vaccination effectively prevented the incidence of abnormal coagulation and protected against embolic complications.

The study findings are in line with previous reports indicating that eosinophil levels were significantly higher in vaccinated patients as compared to unvaccinated individuals. Comparatively, monocyte levels were low, which could be due to the protective effect of the vaccine on cytokine storms that are frequently observed in severely infected patients.

Typically, a decline in lymphocytes, particularly CD8+ T-cells, could be a predictor of COVID-19 severity and clinical worsening. Interestingly, vaccinated COVID-19 patients had significantly increased levels of CD8+ lymphocytes as compared to unvaccinated patients. No significant difference in CD8+ lymphocyte levels was observed in individuals who received two or three doses of the vaccine.

The incidence of hyponatremia was mostly prevented in the vaccinated group due to higher plasma sodium levels as compared to the unvaccinated group.

A key limitation of the current study was the small size cohort that was obtained from a single center. The time of the last dose of vaccination was not available for all participants, thus limiting the researchers ability to determine the association between vaccination-infection interval and disease severity.

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Chinese study determines the real-world effectiveness of COVID-19 vaccines - News-Medical.Net

Uncommon Side Effects of COVID-19 Vaccination in the Pediatric Population – Cureus

October 15, 2022

The Corona Virus Disease 2019 (COVID-19) pandemic has resulted in widespread health, social, and economic impacts [1]. It also led to the rapid development and emergency use authorizations of the vaccine against coronavirus (SARS-CoV-2)[2]. The vaccines underwent an expedited review process and were released for general use to control the pandemic. The evaluation of the side effect profiles followed proper procedures, but the sample groups, especially in children, were not as extensive as prior vaccines, possibly due to the newer form of vaccines and urgency at the time [3]. There have been isolated studies about vaccines and certain adverse outcomes [4]. Similar analyses were performed for the adult population [5]. Still, a detailed evaluation of population-level reporting in the pediatric age group is lacking. We aim to review the reported side effects for the pediatric age group to inform the clinicians and the general population about possible side effects and provide detailed information for objective decision-making.

With the vaccine deployment, the Centers for Disease Control and Prevention (CDC) also created a section for the COVID-19 vaccines in the Vaccine Adverse Event Reporting System (VAERS) [6]. Patients/parents/guardians, and/or healthcare providers reported suspected side effects to the VARES. The VAERS data is openly available for researchers. The decision was made to limit the search scope to the Delaware state and the year 2021 due to resource limitations. Due to the dataset format, the age group was limited to 6-17 years.

We queried the VAERS system with the terms listed below in Table 1.

We performed a literature search in the PubMed index and Google scholar for each side effect under consideration for this article. The Search terms used were COVID-19 OR SARS-CoV-2 OR COVID AND vaccines or vaccination AND adverse Effects OR side Effects AND myocarditis, stroke, seizure, menstrual disorder, chest pain, allergic reaction,appendicitis, behavioral, Multisystem inflammatory syndrome in children(MIS-C), AND hematuria.

We included the following article types: Case reports, case series, cohort studies, and clinical trials. We also reviewed the Food drug administration (FDA), and Centers for Disease Control (CDC) website information. The Institutional Review Board of Inspira Health reviewed and approved the study protocol, File #2022-05-003.

The final cohort included 111 patients. Life-threatening events such as stroke and seizures were rare, and none of the reports included death. Further details of the individual report's exact age or racial profile were unavailable in the dataset. Although no direct comparison was made with the number of vaccinations, as per the State of Delaware records, a total of 62013 doses had been administered by 12/31/2021 to the age group of 5-17 years [7]. Acknowledging the dataset limitations and the age group discrepancy, the adverse events reported had an approximate incidence of 0.18% or less than two per 1000 vaccine recipients.

Among the reported events, the majority were concerning the vaccine delivery/administration, including the wrong brand of vaccine or the wrong dose of vaccine administered (n=48). Excluding dosing or administration issues, details of the 63 reports were reviewed (Table 2). The key part to note is that given that some cases had reported multiple complaints, the total side effects reported below will be more than the 63 total reports.

Some of the selected side effects, based on importance or uncommon but serious nature, are discussed in detail below, with a literature review regarding the topic providing further commentary. We created a citation [8] to refer to the resulting dataset for ease of expression.

As per the report received from a healthcare professional, after an unspecified vaccination duration, one patient reported COVID-like symptoms, fever, vomiting, rash, and diarrhea [8]. After a few days, the patient developed respiratory, gastrointestinal, dermatologic, and neurologic symptoms, requiring hospitalization, and was diagnosed with MIS-C.

According to Levy et al. study, a single COVID-19 vaccine injection to MIS-C onset interval was 25 days [9]. However, in Levy et al. study, there are no MIS-C cases in fully vaccinated children. After SARS-CoV-2 infection, a mean 28-day delay was noticed to MIS-C onset [10]. The incidence of MIS-C was one per million in individuals who received one or more doses of the COVID-19 vaccine compared to 200 per million cases of MIS-C in unvaccinated individuals [11].

Appendicitis

A patient received the BNT162b2 vaccine a few days before presenting with an upset stomach and vomiting [8]. The patient was diagnosed with appendicitis and underwent an appendectomy.

Cases of appendicitis have been reported post-COVID-19 vaccination [12,13]. One possible mechanism of appendicitis is the inflammatory enlargement of lymph nodes in the abdomen following the COVID-19 vaccination [14]. Out of 43,448 participants, eight in the vaccine group suffered from appendicitis following COVID-19 vaccination, and four in the placebo group suffered appendicitis [13]. However, these cases of appendicitis showed no direct association with vaccination, as the frequency of appendicitis post-COVID-19 vaccination was not higher than expected within the general population [13].

Hematuria

An adolescent male reported hematuria two times after his BNT162b2 vaccine. During these episodes, he also had mild stingy sensations with urination [8].

A study reported 27 cases of gross hematuria after the COVID-19 vaccine [15]. Seventy percent of those had a prior diagnosis of immunoglobulin A nephropathy. This study suggested no real progression of hematuria to severe kidney dysfunction.

Stroke

One patient was reported to have had a stroke 28 days after the BNT162b2 vaccination [8]. The patient presented with right-sided weakness and paresthesias, acute embolic stroke, and pulmonary embolism. The patient was later found to have a patent foramen ovale. The additional contributing factor was considered to be the use of oral contraceptives.

The COVID-19 infection is associated with hypercoagulability due to the pro-inflammatory impact and effect on the coagulation cascade [16]. Stroke has been reported with the COVID-19 vaccination as well. Kolahchi et al. summarized eight cases of patients having stroke outcomes with the administration of mRNA vaccination, with the youngest being 36 years of age [17]. The possible pathophysiology for stroke was a combination of atherosclerotic disease and pro-inflammatory status [18].

Seizures

Four cases of seizures were reported [8], although the reports do not clarify any prior history of seizures, limiting the causal association.

Case 1: The patient received the vaccine, and the next day, the patient had a headache and a temperature of 100.0 F. The patient then had one episode of a seizure lasting 30 seconds, described as the face getting pale, jaw stuck open, and clicking noises, with eyes open and staring up. The patient urinated on herself. After the seizure episode, the patient returned to a normal state.

Case 2: The patient had a seizure two weeks after receiving the vaccine. The patient initially experienced minor undefined seizure episodes, eventually worsening to a full tonic-clonic state. The patient required hospitalization and received anti-seizure medications.

Case 3: The patient had vomiting and focal seizures seven days after receiving the vaccine. No further data was available in the report.

Case 4: The patient started having involuntary movements of arms and legs along with eyes rolling behind his head, with episodes lasting 5 to 10 seconds. The time since vaccination was not specified. The patient initially had only a few episodes, and later, the frequency increased to about 35 seizures-like activities daily. The patient had unremarkable MRI and EEG and was treated with Trileptal.

COVID-19 vaccination has been associated with common neurological symptoms such as dizziness, myalgia, paresthesia, and headaches [19]. These were mostly acute and transient. The incidence rate of COVID-19 vaccine-related seizures was reported to be 3.19 seizures per 100,000 persons per year, and the COVID-19 vaccine increased the risk of new-onset seizures by >30-fold when compared to the influenza vaccine [20]. Most seizures typically occur within two days of vaccination, including influenza and COVID-19. Therefore, caution for those with prior history of seizures is advised.

Menstrual Disorders

A total of five reports were noted for patients with alterations in their menstrual periods [8].

Case 1: The patient received her first BNT162b2 vaccine one month after her menarche and her second dose three weeks later. The patient reported her third menses onset was one day before her second BNT162b2 vaccine. She noticed dysfunctional uterine bleeding, dyspnea on exertion, lightheadedness, and pallor. The patient was hospitalized for symptomatic anemia, requiring a blood transfusion.

Case 2: The patient reported not having a menstrual cycle for two months since getting the COVID-19 vaccine. The patient states that she was due before her initial vaccine dose; however, her menstrual period did not arrive. The pregnancy test was negative. The patient tolerated the BNT162b2 vaccine without any other issues. Other reported cases were similar in presentation to those above.

The Edelman et al. study included 3,959 individuals and reported that compared to the unvaccinated population, the menstrual cycle length was noted to have changed by less than one day in women who received both doses of the COVID-19 vaccine [21]. These changes in the menstrual cycle were noted to be transient. The changes in cycle length did not persist over time [22]. Historically, about 75% of adolescents were affected by menstruation disorders years before COVID-19 and its vaccines [23]. Therefore, reports about COVID-19 vaccination and menstruation disorders should be considered cautiously.

Chest Pain

A total of 11 cases reported chest pain [8].

Case 1: The patient complained of stabbing left-sided chest pain two hours after receiving the first BNT162b2 vaccine and had pain and swelling at the injection site. She denied any history of sarcoidosis, lupus, TB exposure, or other autoimmune diseases. The chest pain and fatigue persisted the following week. The echocardiogram, and blood tests, including troponin, were within normal range, except for elevated Creatinine Kinase (CK) levels at 831 U/L. Repeat testing a few days later noted CK levels had normalized to 76 U/L, and the chest X-ray noted mild right middle lobe atelectasis possibly related to possible viral illness and/or underlying inflammatory process. This further clarifies that this patient likely had the symptoms secondary to viral illness and less likely due to the vaccine. Over the next few days, the patient reported improving her chest pain and denied fatigue, palpitations, dizziness, or myalgia.

Case 2: Three weeks after receiving the second BNT162b2 vaccine, the patient developed chest pain and shortness of breath during sports practice, resolving with rest without recurrence. The patient was evaluated in ER and discharged without needing further intervention.

Case 3: The patient with a history of asthma and food allergies reported wheezing and chest pain one hour after receiving the BNT162b2 vaccine. Symptoms resolved without significant intervention.

Similarly, in Case 4, a patient had reported chest pain following the second dose of the COVID-19 vaccine, which resolved by itself. The other cases were with symptoms similar to those above, with workups negative for myocarditis and normal troponin and BNP levels.

Multiple patients have reported chest pains after the COVID-19 vaccinations, with the majority being noncardiac [24]. Costochondritis is an inflammation of the costal cartilage, a benign cause of reproducible sternal chest pain [25]. This condition might resolve spontaneously or require a short treatment with nonsteroidal anti-inflammatory drugs such as ibuprofen. The Costochondritis symptoms due to COVID-19 infection are more severe than COVID-19 vaccine-related costochondritis [25,26].

Myocarditis

Myocarditis was reported in three cases [8]. Cases 1 and 2 initially presented with chest pain, palpitations, and elevated troponins three days after receiving the second BNT162b2 vaccine. Electrocardiogram (EKG) and echocardiogram were normal in both cases.

Case 3: Chest pain, elevated troponin, shortness of breath, and fatigue was noted 17 days after receiving the first BNT162b2 vaccine. All three instances resolved symptoms with oral nonsteroidal anti-inflammatory drugs (NSAIDs).

Immune response against infection or some other trigger that results in inflammation of the heart muscles is known as myocarditis [27]. Patients with myocarditis usually complain of chest pain, shortness of breath, palpitations, and dyspnea on exertion and have lab evidence of myocardial injury. Myocarditis risk factors include young adults, male gender, diabetes, HIV infection, end-stage kidney disease, and chest injury. The COVID-19 vaccine correlates with myocarditis in pediatric and adult populations [28]. Myocarditis and pericarditis are also seen with other vaccines like smallpox [29] and influenza [30,31].

Cases of myocarditis after receiving the COVID-19 vaccine typically occur within one week of vaccination. Most patients' symptoms resolve themselves with rest and pain medications like NSAIDs [25]. These patients should also follow up with a cardiologist before returning to exercise or sports activities [32].

Allergic Reactions

The key cases with reports of allergic reactions are summarized below [8]. Case 1 was an 11-year-old patient with reported acute onset of swelling of hands and feet, redness, and severe itching associated with itchy red skin on the body. Cases 2 and 3 reported sudden onset of itchy hives all over the body after a few days from vaccination. Case 4 reported a local reaction, with raised erythematous itchy, and painful swelling at the injection site and down on the arm for four days. Case 5 reported acute onset of eyelid redness and swelling, congestion, with red spots on the chest and back. Case 6 reported acute onset of difficulty breathing, throat tightness, and tingling in lips, ears, and throat 10 minutes after vaccination. No breathing compromise was noted. Case 7 reported shakes, redness, throat tightness, and itching. Prior history of allergic reactions to vaccines was not reported in any of the cases. All these cases reported improvement in symptoms with antihistamine administration.

Several studies have reported various cutaneous reactions after BNT162b2 and mRNA-1273 (Moderna) vaccines [33,34]. One possible mechanism of post-COVID-19 vaccine-induced skin lesions is an allergic reaction to vaccine components, with mast cell degranulation causing severe rash, angioedema, and anaphylaxis [35]. Similarly, influenza vaccinations in 2009 were noted to have reports of 10.7 hypersensitivity reactions per million vaccine doses distributed [36]. Those with prior history of allergic reactions were noted to have a higher risk of allergies to mRNA vaccines [37].

Behavioral Issues

A 15-year-old female with a history of pediatric acute-onset neuropsychiatric syndrome (PANS), mast cell activation syndrome, postural orthostatic tachycardia syndrome, obsessive-compulsive disorder (OCD), withholding food, and head-banging behaviors after a few hours of receiving the second COVID-19 vaccine, experienced PANS and OCD symptoms and worsening of behavioral symptoms [8]. She was treated with NSAIDs and an antihistamine (Cetirizine), with the resolution of symptoms a few hours later.

The development of psychological issues has been reported after vaccination, with the influenza vaccine [38] and the yellow fever vaccine [39], including depression, anxiety, and psychosis. The pathophysiology of vaccination-induced psychological/behavioral issues is not entirely understood. However, vaccinations like COVID-19, influenza, etc., stimulate pro-inflammatory cytokines, which have been associated with neuropsychiatric symptoms [40,41].

Fluctuation of Blood Sugar Levels

A 16-year-old diabetes type-1 patient reported a fluctuation in blood glucose level the next day after the vaccine [8]. This was addressed with the sick day insulin plan to control her sugar level.

The COVID-19 vaccine stimulates the immune system to a milder degree than the COVID-19 infection itself, causing stress and affecting hormone levels such as adrenaline, growth hormone, and cortisol, leading to hyperglycemia [42]. Type-1 and Type-2 diabetes patients cannot rapidly counteract high glucose levels, leading to higher fluctuations than patients who do not have diabetes [43]. Immune response-mediated cytokine release can affect blood glucose levels, leading to insulin resistance within tissues [44]. Blood sugar fluctuations after COVID-19 vaccines were noted to be transient, lacking any significant glycemic control impact, with the return to baseline a few days after vaccination [45,46].

Otological Symptoms

One patient reported ringing in the ears, lightheadedness, nausea, and spotty vision for a few minutes after the vaccine administration. The patient had a history of similar symptoms after influenza vaccination. Another patient reported muffled hearing, lightheadedness, and nausea, which resolved in a few minutes [8].

In the Wichova et al. study, 30 patients had new or exacerbated otological symptoms after COVID-19 vaccination. Twelve patients in that study received the Pfizer vaccine, and 18 received the Moderna vaccine. Of 30 patients, 83% reported hearing loss, 50% reported tinnitus, 26% reported dizziness, and 16% reported vertigo [47]. As per the systematic review, the pulled estimate of prevalence was 7.6% for hearing loss, 14.8% for tinnitus, and 7.2% for vertigo based on retrospective recall of symptoms [48].

Abnormal Liver Function Test Results

One patient reported an elevated bilirubin level of 2.04 after the first dose of the Pfizer vaccine [8]. Liver enzymes were not elevated. The patient had reported nausea and reduced appetite for a week after vaccination.

Autoimmune hepatitis after vaccination is rare, and most cases improve after steroid treatment [49,50]. It is possible that, in predisposed patients, COVID vaccines may unmask autoimmune diseases [51]. Antibodies against the spike protein were noted to have affinity against transglutaminase 3, transglutaminase 2, anti-extractable nuclear antigen, nuclear antigen, and myelin basic protein [52].

Multiple COVID-19 vaccine-related side effects are reported in the pediatric population in our reports and similarly in the available literature. Those of most common or clinical relevance, such as rare side effects like myocarditis, costochondritis, hematuria, menstrual disorder, stroke, etc., are summarized above, including the discussion about those in contrast to the reviewed literature.

Per the CDC, VAERS received 9,246 adverse event reports in the age group of 12 to 17 yearsby 06/16/2021 for Pfizer-BioNTech vaccination [53]. Of these, 90.7% of accounts were nonserious, while 9.3% were serious adverse events, including myocarditis (4.3%). Per this Hause et al. report, adolescents reported local (63.4%) and systemic (48.9%) reactions. During the 3/11/21 to 12/19/21 period, for children aged 5-11 years, VAERS received 4,249 reports of adverse events in this age group, 97.6%of which were not serious [54]. The majority of these were local (57.5%). The systemic reactions, including fatigue and headache, were reported in 40.9%.

We postulate the low prevalence reported in our dataset (approximately <0.2%) to be likely secondary to underreporting minor adverse effects, especially after the initial few months of vaccinations, and some side effects became commonly accepted.

We have no intention of repudiating the overwhelming public health benefits of the COVID-19 vaccines. Vaccines play a major role in controlling the spread and impact of infectious diseases. Considering COVID-19 infection and its complications, vaccination in the pediatric population and pregnant women is needed to minimize the ongoing spread and evolution of the COVID-19 pandemic in the pediatric population [55].

Severe allergic reactions are contraindications for the future administration of the said vaccine [56]. Similarly, careful consideration is also required after the occurrence of significant side effects.Hesitancy against vaccines is common in public and among healthcare workers, with post-vaccination side effects being the key barrier [57]. Open discussion about the possible side effects and reinforcing the individual, family, and community benefits are key to promoting acceptance [58]. Addressing the unique barriers to vaccine acceptance based on community dynamics, sociocultural factors, and vaccine criticism while providing well-informed messaging is vital [59, 60]. For example, appropriately framing the side effect with comparative risk labeling describing the risks associated with COVID-19 or other viral infections can improve vaccine acceptance [61].

There is increasing consensus against mandatory vaccination of healthy children for ethical reasons [62]. Our study also supports this because even though very rare, as discussed above, the COVID-19 vaccine has been correlated with serious side effects and hospitalizations in otherwise healthy children. Especially now that the COVID-19 virus is moving from the pandemic to an endemic disease. We recommend thoroughly pre-screening children before the next vaccination or booster dose and allowing the guidelines to be individualized.

We acknowledge the following limitations. a) This review summarises the reported adverse events. Given the narrative nature of the data, it should not be considered a causal association. It carries the inherent limitations of voluntarily reported data without validation. b). Reporting bias and lack of uniformity in the provided information. c). Lack of clinical correlation or individual clinical data. d). Available data is focused on acute or short-term adverse events, and long-term side effects cannot be assessed. Most reports have been in the adult population, and direct comparison is not recommended. e). An analysis of a larger population or a prospective study is needed to understand the side effects better.

Despite the limitations above, it is crucial to overview the already reported adverse events to make informed decisions and take preventive measures for those at-risk, such as the history of allergic reactions, diabetes, neurological, or cardiac conditions. There is a need for further focused studies and long-term assessment of the vaccine-related outcomes to provide further evidence to draw any definitive relationship. Patients with similar reported side effects in the past with other medications or identical health conditions need to be advised of additional caution when considering COVID-19 vaccinations.

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Uncommon Side Effects of COVID-19 Vaccination in the Pediatric Population - Cureus

FACT CHECK: Did Pfizer lie about testing COVID-19 vaccine’s ability to prevent transmission before roll out? – WCPO 9 Cincinnati

October 15, 2022

CLAIM: Pfizer admitted to the European Parliament that it had not tested the ability of its COVID-19 vaccine to prevent transmission of the virus before it entered the market, proving the company lied about this earlier in the pandemic.

APS ASSESSMENT: Missing context. Janine Small, president of international markets at Pfizer, told the European Parliament on Monday that Pfizer did not know whether its COVID-19 vaccine prevented transmission of the virus before it entered the market in December 2020. But Pfizer never claimed to have studied the issue before the vaccines market release.

THE FACTS: After Small testified before the European Parliaments Special Committee on the COVID-19 Pandemic, misleading claims about whether Pfizer knew the impact of its COVID-19 vaccine on preventing transmission spread widely on social media.

Rob Roos, a Dutch European Parliament member who asked Small a question about transmission at the hearing, tweeted: BREAKING: In COVID hearing, #Pfizer director admits: #vaccine was never tested on preventing transmission. Get vaccinated for others was always a lie. The only purpose of the #COVID passport: forcing people to get vaccinated. The world needs to know. Share this video!

The tweet, which included a video showing the exchange between Roos and Small, had received more than 232,000 likes and more than 166,000 shares by Thursday.

Other social media posts about the hearing used the hashtag #PfizerLiedPeopleDied.

At the hearing (which you can watch by clicking here), Roos asked Small whether Pfizer had tested its COVID-19 vaccine for its ability to prevent transmission of the virus prior to its market release. Small answered: No. We had to really move at the speed of science to really understand what is taking place in the market. She went on to explain why Pfizer moved quickly to develop a COVID-19 vaccine as the virus spread worldwide.

While Roos and many others framed this as a new revelation, Pfizer never claimed that its clinical trial, upon which the vaccine was authorized for use, evaluated the shots effect on transmission. In fact, shortly before the vaccines release, the companys CEO emphasized that this was still being evaluated.

A study funded by Pfizer and German vaccine maker BioNTech published in the New England Journal of Medicine on Dec. 10, 2020, a day before the Food and Drug Administration gave Pfizers COVID-19 vaccine emergency use authorization, did not include data about the vaccines effectiveness at reducing transmission of the virus.

Instead, it reported that two doses of the vaccine provided 95% protection against contracting symptomatic COVID-19 in people 16 and older. Pfizer CEO Albert Bourla also said in a December 2020 interview with NBC News that it was still unclear whether vaccinated individuals could carry the virus and transmit it to others.

I think this is something that needs to be examined, he told the network. We are not certain about that right now.

The FDA stated in a Dec. 11, 2020, press release announcing the authorization of Pfizers COVID-19 vaccine that at this time, data are not available to make a determination about how long the vaccine will provide protection, nor is there evidence that the vaccine prevents transmission of SARS-CoV-2 from person to person.

A Pfizer spokesperson told The Associated Press that its clinical trial was designed to evaluate the efficacy of its COVID-19 vaccine in preventing disease caused by the COVID-19 virus, including severe illness.

Stopping transmission was not a study endpoint, the spokesperson wrote in an email.

Asked for comment, Roos told the AP that he was not making a point about Pfizer, but about government mandates for the COVID-19 vaccines.

I take fundamental rights seriously, Roos wrote in an email. For governments to infringe on them, they need a massive amount of evidence to prove the necessity. In this case, it was not even a part of the Pfizer trials. He said that such mandates were based on no evidence.

But experts and research say that the COVID-19 vaccines have provided benefits in terms of limiting infections and transmission, at least with earlier variants of the virus and for a period of time after being vaccinated.

Dr. Walter Orenstein, associate director of the vaccine center at Emory University, told the AP that the fact that Pfizer did not address the vaccines impact on transmission during clinical trials is not unusual, because transmission is a complex metric to measure.

Its much more difficult to evaluate impact on transmission, Orenstein, a professor of infectious diseases at the Emory School of Medicine, wrote in an email. What is usually done is a randomized placebo controlled study, in which the recipients are blinded (i.e., do not know whether they received placebo or vaccine.

Public officials have suggested on multiple occasions that COVID-19 vaccines prevent transmission, but thats an overstatement. For example, in an October 2021 speech in Illinois, President Joe Biden said: Were making sure healthcare workers are vaccinated, because if you seek care at a healthcare facility, you should have the certainty thatthe people providing that care are protected from COVID and cannot spread it to you.

While the vaccines do not eliminate all transmission, they can help. Studies done after distribution of the COVID-19 vaccines began, including research by Pfizer, did find that the companys shot reduced asymptomatic infections in addition to symptomatic cases with earlier variants of the virus. Researchers in the United Kingdom reported in a February observational study that Pfizers vaccine helped cut transmission of the alpha and delta variants.

Our study from earlier in the year shows that the Pfizer vaccine reduces transmission from people with breakthrough infections, at least in the 3 months post vaccine which we studied, Dr. David Eyre, a professor of infectious diseases at the University of Oxford and lead author of the study, wrote in an email.

Experts have told the AP that while the original COVID-19 vaccines provide less protection against infection with the highly contagious omicron variant, they still protect against serious outcomes.

The CDC stated in an August report that receiving only the first one or two doses of a COVID-19 vaccine provides minimal protection against infection and transmission and that being up to date on all recommended booster doses provides a transient period of increased protection against infection and transmission after the most recent dose, although protection can wane over time.

Dr. Paul Offit, a member of the FDAs Vaccines and Related Biological Products Advisory Committee, explained that while the vaccines do provide neutralizing antibodies, which help protect against infection, those kinds of antibodies quickly wane even as protection against serious illness continues to last.

It is fair to say that when you get a vaccine that clearly decreases your chance of getting infected, it does, said Offit, who is also the director of the Vaccine Education Center at the Childrens Hospital of Philadelphia. And therefore it decreases your chance of spreading it to others. But its not in any way absolute.

Offit added that messaging to the public around the vaccines early on was flawed and should have been focused on their core benefit preventing serious illness and hospitalization since many would later cast doubt on the vaccines success because of breakthrough infections.

___

This is part of APs effort to address widely shared misinformation, including work with outside companies and organizations to add factual context to misleading content that is circulating online. Learn more about fact-checking at AP.

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FACT CHECK: Did Pfizer lie about testing COVID-19 vaccine's ability to prevent transmission before roll out? - WCPO 9 Cincinnati

COVID-19 vaccination reduced the severity of the Omicron-driven pandemic wave in Saudi Arabia – News-Medical.Net

October 15, 2022

In a recent study published in the Journal of Infection and Public Health, researchers conducted a retrospective study of all coronavirus disease 2019 (COVID-19) cases from a single hospital in the Kingdom of Saudi Arabia (KSA) between December 25, 2021, and February 30, 2022.

They described the epidemiology and clinical characteristics of COVID-19 patients during the third pandemic wave when the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron variant was predominant.

The KSA had managed to control the spread of SARS-CoV-2 within the country to a large extent through widespread vaccination programs. With the emergence of Omicron, the daily reported cases in the KSA surged to 4000/day from less than 100/day in the preceding months.

Although compared to Delta, Omicron caused less severe infections, fewer hospitalizations, intensive care unit (ICU) admissions, and much-reduced mortality, there was an urgent need to evaluate its effects in the general population.

In the present study, researchers reviewed all COVID-19 cases from a single medical center in KSA and gathered data to study the characteristics of patients during the Omicron wave. This data encompassed their demographics, clinical symptoms, pre-existing medical conditions, COVID-19 vaccination status, date of last vaccination, and SARS-CoV-2 infection. Further, the researchers assessed whether or not these COVID-19 patients required hospital or ICU admission.

For statistical analyses, they first summarized data as numbers and percentages. They compared categorical data using a chi-square test, including admitted and non-admitted patients and gender-based data with other covariates.

A binary logistic regression analysis helped the researchers model multiple covariates with admission status and gender. Furthermore, they constructed a Boxplot of the cycle threshold (CT) values of SARS-CoV-2 reverse transcriptase-polymerase chain reaction (RT-PCR) with COVID-19 vaccine doses. Finally, the team used Kaplan-Meier curve analysis to determine the days from the last COVID-19 vaccine to the subsequent occurrence of SARS-CoV-2 infection.

The final study analysis covered 400 Omicron-infected patients, of which 55% were males, and the remaining were females. The most common pre-existing medical conditions were diabetes mellitus and hypertension, 10.5% and 7.5%. The most striking feature of the Omicron wave was the significantly lower hospitalization rate (only 14%) compared to prior pandemic waves. Only 3.5% and 2% of 400 Omicron-infected patients required ICU admission andmechanical ventilation, respectively.

Further, it was inversely related to the number of COVID-19 vaccine doses. In a binary logistic analysis, while hospital admission was significantly associated with headache and sore throat, fever and diabetes mellitus were inversely associated with hospital admission.

The most common symptoms observed in the study of patients infected with Omicron were sore throat, cough, fever, and headache, observed in 39.8%, 39.5%, 33%, and 30.5% of patients, respectively. The clinical presentation and comorbidities did not change with the patient's gender during the Omicron-driven pandemic wave. However, the occurrence of sore throat in a binary logistic regression showed a higher rate among males with an OR of 2.014.

Regardless of the vaccination status, more Omicron-infected than Delta-infected patients experienced sore throats (70.5% vs. 60.8%). Intriguingly, these patients also had odynophagia; however, anosmia, a pathognomonic symptom of previous SARS-CoV-2 variants, was markedly low in Omicron-infected patients.

Across male and female patients, the average time to SARS-CoV-2 infection from the last vaccination was 131.60 days. The average CT value was higher in the recipients of two or three vaccine doses than the recipient of one dose of the COVID-19 vaccine; however, this difference did not reach a statistical difference.

The observed differences during different COVID-19 pandemic waves likely reflected differences in the study population or the interaction between the factors and the vaccination.

The current study remarkably depicted the epidemiological and clinical characteristics of COVID-19 patients during the Omicron wave in KSA. They had a milder disease and required less hospitalization and less ICU admission. Since most patients had received COVID-19 vaccines, it showed the importance of COVID-19 vaccination in limiting disease severity and decreasing the need for hospitalization.

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COVID-19 vaccination reduced the severity of the Omicron-driven pandemic wave in Saudi Arabia - News-Medical.Net

Risk of thyroid dysfunction associated with mRNA and inactivated COVID-19 vaccines: a population-based study of 2.3 million vaccine recipients – BMC…

October 15, 2022

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