Global burden of vaccine-associated cutaneous immune-related adverse events, 1968–2024: An international pharmacovigilance study DOI
Jaehyeong Cho,

Hyesu Jo,

Damiano Pizzol

et al.

Life Cycle, Journal Year: 2024, Volume and Issue: 4

Published: Nov. 22, 2024

Language: Английский

Incidence and management of the main serious adverse events reported after COVID‐19 vaccination DOI Creative Commons
Teresa Padilla‐Flores, Alicia Sampieri, Luis Vaca

et al.

Pharmacology Research & Perspectives, Journal Year: 2024, Volume and Issue: 12(3)

Published: June 1, 2024

Coronavirus disease 2019 (COVID-19) caused by the severe acute respiratory syndrome coronavirus 2n first appeared in Wuhan, China 2019. Soon after, it was declared a pandemic World Health Organization. The health crisis imposed new virus and its rapid spread worldwide prompted fast development of vaccines. For time human history, two vaccines based on recombinant genetic material technology were approved for use. These mRNA applied massive immunization programs around world, followed other more traditional approaches. Even though all tested clinical trials prior to their general administration, serious adverse events, usually very low incidence, mostly identified after application millions doses. Establishing direct correlation (the cause-effect paradigm) between vaccination appearance effects has proven challenging. This review focuses main observed vaccination, including anaphylaxis, myocarditis, vaccine-induced thrombotic thrombocytopenia, Guillain-Barré syndrome, transverse myelitis reported context COVID-19 vaccination. We highlight symptoms, laboratory tests required an adequate diagnosis, briefly outline recommended treatments these effects. aim this work is increase awareness among healthcare personnel about events that may arise post-vaccination. Regardless ongoing discussion safety must be promptly treated effectively reduce risk complications.

Language: Английский

Citations

9

Events supposedly attributable to vaccination or immunization of COVID-19 vaccines in Brazil: a cross-sectional study DOI Creative Commons
Paloma Cristina Pimenta, Vitoria Gabriele Souza Geraldine, Túlio M. Lima

et al.

Deleted Journal, Journal Year: 2025, Volume and Issue: 22(1)

Published: Jan. 2, 2025

Abstract COVID-19 vaccines effectively reduce morbidity and mortality but are associated with Events Supposedly Attributable to Vaccination or Immunization (ESAVI). This cross-sectional study examined the incidence characteristics of ESAVI in Brazil during 2021, using data from e-SUS Notifica Vacivida. Among 109,424 reports, rates were 30.82 83.08 symptoms per 100,000 doses. Most reports involved women (70.83%), individuals aged 30–39, residents southern region. Common included headache, fever, myalgia. AstraZeneca accounted for 56.79% cases. Non-severe cases predominated (95.03%), 78.7% classified as “product-related according literature.” Mortality was rare (0.03%), a significant association identified between DNA deaths (χ 2 = 4.333; p 0.037; OR 2.673; 95% CI 1.020–7.007). Regional disparities evident, higher incidences South Southeast. Underreporting non-severe remains challenge. Logistic regression showed lower odds severe among adults Black/Brown individuals, while Pfizer initial doses linked odds. These results highlight safety emphasizing need strengthened post-vaccination surveillance address regional disparities, health inequities, vaccine hesitancy.

Language: Английский

Citations

0

A SARS-CoV-2 mucosal nanovaccine based on assembly of maltodextrin, STING agonist and polyethyleneimine DOI
Yu Tian, Liang Hu, Qingrui Huang

et al.

International Journal of Biological Macromolecules, Journal Year: 2025, Volume and Issue: unknown, P. 139395 - 139395

Published: Jan. 1, 2025

Language: Английский

Citations

0

Nanotechnology Assisted Strategies to Tackle COVID and Long-COVID DOI
Keshaw Ram Aadil,

Khushboo Bhange,

Gita D. Mishra

et al.

BioNanoScience, Journal Year: 2025, Volume and Issue: 15(2)

Published: Feb. 4, 2025

Language: Английский

Citations

0

COVID-19 Modified mRNA “Vaccines”: Lessons Learned from Clinical Trials, Mass Vaccination, and the Bio-Pharmaceutical Complex, Part 2 DOI Creative Commons
M. Nathaniel Mead, Stephanie Seneff, Jessica Rose

et al.

International Journal of Vaccine Theory Practice and Research, Journal Year: 2024, Volume and Issue: 3(2), P. 1275 - 1344

Published: Aug. 16, 2024

The COVID-19 modified mRNA (modmRNA) lipid nanoparticle-based “vaccines” are not classical antigen-based vaccines but instead prodrugs informed by gene therapy technology. Of considerable note, these products have been linked to atypical adverse and serious event profiles. As discussed in Part 1, health-related risks drawbacks were drastically misreported underreported the Pfizer Moderna trial evaluations of genetic products. Now 2, we examine main structural functional aspects injectables. modmRNA injectable introduce a unique set biological challenges human body with potential induce an extensive range adverse, crippling, life-threatening effects. Based on fact that there is no current method quantify host (cell-based) spike protein production vivo following injection prodrugs, standard “dose”. This part due differences output, which depends cell metabolism transfection efficiency. It therefore difficult predict profiles individual basis, considering millions adults across world reported severe events context products, valid concerns raised regarding infants younger age groups for whom poses only minimal risks. We address process-related impurities inherent mass posed contaminants. then categorize principal associated brief systems-based synopsis each six domains harms: (1) cardiovascular, (2) neurological, (3) hematologic; (4) immunological, (5) oncological, (6) reproductive. conclude discussion primary public health regulatory issues arising from this evidence-informed synthesis literature reiterate urgency imposing global moratorium modmRNA-LNP-based platform.

Language: Английский

Citations

2

Safety of COVID-19 Vaccines among People with History of Allergy: A European Active Surveillance Study DOI Creative Commons
Nicoletta Luxi, Francesco Ciccimarra, Chiara Bellitto

et al.

Vaccines, Journal Year: 2024, Volume and Issue: 12(9), P. 1059 - 1059

Published: Sept. 17, 2024

Conventional vaccines rarely cause severe allergic reactions. However, the rapid development and approval of COVID-19 left limited initial data on their adverse reactions, particularly in individuals with a history allergy. The aim this study was to assess compare safety profile different doses brands subjects allergy vs. those without

Language: Английский

Citations

1

An improvement of the safety profile of SARS‐CoV‐2 vaccines is desirable DOI Creative Commons
Josef Finsterer

Pharmacology Research & Perspectives, Journal Year: 2024, Volume and Issue: 12(5)

Published: Sept. 12, 2024

Language: Английский

Citations

0

Characteristics of Oral Adverse Effects following COVID-19 Vaccination and Similarities with Oral Symptoms in COVID-19 Patients: Taste and Saliva Secretory Disorders DOI Creative Commons
Hironori Tsuchiya, Maki Mizogami

Medical Principles and Practice, Journal Year: 2024, Volume and Issue: unknown, P. 1 - 33

Published: Dec. 19, 2024

Although COVID-19 vaccines exhibit diverse side effects, taste and saliva secretory disorders have remained poorly understood despite their negative impact on the overall quality of life. The present study aimed to characterize oral adverse effects following vaccination assess similarities with symptoms in patients. A literature search was conducted databases, including PubMed, LitCovid, Google Scholar, retrieve relevant studies. narrative review indicated that a certain number vaccinated people develop ageusia, dysgeusia, hypogeusia, xerostomia, dry mouth, while they are rare compared symptoms. prevalence varies by country/region such geographical differences may be related type vaccine used. Similar SARS-CoV-2 infection, adversely affects perception salivary secretion females older subjects more frequently than males younger subjects. Their impairments mostly appear withing three days after vaccination, bitter is specifically impaired some cases. Considering share characteristics patients, it speculated spike protein derived from infection pathophysiologically responsible for disorders. This because has potential interact ACE2 expressed cells, produce proinflammatory cytokines, form antiphospholipid antibodies. Our results do not deny advantage but attention should paid post-vaccination addition

Language: Английский

Citations

0

Global burden of vaccine-associated cutaneous immune-related adverse events, 1968–2024: An international pharmacovigilance study DOI
Jaehyeong Cho,

Hyesu Jo,

Damiano Pizzol

et al.

Life Cycle, Journal Year: 2024, Volume and Issue: 4

Published: Nov. 22, 2024

Language: Английский

Citations

0