Global COVID-19 Vaccine Summary: Side Effects
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Microsoft Outlook
Morris, Max From: Morris, Max Sent: Monday, March 22, 2021 11:38 PM To: Morris, Max Subject: 03/22/2021 Coronavirus Daily Recap This email is provided for informational, non-commercial purposes only. Use or reliance on the information contained in this email is at your sole risk. This email is not provided by or affiliated in any way with Ally Financial Inc. These updates are being shared to multiple organizations, individuals and lists who/which are bcc’d. Best effort we are sending Daily updates during the business week, typically in the evening, a Weekend Recap on Monday mornings, and any significant breaking news events provided anytime. Please note some numbers included in the Statistics and news stories come from various sources and so can vary as they are constantly changing and not reported at the same time. All communications are TLP GREEN and can be shared freely. Know someone who might want to be added to our Updates? Of course ask them first, and then have them send us an email to [email protected]. Live the message, share the message: Be safe – Stay home and limit travel as much as possible, self-quarantine if you or any members of your family are or may be sick, if you go out wear your mask – the right way, ensure safe social distancing, and practice good hygiene – wash your hands, avoid touching your face, and sanitize used items and surfaces. Need to find a vaccine? Here are a few good sites and resources we have come across that may help: CDC Vaccine Finder – https://vaccinefinder.org/ [Free government website where users can search for pharmacies and providers that offer vaccinations, currently limited number of states but expanding] Dr. -
COVID-19 Vaccines: Update on Allergic Reactions, Contraindications, and Precautions
Centers for Disease Control and Prevention Center for Preparedness and Response COVID-19 Vaccines: Update on Allergic Reactions, Contraindications, and Precautions Clinician Outreach and Communication Activity (COCA) Webinar Wednesday, December 30, 2020 Continuing Education Continuing education will not be offered for this COCA Call. To Ask a Question ▪ All participants joining us today are in listen-only mode. ▪ Using the Webinar System – Click the “Q&A” button. – Type your question in the “Q&A” box. – Submit your question. ▪ The video recording of this COCA Call will be posted at https://emergency.cdc.gov/coca/calls/2020/callinfo_123020.asp and available to view on-demand a few hours after the call ends. ▪ If you are a patient, please refer your questions to your healthcare provider. ▪ For media questions, please contact CDC Media Relations at 404-639-3286, or send an email to [email protected]. Centers for Disease Control and Prevention Center for Preparedness and Response Today’s First Presenter Tom Shimabukuro, MD, MPH, MBA CAPT, U.S. Public Health Service Vaccine Safety Team Lead COVID-19 Response Centers for Disease Control and Prevention Centers for Disease Control and Prevention Center for Preparedness and Response Today’s Second Presenter Sarah Mbaeyi, MD, MPH CDR, U.S. Public Health Service Clinical Guidelines Team COVID-19 Response Centers for Disease Control and Prevention National Center for Immunization & Respiratory Diseases Anaphylaxis following mRNA COVID-19 vaccination Tom Shimabukuro, MD, MPH, MBA CDC COVID-19 Vaccine -
COVID-19 Vaccination Programme: Information for Healthcare Practitioners
COVID-19 vaccination programme Information for healthcare practitioners Republished 6 August 2021 Version 3.10 1 COVID-19 vaccination programme: Information for healthcare practitioners Document information This document was originally published provisionally, ahead of authorisation of any COVID-19 vaccine in the UK, to provide information to those involved in the COVID-19 national vaccination programme before it began in December 2020. Following authorisation for temporary supply by the UK Department of Health and Social Care and the Medicines and Healthcare products Regulatory Agency being given to the COVID-19 Vaccine Pfizer BioNTech on 2 December 2020, the COVID-19 Vaccine AstraZeneca on 30 December 2020 and the COVID-19 Vaccine Moderna on 8 January 2021, this document has been updated to provide specific information about the storage and preparation of these vaccines. Information about any other COVID-19 vaccines which are given regulatory approval will be added when this occurs. The information in this document was correct at time of publication. As COVID-19 is an evolving disease, much is still being learned about both the disease and the vaccines which have been developed to prevent it. For this reason, some information may change. Updates will be made to this document as new information becomes available. Please use the online version to ensure you are accessing the latest version. 2 COVID-19 vaccination programme: Information for healthcare practitioners Document revision information Version Details Date number 1.0 Document created 27 November 2020 2.0 Vaccine specific information about the COVID-19 mRNA 4 Vaccine BNT162b2 (Pfizer BioNTech) added December 2020 2.1 1. -
Considerations for Causality Assessment of Neurological And
Occasional essay J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp-2021-326924 on 6 August 2021. Downloaded from Considerations for causality assessment of neurological and neuropsychiatric complications of SARS- CoV-2 vaccines: from cerebral venous sinus thrombosis to functional neurological disorder Matt Butler ,1 Arina Tamborska,2,3 Greta K Wood,2,3 Mark Ellul,4 Rhys H Thomas,5,6 Ian Galea ,7 Sarah Pett,8 Bhagteshwar Singh,3 Tom Solomon,4 Thomas Arthur Pollak,9 Benedict D Michael,2,3 Timothy R Nicholson10 For numbered affiliations see INTRODUCTION More severe potential adverse effects in the open- end of article. The scientific community rapidly responded to label phase of vaccine roll- outs are being collected the COVID-19 pandemic by developing novel through national surveillance systems. In the USA, Correspondence to SARS- CoV-2 vaccines (table 1). As of early June Dr Timothy R Nicholson, King’s roughly 372 adverse events have been reported per College London, London WC2R 2021, an estimated 2 billion doses have been million doses, which is a lower rate than expected 1 2LS, UK; timothy. nicholson@ administered worldwide. Neurological adverse based on the clinical trials.6 kcl. ac. uk events following immunisation (AEFI), such as In the UK, adverse events are reported via the cerebral venous sinus thrombosis and demyelin- MB and AT are joint first Coronavirus Yellow Card reporting website. As of ating episodes, have been reported. In some coun- authors. early June 2021, approximately 250 000 Yellow tries, these have led to the temporary halting of BDM and TRN are joint senior Cards have been submitted, equating to around authors. -
National Emergency Management Organisation (Nemo) Ministry of National Security St
NATIONAL EMERGENCY MANAGEMENT ORGANISATION (NEMO) MINISTRY OF NATIONAL SECURITY ST. VINCENT AND THE GRENADINES WEST INDIES Tel: 784-456-2975, Fax: 784-457-1691, Email: [email protected] or [email protected] ______________________________________________________________________________ ___________________________________________________________________________________________________________________ HEALTH SERVICES SUBCOMMITTEE PROTOCOL FOR THE ENTRY OF FULLY VACCINATED TRAVELLERS TO ST. VINCENT AND THE GRENADINES – revised 10/08/2021 AIM: The safe entry of travellers to St. Vincent and the Grenadines in a manner that reduces the risk of the importation and subsequent transmission of COVID-19 in St. Vincent and the Grenadines. OBJECTIVES: 1. To establish the risk of the arriving traveller introducing new COVID-19 cases to SVG; 2. To minimize exposure of residents of SVG to new COVID-19 cases; 3. Early identification of potential exposure to COVID-19 and 4. Early containment of new COVID-19 cases. ESTABLISH RISK OF ARRIVING TRAVELLER: The arriving traveller will: 1. Complete the Pre-Arrival Form available at health.gov.vc And the Port Health Officer will: 1. Review Port Health form for each arriving passenger. 1 PHASED PROCESS OF ENTRY OF FULLY VACCINATED TRAVELERS TO ST. VINCENT AND THE GRENADINES: TESTING & QUARANTINE: PHASE #16 - Commencing Wednesday, August 11, 2021: 1. Where ‘Fully Vaccinated Travelers’ are those persons who: a. Have completed a vaccination regimen with one of the following COVID-19 vaccines recognized by the Ministry of Health, Wellness and the Environment of St Vincent and the Grenadines: i. AstraZeneca – Oxford AstraZeneca (Vaxzevria), COVISHIELD, AstraZeneca COVID-19 vaccine by SK Bioscience; ii. Pfizer-BioNTech COVID-19 vaccine; iii. Moderna COVID-19 vaccine; iv. -
Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS)
Grant Final Report Grant ID: R18 HS 017045 Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS) Inclusive dates: 12/01/07 - 09/30/10 Principal Investigator: Lazarus, Ross, MBBS, MPH, MMed, GDCompSci Team members: Michael Klompas, MD, MPH Performing Organization: Harvard Pilgrim Health Care, Inc. Project Officer: Steve Bernstein Submitted to: The Agency for Healthcare Research and Quality (AHRQ) U.S. Department of Health and Human Services 540 Gaither Road Rockville, MD 20850 www.ahrq.gov Abstract Purpose: To develop and disseminate HIT evidence and evidence-based tools to improve healthcare decision making through the use of integrated data and knowledge management. Scope: To create a generalizable system to facilitate detection and clinician reporting of vaccine adverse events, in order to improve the safety of national vaccination programs. Methods: Electronic medical records available from all ambulatory care encounters in a large multi-specialty practice were used. Every patient receiving a vaccine was automatically identified, and for the next 30 days, their health care diagnostic codes, laboratory tests, and medication prescriptions were evaluated for values suggestive of an adverse event. Results: Restructuring at CDC and consequent delays in terms of decision making have made it challenging despite best efforts to move forward with discussions regarding the evaluation of ESP:VAERS performance in a randomized trial and comparison of ESP:VAERS performance to existing VAERS and Vaccine Safety Datalink data. However, Preliminary data were collected and analyzed and this initiative has been presented at a number of national symposia. Key Words: electronic health records, vaccinations, adverse event reporting The authors of this report are responsible for its content. -
COVID-19 Vaccineadmin VAERS
Reporting a Suspected Vaccine Adverse Event Indian Health Service, National Pharmacy & Therapeutics Committee CAPT Matthew Clark, MD, FAAP, FACP, Chair CAPT Ryan Schupbach, PharmD, BCPS, CACP, Vice Chair CAPT Christopher Lamer, PharmD, MHS, BCPS, CDE, Director of Pharmacovigilance October 2020 Potential New Vaccine for COVID-19 • Operation Warp Speed (OWS) • Collaboration between the Federal Government and biopharmaceutical companies to develop medications, diagnostic tests, and vaccines. • Shortened timelines but safety and efficacy are the primary focus. • Vaccines must be at least 50% effective for FDA EUA or approval. • Vaccines must be safe, and benefits of immunization must outweigh any risks of adverse events. • Continued need for influenza immunization • Continued need for scheduled immunizations https://www.hhs.gov/coronavirus/explaining-operation-warp-speed/index.html 2 Vaccine Safety: Common Adverse Events Vaccines are considered to be safe and effective with most common adverse events being mild and are signs that the body is developing immunity: • Pain, swelling, or redness where the shot was given • Mild fever • Chills • Feeling tired • Headache • Muscle and joint aches https://www.vaccines.gov/basics/safety/side_effects 3 Vaccine Safety: Serious Adverse Events More serious side effects are rare but can occur. Some examples are: • Anaphylaxis (0.65 cases/1 million vaccinations) • Thrombocytopenia from Rubella vaccine (1 case/40,000 vaccinations) • Orchitis from Mumps vaccine (0.3 cases/1 million vaccinations) • Intussusception from Rotavirus vaccine (1 case/100,000 vaccinations) • Guillain-Barre from flu vaccine (1 case/1.25 million vaccinations; association is stronger with flu infection than the vaccine) Spencer JP, Trondsen Pawlowski RH, Thomas S. Vaccine Adverse Events: Separating Myth from Reality. -
COVID Vaccine Quick Reference Chart for Timeline
Pfizer-BioNTech Moderna Johnson & Johnson Novavax Oxford-AstraZeneca Sputnik V CureVac Sinopharm's BBIBP-CorV MOA mRNA vaccine mRNA vaccine Adenovirus vector vaccine Protein-based vaccine Adenovirus vector vaccine Adenovirus vector vaccine mRNA vaccine Inactivated virus Dosing 2 doses, 21 days apart 2 doses, 28 days apart 1 dose 2 doses, one month apart 2 doses, three months apart Sputnik Light requires one dose. 2 doses, four weeks apart 2 doses, three weeks apart Schedule The vaccine has been In a press release, the Gamaleya National D shown to be 89.3% effective Center of Epidemiology and Microbiology in in large-scale UK trials. Moscow claimed a large-scale Russian e 72% in the U.S. and 66% globally 76% in a U.S. study against Significantly, it is the first study saw 92% efficacy for its vaccine. t against moderate-to-severe symptomatic COVID-19; 100% 95% at least 7 days after 94.1% at least 14 days jab shown to be effective However, other scientists have voiced Efficacy results are presumed to 78% according to the World Health Efficacy disease; 85% effective against effective severe disease; 85% a dose 2 after dose 2 against the new UK variant concerns this claim is based on too few be released in May 2021. Organization severe disease, 28 days after a efficacy against symptomatic of COVID-19 in such a trial. cases. Although the vaccine was trialled on i single dose. COVID-19 in those 65+ 96% against original 18,000 people, the efficacy claim has been l coronavirus, 86% against B. -
Periodic Update on AEFI
CONSOLIDATED REGIONAL AND GLOBAL INFORMATION ON ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEFI) AGAINST COVID-19 AND OTHER UPDATES Thirteenth report WASHINGTON, DC Updated: 10 May 2021 1 OFFICIAL REPORTS ON PHARMACOVIGILANCE PROGRAMS CANADA • As of 30 April 2021, 13,420,198 doses of the COVID-19 vaccines of Pfizer-BioNTech, Moderna, Oxford- AstraZeneca, and the vaccine Covishield (AstraZeneca manufactured by the Serum Institute of India), had been administered. • A total of 4,548 individual reports of one or more adverse events (0.034% of doses administered) were received. Of these, 748 were considered serious events (0.006% of doses administered), with anaphylaxis being the one most frequently reported. • Of total reports, there were 2,072 non-serious and 520 serious events associated with the Pfizer-BioNTech vaccine. For the Moderna vaccine, 1,457 non-serious and 103 serious events were reported; for Covishield, there were 201 non-serious and 48 serious events, and for Oxford-AstraZeneca, 65 non-serious events and 62 serious events. • A total of 13,596 adverse events following immunization (AEFI) were reported, with 4,548 reports with one or more events. The most frequently reported non-serious adverse events were injection-site reactions, paresthesia, itching, hives, headache, hypoesthesia, and nausea. There were 61 reports of anaphylaxis. • Although 55% of vaccine doses were administered to women as of 30 April, and 45% to men, most of the reported adverse events were in women (84.3% of total doses). At the same time, 43.0% of total events were reported for people between the ages of 18 and 49, who account for 24% of people vaccinated. -
Comparative Characteristics of the Main Coronavirus Vaccines
Acta Scientific MICROBIOLOGY (ISSN: 2581-3226) Volume 4 Issue 9 September 2021 Editorial Comparative Characteristics of the Main Coronavirus Vaccines Pavel F Zabrodskii* Received: June 23, 2021 Saratov Medical University "REAVIZ", Saratov, Russian Federation Published: August 01, 2021 *Corresponding Author: Pavel F Zabrodskii, Saratov Medical University "REAVIZ", © All rights are reserved by Pavel F Saratov, Russian Federation. Zabrodskii. Since the beginning of the epidemic, vaccine development has been a priority for all developed countries. According to WHO (26 adenovirus rather than human adenovirus should reduce the risk virus. The fact that the vaccine was developed using chimpanzee January 2021), more than 60 vaccines worldwide are already in of allergic reactions and severe side-effects. However, the disadvan- clinical trials. More than 170 are being tested on animals. There tage of this product, as with all vector vaccines, is that the technol- ogy itself is new and has not previously been used in health care. One of the pluses for vector drug manufacturers is their speed of are 22 vaccines that have made it through the final phase of testing. creation. The vaccine is registered for use in the European Union. It The vaccine, developed by US company “Pfizer” and its German is licensed for emergency use in another 20 countries. clinical trials ended on 9 November 2020. In addition to EU coun- partner “BioNTech”, has been registered first in the EU. Phase III - ceutical company Sinovac Biotech, which has shown controversial tries, the vaccine is used in Australia, Saudi Arabia, Switzerland, “CoronaVac” is an inactivated vaccine from Chinese biopharma - Norway, Iceland, Serbia and some other countries. -
The Fast Approval and Slow Rollout of Sputnik V: Why Is Russia's Vaccine
Article The Fast Approval and Slow Rollout of Sputnik V: Why Is Russia’s Vaccine Rollout Slower than That of Other Nations? Elza Mikule 1,*,† , Tuuli Reissaar 1,† , Jennifer Villers 1,† , Alain Simplice Takoupo Penka 1,† , Alexander Temerev 2 and Liudmila Rozanova 2 1 Global Studies Institute, University of Geneva, 1205 Geneva, Switzerland; [email protected] (T.R.); [email protected] (J.V.); [email protected] (A.S.T.P.) 2 Institute of Global Health, University of Geneva, 1202 Geneva, Switzerland; [email protected] (A.T.); [email protected] (L.R.) * Correspondence: [email protected] † These authors contributed equally. Abstract: The emergence of the SARS-CoV-2 pandemic in the beginning of 2020 led to the deployment of enormous amounts of resources by different countries for vaccine development, and the Russian Federation was the first country in the world to approve a COVID-19 vaccine on 11 August 2020. In our research we sought to crystallize why the rollout of Sputnik V has been relatively slow considering that it was the first COVID-19 vaccine approved in the world. We looked at production capacity, at the number of vaccine doses domestically administered and internationally exported, and at vaccine hesitancy levels. By 6 May 2021, more first doses of Sputnik V had been administered Citation: Mikule, E.; Reissaar, T.; abroad than domestically, suggesting that limited production capacity was unlikely to be the main Villers, J.; Takoupo Penka, A.S.; reason behind the slow rollout. What remains unclear, however, is why Russia prioritized vaccine Temerev, A.; Rozanova, L. -
Recommendations for Improving Adult Vaccination Rates and Reporting Within Community Pharmacy Practice
Recommendations for Improving Adult Vaccination Rates and Reporting within Community Pharmacy Practice The purpose of this white paper is to provide best practice recommendations for improving adult vaccination rates and reporting. The intended audience for this white paper includes pharmacists practicing in community settings. This white paper was developed by the Pharmacy Quality Alliance (PQA) Adult Immunization Task Force and reviewed through a consensus-based process. The Task Force was sponsored by PFIZER®. September 2016 TABLE OF CONTENTS INTRODUCTION ....................................................................................................................................................... 4 RECOMMENDATIONS ............................................................................................................................................ 5 1. Immunization Screening Opportunities ...................................................................................... 5 A. Query immunization information systems ................................................................................. 5 B. Assess immunization status by utilizing the pharmacy dispensing system ............................. 6 C. Conduct immunization status screening during point-of-care activities (e.g., health screenings, yearly influenza vaccination administration, or refill pick-up) .............................. 7 D. Include immunization status screenings when performing medication therapy management services ..................................................................................................................