0000088968 00000 n 0000004761 00000 n The AstraZeneca vaccine is based on time-tested technology that employs a harmless cold virus (called adenovirus) that has been genetically modified to stimulate an immune response against the coronavirus. %%EOF Messenger RNA (mRNA) Nucleoside-modified mRNA encoding the viral spike (S) glycoprotein of SARS-CoV-2. >!V9j5LYHCz. ;BV 0000009283 00000 n 2.What should I know before I am given this COVID-19 vaccine Warnings You shouldnot receiveCOVID-19 Vaccine . The majority of recipients were White (75.5%), 10.1% were Black and 3.5% were Asian; 55.8% were female and 44.2% male. 0000003223 00000 n This means that it is essentially sodium-free. The Astra Zeneca vaccine remains a suitable option as a heterologous booster to primary series vaccination with a different vaccine. b AV Q4 8=0 ) /ID [<46442D36362D36432D33412D43412D36>] According to the vaccine's safety profile within the product information, the most common side effects include mild-to-moderate symptoms of one or more of the following: headache (52.6%) fatigue . 0000011249 00000 n %%EOF Most people have been exposed to them in their lives. The AstraZeneca vaccine remains a safe and effective choice to protect against COVID-19, and will protect against severe outcomes from getting infected with COVID-19, including illness, hospitalization and death. Older people have been prioritized to receive COVID-19 vaccines in many areas of the world. "A Simple Breakdown of the Ingredients in the COVID Vaccines." 11 Jan 2021. After the first dose is withdrawn, the vaccine should be used as soon as practically possible and within 6 hours. endobj Dont worry we wont send you spam or share your email address with anyone. endstream endobj 819 0 obj <>/Metadata 27 0 R/Outlines 44 0 R/Pages 815 0 R/StructTreeRoot 48 0 R/Type/Catalog/ViewerPreferences<>>> endobj 820 0 obj <. z(2$bW*; ! endstream endobj 73 0 obj <>/Font<>/ProcSet[/PDF /Text /ImageB /ImageC /ImageI]/XObject<>>>/Rotate 0/Type/Page>> endobj 74 0 obj <> stream endobj After vaccination, the surface spike protein is produced, priming the immune system to attack the virus if it later infects the body, protecting it against COVID-19. (Centers for Disease Control and Prevention). The severity and intensity of local and systemic reactions was highest on day 1 after vaccination. Discard the vial and do not combine residual vaccine from multiple vials. x]n@@eH%/Vu1]}sn\H6:ypen^mVU}m)QmB9ciMeT{ed#NtQwv/ ,6aYmk}*Oko8/q1(z h^ONc! 55 0 obj Function. 346 0 obj <> endobj endstream endobj startxref 0 %%EOF 72 0 obj <>>> endobj 95 0 obj <> stream Safety data sheet. 0 It has been adjusted to work as a delivery system for the vaccine. a severe headache that is not relieved with simple painkillers or is getting worse or feels worse when you lie down or bend over, an unusual headache that may be accompanied by blurred vision, confusion, difficulty with speech, weakness, drowsiness or seizures (fits), rash that looks like small bruises or bleeding under the skin beyond the injection site, or any unexplained bleeding. United Kingdom, MedImmune Pharma B.V., Nijmegen FDA Approved: No 6. 3. It will take only 2 minutes to fill in. The COVID-19 vaccines currently approved for use in the UK are: Moderna (Spikevax) Pfizer/BioNTech (Comirnaty) Novavax (Nuvaxovid) AstraZeneca (Oxford) (not available) Janssen (Johnson & Johnson) (not available) Valneva (Valneva) (not available) Which vaccine will I get? 0000003465 00000 n Keep this medicine out of the sight and reach of children. During use it can be stored from 2C to 25C. 0000103790 00000 n 0000104953 00000 n Tell your doctor, pharmacist or nurse before vaccination: If you are not sure if any of the above applies to you, talk to your doctor, pharmacist or nurse before you are given the vaccine. We also use cookies set by other sites to help us deliver content from their services. If you miss an appointment for your second injection of COVID-19 Vaccine AstraZeneca This product contains genetically modified organisms (GMOs). The overall safety of COVID-19 Vaccine AstraZeneca is based on an interim analysis of pooled data from four clinical trials conducted in the United Kingdom, Brazil, and South Africa. trailer <<082F7B1BF056430DB0F4C36E6FE6E521>]/Prev 207227>> startxref 0 %%EOF 96 0 obj <>stream 0000132021 00000 n 0000001096 00000 n This is due to the fact that this group is less likely to respond adequately to vaccination following a standard primary All 28 developed different types of clots, or thromboses, five to 16 days after vaccination, and all had made antibodies against platelets. 0000007231 00000 n This is the same type of vaccine that flu and the Middle East Respiratory Syndrome vaccines have used for years. xref %PDF-1.7 Each vial contains 10 doses of 0.5 ml. This phase also helps researchers understand how well a vaccine works over a longer time frame and how safe it is for the population. 3.What if I am taking, have recently taken or might take other medicinesor vaccination series and are at higher risk of severe COVID-19 disease. 0000055209 00000 n The Astra-Zeneca vaccine can be offered to people who have had COVID-19 in the past. 0000003743 00000 n 0000015824 00000 n The Janssen COVID-19 Vaccine includes the following ingredients: recombinant, replication-incompetent adenovirus type 26 expressing the SARS -CoV-2 spike protein, citric acid The AstraZeneca vaccine is made from an adenovirus that has been changed in the lab so it can't cause harm. 0000054208 00000 n WHO recommends focusing on achieving high first dose coverage by extending the inter-dose interval, whilst continuing to maximize second dose coverage of vulnerable groups in the context of variants of concern. For countries considering heterologous schedules, WHO has made recommendations to ensure equivalent or favourable immunogenicity or vaccine effectiveness for heterologous versus homologous schedules: When considering booster vaccination after having been vaccinated with ChAdOx1-S [recombinant] COVID-19 [Astra Zeneca] vaccine for the primary series, SAGE considers using a different type of COVID-19 vaccine for a third dose a more favourable option. 0000107012 00000 n endstream endobj startxref L-histidine hydrochloride monohydrate (amino acid) Magnesium chloride hexahydrate (salt) Polysorbate 80 (surfactant) Ethanol (alcohol) Sucrose (sugar) Sodium chloride (salt) Disodium edetate dihydrate (salt) Water for injections (diluent) The vaccine does not include any human or animal products, thimerosal, gelatin, or formaldehyde. 0 The last nine ingredients on the list are called 'excipients.' }wfydUj_mr\]]s=']O_Od>MdD.PHTpo This article has been translated from its original language. Andrew Pollard has been leading the Oxford vaccine clinical trials in the UK, Brazil, and South Africa. COVID-19 Vaccine AstraZeneca is given as an injection of 0.5 ml into a muscle (usually in the upper arm). If you forget to go back at the scheduled time, ask your doctor, pharmacist or nurse for advice. Store in a refrigerator (2C to 8C). %PDF-1.7 % To get around the problem, scientists used virus from a chimpanzee to ensure people would not have any natural immunity to it. None of the ingredients in this vaccine can cause COVID-19. 0000002028 00000 n The EU has lost a legal battle over its attempt to force AstraZeneca to deliver 120 million doses of its vaccine to the bloc, by the end of June. Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take, any other medicines or vaccines. In this vaccine ,polysorbate 80 works to separate the listed ingredient of water from other oil-based ingredients. 0000100169 00000 n hb```(1A;B% dose regimen of this vaccine is believed to be more protective against variants of concern than a single dose alone. The need for, and timing of, booster doses for children aged 5-11 years has not yet been determined. % If you are immunocompromised and receive a third dose of COVID-19 Vaccine AstraZeneca, it may still not provide full immunity to COVID-19 and you should continue to maintain physical precautions to help prevent COVID-19. EDTA is not listed as an ingredient in the Johnson &. COVID-19 Vaccine AstraZeneca is a vaccine used for preventing COVID 19, caused by a virus called coronavirus (SARS-CoV-2). The easiest way to lookup drug information, identify pills, check interactions and set up your own personal medication records. 0000098136 00000 n Andrew Pollard was in a French taxi when he realised what was coming. If your fever is high and lasts longer than two or three days, or you have other persistent symptoms, this might not be due to side effects of the vaccine and you should follow appropriate advice according to your symptoms. LYpeP4 &=C&CBzLL3y20gah!A '1>ederj4+e@Zg Rc`TaPa`2R6r G2p T A third injection may be given at least 8 weeks after the second injection if advised by your doctor. The final stage (Phase III) provides the vaccine to thousands of people from the target population to see how safe and effective it is. 0000004240 00000 n The goal of this stage is to identify the most effective dosages and schedule for Phase III trials. /Info 87 0 R 870 0 obj <>stream Liverpool, L24 9JW To help pregnant women make this assessment, they should be provided with A new investigational treatment for COVID-19: Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. stream People under the age of 40 are to be offered an alternative to the Oxford-AstraZeneca vaccine in the UK as a precaution, after a review of all the latest evidence by vaccine advisers and safety . COVID-19 Vaccine AstraZeneca contains genetically modified organisms (GMOs). When these blood clots do occur, they may be in unusual or atypical locations (e.g. Each vial contains 8 doses of 0.5 ml. Vaccine efficacy tended to be higher when the interval between doses was longer. If you experience any of the following from around 4 days after vaccination you should seek medical advice urgently: Tell your doctor, pharmacist or nurse if you experienced a blood clot occurring at the same time as low levels of platelets after receiving a previous dose of the vaccine. However, it is not confirmed whether these events were due to the vaccine. Statement of the WHO Global Advisory Committee on Vaccine Safety (GACVS) COVID-19 subcommittee on safety signals related to the AstraZeneca COVID-19 vaccine, Interim statement of the COVID-19 subcommittee of the WHO Global Advisory Committee on Vaccine Safety on AstraZeneca COVID-19 vaccine, The Janssen Ad26.COV2.S COVID-19 vaccine: What you need to know, The Moderna COVID-19 (mRNA-1273) vaccine: what you need to know, The Pfizer BioNTech (BNT162b2) COVID-19 vaccine: What you need to know, The Sinovac-CoronaVac COVID-19 vaccine: What you need to know, The Sinopharm COVID-19 vaccine: What you need to know, The Novavax vaccine against COVID-19: What you need to know, The Bharat Biotech BBV152 COVAXIN vaccine against COVID-19: What you need to know, Independent Oversight and Advisory Committee, WHO Strategic Advisory Group of Experts on Immunization (SAGE), Strategic Advisory Group of Experts on Immunization, Interim recommendations for use of the ChAdOx1-S [recombinant] vaccine against COVID-19 (AstraZeneca COVID-19 vaccine AZD1222 Vaxzevria, SII COVISHIELD), The Oxford/AstraZeneca (ChAdOx1-S [recombinant] vaccine) COVID-19 vaccine: what you need to know, Uncommon (infrequent) >1/1000 and < 1/100, The Astra-Zeneca vaccine recommendations have also been modified to indicate that either of the mRNA COVID-19 vaccines (Pfizer or Moderna) can be used as a second dose following a, The Astra-Zeneca vaccine can be used as a. Moderna bivalent COVID-19 vaccine. endstream endobj 75 0 obj <> stream 0000002484 00000 n Dont include personal or financial information like your National Insurance number or credit card details. AstraZeneca-Oxford vaccine was 76% effective at preventing symptomatic COVID-19 two weeks after the second dose and was 100% effective in stopping severe disease and hospitalization in a. Something went wrong while submitting the form. Published: 2021-05-07. WHO will continue to review these rare reports of GBS and to work closely with national regulators to manage potential risks. Excipients are the non-active ingredients that are added to the vaccine for a variety of reasons. 779 0 obj <> endobj 0000015637 00000 n 0000001605 00000 n 0000015344 00000 n 0000012193 00000 n COVID-19 Vaccine AstraZeneca stimulates the bodys natural defences (immune system). Some of the information might be out of date or no longer relevant. %PDF-1.6 % AstraZeneca vs. Sinovac side effects. Vaccines are tested and studied in multiple phases (phased testing) to determine if they are safe and work to prevent illness. 0000001732 00000 n 0000054470 00000 n 569 0 obj <>/Filter/FlateDecode/ID[<422DFA914F61AD45909E39C193482A39>]/Index[548 34]/Info 547 0 R/Length 105/Prev 177378/Root 549 0 R/Size 582/Type/XRef/W[1 3 1]>>stream i; "32tBa;CC'd&@u^?^02/g`8Ea?U Of the participants who received AZD1222 without paracetamol, 328 (67%) reported mild to moderate pain after vaccination, and 403 (83%) reported site tenderness. 0000005805 00000 n Read all of this leaflet carefully before the vaccine is given because it contains important information for you. JZD| Getty Images. This type of vaccine development technology has been tested for many other diseases such as influenza (flu) and Middle East respiratory syndrome coronavirus (MERS-CoV). 0000007190 00000 n Active ingredients Added ingredients Products used in the manufacture of the vaccine Growing the active ingredients Further information The information on this page is based on the best information that we can find from the available literature. Active ingredient: 0000014217 00000 n &Va(f+0&+FIcDHoL The AstraZeneca vaccine does contain polysorbate. 0000004159 00000 n 0000000016 00000 n RZ%L ?Gss0~ls"+?H~9~ ~~g5-?K~=2_H This publication is available at https://www.gov.uk/government/publications/regulatory-approval-of-covid-19-vaccine-astrazeneca/information-for-uk-recipients-on-covid-19-vaccine-astrazeneca, Regulation 174 Information for UK recipients, COVID-19 Vaccine AstraZeneca solution for injection The AstraZeneca vaccine has an efficacy of 72% against symptomatic SARS-CoV-2 infection, as shown by the primary analysis of data irrespective of interdose interval from trial participants who received 2 standard doses with an interval varying from about 4 to 12 weeks. Produced in genetically modified human embryonic kidney (HEK) 293 cells. Younger patients may be more likely to experience anaphylaxis. This Oxford-AstraZeneca vaccine uses the ChAdOx1 technology, which has been developed and optimised by the Jenner Institute over the last 10 years. The solution is colourless to slightly brown, clear to slightly opaque. 0000100043 00000 n 0000006565 00000 n AstraZeneca is a member of Covax, a global initiative aiming to distribute two billion vaccine doses to 92 low- and middle-income countries at no more than $3 a dose. x P^0^N&8:Cssfo"E$hq(#^G78@ Browse our homepage for up to date content or request information about a specific topic from our team of scientists. None of the ingredients in this vaccine can cause COVID-19. COVID-19 Vaccine (ChAdOx1-S* recombinant) 5 10^10 viral particles (vp). Vaccines are widely used to prevent infections, and most traditional vaccines that target viruses are made from dead or attenuated live viruses (viruses that have been altered so they are not harmful) to help people develop immunity without becoming ill. The AstraZeneca vaccine uses a harmless, weakened animal virus (called a viral vector) that contains the genetic code for the coronavirus spike protein. Data sources include IBM Watson Micromedex (updated 5 Feb 2023), Cerner Multum (updated 22 Feb 2023), ASHP (updated 12 Feb 2023) and others. "It can't give you an infection. No substantive data are available related to impact of the vaccine on transmission or viral shedding. 0000003094 00000 n . hbbd```b``5d4d""A$a0DEE4$U0 The benefits of booster vaccination are recognized following increasing evidence of waning vaccine effectiveness against mild and asymptomatic SARS-CoV-2 infection over time. health workers and immunocompromised persons should be prioritised. If you are not sure, talk to your doctor, pharmacist or nurse. hb``g``oc`c` @1v=k}u F'SUNZ endstream information about the risks of COVID-19 in pregnancy, the likely benefits of vaccination in the local epidemiological context, and the current limitations of safety data in pregnant women. Preservatives in this vaccine are disodium edetate dihydrate and ethanol. Once this enters the body, it tells your cells to make copies of the spike protein. Additional Information If you have questions, visit the website or call the telephone number provided 56 0 obj Spills should be disinfected using agents with activity against adenovirus. <>/Metadata 30 0 R>> Guillain-Barr syndrome (GBS) has been reported very rarely following vaccination. Some people have reported a sudden feeling of cold with shivering/shaking accompanied by a rise in temperature, possibly with sweating, headache (including migraine-like headaches), nausea, muscle aches and feeling unwell, starting within a day of having the vaccine and usually lasting for a day or two. 0000004065 00000 n What COVID-19 Vaccine AstraZeneca is and what it is used for COVID-19 Vaccine AstraZeneca is a vaccine used for preventing COVID-19, caused by a virus called coronavirus (SARS-CoV-2). 0000102371 00000 n 346 65 M Ms CZHto ) Overall, among the participants who received COVID-19 Vaccine AstraZeneca, 90.3% were aged 18 to 64 years and 9.7% were 65 years of age or older. It is important that you return for your second injection of COVID-19 Vaccine AstraZeneca. . COVID-19 Vaccine AstraZeneca contains sodium and alcohol (ethanol) This medicine contains less than 1 mmol sodium (23 mg) per dose of 0.5 ml. It's only capable of delivering the DNA," he said. Such reactions may include a combination of any of the following symptoms: In clinical studies with the vaccine, fewer side effects were reported after the second dose and those that were reported were milder in nature when compared to after the first dose. 0000093244 00000 n Route of administration Intramuscular injection. 0000006617 00000 n However, a mild fever or infection, like a cold, are not reasons to delay vaccination; If you have ever had a condition known as heparin-induced thrombocytopenia and thrombosis (HITT or HIT type 2), or a blood clot in the sinus veins in the brain; If you have a problem with bleeding or bruising, or if you are taking a blood thinning medicine (anticoagulant); If your immune system does not work properly (immunodeficiency) or you are taking medicines that weaken the immune system (such as high-dose corticosteroids, immunosuppressants or cancer medicines). Interim results were published in. AstraZeneca has updated the efficacy result of its coronavirus vaccine trial in the US, after health officials insisted they wanted to include the latest information. . serious nerve inflammation, which may cause paralysis and difficulty breathing (Guillain-Barr Possible side effects 5. 0000002960 00000 n Keep vials in outer carton to protect from light. endstream endobj 549 0 obj <. This medicinal product has been given authorisation for temporary supply by the UK Department of Health and Social Care and the Medicines & Healthcare products Regulatory Agency. For the Oxford-AstraZeneca vaccine, 30 cases of anaphylaxis have been confirmed . 0000083589 00000 n Following widespread use of the vaccine there have been extremely rare reports of blood clots in combination with low level of blood platelets. . /Size 89 /Prev 149222 No data are currently available in individuals with a weakened immune system or who are taking chronic treatment that suppresses or prevents immune responses. 0000107040 00000 n COVID-19 Vaccine AstraZeneca is given to adults aged 18 years and older. The AstraZeneca COVID-19 vaccine, now called Vaxzevria, is a viral vector vaccine, just like the Johnson & Johnson vaccine. In the trial, 543 participants received AZD1222 (56 also received a prophylactic dose of the pain killer paracetamol), and 534 received MenACWY, a comparator meningococcal conjugate vaccine. 0000018147 00000 n AstraZeneca's Oxford vaccine trial to resume, the university says The document, which is labeled an "initial report," describes how the study participant had trouble walking, weakness and pain. Neither Pfizer nor Moderna . COVID-19 Vaccine AstraZeneca contains sodium and alcohol). Information about the Moderna coronavirus vaccine, including a full list of ingredients and side effects, is available: Information on the Moderna COVID-19 vaccine. 0000009792 00000 n This is not enough to cause any noticeable effects. Epub 2020 Dec 8. According to the information that AstraZeneca and the University of Oxford presented to the United Kingdom's vaccine regulatory agency, this vaccine contains: The vaccine does not include any human or animal products, thimerosal, gelatin, or formaldehyde. 0000016862 00000 n 0000003890 00000 n AstraZeneca's active ingredient is a non-infectious chimpanzee adenovirus, which Professor Pouton described as a "delivery system" for a DNA payload, which contains code to produce the SARS-CoV-2 spike protein, into the body's cells. SAGE has reviewed all available data on the performance of the vaccine in the settings of variants of concern. 0000006047 00000 n Talk to the healthcare provider if you have questions. The Oxford-AstraZeneca vaccine contains no pork products or by-products. 0000085176 00000 n syndrome [GBS]), rapid swelling under the skin in areas such as the face, lips, mouth and throat (which may cause difficulty in swallowing or breathing) (angioedema), capillary leak syndrome (a condition causing fluid leakage from small blood vessels), very low levels of blood platelets (immune thrombocytopenia) that can be associated with bleeding (see section 2, Blood disorders), blood clots in the brain, not associated with low level of blood platelets (see section 2, Blood disorders), inflammation of the spinal cord which may cause muscle weakness, localised or radiating back pain, bladder and bowel symptoms and changes in sensation (transverse myelitis). The Oxford-AstraZeneca vaccine contains no thimerosal, mercury, or aluminum. CLS is a serious, potentially fatal condition causing fluid leakage from small blood vessels (capillaries) resulting in rapid swelling of the arms and legs, sudden weight gain and feeling faint (low blood pressure). 54 0 obj Vaccine Maker Halts Trial Following Unexplained Illness in Volunteer, Details Emerge on Unexplained Illness in AstraZeneca COVID Vaccine Trial, A Study of a Candidate COVID-19 Vaccine (COV001), New Vaxzevria Data Further Support its Use as Third Dose Booster, Vaxzevria Significantly Boosted Antibody Levels Against Omicron, Vaxzevria is Highly Effective After One Dose Against Severe Disease or Hospitalisation Caused by Beta and Delta Variants of Concern, Vaxzevria Induced Immunity for at Least One Year Following a Single Dose and Strong Immune Responses Following Either a Late Second Dose or a Third Dose, COVID-19 Vaccine AstraZeneca Effective Against Delta (Indian) Variant, AstraZeneca COVID-19 Vaccine Vaxzevria Authorised for Emergency Use in Japan, AZD1222 US Phase III Primary Analysis Confirms Safety and Efficacy, AZD1222 US Phase III trial Met Primary Efficacy Endpoint in Preventing COVID-19 at Interim Analysis, UK and EU Regulatory Agencies Confirm COVID-19 Vaccine AstraZeneca is Safe and Effective, Update on the Safety of COVID-19 Vaccine AstraZeneca, AstraZeneca Advances Mass Global Rollout of COVID-19 Vaccine Through COVAX, AstraZeneca COVID-19 Vaccine Authorised for Emergency Use by the World Health Organization, COVID-19 Vaccine AstraZeneca Confirms 100% Protection Against Severe Disease, Hospitalisation and Death in the Primary Analysis of Phase III Trials, COVID-19 Vaccine AstraZeneca Authorised for Use in the EU, COVID-19 Vaccine AstraZeneca Recommended for Use in the EU, Serum Institute of India Obtains Emergency Use Authorisation in India for AstraZenecas COVID-19 Vaccine, AstraZenecas COVID-19 Vaccine Authorised for Emergency Supply in the UK, AZD1222 Oxford Phase III Trials Interim Analysis Results Published in The Lancet, AZD1222 Vaccine Met Primary Efficacy Endpoint in Preventing COVID-19, FDA Authorises Restart of the COVID-19 AZD1222 Vaccine US Phase III Trial, COVID-19 Vaccine AZD1222 Clinical Trial Resumed in Japan, Follows Restart of Trials in the UK, Brazil, South Africa and India, COVID-19 Vaccine AZD1222 Clinical Trials Resumed in the UK, Statement on AstraZeneca Oxford SARS-CoV-2 Vaccine, AZD1222, COVID-19 Vaccine Trials Temporary Pause, AstraZenecas Scientific and Social Commitment for COVID-19 Vaccine AZD1222, Development of COVID-19 Vaccine AZD1222 Expands into US Phase III Clinical Trial Across All Adult Age Groups, AstraZeneca Australia & New Zealand Response to the COVID-19 Pandemic, AstraZeneca Concludes Agreement with the European Commission for the Supply of up to 400 Million Doses of AZD1222 COVID-19 Vaccine, COVID-19 Vaccine AZD1222 Showed Robust Immune Responses in All Participants in Phase I/II Trial, Cobra Signs Supply Agreement with AstraZeneca for Manufacture of COVID-19 Vaccine Candidate, AstraZeneca to Supply Europe With Up To 400 Million Doses of Oxford Universitys COVID-19 Vaccine At No Profit, AstraZeneca Takes Next Steps Towards Broad and Equitable Access to Oxford Universitys COVID-19 Vaccine, AstraZeneca Advances Response to Global COVID-19 Challenge as it Receives First Commitments for Oxfords Potential New Vaccine, Investigational ChAdOx1 nCoV-19 Vaccine Protects Monkeys Against COVID-19 Pneumonia, AstraZeneca and Oxford University Announce Landmark Agreement for COVID-19 Vaccine. 80 works to separate the listed ingredient of water from other oil-based ingredients multiple vials n & Va f+0! May be more likely to experience anaphylaxis now called Vaxzevria, is a viral vector vaccine, just the. ] ] s= ' ] O_Od > MdD.PHTpo this article has been translated astrazeneca vaccine ingredients pdf its language... Aged 18 years and older talk to your doctor, pharmacist or nurse if you miss appointment... Vaccine from multiple vials contains 10 doses of 0.5 ml into a muscle ( usually in upper. Different vaccine is essentially sodium-free wont send you spam or share your email address with anyone years has not been. During use it can be offered to people who have had COVID-19 in the settings of variants of.! Spam or share your email address with anyone of children effective dosages and schedule for phase III trials dose. Be higher when the interval between doses was longer the settings of variants of concern 30. Personal medication records minutes to fill in, ask your doctor, pharmacist or nurse for advice a French when. 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