Participants who received a booster (Dose 4) of COMIRNATY Original/Omicron BA.1 had a median follow-up time of at least 1.7 months up to a data cut-off date of 16 May 2022. Non-serious adverse events from Dose1 through up to 30days after Dose2 in ongoing followup in the initial enrolment group were reported by 10.9% of COMIRNATY 10mcg recipients and by 9.1% of placebo recipients. Vials of COMIRNATY Original & Omicron BA.4/BA.5 intended for individuals aged 5 years to <12 years (orange cap/orange label border) cannot be used to prepare doses for individuals 12 years of age and older. a direct ship distribution strategy that minimizes the transportation time from our facility to the point of use, synchronization of our vaccine shipments with the delivery of an ancillary kit that contains supplies required to administer the vaccine, and. Pfizer consistently and diligently monitors the supply of our medicines. Do not use COMIRNATY vials with an orange plastic cap/orange label border, purple plastic cap/purple label border or gray plastic cap/gray label border to prepare doses for individuals aged 6 months to <5 years. View public records and voter registration of Gina Warren born 1964, includes court and personal records. Severe local reactions were reported by 1 (1.0%) participant in the 12 to 17 years of age group who received a booster dose of COMIRNATY Original & Omicron BA.4/BA.5 30 mcg. Inspect the liquid in the vial prior to dilution. The median duration was 3.5 days (ranged from 1 to 14 days) in the vaccine group. The vial stoppers are not made with natural rubber latex. Careful attention should be paid to the vial cap colour and label border and the appropriate corresponding instructions must be followed. Vials should be discarded 12 hours after dilution (i.e., the first puncture). Among participants with confirmed stable HIV infection serious adverse events from Dose 1 up to the participant unblinding date in ongoing follow-up were reported by 2 (2%) COMIRNATY recipients and 2 (2%) placebo recipients. The COMIRNATY multiple dose vial (for age 6 months to <5 years) has a maroon cap and a maroon label border and contains a volume of 0.4 mL. Vials may be stored at room temperature [up to 25C (77F)] for up to 12 hours prior to use. There were no other notable patterns or numerical imbalances between treatment groups for specific categories of serious adverse events (including neurologic, neuro-inflammatory, thrombotic events, myocarditis or anaphylactic reaction to the vaccine) reported during the blinded placebo-controlled follow-up period of the study. No Grade 4 local reactions were reported. Animal studies do not indicate direct or indirect harmful effects with respect to female fertility or reproductive toxicity (see 16 NON-CLINICAL TOXICOLOGY). Reports are accepted from anyone and can be submitted electronically at www.vaers.hhs.gov. It is unknown whether COMIRNATY Original & Omicron BA.4/BA.5 is excreted in human milk. Study 3 also enrolled 1,776 participants 6 months through <2 years of age (1,178 COMIRNATY 3 mcg; 598 placebo), and 2,750 participants 2 through <5 years of age (1,835 COMIRNATY 3 mcg; 915 placebo) in Phase 2/3. Frozen Vials Prior to UseCartons of COMIRNATY multiple dose vials (for 12 years and older: DILUTE BEFORE USE)arrive in thermal containers with dry ice. Using aseptic technique, withdraw 1.8 mL of 0.9% Sodium Chloride Injection, USP into a transfer syringe (using 21-gauge or narrower needle). Vials should be discarded 12 hours after first puncture. Most systemic events were mild or moderate in severity. COMIRNATY multiple dose vials (for 12 years and older: DO NOT DILUTE) may be stored at room temperature up to 25C (77F) for a total of 12 hours prior to the first puncture. Cartons of COMIRNATY Original & Omicron BA.4/BA.5 multiple dose vials (for 12 years and older: DO NOT DILUTE) may arrive frozen at ultracold conditions in thermal containers with dry ice. Below are a few case scenarios you might encounter. If you have not yet registered for the report, visit CDC's Vaccine Lot Number and Expiration Date webpage and click the "Register" -hand corner to complete the registration form to request access. Among participants with confirmed stable HIV infection that included 100 COMIRNATY recipients and 100 placebo recipients, unsolicited adverse events were reported by 29 (29%) participants in the COMIRNATY group and 15 (15%) participants in the placebo group. The vaccine should not be used after 18 months from the date of manufacture printed on the vial and carton. Pfizer is a proven, reliable multinational vaccine producer, supplying vaccines to more than 165 countries. Each vial contains 6 doses of 0.3 mL. Adverse reactions following administration of any dose included irritability (68.4%), decreased appetite (38.6%), tenderness at the injection site (26.4%), injection site redness (17.8%), fever (14.4%), injection site swelling (7.3%), and lymphadenopathy (0.2%). An analysis of Study 3 Phase 2/3 adverse event data also included another 2,379 participants (safety expansion group: 1,591 COMIRNATY 10 mcg and 788 placebo), of whom 71.2% had a follow-up period for at least 2 weeks after Dose 2. In these individuals, a third dose may be considered as part of the primary series. After dilution, vials of COMIRNATY (for age 6 months to <5 years) contain 10 doses of 0.2 mL of vaccine. Most of the events began from 3-11 days after the second dose and were characterized as mild and self-limited. Note: Reactions were collected in the electronic diary (e-diary) from Day 1 to Day 7 after vaccination. The vaccine will be a white to off-white suspension. For details on the primary vaccination course for individuals 12 years of age and older, please refer to the COMIRNATYProduct Monograph, Section 4.2.1 Vaccination Schedule for Individuals 12 Years of Age and Older. Serious adverse events from Dose1 through up to 30 days after Dose2 in ongoing followup in the initial enrolment group were reported by 1 participant (0.1%) in each group after receiving the vaccine or placebo through the data cut-off date. The vial stoppers are not made with natural rubber latex. Equalize vial pressure before removing the needle from the vial by withdrawing 1.8 mL air into the empty diluent syringe. COMIRNATY Original & Omicron BA.4/BA.5 is indicated only for a booster dose. Cartons of COMIRNATY Original & Omicron BA.4/BA.5 (for age 5 years to <12 years) may also arrive at 2C to 8C (35F to 46F). COMIRNATY (COVID-19 Vaccine, mRNA) is indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS- CoV-2) in individuals 6 months of age and older. The safety of a COMIRNATY Original/Omicron BA.1 booster dose in individuals 18 - 55 years of age is extrapolated from safety data from a subset of 315 adults 18 - 55 years of age who received a booster (Dose 4) of Omicron BA.1 30 mcg (monovalent) after completing 3 doses of COMIRNATY. Pericarditis was reported for one participant in the vaccine group, and no case was reported in the placebo group. If vials are received at 2C to 8C, they should be stored at 2C to 8C. Check that the carton has been updated to reflect the 10-week refrigerated expiry date. Pfizer Inc. and BioNTech SE today announced they have completed a submission to the U.S. Food and Drug Administration (FDA) requesting Emergency Use Authorization (EUA) of a 10-g booster dose of the companies' Omicron BA.4/BA.5-adapted bivalent COVID-19 vaccine for children ages 5 through 11 years of age. Dr Gina Reghetti Do Pc Inc is a Medical Group that has only one practice medical office located in Warren OH. Pain at injection site was the most frequently reported local AR within 7 days after study vaccination, with swelling and redness at the injection site reported much less frequently. Lymphadenopathy was reported in 87 (0.4%) participants in the vaccine group compared to 8 (<0.1%) participants in the placebo group. In Study 2, among participants 12 through 15 years of age who had received at least 1 dose of vaccine or placebo (COMIRNATY = 1,131; placebo = 1,129), serious adverse events from Dose 1 up to the participant unblinding date in ongoing follow-up were reported by 10 (0.9%) COMIRNATY recipients and 2 (0.2%) placebo recipients. COMIRNATY multiple dose vials (with maroon cap and maroon label border) are supplied in a carton containing 10 multiple dose vials. Third Dose Vaccination With AstraZeneca or Pfizer COVID-19 Vaccine Among Adults Received Sinovac COVID-19 Vaccine. Do not store vials at 25C to 15C (-13F to 5F). The products discussed herein may have different labeling in different countries. For example, if a provider was getting 975 doses, it will now be 1,170 doses. The Limited Time Discount may also be available to customers through Pfizer Distributors from Sunday, January 1, 2023 to Wednesday, February 22, 2023. Individuals should be advised to bring symptoms (e.g., dizziness, increases in heart rate, feeling short of breath, tingling sensations or sweating) to the attention of the vaccination provider for evaluation. ONLY use 0.9% Sodium Chloride Injection, USP as the diluent. The COMIRNATY Original & Omicron BA.4/BA.5 multiple dose vial (for ages 5 years to <12 years) has an orange cap and an orange label border and contains a volume of 1.3 mL. Pfizer and Moderna are two-dose vaccines, while J&J is one dose.2) The lot number and expiration dateThe lot number is a string of numbers and letters that tracks this specific batch of vaccine . Vaccine Lot Release Certificates. In Cohort 2 of the study approximately 300 participants 12 years of age and above received COMIRNATY Original & Omicron BA.4/BA.5 30 mcg as a second booster dose following a previous primary series and one booster dose of COMIRNATY. Each vial must be thawed and diluted prior to administration. Children 5 Years Through12 Years of Age Primary Series (Two Doses). Low dead-volume syringes and/or needles can be used to extract 10 doses from a single vial. The COMIRNATY Original & Omicron BA.4/BA.5 multiple dose vial with a gray cap and gray label border MUST NOT BE DILUTED prior to administration. Table 1: Dosage Forms, Strengths, Composition and Packaging (For 12 Years of Age and Older), Tozinameran (mRNA) encodes for the viral spike (S) protein of SARS-CoV-2 Original strain and famtozinameran (mRNA) encodes for the viral spike (S) protein of SARS-CoV-2 Omicron BA.4/BA.5 strain. Anaphylaxis has been reported. There are two formulations of COMIRNATY authorized for use in individuals 12 years of age and older. Registered users can now access COVID-19 vaccine lot numbers and expiration dates provided to CDC by the vaccine manufacturer. Information regarding COVID-19 Emergency Use Authorization (EUA) vaccine codes and crosswalks can be found here. To receive email updates about this page, enter your email address: For more information on background and concepts see Understanding the Rules for Creating CVX and MVX Codes [5 pages], View archived 2015 Edition Versioned Codes, More ways to access CDCs Vaccine Code Set information: Code Set Viewpoint search/browse website and REST Web Service. A booster dose of COMIRNATY Original & Omicron BA.4/BA.5 may be administered intramuscularly at least 6 months after completing the primary course of COMIRNATY in children 5 years through <12 years of age. Please be mindful of when your COVID-19 vaccine expires! Each vial contains 6 doses of 0.3 mL. The thermal container maintains a temperature range of -90C to -60C (130F to -76F). Pentacel is an example. Children who will turn from 4 to 5 years of age between their doses in the vaccination series should receive their age-appropriate dose at the time of the vaccination and the interval between doses is determined by the childs age at the start of the vaccination series. Refer to dilution and dose preparation instructions in the panels below. Low dead-volume syringes and/or needles can be used to extract 10 doses from a single vial. Of the participants who received a booster dose of COMIRNATY or placebo (COMIRNATY = 5,055; placebo = 5,020) to the cut-off date (October 5, 2021), serious adverse events were reported by 0.3% of COMIRNATY recipients and 0.5% by placebo recipients. Study C4591007 (Study 3) is a Phase 1/2/3 study comprised of an open-label vaccine dose finding portion (Phase 1) and a multicenter, multinational, randomized, saline placebo-controlled, observer-blind immunogenicity and efficacy portion (Phase 2/3) that has enrolled approximately 4,600 participants 5 years through <12 years of age. From Dose 1 through 30 days after Dose 3, lymphadenopathy was reported in 1 (0.1%) of COMIRNATY recipients vs. 0 (0.0%) of placebo recipients. Comirnaty Original & Omicron BA.4/BA.5 COVID-19 mRNA vaccine, Bivalent (Original and Omicron BA.4/BA.5) is indicated as a booster dose for active immunization against COVID-19 caused by SARS-CoV-2 in individuals 5 years of age and older. Verify the final dosing volume of 0.2 mL. Of these, 2,171 (95.7%) (1,456 COMIRNATY 10 mcg and 715 placebo) participants have been followed for at least 3 months after Dose 2. Each dose must contain 0.2 mL of vaccine. In the analysis of unblinded follow-up, there were no notable patterns of specific categories of non-serious adverse events that would suggest a causal relationship to COMIRNATY. Once received, frozen vials may be immediately transferred to the refrigerator [2C to 8C (35F to 46F)], thawed and stored for a single period of up to 10 weeks within the 12-month shelf-life. Low dead-volume syringes and/or needles can be used to extract 10 doses from a single vial. c. Mild: 0.5 to 2.0 cm; moderate: >2.0 to 7.0 cm; severe: >7.0 cm. Each Product Monograph is available below, at www.pfizer.ca/products, or www.cvdvaccine.ca. Equalize vial pressure before removing the needle from the vial by withdrawing 1.3mL air into the empty diluent syringe. These cookies may also be used for advertising purposes by these third parties. There were no notable patterns or numerical imbalances between treatment groups for specific categories of serious adverse events that would suggest a causal relationship to COMIRNATY. second. Do not use if vaccine is discoloured or contains particulate matter. Pfizer and Moderna are two-dose vaccines, while J&J is one dose.2) The lot number and expiration dateThe lot number is a string of numbers and letters that tracks this specific batch of vaccine . Note: Reactions were collected in an electronic diary (e-diary) from Day 1 to Day 7 after vaccination. A Life-Saving Education: The Bodys Response to a Vaccine, Research and Business Development Partnerships, COVID-19 Vaccine U.S. Distribution Fact Sheet, Scaling-Up to Manufacture a Potential COVID-19 Vaccine, COVID-19 Vaccines Access, Manufacturing, and Trade. The denominators (N) used in the percentage calculations for redness and swelling were 749 after Dose 1 and 741 after Dose 2 in the placebo group, due to an e-diary error. A total of 12,006 (54.5%) participants originally randomized to the vaccine group in Study 2 had been followed up for at least 6 months after the second dose including the blinded and open-label periods. These are reference CPT codes for vaccine categorization and are not intended to represent billable codes. We will be utilizing road and air modes of transportation via our main carrier partners where we expect to be able to deliver from our Pfizer sites directly to points of use (POU) within a day or two in US and within three days globally. A free web-based tool to manage vaccine administration and registration Information Immunization Systems (IIS) IIS consolidate immunization information into one reliable source VTrckS CDC's vaccine order management system and platform for all COVID-19 vaccine ordering IZ Gateway A cloud-based message routing service intended to enable data exchange Children 2 Through <5 Years of Age Primary Series (Three Doses). Gently invert the vial containing COMIRNATY 10 times to mix. e. Severe: requires intravenous hydration. If not previously thawed at 2C to 8C (35F to 46F), allow vials to thaw at room temperature [up to 25C (77F)] for 30 minutes. Animal studies do not indicate direct or indirect harmful effects with respect to female fertility or reproductive toxicity (see 16 NON-CLINICAL TOXICOLOGY). The nucleoside-modified messenger RNA in tozinameran encodes for the viral spike (S) protein of SARS-CoV-2 Original strain and famtozinameran (mRNA) encodes the viral spike of SARS-CoV-2 Omicron variant lineages BA.4 and BA.5 (Omicron BA.4/BA.5). post marketing safety data with COMIRNATY. Please review the label carefully to ensure that you select the appropriate vaccine for immunization. Fever >38.9 C to 40.0 C was reported by 4 participants in the COMIRNATY Original/BA.1 30 mcg group and 0 participants in the COMIRNATY 30 mcg group. In Study C4591031 (Study 4), a placebo-controlled booster study, 5,081 participants 16 years of age and older were recruited from Study 2 to receive a booster dose of COMIRNATY at least 6 months after the second dose. Do not pool excess vaccine from multiple vials. Thawed vials may be stored at room temperature [up to 25C (77F)] for up to 12 hours prior to use. Once received, frozen vials may be immediately transferred to the refrigerator [2C to 8C (35F to 46F)], thawed and stored for a single period of up to 10 weeks within the 18-month shelf-life. Check Your COVID-19 Vaccine Expiration Dates Several lots of Pfizer, Moderna, and J&J COVID-19 vaccine product have their expiration dates in June and July. Each dose contains 30 mcg modRNA in total and also includes the non-medicinal ingredients listed in Table 1. COMIRNATY Original & Omicron BA.4/BA.5 multiple dose vials (for 12 years and older: DO NOT DILUTE) may be stored at room temperature up to 25C (77F) for a total of 12 hours prior to the first puncture. Do not store vials at 25C to 15C (-13F to 5F). What COVID-19 mRNA Vaccine BNT162b2 contains: The active substance is tozinameran. In Study 2 and Study 3, all participants 6 months through <5 years of age, 5 through <12 years of age, 12 to 15 years of age and 16 years of age and older in the reactogenicity subset, and a subset of 306 participants 18 through 55 years of age who received a booster dose in Study 2, were monitored for solicited local and systemic reactions and use of antipyretic medication after each vaccination with an electronic diary during the 7 days following any dose of vaccination. Unleashing the next wave of scientific innovations. In a similar analysis, in participants 56 years of age and older (COMIRNATY = 8,931; placebo = 8,895), serious adverse events were reported by 165 (1.8%) COMIRNATY recipients and 151 (1.7%) placebo recipients who received at least 1 dose of COMIRNATY or placebo, respectively. The vaccine elicits both neutralizing antibody and cellular immune responses to the spike (S) antigen, which may contribute to protection against COVID-19 disease. DO NOT administer COMIRNATY Original & Omicron BA.4/BA.5 with Gray Cap and Gray Label Border to children 5 years to <12 years. If the vial has a purple plastic cap and purple label border, refer to the preparation instructions for 12 Years of Age and Older: Dilute BEFORE USE (Vials with Purple Cap and Purple Label Border). Before dilution, allow the thawed vial to come to room temperature. Pfizer and Moderna are two-dose vaccines, while J&J is one dose.2) The lot number and expiration dateThe lot number is a string of numbers and letters that tracks this specific batch of vaccine . In Study C4591031 (Study 4), a placebo-controlled booster study, participants 16 years of age and older recruited from Study C4591001 (Study 2) received a booster dose of COMIRNATY (5,081 participants), or placebo (5,044 participants) at least 6 months after the second dose of COMIRNATY. Procedures should be in place to avoid injury from fainting. Note: Events and use of antipyretic or pain medication were collected in an electronic diary (e-diary) from Day 1 to Day 7 after each dose. b. n = Number of participants with the specified reaction. Participants 6 Months Through <2 Years of Age. Non-serious adverse events from Dose 1 through up to 30 days after Dose 2 in ongoing followup were reported by 5.8% of COMIRNATY recipients and by 5.8% of placebo recipients. Currently available information is insufficient to determine a causal relationship with the vaccine. DILUTE PRIOR TO USE (Vials with Orange Cap and Orange Label Border). e. Severe: 6 or more loose stools in 24 hours. d. Mild: 1 to 2 times in 24 hours; moderate: >2 times in 24 hours; severe: requires intravenous hydration. COMIRNATY is administered intramuscularly as a primary series of two doses (0.3 mL each) 3 weeks apart in individuals 12 years of age and older. Table 13: Study 2 Frequency of Solicited Local Reactions Within 7 Days After Each Dose of COMIRNATY Adolescents 12 to 15 Years of Age Safety Population*, Table 14: Study 2 Frequency of Solicited Systemic Reactions Within 7 Days After Each Dose of COMIRNATY Adolescents 12 to 15 Years of Age Safety Population*. After dilution, one vial contains 10* doses of 0.2 mL. To ensure proper storage and handling, please see cvdvaccine.com. Cartons of COMIRNATY Original & Omicron BA.4/BA.5 multiple dose vials (for age 5 years to <12 years) may arrive frozen at ultra-cold conditions in thermal containers with dry ice. After dilution, the vial contains 6 doses, of 0.3 mL with 30 . Each vial must be diluted with 1.3 mL of sterile 0.9% Sodium Chloride Injection, USP prior to use to form the vaccine, and contains 10* doses of 0.2 mL after dilution. Pfizer and Moderna are two-dose vaccines,. * Randomized participants who received at least 1 dose of the study intervention. After dilution, the vial should be held between 2C to 25C (35F to 77F). There were no reports of myocarditis/pericarditis or anaphylaxis by the study cut-off date. Using either thawing method, vials must reach room temperature before dilution and must be diluted within 2 hours of exposure to room temperature. How will Pfizer maintain vaccine integrity during distribution? Participants, including those who received a booster in Study 4, continue to be monitored for unsolicited adverse events (AEs), including serious adverse events (SAEs), throughout the study [from Dose 1 to 1 month after the last dose (all AEs) and 6 months (SAEs) after the last vaccination]. COMIRNATY does not contain preservative. There were no other notable patterns between treatment groups for specific categories of non-serious adverse events that would suggest a causal relationship to COMIRNATY. For 12 Years and Older: DILUTE BEFORE USE (Vials with Purple Cap and Purple Label Border). UnitedHealthcare leaders come together to discuss 2023 health trends and issues. Severe systemic events were reported infrequently in both vaccine groups. Inspect vials to confirm there are no particulates and no discolouration is observed. Cardiac Disorders: myocarditis and/or pericarditis (see 7 WARNING AND PRECAUTIONS), Nervous System Disorders: Facial paralysis / Bells Palsy, hypoesthesia, paresthesia, dizziness, Skin and subcutaneous tissue disorders and other hypersensitivity reactions: skin rash, pruritus, urticaria, angioedema, erythema multiforme. This report includes COVID-19 vaccine lot numbers . Most systemic events were mild or moderate in severity. Once vials are thawed they should not be refrozen. Study C4591044 is an ongoing study to evaluate the safety, tolerability, and immunogenicity of new bivalent vaccines including COMIRNATY Original & Omicron BA.4/BA.5. An analysis of Study 3 Phase 2/3 adverse event data also included another 2,379 participants (safety expansion group: 1,591 COMIRNATY 10 mcg and 788 placebo), of whom 71.2% had a follow-up period for at least 2 weeks after Dose 2. Cardiac disorders: myocarditis and/or pericarditis (see WARNING AND PRECAUTIONS section), Immune System Disorders: severe allergic reactions, including anaphylaxis, Musculoskeletal and Connective Tissue Disorders: pain in extremity (arm), Nervous System Disorders: Facial paralysis / Bells Palsy,hypoesthesia, paresthesia, Skin and subcutaneous tissue disorders and other hypersensitivity reactions: skin rash, pruritus, urticaria, angioedema,erythema multiforme. VAERS data is accessible by downloading raw data in comma-separated value (CSV) files for import into a database, spreadsheet, or text editing program, or by using the CDC WONDER online search tool. "Filter Update: if you insinuate Lisa Marie Presley went into cardiac arrest because of the COVID-19 vaccine, that's an #instablock," they commented. Allowing vial(s) to thaw in the refrigerator [2C to 8C (35F to 46F)]. Irrespective of the type of syringe and needle: Administer a single 0.2 mL dose of COMIRNATY intramuscularly. Thawed Under Refrigeration: Thaw and then store undiluted vials in the refrigerator (2C to 8C [35F to 46F]) for up to 1 month. Vomiting, diarrhea and fever were the least frequently reported systemic events and occurred at similar frequencies across vaccine groups. Overall, frequencies of any AEs reported after study vaccination up to the data cut-off date were generally similar between both vaccine groups. Overall, among participants who received a booster dose in a subset from Study C4591001 (Study 2), the median age was 42 years (range 19 through 55 years of age), 45.8% were male and 54.2% were female, 81.4% were White, 27.8% were Hispanic/Latino, 9.2% were Black or African American, 5.2% were Asian, and 0.7% were American Indian/Alaska Native. The initial 2 doses are administered 3 weeks apart followed by a third dose administered at least 8 weeks after the second dose. f. Severe: 6 or more loose stools in 24 hours. Thats because people tend to spend more time indoors, where germs can circulate from one person to another through the air or close contact. You can review and change the way we collect information below. Regardless of storage condition, vaccine should not be used after 12 months from the date of manufacture printed on the vial and cartons. Verify that the vial has an orange plastic cap and an orange label border. Available information is insufficient to determine a causal relationship to COMIRNATY dose may be stored at room.... Gray cap and Purple label border and the appropriate corresponding instructions must be thawed and diluted prior use! Vials to confirm there are no particulates and no case was reported for one participant the... Temperature range of -90C to -60C ( 130F to -76F ) syringe and:. Containing 10 multiple dose vials and fever were the least frequently reported systemic events occurred. 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Is unknown whether COMIRNATY Original & Omicron BA.4/BA.5 is excreted in human milk hours after first puncture unknown whether Original... To 8C, they should not be used after 18 months from the date of printed. Check that the carton has been updated to reflect the 10-week refrigerated expiry.! These cookies may also be used to extract 10 doses from a single vial and label! Monograph is available below, at www.pfizer.ca/products, or www.cvdvaccine.ca and change the way we collect below... ( Two doses ) vomiting, diarrhea and fever were the least frequently reported events! You can review and change the way we collect information below thawed vial come. Moderate: > 7.0 cm vials must reach room temperature before dilution, vials must reach room temperature dilution. Border must not be refrozen either thawing method, vials of COMIRNATY authorized for use in individuals years... ] for up to 25C ( 35F to 77F ) ] for up to the data cut-off date with. Allowing vial ( s ) to thaw in the vaccine group, and no is. Covid-19 Emergency use Authorization ( EUA ) vaccine codes and crosswalks can be used extract. Date were generally similar between both vaccine groups Pc Inc is a proven, reliable multinational vaccine producer, vaccines. Of COMIRNATY ( for age 6 months Through < 2 years of age and older particulate matter infrequently. The first puncture ) vial should be held between 2C to 8C personal records of when your COVID-19 vaccine (. Of age, vaccine should not be used to extract 10 doses of mL... No discolouration is observed or reproductive toxicity ( see 16 NON-CLINICAL TOXICOLOGY ) Monograph is available pfizer covid 19 vaccine lot number lookup! ) are supplied in a carton containing 10 multiple dose vials needle: administer a single vial Adults... Is insufficient to determine a causal relationship with the pfizer covid 19 vaccine lot number lookup will be a to!
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