A VIS یا Vaccine Information Statement یک سند است که توسط CDC تهیه شده و دریافتکنندگان واکسن - یا والدین یا نمایندگان قانونی آنها - را در مورد فواید و خطرات واکسنی که دریافت میکنند، آگاه میسازد. تمام ارائهدهندگان واکسن، دولتی یا خصوصی، طبق قانون آسیبهای دوران کودکی ناشی از واکسن https://www.govinfo.gov/content/pkg/USCODE-2010-title42/pdf/USCO
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07/29/2026
Supporting Files
Centers for Disease Control and Prevention (U.S.) (2021). واکسن MMRV (سرخک، اوریون، سرخجه و آبلهمرغان): آنچه باید بدانید [2021].
Centers for Disease Control and Prevention (U.S.) "واکسن MMRV (سرخک، اوریون، سرخجه و آبلهمرغان): آنچه باید بدانید [2021]" (2021)
Centers for Disease Control and Prevention (U.S.) "واکسن MMRV (سرخک، اوریون، سرخجه و آبلهمرغان): آنچه باید بدانید [2021]" , 2021
A VIS یا Vaccine Information Statement یک سند است که توسط CDC تهیه میشود و دریافتکنندگان واکسن - یا والدین یا نمایندگان قانونی آنان - را در مورد فواید و خطرات واکسنی که دریافت میکنند، آگاه میسازد. همه ارائهدهندگان واکسن، چه دولتی و چه خصوصی، مطابق با قانون صدمات دوران کودکی ناشی از واکسن https://www.govinfo.gov/content/pkg/USCODE-2010-title42/
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07/29/2026
Supporting Files
Centers for Disease Control and Prevention (U.S.) (2021). واکسن MMRV (سرخک، اوریون، سرخجه و چیچک): آنچه باید بدانید [2021].
Centers for Disease Control and Prevention (U.S.) "واکسن MMRV (سرخک، اوریون، سرخجه و چیچک): آنچه باید بدانید [2021]" (2021)
Centers for Disease Control and Prevention (U.S.) "واکسن MMRV (سرخک، اوریون، سرخجه و چیچک): آنچه باید بدانید [2021]" , 2021
A VIS বা Vaccine Information Statement হল CDC কর্তৃক প্রস্তুত একটি নথি, যা টিকা গ্রহণকারীদের - অথবা তাদের বাবা-মা বা আইনগত প্রতিনিধিদের - তারা যে টিকা গ্রহণ করছেন তার উপকারিতা এবং ঝুঁকি সম্পর্কে জানায়। সকল টিকা প্রদানকারী, সরকারি বা বেসরকারি, National Vaccine Childhood Injury Act https://www.govinfo.gov/content/pkg/USCODE-2010-title42/pdf/USCODE-2
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07/29/2026
Supporting Files
Centers for Disease Control and Prevention (U.S.) (2021). MMRV টিকা (হাম, মাম্পস, রুবেলা এবং জলবসন্ত): আপনার জানা প্রয়োজন [2021].
Centers for Disease Control and Prevention (U.S.) "MMRV টিকা (হাম, মাম্পস, রুবেলা এবং জলবসন্ত): আপনার জানা প্রয়োজন [2021]" (2021)
Centers for Disease Control and Prevention (U.S.) "MMRV টিকা (হাম, মাম্পস, রুবেলা এবং জলবসন্ত): আপনার জানা প্রয়োজন [2021]" , 2021
A VIS կամ Պատվաստանյութի տեղեկատվական հայտարարություն CDC-ի կողմից մշակված փաստաթուղթ է, որը տեղեկացնում է պատվաստանյութ ստացողներին - կամ նրանց ծնողներին կամ օրինական ներկայացուցչին - այն պատվաստանյութի օգուտների և ռիսկերի մասին, որը նրանք ստանում են։ Բոլոր պատվաստանյութ տրամադրողները, պետական թե մասնավոր, պարտավոր են՝ ըստ Պատվաստանյութերից երեխան
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07/29/2026
Supporting Files
Centers for Disease Control and Prevention (U.S.) (2021). MMRV պատվաստանյութ (կարմրախտ, խոզակ, կարմրուկ և ջրծաղիկ). Ինչ է անհրաժեշտ לדעת [2021].
Centers for Disease Control and Prevention (U.S.) "MMRV պատվաստանյութ (կարմրախտ, խոզակ, կարմրուկ և ջրծաղիկ). Ինչ է անհրաժեշտ לדעת [2021]" (2021)
Centers for Disease Control and Prevention (U.S.) "MMRV պատվաստանյութ (կարմրախտ, խոզակ, կարմրուկ և ջրծաղիկ). Ինչ է անհրաժեշտ לדעת [2021]" , 2021
July 30, 2026
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Surveillance Summaries: Morbidity and Mortality Weekly Report (MMWR)
Invasive mold diseases (IMDs) are rare, life-threatening infections that primarily affect persons with immunocompromising conditions. The most common molds associated with IMDs are Aspergillus spp., Mucorales (e.g., Mucor spp., Rhizomucor spp., and Rhizopus spp.), Fusarium spp., and Scedosporium spp. IMDs can affect the lungs, sinuses, skin, centra
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07/29/2026
"Morbidity and Mortality Weekly" (2026). Morbidity and Mortality Weekly Report (MMWR): Surveillance Summaries. 75(5).
"Morbidity and Mortality Weekly Report (MMWR): Surveillance Summaries / Vol. 75 / No. 5, July 30, 2026" Morbidity and Mortality Weekly Report (MMWR): Surveillance Summaries 75, no. 5 (2026)
"Morbidity and Mortality Weekly Report (MMWR): Surveillance Summaries / Vol. 75 / No. 5, July 30, 2026" Morbidity and Mortality Weekly Report (MMWR): Surveillance Summaries, vol. 75, no. 5, 2026
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division
2026/07/01
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National Center for Immunization and Respiratory Diseases (NCIRD)
Proper vaccine storage and handling practices are essential for protecting patients by ensuring product efficacy and quality, preventing unnecessary revaccination, minimizing vaccine wastage, and ensuring a viable vaccine supply. Ultimately, adhering to vaccine storage and handling guidelines helps improve patients' health by preventing disease.The
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07/28/2026
CurrentSupporting Files
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division (2026). Vaccine Storage and Handling Toolkit Addendum: for SNS-suppled Jynneos [2026/07].
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit Addendum: for SNS-suppled Jynneos [2026/07]" (2026)
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit Addendum: for SNS-suppled Jynneos [2026/07]" , 2026
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division
2026/07/01
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National Center for Immunization and Respiratory Diseases (NCIRD)
Proper vaccine storage and handling practices are essential for protecting patients by ensuring product efficacy and quality, preventing unnecessary revaccination, minimizing vaccine wastage, and ensuring a viable vaccine supply. Ultimately, adhering to vaccine storage and handling guidelines helps improve patients' health by preventing disease.The
...
07/28/2026
CurrentSupporting Files
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division (2026). Vaccine Storage and Handling Toolkit: Key Resources [2026/07].
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit: Key Resources [2026/07]" (2026)
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit: Key Resources [2026/07]" , 2026
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division
2026/07/01
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National Center for Immunization and Respiratory Diseases (NCIRD)
Proper vaccine storage and handling practices are essential for protecting patients by ensuring product efficacy and quality, preventing unnecessary revaccination, minimizing vaccine wastage, and ensuring a viable vaccine supply. Ultimately, adhering to vaccine storage and handling guidelines helps improve patients' health by preventing disease.The
...
07/28/2026
CurrentSupporting Files
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division (2026). Vaccine Storage and Handling Toolkit [2026/07].
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit [2026/07]" (2026)
Centers for Disease Control and Prevention (CDC) (U.S.). National Center for Immunization and Respiratory Diseases. Immunization Services Division "Vaccine Storage and Handling Toolkit [2026/07]" , 2026
Centers for Disease Control (U.S.). Food and Drug Administration
2010
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H1N1 Flu Update
Special VAERS update detailing an increased signal of febrile seizure reports in children aged 6-23 months following Fluzone TIV vaccination, including case characteristics, timing, severity, and no changes to vaccine recommendations.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2010). UPDATE: Vaccine Adverse Event Reporting System (VAERS) Data on Febrile Seizures after Vaccination with Fluzone®, a 2010-2011 Trivalent Inactivated Vaccine, in Children: Data through December 13, 2010.
Centers for Disease Control (U.S.). Food and Drug Administration "UPDATE: Vaccine Adverse Event Reporting System (VAERS) Data on Febrile Seizures after Vaccination with Fluzone®, a 2010-2011 Trivalent Inactivated Vaccine, in Children: Data through December 13, 2010" (2010)
Centers for Disease Control (U.S.). Food and Drug Administration "UPDATE: Vaccine Adverse Event Reporting System (VAERS) Data on Febrile Seizures after Vaccination with Fluzone®, a 2010-2011 Trivalent Inactivated Vaccine, in Children: Data through December 13, 2010" , 2010
Centers for Disease Control (U.S.). Food and Drug Administration
2016
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H1N1 Flu Update
Season overview listing 2016-17 vaccine types, ACIP vote against LAIV use for the season, newly licensed Fluad and expanded Flublok approval, febrile seizure information, and VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2016). 2016-2017 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2016-2017 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2016)
Centers for Disease Control (U.S.). Food and Drug Administration "2016-2017 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2016
Centers for Disease Control (U.S.). Food and Drug Administration
2015
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H1N1 Flu Update
Season overview listing 2015-16 vaccine types, ACIP removal of LAIV preferential recommendation for children, LAIV warnings/precautions, egg-allergy guidance, febrile seizure information, and VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2015). 2015-2016 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2015-2016 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2015)
Centers for Disease Control (U.S.). Food and Drug Administration "2015-2016 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2015
Centers for Disease Control (U.S.). Food and Drug Administration
2014
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H1N1 Flu Update
Season overview noting unchanged 2014-15 vaccine formulation from prior year, describing available vaccine types (IIV3, IIV4, LAIV, cell-based, recombinant), egg-allergy guidance, febrile seizure monitoring history, and VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2014). 2014-2015 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2014-2015 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2014)
Centers for Disease Control (U.S.). Food and Drug Administration "2014-2015 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2014
Centers for Disease Control (U.S.). Food and Drug Administration
2013
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H1N1 Flu Update
Season overview describing the expanded range of 2013-14 influenza vaccines (IIV3, IIV4, LAIV, cell-based, recombinant), egg-allergy guidance, febrile seizure monitoring history and findings through 2012-13, and VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2013). 2013-2014 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2013-2014 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2013)
Centers for Disease Control (U.S.). Food and Drug Administration "2013-2014 Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2013
Centers for Disease Control (U.S.). Food and Drug Administration
2012
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H1N1 Flu Update
Season overview describing 2012-13 vaccine formulation changes, available vaccine types (TIV, Fluzone High Dose, LAIV, intradermal), follow-up on 2010-11 febrile seizure study findings, egg-allergy vaccination guidance, and VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2012). 2012-2013 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2012-2013 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2012)
Centers for Disease Control (U.S.). Food and Drug Administration "2012-2013 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2012
Centers for Disease Control (U.S.). Food and Drug Administration
March 7, 2011
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H1N1 Flu Update
Monthly VAERS summary of adverse event reports following 2010-2011 trivalent influenza vaccination, including counts of serious events, deaths, GBS, and febrile seizure signal in children, as of January 25, 2011.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2011). Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System :Data through Jan. 25, 2011.
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System :Data through Jan. 25, 2011" (2011)
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System :Data through Jan. 25, 2011" , 2011
Centers for Disease Control (U.S.). Food and Drug Administration
January 21, 2011
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H1N1 Flu Update
Monthly VAERS summary of adverse event reports following 2010-2011 trivalent influenza vaccination, including counts of serious events, deaths, GBS, and febrile seizure signal in children, as of December 14, 2010.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2011). Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System:Data through December 14, 2010.
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System:Data through December 14, 2010" (2011)
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System:Data through December 14, 2010" , 2011
Centers for Disease Control (U.S.). Food and Drug Administration
February 4, 2010
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H1N1 Flu Update
Monthly VAERS summary of adverse event reports following 2010-2011 trivalent influenza vaccination, including counts of serious events, deaths, GBS, and febrile seizure signal in children, as of December 28, 2010.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2010). Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through December 28, 2010.
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through December 28, 2010" (2010)
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through December 28, 2010" , 2010
Centers for Disease Control (U.S.). Food and Drug Administration
April 5, 2010
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H1N1 Flu Update
Monthly VAERS summary of adverse event reports following 2010-2011 trivalent influenza vaccination, including counts of serious events, deaths, GBS, and febrile seizure signal in children, as of February 25, 2011.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2010). Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through Feb. 25, 2011.
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through Feb. 25, 2011" (2010)
Centers for Disease Control (U.S.). Food and Drug Administration "Summary of 2010-2011 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System: Data through Feb. 25, 2011" , 2010
Centers for Disease Control (U.S.). Food and Drug Administration
2011
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H1N1 Flu Update
Season overview noting the 2011-12 vaccine formulation is unchanged from 2010-11, describes available vaccine types (TIV, LAIV, new intradermal product), references prior season's febrile seizure signal, and provides VAERS WONDER search instructions.
07/28/2026
Centers for Disease Control (U.S.). Food and Drug Administration (2011). 2011-2012 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS).
Centers for Disease Control (U.S.). Food and Drug Administration "2011-2012 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" (2011)
Centers for Disease Control (U.S.). Food and Drug Administration "2011-2012 Trivalent Influenza Vaccine Data from the U.S. Vaccine Adverse Event Reporting System (VAERS)" , 2011
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