Winter weather slows delivery of vaccine doses across US | WNT

Vaccinations have been postponed or cancelled in at least 40 states due to weather. In other news, Pfizer announced it is testing its vaccine on pregnant women around the world.

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28 thoughts on “Winter weather slows delivery of vaccine doses across US | WNT

  1. CRAZY…. Vaccines typically contain many of the following fillers:

    aluminum hydroxide * aluminum phosphate * ammonium sulfate * amphotericin B * animal tissues: pig blood, horse blood, rabbit brain, * dog kidney, monkey kidney, * chick embryo, chicken egg, duck egg * calf (bovine) serum * betapropiolactone * fetal bovine serum * formaldehyde * formalin * gelatin * glycerol * human diploid cells (originating from human aborted fetal tissue) * hydrolized gelatin * mercury thimerosol (thimerosal, Merthiolate(r)) * monosodium glutamate (MSG) * neomycin * neomycin sulfate * phenol red indicator * phenoxyethanol (antifreeze) * potassium diphosphate * potassium monophosphate * polymyxin B * polysorbate 20 * polysorbate 80 * porcine (pig) pancreatic hydrolysate of casein * residual MRC5 proteins * sorbitol * tri(n)butylphosphate, * VERO cells, a continuous line of monkey kidney cells, and * washed sheep red blood.
    Common sense and a thinking brain will clearly tell people/parents, that most of these are ingredients that are not safe ( and at the very least questionable) for injection into the body, let alone the vaccine dose schedule suggested for babies and children. Does anyone really want these chemicals, animal and insect DNA injected directly into their blood stream?

  2. Testing on Pregnant Women! Vaccines typically contain many of the following fillers:

    aluminum hydroxide * aluminum phosphate * ammonium sulfate * amphotericin B * animal tissues: pig blood, horse blood, rabbit brain, * dog kidney, monkey kidney, * chick embryo, chicken egg, duck egg * calf (bovine) serum * betapropiolactone * fetal bovine serum * formaldehyde * formalin * gelatin * glycerol * human diploid cells (originating from human aborted fetal tissue) * hydrolized gelatin * mercury thimerosol (thimerosal, Merthiolate(r)) * monosodium glutamate (MSG) * neomycin * neomycin sulfate * phenol red indicator * phenoxyethanol (antifreeze) * potassium diphosphate * potassium monophosphate * polymyxin B * polysorbate 20 * polysorbate 80 * porcine (pig) pancreatic hydrolysate of casein * residual MRC5 proteins * sorbitol * tri(n)butylphosphate, * VERO cells, a continuous line of monkey kidney cells, and * washed sheep red blood.
    Common sense and a thinking brain will clearly tell people/parents, that most of these are ingredients that are not safe ( and at the very least questionable) for injection into the body, let alone the vaccine dose schedule suggested for babies and children. Does anyone really want these chemicals, animal and insect DNA injected directly into their blood stream?

  3. 501 deaths + 10,748 other injuries reported following COVID vaccine, latest CDC data show

    The numbers reflect the latest data available as of Jan. 29 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453 were from the U.S. The average age of those who died was 77, the youngest was 23.

    Fri Feb 5, 2021 – 9:56 pm EST

    By Children’s Health Defense

    February 5, 2021 (Children’s Health Defense) — As of Jan. 29, 501 deaths — a subset of 11,249 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between Dec. 14, 2020, and Jan. 29, 2021.

    VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

    As of Jan. 29, about 35 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental.
    According to the latest data, 453 of the 501 reported deaths were in the U.S. Fifty-three percent of those who died were male, 43% were female, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest reported death was of a 23-year-old. The Pfizer vaccine was taken by 59% of those who died, while the Moderna vaccine was taken by 41%.

    The latest data also included 690 reports of anaphylactic reactions to either the Pfizer or Moderna vaccines. Of those, the Pfizer vaccine accounted for 76% of the reactions, and the Moderna vaccine for 24%.

    As The Defender reported today, a 56-year-old woman in Virginia died Jan. 30, hours after receiving her first dose of the Pfizer vaccine. Doctors told Drene Keyes’ daughter that her mother died of flash pulmonary edema likely caused by anaphylaxis. The death is under investigation by Virginia’s Office of the Chief Medical Examiner and the CDC.

    Last week, the CDC told USA TODAY that based on “early safety data from the first month” of COVID-19 vaccination the vaccines are “as safe as the studies suggested they’d be” and that “everyone who had experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated.

    Other vaccine injury reports updated this week on VAERS include 139 cases of facial asymmetry, or Bell’s palsy type symptoms, and 13 miscarriages.

    The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (20 deaths), 037K20A (21 deaths) and 011J2A (16 deaths), 025J20A (16 deaths) . For Pfizer, the lot numbers associated with the most reports of deaths were: EK5730 (10 deaths), EJ1685 (23 deaths), EL0140 (19 deaths), EK 9231 (17 deaths) and EL1284 (13 deaths). For 135 of the reported deaths, the lot numbers were unknown.

    The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

    While the VAERS database numbers are sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.

    According to the VAERS website, healthcare providers are required by law to report to VAERS:

    • Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination

    • An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine

    • The CDC says healthcare providers are strongly encouraged to report:

    • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event

    • Vaccine administration errors

    • However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.

    • Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

    • Historically, fewer than fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure,” including in a December 2020 letter to Dr. David Kessler, former FDA director and now co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed.

    A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

    CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.

    Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

    © February 5, 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

    LifeSiteNews has produced an extensive COVID-19 vaccines resources page. View it here.

  4. 501 deaths + 10,748 other injuries reported following COVID vaccine, latest CDC data show

    The numbers reflect the latest data available as of Jan. 29 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453 were from the U.S. The average age of those who died was 77, the youngest was 23.

    Fri Feb 5, 2021 – 9:56 pm EST

    By Children’s Health Defense

    February 5, 2021 (Children’s Health Defense) — As of Jan. 29, 501 deaths — a subset of 11,249 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between Dec. 14, 2020, and Jan. 29, 2021.

    VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

    As of Jan. 29, about 35 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental.
    According to the latest data, 453 of the 501 reported deaths were in the U.S. Fifty-three percent of those who died were male, 43% were female, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest reported death was of a 23-year-old. The Pfizer vaccine was taken by 59% of those who died, while the Moderna vaccine was taken by 41%.

    The latest data also included 690 reports of anaphylactic reactions to either the Pfizer or Moderna vaccines. Of those, the Pfizer vaccine accounted for 76% of the reactions, and the Moderna vaccine for 24%.

    As The Defender reported today, a 56-year-old woman in Virginia died Jan. 30, hours after receiving her first dose of the Pfizer vaccine. Doctors told Drene Keyes’ daughter that her mother died of flash pulmonary edema likely caused by anaphylaxis. The death is under investigation by Virginia’s Office of the Chief Medical Examiner and the CDC.

    Last week, the CDC told USA TODAY that based on “early safety data from the first month” of COVID-19 vaccination the vaccines are “as safe as the studies suggested they’d be” and that “everyone who had experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated.

    Other vaccine injury reports updated this week on VAERS include 139 cases of facial asymmetry, or Bell’s palsy type symptoms, and 13 miscarriages.

    The Moderna vaccine lot numbers associated with the highest number of deaths were: 025L20A (20 deaths), 037K20A (21 deaths) and 011J2A (16 deaths), 025J20A (16 deaths) . For Pfizer, the lot numbers associated with the most reports of deaths were: EK5730 (10 deaths), EJ1685 (23 deaths), EL0140 (19 deaths), EK 9231 (17 deaths) and EL1284 (13 deaths). For 135 of the reported deaths, the lot numbers were unknown.

    The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

    While the VAERS database numbers are sobering, according to a U.S. Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.

    According to the VAERS website, healthcare providers are required by law to report to VAERS:

    • Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination

    • An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine

    • The CDC says healthcare providers are strongly encouraged to report:

    • Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether or not it is clear that a vaccine caused the adverse event

    • Vaccine administration errors

    • However, “within the specified time” means that reactions occurring outside that timeframe may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare provider.

    • Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

    • Historically, fewer than fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense has previously referred to as an “abject failure,” including in a December 2020 letter to Dr. David Kessler, former FDA director and now co-chair of the COVID-19 Advisory Board and President Biden’s version of Operation Warp Speed.

    A critic familiar with VAERS’ shortcomings bluntly condemned VAERS in The BMJ as “nothing more than window dressing, and a part of U.S. authorities’ systematic effort to reassure/deceive us about vaccine safety.”

    CHD is calling for complete transparency. The children’s health organization is asking Kessler and the federal government to release all of the data from the clinical trials and suspend COVID-19 vaccine use in any group not adequately represented in the clinical trials, including the elderly, frail and anyone with comorbidities.

    Children’s Health Defense asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.

    © February 5, 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.

    LifeSiteNews has produced an extensive COVID-19 vaccines resources page. View it here.

  5. willing to shove this crap in your body, when u have no idea, what the side effects are, it takes 20 years to know this, well big parma, loves you all that take it, they will make all the cashola, they set out to make, ohhhh, and no matter what u CANNOT sue them~

  6. DEAR AMERICA🌹OUR (:GRANDMAS GRANDPAS, MOMS ) AND DADS DIED R.I.P🌹IN ( NURSING HOMES, ASSIST LIVING COMMUNITIES ) AND ( SOCIAL SERVICES ) HOME CARE ACROSS THIS NATION FROM THE VIRUS 🤑 AND VACCINES 🤮 THE NUMBER OF DEATHS FROM THE VACCINES NOR IT'S LONG-TERM EFFECTS HAS BEEN READILY REPORTED OR MADE PUBLIC TO THE AMERICAN PEOPLE 🤔 I BLAME THE FEDERAL GOVERNMENT ( GLOBALIST ) BILL GATES DEPOPULATION AGENDA 2021 😭 THEY HAVE TOUCHED THE ( HEART ) OF THE MOST HIGH GOD ( MANKIND )🌹HIS JUDGEMENT IS HERE AND HIS WRATH IS SURE 🎯

  7. EMERGENCY USE AUTHORIZATION (EUA) OF THE MODERNA COVID-19 VACCINE FACT SHEET
    https://www.fda.gov/media/144638/download
    https://www.modernatx.com/covid19vaccine-eua/recipients/
    1, It is your choice to receive or not receive the Moderna COVID-19 Vaccine. Should you decide not to receive it, it will not change your standard medical care.

    2, The Moderna COVID-19 Vaccine is an unapproved vaccine.

    3, The Moderna COVID-19 Vaccine has not undergone the same type of review as an FDA- approved or cleared product.

    4, "The Moderna COVID-19 Vaccine may not protect everyone"

    5, The duration of protection against COVID-19 is currently unknown

    6, "A severe allergic reaction would usually occur within a few minutes to one hour after getting a dose of the Moderna COVID-19 Vaccine" Signs of a severe allergic reaction can include:
    •Difficulty breathing
    •Swelling of your face and throat
    •A fast heartbeat
    •A bad rash all over your body
    •Dizziness and weakness

    These may not be all the possible side effects of the Moderna COVID-19 Vaccine. Serious and unexpected side effects may occur. The Moderna COVID-19 Vaccine is still being studied in clinical trials

    7, Call 9-1 -1, or go to the nearest hospital If you experience a severe allergic reaction

    8, The EUA for the Moderna COVID-19 Vaccine is in effect for the duration of the COVID-19 EUA declaration justifying emergency use of these products, unless terminated or revoked (after which the products may no longer be used).

  8. We need to do the nation, for free, a favor and create our own solutions, too. Vaccines shouldn’t be the only solution in our country. We the people had done it before without congress’ approval. We just need the entire nation to agree to do the nation, for free, a favor. If the trains and train tracks and roads and houses and a bunch of other things were built for free when this nation was built, and The White House was also built by people for free, we need to create something as a nation for free. Like when the nation was just born.

  9. The Biden Administration is Adam Bull-Schiffing the beautimous vaccination plan the Trump Administration laid out for them. It would have helped if old Joe would have waited to donate his brain to Science until after he no longer needed it.

  10. "Winter weather slows delivery of (Covid) vaccine doses across US" thereby motivating us, the people of America, to redouble our efforts to rapidly find out at any given moment, including even while On-Line, who among us are unwittingly contagious (i.e. pre-symptomatic or asymptomatic) in order to #ConvinceItForward for them to call their doctor and to self-quarantine per CDC guidelines in hopes of stopping this pandemic instead of having more #MourningInAmerica. Thus, we're hoping for the best while preparing for the worse-case scenario of the #UKvariant strain(s) mutations and others like the South African, Brazilian, Californian & #Cluster5Mink mutations rendering current vaccines no longer effective.

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