CDC Signs Off on COVID Vaccine Boosters for Kids Ages 5–11
Video Credit: Wibbitz Top Stories - Duration: 01:31s - Published
CDC Signs Off on COVID Vaccine Boosters for Kids Ages 5–11
CDC Signs Off on COVID Vaccine Boosters , for Kids Ages 5–11.
CNN reports that on May 19, the CDC's
Advisory Committee on Immunization Practices (ACIP)... .
... voted in support of recommending an additional Pfizer shot for 5- to 11-year-olds who've received their first two doses.
The vote was 11-1 with 1 abstention.
CNN reports that the FDA authorized
the booster dose earlier this week.
Children within this age group are advised to wait at least five months after receiving their two-dose regimen before getting a booster shot.
CNN reports a fourth dose is recommended for children who are immunocompromised.
.
According to Pfizer, a trial of 4,500 children ages 5-11 showed Omicron-fighting antibodies were 36 times stronger upon receiving a booster.
The company also says
no new safety issues were detected.
On May 16, the American Academy of Pediatrics reported that COVID cases in U.S. children rose 76%
the previous week compared to two weeks prior.
CDC Director Dr. Rochelle Walensky gave opening remarks before the ACIP's vote.
The sadness I feel for
lives lost, the families
devastated and the
communities changed
is steep.
We have the
tools we need to protect
these people from severe
disease and prevent any
more tragic deaths, Dr. Rochelle Walensky, via opening remarks
before the ACIP's vote, via CNN
COVID is now an "inconvenience" for most people rather than "life-threatening", the World Health Organisation's special envoy on the virus has told Sky News. Sky News
In last 24 hours, 21 people died of Covid in India. Maharashtra witnessed 5 deaths, 4 people died in Delhi while 6 deaths were reported from Kerala. DNA
Pfizer’s COVID Booster Shot , for 5 to 11 Year Olds, Authorized by FDA.
NBC News reports on May 17, the Food
and Drug Administration (FDA)...
… announced it had authorized Pfizer-BioNTech's coronavirus
booster dose for 5 to 11 year olds.
The FDA says eligible recipients of a booster dose could receive the extra shot starting five months after their initial two-dose series.
Per NBC News, Pfizer's booster shot for
5 to 11 year olds is 10 micrograms ... .
... a third of the dosage given
to citizens 12 and older.
Following the FDA's ruling, it is now up
to the Centers for Disease Control and Prevention (CDC) to recommend how to implement boosters for the age group.
CDC data shows less than one third
of 5 to 11 year olds in the United States
have recieved the primary series of
a COVID-19 vaccine.
Experts say booster shots offer
better protection against the omicron
strain and its associated subvariants.
The CDC's Advisory Committee on Immunization Practices will reportedly discuss booster shots on May 19.
Dr. Rochelle Walensky, the Director of the CDC, should have her final recommendation following the committee's discussion
Credit: Wibbitz Top Stories Duration: 01:30Published
CDC Warns of COVID 'Rebound' , After Taking Paxlovid.
Paxlovid can be prescribed for those who may have a high risk of being hospitalized with COVID. .
But CDC Director Dr. Rochelle Walensky recently revealed that those who take it can have "rebound" symptoms.
If you take Paxlovid, you might get symptoms again, Dr. Rochelle Walensky, CDC Director,
via CBS News.
We haven't yet seen anybody who has returned with symptoms needing to go to the hospital. , Dr. Rochelle Walensky, CDC Director,
via CBS News.
So, generally, a milder course, Dr. Rochelle Walensky, CDC Director,
via CBS News.
Dr. Walensky maintains that the drug is useful in
preventing COVID illness that requires hospitalization.
Data from the CDC shows that Paxlovid prevents death and hospitalization for unvaccinated COVID patients by up to 90 percent.
Health officials are unsure as to the cause of COVID rebound in patients who have taken Paxlovid.
One health official described their experience with contracting COVID, taking the drug and getting sick again.
I was totally shocked. I did not expect that. , Dr. David Ho, Infectious Disease Expert,
via CBS News.
And that's because I had tested negative six consecutive days, including two PCR, Dr. David Ho, Infectious Disease Expert,
via CBS News.
In order to prevent infecting others,
Dr. Walensky says that those who experience COVID rebound should take standard virus precautions.
They should test. They should put their mask back on. , Dr. Rochelle Walensky, CDC Director,
via CBS News.
And if their test is positive,
restart the isolation protocol, Dr. Rochelle Walensky, CDC Director,
via CBS News
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CDC Says One-Third of Americans , Should Be Wearing Masks.
CNN reports that the U.S. Centers for Disease Control and Prevention (CDC) is urging local officials to encourage their constituents to mask up.
Currently, over 32% of Americans live
in regions experiencing medium to high
COVID-19 community levels.
Per CDC data, 9% of Americans live in areas with high COVID-19 community levels.
23% of citizens are currently living
in areas with a medium amount of
coronavirus transmission.
We urge local leaders to
encourage the use of prevention strategies like masking in public indoor settings and increasing
access to testing and to treatment. , Dr. Rochelle Walensky, CDC Director, via CNN.
In areas where community levels are high, everyone should be using prevention measures and wearing a mask in public indoor settings. , Dr. Rochelle Walensky, CDC Director, via CNN.
As of May 18, nearly 4.25% of counties in the
United States have soaring COVID-19 community levels. .
As we’re currently seeing
a steady rise of cases in parts of the country... , Dr. Rochelle Walensky, CDC Director, via CNN.
... we encourage everyone
to use the menu of tools we have today to prevent further infection and severe disease, , Dr. Rochelle Walensky, CDC Director, via CNN.
... including wearing a mask, getting tested, accessing treatments early if infected and getting vaccinated or boosted, Dr. Rochelle Walensky, CDC Director, via CNN
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Increase in US COVID Rates , Prompts Health Officials
to Urge Mask-Wearing, in Some Areas.
Federal health officials presented an assessment from the White House on May 18.
Speaking were Dr. Ashish Jha, the
White House COVID response coordinator, .
and Dr. Rochelle P. Walensky, the director of the Centers for Disease Control and Prevention (CDC).
We urge local leaders to encourage the use of prevention strategies like masking in public indoor settings.., Dr. Rochelle P. Walensky, CDC Director,
via 'The New York Times'.
... and increasing access to testing and treatment
for individuals, Dr. Rochelle P. Walensky, CDC Director,
via 'The New York Times'.
The COVID briefing was the first to be conducted from the White House in six weeks.
According to federal data, hospital admissions related to COVID have increased by 20 percent over the past week.
The Northeastern U.S. has experienced the most dramatic increase in cases.
Dr. Jha urged Congress to approve additional COVID aid to address the rising cases and a potential wave in the fall.
Experts weighed in, stating that now is a good time
to reimplement prevention measures.
We’re seeing rising cases and hospitalizations and testing positivity rates; now is not the time to end these flexibilities that allow great access to care, Ashley Thompson, American Hospital Association, via 'The New York Times'.
We are not out of the woods yet, Ashley Thompson, American Hospital
Association, via 'The New York Times'.
We could be entering a period where we have an increased number of cases but a substantially decreased severity of illness, Dr. Michael T. Osterholm, University of Minnesota,
via 'The New York Times'.
... so that we see fewer hospitalizations and many
fewer deaths, Dr. Michael T. Osterholm, University of Minnesota,
via 'The New York Times'
Credit: Wibbitz Top Stories Duration: 01:30Published
FDA Panel , Endorses
COVID Vaccines, for Children Under 5.
On June 15, an advisory panel to the United States
Food and Drug Administration voted to recommend
two COVID-19 vaccines for kids ages 5 and under.
Yahoo reports that both Pfizer/BioNTech
and Moderna were under review by the panel. .
The unanimous FDA panel vote
is the first step in what is predicted
to be a quick authorization process.
According to Yahoo, data from trials shows
that both vaccines continue to protect against severe disease, hospitalization and death.
According to Yahoo, data from trials shows
that both vaccines continue to protect against severe disease, hospitalization and death.
Yahoo reports that parents now
have two options for how
to vaccinate their children.
Pfizer's vaccine for kids is delivered in three,
three-microgram doses, while Moderna's vaccine
is delivered in two shots of a 25-microgram dose.
Our robust clinical study shows that
three doses can provide protection for
the circulating Omicron variant and
offers promise for protection against
potential future waves of COVID-19, Dr. Bill Gruber, Pfizer's Vaccine Clinical Research
and Development head, via Yahoo.
Our robust clinical study shows that
three doses can provide protection for
the circulating Omicron variant and
offers promise for protection against
potential future waves of COVID-19, Dr. Bill Gruber, Pfizer's Vaccine Clinical Research
and Development head, via Yahoo.
The committee’s support today
is imperative to providing a critical tool
for pediatricians, parents, and caregivers
who eagerly await an option
for children under five, Dr. Bill Gruber, Pfizer's Vaccine Clinical Research and Development head, via Yahoo.
Both companies are now awaiting approval from
the FDA and the CDC which will hold an advisory
committee meeting on the topic over the weekend.
Credit: Wibbitz Top Stories Duration: 01:30Published
Anthony Fauci, Tests Positive
for COVID.
The National Institute of Allergy and Infectious Diseases (NIAID) released a statement on
Dr. Fauci's positive COVID test on June 15.
He is currently experiencing
mild symptoms, NIAID, via statement.
The statement specified that Fauci "is fully vaccinated and has been boosted twice.".
Dr. Fauci's diagnosis was confirmed by a rapid antigen test. He is being treated with Paxlovid.
Dr. Fauci is the Chief Medical Advisor
to President Joe Biden.
He has not recently been in contact
with the president.
He has not recently been in close contact with President Biden or other senior government officials, NIAID, via statement.
The NIAID statement also specified how he will approach the coming days.
Dr. Fauci will follow the COVID-19 guidelines of the Centers for Disease Control and Prevention and medical advice from his physician and return to the NIH when he tests negative, NIAID, via statement.
Fauci has consistently urged caution when faced with social encounters.
Each of us, in our own personal way, has to make an assessment of what risk you’re willing to accept about getting infected, Anthony Fauci, via CNN.
He recently declined attendance at the White House Correspondents' Dinner.
In general, the risk is low, but I made a personal assessment. I’m 81 years old, and if I get infected, I have a much higher risk, Anthony Fauci, via CNN.
Recently, Dr. Fauci revealed that he has not had a day off since the beginning of the pandemic
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US To End , COVID Testing
Requirement , for Air Travelers.
CNN reports that on June 10, the Biden administration will announce that the CDC will lift the restriction
for air travelers entering the country.
The change will reportedly go into
effect at midnight on June 12.
CNN reports that the travel industry had lobbied against the requirement for months.
claiming the protocol wasn't necessary anymore "based on the science and data.".
It has been in place
since January 2021.
But since new COVID variants are
continuously arising, the CDC will re-examine the decision to end testing in 90 days.
Roger Dow, U.S. Travel Association President, commended the decision.
Prior to the pandemic, travel was one of our nation's largest industry exports. , Roger Dow, U.S. Travel Association President, via CNN.
The lifting of this requirement will enable the industry to lead the way toward a broader U.S. economic and jobs recovery, Roger Dow, U.S. Travel Association President, via CNN
Credit: Wibbitz Top Stories Duration: 01:30Published
Moderna Says New Booster , Shows 'Superior' Omicron Response.
NPR reports Moderna claims its most recent vaccine candidate has shown a "superior neutralizing
antibody response" when compared to its first vaccine.
It is "bivalent," engineered to
target two different antigens.
Per NPR, Moderna intends to make its
newest booster available in fall 2022.
We are submitting our
preliminary data and analysis to regulators with the hope that the Omicron-containing bivalent booster will be available in the late summer. , Stéphane Bancel, Moderna CEO, via statement.
Due to a higher antibody response, Moderna believes its newest vaccine will offer protection that is "more durable over time" against Omicron.
Due to a higher antibody response, Moderna believes its newest vaccine will offer protection that is "more durable over time" against Omicron.
Moderna officials think their new vaccine could potentially offer protection for one year.
As new variants continuously arise, Moderna officials
hope the new bivalent vaccine can counter the
more contagious strains taking hold in the United States.
As new variants continuously arise, Moderna officials
hope the new bivalent vaccine can counter the
more contagious strains taking hold in the United States.
According to the Centers for Disease
Control and Prevention (CDC), two new
subvariants of Omicron, BA.4 and BA.5,
are spreading quickly across the country.
Experts say another wave of coronavirus
is bound to occur next winter as cold weather drives citizens back indoors
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CDC Ramps Up Monkeypox Alert , to Level 2 .
The Center for Disease Control and Prevention (CDC) raised the level of alert concerning monkeypox on June 6.
Known global cases of the virus have exceeded 1,000 across 29 countries.
An alert level of three, the highest level, would recommend against travel that is non-essential.
The agency is encouraging the public to “practice enhanced precautions” to curb the spread of the virus.
New guidance issued from the CDC recommends that individuals avoid close contact with other infected people and infected animals.
According to reporting on the new guidance, those with visible skin legions could be more infectious. .
According to the World Health Organization, the virus has been circulating undetected for “weeks, months or possibly a couple of years.”.
Experts say that the ease of international travel is likely a significant reason as to why the virus has spread.
Diseases that were locally spread are now able to make their way across countries and continents much more easily, Professor Eyal Leshem, Sheba Medical Center,
via CNBC.
Meanwhile, interaction between humans and animals has
also amplified. , Professor Eyal Leshem, Sheba Medical Center,
via CNBC.
Experts also say that climate change has likely played a role in the speed at which the virus has spread.
Climate change has forced some animals into closer contact with humans, you will see more of these types of diseases, Professor Eyal Leshem, Sheba Medical Center,
via CNBC.
Monkeypox infections are considered rare and the threat to the general public remains low.
Symptoms of the virus include headache, fever, swelling, back-pain, and muscle ache
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Pfizer Says Updated COVID-19 Shot , Effective Against Omicron.
NBC News reports Pfizer announced on
June 25 that its updated coronavirus vaccine
better targets the omicron variant.
Experts say while current vaccines offer ample protection against new variants, .
their effectiveness has waned
in the age of omicron.
The Food and Drug Administration has considered ordering altered vaccines, .
hoping a modified recipe could offer
more protection when coronavirus
surges again this fall and winter.
Pfizer says after studying over 1,200 adults who had received three vaccine doses.
officials say each of their vaccines
showed a substantial increase in omicron-resistant antibodies.
Based on these data,
we believe we have two
very strong omicron-
adapted candidates. , statement from Pfizer CEO Albert Bourla, via NBC News.
Pfizer's tweaked shot shows a 9 to 11-fold increase in omicron-fighting antibodies.
almost 1.5 times higher than
the company's initial dose
Credit: Wibbitz Top Stories Duration: 01:30Published
Pfizer's COVID Vaccine
for Kids Under 5 , Moves Closer to FDA Approval .
Pfizer announced on June 1 that its application to the Food and Drug Administration (FDA) for the vaccine was complete.
Pfizer announced on June 1 that its application to the Food and Drug Administration (FDA) for the vaccine was complete.
The three-dose vaccine is for children between the ages of six months and five years.
Pfizer released a statement detailing the application.
Pfizer and BioNTech completed a rolling application to the U.S. Food and Drug Administration (FDA) for emergency use authorization (EUA)... , Pfizer Statement, via ABC News.
... of the 3-µg [microgram] dose of the Pfizer-BioNTech COVID-19 Vaccine.., Pfizer Statement, via ABC News.
... for children 6 months through
4 years of age (also referred to as
6 months to under 5 years of age) on June 1, 2022, Pfizer Statement, via ABC News.
Pfizer reported an 80 percent effectiveness rate in children in May.
The FDA also released a statement on June 1, confirming that the agency had accepted the Pfizer application.
We recognize parents are anxious to have their young children vaccinated against COVID-19... , FDA Statement, via ABC News.
... and while the FDA cannot predict how long its evaluation of the data and information
will take, , FDA Statement, via ABC News.
... we will review any EUA request we receive as quickly as possible using a science-based approach, FDA Statement, via ABC News.
According to a poll conducted by the
Kaiser Family Foundation in April of this year.
... just 18 percent of parents intend to have their children vaccinated once the vaccine is approved.
27 percent of parents stated that they will "definitely not" vaccinate their children against COVID
Credit: Wibbitz Top Stories Duration: 01:31Published
Pfizer’s 3-Dose Vaccine , 80% Effective Against Omicron, Infection for Youngest Children.
ABC News reports new data shows
Pfizer's 3-dose vaccine is 80% effective against omicron infections in children
five years old and younger.
In all age groups, Pfizer's coronavirus
vaccine has been less effective against
mild breakthrough infections.
but has been shown to offer high protection against severe disease and death.
Experts say Pfizer's announcement offers reassurance to parents who wish to protect their children against coronavirus.
We are pleased that our formulation for the youngest children, which we carefully selected to be one-tenth of
the dose strength for adults ... , statement from Albert Bourla, chairman CEO Pfizer, via ABC News.
... was well tolerated
and produced a strong immune response. , statement from Albert Bourla, chairman CEO Pfizer, via ABC News.
After two years without a vaccine for young children, many pediatricians and parents intend to vaccinate as soon as possible.
However, recent polls have shown over 50% of parents feel they need more information before their children receive a COVID-19 shot.
Parents should also be
aware that this preliminary
data will be supplemented by additional data in June ... , Dr. Alok Patel, pediatric hospitalist Stanford Children's Health, via ABC News.
... which will then be
thoroughly reviewed by
both the FDA and the CDC. , Dr. Alok Patel, pediatric hospitalist Stanford Children's Health, via ABC News
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FDA To Pull Juul E-Cigarettes , off US Market.
Fox News and other outlets report that the Food and Drug Administration (FDA) is gearing up to order Juul Labs Inc.
to remove its e-cigarettes from store shelves in America.
Fox News and other outlets report that the Food and Drug Administration (FDA) is gearing up to order Juul Labs Inc.
to remove its e-cigarettes from store shelves in America.
The announcement is expected to come
as data presented by Juul has been
under review for nearly two years. .
The announcement is expected to come
as data presented by Juul has been
under review for nearly two years. .
Fox News reports that four years ago,
the vaping company came under fire for
its fruity flavors and marketing direction.
Fox News reports that four years ago,
the vaping company came under fire for
its fruity flavors and marketing direction.
Fox News reports that four years ago,
the vaping company came under fire for
its fruity flavors and marketing direction.
Critics say underage vaping surged as a result.
Juul has since cut back on its marketing,
and in 2019, the company stopped selling
fruity, sweet cartridge flavors. .
Still, sales have dramatically declined
for the e-cigarette manufacturer. .
The sale of all fruity e-cigarette flavors
has since been banned by the FDA.
Juul's impending departure would pave the way for
Reynolds American Inc. and NJOY Holidings Inc. to corner the tobacco-flavored segment of the e-cigarette market.
Juul's impending departure would pave the way for
Reynolds American Inc. and NJOY Holidings Inc. to corner the tobacco-flavored segment of the e-cigarette market.
Juul's impending departure would pave the way for
Reynolds American Inc. and NJOY Holidings Inc. to corner the tobacco-flavored segment of the e-cigarette market.
Fox News reports Juul will be able to file an appeal through the FDA, take the matter to court or file a new application with revised products. .
Fox News reports Juul will be able to file an appeal through the FDA, take the matter to court or file a new application with revised products.
Credit: Wibbitz Top Stories Duration: 01:30Published
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