COVID Vaccination Rate Falls Short of July 4th Goal

In the opening days of President Joe Biden’s administration, he set a goal of having a 70% vaccination rate for eligible people before the Independence Day holiday in the United States. The country ended up falling just short of that goal, reaching 67% by July 4th.

Although the three percentage points aren’t that far off the desired number, they could have been reached or exceeded. The U.S. South has staggering low vaccination statistics, even with the Delta variant surge that happened during the summer.

Alabama had only 34% of its population fully vaccinated by the end of July. Arkansas wasn’t much better at 36%, while Louisiana had its figures at 37%.

The Delta Variant Caused a Surge of Vaccination Requests

When the Delta variant surges through the U.S. South, it became apparent that the most vulnerable people were those who hadn’t been vaccinated.

Over 90% of the registered infections came from those who hadn’t gotten a COVID shot or hadn’t completed their series. The percentage of hospitalizations was even higher.

Getting the word out about how transmissible the Delta variant is compared to the original coronavirus infections helped to push vaccination rates above 100% over the previous month. 

When all Americans are accounted for in every age group, about 50% were fully vaccinated by the end of July. 

Biden’s goal could have been reached if states like Wyoming, Idaho, Louisiana, Arkansas, Mississippi, and Alabama had hit 50% instead of being under 40%. For now, the best option we have is to wear a mask, stay socially distant, and stay healthy.

For some people, products like Neurobiologix and Quicksilver Scientific can work to potentially give their immune systems an extra boost to reach that goal. 

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15 Million COVID-19 Vaccines Ruined After Ingredient Mix-up

Although the United States exceeded its vaccination goals since February 2021, the outcome hasn’t been flawless. A factory mix-up ruined up to 15 million doses of the single-shot Johnson & Johnson vaccine when a subcontractor mixed the ingredients from it with the AstraZeneca product.

Since the AstraZeneca vaccine is not available for distribution in the United States, the product was not usable.

The plant is run by Emergent BioSolutions, which partners with both single-shot producers. Regulators attributed the issue to human error, causing Johnson & Johnson to step up quality control procedures at the facility.

One Shot Speeds Up the Immunity Process in the United States

Although the two-shot vaccines for COVID-19 came out first, the Johnson & Johnson product receives a lot of credit for speeding along the immunity-building process in the United States. Once someone gets this shot, they’re considered immune after two weeks.

The setback was a major embarrassment for both companies involved in vaccine production. It would soon be followed by revelations that a rare side effect of the Johnson & Johnson vaccine involves blood clots that can appear three weeks after it gets administered.

To make up for the gap in vaccination opportunities, Pfizer started shipping its doses early. Moderna requested approval to send vials with 15 shots instead of ten to bolster the stock even further.

None of the tainted doses ever left the production facility. The mishap was reported to regulators immediately, and steps are in place to prevent future lapses.

The error has not affected any of the already delivered Johnson & Johnson doses. Additional deliveries from the Baltimore facility continue to remain in question.

$1.6 Billion Awarded to Novavax for a Coronavirus Vaccine

Novavax made headlines in 2020 because the company received $1.6 billion from the Trump Administration. The funds are the largest contract of its type for this struggling organization, one which has never brought a usable vaccine to the marketplace.

Why did Novavax get so much attention when other pharmaceutical companies with a better record of success were on the same path? In a rare move of bipartisanship in American politics, executives from the Bill and Melinda Gates Foundation promoted this small biotech company’s potential.

Republican officials in the White House agreed. The company uses moth cells to create crucial molecules faster than a typical vaccine, providing an advantage during the pandemic era that other companies couldn’t match.

The Company Was on the Verge of Collapse

Novavax made the push to the federal government for the $1.6 billion award after receiving almost $400 million from the Coalition for Epidemic Preparedness Innovations, headed by Dr. Richard Hatchett.

The funds are a dramatic turnaround for a company that was on the verge of collapse. After receiving the award, stock prices surged 30% almost overnight.

Novavax was on the verge of collapse. Their leading vaccine candidate was a product intended to prevent a deadly virus in newborns. It had failed for the second time in three years, causing the stock to trade so low that NASDAQ was threatening to delist it.

The company was raising cash by selling its manufacturing facilities.

How could the agency get so much money so quickly to produce a successful vaccine that it had never done before? The answer lies in a secretive mission called Operation Warp Speed.

What Is Operation Warp Speed?

Operation Warp Speed is a public-private partnership (PPP) initiated by the Trump Administration in April 2020. The goal of this effort was to accelerate the development, manufacturing, and distribution of vaccines to stop COVID-19. 

Congress allocated about $10 billion for this effort, including $3 billion for research through the National Institutes of Health.

Novavax received the $1.6 billion offer with one condition: it had to prove that its clinical trials were successful. If that happened, the money would help them to produce 100 million doses of the vaccine.

BioNTech and Pfizer received a $2 billion order with the same stipulation, getting 100 million doses of a safe and effective COVID-19 vaccine. In July 2020, GSK and Sanofi got funding of $2.1 billion.