INDIA: COVID-19 CASES PLUMMET AS THE COUNTRY TURNS TO IVERMECTIN AND HYDROXYCHLOROQUINE

India: COVID-19 cases plummet as the country turns to Ivermectin and hydroxychloroquine (H/T: The Free)

UPDATED May 17, 2021 – State of Tamil Nadu halts use of Ivermectin. Just like that, despite Ivermectin saving lives, The Hindu is reporting that the state health department removed Ivermectin from its case management protocols. This is murder with malice, no matter how you slice it.

More information and charts:

India Just Became Latest Country to Approve Use of Ivermectin to Treat Covid-19

Feds target Steve Bannon-linked company for the ‘unlawful spreading of COVID-19 misinformation’

Feds target Steve Bannon-linked company for the ‘unlawful spreading of COVID-19 misinformation’

DOJ Statement: Justice Department and FTC Announce Action to Stop Deceptive Marketing of Purported COVID-19 Treatments

I don’t understand why Congress even had to make it law, considering the following (I’m not saying that either help or not): 🤦🏼‍♀️

In 1994, the Dietary Supplements Health and Education Act was passed which established the guidelines for dietary supplement labeling claims for the FDA. This act requires labeling claims to be “truthful, not misleading and substantiated.” Likewise, the FTC has its own legislation under the Enforcement Policy Statement on Food Advertising which applies to supplements as well as food. This act defers to the FDA’s ruling on what is considered to be truthful, not misleading and substantiated and defines a deceptive ad as “one that contains a misrepresentation or omission that is likely to mislead consumers acting reasonable under the circumstances to their detriment.”

Generally, a claim that is made on a dietary supplement must be backed by scientific evidence to be considered for inclusion on a label by the FDA. For FTC requirements, these same requirements must be met, however any claims that can be inferred from the advertising or anything that is implied by claims made must also be truthful and substantiated. It is important to be meticulous in label creation to ensure compliance with these laws. Unless you are well versed in FDA and FTC regulations, it is extremely important to consult with an label consultant to ensure that no label claims may be subject to disciplinary action by these federal agencies.

False Advertising in Dietary Supplements

Latest VAERS Data Show Reports of Blood Clotting Disorders After All Three Emergency Use Authorization Vaccines

Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed reports of blood clots and other related blood disorders associated with all three vaccines approved for Emergency Use Authorization in the U.S. — Pfizer, Moderna and Johnson & Johnson (J&J). So far, only the J&J vaccine has been paused because of blood clot concerns.

Latest VAERS Data Show Reports of Blood Clotting Disorders After All Three Emergency Use Authorization Vaccines

H/T: The Free

Related:

If J&J Coronavirus Vaccine Shots Are Halted Because of Blood Clots, Why Not Moderna and Pfizer-BioNTech Also?

EUA: May Employers and Universities Require COVID-19 Vaccinations?

May Employers and Universities Require COVID-19 Vaccinations?

“At present, there is nothing in federal law that should preclude vaccination requirements for returns to workplaces and campuses.”

Federal law prohibits employers and others from requiring vaccination with a Covid-19 vaccine distributed under an EUA

When the FDA grants emergency use authorization for a vaccine, many questions about the product cannot be answered. Given the open questions, when Congress granted the authority to issue EUAs, it chose to require that every individual should be allowed to decide for himself or herself whether or not to receive an EUA product. The FDA and CDC apparently consider this fundamental requirement of choice important enough that even during the height of the Covid-19 pandemic they reinforced that policy decision when issuing their guidance related to the Covid-19 vaccines.

[2020] You can’t sue Pfizer or Moderna if you have severe Covid vaccine side effects. The government likely won’t compensate you for damages either

You can’t sue Pfizer or Moderna if you have severe Covid vaccine side effects. The government likely won’t compensate you for damages either

You also can’t sue the Food and Drug Administration for authorizing a vaccine for emergency use, nor can you hold your employer accountable if they mandate inoculation as a condition of employment.

In February, Health and Human Services Secretary Alex Azar invoked the Public Readiness and Emergency Preparedness Act. The 2005 law empowers the HHS secretary to provide legal protection to companies making or distributing critical medical supplies, such as vaccines and treatments, unless there’s “willful misconduct” by the company. The protection lasts until 2024.

US Vaccine Imperialism Backfires

By Herman Tiu Laurel (Part 1: mRNA’s yet Unchartered Waters)

It took me some time to ascribe as “imperialism” the US behavior on its vaccine promotion efforts, but after reviewing the course of events since the start of the Covid-19 crisis I found this as an inescapable fact – the US has tried to impose on the world its new vaccine development, its parameters for defining “efficacy” and its pernicious propaganda efforts at putting down other countries’ vaccine projects.

US Vaccine Imperialism Backfires