The TGA has banned a safe and effective COVID-19 treatment. One that could end the pandemic and save lives today.
A treatment that’s safer than paracetamol*
Australian scientists discovered it killed SARS-COV-2 stone cold in 48 hours.
It has an unparalleled safety profile with 3.7 billion doses administered in humans over 35+ years and it’s won a Nobel Prize for treating infections.
It’s called ivermectin. The problem?
It’s banned for use in the treatment and prevention of COVID-19
Why has ivermectin been banned?
- It’s off-patent & very cheap which means extremely small profit for pharmaceutical companies.
- Newly patented COVID drugs/vaccines have made and will continue to make billions of dollars.
- Emergency use of new COVID medicines can only be granted when no alternatives are available.
Responses
I have 2 friends one was in his 20’s one was 67…both died from heart attack both had been jabbed. We must unite!
It is being administered a Liverpool Hospital. There is picture proof on the net from a COVID patient who was at the hospital.
Signature confirmed – Verification succeeded!
Successfully signed petition EN3364.
Signed and posted on
This has never been about public health. It’s about controlling every move you make and submitting to authority.
Signed and shared!
Video unavailable?? however, watch Discernible on youtube for dictator dans new powers he wants, permanent emergency powers!! WTF
Many healthy people i know took that shit and are now suffering with adverse reactions
Worth a read ….
Risk Assessment and Risk Management Plan
for
DIR 180
Commercial supply of a genetically modified
COVID-19 vaccine
Applicant: AstraZeneca Pty Ltd
February 2021
https://www.ogtr.gov.au/sites/default/files/2021-06/dir180-full_risk_assessment_and_risk_management_plan.pdf
“Previous clinical trials Phase 1/2 clinical trial with the GM vaccine ChAdOx1-S [recombinant] (also
known as AZD1222, ChAdOx1 nCoV-19) was conducted and completed in the
United Kingdom (UK) to test the safety of the vaccine in adults aged 18-55
years.
Current approvals • Clinical trials with the GM vaccine ChAdOx1-S [recombinant] (also known as
AZD1222, ChAdOx1 nCoV-19) are approved and are currently ongoing in
several overseas jurisdictions including the UK, the United States (US),
1 The title of the licence application submitted by AstraZeneca is “Commercial release of a COVID-19 vaccine
AstraZeneca to Prevent Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)”.
DIR 180 – Risk Assessment and Risk Management Plan (February 2021) Office of the Gene Technology Regulator
Summary II
Brazil, South Africa, Argentina, Chile, Colombia, Japan, Peru and the
Russian Federation.
• The GM vaccine may be manufactured in Australia under a licence for
Dealings Not involving Intentional Release (DNIR) of a GMO into the
environment (DNIR-630 and DNIR-632) or imported under a Notifiable Low
Risk Dealing authorisation.
• The GM vaccine is currently approved for emergency use in several
countries including the UK, Argentina, Brazil, El Salvador, India, Dominican
Republic, Mexico, Morocco and Pakistan.
• The GM vaccine has been approved for commercial use in the European
Union.
Proposed locations Australia-wide
Primary purpose Commercial supply of the GM COVID-19 vaccine”