Wuhan Coronavirus Thread

Is coronavirus a biological warfare agent released by China?

  • yes

    Votes: 175 89.3%
  • no

    Votes: 21 10.7%

  • Total voters
    196

Kumata

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➕ℹ https://bit.ly/3CcC1nn
Translated from Spanish by
#Covaxin| Four hundred thousand doses arrive in the country

It is an acquisition of the Government of Paraguay, through the Paraguay-Taiwan Bilateral Cooperation Fund.

This platform is approved by the WHO for emergency use.
Most probably supplied via that UN alliance...forget the name..
 

ezsasa

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a bit amusing for coupta himself and his bunch in this interview refer themselves as "We" when asking questions. "We" as in, since the program is a success they are attaching themselves to the Government success story(AIIMS and ICMR are a govt organisation).

Other days on other topics, they don't refer themselves as "We".
==============
Off The Cuff with Prof (Dr) Balram Bhargava, Director General, ICMR

 

Hari Sud

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Belligerent Chinese just got away from owning responsibility of inventing and spread Coronavirus virus. Even Biden with huge hoopla involving intelligence agencies six months back has backed away. Chinese have grown economically so powerful that they can turn off any investigation. The Biden intelligence agency report said that they had information but not enough to fully hold China responsible. In the meantime Pfizer, Moderna, AsterZeneca grew rich with half fast developed vaccine. The world lost $2 trillion in the spread of the virus and its after affects. The virus is still around and inflicting more damage on mankind.

if Joe Biden was a strong president then he could have stopped all trade until Chinese came out with full details of the virus invention. But now American economy is badly intertwined with cheap but worthless Chinese products and hence Biden is prepared to accept the damage which even now the Corona virus is inflicting on America and rest of the. …….. Chinese, you have done well.
 

Kumata

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Belligerent Chinese just got away from owning responsibility of inventing and spread Coronavirus virus. Even Biden with huge hoopla involving intelligence agencies six months back has backed away. Chinese have grown economically so powerful that they can turn off any investigation. The Biden intelligence agency report said that they had information but not enough to fully hold China responsible. In the meantime Pfizer, Moderna, AsterZeneca grew rich with half fast developed vaccine. The world lost $2 trillion in the spread of the virus and its after affects. The virus is still around and inflicting more damage on mankind.

if Joe Biden was a strong president then he could have stopped all trade until Chinese came out with full details of the virus invention. But now American economy is badly intertwined with cheap but worthless Chinese products and hence Biden is prepared to accept the damage which even now the Corona virus is inflicting on America and rest of the. …….. Chinese, you have done well.
Joe was appointed by eleven.... So much for being strong president..
 

ezsasa

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a bit amusing for coupta himself and his bunch in this interview refer themselves as "We" when asking questions. "We" as in, since the program is a success they are attaching themselves to the Government success story(AIIMS and ICMR are a govt organisation).

Other days on other topics, they don't refer themselves as "We".
==============
Off The Cuff with Prof (Dr) Balram Bhargava, Director General, ICMR

Probably this explains why coupta was being extra nice to Dr. Bhargava.
Coupta knows the implications of these statements, while the "RW" folks are stuck in their political current affairs.
==============
How Macaulay Putras Ridiculed Covaxin and Data Proved Them Wrong

The Phase III human clinical trials of Covaxin began in mid-November 2020, involving 26,000 volunteers, between 18 and 98 years of age, across 21 sites. It was India’s first and only Phase III study for a COVID-19 vaccine, and the largest Phase III efficacy trial ever conducted here for any vaccine. The study included 2,433 participants over the age of 60 and 4,500 with co-morbidities.

The interim results of the trial released in late April 2021, showed an efficacy of 100 per cent against severe COVID-19 disease; the efficacy of protection from asymptomatic COVID-19 infection was 78 per cent, putting it at par with other global front-runner vaccines. The analysis was on a data set of 127 Covid-positive volunteers.

Data from 25,800 participants, half of whom received the vaccine and the other half a placebo, also showed that the vaccinated candidate was safe and well tolerated. A review of the safety database showed that severe, serious and medically attended adverse events occurred at low levels and were balanced between vaccine and placebo groups. This was again published in The Lancet.

Analysis from the NIV indicated that vaccine-induced antibodies could neutralize the known variants of concern including the delta variant.


This was all excellent news! Those results will always be a matter of great pride to us at the ICMR, which I will cherish for the rest of my life. There were critics who said that we had to complete Phase III before giving the vaccine to humans, before it could be given to the nation. But there is a Gazette notification of 19 March 2019, which is pre-COVID, and it said that in national interest, if a product has successfully undergone the Phase II trial, it can be deployed. In other words, emergency authorization can be given. And that rule was invoked by the Drugs Controller on 2 January 2020, when approval for Covaxin was issued.

The leadership had about, I would say, more than 15 meetings with various chief ministers of different states. And at that point in time, we had to participate and any question that was put forward for the vaccine or for the testing would come to me. So we were all on our toes at every level. But there was no question after the Emergency Use Authorization (EUA) happened. We were only asked how we could help out; the government would help the company to scale it up.

As we battled one challenge after another and found ways to deal with them, and firmed our resolve to have an Indian vaccine, a tiny section of our population—the so-called experts in the media and elsewhere—began to raise doubts on our ability. It was not the first time that an Indian initiative was being ridiculed even before it had the opportunity to succeed. But it was disgraceful that it should happen at a time when our scientists and researchers were showing a steely determination to find a solution to the pandemic.

It was the Macaulay-mindset at work. What had T.B. Macaulay done? He framed India’s education policy. He said that if the East India Company had to rule over this country, we have to systematically destroy its education system, drilling every Indian’s mind that the Indian education system is inferior to that of the British. This was instilled in 1834 in every Indian’s mind. It is this Macaulay mindset which is responsible for every Indian critic in India who feels that anything Indian can never work.

And that’s why I told Bharat Biotech in a lighter vein, that they should name their company after ‘another country’ Biotech not Bharat, for acceptability from the Macaulay-minded people! It was something I mentioned during my depositions before the Department Related Parliamentary Standing Committee on Health and Family Welfare and the parliamentary standing committee on ‘COVID-19 pandemic response, India’s contribution and the way forward’. I would like to put on record that the members of these panels were most supportive and praised the efforts of the ICMR. Cutting across party lines, they were also of the opinion that the work that the ICMR had done was phenomenal.

Once the Phase III clinical results came out, it laid to rest the criticism of the cynics. It is the vaccine which has more than 10 full scientific publications in top international journals, all featuring only Indian authors.

The approvals for Covaxin, contrary to criticism, were purely data-driven. Phase II trials established beyond doubt the immunogenicity of the vaccine. No responsible Subject Expert Committee (SEC) approves vaccines without adequate data, and those involved with the approval were all responsible people. Experts had taken into account the alpha variant of SARS-Cov-2 before granting approval to Covaxin. And because Covaxin is a whole-virus inactivated vaccine, as I mentioned earlier, it is equipped to target all parts of the virus instead of just partially. The virus is known to have undergone mutations in the spike protein also, and drug makers such as Pfizer Inc. have admitted that it needs about four to six weeks to make tweaks to their vaccine to adjust to the new mutations.

 

sorcerer

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Research reveals long term benefits of Covaxin


NEW DELHI: A research led by the National Institute of Immunology, apart from several other government institutions, has for the first time confirmed Covaxin-induced immune memory, indicating that the COVID-19 vaccine is capable of ensuring long term protection against severe disease.


The study, funded by the Centre's department of biotechnology has shown that T and B cell memory responses generated by Covaxin measures similar to the memory responses generated by the natural infection.

 

Cheran

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United Kingdom: Covaxin to be recognised as a valid Coronavirus vaccine from November 22 onwards

As of now, the United Kingdom has recognised the following vaccines. now include Oxford-AstraZeneca (Covishield), Moderna, Janssen, Pfizer BioNTech, Sinovac, Sinopharm Beijing and Covaxin.

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CC - Darbaris, Jhollachaps, Media coolies, coconuts, etc
 

here2where

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First real-world study: Covaxin effectiveness 50%


Covaxin Only 50% Effective Against Symptomatic Covid-19 in Real-world Assessment


did pfizer/moderna call lancet recently?
 

tommy

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First real-world study: Covaxin effectiveness 50%


Covaxin Only 50% Effective Against Symptomatic Covid-19 in Real-world Assessment


did pfizer/moderna call lancet recently?
That was not a randomized control study. It was conducted among high risk population. Do we have any such data for Pfizer, moderna or even covishield. The actual study itself never calls it a real-world assessment. :frusty:
 

indiatester

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Cheran

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Please listen to the full videi.


Study shows the possibility of coronary diseases increase significantly after receiving mRNA Covid-19 vaccines from Pfizer and Moderna

According to the study presented at the Scientific Sessions of the American Heart Association annual conference, PULS score increases from 11% 5-year ACS risk to 25% 5 year ACS risk after the second dose of mRNA vaccine
 

doreamon

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Please listen to the full videi.


Study shows the possibility of coronary diseases increase significantly after receiving mRNA Covid-19 vaccines from Pfizer and Moderna

According to the study presented at the Scientific Sessions of the American Heart Association annual conference, PULS score increases from 11% 5-year ACS risk to 25% 5 year ACS risk after the second dose of mRNA vaccine
But IIT IIM alumni Chetan Bhagat and anti fascist journalist influencers were in favour of pfizer . So i ll go with it 😊 .
 

temujin

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Pfizer vaccine efficacy study in Israel
Be****d took not one or two but three doses of Pfizer yet down with quite a bad bout of CoviD. Booster received 2 months ago so should have increased protection from symptomatic infection to 99.99% or whatever fantasy figure Pfizer execs dreamt up. Vaccines undoubtedly reduce the severity of infection and risks of death/hospitalisation (although more sceptical of Pfizer considering the CoviD trajectory in Europe) but all these outlandish claims of 99% efficacy were clearly marketing guff
 

asianobserve

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South Africa variant 500 times more infectious than Delta!


And already the most dominant variant in South Africa.


And 2 cases are now discovered in Hongkong!

 

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