2021年11月5日金曜日

ワクチンサマナの皆様にファイザー社から実質的に今後、コロナワクチン接種の必要無しのBad News!(爆wwwwww

 

BREAKING NEWS: Pfizer says its 'extraordinary' new COVID pill cuts risk of hospitalization and death by almost 90% among adults at high risk of a serious reaction to the virus

  • Drug giant announced results on Friday
  • Study on 775 COVID patients found pill reduced hospitalization and death rates by 89 per cent compared to patients giving a dummy pill
  • Results of independent study were so impressive Pfizer halted it early to seek approval for its usage  
  • It wants the Food and Drug Administration to authorize the treatment ASAP
  • Rival manufacturer Merck's COVID pill is already under consideration by FDA 

Pfizer released preliminary results Friday of its study of 775 adults. Patients taking the company's drug along with another antiviral had an 89% reduction in their combined rate of hospitalization or death after a month, compared to patients taking a dummy pill. Fewer than 1% of patients taking the drug needed to be hospitalized and no one died. In the comparison group, 7% were hospitalized and there were seven deaths.

'We were hoping that we had something extraordinary, but it´s rare that you see great drugs come through with almost 90% efficacy and 100% protection for death,' said Dr. Mikael Dolsten, Pfizer´s chief scientific officer, in an interview.

Study participants were unvaccinated, with mild-to-moderate COVID-19, and were considered high risk for hospitalization due to health problems like obesity, diabetes or heart disease. Treatment began within three to five days of initial symptoms, and lasted for five days.

Pfizer reported few details on side effects but said rates of problems were similar between the groups at about 20%. 

Currently all COVID-19 treatments used in the U.S. require an IV or injection. Competitor Merck´s COVID-19 pill is already under review at the Food and Drug Administration after showing strong initial results, and on Thursday the United Kingdom became the first country to OK it.

Pfizer said it will ask the FDA and international regulators to authorize its pill as soon as possible, after independent experts recommended halting the company´s study based on the strength of its results. Once Pfizer applies, the FDA could make a decision within weeks or months.

Researchers worldwide have been racing to find a pill against COVID-19 that can be taken at home to ease symptoms, speed recovery and reduce the crushing burden on hospitals and doctors.

An independent group of medical experts monitoring the trial recommended stopping it early, standard procedure when interim results show such a clear benefit. The data have not yet been published for outside review, the normal process for vetting new medical research.

Top U.S. health officials continue to stress that vaccination will remain the best way to protect against infection. But with tens of millions of adults still unvaccinated - and many more globally - effective, easy-to-use treatments will be critical to curbing future waves of infections.

The FDA has set a public meeting later this month to review Merck´s pill, known as molnupiravir. The company reported in September that its drug cut rates of hospitalization and death by 50%. Experts warn against comparing preliminary results because of differences in studies.

Although Merck's pill is further along in the U.S. regulatory process, Pfizer's drug could benefit from a safety profile that is more familiar to regulators with fewer red flags. While pregnant women were excluded from the Merck trial due to a potential risk of birth defects, Pfizer´s drug did not have any similar restrictions. The Merck drug works by interfering with the coronavirus' genetic code, a novel approach to disrupting the virus.

Pfizer´s drug is part of a decades-old family of antiviral drugs known as protease inhibitors, which revolutionized the treatment of HIV and hepatitis C. The drugs block a key enzyme which viruses need to multiply in the human body.

The drug, which has not yet been named, was first identified during the SARS outbreak originating in Asia during 2003. Last year, company researchers decided to revive the medication and study it for COVID-19, given the similarities between the two coronaviruses.

The U.S. has approved one other antiviral drug for COVID-19, remdesivir, and authorized three antibody therapies that help the immune system fight the virus. But they have to be given by IV or injection at hospitals or clinics, and limited supplies were strained by the last surge of the delta variant.

https://www.dailymail.co.uk/news/article-10169007/New-COVID-19-pill-cut-hospital-death-risk-90.html



これでもうワクチンパスポートも接種義務化も必要無し!


ワクチンサマナの梯子を外して逃げに入ったな!ファイザー!(爆wwwwwwwww

 

4 件のコメント:

GABRIEL さんのコメント...

データの捏造改竄隠蔽
そんなワクチンであっても

ワクチンサマナは
薬物中毒者の如く
コロナワクチン以外の
インフルワクチンやら
コロナ治療薬etcを
渇望する人生になるような(苦

匿名 さんのコメント...

w
VIDs大屠殺モードっすねw

匿名 さんのコメント...

えー商売上手だなー(巨大棒)

匿名 さんのコメント...

キタ――(゚∀゚)――!!

パスポート意味なしwww

飲み薬もどうせヤバイやつだから飲まないけれど、
「飲んだって」言って逃げられるw

この茶番も終了ですねw