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UPDATE 3-J&J COVID-19 vaccine under EU review over blood clots

UPDATE 3-J&J COVID-19 vaccine under EU review over blood clots

更新3-強生新冠肺炎疫苗正在接受歐盟對血栓的審查
路透社 ·  2021/04/10 01:25

* EMA says no causal link yet of blood clots to either vaccine
   * Four cases of blood clots in recipients of J&J shots
   * J&J says working with regulators to assess data on its vaccine
   * Probe of AstraZeneca vaccine and blood clots already ongoing

(Recasts, adds details, expert comment)
By Pushkala Aripaka and Julie Steenhuysen
April 9 (Reuters) - Europe's drug regulator said on Friday
that it is reviewing rare blood clots in four people in the
United States who received Johnson & Johnson's COVID-19
vaccine.
The European Medicines Agency's safety committee has also
been looking at how AstraZeneca's COVID-19 vaccine is
associated with very rare cases of unusual blood clots and said
it was now reviewing reports of capillary leak syndrome in
people given AstraZeneca's vaccine.
Johnson & Johnson (J&J) said it was aware of the rare
reports of blood clots in individuals given its COVID-19
vaccine, and was working with regulators to assess the data and
provide relevant information.
"At present, no clear causal relationship has been
established between these rare events and the Janssen COVID-19
vaccine," the company said in an emailed statement.
Of the four serious cases of clotting and low platelets,
three occurred in the United States during the rollout of J&J's
vaccine from its Janssen unit, the European Medicines Agency
(EMA) said. That was in addition to one person who died from a
clotting disorder reported in J&J's clinical trial.
Nearly 5 million people in the United States had received
J&J's vaccine as of Thursday morning, according to the U.S.
Centers for Disease Control and Prevention.
The report from the European Medicines Agency is the first
to mention a probe of blood clots associated with the J&J
vaccine.
The U.S. Food and Drug Administration said it would respond
shortly to a request for comment.
It follows a probe of blood clots in the brain reported in
people given the AstraZeneca vaccine that have caused some
European countries to change their vaccine recommendations.
In its report on Friday, EMA's safety committee said unusual
blood clots linked with low blood platelets should be listed as
very rare side effects of the AstraZeneca vaccine.
It has also started to investigate reports of capillary leak
syndrome - which causes blood vessel swelling and a drop in
blood pressure - in five people who received the AstraZeneca
vaccine. The safety panel said it was not clear whether these
were linked with the vaccine. AstraZeneca did not immediately
respond to a request for comment.
Ian Douglas, a professor of pharmacoepidemiology at London
School of Hygiene & Tropical Medicine, said the reports were
part of a normal process in which the EMA's safety committee
reviews important safety signals as they arise.
"It’s too early to comment on the signal of capillary leak
with the AZ vaccine, or clots with the Janssen vaccine, but from
what we’ve seen in the last few weeks, the EMA’s PRAC
(Pharmacovigilance Risk Assessment Committee) will doubtless
assess all the evidence they have as thoroughly and quickly as
possible," he said.
Some countries in Europe and Asia have restricted the use of
AstraZeneca's vaccine, Vaxzevria, in younger people following an
update by EU and UK regulators this week that found a link
between the events and the shot. Regulators have said the
benefits of the vaccine outweigh the risks.
Dr. Jesse Goodman, an infectious disease expert at
Georgetown University in Washington D.C. and a former chief
scientist for the U.S. Food and Drug Administration, said in a
briefing on Thursday that he was "fairly convinced" the brain
blood clots were linked with the AstraZeneca vaccine, but said
the events are rare and the risk during an active outbreak from
COVID "is much higher."
J&J's single-dose vaccine has been approved for EU use, but
a rollout is yet to begin. It is mainly being used in the United
States currently.
The J&J and AstraZeneca shots are two of the four approved
COVID-19 vaccinations in Europe.


/><^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
COVID-19 Global Cases Tracker
COVID-19 Global Vaccinations Tracker
FACTBOX-Some countries limit AstraZeneca vaccine use after
possible link to blood clots
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(Reporting by Pushkala Aripaka, Manas Mishra in Bengaluru, Kate
Kelland in London, Julie Steenhuysen in Chicago, Deena Beasley
in Los Angeles; Editing by Shinjini Ganguli, Hugh Lawson and
Susan Fenton)
((Pushkala.A@thomsonreuters.com; Twitter: @pullthekart; Mobile:
+91 852 751 3793 ;)

*EMA表示,目前還沒有血液凝塊與這兩種疫苗的因果聯繫*接受強生針劑注射的人有四例血液凝塊*強生表示與監管機構合作評估其疫苗的數據*對阿斯利康疫苗和血栓的調查已經在進行中(重鑄,添加細節,專家評論)作者:Pushkala Aripaka和Julie Steenhuysen路透4月9日電-歐洲藥品監管機構週五表示他們正在檢查四個人罕見的血液凝塊。收到強生新冠肺炎的美國人疫苗。歐洲藥品管理局(European Medicines Agency)的安全委員會也我一直在關注阿斯利康的新冠肺炎疫苗與罕見的不尋常血液凝塊有關,他説它現在正在審查關於#年毛細血管滲漏綜合徵的報告。人們接種了阿斯利康的疫苗。強生(J&J)表示,它意識到了這種罕見的關於服用新冠肺炎的個體出現血栓的報道疫苗,並正在與監管機構合作評估數據和提供相關信息。“目前還沒有明確的因果關係。建立在這些罕見事件和揚森新冠肺炎之間疫苗。“該公司在一份電子郵件聲明中説。在四例嚴重的凝血和血小板減少的病例中,其中三起發生在強生推出期間的美國來自其Janssen部門-歐洲藥品管理局(European Medicines Agency)的疫苗(EMA)稱。此外,還有一人死於強生的臨牀試驗報告了凝血障礙。美國有近500萬人收到了根據美國食品和藥物管理局的數據,強生的疫苗截至週四上午。疾病控制和預防中心。來自歐洲藥品管理局的這份報告是第一份提到一項與強生有關的血液凝塊的調查疫苗。美國食品和藥物管理局(FDA)表示,將對此做出迴應很快回復了記者的置評請求。在此之前,據報道,一項關於大腦中血液凝塊的探針注射阿斯利康疫苗的人已經引起了一些歐洲國家改變他們的疫苗建議。在週五的報告中,EMA的安全委員會表示,不同尋常的是與低血血小板有關的血液凝塊應列為阿斯利康疫苗非常罕見的副作用。它還開始調查有關毛細管泄漏的報道。綜合徵-會導致血管腫脹和血流量下降血壓-在5名接受阿斯利康治療的人中疫苗。安全小組表示,目前還不清楚這些與疫苗有關。阿斯利康沒有立即做出迴應。回覆置評請求。伊恩·道格拉斯(Ian Douglas),倫敦大學藥物流行病學教授衞生與熱帶醫學院表示,這些報告是作為EMA安全委員會正常程序的一部分在重要的安全信號出現時對其進行檢查。“現在評論毛細管泄漏的信號還為時過早。使用AZ疫苗,或使用Janssen疫苗凝塊,但來自我們在過去幾周所看到的,EMA的PRAC(藥物警戒風險評估委員會)無疑會對他們掌握的所有證據進行全面、快速的評估有可能。“他説。歐洲和亞洲的一些國家已經限制使用阿斯利康(AstraZeneca)的Vaxzevria疫苗在年輕人中應用歐盟和英國監管機構本週發佈的最新數據發現了兩者之間的聯繫在事件和槍擊之間。監管機構表示,疫苗的益處大於風險。傑西·古德曼(Jesse Goodman)博士是一名傳染病專家華盛頓特區的喬治敦大學和一位前校長美國食品和藥物管理局的科學家在一份報告中説週四的簡報説他“相當確信”大腦血液凝塊與阿斯利康疫苗有關,但表示這些事件很少見,在活躍的疫情爆發期間的風險來自“COVID”要高得多。強生的單劑疫苗已獲準在歐盟使用,但新產品的推出還沒有開始。它主要在美國使用。目前在美國。強生和阿斯利康是獲得批准的四種疫苗中的兩種歐洲的新冠肺炎疫苗接種。/>新冠肺炎全球案例追蹤新冠肺炎全球疫苗接種跟蹤者FACTBOX-一些國家在以下情況下限制阿斯利康疫苗的使用可能與血栓有關 ^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^>(Pushkala Aripaka,Manas Mishra在孟加拉國報道,Kate凱蘭(Kelland)倫敦,朱莉·斯蒂芬森(Julie Steenhuysen)芝加哥,蒂娜·比斯利在洛杉磯;編輯:Shinsini Ganguli,Hugh Lawson和蘇珊·芬頓(Susan Fenton)(Pushkala.A@thomsonreurs.com;Twitter:@Pullthekart;手機:+91 852 751 3793 ;)

譯文內容由第三人軟體翻譯。


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