This article is from the source 'rtcom' and was first published or seen on . It last changed over 40 days ago and won't be checked again for changes.

You can find the current article at its original source at https://www.rt.com/news/521616-ema-johnson-covid-vaccine-blood-clots/

The article has changed 4 times. There is an RSS feed of changes available.

Version 2 Version 3
EMA says J&J Covid-19 vaccine benefits outweigh the risks despite finding possible link to rare blood clots EMA says J&J Covid-19 vaccine benefits outweigh the risks despite finding possible link to rare blood clots
(30 days later)
The European Medicines Agency (EMA) has given its backing to the Johnson & Johnson Covid-19 vaccine, saying the overall benefit-risk remains positive, despite warning about the very rare possible side effect of blood clots.The European Medicines Agency (EMA) has given its backing to the Johnson & Johnson Covid-19 vaccine, saying the overall benefit-risk remains positive, despite warning about the very rare possible side effect of blood clots.
The EU drug regulator’s safety committee conducted an investigation into the side effects of the Johnson & Johnson vaccine after the US Food and Drug Administration (FDA) suspended its use in America earlier this month “out of an abundance of caution.”The EU drug regulator’s safety committee conducted an investigation into the side effects of the Johnson & Johnson vaccine after the US Food and Drug Administration (FDA) suspended its use in America earlier this month “out of an abundance of caution.”
The FDA’s move led to Johnson & Johnson delaying its rollout of the vaccine throughout Europe to allow for a full assessment of the risks, with the EMA looking into all eight complaints of clots – including one fatal – from among the 7 million doses administered in the US.The FDA’s move led to Johnson & Johnson delaying its rollout of the vaccine throughout Europe to allow for a full assessment of the risks, with the EMA looking into all eight complaints of clots – including one fatal – from among the 7 million doses administered in the US.
Having conducted its review, the EMA said on Tuesday that a warning about “very rare cases of unusual blood clots with low blood platelets” should be added to the list of side effects for the vaccine, but that overall the benefits outweigh the risks.Having conducted its review, the EMA said on Tuesday that a warning about “very rare cases of unusual blood clots with low blood platelets” should be added to the list of side effects for the vaccine, but that overall the benefits outweigh the risks.
The decision was welcomed by the president of the EU Commission, Ursula von der Leyen, who tweeted a message calling the EMA’s announcement “good news for the roll-out of vaccination campaigns.”The decision was welcomed by the president of the EU Commission, Ursula von der Leyen, who tweeted a message calling the EMA’s announcement “good news for the roll-out of vaccination campaigns.”
European Commissioner for Health and Food Safety Stella Kyriakides shared similar sentiments, stating in light of the EMA’s ruling: “I urge EU Member States to follow the opinion of our experts. Vaccinations save lives.”European Commissioner for Health and Food Safety Stella Kyriakides shared similar sentiments, stating in light of the EMA’s ruling: “I urge EU Member States to follow the opinion of our experts. Vaccinations save lives.”
The EMA will continue to monitor the vaccine’s safety as new data becomes available, but the decision should now facilitate its use across Europe, allowing states to bolster Covid-19 inoculation rollouts, which have been hampered by delays and supply issues. Meanwhile, US authorities are due to meet on Friday to discuss the possible resumption of the vaccine there.The EMA will continue to monitor the vaccine’s safety as new data becomes available, but the decision should now facilitate its use across Europe, allowing states to bolster Covid-19 inoculation rollouts, which have been hampered by delays and supply issues. Meanwhile, US authorities are due to meet on Friday to discuss the possible resumption of the vaccine there.
Like this story? Share it with a friend!Like this story? Share it with a friend!
Dear readers and commenters,
We have implemented a new engine for our comment section. We hope the transition goes smoothly for all of you. Unfortunately, the comments made before the change have been lost due to a technical problem. We are working on restoring them, and hoping to see you fill up the comment section with new ones. You should still be able to log in to comment using your social-media profiles, but if you signed up under an RT profile before, you are invited to create a new profile with the new commenting system.
Sorry for the inconvenience, and looking forward to your future comments,
RT Team.