EU Regulator Approves Johnson & Johnson COVID Vaccine

The Hague, March 11 (AFP/APP):The European Union’s medicines regulator approved the single-shot Johnson & Johnson coronavirus vaccine on Thursday — the fourth jab to get the green light for the 27-nation bloc.

The decision offers a boost for the EU’s sluggish vaccination programme even if reports say the first shipments of J&J doses may not arrive in European countries until April. “With this latest positive opinion, authorities across the European Union will have another option to combat the pandemic and protect the lives and health of their citizens,” European Medicines Agency (EMA) chief Emer Cooke said in a statement.

“This is the first vaccine which can be used as a single dose.”

Clinical trials involving volunteers in the United States, South Africa and South American countries found the Johnson & Johnson vaccine was 67 percent effective at preventing people from getting Covid-19, the EMA said. Side effects were “usually mild or moderate” and cleared within a couple of days, including pain at the injection site, headache, tiredness, muscle pain and nausea.

The European Commission welcomed the news and said it would grant formal authorisation “shortly” for the vaccine produced by the US pharma giant’s European subsidiary Janssen.

“This marks another key step towards ensuring that all citizens can access safe and effective vaccinations as soon as possible,” Health Commissioner Stella Kyriakides tweeted.

The EU has so far approved three vaccines — Pfizer-BioNTech, Moderna and AstraZeneca-Oxford. Three other vaccines are under “rolling review” by the Amsterdam-based EMA — Novavax, CureVac and Russia’s Sputnik. As well as being the first that requires a single injection as opposed to two, the Johnson & Johnson vaccine is easier to store.

The J&J shot however, appears less protective than Pfizer and Moderna’s regimes, which both have an efficacy of around 95 percent against all forms of COVID19 from the classic coronavirus strain.

Bumpy strategy

The EU has been struggling with a disappointing vaccination rollout that started in January and faltered because of a shortage of doses produced by the three suppliers so far. The head of the EU’s vaccine supply task force, Thierry Breton, said on Tuesday the EU’s “bumpy” vaccine strategy should be augmented by the addition of the Johnson & Johnson jab. Reported production shortfalls in the United States by Johnson & Johnson would not impact the EU because Brussels had made contingency plans for all vaccines, he said.

“Do not believe that because one company has a problem that overall it will jeopardise the whole programme,” said Breton, the EU’s industry commissioner.

Europe’s vaccination strategy faced fresh problems on Wednesday as Denmark, Norway and Iceland said they were temporarily suspending the use of AstraZeneca’s Covid-19 vaccine after some patients developed blood clots. Norway and Iceland are not in the EU but are covered by the EMA. Austria, Estonia, Latvia, Lithuania and Luxembourg have separately suspended the use of a particular batch of AstraZeneca vaccines after a 49-year-old nurse died of “severe blood coagulation problems” in Austria following a jab.

The EMA said Denmark’s move was “precautionary” and there appeared to be no higher risk of blood clots in those vaccinated against Covid-19.

“The information available so far indicates that the number of thromboembolic events in vaccinated people is no higher than that seen in the general population,” the EMA told AFP by email when asked about the suspension.

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