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South Korea's Ryu Hae-ran wins Women's PGA Championship
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Canada reach World Cup last 16 as late strike sinks South Africa
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Asia's World Cup falls apart with just two teams remaining
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Stokes announces shock England exit as New Zealand eye series win
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Bromell upsets Lyles, Duplantis shines at Paris Diamond League
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CAF president Motsepe hails African World Cup successes
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South Korea coach quits after early World Cup exit
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Stokes out for 30 in final Test innings after shock England retirement
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Hamilton laments lack of power and poor tyre performance
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Iran warns ships not to bypass its chosen Hormuz route
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Russell holds off Verstappen to win Austrian Grand Prix
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Serena blasts drug test rules ahead of Wimbledon return
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England captain Stokes to retire from international cricket
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Ogier wins Acropolis Rally to close in on Evans
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South Africa maintain World Cup semi-final hopes with nervy win over Bangladesh
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South Korea president apologises after World Cup group-stage exit
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Japan's Ogura wins maiden MotoGP as Bezzecchi crashes in Assen
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Bergs wins Eastbourne final to clinch first ATP title
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Ravindra and Mitchell strengthen New Zealand's grip on England decider
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Iran warns challenge to Hormuz routes will spike Middle East tensions
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BIS warns 'pressure points' putting global economy at risk
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US drug regulator limits use of J&J Covid vaccine
The US said Thursday only adults who "have personal concerns" about mRNA vaccines, access issues or medical reasons for refusing them may now receive the Johnson & Johnson Covid shot, which has been linked to a rare but serious clotting condition.
The vaccine, which was authorized as a single shot, is less protective than those developed by Pfizer and Moderna, and in December the Centers for Disease Control and Prevention advised the public to steer clear.
Thursday's decision by the Food and Drug Administration builds on that recommendation by limiting the J&J vaccine's emergency use authorization.
"Today's action demonstrates the robustness of our safety surveillance systems and our commitment to ensuring that science and data guide our decisions," said FDA scientist Peter Marks in a statement.
Sixty US cases of thrombosis with thrombocytopenia syndrome (TTS), which produces rare and potentially life-threatening blood clots with low levels of blood platelets, had been reported by March 18, with nine deaths.
Symptoms begin approximately one to two weeks following administration, and the condition -- which can cause life-long impacts even when not fatal -- occurs more frequently in premenopausal women.
Concerns over the vaccine have already limited uptake: Only 18.7 million doses have been administered in the United States, or about 3.2 percent of the total 577 million.
But the FDA stopped short of an outright de-authorization, with Marks acknowledging the impact a ban might have on global use of the vaccine, as well as concerns some may have specifically against mRNA vaccines, rather than the adenovirus vector platform J&J uses.
There are certain health-based justifications for not taking an mRNA vaccine -- such as rare instances of heart inflammation in adolescent males and young men -- although these are usually transient in nature and the vast majority affected recover completely.
However, anti-vaccine groups have also raised more general objections against mRNA vaccines, which are tied to conspiracy theories.
Although those types of concerns are not rooted in evidence, the exemption to use J&J's shot nonetheless extends to "individuals who have personal concerns with receiving mRNA vaccines and would otherwise not receive a Covid-19 vaccine," the FDA's statement said.
R.Chavez--AT