The agency said last month it received applications from over 500 companies covering more than 6.5 million tobacco products. E-cigarettes have operated in a regulatory gray area for years. The products, which vaporize a nicotine-laced liquid, have been available in the United States since at least 2007, but the FDA did not formally get jurisdiction over the industry until May 2016.
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Nerve disorder listed as ‘very rare’ side effect of AstraZeneca jab
Guillain-Barre Syndrome was a “very rare” side effect, occurring in under one in 10,000 people, it added. The disorder is a nerve inflammation that may cause temporary paralysis and difficulty breathing. In the United States, the very rare syndrome affects an estimated 3,000 to 6,000 people each year and most go on to recover.
The US Food and Drug Administration also warned in July of an “increased risk” of developing the neurological syndrome with Johnson & Johnson’s dose. Both regulators stressed that the vaccine’s benefits outweighed the potential
India logs 34,973 new COVID-19 cases, 260 deaths
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