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...according to the Food and Drug Administration....
...A decision from the US Food and Drug Administration on Eli Lilly’s donanemab drug was originally due by the end of the first quarter but the breakthrough medicine will now be subject to a further review...
...A decision on Eli Lilly’s donanemab drug from the US Food and Drug Administration was originally due by the end of the first quarter, but the medicine will now be subject to a further review by an advisory...
...The US Food and Drug Administration says there is a shortage of Novo Nordisk’s and Eli Lilly’s diabetes drugs, while Belgium has banned the off-label use of Novo Nordisk’s diabetes drug for obesity treatments...
...These will be the first results from a study designed around landmark US Food and Drug Administration guidelines for researching psychedelics that were outlined last year, a decision that encouraged investors...
...The US Food and Drug Administration will allow Florida to import medicines from Canada, making it the first state to capitalise on rules designed to lower the cost of prescription drugs....
...The US Food and Drug Administration on Friday approved the world’s first ever two gene therapies to treat patients with sickle cell disease....
...The rush to secure manufacturing capacity comes as Wegovy and Mounjaro, which is also commonly prescribed off-label for weight loss, are in short supply, according to the US Food and Drug Administration....
...on behalf of the Food and Drug Administration....
...The Food and Drug Administration on Wednesday approved Zepbound for obese and overweight adults. About 70 per cent of adults in the US are obese or overweight, the FDA said....
...“There’s been a lot of noise about drugs that are illicit or copies or compounded versions of Zepbound or other weight loss drugs and that’s concerning to us and I think it’s concerning to patients, so by...
...The US Food and Drug Administration and the UK’s Medicines and Healthcare products Regulatory Agency said patients in clinical trials of Lilly’s tirzepatide had seen “significant” weight loss compared with...
...Brian Lian, Viking’s chief executive, said the company would meet regulators at the US Food and Drug Administration to assess next steps by the middle of the year....
...The so-called consent degree, the terms of which were agreed with the US Department of Justice on behalf of the US Food and Drug Administration, is subject to approval from the relevant US court, the company...
...On Tuesday, the US Food and Drug Administration issued a “device safety communication” about DreamStation 2. Philips launched this gadget three years ago to replace the discredited predecessor....
...“Drug trafficking gangs such as Los Choneros, many with ties to powerful drug cartels in Mexico, threaten the lives and livelihoods of communities in Ecuador and throughout the region,” Brian Nelson, the...
...Zepbound generated $175.8mn in worldwide sales in the fourth quarter, after only being approved for use by the US Food and Drug Administration in November....
...The US Food and Drug Administration gave approval for the trials in May....
...US taxpayers are in line to save $160bn over the next decade as the Biden administration announced that dozens of pharmaceutical companies would be penalised for raising drug prices faster than inflation...
...Last year the US food and drug watchdog sent Mead Johnson and two other formula manufacturers warning letters over their baby formula manufacturing standards, after Reckitt was forced to recall several batches...
...Food and Drug Administration said on Monday....
...The chief attraction is Karuna’s new schizophrenia treatment KarXT, which it has submitted to the US Food and Drug Administration with an anticipated decision to be made by next September....
...The Novo Nordisk drugs have been several decades in the works and Wegovy was first approved in the US in 2021....
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