Hints and tips:
Related Special Reports
...according to the Food and Drug Administration....
...“There’s always a tension between the human health people and animal health people,” said Scott Gottlieb, a former US Food and Drug Administration commissioner....
...The Department of Health and Human Services first recommended the agency remove cannabis’s schedule-1 classification last year, but the DEA’s determination was the next big hurdle....
...The US Food and Drug Administration advises against consuming raw (unpasteurised) milk products, to guard against pathogens such as salmonella and E-coli; H5N1 is now also on the list....
...Leqembi, priced at $26,500 a year, was the first drug with a black-box warning — the most severe designation about possible side effects — to be granted full approval by the US Food and Drug Administration...
...of Health and Human Services submitting a recommendation to the Drug Enforcement Agency last August (reported about then by Bloomberg and fully revealed in January by Texan lawyer Matthew Zorn) that cannabis...
...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...
...The US Food and Drug Administration last year approved over-the-counter sales of Narcan — the branded version of naloxone, a nasal spray used to reverse opioid overdoses — in the hope that greater access...
...The US Food and Drug Administration recently approved the first-ever drug designed specifically for the most common liver disease, metabolic dysfunction-associated steatohepatitis or mash, developed by Madrigal...
...to a US Food and Drug Administration database tracking shortages....
...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...
...In 2021, Philips recalled certain machines used to treat sleep apnoea after it was found that foam used in the devices could break down and be inhaled or swallowed, according to the US Food and Drug Administration...
...“The climate crisis has numerous impacts on ecosystems, human health, animal health and food production, which also affect AMR,” according to a report titled “Bracing for Superbugs” published last year by...
...According to a Food and Drug Administration database tracking drug shortages, lower doses of Wegovy have limited availability at present but higher doses and Ozempic injections are in good supply....
...Eli Lilly said that it plans to submit the results to the US Food and Drug Administration and other medicine regulators worldwide to seek approval for tirzepatide as a sleep apnoea treatment beginning this...
...and departments, both nationally and globally....
...It also puts fresh pressures on clean water and food supplies, hygiene and health systems — notably in parts of the country ravaged by civil war and poorly resourced ever since....
...The US Federal Drug Administration has disputed that finding (it first approved the artificial sweetener in 1974), noting that “aspartame is one of the most studied food additives in the human food supply...
...GSK, AstraZeneca, Novo Nordisk and Novartis were among 10 companies to receive letters from the FTC on Tuesday informing them that the agency had disputed a number of patents with the Food and Drug Administration...
...But the warming of the planet is delivering another equally alarming threat to human health and wellbeing....
...AI has the potential to significantly transform employment in many aspects of healthcare — from basic research to clinical care, patient monitoring and medical administration....
...Cultivated meat businesses argued they undergo close scrutiny by the US Food and Drug Administration and the US Department of Agriculture before products can be eaten....
...Part of the aim of the metformin trial is to persuade the US Food and Drug Administration to approve ageing as an “indication”, to signify that it can be “treated”....
...on behalf of the Food and Drug Administration....
...A Humira biosimilar from Teva Pharmaceuticals working with Alvotech earlier this year became the first drug that the US Food and Drug Administration granted interchangeable status, which lets pharmacists...
International Edition