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Jun 13, 2024
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they sued the fda. othe conscious otection but that's happening far dowm at the hospital level and the only way to prida remedy based on this injuryaso grant this nationwide relief that is so far removed from fda's regulatory authory 's ultimately requiring all women everywhere to change the use of this drug. it's worth stepping back finally and taking the profoun mh between a serious injury in a remedy thaondents obtained. they have said that theyr that there might be some emergency-room doctor somewhere someye might be presented with some woman who is suffering anncredibly rare complication at the doctor might have to provide tatment notwithstanding the conscious protection. materialized to what the court did is to guard against at rete risk and nationwide relief for sticks access to mifepristone to every single minus country thataus harm. it harms the pharmaceutical industry whichsounding alarm bells in this sen saying this wouldestabilize improving and regulating drugs and it harms women who need ac
they sued the fda. othe conscious otection but that's happening far dowm at the hospital level and the only way to prida remedy based on this injuryaso grant this nationwide relief that is so far removed from fda's regulatory authory 's ultimately requiring all women everywhere to change the use of this drug. it's worth stepping back finally and taking the profoun mh between a serious injury in a remedy thaondents obtained. they have said that theyr that there might be some emergency-room...
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Jun 11, 2024
06/24
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the problem here is they sued the fda. the fda has nothing to do with it -- with the enforcement of protection. that is all happening far downstream. d the only way to provide a remedy therefore was to grt this kind of nationwide release that is so far removed from the regulatory authorities that it is ultimaty requirement all women everywherto change for this drug. i think it is worth stepping ba a thinking about the profoundistch between tt injury and the remedy of the response obtained. they said the fear that there might be se ergency room doors who may be presented with incredibly rare applications and the doctor ma have to provide treatment -- we don't think that harm has materializedutith the court date is entered sweeping nationwide belief that restricts access for everyine woman in this country and that causes profound harm. harm the agenc it harms the part of it -- it harms the pharmaceutical industry saying that this would be -- destabilize the system for approving and regulatingrugs. the court should reverse in
the problem here is they sued the fda. the fda has nothing to do with it -- with the enforcement of protection. that is all happening far downstream. d the only way to provide a remedy therefore was to grt this kind of nationwide release that is so far removed from the regulatory authorities that it is ultimaty requirement all women everywherto change for this drug. i think it is worth stepping ba a thinking about the profoundistch between tt injury and the remedy of the response obtained. they...
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Jun 10, 2024
06/24
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its entirely consistent with fda number in 2020, the fda said the emperor visit was necessary to preserve women's al because the impression visit is the best opportunity to examine things like -- thingbserve pregnancy and age of consent. because the general said that initial impression visit that had no requirement of an ulasound or any effort to detect fetal heartbe except it would not necessilgive inaccurate read gtational age. so i would not necessarily be eliminated? >> i think the fda'undated shows that race didn't up. if you look at the study, it shows a nearly threefold increa when you have -- when you removed it. it was about 2.1 without. >> when they remove this, it took away the opportuny do that. i think a cog -- medical orgazaons that created that are best practice. what is allowed under this a couple of screening questions. i do think that is nearly as good as an in-person exam. quest let's say that -- let's just carve out and putside this -- explain to me what addion costs you might have incurred or what your resources had diverted in aayhat would set aside havens. >> puttin
its entirely consistent with fda number in 2020, the fda said the emperor visit was necessary to preserve women's al because the impression visit is the best opportunity to examine things like -- thingbserve pregnancy and age of consent. because the general said that initial impression visit that had no requirement of an ulasound or any effort to detect fetal heartbe except it would not necessilgive inaccurate read gtational age. so i would not necessarily be eliminated? >> i think the...
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Jun 30, 2024
06/24
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fda wanted to regmo.so fda set y management maturity program.n document at ■r manufacturers are good. but if the demand is not there. if people are not paying a little bit more for reliable drugs, then those steps have a hard ■htime getting a response in the industry. if■c tmanufacturing at this higr of being reliable, then the fda steps by themselves will not make a big difference. it is necessary and not sufficient. that's where cms comes in. cms not just pay for medical services, i used to tell my staff and i was there, you are the nation' agent how we pay mas such a big and cms right these optimal drugs, there is a whole bundle payment that doesn't pay a attention to whether or not the supply is ab senate financer proposals, some other similar proposals out there, are all about how can we change that? just like cms focuses have relic records, adequate staffing. is the least burdensome way to hel give hospitals financial support they need and the accountability for having reliable supply of drugs, too? kathleen: i know that your report on the
fda wanted to regmo.so fda set y management maturity program.n document at ■r manufacturers are good. but if the demand is not there. if people are not paying a little bit more for reliable drugs, then those steps have a hard ■htime getting a response in the industry. if■c tmanufacturing at this higr of being reliable, then the fda steps by themselves will not make a big difference. it is necessary and not sufficient. that's where cms comes in. cms not just pay for medical services, i...
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Jun 15, 2024
06/24
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fda from treatment. the technologies and many more innovations researched and developed some of which to find bridges eat treatment but doesn't do a lot more to be done. just over 40 years ago, only 38 drugs were fda approved. degree alone they were approved by the fda and get them intentionally. our job is to be sure it's ready and the market continues. i'm concerned we don't continue to encourage, we will be harming the potential for development. many of the bills before us today provide the necessary to ensure normal therapy continued to be accessible for patients as rapidly as possible as we work to carry out that, we were carefully today to ensure doesn't have this effect. we need to make sure constructs are approved, patients can actually access them. concentrated at or limited and it may come down to whether the patient can't afford to travel and receive life-saving. patient axis act will make these cost more manageable in the case of a child, parent, and the care they need allowing drug manufactu
fda from treatment. the technologies and many more innovations researched and developed some of which to find bridges eat treatment but doesn't do a lot more to be done. just over 40 years ago, only 38 drugs were fda approved. degree alone they were approved by the fda and get them intentionally. our job is to be sure it's ready and the market continues. i'm concerned we don't continue to encourage, we will be harming the potential for development. many of the bills before us today provide the...
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Jun 13, 2024
06/24
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trying to expand the authority of the fda.e it doesn't. >> michael: we sure hope it doesn't. all right, erielle. thank you very much for bringing that to our attention. this morning we are celebrating the life of one of the greatest basketball players to ever grace the court. jerry west was so good he inspired the silhouette on the league's logo. we have more on his life and legacy. good morning again, will. >> reporter: it's hard to overstate the impact that jerry west had on basketball and nearly impossible to lift his myriad accomplishments as a player, as an kpeb executive as a representative of the game for decades. today the nba and fans everywhere are commemorating the life of the logo. jerry west cut a singular figure in basketball for over 60 years. after starring in college for his home state west virginia mountaineers, west won a gold medal for team usa at the 1960 rome olympics. >> there has never been a thrill in my life than winning a gold medal for our basketball team. >> reporter: an all star in each of his 14
trying to expand the authority of the fda.e it doesn't. >> michael: we sure hope it doesn't. all right, erielle. thank you very much for bringing that to our attention. this morning we are celebrating the life of one of the greatest basketball players to ever grace the court. jerry west was so good he inspired the silhouette on the league's logo. we have more on his life and legacy. good morning again, will. >> reporter: it's hard to overstate the impact that jerry west had on...
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Jun 15, 2024
06/24
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because the fda also valley.ely come up an independent review asked for by the fda commissioner found that the fda has never told companies precisely what is required to get these products approved it on the market. they were not following the size and are simply ignoring it. griff: tony this talk about the problem what it is for the youth we've been showing you if you fox packed through the bottom and we can put up over there 2 million young youth using these e-cigarette progress products and bringing down the up 10 percent of the high school students, and over four and a half of them are middle schoolers said that is concerning. tony: of course is concerning we been talking about this issue for years draft in advocating on the hill, for commonsense reforms that would actually address the issues new marketing for the good news is that i was able to share with the committee, this topic talk about is affected 2019, president trump is being asked to be all flavored he cigarettes and needed something about smarter.
because the fda also valley.ely come up an independent review asked for by the fda commissioner found that the fda has never told companies precisely what is required to get these products approved it on the market. they were not following the size and are simply ignoring it. griff: tony this talk about the problem what it is for the youth we've been showing you if you fox packed through the bottom and we can put up over there 2 million young youth using these e-cigarette progress products and...
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Jun 13, 2024
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this does not credit the fda's approval of mifepristone.simply says these are not the right plaintiffs to bring this case, and the anti-abortion movement is going to find the right plaintiffs. and lisa mentioned that unnamed law professor, it's me, hi, i'm the unnamed law professor. i think she's exactly right. they're going to look for women who were injured by mifepristone. if they can't find women, doctors who have very clear economic injuries or who have been denied conscience protections and have had to provide mifepristone against their conscience wills. that is going to be coming down the pike. what no one has talked about in this 38-page opinion is that it was unanimous but justice clarence thomas, one of the most stalwart objectors to abortion on the court filed a separate concurrence, and in that concurrence he railed against the court's third-party standing doctrine. he said if this particular organization lacks standing, then other organizations including abortion providers, abortion clinics who frequently bring lawsuits challen
this does not credit the fda's approval of mifepristone.simply says these are not the right plaintiffs to bring this case, and the anti-abortion movement is going to find the right plaintiffs. and lisa mentioned that unnamed law professor, it's me, hi, i'm the unnamed law professor. i think she's exactly right. they're going to look for women who were injured by mifepristone. if they can't find women, doctors who have very clear economic injuries or who have been denied conscience protections...
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Jun 10, 2024
06/24
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but, of course, it all depends on, on the fda's approval. and the hope would be i think it's less about the demand of the drug and more about the accessibility of getting it through health systems and having, having access to all of the other treatment that, and testing pieces that need to be given like a, like a pet scan and, and other sorts of evaluations, because these do have to be given to people that have that biological evidence of alzheimer's disease that build up of amyloid. and so it requires a little bit more testing. it also means that we need to think of ways to make sure that this has accessibility to everyone, not just those that live within a 45 mile radius of a large health system. >> very interesting. well, all of this, the potential to be groundbreaking. claire. that's all the time we have for now. thank you for joining us. >> thank you very much. >> up next, apple's taking a bite out of ai. cnet technology reporter abrar al-hadi joins us next to share all the reveals from apple's worldwide developer co ♪ do what you want
but, of course, it all depends on, on the fda's approval. and the hope would be i think it's less about the demand of the drug and more about the accessibility of getting it through health systems and having, having access to all of the other treatment that, and testing pieces that need to be given like a, like a pet scan and, and other sorts of evaluations, because these do have to be given to people that have that biological evidence of alzheimer's disease that build up of amyloid. and so it...
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Jun 27, 2024
06/24
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implications are in a world without chevron. >> if we think about this historically, how we got the fda, it is not something that the framers, the founders thought of. it's not something that the pilgrims brought over, so to speak, what does it come out of? it comes out of a crafty, thoughtful journalist writer who was spending time on the south side of chicago a century ago and looking at meat-packing plants and what he is finding in the meat-packing plants is so horrific, so deeply horrific, what is going into the sausages -- it is redmeat, it is spoiled stuff. it's moldy. it's horrible. the book, "the jungle" comes out of that. this is what americans are eating. who is going to regulate the stuff he's talking about and it's from writing about the slop, writing about the infections, writing about the horrific conditions that those meat-packing workers are living under, and to be honest, we are still kind of in that space. there have been these in-depth studies. we can defer that conversation for another panel but what meat- packing looks like in the united states still today but this
implications are in a world without chevron. >> if we think about this historically, how we got the fda, it is not something that the framers, the founders thought of. it's not something that the pilgrims brought over, so to speak, what does it come out of? it comes out of a crafty, thoughtful journalist writer who was spending time on the south side of chicago a century ago and looking at meat-packing plants and what he is finding in the meat-packing plants is so horrific, so deeply...
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Jun 13, 2024
06/24
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the fda authority being challenged is a real concern. we just saw this week the idm of ivf being challenged, the idea of personhood is now being interjected too many legal opinions across many different states, this idea that a fetus has personhood is now going to create a challenge to ivf. everybody mark this, this show right now. we are going to have ivf challenges that will go to the supreme court because it is something that has been a recognized and safe medical procedure, going to be a problem. that is why this is, to dahlia's point, the spigot hasn't been turned off. we all need to be concerned that we don't have activist judges that are allowing plaintiffs that don't have standing or allowing issues that don't exist to be created simply for the purpose to get in front of the supreme court that has a 6-3 conservative majority. now i will flip it to dahlia to talk about the comstock act. >> very quickly, the comstock act is a zombie law. we thought it was defunct, it was an anti-vice statute that allowed the government to path thro
the fda authority being challenged is a real concern. we just saw this week the idm of ivf being challenged, the idea of personhood is now being interjected too many legal opinions across many different states, this idea that a fetus has personhood is now going to create a challenge to ivf. everybody mark this, this show right now. we are going to have ivf challenges that will go to the supreme court because it is something that has been a recognized and safe medical procedure, going to be a...
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Jun 13, 2024
06/24
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the fda could change its decision about mifepristone. so, you know, i think this issue is far from definitively resolved, even though this case is over an anti-abortion rights group outside the supreme court today. >> obviously, we were disappointed. so the court ruled against the alliance for hippocratic medicine, but we weren't super surprised. that was what we expected, and we're going to be back. >> and a spokeswoman for danco, the maker of mifepristone, says they are pleased with the high court's decision today, calling it an incredibly important case. perry russom abc news at the supreme court. >> now, even as the medication abortion options remain available for now, new numbers out today show that ever since the high court overturned roe v wade two years ago, traveling out of state for surgical abortions has skyrocketed. joining us live now to talk about the first in-depth look at this trend, kelly baden, vice president of public policy for guttmacher institute. that's a research and policy organization that was once part of plann
the fda could change its decision about mifepristone. so, you know, i think this issue is far from definitively resolved, even though this case is over an anti-abortion rights group outside the supreme court today. >> obviously, we were disappointed. so the court ruled against the alliance for hippocratic medicine, but we weren't super surprised. that was what we expected, and we're going to be back. >> and a spokeswoman for danco, the maker of mifepristone, says they are pleased...
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Jun 22, 2024
06/24
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KDTV
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la fda autorizÓ un cigarrillo electrÓnico mentolado, argumentando que es malo para la salud pero queiene tÉrmino medio. reportera: la fda autorizÓ el primer cigarrillo electrÓnico mentolado bajo el argumento de que es malo para la salud, pero es menos nocivo para un fumador que trata de dejar de fumar. un cardiÓlogo dice que es malo el fumar y no tiene tÉrminos medios. >> las personas que estÁn tratando de dejar de fumar, posiblemente sea algo que es menos daÑino que el cigarro y puede ser un sustituto, pero el consejo que le doy a cualquier persona es que no pongan nada de fumar en su boca. va a traer consecuencias de salud. reportero: la fda citÓ un estudio hecho por la empresa de tabaco que produce cigarrillos mentolados. la fda dice que segÚn su revisiÓn cientÍfica los adultos fumadores se benefician al reemplazar el cigarrillo electrÓnico mentolado que tienen menos sustancias nocivas. >> hay un aumento de infartos. hay una disfunciÓn en las arterias. hay un aumento de infartos cerebrales. puede causar asma. puede causar daÑos al pulmÓn. puede causar cÁncer de pulmÓn. esto no es
la fda autorizÓ un cigarrillo electrÓnico mentolado, argumentando que es malo para la salud pero queiene tÉrmino medio. reportera: la fda autorizÓ el primer cigarrillo electrÓnico mentolado bajo el argumento de que es malo para la salud, pero es menos nocivo para un fumador que trata de dejar de fumar. un cardiÓlogo dice que es malo el fumar y no tiene tÉrminos medios. >> las personas que estÁn tratando de dejar de fumar, posiblemente sea algo que es menos daÑino que el cigarro y...
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Jun 26, 2024
06/24
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that is where you get■-;f the issue of how far ahead to the fda look? do we have on staff to make sure we can have them all around the world? they are all around the world, but do we have enough people, quitis there so even if ite the is not produced here, we don't have these shutdnskathleen: is o address that? act is hoping to map of all of this, the supply chain in one place, health and human services. then, have the experts -- i would not congres count congress in that. the peth doing as it relates to productive manufacturing. if you have the data that you understand where the vulnerabilities at, maybe you can address those. kathleen: let's talk about the generics specifically. you have highlighted how they have these issues. in particular, what we need to do.■7i hear so many people say s quality. instead of having this race to the bottom on pricing, you have to find a way to reward qualy. thoughts on that? how do we do that? rep. bucshon: free market econot is a difficult challenge. because, of course,n these medications and there are various degree
that is where you get■-;f the issue of how far ahead to the fda look? do we have on staff to make sure we can have them all around the world? they are all around the world, but do we have enough people, quitis there so even if ite the is not produced here, we don't have these shutdnskathleen: is o address that? act is hoping to map of all of this, the supply chain in one place, health and human services. then, have the experts -- i would not congres count congress in that. the peth doing as...
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Jun 13, 2024
06/24
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way fda regulates medicines with threaten the pharmaceutical industries bloody to depend on the fda as the key regulator of medicines, gym all right, make sure we're all very significant development coming out of the supreme court. >> i want to bring in gloria borger, who's with me here in the studio. glory. i mean, this, this is a major development. i mean, obviously if the supreme court had had done something to take away access to mifepristone. this would have just sent shock waves right around the country no more than half of the women terminating pregnancies in this country right now, use this pill yeah. and so that would have had a huge effect. also, the people who petitioned the court wanted a prescription for this drug to have to be done in person as mega was saying person to dr. rather than get just getting it at your pharmacy, are doing it virtually. and that would be the case. and so, you know, as paula was saying, they didn't decide the case, they decided that people who brought the case didn't have standing butt to bring the case, but it has the same impact, which is th
way fda regulates medicines with threaten the pharmaceutical industries bloody to depend on the fda as the key regulator of medicines, gym all right, make sure we're all very significant development coming out of the supreme court. >> i want to bring in gloria borger, who's with me here in the studio. glory. i mean, this, this is a major development. i mean, obviously if the supreme court had had done something to take away access to mifepristone. this would have just sent shock waves...
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Jun 3, 2024
06/24
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KDTV
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actualmente estÁn esperando que lo apruebe la fda.uchas gracias, saludos a todos. Éste es un mÉtodo excelente que promete ser una muy buena opciÓn para todos los hombres para ayudarle a las mujeres a llevar esta responsabilidad de la anticoncepciÓn. la efectividad sobre lo que sea evaluado en un 86%, a diferencia de los otros mÉtodos que se habÍa intentado hacer en el pasado, este mÉtodo es mucho mÁs rÁpido en desarrollar el bloqueo de la producciÓn del espermatozoide. es algo muy bueno que se puede venir dentro de poco para nosotros los hombres. borja: a diferencia de las pÍldoras, inyecciones, parches que ya estÁn disponibles sobre todo para las mujeres, esto es un gel, como hombre me gustarÍa saber cÓmo funciona y si podrÍa tener algÚn tipo de efecto secundario. ¿quÉ piensa usted, doctor? >> excelente pregunta. lo que se ha visto es un ligero aumento del peso en alguna de las personas, pero este peso puede que se aumenta debido a una persona sedentaria con parece ser que no es el mÉtodo como tal, hay alguna reacciÓn alÉrgica tÓpica
actualmente estÁn esperando que lo apruebe la fda.uchas gracias, saludos a todos. Éste es un mÉtodo excelente que promete ser una muy buena opciÓn para todos los hombres para ayudarle a las mujeres a llevar esta responsabilidad de la anticoncepciÓn. la efectividad sobre lo que sea evaluado en un 86%, a diferencia de los otros mÉtodos que se habÍa intentado hacer en el pasado, este mÉtodo es mucho mÁs rÁpido en desarrollar el bloqueo de la producciÓn del espermatozoide. es algo muy...
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Jun 13, 2024
06/24
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CNNW
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this makes the fda commissioner position of very political one in the next election, because an fda commissioner could come in and direct the agency then to sort of peel back some of the things that they have allowed in terms of access to mifepristone. this is one of two pills used in medication abortion. medication abortion is the most common way that people access abortion in the united states accounted for 63% i've abortions in 2023, there were 1 million abortions that year according to guttmacher institute datas, lets more than 600,000 people who are accessing this pill. now if mifepristone access were rolled back, it wouldn't disappear from the market completely if the supreme court had ruled in the opposite way today, but it would have made it very difficult to get through telemedicine something that has become an increasing way that people access medication, abortion in the united states. but as we've heard from all of your experts, it does not sound like this challenge is done either. it could come back through the courts with different plaintiffs who may have a better argum
this makes the fda commissioner position of very political one in the next election, because an fda commissioner could come in and direct the agency then to sort of peel back some of the things that they have allowed in terms of access to mifepristone. this is one of two pills used in medication abortion. medication abortion is the most common way that people access abortion in the united states accounted for 63% i've abortions in 2023, there were 1 million abortions that year according to...
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Jun 30, 2024
06/24
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CSPAN
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number one, quality related sucan the fda keep up and make sure the manufacstandards? they are not. and, who controls the export of the aical ingredient? it can get tied up in geopolitical dispu like seen during covid with the chinese. , not as much with india because they're democracy and a like-minded country. we did seeh÷ with carbon platin, there was a quality issue. into the issue of how far ahead to the k? how many people do we have on staff to make sure we can have the world? they are all around the world, but do we have enough people, enough funding to make sure the quality is there so even if it is not produce't have these shutdowns. kathleen:s that? rep. bucshon: the act to have a map of all ofhi the supply chain in one place, health and human svices.then, hi would not congress -- count cong i that. the experts that know what they are doing as it relates to distribution, productive manufacturing. the data that you understand where the vulnerabilities at, maybe you can address those. kathleen: let's talk about the ge■gri specifically. you have highlighted how
number one, quality related sucan the fda keep up and make sure the manufacstandards? they are not. and, who controls the export of the aical ingredient? it can get tied up in geopolitical dispu like seen during covid with the chinese. , not as much with india because they're democracy and a like-minded country. we did seeh÷ with carbon platin, there was a quality issue. into the issue of how far ahead to the k? how many people do we have on staff to make sure we can have the world? they are...
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Jun 20, 2024
06/24
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KGO
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keytruda is known to treat cancer, fda-approved for 17 types of cancer.ced nonsquamous, non-small cell lung cancer, where keytruda is approved to be used with certain chemotherapies as your first treatment if you do not have an abnormal “egfr” or “alk” gene. keytruda can cause your immune system to attack healthy parts of your body during or after treatment. this may be severe and lead to death. see your doctor right away if you have cough, shortness of breath, chest pain, diarrhea, severe stomach pain, severe nausea or vomiting, headache, light sensitivity, eye problems, irregular heartbeat, extreme tiredness, constipation, dizziness or fainting, changes in appetite, thirst, or urine, confusion, memory problems, muscle pain or weakness, fever, rash, itching, or flushing. there may be other side effects. tell your doctor about all your medical conditions, including immune system problems, if you've had or plan to have an organ, tissue, or stem cell transplant, received chest radiation or have a nervous system problem. depending on the type of cancer, keyt
keytruda is known to treat cancer, fda-approved for 17 types of cancer.ced nonsquamous, non-small cell lung cancer, where keytruda is approved to be used with certain chemotherapies as your first treatment if you do not have an abnormal “egfr” or “alk” gene. keytruda can cause your immune system to attack healthy parts of your body during or after treatment. this may be severe and lead to death. see your doctor right away if you have cough, shortness of breath, chest pain, diarrhea,...
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Jun 11, 2024
06/24
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the fda will make the final decision later on this year. >>> and the fda is warning people from eatingate. it says the shellfish may be contaminated with toxins that cause paralytic issues. at least 31 people have been sickened in oregon. the fda says to avoid baked shellfish and clams since the end of last month. >>> and a diet that's good for you may also be good for the planet. a new study in the american journal of clinical nutrition found those who eat more plants and less processed foods can lower their risk of early death by 30%. the so-called planetary health diet also had lower greenhouse gas emissions. the diet encourages eating nuts, beans, fruits, vegetables, and less meat and sugar. >>> coming up only on "cbs mornings," we will reveal oprah winfrey's newest book club selection. winfrey's latest good club selection. and who are anti-achr antibody positive, season to season, ultomiris is continuous symptom control, with improvement in activities of daily living. it is reduced muscle weakness. and ultomiris is the only long-acting gmg treatment with the freedom of just 6 to 7
the fda will make the final decision later on this year. >>> and the fda is warning people from eatingate. it says the shellfish may be contaminated with toxins that cause paralytic issues. at least 31 people have been sickened in oregon. the fda says to avoid baked shellfish and clams since the end of last month. >>> and a diet that's good for you may also be good for the planet. a new study in the american journal of clinical nutrition found those who eat more plants and...
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Jun 13, 2024
06/24
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right now, there are only 23 e-cigarette products that are approved by the fda in new york.hansen, ktvu, fox two news new at five tonight, the republican majority in the house voted to hold attorney general merrick garland in contempt of congress. >> gop lawmakers took issue with garland's refusal to turn over audio of president biden's interview in his classified documents case. today's vote is largely symbolic, as the white house issued executive privilege over the audio shielding it from congress, garland saying in a statement, quote, it is deeply disappointing that this house of representatives has turned a serious congressional authority into a partizan weapon. today's vote disregards the constitutional separation of powers. the justice department's need to protect its investigative actions, and the substantial amount of information we have provided to the committees. >> the white house held its first press briefing today since hunter biden was convicted in his federal gun trial, and a spokesperson did not rule out a commutation. president biden has ruled out pardoning
right now, there are only 23 e-cigarette products that are approved by the fda in new york.hansen, ktvu, fox two news new at five tonight, the republican majority in the house voted to hold attorney general merrick garland in contempt of congress. >> gop lawmakers took issue with garland's refusal to turn over audio of president biden's interview in his classified documents case. today's vote is largely symbolic, as the white house issued executive privilege over the audio shielding it...
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Jun 11, 2024
06/24
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but, of course, it all depends on, on the fda's approval.ope would be i think it's less about the demand of the drug and more about the accessible of getting it through health systems, and having having access to all of the other treatment, and testing pieces that need to be given like a, like a pet scan and, and other sorts of evaluations, because these do have to be given to people that have that biological evidence of alzheimer's disease that build up of amyloid. and so it requires a little bit more testing. it also means that we need to think of ways to make sure that this has accessibility to everyone, not just those that live within a 45 mile radius of a large health system. >> a lot of good information in there, as you can tell. you can watch live interviews like that every weekday at 3 p.m. right here on abc seven. >> the heat will be with us tomorrow. sandhya has a preview of the temperatures to expect where you live. >> plus building a better bay area one snapshot at a time. the new contest trying to protect a beautiful space throu
but, of course, it all depends on, on the fda's approval.ope would be i think it's less about the demand of the drug and more about the accessible of getting it through health systems, and having having access to all of the other treatment, and testing pieces that need to be given like a, like a pet scan and, and other sorts of evaluations, because these do have to be given to people that have that biological evidence of alzheimer's disease that build up of amyloid. and so it requires a little...
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Jun 13, 2024
06/24
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CNNW
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on women who need this drug on the fda. it's regulatory powers, something that at the supreme court had opted to weigh in could have enormous implications for the entire pharmaceutical industry and other medical devices then also potentially impact on the 2024 race but they have effectively sidestep to this issue standing is a technical aspect of what you need to bring a case and they're saying that the people who brought this challenge did not have standing. they've not illustrated that they have an injury. if they have a complaint or a concern about and if a person stone justice kevin and the other justices suggested that they go color congress person to talk about legislative solutions or go through the executive branch. but this is not the way they can bring a case to the supreme court, but i fully expect that others who may have standing will try to challenge the same issue and then eventually the supreme court may opt to weigh in. but here they have preserve the status quo not shocking based on what we saw an oral arg
on women who need this drug on the fda. it's regulatory powers, something that at the supreme court had opted to weigh in could have enormous implications for the entire pharmaceutical industry and other medical devices then also potentially impact on the 2024 race but they have effectively sidestep to this issue standing is a technical aspect of what you need to bring a case and they're saying that the people who brought this challenge did not have standing. they've not illustrated that they...
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Jun 26, 2024
06/24
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that is where you get■ into the issue of how far ahead to the fda look?o mae them all around the world? they are all around the but do we have enough people, enough funding to make sure ■ñ quality is there so even if it is not produced here, we don't have these shukathleen: is thero address tt?rep. bucshon: the acg e map of all of this, the supply chain in one place, health and human services. then, have thets -- i would not congress in that. exathey are doing as it relates to supply chain, distribution, productive manufacturing. understand where the vulnerabilities at, maybe you can esose. kathleen: let's talk about the generics specifically. you haveighlighted how they have these issues. in particular, what we need to do. i hear so many people say it is quality. ttom on pricing, you have to find a way to reward itwhat ? how do we do that? rep. bucshon: have to but it is a free market economy and it is a difficult challenge. because, of course, people are dependent on these medications and there are various of the ability of people to afford them. whr th
that is where you get■ into the issue of how far ahead to the fda look?o mae them all around the world? they are all around the but do we have enough people, enough funding to make sure ■ñ quality is there so even if it is not produced here, we don't have these shukathleen: is thero address tt?rep. bucshon: the acg e map of all of this, the supply chain in one place, health and human services. then, have thets -- i would not congress in that. exathey are doing as it relates to supply...
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Jun 15, 2024
06/24
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KRON
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and now the fda is making changes to vaccine requirements to target the strain of covid.re most worried about. you probably noticed an increase of positive covid cases among friends and family. luke willis of san francisco recently posted on instagram to tell his followers about his recent bout with the virus. >> had swelling, incredible fever night sweats like all the things. it was really i wish i had gotten a booster. >> it's an unfortunate trend that's happening all over the country. according to infectious disease expert at ucsf doctor peter chin. hong. if you look at the country, for example, there's been about 15% increase in emergency department visits >> over the last week, the strain of covid that the food and drug administration is most concerned about is called kp too, which accounts for just over 22% of cases in the u.s. not the majority, but the fda has advised drugmakers like pfizer and moderna to update their covid vaccines to target that strain because they believe it will account for the majo o
and now the fda is making changes to vaccine requirements to target the strain of covid.re most worried about. you probably noticed an increase of positive covid cases among friends and family. luke willis of san francisco recently posted on instagram to tell his followers about his recent bout with the virus. >> had swelling, incredible fever night sweats like all the things. it was really i wish i had gotten a booster. >> it's an unfortunate trend that's happening all over the...
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Jun 13, 2024
06/24
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KRON
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so called the store or right near the fda's headquarters. >> i can't go through every single product on that. will tell you that it's a >> the point here is this is a shelf full. a potentially dangerous substances in a store in the shadow of the fda building. >> according to a cdc report, e-cig usage went down among high school students between 2022 2023. but lawmakers know many kids are already addicted to vaping. i couldn't spend quality time with my friends without thinking about when we're going to get our next hit. new jersey senator cory booker is concerned about the overwhelming number of the e 6 sold in the u.s. that are marketed towards kids and come from china. do they pose a threat? could they pose a threat? i would say that any of the products, regardless of whether coming from china are not could. the fda says it has a system to review what's in the e 6 that come from abroad. >> but it is overwhelmed by millions of applications for product approval reporting in washington. i'm basil, all right now to our 4 zone forecast as we get a live look outside right now at. >> our
so called the store or right near the fda's headquarters. >> i can't go through every single product on that. will tell you that it's a >> the point here is this is a shelf full. a potentially dangerous substances in a store in the shadow of the fda building. >> according to a cdc report, e-cig usage went down among high school students between 2022 2023. but lawmakers know many kids are already addicted to vaping. i couldn't spend quality time with my friends without thinking...
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Jun 16, 2024
06/24
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them the fda about?hat was the most important issue here altogether, kira much more than mifepristone, which was important in itself. what the supreme court might have done with the fda. and again, we don't know the jury's out. but for now, this this issue has been dodged. and ever since roe was overturned, this has been a hot button issue in the us once again. so do you think this decision or non-decision means that the abortion issue will remain an issue for the supreme court and all likelihood, yes. and sooner than we think. look next year, of course we could. we could very well have a woman who has been harmed, who claims she's been harmed by the drug come, go bring a case before the supreme court, in which case it probably would decide it one way or the other. but more important than that, cure, we have another case on the court's docket that they're likely to decide later this month. it's called idaho versus the united states. what is that all about? well, there's the state of idaho passed a very,
them the fda about?hat was the most important issue here altogether, kira much more than mifepristone, which was important in itself. what the supreme court might have done with the fda. and again, we don't know the jury's out. but for now, this this issue has been dodged. and ever since roe was overturned, this has been a hot button issue in the us once again. so do you think this decision or non-decision means that the abortion issue will remain an issue for the supreme court and all...
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Jun 5, 2024
06/24
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the fda will still make a decision. this will come on or about august 11.ere was a recent analysis on how this shakes out. 88% of the time, the fda does not follow its advisory committee. they tend, when they reject what the advisory committee says, too biased toward approval, and what is interesting about this one is there is a lot of congressional support here. this affects veterans, and it is a bipartisan issue. republicans and democrats have been pressuring and sending letters to the veterans administration, encouraging it to do what it can to further these studies. it is a frustrating thing. ptsd affects 13 million americans and there are not a lot of tools in the toolbox. geoff: miles o'brien, thank you for walking us through this important story. we appreciate it. >> you're welcome. ♪ amna: headlines around higher education this year have centered on protests, free speech, and student safety, but some important changes on the academic and admissions front have gotten less attention, including some schools turning back to standardized testing after de
the fda will still make a decision. this will come on or about august 11.ere was a recent analysis on how this shakes out. 88% of the time, the fda does not follow its advisory committee. they tend, when they reject what the advisory committee says, too biased toward approval, and what is interesting about this one is there is a lot of congressional support here. this affects veterans, and it is a bipartisan issue. republicans and democrats have been pressuring and sending letters to the...
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Jun 2, 2024
06/24
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one of the things the fda showed is that r.j. reynolds had applied for a patent to double the levels of nicotine in cigarets. that was a new fact that people had known before. another thing that fda commissioner david kessler brought out was that while up to 15% of people got addicted to alcohol when it came to cigarets, the addiction levels were 75 to 90% of smokers. those were new facts that waxman was trying to get out to public. but we had been discussing the effects of smoking since the 1950s, hadn't. and, of course, the famous surgeon general's report in the early sixties came out. that's true. the very first report that came out that linked smoking to cancer was in 1953. and there was a bigger report in 1954, in. the first big report in the united states, 1964. that u.s. surgeon general's report linking a to cancer. so yeah, those warnings had been out there, but not a lot of people pay attention to them and one of the things that mr. waxman tried to do was publicize those findings in the hearings that he held to get the w
one of the things the fda showed is that r.j. reynolds had applied for a patent to double the levels of nicotine in cigarets. that was a new fact that people had known before. another thing that fda commissioner david kessler brought out was that while up to 15% of people got addicted to alcohol when it came to cigarets, the addiction levels were 75 to 90% of smokers. those were new facts that waxman was trying to get out to public. but we had been discussing the effects of smoking since the...
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Jun 11, 2024
06/24
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KGO
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the fda still has to give final approval for the new drug. >> meantime, the fda is teaming up with the department of justice to crack down on the sale of illegal vapes. they're creating a task force to enforce tobacco laws, which can result in felony convictions, criminal fines as well. it comes just after the fda sent out over a thousand warning letters to distributors and manufacturers behind illegal tobacco products, including e-cigarettes. in december, the agency seized about 1.4 million units of unauthorized e-cigarette products. >> more money in more places for more fireworks. that's what san mateo county is hoping to continue again this year, with its second ever anonymous firework buyback event. this year, there's even more cash up for grabs. so as the summer heats up, abc seven news reporter lauren martinez shows us how it'll all work. >> ahead of this year's 4th of july, people can get a cash reward for turning in illegal fireworks during the month of june, the san mateo county sheriff's office will hold three buyback events. >> our hope is to just enhance community safety, s
the fda still has to give final approval for the new drug. >> meantime, the fda is teaming up with the department of justice to crack down on the sale of illegal vapes. they're creating a task force to enforce tobacco laws, which can result in felony convictions, criminal fines as well. it comes just after the fda sent out over a thousand warning letters to distributors and manufacturers behind illegal tobacco products, including e-cigarettes. in december, the agency seized about 1.4...
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Jun 12, 2024
06/24
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KTVU
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right now, there are only 23 e-cigarette products that are approved by the fda in new york.en, ktvu, fox two news, ktvu, fox two news at five starts now. >> now at 5:00, an increase in cameras showing signs of success in san francisco. police touting the results of their new license plate readers. despite the privacy concerns. >> automated license plate readers are by definition, mass surveillance. >> the police are monitoring. somebody's got to. somebodys got to see what's going on in the neighborhood at night. >> mixed reaction to the new numbers tonight. good evening. >> i'm julie julie haener and i'm mike mibach. tonight, city leaders looking to push back against the narrative that crime has no consequences in san francisco. >> ktvu christien kafton joins us now. he's live in the city. and christian backers of the cameras say they've already taken numerous criminals off the streets. >> yeah. that's right. right now there are about 100 cameras that look just like this one scattered throughout san francisco. supporters say those cameras are working to help track down crimi
right now, there are only 23 e-cigarette products that are approved by the fda in new york.en, ktvu, fox two news, ktvu, fox two news at five starts now. >> now at 5:00, an increase in cameras showing signs of success in san francisco. police touting the results of their new license plate readers. despite the privacy concerns. >> automated license plate readers are by definition, mass surveillance. >> the police are monitoring. somebody's got to. somebodys got to see what's...
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Jun 22, 2024
06/24
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and so like the fda should just move ahead. yeah. so i mean, for better or for worse in my current role, i can't get too far editorializing there. but but on the other hand, like, you know, as somebody who spent lot of time thinking about these issues, i'm kind of glad that i'm not in a prescriptive because the answers are really hard. but i do think the the point that people are already doing you know whether it's on their own at home and sort of self-medicating and taking matters into their own hands or know hiring a sitter off some website or, finding somebody on reddit or, you know, instagram becomes kind of their guide. like the reality is this is already happening. the reality is we're in environment where people perceive that the legal of acquiring or growing and selling these compounds is relatively because law enforcement is a lot more with far more addictive and destructive drugs like opioids. i think that is really the world as it exists you know people are going on these retreats these retreats and these experiences are b
and so like the fda should just move ahead. yeah. so i mean, for better or for worse in my current role, i can't get too far editorializing there. but but on the other hand, like, you know, as somebody who spent lot of time thinking about these issues, i'm kind of glad that i'm not in a prescriptive because the answers are really hard. but i do think the the point that people are already doing you know whether it's on their own at home and sort of self-medicating and taking matters into their...
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Jun 3, 2024
06/24
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one of the things the fda showed is that r.j. reynolds had applied for a patent to double the levels of nicotine in cigarets. that was a new fact that people had known before. another thing that fda commissioner david kessler brought out was that while up to 15% of people got addicted to alcohol when it came to cigarets, the addiction levels were 75 to 90% of smokers. those were new facts that waxman was trying to get out to public. but we had been discussing the effects of smoking since the 1950s, hadn't. and, of course, the famous surgeon general's report in early sixties came out. that's true. the very first report that came out that linked smoking to cancer was in 1953. and there was a bigger report in 1954, in. the first big report in the united states, 1964. that u.s. surgeon general's report linking a to cancer. so yeah, those warnings had been out there, but not a lot of people pay attention to them and one of the things that mr. waxman tried to do was publicize those findings in the hearings that he held to get the word
one of the things the fda showed is that r.j. reynolds had applied for a patent to double the levels of nicotine in cigarets. that was a new fact that people had known before. another thing that fda commissioner david kessler brought out was that while up to 15% of people got addicted to alcohol when it came to cigarets, the addiction levels were 75 to 90% of smokers. those were new facts that waxman was trying to get out to public. but we had been discussing the effects of smoking since the...
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Jun 4, 2024
06/24
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KQED
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miles: it's a complicated one for the fda.lking about a treatment regime that involves the drug plus a very elaborate set of psychotherapy and the fda, interestingly, does not regulate secretary. in addition, the psychotherapy was not standardized. the study also had a very fundamental problem which is to say it could not be properly blinded. those who receive mdma, ecstasy -- sugar pill. you know you did not. it was very difficult to get really objective results because the psychological factor of knowing that you have had it favors a favorable outcome or response, i should say and in addition to that, the company overlooked problems more so the committee determined, overlooked problems in his pursuit of approval of this drug. it really was a surprising decision particularly given what we have heard over the years from many of the center ice who have described this drug in this therapy as a life-changing experience. cj harden is a former army helicopter mechanic and machine gun and who faced imminent death in iraq and also af
miles: it's a complicated one for the fda.lking about a treatment regime that involves the drug plus a very elaborate set of psychotherapy and the fda, interestingly, does not regulate secretary. in addition, the psychotherapy was not standardized. the study also had a very fundamental problem which is to say it could not be properly blinded. those who receive mdma, ecstasy -- sugar pill. you know you did not. it was very difficult to get really objective results because the psychological...
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Jun 6, 2024
06/24
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CNBC
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it's the only fda-approved treatment to slow ga in as few as 6 doses per year.ection, or active swelling in or around your eye that may include pain and redness. syfovre can cause serious side effects, such as eye infection and retinal detachments, severe inflammation of vessels in the retina which may result in severe vision loss, wet amd, eye inflammation, and an increase in eye pressure. most common side effects are eye discomfort, wet amd, small specks floating in vision, and blood in the white of the eye. tell your doctor right away if you have any side effects. every moment counts—act now to slow ga with syfovre. ask your retina specialist about syfovre. >>> welcome back to "fast money." robinhood topping the tape after splashing $200 billion on bitstamp. it accelerating robinhood's push into digital assets. bitstamp, popular in europe and asia, gives robinhood a foothold abroad. robinhood now up more than 80% this year, at its highest since december 2021. as dan aptly pointed out during the break, you've been on this train forever, guy. >> we've done a de
it's the only fda-approved treatment to slow ga in as few as 6 doses per year.ection, or active swelling in or around your eye that may include pain and redness. syfovre can cause serious side effects, such as eye infection and retinal detachments, severe inflammation of vessels in the retina which may result in severe vision loss, wet amd, eye inflammation, and an increase in eye pressure. most common side effects are eye discomfort, wet amd, small specks floating in vision, and blood in the...
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Jun 20, 2024
06/24
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KRON
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to revive a lawsuit that accuses the fda of illegally bring the drug to market last week. the supreme court struck the lawsuit down. the justices unanimously ruled anti-abortion doctors did not have grounds to sue the fda. the decision based on a legal technicality allows the fda to continue this reckless disregard women's health. >> and as for now, the attorneys general are pushing to ban the drug nationwide. missouri republican senator josh hawley also has been of erin hawley. >> this is the suit is necessary to keep the drug out state with abortion bans like missouri. i don't want the federal government coming in over top of our voters and saying never mind what you want. we're going to mail and chemical abortion drugs into your state. that's wrong. >> for kansas, the legal challenges were complicated in 2022 voters there chose not to restrict abortion access kansans. we have been. so clear kansas democratic congresswoman davids calls the push to ban mifepristone extreme. they're attacking something that has been safely and effectively used for. the wiles says move up.
to revive a lawsuit that accuses the fda of illegally bring the drug to market last week. the supreme court struck the lawsuit down. the justices unanimously ruled anti-abortion doctors did not have grounds to sue the fda. the decision based on a legal technicality allows the fda to continue this reckless disregard women's health. >> and as for now, the attorneys general are pushing to ban the drug nationwide. missouri republican senator josh hawley also has been of erin hawley. >>...
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Jun 13, 2024
06/24
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the drug has been handled by th fda. >> bill: that could be a boomerang case coming back. standby in case there's more coming up momentarily. >> dana: , kellyanne, you have seen, you're no stranger to this , the democrats trying to make abortion the front and center issue of their campaign and their policies. will this supreme court decision , to at least take one part of that off the table? >> no, i think they will look a an opportunity to triple dharma that per the challenge for the democrats is they are for abortion anytime anywhere, read the party platform to verify that part i hope president trum and whoever he picks will be robust at least in exposing that . here is what i would do, i woul have a science conversation at this point with america. i would tell them that the same democrats that knew enough to mask up our five -year-old for the better part of two school years, look at a five -month-ol sonogram in pretend they don't see a baby sucking its thumb an the male organ on display. if babies are being born and th state when harris states of california, she went ho
the drug has been handled by th fda. >> bill: that could be a boomerang case coming back. standby in case there's more coming up momentarily. >> dana: , kellyanne, you have seen, you're no stranger to this , the democrats trying to make abortion the front and center issue of their campaign and their policies. will this supreme court decision , to at least take one part of that off the table? >> no, i think they will look a an opportunity to triple dharma that per the challenge...