the fda. these actions do not allow us to recover monetary penalties, limiting their deterrent effect in some circumstances. but they are an important tool inappropriate cases. the department has secured injunctions against six entities, continues to litigate against another and just yesterday filed a proposed consent decree in our most recent case. we stand ready to act on additional referrals in consultation with the fda. we recognize that illegal distribution and sale of e-cigarettes is a complex and evolving problem that poses a grave threat to public health and safety. it demands urgency. while some progress has been made, there is still much work ahead of us. that is why earlier this week, the department and fda announced the creation of a multiagency task force with the sole purpose of addressing the threat posed by the sale of illegal e-cigarettes. the task force combines the expertise of multiple law enforcement partners, including atf, the u.s. postal inspection service, the u.s. mar

fda's decisions in court. the fda and over 80 legal challenges filed by manufacturers and will many of those matters have yet to be decided, we've revealed more than a dozen cases including any decision and seven court of appeal. the case in which we have received a significant adverse decision in the fifth circuit, that affirmative seeking review supreme court. the department also plays an important role in enforcing the tobacco control act. for example of the fda pursued monetary penalties against over 55 manufacturers, and 100 retailers and sent warning letters to hundreds more. all of thef, department cannot impose penalties itself, we are prepared to assist the fda and collection actions to ensure compliance. additionally, they partnered with the fda and significant enforcement actions. this includes the first mistake seizure of unauthorized e-cigarette, which included more than 45000 illegal e-cigarette. we also have the authority to bring civil injunction actions and matters referred to the department b

they sued the fda. fda has nothing to do with enforcement of the conscious protection but that's happening far downstream at the hospital level and the only way to provide a remedy based on this injury was to grant this nationwide relief that is so far removed from fda's regulatory authority it's ultimately requiring all women everywhere to change the use of this drug. it's worth stepping back finally and taking the profound mismatch between a serious injury in a remedy that respondents obtained. they have said that they fear that there might be some emergency-room doctor somewhere someday he might be presented with some woman who is suffering an incredibly rare complication at the doctor might have to provide treatment notwithstanding the conscious protection. we don't think that harm is materialized to what the court did is to guard against that remote risk and nationwide relief for sticks access to mifepristone to every single minus country that causes harm. it harms the pharmaceutical industry which

fda wanted to regulate more. so fda set up that quality management maturity program. steps where they can document at least on a pilot basis which manufacturers are good. but if the demand is not there. if people are not paying a little bit more for reliable supply, not just quality drugs, then those steps have a hard time getting a response in the industry. if they can't sustain their manufacturing at this higher cost 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's largest public health agent how we pay makes such a big difference and cms right now especially for these optimal drugs, there is a whole bundle payment that doesn't pay a attention to whether or not the supply is reliable or not. the senate finance bill, our proposals, some other similar proposals out there, are all about how can we change that? just like cms focuses on you have to have reliable electronic re

fda want you just regulate more pics of the fda sit up like i said that quality management surety program and steps for they can kind of document at least on a pilot basis which manufacturers are good, but if the demand isn't there, if people aren't paying a little bit more for reliable supply, not just quality drugs, those steps have a hard time getting a response in industry but they can't, if they can't sustain their manufacturing at this higher cost of being reliable, then the fda steps by themselves aren't going to make a big difference. so it is a necessary step. that is where cms comes in. cms not just pays for medical services. i used to tell my staff when i was there you are the nation's largest public health agency because how we pay makes such a big difference. at cms right now, has paid for, especially for these hospital drugs, it is a whole bundle payment that doesn't pay a lot of attention to whether or not the supply is reliable or not. and the senate finance bill, our proposals, some other some alone proposals that are out there all about well, how can we change that, have

again on the fda side when you have a peanut corporation of america, those inspections are set by fda. host: rick from pennsylvania. republican line. you are on. caller: hello. where i go boar's head is popular. are they pulling just some of the meats from boar's head or are they pulling all of them? thank you? guest: that is a great question and i would occurred you -- encourage you to ask the retailer if they have pulled the appropriate products. 7 million pounds have been recalled with certain production dates. but sometimes retailers miss them. there have been cases where they have recalled products that are still being sold. it should not be. if you are concerned at the other thing i would encouraged -- the other thing i would encourage you to do is check your refrigerator because the sell by date is into october. if it is in your refrigerator thrown away or take it back to the retailer and be sure to clean and sanitize your refrigerator. listeria loves to grow at cold temperatures. so most pathogens if you put stuff in the refrigerator it will kill the pathogen but the pathogen

that the fda didn't spend enough time figuring out what was going on with it. as the fda started making changes over the years, that they again were not really taking safety into account. weren't worrying about women's health in the way that these folks did. that there should at the very minimum, they weren't going to take it off the market altogether. that they needed to roll back some of the changes. so changes for instance saying you could go up to 10 weeks instead of having to only stop at seven weeks. changes saying he no longer had to go to the doctor's office three times or more. saying that the physicians basically had to stop the medication themselves. just all sorts of things. all of which were political in the very first instance. as soon as this medication got approved in the united states. which took far longer than it should have because it had been approved elsewhere long before that. a lot of the rules that were put in place put in place to make it as hard as possible to access it. i have been talking for a long time but i just want to say a cou

>> well, we need to work with the fda. this is a hypothetical. you have two manufacturing facilities and one of them has to shut down. the other facility is to have the latitude to at least temporarily produce more of a certain medication per day or per week. right? above and beyond what they are certified by the fda to produce. so there needs to be a little more flexibility there were he can ramp up. and that is one of the things coming out of covid. things like masks and all these other things. not just drugs. we need to have that kind of resiliency where if we need these things we have the abilities built in, with probably some federal support, built in so that we can expand our capacity in the short run. and we may have to make sure that all of the federal agencies have the federal flexibility to allow that. and still keep the quality there. and so resiliency within our own country is important. no doubt. >> you mentioned federal support. other countries. china. india. they subsidize a lot of what they're pharmaceutical companies do. we do no

justification for the fda to regulate cigarets as a drug.lso want to talk to you about the real issue before the american people and this subcommittee. the real issue is should cigaret be outlawed. let's make no mistake about it. the goal of the anti smoking >> . >> this morning i intend to show you how they hope to achieve that goal. first i want to address the charge that reynolds tobacco manipulates the level of nicotine and its products. the implication is that we are somehow doing something sinister or two addicted smokers are to keep them addicted. we do not. we do reduce the amount of nicotine in our products. we do monitor and measure tar and nicotine yield because we are required to publish those figures in our advertising. and we need to maintain the consistent taste and quality of ourrand brand which our customers expect. but we do not do anything to smokers or to keep them helped. let me repeat, we do not manipulate nicotine two addicted smokers. we know more manipulate nicotine then coffee manufacturers manipulate caffeine. ther

so why is the fda behind? during covid, it stopped all but the most critical inspections. it's trying to catch up with far fewer employees. more than 200 inspection jobs are currently unfilled. many former employees left for higher paying jobs in the private sector. >> we have a lot of work to do as long as the marketplace is working the way it is. >> the fda insists the u.s. drug supply is the safest in the world, but it hasn't said when it expects to complete those overdue inspections. rhiannon andrew. >> andrea. thank you. more rain and flooding is expected on the gulf coast. we've seen dozens of high water rescues in texas this week. people clinging to trees. louisiana to northern florida are at risk today. let's check your friday forecast. >> good morning. we're dealing with some drenching rain across the gulf coast states, new orleans. we're very concerned about flooding for you. also georgia and alabama into south carolina late this evening. soaking rain. some of you in southern louisiana will see between 8 and 12in of rain for the storm. total from what fell at mid

the fda says is quizzing on this earlier you meet fda approval for a doctor to describe and get the reimbursement they looked often it's now been safe. those are couple of things will open it up it. >> a. >> thank you for those first questions. who is the target we have for this? an ideal world we went to draw on the form or other pharmaceutical and get them interested in this. that made it like 50 years ago for them all the data already. you see it being easy for them to pick it up and do the research. we want this to be open to nontraditional as well the slot of nonprofits in the space right now this academic research happening. the challenge is the fda approval requirement which i think is more suited for firms that have xmas with that process. that is similar what we are thinking of here. as far as the pilots and you are raising a good point i don't think we thought through the specifics of it enough. there could be a way say for example to run the pilot program. you know how many are in place. that's a really good point. this is when i was prepared to get. this is a question we've gotten a l

that is where you get into the issue of how far ahead to the fda look? how many people 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, enough funding to make sure the quality is there so even if it is not produced here, we don't have these shutdowns. kathleen: is there a maps act to address that? rep. bucshon: the act is hoping to have a map of all of this, the supply chain in one place, health and human services. then, have the experts -- i would not congress -- count congress in that. the experts that know what they are doing as it relates to supply chain, distribution, 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. i hear so many people say it is quality. instead of having this race to the bottom on pricing, you have to find a way to reward quality. what

the fda says is quizzing on this earlier you meet fda approval for a doctor to describe and get the reimbursement they looked often it's now been safe. those are couple of things will open it up it. >> a. >> thank you for those first questions. who is the target we have for this? an ideal world we went to draw on the form or other pharmaceutical and get them interested in this. that made it like 50 years ago for them all the data already. you see it being easy for them to pick it up and do the research. we want this to be open to nontraditional as well the slot of nonprofits in the space right now this academic research happening. the challenge is the fda approval requirement which i think is more suited for firms that have xmas with that process. that is similar what we are thinking of here. as far as the pilots and you are raising a good point i don't think we thought through the specifics of it enough. there could be a way say for example to run the pilot program. you know how many are in place. that's a really good point. this is when i was prepared to get. this is a question we've gotten a l

and congressman grace meng says the fda listens. now the agency is doing a risk assessment to evaluate whether tampon users are exposed to the toxic metals and whether that poses health risks. it's really important that we do ask the scientific questions and that we prioritize funding and research to answer that, especially because we know that there are some harmful and toxic chemicals present in those products. once the fda gets more data, congresswoman manx as leaders will be able to make policy accordingly and women will be able to make more informed health decisions. we as consumers. >> and america have a right to know what we are putting inside our bodies. the fda is promising to share its findings with the public in washington. i'm hannah brandt. >> let's take a peek outside at the san mateo bridge, the hustle home on a thursday. slow going on the left there heading into the east bay, you know, but at least the weather is pleasant for folks as they're trudging along, right? kathy? >> yes, let's look at another bridge about th

finally there is no c justification for the fda to regulate cigarettes as a drug.want to talk to you about the real issue before the american people and the subcommittee. the real issue is, should cigarettes be outlawed? let's make no mistake about it. the goal of the antismoking industry is to bring back prohibition. i intend to show you how they hope to achieve thatrs goal. but first i want to address the charge reynolds tobacco manipulates the level of nicotine in its products. the implication is that we are somehow doing something sinister to addictive smokers or keep them addicted. we do not. we do reduce the amount of nicotine and our products. we do monitor and because we are required and or advertising. we do maintain the consistent taste and quality of our brands which our customers. expect. but we do not do anything to hook smokers or keep them hooked. let me repeat, we do not manipulate nicotine to we know nicotine and cigarettes andro coffee manufacturers manipulate caffeine in their products. there is nothing sinister about it. the subcommittee should

one of theda things the fda shod is that r.j. reynolds had applied forfo a patent to double the levels of nicotine in cigarettes. that was a new fact that people had not known before. another thing that fda commissioner david kessler rot outo was that while up to 50% of people got addicted to alcohol, when he came to cigarettes the addiction levels were 75-90% of smokers. those were new facts that waxman was trying to get out to the public. >> host: but we've been t discussing the effects of smoking since the 1950s. the famous surgeon general support in your 60s came out. >> guest: that's true. the very first report that came out that link smoking to cancer was in 1953 and there was a bigger report in 1954 in england. the first big report in the united states was 1964. that u.s. surgeon general report linking smoking to cancer. soee yeah, those warnings had bn out of there and not a lot of people paid attention to them. one of the things mr. waxman tried to do was emphasize those findings in a hearing study help to get the word o

and congressman grace meng says the fda listens. the agency is doing a risk assessment to evaluate whether tampon users are exposed to the toxic metals and whether that poses health risks. it's really important that we do ask the scientific questions and that we prioritize funding and research to answer that, especially because we know that there are some harmful and toxic chemicals present in those products. once the fda manx as leaders w1ll be able to make policy accordingly and women will be able to make more informed health decisions. we as consumers. >> and america have a right to know what we are putting inside our bodies. the fda is promising to share its findings with the public. >> in washington, i'm hannah brandt. >> pesky problem in the south bay. still ahead at 2 mosquitoes that still need to be dealt with and using air be dealt with and using air pods in the world of medicine. alright. what's the definition of character to you? umm... would you be a superhero or a supervillain? if you could say one thing to big tobacco,

the fda says is quizzing on this earlier you meet fda approval for a doctor to describe and get the reimbursement they looked often it's now been safe. those are couple of things will open it up it. >> a. >> thank you for those first questions. who is the target we have for this? an ideal world we went to draw on the form or other pharmaceutical and get them interested in this. that made it like 50 years ago for them all the data already. you see it being easy for them to pick it up and do the research. we want this to be open to nontraditional as well the slot of nonprofits in the space right now this academic research happening. the challenge is the fda approval requirement which i think is more suited for firms that have xmas with that process. that is similar what we are thinking of here. as far as the pilots and you are raising a good point i don't think we thought through the specifics of it enough. there could be a way say for example to run the pilot program. you know how many are in place. that's a really good point. this is when i was prepared to get. this is a question we've gotten a l

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. the 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, e 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 word

there is one word of caution, though from the fda. they say over-the-counter hearing aids are not a treatment for people with severe hearing loss. they say those individuals should still consult with a health care professional. okay, back to our first alert weather right now giving you a live look outside. nice and dry outside. but you know it's going to start to cool down. let's check back in with meteorologist jessica burch. >>all right. well look at the east bay right now with those clear skies. that's the case as we head into this afternoon. we're still warming up right now all the way into the 90s today, into areas like walnut creek and concord. antioch. a similar trend. head up into the north bay if you want to go up to wine country this weekend, we have seconds for now. but all of us, especially in our inland areas, we're going to cool down fast. more fall like weather right around the corner as we head into this weekend, 60 still holding on tight to the coast this weekend 80 down in the santa clara valley will quickly turn int

the fda says the rate of teens using vapes fell below 6% this year. in their latest survey.down from 7.7% in 2023. about 1.6 million students reported vaping last month. that is about one third the number in 2019, when underage vaping peaked. officials say that the drop in vaping did not lead to a rise in other tobacco products, being used, such as nicotine pouches. >> the fda is struggling to inspect pharmaceutical manufacturing firms, which are overdue for required examinations. that's according to an investigation by the associated press, which found fda inspectors have not returned to about 2000 facilities that produce drugs taken by americans since before the covid 19 pandemic. the discovery is raising concerns that there could be risks of contamination and issues in drugs going unnoticed. >> i was hoping current fda inspections would be higher than than pre-covid, because i thought the fda would be catching up, but they're still behind. we need the fda to conduct these inspections, or we need some other mechanism to ensure the safety and efficacy of these medicines. >>

la fda aprobÓ hoy la primera vacuna contra la influenza que no necesita ser aplicada por personal mÉdico en la comodidad de tu casa sin necesidad de jeringas. asÍ empezamos. noticias telemundo en la noche con arantza loizaga. buenas noches les saluda sonia sÁnchez. en ausencia de aranza luizaga comenzamos con las imÁgenes del tiroteo en el metro de nueva york, que el domingo dejÓ a dos pasajeros heridos, uno de ellos muy grave. los videos son clave porque la balacera ha desencadenado una ola de protestas en contra de la reacciÓn de la policÍa a un sospechoso que no habÍa pagado su boleto y que se resistiÓ a ser detenido. karla amezola tiene el informe. son las imÁgenes de las cÁmaras corporales de la policÍa de nueva york. en el momento en que oficiales disparan en la plataforma del tren, hiriendo a pasajeros inocentes. ahÍ estÁn. todo iniciÓ cuando la policÍa persigue a derek michaels, quien presuntamente se saltÓ el torniquete de la estaciÓn sin pagar. agentes le ordenan detenerse, pero siguen despuÉs. segÚn la policÍa, sacÓ un cuchillo con el que los amenazÓ. lanzaron descargas elÉctr

and congressman grace meng says the fda listens. agency is doing a risk assessment to evaluate whether tampon users are exposed to the toxic metals and whether that poses health risks. it's really important that we do ask the scientific questions and that we prioritize funding and research to answer them, especially because we know that there are some harmful and toxic chemicals present in those products. once the fda gets more data, congresswoman manx as leaders will be able to make policy accordingly and women will be able to make more informed health decisions. we as consumers. >> and america have a right to know what we are putting inside our bodies. the fda is promising to share its findings with the public in washington. i'm hannah brandt. >> still ahead, a decades-old san francisco market closing its doors. what the owners. let me play. their decision to shut down. also, apple air-pods now contributing to new health care technology. we explain. >> today, the fda authorized the first over-the-counter hearing aids software and

. >> reporter: in an industry first the fda agreed this helped extend the years in dogs. >> they ared to claims to things and not knowing whether you should believe them or not, but when the fda puts you through the hoops, you have more confidence. >> reporter: mckenzie keeps one beloved pup at top of mind as his medication gets closer to full dad approval. >> grommet was a 75-pound has been mix and lived to age 15. ultimately, i had to put him to sleep because of the wear and tear of age made it hard for him to walk and go through every day life. >> >> reporter: the drug could come in an injectable or daily pill and mckenzie says he's confident enough in the product that once it's ready he plans to give it to his own pups, brody and kaloni. >> sure, we want our dogs to live longer and be healthy as long as possible. that's the focus of what we're trying to accomplish more than anything else. >> the company hopes to receive full fda approval in 2025 and have it ready for distribution as quickly as possible. >>> now to a development in women's health, a new regulation from the fda wen

the samsung galaxy watch has a similar fda clearance. new sleep apnea detection feature will be available in the apple watch series nine, ten, and ultra two. but you don't have to buy a watch to know there's a problem. doctor dasgupta says. chronic snoring and feeling tired all the time are reasons to talk to your doctor. denise teodoro, abc seven news. >> all right, and remember, abc seven is streaming 24 over seven. get the abc seven bay area app and join us whenever you want, wherever you are. with that, we say thank you so much for joining us today for abc seven news at three. world news tonight with david muir starts right now. and i'll see you back here for abc seven news at four. bye bye. >>> tonight, breaking news as we come on the air. reports a judge has been shot and killed in his chambers. the breaking developments unfolding right now. the governor of kentucky moments ago revealing the judge was fatally shot in his chambers late today. what we now know about the judge's

i thought the fda would be catching up, but they're still behind.rall, about 42% of all drug making factories have gone without fda inspection since 2019. >> under federal guidelines, factories that haven't been inspected for five years or more are considered a, quote, significant risk for contamination and poor quality. now lawmakers are asking tough questions about how the backlog happened and whether a congressional push is needed to get the fda to step up inspections. >> in the absence of regulatory inspections and actions that we've seen numerous quality control failures. >> it is past time the fda addresses these issues. people's lives depend on it. >> most of the plants overdue for inspections are in the u.s, but more than 300 are overseas, mostly in china and india. in new york, cb cotton, ktvu, fox two news, san francisco international is now tracking confused passengers in its legal fight against the recent airport ban brand in oakland, according to sfgate. >> airport managers in san francisco say they have proof. six people in june confus

it says they're not elevated for fda clearance. tested the feature on roughly 1400 people and then compared it against the gold standard medical sleep test. and apple says the watch correctly alerted people who had apnea 66% of the time. and while it doesn't diagnose sleep apnea, it can indicate something is going on. other devices like the ring and fitbit give warnings about apnea, and the samsung galaxy watch has a similar fda clearance. but with the samsung watch, you have to actively set up an apnea evaluation. while the apple watch does it automatically. the apple watch nine and ten and the ultra two will work with this feature. the watch monitors you for a month before popping up any alerts and apple says if you do get a notification, talk to your doctor. now, many people are wondering, though, how am i supposed to sleep with the watch on? that's normally when i charge it. apple says the apple watch ten has fast charging, so you can get 80% of a charge in just 30 minutes, so maybe you give it two quick charges a day and you'r

i thought the fda would be catching up, but they're still behind.erall, about 42% of all drug making factories have gone without fda inspection since 2019. >> under federal guidelines, factories that haven't been inspected for five years or more are considered a, quote, significant risk for contamination and poor quality. now, lawmakers are asking tough questions about how the backlog happened and whether a congressional push is needed to get the fda to step up inspections in the absence of regulatory inspections and actions that we've seen, numerous quality control failures. >> it is past time the fda addresses these issues. people's lives depend on it. >> most of the plants overdue for inspections are in the u.s, but more than 300 are overseas, mostly in china and india. in new york, cb cotton, ktvu, fox two news. >> now to another health matter. teen use of e-cigarettes has fallen to a ten year low. the fda says the rate of teens using vapes fell below 6% this year in its latest survey. that's down from 7.7% back in 2023. we welcome now for more

the fda expanding approval of a drug for met static cancer. one woman shares how it saved her life. >>> and a family gives a vietnam veteran the gravestone they always thought he deserved after a 50-year effort. it's wednesday, september 18. "early today" starts right now. good morning. i'm frances rivera. sean "diddy" combs remains behind bars this morning. the music mogul facing a slough of charges, including sex trafficking and racketeering. he will be back inside a courtroom for an appeal hearing after he was denied bail. the indictment against combs has been unsealed. and some of the details you're about to hear are graphic. chloe melas has this report. >> reporter: sean diddy combs behind bars. a federal judge denying the music mogul bail following his arrest and indictment as the prosecutor alleges he is dangerous and poses an ongoing threat to the safety of the community. in comporturt, combs pleading n guilty to several counts. >> sean combs led and participated in criminal activity, including sex trafficking, forced labor, kidnapping

like the fda has standardized the notification.ed to standardized insurance coverage for women. >> joanne pushkin, executive director of breast info.org and advocate and breast cancer survivor. thank you for joining us. ♪ lisa: a group of parents in gaza have described heartbreak as they remain separated from their babies who were born prematurely in jerusalem over a year ago. he needed specialized care and their parents were supposed to reunite with them. but the war has kept them separated, meaning shaky video calls and the closest contact they have with the children are from those calls. rachel younger has this report from jerusalem. >> meet triplets, a handful of mischief at almost 30 months old. and little --, who was born a few weeks before them. it should be their parents playing with them. unbelievably, having born just outside gaza and now stuck on different sides of the impenetrable wall that surrounds it. the only time they get to see their faces are during the fleeting minutes they get a connection to one of the most da

the fda addresses these issues. people's lives depend on it. agency officials say their work has been hampered by difficulties recruiting and retaining inspectors who face a grueling schedule of overseas travel. >> and still ahead on the news at 6, another hot one today, some cities in the bay. we're triple digits. chief meteorologist kathy trafton rather will have a look ahead. plus, several small businesses destroyed by an overnight fire in san jose. will hear from the owners and it's a fight against childhood >> it's a matter of saving lives. that's the message today from san francisco assemblymember matt haney talking about a bill focused on the opioid crisis and getting folks help they desperately need kron four's terisa stasio reports. >> this assembly bill proposes a long list of measures that sponsors say could make a transformational difference from those suffering from opioid addiction. new policies to protect lives. that's the goal behind assembly bill. 2015 now before governor newsom. this will save lives. it will greatly increase t

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keytruda is known to treat cancer, fda-approved for 17 types of cancer. of those cancers is advanced 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

reportero: la nueva disposiciÓn de la fda serÁ uniforme para todas las clÍnicas y hospitales de estados de la tomografÍa y tomar acciones para prevenir el cÁncer de mama. maity: el ipod 16 marca el inicio. con el iphone 16 podrÁ generar imÁgenes gracias a un potente procesador diseÑado para tener inteligencia artificial. a partir del 20 de septiembre estarÁ disponible por 799 dÓlares. eliÁn: el hecho de que edmundo gonzÁlez se haya ido a espaÑa,trae dudas y confusiÓn. reportero: tras la salida de edmundo gonzÁlez, exiliado en espaÑa, trae dudas. >> las pocas esperanzas que uno tenÍa se fueron con Él. reportero: marÍa corina machado hizo su declaraciÓn virtual. >> yo he decidido permanecer en venezuela y acompaÑar la lucha desde aquÍ. reportero: una lucha donde nicolÁs maduro estÁ alcanzando su objetivo. >> estamos frente a un choque de trenes, es el peor de los escenarios que podrÍamos preveer para la situaciÓn pos electoral. reportero: con el ganador de las elecciones electorales exiliado en madrid tras abandonar el paÍs tras las amenazas del rÉgimen. >> mi salida de caracas estuvo rod

elian: la fda aprueba una innovadora vacuna contra la gripe y no necesita inyecciÓn.ndo la aplicas tÚ mismo o un trabajador de la salud. estÁ disponible para personas de 2 a 49 aÑos. los pacientes con receta mÉdica podrÁn pedirla el ine a partir del prÓximo aÑo. seguimos hablando de salud. aumentan los casos de un virus respiratorio que puede causar una parÁlisis. los niÑos son los mÁs vulnerables. se propaga cuando un enfermo 12 o estornuda. ante los sÍntomas son parecidos a los de la influenza, una infecciÓn severa se puede manifestar de forma similar a la poliomielitis. sÓlo se han reportado 13 casos en 10 estados del paÍs. nuevas frases revelan que delitos callejeros cayeron de 2022 al 2023. la reducciÓn mÁs drÁstica es en los asesinatos. las violaciones en mÁs de un 1%, pero los delitos de odio en menos de un 1%. menos de un 1%. vestida de novia y sobre i think we need a bigger yard, with our credit? ow, ow, ow, ow. credit karma can show us how to improve our credit for free, then we can get a place with a bigger yard. yay. intuit credit karma. download the app t

that could be done through what we did at fda, which was bringing the stakeholders up.wasn't a bill of rights. i forget what we called it, but it was basically like a white paper that we generated. we generated content. that is going on now. i don't think it is as visible at a high level of effort to do that. keagan: is there anyone being left out of the debate or discussion that needs to be heard? dr. gottlieb: i think the one group that was absent from our discussion and may be the are here today is some of the child safety groups. i think they have a lot of awareness of what is going on. they have more proximity to some of the parental organizations. they also have the ability to convene stakeholders at a local level. if you kind of have a common toolbox ultimately, you are going to need to get parents educated on how to make use of these tools. that can be led at a local level. schools can be leading some of this discussion. maybe even requiring it. educate them, but maybe even at a local school level. you could see schools just as likely if you were going to allow

elian: la fda ha aprobado una vacuna a erosiÓn nasal contra la gripe. podrÁn pedirla el ine a partir del prÓximo aÑo. seguimos hablando de salud. aumentan los casos de un virus respiratorio que puede causar una parÁlisis. los niÑos son los mÁs vulnerables. se propaga cuando un enfermo 12 o estornuda. ante los sÍntomas son parecidos a los de la influenza, una infecciÓn severa se puede manifestar de forma similar a la poliomielitis. sÓlo se han reportado 13 casos en 10 estados del paÍs. nuevas frases revelan que delitos callejeros cayeron de 2022 al 2023. la reducciÓn mÁs drÁstica es en los asesinatos. las violaciones en mÁs de un 1%, pero los delitos de odio en menos de un 1%. vestida de novia y sobre estos momentos son para la familia y los seres queridos, no para lavar platos sucios. déjaselos a finish ultimate. es eficaz en manchas de quemado, incluso sin enjuagarlas, o la comida corre por nuestra cuenta. el $2 $4 $6 $8 value menu ha vuelto del más allá. mata el hambre con ofertas para morir como el everyday value slam, y mucho más. el $2 $4 $6 $8 val

the fda approving the first flu vaccine you can give to yourself at home. how it works. >>> and the remarkable milestone seen by millions. some now asking, was it the greatest game of all-time? who is our "person of the week"? >> david: good evening, and it's great to have you with us as we year the end of another week together here. we'll have more on that judge shot and killed in the courthouse. authorities tonight now say it was the sheriff who killed him, and what we've learned. >>> we do begin with the race for the white house. 46 days to go to the election, and the fierce fight tonight in the key battlegrounds. vice president kamala harris in atlanta, her emotional comments today about the death of a mother who she says could not get care in time after reports medical help was delayed because of that state's strict abortion ban. >>> the major headline also from georgia tonight, that state's election board ordering the manned-counting of all ballots, likely delaying results on election night in what could already be a very close election. >>> former tr

the fda approving the first at-home flu vaccine.ourself. and i chose breztri for my copd, i had bad days. [cough] flare-ups that could permanently damage my lungs. with breztri, things changed for me. breztri gave me better breathing. starting within 5 minutes, i noticed my lung function improved. it helped improve my symptoms, and breztri was even proven to reduce flare-ups, including those that could send me to the hospital. so now i look forward to more good days. breztri won't replace a rescue inhaler for sudden breathing problems. it is not for asthma. tell your doctor if you have a heart condition or high blood pressure before taking it. don't take breztri more than prescribed. breztri may increase your risk of thrush, pneumonia, and osteoporosis. call your doctor if worsened breathing, chest pain, mouth or tongue swelling, problems urinating, vision changes, or eye pain occur. can't afford your medication? astrazeneca may be able to help. ask your doctor about breztri. (vo) memory and thinking issues keep piling up? astrazene