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

and the fda convened this committee of outside advisers.as quite split on what to recommend to the fda. the committee ted against the proposition that the device was proven effective. however, it voted that the benefits outweigh the risks. ultimately, the fda approved it for a somewhat narrower universe of patients than originally proposed. ali: i should note that the fda, has a statement that says, that, the agency believes that the overall benefits of this device continue to outweigh the risks, in these patients and that, abbott's recall strategy was appropriate and adequate. much left to discuss, but we have to leave it tre. david hilzenrath with, kff. thank you so much for coming in. >> thank you. ali. great to be here. ♪ john: and that is pbs news week on for this sunday. for all of my colleagues, thanks for joining us. have a good week. >> paper -- major funding for pbs news week and has been provided by. ♪ and with the ongoing support of these individuals and institutions. ♪ this program was made possible by the corporation for publi

>> the comstock provisions don't fall within fda or the fda under the ftca can only maintain restrictions under the program is necessary to insure safety pin 2021 what they determined if you don't need dispensing for safe use of the ftc did not independently require that recent prescription and can be imposed once that determination was made. fda was not affirmatively approving in violation of comstock even if you interpreted it that way and at the very least i don't think it was fda's responsibility to consider that or could it have under that statute. didn't do anything about it and this is a prominent provision and not some obscure subsection of a complicated obscure lot. they knew about it and everybody knew about it. shouldn't they have the least address to? to have answers to the air currents made on the other side and shouldn't the fda at least and we considered those and provide some kind of an exclamation? >> let me give two responses one is i don't think it's even permissible for fta to maintain the restriction because of comstock pretty good look at the statutory section here t

the fda are highly skewed towards avoiding risks.ere's a tendency us to have drugs that are safer, but not to have drugs that are effective. now i've heard remarkable statements from some of these committees in considering drugs. one has seen the statement. there are not enough patients with disease of this severity to warrant marketing. this drug for general use. now, that's fine if what you're trying to do is to minimize drug toxicity for the whole population. but if you happen to be one of these, not enough patients and you have a disease that is of high severity or disease, that's very rare, then that's just tough on you. for ten years. mrs. estero dean suffered from severe asthma. the medication she received serious side effects. her condition was getting worse, but the drug her doctor preferred was prohibited by the fda. so twice a year mrs. usdin had to out on a journey. i had been very sick. i had been in and out of the hospital several times. and they couldn't seem. to find a way to control the asthma. and i had to change li

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

preferred was prohibited by the fda.o set out on a journey. >> i had been very sick. i'd been in and out of the hospital several times they could not seem to find a way to control the asthma i had to change my lifestyle once i was out even for a short time. mainly because the court's own e derivatives were softening the bones and causing a puffiness of the face and other changes in my body. the doctors were pretty anxious to get me off the cortisone derivative. >> the drug her doctor wanted her to have have been available for use for five years in canada. once across the border could make use of a prescription that she had obtained from a canadian doctor. all she had to do which any pharmacy there she could buy the drug that was totally prohibited in her own country the drug worked immediately both because of the shortness of breath being resolved and also because now we do not have to worry about so much about the softening of the bones. fortunately once i got that medicine very quickly everything sort of reverted back

user fees only make up 47% of the fda. from the food's program comes from mostly federal appropriations and 1% of user fees. rachel: it's important to note that in the food coloring topic that food coloring is notes allowed in europe and my daughter served a semester in rrome and was eating the food in her cafeteria and felt bad and comes home and feels good and went to rome for a semester and never felt better. something is wrong with our food supply. we are making our citizens fatter, sicker. we have more -- we spend more than any other country on healthcare and yet we have our citizens are sicker and starting at a very young age and starting with formula and putting them on processed foods. all the way to adulthood and no wonder we're dying sooner and having bad outcomes. this is a sleeper issue and both of you have wives that ware a lot about your diet. is this issue an issue for women? will: i do know this is a sleeper issue. i don't think -- what i think, i think the curious part of me is very into this topic. to the

says it is. >> we want the fda to make sure doctors are prescribing this in a safe way. that's all that we've ever said, and i believe that that is how president trump feels about this. agains yo again, you want the states to make these determinations and you want to make sure the fda is ensuring these are safe. >> it's been on the market for decades, and they say it is safe, but would -- >> anti-biotics are safe, but we want to make sure they're prescribed by doctors and the doctors are monitoring this stuff. >> sure. >> so people don't get hurt. >> of course. >> we've talked now for i think six questions now about abortion -- >> i'm city tstill trying to ge clear answer. >> i gave you one. >> where that commissioner stands on this drug, would that determine whether or not they are chosen to be put in this key role? >> i think president trump has clearly said there are no litmus tests on this particular issue. he just wants to make sure that drugs are safe and effective before they're out there on the market and of course, that doctors are properly controlling this stuf

>> the fda allows for this. if the patient needs medication and it's on shortage the only way they'll be able to get it is to come to a compounding pharmacy and let the pharmacy make it for them. >> reporter: it's a little-understood part of the multibillion-dollar weight loss drug industry. federal law allows state-licensed compounding pharmacies to dispense drugs that are essentially a copy of fda-approved medications. only to patients with a prescription and only for medications in shortage, which includes wegovy and zepbound. compounding pharmacies often sell them at a steep discount. usually $100 to $400 per month, compared to roughly $1,000 for the name brands without insurance. elizabeth kenley needed to lose 50 pounds for a double knee replacement. she struggled to find the brand name drugs in stock and at a price she could afford. >> how are you doing? >> reporter: so her primary care provider suggested a compounded version. >> did you have some questions? >> i had a lot of questions. i was a little ner

bring on the day. >> david: to the index, the fda >> david: to "the index," the fda approving the firstee drug to treat life threatening allergic reactions to food or bee stings. a nasal spray called neffy will help slow anaphylaxis. it should be available here in the u.s. within eight weeks. a welcome change. >>> when we come back, harrison ford, angela bassett, jamie lee curtis and kelly ripa, the big honor in a moment here. we're still going for that perfect pizza. and with higher stroke risk from afib not caused by a heart valve problem,... ...we're going for a better treatment than warfarin. eliquis. eliquis reduces stroke risk. and has less major bleeding. over 97% of eliquis patients did not experience a stroke. don't stop taking eliquis without talking to your doctor as this may increase your risk of stroke. eliquis can cause serious and in rare cases fatal bleeding. don't take eliquis if you have an artificial heart valve or abnormal bleeding. while taking, you may bruise more easily... ...or take longer for bleeding to stop. get help right away for unexpected bleeding or unusu

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 cose, the famous surgeonenal'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 ou

the fda., you know, we invent the product. that's why there's a premium for the real think made by lilly. >> stephanie joins us now in studio. how much more difficult is for the patients to give the shots with the vials? >> well, there are other medications that use syringes like insulin and fertility drugs but it is definitely a little bit more difficult. patients have to actually draw the dose into a syringe, and for some people that's kind of a daunting thing to have to do. >> all right. stephanie gosk with the new developments tonight. thank you. >> you're welcome. >>> coming up, why some are seeing a champagne super nova in the sky tonight. what oasis just told fans. (vo) you might be used to living with your albuterol asthma rescue inhaler, but it's a bit of a dinosaur, because it only treats your symptoms, not inflammation. treating both symptoms and inflammation with rescue is supported by asthma experts. finally, there's a modern way to treat symptoms and asthma attacks. airsupra is t

>> the fda allows this. a shortage, the compounding pharmacy can make it for them. >> reporter: federal law allows state-licensed compounding pharmacies to dispense drugs that are essentially a copy of fda-approved medications. only to patients with a prescription, and only for medications in shortage, which includes wegovy and zepbound. compounding pharmacies often sell them at a steep discount, usually $100 to $400 per month, compared to roughly $1,000 for the name brands without insurance. elizabeth kenley needed to lose 50 pounds for a double knee replacement. she struggled to find the brand name drugs in stock and at a price she could aifford. so her primary care provider suggested a compounding pharmacy. >> i was a little nervous, but i did talk to my doctor about it a lot. and then i went and talked to the compounding pharmacy. >> reporter: and it's working. she's lost about 25 pounds. >> you've had just mild, mild side effects. >> reporter: primary care provider, leanne owens, once a skeptic herself,

the fda rejected mdma assisted therapy friday that the fda and said no. >> to this revolutionary treatment, you news, california congressman lou correa says the psychedelic drug known as ecstasy shows real promise in easing veterans, ptsd. they told me never do it again. but i confronted might might even some speak, gotten cured and i'm ready to move correa and 60 of his colleagues in the house signed a bipartisan letter to president biden last week highlighting the benefits of the treatment. >> the fda's decision comes after its advisory panel in june recommended against approval calling the drug's effectiveness. unproven actually look at the science surprising at all. doctor kevin sabet with the foundation for drug policy solutions says the fda made the right move. these are very powerful mind conscious is altering substances >> and we need to really take a lot of care with them. so says mdma may be helpful for some, but the broader data doesn't show it's safe and effective. long term. >> he says it's also hard to study these placebos often fail because you kind of know whether you're ta

keytruda is known to treat cancer, fda-approved for 17 types of cancer. one 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 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. dependi

group, ahm, which opposes abortions, had n standing to file suit and failed to show harm from the fda's actions concerning the pill. oral argument was heard back in march. tune in for this and oer supreme court rulings all this week at 9:00 p.m. eastern on c-sp. you can also find all of our preme court coverage on our website, c-span.org/supremecourt. anno vice president harris governor tim walls began itota southeastern georgia speaking voters in rural pockets of the battleground s they were greeted at the airport by students from - they then madeir way to liberty county high school where metith members of the hool's marching band and were d with a song. their next stop was that sand fly barbecue in savannah. [cheers] >> thank you, everybody. thank you so much. [cheers and applause] [indiscernible] ♪ [applause] >> i would like to thank our distinguished guests for visiting here. [applause] we are honored to have you visit our school. right now i am going to turn over to right now, minnesota governor, but our future vice president, coach tim walz. [applause] gov. walz: thank you all. th

this is the first time they've tried to seek fda approval and even though the fda said no, it kind ofback because they didn't approve it. they had a few reasons number one, the way the study was conducted, over 100 adults that had ptsd, they had used mdma before, and they're saying they didn't look at health effects and the blind study like they normally do there are concerns >> was it just about how the study was conducted? does the treatment itself look promising? and how does it compare to other treatments that are out there? >> the treatment looks very promising, and there's actually three different things that are out there, ketamine, sill sigh b bin, these are called the psychedelics, they basically open the door so people who are reluctant to bring to surface these feelings they have or these past events can do that now safely, but then they have to have therapy associated with that that's where the fda got confused let's try to figure that out moving forward. >> there are 13 million americans who live with ptsd what does it mean for patients what do they speexperience >> it ca

the fda is telling the company they'll need to run an additional trial and resubmit it for fda approvaldly needed for people for ptsd. treatments are badly needed. talk therapy and antidepressant s help a third of patients. this is minor setback for now. veterans, lawmakers have been calling to allow mdma for help. >> thanks so much. >>> coming up the u.s. sending more firepower to the middle east as tensions soar following a deadly air strike. before a fresh round ofeace p oh-ho-ho, look at that jet stream. [ whistles ] weather. oh, boy. yep, they're calling it an atmospheric river. it is coming down. [ cellphone buzzes, chimes ] oh, flood warning in louisiana. are they obsessed? oh, yeah. the stuff they do on the green screen, unbelievable. they said 10% chance of rain. -seems more like 40% to me. -no. it has nothing to do with the dew point. progressive can't save you from becoming your parents, but we can save you money when you bundle home and auto with us. what are those, cumulus clouds? missing out on the things you love because of asthma? get back to better breathing with fasenr

if elected to the white house, they say loud and clear that their plan is to instruct the fda to, quote quote. how did donald trump quote it again? >> you could do things that would supplement, absolutely. those things are pretty open and humane but you have to have a vote. >> that word salad responses no action because republicans are painfully aware of the fact of being the party that bans abortion is hanging around their necks like a political and. they are not softening policy positions around abortion, there softening the way that they talk about it and they hope that voters don't notice the difference but tonight in arizona, vice president harris made the difference very clear. >> just yesterday in a press conference, we got a fresh reminder of what donald trump's 2025 agenda would do, it would ban medication abortion in every state. but we are not going to let that happen. because we trust women! >> joining us is the president and ceo of reproductive freedom for all. thank you for being here. i have to say in all the years i covered the issue of abortion, i have never seen this,

and that's what the fda is saying.y issued a warning in 2023, lots of these forms of ketamine are out there, unregulated. we don't know the strength of ketamine in these oral forms that might be used for pain or might be used for depression that people are taking and buying from untrustworthy sources. that are not regulated. as a result, concerns like respiratory depression are really paramount here and that's appears what happened here, a dose of ketamine was taken that was a lot higher than it was anticipated, i'm speculating a bit, but that caused respiratory depression. >> thank you so much for being with us this morning. >>> up next, an update on ernesto's impact on puerto rico as forecasters warn it could strengthen to a cat 3 storm in 24 hours. >>> plus, pop superstar taylor swift is set to take the stage in london for her first show after last week's foiled terror plot in austria. we'll take you to the sold out stadium next. you're watching "jose diaz-balart reports" on msnbc. nt you're watching "jose diaz-bala

. ♪ [mÚsica] ♪ principalmente, la ketamina es una droga aprobada por la fda para su uso anestÉsico eno, siempre con un doctor . esta medicina puede causar efectos alucinÓgenos, distorsiÓn a la vista, y el sonido, y parece que la persona se siente cÓmodo desorientada. la dea asegura que la ketamina se ha fabricado de manera ilegal durante dÉcadas como droga recreativa. cambiamos el tema, tenemos un ojo puesto en venezuela, porque este sÁbado serÁ realmente un dÍa importante. la oposiciÓn se estÁ organizando para esta gran protesta que tiene alineada para maÑana y mÁs de 300 ciudades del mundo. al tiempo que su lÍder marÍa corina machado ha rechazado categÓricamente la propuesta de celebrar nuevas elecciones como han pedido los presidentes de brasil y de colombia. conversamos sobre este tema con joan merchan, periodista venezolano y productor de "al punto", con jorge ramos, sabemos que estÁis preparando un especial para este domingo en "al punto", me gustarÍa conversar contigo sobre quÉ estÁ pasando con esa salida negociada de maduro del poder. ¿crees que es viable? >> gracias por la in

the fda rejected mdma assisted therapy friday that the fda said no.o this revolutionary treatment. the sad news, california congressman lou correa says the psychedelic drug known as ecstasy shows real promise in easing veterans, ptsd. they told never do it again. but i confronted might might even some speak. i've gotten cured and i'm ready to correa and 60 of his colleagues in the house signed a bipartisan letter to president biden last week highlighting the benefits of the treatment. >>the fda's decision comes after its advisory panel in june recommended against approval calling the drug's effectiveness. unproven actually look at the science. this isn't surprising at all. doctor kevin sabet with the foundation for drug policy solutions says the fda made the right move. these are very powerful mind altering conscious is altering substances and we need to really take a lot of care with them. summit says mdma may be helpful for some, but the broader data doesn't show it's safe and effective. long term. he says it's also hard to study these placebos ofte

the fda citing a lack of data and requesting additional trials.aker lykos therapeutics says it plans to request a meeting with the fda to ask the agency to reconsider the decision. >>> all right, time for another check of the weather now with somara theodore, and she's right here with the weather. and it's looking really beautiful in florida, somara. >> somara: it is. you know, all eyes all week have been on debby, rightfully so, but as debby departs, now we're talking about the heat, and this is lauderdale-by-the sea. good morning, florida. all right. so let's talk numbers, shall we? you are under a heat advisory in the state of florida. parts of georgia into south carolina and even in texas, we have triple-digit feel-like temperatures today. it feels like 111 in corpus christi. houston, 103. miami feeling like 107 degrees. crank up the heat, right? so, over the next three days these heat index values stick around. so it's going to feel hot over like houston, new orleans feeling like 105 on monday. even atlanta, 93 degrees on monday. 96 is what i

meaning can the fda ban this drug? there are many things i humane basis you can do outside of that. what does that refer to? i have no idea but you also have to get a vote and people are going to have to decide. what is that answer? it is not coherent, it is meaningless. not for lack of effort by garrett. and then a spokesperson -- what it seems to say is again, donald trump says yeah, he would be open to the fda banning the use of mifepristone which is used in half of abortions nationwide in the trunk campaign came in today to blame the answering the question, the press conference being cold, difficulty here which was their undoing. atrium campaign spokesperson i think not on the record, not named, said his position on the abortion medication, mifepristone, means the same. the supreme court unanimously decided on the issue and that matter is settled. that doesn't answer the actual question because the supreme court first about did not really decide on it, they kicked it and punted on standing ground. the supreme court ruling as the washington post points out has no bearing on wheth

but the fda is now warning that those compounds have led to accidental overdoses. >> reporter: the ads are everywhere. >> to lose 15% of your body weight. >> reporter: many companies promising weight loss drugs for way less money than name brand prescriptions. >> for as little as 199 per month including options compounded in the usa. >> reporter: for becky chairs the deal was too good to pass up. >> $295 a month or something. let's see how it goes. >> reporter: the family therapist says she got a prescription for compounded semaglutide online but when she received her first shipment from a compounding pharmacy she misunderstood the instructions and accidentally overdosed. >> my first dose was really supposed to be like .5 units. like really tiny dose. and i gave myself five times the dose. 9:00 at night i was going man, i'm feeling sick. >> reporter: because name brands like ozempic are on the fda's drug shortage list compounded versions of semaglutide are allowed on the market. compounding pharmacists can alter or combine medications and tailor them to individual

este jueves la fda aprobÓ la de moderna y la de pfizer. con una nueva fÓrmula para atacar a las variantes que circulan actualmente y brindar una mejor protecciÓn contra las consecuencias graves del covid 19, incluidas la hospitalizaciÓn y la muerte. la recomendaciÓn de las autoridades de salud es que todas las personas mayores de seis meses reciban una vacuna de covid actualizada este aÑo. >> la mayorÍa de la poblaciÓn es vulnerable, verdad? porque tenemos mucha obesidad, tenemos mucho diabetes, alta presiÓn. >> marÍa, quien dice se ha inmunizado tres veces, no piensa recibir una vacuna mÁs. >> no hay demasiado mal con la primera vacuna que me puse despuÉs, la segunda sÍ me dio, pero ya no tanto. >> la aprobaciÓn se da en medio de una nueva ola de cs de covid en el paÍs este verano. de acuerdo con los cdc, los casos positivos aumentaron un 18% de la semana del 10 de agosto de este aÑo, comparada con la semana del 19 de agosto del 2023. las vacunas actualizadas estarÁn disponibles en los prÓximos dÍas en farmacias y consultorios mÉdicos. si

the fda says the efforts of their last cut helped infighting, diet related chronic diseases. is seeking voluntary cooperation from major food makers to help achieve these levels. fast food chains would also likely be affected by the law. 2 new bills and prices are back on the rise with the now familiar cause being cited as the reason it's the avian flu that's behind it. researchers at purdue university say avian influenza also known as bird flu is the main cause of the price spike prices rose about 20% in july compared to the same time out last year, making the average price for a dozen eggs, $3.8. one researcher says that consumers could see some breaks in prices since future seasons. i'm less likely to have severe bird flu outbreaks. >> coming up, secretary of state antony blinken is in israel for what could be his most consequential trip for the possibility of a cease-fire stands now. plus, willie brown, is he going to sue donald trump were the things he said about him. we'll hear from the former san francisco mayor vicki caught up with. willie brown. and it's day one of t

tras la aprobaciÓn de la fda. vacunas se debilita con el tiempo. por eso, funcionarios federales de salud recomiendan recibir una vacuna anual actualizada contra el covid 19. este jueves la fda aprobÓ la de moderna y la de pfizer. sixto, quien tiene 64 aÑos, asegura que ha recibido todas las vacunas, que nunca se ha enfermado de covid y que sÍ se pondrÍa la actualizada porque mi salud me interesa. >> quiero vivir mÁs tiempo. >> la fda precisÓ en un comunicado que las vacunas se han actualizado con una nueva fÓrmula para atacar a las variantes que circulan actualmente y brindar una mejor protecciÓn contra las consecuencias graves del covid 19, incluidas la hospitalizaciÓn y la muerte. la recomendaciÓn de las autoridades de salud es que todas las personas mayores de seis meses reciban una vacuna de covid actualizada este aÑo. >> la mayorÍa de la poblaciÓn es vulnerable, verdad? porque tenemos mucha obesidad, tenemos mucho diabetes, alta presiÓn. >> marÍa, quien dice se ha inmunizado tres veces, no piensa recibir una

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, they're not approved by the fda.addition to that, we invent the product. that's why there's a premium for the real thing made by lilly. >> reporter: some have been and rehen s re apprehensive. it could be something that keeps people from taking advantage of this new option. back to you. >> stephanie, thank you. >>> still to come. e keanu reeves joins the latest big screen adventure. >>> and will a big star return >>> and will a big star return to the ranchule a day. you are bountiful, it's in your nature. the first time you try bounce, ? s you: your laundry feels way fresher and less wrinkled... you start to wonder... if i put a sheet of bounce on my boss, will it make his wrinkles smoother? bounce can't do it all, but for better laundry... ♪ put a sheet on it ♪ ♪ with bounce ♪ swiffer duster traps 4x more dust for a clean even mom approves of. that reach! ♪♪ making hard to reach. so easy! swiffer, [wow!] the mother of all cleans! ♪♪ okay everyone, our mission is to provide complete, balanced nutrition for strength a

pronto. >> millones de dosis de la nueva vacuna contra el covid 19 se distribuirÁn luego de que la fdamergencia, hasta bebÉs de seis meses, pero las ayudas de la pandemia ya no estÁn vigentes, y no todos califican para una vacuna gratuita. depende de cada caso y si la persona tiene condiciones preexistentes. las vacunas para la influenza tÍpicamente demoran hasta dos semanas para llegar a la protecciÓn total. >> importante informaciÓn. llegamos al final de noticias univisiÓn 14 a las seis. gracias por su compaÑÍa. recuerde nuestra cita con mÁs informaciÓn local a las 11. buena tarde. elian: kamala harris entra en la tapa crucial de sumar votos tras su promesa de gobernar para todos los estadounidenses. [habla en inglÉs] elian: se alista para su choque frontal con donald trump en su prÓximo debate presidencial.

so the fda has now approved the first nasal spray version. it's called nephi. you can see the device there. it's the exact same device that's used to administer narcan or nasal spray, naloxone for an opioid overdose. so you scored it up the nostril. >> it can be administered again if needed, into the same nostril. >> the fda has proved it for adults and children who weigh more than 66 pounds, the company's ceo told me on friday, they also are about to file for approval of a lower dose for children who way down to 33 pounds. and this is expected to be available to folks within about eight weeks. now, it's approved based on tests showing similar levels of epinephrine in the blood as when you use an injectable form like an epipen or a similar model. they also saw similar reactions and heart rate and blood pressure so a lot of folks are very excited about potentially being able to use an option rican square root up the nose. you don't have to use a needle, jessica, yeah. that is a game and changer for sure. what about the cost yeah. >> that has been something that

the first to be approved by the fda was adocanamab in 2021.drug is given intravenously, but dr. rezai told us it works slowly. >> typically, you go into the clinic and get an iv and have the antibody infusion over one to two hours and have to do it once a month or twice a month for 18 months or longer, and during those 12 to 18 months, the brain is continuing to progress. alzheimer's is not going away. >> it takes so long, because the drugs have a hard time getting through something called the blood/brain barrier. this tight filter of cells line the blood vessels to keep toxins from leaking into the brain, but it also prevents almost all of the medication from getting in, too. >> we think that that's what's causing the disruption. >> reporter: dr. rezai thought he could solve that problem with ultrasound. the same technology that's been used for 70 years to give doctors a view of orr gans and e ta fetal development. he chose ultrasound because it easily penetrates the skull and can be focused like sunlight through a magnifying class to help op

according to the fda that is not the case right now.s maybe in the future that will become fda approved and provide treatment for those in need. jon: whatever we can do to make life better for our veterans who are suffering we should do. doctor jenness. much more effective for coming up. ♪ new centrum menopause supplements help unpause life when symptoms pause it. with a multivitamin plus hot flash support. daily zz for quality sleep. and enxtra for focus and clarity. centrum, powered by clinically studied ingredients. i couldn't get my hair done. then psoriatic arthritis. cosentyx works on both for me. people with psoriasis on the scalp have a 4 times higher risk for psoriatic arthritis. serious allergic reactions, severe skin reactions that look like eczema, and an increased risk of infections, some fatal, have occurred. tell your doctor if you have an infection or symptoms, had a vaccine or plan to, or if ibd symptoms develop or worsen. still workin' for me. ♪see me.♪ no one should have to choose between good vision and great value,