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Jun 28, 2017
06/17
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KQED
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eye 142
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this is a fda-approved product... >> narrator: dr.ston mason is a harvard university researcher. here, he's comparing prescription-quality fish oil to the oil found in over-the-counter supplements. >> and give it a smell. >> it smells a little bit fishy, but not bad. >> right. you're gonna have always some smell. >> narrator: one of the issues with fish oil is it's delicate. it's extracted as a byproduct from oily fish like anchovies. as the fish get crushed, the oil is exposed to oxygen, and it doesn't take much oxygen to turn the oil rancid. >> this is a common supplement for fish oil. see what that smells like. >> oh... >> what? >> that doesn't smell good. that smells like it's going bad. >> yeah, right. it's a very strong fishy smell. >> narrator: if it was simply an odor issue, that would be one thing, but oxidized oil contains oxidized lipids, one of the building blocks of cells. we've long known that lipids, when oxidized, can be harmful. >> so an oxidized lipid triggers inflammatory responses within our body, particularly in o
this is a fda-approved product... >> narrator: dr.ston mason is a harvard university researcher. here, he's comparing prescription-quality fish oil to the oil found in over-the-counter supplements. >> and give it a smell. >> it smells a little bit fishy, but not bad. >> right. you're gonna have always some smell. >> narrator: one of the issues with fish oil is it's delicate. it's extracted as a byproduct from oily fish like anchovies. as the fish get crushed, the...
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91
Jun 21, 2017
06/17
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CSPAN3
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eye 91
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fda's reach is vast. the agency has authority over more than 300,000 foreign establishments, and 185,000 domestic establishments ranging from food processing plants, to facilities that manufacture life-saving medications. in addition to facilities themselves, the fda is tasked with the regulatory responsibility of individual products. and delivering these regulatory responsibilities your private-sector partners expect transparency and certainty from the fda. when i speak to small businesses, and ag producers in north dakota, their overwhelming concerns is that often overly burdensome regulations coming out of washington, d.c. can stifle innovation, and hinder their ability to create jobs. while we all support the fda's mission, we must also be mindful of these concerns. i believe the fda must avoid the trappings of one size fits all solutions and i urge you and your staff to take a common-sense approach in regard to the budget request itself. i'm concerned that this request relies on a significant increas
fda's reach is vast. the agency has authority over more than 300,000 foreign establishments, and 185,000 domestic establishments ranging from food processing plants, to facilities that manufacture life-saving medications. in addition to facilities themselves, the fda is tasked with the regulatory responsibility of individual products. and delivering these regulatory responsibilities your private-sector partners expect transparency and certainty from the fda. when i speak to small businesses,...
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Jun 10, 2017
06/17
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WUSA
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the fda told us this is all perfectly legal. all drugs like this are considered new just because no other company bothered to ask for fda approval until now. >>> a mom and five kids, they thought they were getting an award at tonight's national games. it turned out to be so much more. dad came home. lieutenant commander chris shedder was overseas on his fourth tour of duty. but tonight he surprised amy his wife and kids, miles, emerson, and emile y'all before the first pitch. >> now they get to spend the weekend together and beyond. >> the matter anymore, did it. >> it didn't turn out well, but that's coming up in sports. >> highlight,. >> great finish to the week and now just really hot here. some heat tomorrow, but i think the real heat comes in sunday, monday, tuesday and wednesday. let's talk about what is happening. high of 85 and today high of 84, little late on the drum roll, but okay, difference, zero, going 90 tomorrow for my guarantee. the jet stream is going way north. high pressures, bermuda high situation. upper lev
the fda told us this is all perfectly legal. all drugs like this are considered new just because no other company bothered to ask for fda approval until now. >>> a mom and five kids, they thought they were getting an award at tonight's national games. it turned out to be so much more. dad came home. lieutenant commander chris shedder was overseas on his fourth tour of duty. but tonight he surprised amy his wife and kids, miles, emerson, and emile y'all before the first pitch. >>...
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491
Jun 10, 2017
06/17
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KNTV
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for first time, the fda tells a drug company to pull an opioid off the market, taking action as so many families are caught in the epidemic. >>> are there more stolen secrets? new allegations in the case of the nsa contractor accused of leaking classified information. what prosecutors say she told her mother that has them so concerned. >>> and team spirit. why a girl got booted from a soccer game, and how her teammates rallied around her that has people across america cheering them on. "nightly news" begins right now. >>> good evening to our viewers in the west. it's great to have you with us on this friday. president trump broke his silence on the james comey testimony today, spinning comey's mixed bag of conclusions, hunches, and outright allegations into a good day for him and a bad one for the fbi boss he fired. a defiant president today claiming vindication, and saying he's willing to testify under oath about the russia matter, apparently ready to challenge comey's allegation that the president directed him to drop the criminal investigation of his former national security adviser.
for first time, the fda tells a drug company to pull an opioid off the market, taking action as so many families are caught in the epidemic. >>> are there more stolen secrets? new allegations in the case of the nsa contractor accused of leaking classified information. what prosecutors say she told her mother that has them so concerned. >>> and team spirit. why a girl got booted from a soccer game, and how her teammates rallied around her that has people across america cheering...
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Jun 22, 2017
06/17
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CSPAN2
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eye 97
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the fda doesn't have a black-and-white criteria. you have to be approved as being an abuse deterrent formulation. that is one of the challenges. we also have a disconnect in terms of when you look at the commercial coverage policies for the product. so what you generally see is the abuse deterrent formulations are two or three, tier four. in other words you're feeling for us on everything else and there's not kind to the calculation that we need to be considering potential for abuse. the fda has said it's a priority for them to approve the deterrent formulations, yet we have a disconnect when it comes to coverage and payment policies. again, only one tool in the toolkit, but an important one. >> 96% of the drugs and opioids people take routinely, daily, legally do not have any abuse deterrent. >> correct. >> so thick it takes one of my medicine cabinet, there's nothing they are it would keep them from crashing it into snorting it for cooking it and injecting it. >> correct. that's one of the reasons we think it's so important to inc
the fda doesn't have a black-and-white criteria. you have to be approved as being an abuse deterrent formulation. that is one of the challenges. we also have a disconnect in terms of when you look at the commercial coverage policies for the product. so what you generally see is the abuse deterrent formulations are two or three, tier four. in other words you're feeling for us on everything else and there's not kind to the calculation that we need to be considering potential for abuse. the fda...
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Jun 30, 2017
06/17
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CSPAN3
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eye 79
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and the fda just asked a company to remove opana from the market, and hopefully this could signal fda is beginning the change the opioid pistoriuss. it's unclear whether that was based in a change in fda or had something to do with a battle between fda and endo over the naming. there's quite a bit fda could do, and if they start taking the proper steps, it could be very helpful. >> we have about five minutes. i'm going to give you each about half of that. you're the drug czars. i mean you have all the power in the world to change this epidemic. lena, what's your list of policies? >> sounds amazing. first of all, i have to get used to this. first i would ensure that there is treatment on demand. not treatment in three months but treatment at the time that people need and the right treatment. we shouldn't be telling people, well, there's only one thing available. you get methadone or counseling. we should give people the services they need. ensuring treatment on demand. second, i would support those on the front lines with the resources that they need. we in baltimore city work closely
and the fda just asked a company to remove opana from the market, and hopefully this could signal fda is beginning the change the opioid pistoriuss. it's unclear whether that was based in a change in fda or had something to do with a battle between fda and endo over the naming. there's quite a bit fda could do, and if they start taking the proper steps, it could be very helpful. >> we have about five minutes. i'm going to give you each about half of that. you're the drug czars. i mean you...
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Jun 25, 2017
06/17
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CSPAN
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eye 64
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thattp -- the fda requires to medicalontribute training. is showing that they were not able to meet their goal of 80,000 prescribers taking that training over a two-year period. onre needs to be a focus prescribers getting better education about the treatment of pain and addiction. medical schools only spend a handful of hours on how to treat addiction and pain. our view is very strongly that you should -- that positions need the education regarding when it is appropriate to prescribe and opioid. and they are relying on clinical guidelines to prescribed dosage and for how long. other areas we are engaged in -- one of the challenges is a lot -- they have a misconception that because it is prescription, it is safer than heroin. that is not accurate. we need to do a better job of educating the public. we need to discourage people from sharing medication. when a surveyng shows that half of those that theypioids nonmedically, have obtained them from a family or friend. >> let us talk about the medications themselves. pills or other forms. it has
thattp -- the fda requires to medicalontribute training. is showing that they were not able to meet their goal of 80,000 prescribers taking that training over a two-year period. onre needs to be a focus prescribers getting better education about the treatment of pain and addiction. medical schools only spend a handful of hours on how to treat addiction and pain. our view is very strongly that you should -- that positions need the education regarding when it is appropriate to prescribe and...
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Jun 9, 2017
06/17
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BLOOMBERG
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and though has said it is reviewing the fda's request. sign that the nation's opioid crisis has become too big to ignore. let's bring in drew armstrong, bloombergs --rmaceutical procedure news. this is just 4% of their revenue. has the stock reacted so dramatically, and the second thing is, does this open up other pharmaceuticals? drew: to enter the second part of your question first, the fda has indicated and the commissioner has said, we are going to be taking a look at a lot of these issues. the fda does have the legal and say,go out there hey, people are abusing this. if the risks to people who might use it beyond the legitimate users washed over into that, it becomes a big deal here they feel the responsibility to take action because they can. from a legal perspective, there probably is the signal of some risk. keep in mind that several states, several counties and no andhave sued and other manufacturers about how they have abused communities. lawyers and courts are going to listen to that as they attempt to build cases. julia: accep
and though has said it is reviewing the fda's request. sign that the nation's opioid crisis has become too big to ignore. let's bring in drew armstrong, bloombergs --rmaceutical procedure news. this is just 4% of their revenue. has the stock reacted so dramatically, and the second thing is, does this open up other pharmaceuticals? drew: to enter the second part of your question first, the fda has indicated and the commissioner has said, we are going to be taking a look at a lot of these issues....
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Jun 1, 2017
06/17
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CSPAN
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eye 68
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the agreements that fund the fda and the user fee program expire this year. longer be will no able to approve drugs unless it has the fees that come from the drug companies that fund the fda's work. both programs must be re-authorized by congress this year. next creates a vehicle for someone to insert something into that legislation to go after prices because it is a relevant amendment to the user fee legislation. one has to do with the brandeds and one has to do with the generics. that is likely something that will be inserted that will drugss pharmaceutical prices. what will be inserted is unclear. right now, who is going to get hit? pedro: is there a philosophical battle within members of congress about so much sway over an industry and the prices they can set for themselves? mr. lipton: the typical move that congress does is, let's commission somebody to do a study to see how we can lower prices. that is essentially what one piece of the legislation is proposing. program that was passed to try to create more safety but ultimately it has become a way for t
the agreements that fund the fda and the user fee program expire this year. longer be will no able to approve drugs unless it has the fees that come from the drug companies that fund the fda's work. both programs must be re-authorized by congress this year. next creates a vehicle for someone to insert something into that legislation to go after prices because it is a relevant amendment to the user fee legislation. one has to do with the brandeds and one has to do with the generics. that is...
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Jun 24, 2017
06/17
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CSPAN3
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eye 97
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first of all, pharmaceutical is heavily regulated by the fda. so the comparison between pharmaceutical ads and attorney ads i think is apt, and i think we should be as thoughtful and driven as attorney ads as we are about drug ads. >> tradition tale it's been the state bars that regulate this problem. as far as i can tell there's been no complaints and nobodies brought in the cases. and i get my lawyer magazines and i see hundreds of complaints against lawyers every week. lawyers have been complain said about this and that, not calling their clients back, not giving complete information. so i'm just amazed there's not been a case like this. >> so my understanding most consumer related complaints are client driven. and this is an unusual situation because it's not the client that's injured. they're not complaining their lawyer is stealing their fee. because the client is affected, i think that's why there's way fewer complaints than consumer protection might suggest there should be. >> yes, you want to comment. >> let me clarify one issue with re
first of all, pharmaceutical is heavily regulated by the fda. so the comparison between pharmaceutical ads and attorney ads i think is apt, and i think we should be as thoughtful and driven as attorney ads as we are about drug ads. >> tradition tale it's been the state bars that regulate this problem. as far as i can tell there's been no complaints and nobodies brought in the cases. and i get my lawyer magazines and i see hundreds of complaints against lawyers every week. lawyers have...
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Jun 12, 2017
06/17
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CSPAN
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eye 69
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it is incumbent on the on the fda to remove it. fda shocks lawmakers by pulling opioid off the market. the stories said that the fda shocked lawmaker advocates and the pharmaceutical industry when it asked drug maker to pull opioid from store shelves. the agency decision last thursday asking the pharmaceuticals to remove the painkiller opana. it came after years of lawmakers saying the fda approved too many opioids and contributed to a growing epidemic. i have advocated for years for the fda to seek the advice of its expert advisory panel and seriously follow recommendations on the approval of regulations of dangerously addictive drugs. this is from senator joe manchin democrat from west virginia. the agency's decision came after a group of experts voted 18-8 back in march that long acting painkiller was doing more harm than good. let's get a call from gary now. gary is in everest kentucky, democrat. caller: how are you? we're all blessed by the good lord. thank you for taking my call. i live here in in here in in kentucky. 15 mile
it is incumbent on the on the fda to remove it. fda shocks lawmakers by pulling opioid off the market. the stories said that the fda shocked lawmaker advocates and the pharmaceutical industry when it asked drug maker to pull opioid from store shelves. the agency decision last thursday asking the pharmaceuticals to remove the painkiller opana. it came after years of lawmakers saying the fda approved too many opioids and contributed to a growing epidemic. i have advocated for years for the fda to...
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Jun 15, 2017
06/17
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WRC
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the fda said the administration set a maximum daily lead intake at 6 micrograms. why not zero?da said that lead is in food because it is in the environment and it cannot simply be removed from food. doctors discourage parents from worrying too much about the lead in baby food. >> i certainly would not recommend avoiding entire food groups. root vegetables are a healthy choice for babies. >> the fda is currently reviewing that 6 microgram level of lead. >>> stay with us. "news 4 today" continues right now at 5:00 a.m. >>> right now on "news 4 today," lawmakers and their aides targeted. four people shot when a gunman goes on a rampage. >> we are learning about him, his motives and a question he asked before the attack. >> the victims, who they are, their victims and their plans. >>> "news 4 today" starts now. >>> it is 5:00 a.m. good morning, everybody, i'm aaron gilchrist. >> i'm erika gonzalez. eun yang is on assignment. justin finch is live at the field where it happened. >> the lights are on as the investigation continues. we'll get more on that. first though, check on your f
the fda said the administration set a maximum daily lead intake at 6 micrograms. why not zero?da said that lead is in food because it is in the environment and it cannot simply be removed from food. doctors discourage parents from worrying too much about the lead in baby food. >> i certainly would not recommend avoiding entire food groups. root vegetables are a healthy choice for babies. >> the fda is currently reviewing that 6 microgram level of lead. >>> stay with us....
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Jun 24, 2017
06/17
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CNNW
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eye 79
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states, stem cells are partly mired in the controversy regarding fetal stem cells currently hung up in fda regulations and cost prohibitive. tens of millions of dollars to conduct one phase of a trial li this. the team at emery are currently working to raise the funds for the third phase of this trial. but it's risk and reward. even slow progress is still progress. >> now that we understand the limitations of having done this the first time we're developing techniques to try and inject the spinal cord in the mri scanner so there's a lot of details, questions that we would have never asked had we not done the first round of trials. >> six years after the transplant, ed's als progression is slower than normal. it hasn't yet reached his respiratory system. whether the stem cells had something to do with it or not, it's too early to tell. he's still outdoors as much as he can be, traveling the world in his wheelchair. even throwing out the first pitch with his son at a chicago cubs baseball game. >> i was happy to be part of something that looked forward, and then there's that part of all of u
states, stem cells are partly mired in the controversy regarding fetal stem cells currently hung up in fda regulations and cost prohibitive. tens of millions of dollars to conduct one phase of a trial li this. the team at emery are currently working to raise the funds for the third phase of this trial. but it's risk and reward. even slow progress is still progress. >> now that we understand the limitations of having done this the first time we're developing techniques to try and inject...
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Jun 23, 2017
06/17
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CSPAN3
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eye 53
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first of all pharmaceutical advertising is heavily regulated by the fda. these attorney ads are not there only regulated by state bars. so the comparison between pharmaceutical ads and attorney ads i think is apt and we should be as thoughtful and data driven by attorney ads as farm astd. >> who is we. >> attorneys. >> traditionally it's the state bars and state supreme court that regulates this problem. so as far as i can tell there have been no complaints and nobody's brought cases, you know, i get my lawyer magazines and i see hundreds of cases of complaints against lawyers every week. lawyers are complained about for this or that, not calling clients back, not giving them information. i'm amazed there's never a case like this. >> my understanding most complaints are client driven. it's not the clients who are injured. they are not complaining about the lawyers stealing their fees. because it's non-clients i think that's why there is way fewer complaints than consumer protection might suggest. >> yes. you want to comment. >> let me clarify one issue wit
first of all pharmaceutical advertising is heavily regulated by the fda. these attorney ads are not there only regulated by state bars. so the comparison between pharmaceutical ads and attorney ads i think is apt and we should be as thoughtful and data driven by attorney ads as farm astd. >> who is we. >> attorneys. >> traditionally it's the state bars and state supreme court that regulates this problem. so as far as i can tell there have been no complaints and nobody's...
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Jun 28, 2017
06/17
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KPIX
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eye 137
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go to the fda website and file a report if they have an adverse event.ash for me may be more serious problem for you. only way the fda will get a clear picture what is going on with more data. >> great advice. doctor, thank you very much. >>> up next, chicago police officers are charged with a cover-up. >>> three chicago police officers were charged to day with conspiring to cover-up the actions of a white cop who fatally shot a black teenager in 2014. the officers told investigators they saw laquan mcdonald swing a knife at officer jason vandyke. dash cam video showed vandyke shooting mcdonald 16 times as he walked away. vandyke is charged with murder. >>> a report out today says usa gymnastics needs a complete cultural change. following a sex abuse scandal. a former federal prosecutor made 70 recommendations to protect young gymnasts include making sure adults are never alone with minors. former team doctor dr. larry nasser will stand trial for sexual salt of six athletes. >> firefighters battling 20 major wildfires in the west. in arizona a fire teari
go to the fda website and file a report if they have an adverse event.ash for me may be more serious problem for you. only way the fda will get a clear picture what is going on with more data. >> great advice. doctor, thank you very much. >>> up next, chicago police officers are charged with a cover-up. >>> three chicago police officers were charged to day with conspiring to cover-up the actions of a white cop who fatally shot a black teenager in 2014. the officers told...
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Jun 8, 2017
06/17
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KTVU
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. >> 23 and me, i recall back in 2013 the fda told it to stop marketing itself as the genetic testingervice due to the fear that it could be inaccurate and it sounds like they have done an about-face on the ruling. >> reporter: they have. they have come back and said that 23 and me which was designed to give you an idea of your ancestry, traits and things like that, and was really kind of a test for the genetically curious folks that wanted to know a little bit about their genes. they had a little bit overstepped i think initially in offering the medical information that the fda felt there was not enough testing to say that it held up. what they did was to come back a couple of months ago and asking the fda to reconsider and they said yes, you can start sharing information with people, including things like if you have a genetic variance for late onset alzheimer's disease or if you have a genetic variance issue set for parkinson's. they can share that information with you if you want to have that information but the question is what you do with the information because the illnesses do
. >> 23 and me, i recall back in 2013 the fda told it to stop marketing itself as the genetic testingervice due to the fear that it could be inaccurate and it sounds like they have done an about-face on the ruling. >> reporter: they have. they have come back and said that 23 and me which was designed to give you an idea of your ancestry, traits and things like that, and was really kind of a test for the genetically curious folks that wanted to know a little bit about their genes....
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Jun 28, 2017
06/17
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CNBC
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i'm focused on fda right now >> let's talk about an issue that's been surrounding the fda in kind ofoversial issue covering the fda for quite awhile and that is the slow approval process for what people think may be life saving drugs in situations like cancer and situations like illnesses that affect children. is there a way to allow some of these people, some of these patients, to get access to drugs on a faster path without having to go through the full approval process? how do you balance sort of the safety, and the speed issues of these situations for life saving situations >> right well two issues here one is getting drugs on so-called compassionate use before they're approved. we've done a lot in recent years to try to facilitate access to patients who want to get access to a drug who were facing life threatening condition and want to try an experimental drug. there's probably more that we can do we're going to be bringing in a team to look at our programs and related to so-called compassionate use. and then there's also the question of trying to improve the overall efficiency
i'm focused on fda right now >> let's talk about an issue that's been surrounding the fda in kind ofoversial issue covering the fda for quite awhile and that is the slow approval process for what people think may be life saving drugs in situations like cancer and situations like illnesses that affect children. is there a way to allow some of these people, some of these patients, to get access to drugs on a faster path without having to go through the full approval process? how do you...
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Jun 10, 2017
06/17
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KPIX
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the fda warns that the drug is being crushed up and injected by people seeking to abuse it. that has led to several public health problems. >>> one in ten households used a prepaid debit card as their primary card and they don't have the same protections and credit cards. consumerwatch reporter julie watts on new rules that could change that. >> reporter: alvin is one of the millions of americans without a bank account. so his paycheck is direct deposited to a prepaid debit card but when he tried to get his money. >> i was sick. >> reporter: he says someone drained his card leaving him with no way to payment. >> i'm going to get kicked out find a new place to live. >> reporter: when he called the card company he said they said they couldn't do anything. >> i have no idea what to do. i have never been in addition situation. >> reporter: while credit and debit cards do provide protection from fraud when it comes to the prepaid debit cards used by 23 million americans. >> the truth is there wasn't a whole lot of protection. >> reporter: but last year the consumer financial prot
the fda warns that the drug is being crushed up and injected by people seeking to abuse it. that has led to several public health problems. >>> one in ten households used a prepaid debit card as their primary card and they don't have the same protections and credit cards. consumerwatch reporter julie watts on new rules that could change that. >> reporter: alvin is one of the millions of americans without a bank account. so his paycheck is direct deposited to a prepaid debit card...
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Jun 4, 2017
06/17
by
FOXNEWSW
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the number-one-prescribed, fda-approved oral combination treatment for hr+/her2- mbc. . arthel: members of london's muslim community gathering near london bridge, leaving flowers and paying respects to the victims of last night's attack. also ariana grande one love manchester concert happening now, and tomorrow night, a vigil will be held near london bridge, which london mayor sadiq khan will attend. eric: people of all faiths will attend to join in solidarity. tuesday, the british prime minister's house that's 10 downing street, there will be a moment of silence held at 10 downing street. that does it for us on a somber weekend as we are so tragically reminded of the terrorist threat we all face
the number-one-prescribed, fda-approved oral combination treatment for hr+/her2- mbc. . arthel: members of london's muslim community gathering near london bridge, leaving flowers and paying respects to the victims of last night's attack. also ariana grande one love manchester concert happening now, and tomorrow night, a vigil will be held near london bridge, which london mayor sadiq khan will attend. eric: people of all faiths will attend to join in solidarity. tuesday, the british prime...
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44
Jun 10, 2017
06/17
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WTTG
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>> ♪ >> the fda wants the opioid pain killer opona off the market here in the u.s.first time the fda has asked a company to withdraw opioid pain medication due to the public health threat of abuse. the agency says its risk outweigh its benefits. >> meantime the defense will begin its case monday in the bill cosby sex assault trial. prosecution rested its case after five days and 12 witnesses. tmz is reporting cosby's lawyers filed documents asking the judge to allow them to introduce evidence that andrea constand is gay. he reportedly wanted to show the jury he deceived him. prosecutors say it's victim shaming. the judge denied that motion. >> police say there have been dozens of car breaks in just this week. prince george's county police have been tweeting out photos from car break-ins along with the numbers. more than 2300 year to date, that's yearly a 15 percent increase over last year. police say to always lock up your car and not to leave any items laying out or anything visible somebody might want to take. >> there was actually -- before i've heard cops refer
>> ♪ >> the fda wants the opioid pain killer opona off the market here in the u.s.first time the fda has asked a company to withdraw opioid pain medication due to the public health threat of abuse. the agency says its risk outweigh its benefits. >> meantime the defense will begin its case monday in the bill cosby sex assault trial. prosecution rested its case after five days and 12 witnesses. tmz is reporting cosby's lawyers filed documents asking the judge to allow them to...
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78
Jun 7, 2017
06/17
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CNBC
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eye 78
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that same month the fda approved the machine for neurological procedures.er that year they got a thumbs up for a new optional imaging feature and more applications and various surgeries like removing the uterus and fallopian tubes. last year they got approval for a surgical table that moves in tandem with their davinci system along with various new accessories and last week the fda approved the davinci x or 10 this was a big deal because they weren't expecting it to be approved so quickly. the stock continued fabulous performance and the institutions. with the acceleration in numbers. accelerated record growth which is where it stayed so far this year. many of the more complicated new products carried higher margins which is the gross margin. that's what it makes after the cost of goods sold has gone from 66% in 2014 up to 70% last year. you combine faster revenue growth and you get an earnings explosion 19.8% earnings growth in 2013. wow. intuitive surgical may not be a young company anymore. we have excellent numbers for more mature business. as it's matu
that same month the fda approved the machine for neurological procedures.er that year they got a thumbs up for a new optional imaging feature and more applications and various surgeries like removing the uterus and fallopian tubes. last year they got approval for a surgical table that moves in tandem with their davinci system along with various new accessories and last week the fda approved the davinci x or 10 this was a big deal because they weren't expecting it to be approved so quickly. the...
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119
Jun 12, 2017
06/17
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WPVI
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eye 119
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. >> first time the fda asked the company to remove a prescription opioid because of a public health risk of abuse. the details when "action news" continues. >> often criminal acts such as rape, criminal violence could have been >> >> >> general election said the ceo is stepping down after 16 years, he will stay in until his retirement after the year. he took over 2001 four days before the terror attacks. he led the company through the 2008 crisis and financial markets. it was part of the succession plan. john flannery will take over the post in august. >>> in "healthcheck," now, for the first time, the u.s. food and drug administration has asked that a prescription opioid be pulled from the market because of the public health sequences of abuse. the fda asked pharmaceuticals to pull the drug since most users are injecting it since it was approved in 2012. >>> the "action news" team is working on new stories tonight begin agent 4:00 p.m. with temperatures in the 90s, hot coffee is the last thing most of us want in the morning that's where cold brew come in. but you don't have to head
. >> first time the fda asked the company to remove a prescription opioid because of a public health risk of abuse. the details when "action news" continues. >> often criminal acts such as rape, criminal violence could have been >> >> >> general election said the ceo is stepping down after 16 years, he will stay in until his retirement after the year. he took over 2001 four days before the terror attacks. he led the company through the 2008 crisis and...
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Jun 10, 2017
06/17
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a major shake up in the pharmaceutical industry for the first time the fda is asking a company not tol an opioid pain medication. according to reports there's concern because of the drug's potential for obama fda is asking endo pharmaceuticals to withdraw opan rer before the risks outweigh any benefits of pain control. >>> scary moments for delaware couple on the way to the hospital. the wife in labor, the obama ready to come at any moment. well, never made it to the hospital. fox 29's joanne pileggi explains where this baby entered the world. >> reporter: unexpected early delivery on a busy interstate. good thing everything went as well as it could. >> diss pat comes back outread radio and says the baby has been delivered. now i know why they stopped on the side of the road this makes sense now. >> reporter: on the side of the road not just any rode, but i-95 south in delaware. at 3:20 this morning. kirk and sally lawrence were on their way to the hospital. >> next thing, the baby was coming out in the car. bakely by the time we pulled over the baby had been born. we were picking the
a major shake up in the pharmaceutical industry for the first time the fda is asking a company not tol an opioid pain medication. according to reports there's concern because of the drug's potential for obama fda is asking endo pharmaceuticals to withdraw opan rer before the risks outweigh any benefits of pain control. >>> scary moments for delaware couple on the way to the hospital. the wife in labor, the obama ready to come at any moment. well, never made it to the hospital. fox 29's...
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Jun 21, 2017
06/17
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WTTG
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the fda has issued warnings on the reaction of so-called black henna which the fed agency may contain phenyl in die mean also known as ppd which is only permitted for use as a hair diane is known to cause an allergic reaction. if something is too hot outside -- a beach, right? in beach has more hot. sometime it burn the skin. nie large audience has been tattoos henna in the states for roughly a disek aid. back home in india the women typically get tattoos for good luck and for important events like parties or weddings. pay the ton mother's says she's unsure what exactly was used for payton's tattoo, she just heartache for another family. i high little ones are more at risk than adults but we were never washed when we walked into the store. if i only had gone on google before we did i would have saved a the lot of time and heartache. in an attempt to keep track of these actions, the fda can then keep track of what product is causing which problem . in prince william county, marina maracco, fox5 local news. >> the crack down on illegal immigration is hitting close to home. the nonprofit
the fda has issued warnings on the reaction of so-called black henna which the fed agency may contain phenyl in die mean also known as ppd which is only permitted for use as a hair diane is known to cause an allergic reaction. if something is too hot outside -- a beach, right? in beach has more hot. sometime it burn the skin. nie large audience has been tattoos henna in the states for roughly a disek aid. back home in india the women typically get tattoos for good luck and for important events...
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Jun 24, 2017
06/17
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CSPAN
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similarly where the fda, we were undertin
similarly where the fda, we were undertin
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Jun 29, 2017
06/17
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KGO
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and the fda, which regulates medical devices, told us cybersecurity risks are constantly evolving and has been working diligently to address medical device cybersecurity in all phases of a product's life cycle. >> open the chest up. >> reporter: back at the simulation these doctors are frantically working to keep their mock patients alive. >> this has gone from worrisome to official really quickly. >> reporter: everything that could go wrong does. a patient with a pacemaker. it's been hacked. >> we're making first incision. yeah, i feel the itd. >> that's the date of activity right now. >> reporter: all of the pretend patients in this simulation, even the surgical dummies, lived. thanks to these doctors. and while there aren't any known cases of illicit hackers manipulating somebody's pacemaker, jeff and christian are taking no chances. >> do you guys ever look at each other and think it's not bad for a couple of hackers who've gone on to perhaps save a bunch of lives here. >> we're just happy we're not in jail. >> thank you, doctor. good job. appreciate it. >> thank you. >> thank you
and the fda, which regulates medical devices, told us cybersecurity risks are constantly evolving and has been working diligently to address medical device cybersecurity in all phases of a product's life cycle. >> open the chest up. >> reporter: back at the simulation these doctors are frantically working to keep their mock patients alive. >> this has gone from worrisome to official really quickly. >> reporter: everything that could go wrong does. a patient with a...
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Jun 8, 2017
06/17
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CNBC
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the fda has been extremely positive.olutely. >> our first guest would never ever partner with anyone he didn't think would have anything special. talk to us about that. >> it's a great partnership. we're taking regeneron's pd 1 inhibitor. >> very important drug. >> very important drug and combining it with our 54-1 one of my favorite cancers for inovio, we're swinging for the fences. i know you're a baseball fan. >> if the phillies were better i would be even more a fan. you've been at this a long time. you're playing the long game. you admit it's a long game before you get to fruition for everything. >> normally yes. in immunology and cancer there are break through things and fast tracking depends on the data. i'm convinced on the data we have thus 4. 54-1 and pd 1 inhibitor will bring about very good data. >> i don't want to get folks too excited but you have an exciting company. the president of the fatherlies company next door to where i'm from, after the break. think again. this is the new new york. we are building
the fda has been extremely positive.olutely. >> our first guest would never ever partner with anyone he didn't think would have anything special. talk to us about that. >> it's a great partnership. we're taking regeneron's pd 1 inhibitor. >> very important drug. >> very important drug and combining it with our 54-1 one of my favorite cancers for inovio, we're swinging for the fences. i know you're a baseball fan. >> if the phillies were better i would be even more...
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Jun 9, 2017
06/17
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BLOOMBERG
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it's a milestone for the fda.ght against pain drug abuse, regulators have asked endo to stop sales of its opioid painkiller. it's the first time the fda has taken a step like this. drug users have started injecting the medication leading to an outbreak of hepatitis c and hiv. single-parent alphabet is selling part of its company to japan. sellingon what the prices for boston dynamics. softbank is buying japanese robotics company sha. beenlobal forecast has boosted for airline production. get pushedles will to 35,000 over the next few years. timell be driven by first buyers and the opening of new airports. that's your latest bloomberg business flash. trump: president donald has offered rex tillerson the position of mediating the qatar crisis. -- persian gulf monetary monarchy is little but it has for itself as an outside power broker in a volatile region. thanks to vast reserves of natural gas, it enjoys the highest per capita income. soon after president donald trump visited saudi arabia last month, the saudi's an
it's a milestone for the fda.ght against pain drug abuse, regulators have asked endo to stop sales of its opioid painkiller. it's the first time the fda has taken a step like this. drug users have started injecting the medication leading to an outbreak of hepatitis c and hiv. single-parent alphabet is selling part of its company to japan. sellingon what the prices for boston dynamics. softbank is buying japanese robotics company sha. beenlobal forecast has boosted for airline production. get...
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Jun 21, 2017
06/17
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WTTG
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. >> the fda has issued warnings on the so-called black hen a which the agency may also contain ppd which is only permitted for use as a hair sky if something is too hot outside and beach has more hot. sometime it burn the skin. nylon has been tattooing hen a for a decade. back home women typically get hen a tattoos for good luck for weddings or parties. this one is narm. pay the ton's mother says she's unsure what exactly was used for pay the ton's tattoo, she just hopes her story will avoid pain and heartache for another family . i think little ones are more at risk than adults but we were never warne into the store. if i only had gone on google before i did this i would have saved a lot of time and a lot of heartache. >> in an attempt of keeping track of these reactions, the fda recommends that consumers alert the agency if they have any sort of issue with a similar product so that in turn, the fda can then track which products are causing the problems. live tonight in prince william county , marina maracco, fox5 local news. >> good information. still ahead tonight, oj simpson is sched
. >> the fda has issued warnings on the so-called black hen a which the agency may also contain ppd which is only permitted for use as a hair sky if something is too hot outside and beach has more hot. sometime it burn the skin. nylon has been tattooing hen a for a decade. back home women typically get hen a tattoos for good luck for weddings or parties. this one is narm. pay the ton's mother says she's unsure what exactly was used for pay the ton's tattoo, she just hopes her story will...
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Jun 25, 2017
06/17
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CSPAN
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. -- half thethe sba day -- fda. something else in competing health and safety measures? we can split the pie up and look at government paperwork, we can look at government health and safety regulations, and fair -- environmental types, economic regulations and come together and say some of this stuff is tough and if it is tough to deal congress should step in and legislate on that category rather than the agency who bats this around so much. we have to work on the existing regulatory body that is out there and, together with a bipartisan reduction. braddock,e from pennsylvania on the democratic line. caller: good morning. tell you a short story, when i grew up in the early 1960's we used to cap out at dashcam out at lake ontario. there was nothing but clean beaches and everything was fine. back wend year we went couldn't wait to get to the beach. there were dead fish all along the shore with tractors scooping them up and piling them up in burying them. it was a plant upstream that was running whatever it was into the lake, it killed off all these fish. thank out that ric
. -- half thethe sba day -- fda. something else in competing health and safety measures? we can split the pie up and look at government paperwork, we can look at government health and safety regulations, and fair -- environmental types, economic regulations and come together and say some of this stuff is tough and if it is tough to deal congress should step in and legislate on that category rather than the agency who bats this around so much. we have to work on the existing regulatory body that...
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Jun 12, 2017
06/17
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KTVU
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. >>> the fda wants a prescription painkiller off the market. the agency says the opioid painkiller should be halted off in the u.s. the powerful medications risk for abuse outweighs its benefits. the fda is increasing the pharmaceutical company to volunteerly recall the drug. it's the first time they have moved to take the opioid pain medication off the market due to abuse. the number of opioid overdose deaths have quadrupled in the past 15 years. they are reviewing the request in a way of evaluating their options. >>> women with type ii diabetes who take a low dose aspirin may reduce the risk for breast cancer. researchers studied 150 women with type ii diabetes over a 14- year period and found women who took low dose aspirin had nearly a 20% reduction of developing breast cancer. the team notes many of these women were taking aspirin therapy to prevent cardiovascular disease, but might be protecting a new device as well. >>> san francisco today and mother nature forced a change and plan for the thousands of athletes taking part in this year's
. >>> the fda wants a prescription painkiller off the market. the agency says the opioid painkiller should be halted off in the u.s. the powerful medications risk for abuse outweighs its benefits. the fda is increasing the pharmaceutical company to volunteerly recall the drug. it's the first time they have moved to take the opioid pain medication off the market due to abuse. the number of opioid overdose deaths have quadrupled in the past 15 years. they are reviewing the request in a...
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Jun 15, 2017
06/17
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WRC
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the fda says the administration set a maximum daily lead intake at 6 micrograms. why not zero? fda says that lead is in food because it's in the environment and it can't simply be removed from food. doctors are discouraging parents from worrying too much about the lead levels in baby food. >> i certainly would not recommend avoiding entire food groups because of concern of exposure. >> that said the fda is currently reviewing the 6 microgram lead level. >>> good morning, i'm courtney ragan at cnbc headquarters. apple wants to turn your phone into a one stop shop for all of your medical information. cnbc hats learned they are working on creating an itunes for health data. it will be a centralized management system for everything from medical records to prescriptions. apple is reportedly in talks with several hospitals and i.t. health firms. >>> the federal reserve is raising interest rates by a quarter of a percentage point. >> the question many of you may be asking, how will this affect me? news 4 is working for you with the bottom line here. take a look. if you're looking to b
the fda says the administration set a maximum daily lead intake at 6 micrograms. why not zero? fda says that lead is in food because it's in the environment and it can't simply be removed from food. doctors are discouraging parents from worrying too much about the lead levels in baby food. >> i certainly would not recommend avoiding entire food groups because of concern of exposure. >> that said the fda is currently reviewing the 6 microgram lead level. >>> good morning,...
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Jun 10, 2017
06/17
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KPIX
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. >>> the fda has approved a medical device that could help millions living with heart disease. the device is called an echo duo. it combines a stethoscope and antic toe cardiogram. electrocardiogram. >>> we've put it into a simple friendly factor. it is a small device that connects to a physician's mobile devices and captures ecg and heart sounds. >> 28 million americans are living with heart disease. >>> a look at a lifesaving resource coming back to the bay area. i headed out to burialing game to check out the return of a vital service. >> the urgency is great for the patient to get there. >> reporter: it might mean the difference between living and dying. >> ultimately, my job is to get the helicopter and that person there safely. >> reporter: there's a new option for critically ill patients on the peninsula, for the first time in five years, helicopters will be airlifting patients to mills peninsula medical center to be treated for strokes and heart attacks. >> we'll be able to fly patients in who have needs for specialists. >> reporter: the old helipad was demolished when
. >>> the fda has approved a medical device that could help millions living with heart disease. the device is called an echo duo. it combines a stethoscope and antic toe cardiogram. electrocardiogram. >>> we've put it into a simple friendly factor. it is a small device that connects to a physician's mobile devices and captures ecg and heart sounds. >> 28 million americans are living with heart disease. >>> a look at a lifesaving resource coming back to the bay...
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Jun 15, 2017
06/17
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the fda gave them to live next year to comply but a new date is not yet been announced.>>> if you wante to eat the vegetables give them exotic names and they've observed the habits of 28,000 diners over 46 days. they worked with the food service staff to put different labels on the vegetables to see if that would influence the diners decisions and all the vegetables were prepared the same way but labeled differently. the more interesting the name the more likely people work to choose that vegetable over sugar free labeled products or smart choice. they believe this could change the mindset that healthy food taste best. >>> pharmacies may be more aware of the penicillin allergies and the doctors that prescribe the medicines. they analyzed 300 surveys completed by the doctors, nurses, physician assistants and pharmacists with more than 80% of the general practitioners new patients that reported the penicillin allergy should be referred to the allergist. many had never referred the patient or referred only one patient a year to be tested. they said the findings show a need to better educa
the fda gave them to live next year to comply but a new date is not yet been announced.>>> if you wante to eat the vegetables give them exotic names and they've observed the habits of 28,000 diners over 46 days. they worked with the food service staff to put different labels on the vegetables to see if that would influence the diners decisions and all the vegetables were prepared the same way but labeled differently. the more interesting the name the more likely people work to choose...
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Jun 22, 2017
06/17
by
CNBC
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the fda removing opioid painkiller of the markets.on of attention being paid here. >> where is the wrong doing being done the fda is aprovproving any wro labels, the sales people going out and talking to the doctors of addictive risks, what's your theory >> that's right and among other things the facts are and these companies engaging in marketing campaigns towards doctors and consumers that deliberately misrepresents the nature of these drugs. they have spent by the way tens of millions of dollars used front organizations and fake and fraudulent researches convincing these drugs are not highly addictive. they say things that you cannot get addicted from opioids. >> it sounds a lot like smoking, is it not? >> there is $880 million spent by the industry to lobby against stricter regulations for opioid prescriptions. >> $880 million. >> yes, it is been a coordinated campaign, there is no doubt about it the results of that has been mass addiction missouri last year alone 30,000 hospitalizations due to opioids. there is a reason why these
the fda removing opioid painkiller of the markets.on of attention being paid here. >> where is the wrong doing being done the fda is aprovproving any wro labels, the sales people going out and talking to the doctors of addictive risks, what's your theory >> that's right and among other things the facts are and these companies engaging in marketing campaigns towards doctors and consumers that deliberately misrepresents the nature of these drugs. they have spent by the way tens of...
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Jun 13, 2017
06/17
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KTVU
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. >>> the fda wants a prescription painkiller off the mark.gency says the ohii did painkiller p. the fda is requesting endo pharmaceuticals to withdraw the drug. it is the first time the fda has moved to take an opioid pain medication off the market due to the public health threat of abuse. the number of opioid overdose drugs in the u.s. has quadrupled in the past 15 years. endo says it is reviewing the request and a he epees. a low dose aspirin may reduce the risk of developing. they found the women who took low-dose aspirin had a 20% less risk of developing breast cancer. it may be providing a protective affect. the findings appear in the journal of women's health. >>> coming up, a bay area senior unable to sieves diploma with his classmates all because of what he was wearing. now an apology has been issued. we will show you the private ceremony was held today and the outpouring of support. >>> plus, production on the reality tv show "bachelor in paradise" is now suspended over al. >>> we're tracking what's left of the clouds and a big warm-
. >>> the fda wants a prescription painkiller off the mark.gency says the ohii did painkiller p. the fda is requesting endo pharmaceuticals to withdraw the drug. it is the first time the fda has moved to take an opioid pain medication off the market due to the public health threat of abuse. the number of opioid overdose drugs in the u.s. has quadrupled in the past 15 years. endo says it is reviewing the request and a he epees. a low dose aspirin may reduce the risk of developing. they...
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Jun 11, 2017
06/17
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KGO
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ask your doctor about ibrance, the number-one-prescribed, fda-approved oral combination treatment fortime now for our index, and a major nationwide food recall to tell you about tonight. conagra brands recalling canned spaghetti and meatballs. the products mislabeled. they did not say they could contain milk. they were sold under several brands, including chef boyardee. >>> and we're learning tonight tiger woods says he was also taking an anti-anxiety medication when he was arrested for suspicion of dui. woods told arresting officers he was prescribed four medications, including vicodin, when he was found asleep at the wheel of his car. but an unredacted police report obtained by the golf channel says woods told them he also took xanax. the fda says taking xanax with an opioid like vicodin can cause serious complications that could even prove to be fatal. >>> and a florida truck driver in critical condition tonight after his tractor trailer exploded. the explosion caught on camera. you can see it there. the truck's fuel tank rupturing after hitting a guardrail. the 69-year-old driver
ask your doctor about ibrance, the number-one-prescribed, fda-approved oral combination treatment fortime now for our index, and a major nationwide food recall to tell you about tonight. conagra brands recalling canned spaghetti and meatballs. the products mislabeled. they did not say they could contain milk. they were sold under several brands, including chef boyardee. >>> and we're learning tonight tiger woods says he was also taking an anti-anxiety medication when he was arrested...
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Jun 9, 2017
06/17
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CSPAN2
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the fda, what we envisioned in the fda has shifted the resources coming to fda and i think in fact there's $500 million increase in resources coming to fda through a modification and an improvement in the user fee process. >> you are aware of your time, you can submit questions in writing, i'm sure the secretary will submitted.>> if it's okay with you, i think i will yield to senator robert to spend your waitingand i'd like to go after him . >> very gracious. we will go to senator roberts and i'll come back. >> german, i wave . the 10th of an hour or five or six, what are we doing? i'm assuming we're under the five minute rule. i want to get in the weeds a little bit, welcome back. >> good to be back. >> there are statements that you are responsible for people dying in ohio, all of the current problems in the affordable healthcare act over the last three years. reductions in funding inrural areas which of course i'm very much interested in . the entire budget by the president proved to be more accurate omb and the chairman has been chided for not having regular order but what we have today
the fda, what we envisioned in the fda has shifted the resources coming to fda and i think in fact there's $500 million increase in resources coming to fda through a modification and an improvement in the user fee process. >> you are aware of your time, you can submit questions in writing, i'm sure the secretary will submitted.>> if it's okay with you, i think i will yield to senator robert to spend your waitingand i'd like to go after him . >> very gracious. we will go to...
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Jun 12, 2017
06/17
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WRC
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. >> reporter: now a new treatment just approved by the fda could be a game changer for people like felicia who suffer from debilitating arthritis but not ready for surgery. it's called coolief. doctors insert specialized needles that emit radio frequency to stop the pain. this is not getting rid of the arthritis, it's taking care of the pain. >> we're not changing the structure of the knee, but if we get rid of the pain she can be functional. >> reporter: one steady comparing coolief to popular cortisone injections show it not only gave patients more pain relief but that relief lasted longer, about six to 12 months with minimal side effects. coolief cost up to $4,000 and covered by some insurance companies. last month felicia underwent the procedure that lasted le she says the pain relief was instant. >> i can just do things now and i don't even know what i want to do but i know it's everything, you know. >> reporter: because the nerves regrow, the pain can return after six to 12 months but at that point the procedure can be done to stop it again and as felicia told me unless you're living
. >> reporter: now a new treatment just approved by the fda could be a game changer for people like felicia who suffer from debilitating arthritis but not ready for surgery. it's called coolief. doctors insert specialized needles that emit radio frequency to stop the pain. this is not getting rid of the arthritis, it's taking care of the pain. >> we're not changing the structure of the knee, but if we get rid of the pain she can be functional. >> reporter: one steady comparing...
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Jun 12, 2017
06/17
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BBCNEWS
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chief james lingers, did he have a roll in the sacking of fda chiefjames comey? and gets a definitive a nswe rs is tragically, and gets a definitive answers on who met whom on what particular date, and try to get some clear a nswers particular date, and try to get some clear answers from jeff sessions as to his involvement. perhaps meetings that were previously undeclared with russian officials, that he might now wa nt to russian officials, that he might now want to acknowledge. and apart from thisjeff sessions testimony, the donald trump troubled and is back in the headlines, after suffering another defeat in the courts? yes. this is another court that has issued a defeat, and this is because according to the appeal court, the president overstepped his authority in issuing that executive order. this was the revised travel ban, involving a ban on travel for their wool from six mostly muslim nations. it lake this is almost certain go to the us supreme court. —— for people from. the so—called islamic state group has released a video claiming to show is militants mu
chief james lingers, did he have a roll in the sacking of fda chiefjames comey? and gets a definitive a nswe rs is tragically, and gets a definitive answers on who met whom on what particular date, and try to get some clear a nswers particular date, and try to get some clear answers from jeff sessions as to his involvement. perhaps meetings that were previously undeclared with russian officials, that he might now wa nt to russian officials, that he might now want to acknowledge. and apart from...