. >> the fda confirmed the news but will not say which facility it was discovered at. it was found in august and some health experts say this might be a good thing. >> finding it before it's used is very, very good because that means we are doing the right thing. we are trying to identify whether there are any contaminated bloods before they are given. >> the three tests being used to test fo not licensed by the fda but have been allowed on an emergency basis. the fda did not say exactly how many are or are not using the double testing procedure. >>> also a new study in the journal pediatrics shows a rise in snake bites in florida. overall, the study shows more than 1,300 kids suffer snake bites each other. this two-year-old right here is recovering from a rattlesnake bite to the leg. two out of three victims were boys in these bites.

as always at fda has no role in setting drug pricing.but our actions are to enhance competition which has been shown to decrease drug prices. for example, i'd like to go through some of the actions we can take that enhance competition. we often approve multiple drug and therapeutic class. they are separate drugs that, for example, there's a lot of stuff was born and about its out there, say within a class or antihypertensive of certain class, there may be a lot of drugs that compete in the market. also we often approve different versions of a marketed drug wants patent and exclusivity have expired that are not exact copies fund our 505 at two b. program which is not a generic but is part of legislation here these copies also can compete with a marketed drug. under the generics program, multiple more less exact copies of the branded drug can be approved once all exclusivity and patents have expired. we frequently approved several copies at once. for example, very recently we approved a generic crest doors on the same day. so there's a fir

as already said, fda has no role in setting drug pricing.ns serve to enhance competition, which has been shown to decrease drug prices. for example, i would like to go through some of the actions we do take that enhance competition. we often approve multiple drugs in a therapeutic class. they are separate drugs. for example, there are a lot of self lo spohr -- within a class, there may be a lot of drugs that compete in the market. also, we often approve different versions of the marketed drug once the patents have expired that are not exact copies under our 500 b 2 program, which is not generic but part of the legislation. these copies also can compete with the marketed drug. under the generics program, multiple, more less exact copies of a brand of drug can be approved once all exclustivety and patents expire. we frequently approve several copies at once. for example, recently, very recently, we approved eight crestors on the same day. so there's a first generic, but there might be eight first generics. the introduction of multiple copies i

the fda is okay with the.use. if they find the injections are a drug it could table studies issue animal testing and humachine trials before it is available. doctor mc gee says the fda's decision will be ground breaking. >> we're at point we need more research to give patients data. >> and his patients. >> wants history and the fda's decision makers to hear it. >> someone is hurt and they put creating this new thing. it is -- that cool temperature really is. >> reporter: after years of pain he is finally healed. >> it is gone. it was gone in a week. >> reporter: for him the shots hit the bull's eye. >> it is a life changer for me. i can't be happier. it is no different than going in and getting a couple of shots you need for a physical. >> ea and you know you want to get out and around with fantastic weather. >> maria: jerry brown is joining us on a friday. not a bad way to end september. >> reporter: october is going to be the first weekend bad hair days. you know the winds. the temperature range you will love it

i went on the fda's website, people could have problems from nonapproved botox. it could be poisoning, adding the vitamin b 12 injections, it's for a certain use only. and he sharpied out "not for human use". the medical peels were expiration date with a sharpie and wrote a new one. he wanted us to use wart remover on people's faces to pull up , and i began to get really nervous, i started thinking, my license is in general partner, the patients are in jeopardy. >> ?, and the doctor said, i also doing in the area. what the doctor is doing, is, wrong. >> that nurse, nurse "x" joins us on the phone. we call her this, to protect her identity. a lot of eye-opening things you said there. what happened after your findings? >> i decided that they're my employment just for the fact that i was bringing attention to the illegal activities. >> dr. travis: what happened after that? >> i am un called the fda. they're in the middle of investigation. and they're still in business. they're still using illegal products. and as of today, the office is still open. >> had you had ex

>> i think the fda can do more. but this is a brave new world. certainly there were a few people, myself included ten years ago advocating to the fda and various government agencies that you need to watch for these security problems. they did listen, but typically the government reacts on a cycle that's measured in four or five years, not overnight. >> and the meantime for those hospitals caring for patients overnight and healthcare providers and others, are they investing enough themselves in cybersecurity? >> well, i heard from one cio of a large hospital system that he went to his board asking for a $5 million annual budget and the board said how about 6 million. so i think some hospitals are beginning to invest more heavily in cybersecurity. the real problem is they don't -- they have a hard time even knowing what medical devices are at risk. so it's pretty basic right now in the hospital systems. and as far as patients go, personally i think patients are far safer with these devices than -- than not. patients are predisposed to medical risks

if it's found to be a biological treatment using tissue, then the fda is okay with its present use. but if the agency finds stem cell injections are considered a drug, then it could take years of studies, animal testing and human trials before the treatment becomes readily available. dr. mcgee says the fda's decision will be groundbreaking. >> we're at the point now where >> reporter: and his patient -- >> it sounds like something you would see in a movie, doesn't it? >> reporter: -- wants his story told and the demakers to hear it. >> someone is hurt and they put a few injections in there and these cells regenerate and go to the pain and start building and attaching and creating this new thing. it's that cool. it really is. >> reporter: dudley adds after years of pain, he's finally healed. it was literally gone in a week. >> for him, the shots hit the bull's eye. >> it's a life-changer for me. i can't be happier. it's no different than going in and getting a couple of shots you need for a physical. >> wow. that's amazing. we will follow up on progress. >>> firefighters rescue a kit

. >>> also, why the fda is warning the parents against using certain baby teething tablets and gels. tonight. they debate one another in virginia. you'll see that live here on 12 news at 6:00. >>> and then join us for an all new episode of "the voice" on 12 news at 9:00. wireless headphones, the best bang for your buck. and then on 12 news at 10:00, a new feature aimed at protecting the infants in safety seats to the test that is tonight only >>> everyone seems to be buzzing about it. maybe you have been getting the e-mails from southwest airlines about a three-day sale. they're promising one-way fares for as low as $49. >> how likely you will be able to get the bargain basement price ? we sat down at the >> reporter: it turns out you're pretty likely if you about fast. there are some restriction tons flights, but if you are not set on the dates and you don't want to go that far, there are good deals for under $100. want to get away for less than $100? it is possible if you want to go to the right places. >> for short haul flights, i looked today, they were available, pretty widely a

the fda confirms they're 10 news went to five stores. cvs, big lots, winn-dixie, target, and dollar general, none of the stores had these pucks on shelves. walgreens had it in stock, but when we went to buy it, the cashier wouldn't sell it to us. the fda recommends if you have the tablets or the them out. if your child has had seizures, difficulty breathing, you should report that and any other add verse side effects to the fda. >>> running drivers off the road. take a look at this, highway patrol troopers say one man was driving straight at them with no regard for his life or anyone else's. when the man didn't pull over, he led police on a high-speed chase down some dirt roads in southern oklahoma. the medal. many folks were forced off the road. police put out a spike strip which ultimately got the driver to slow down. but he almost ran over a trooper while they were trying to take him into cust can i. >>> two months after historic flooding in louisiana, it's fast becoming a sellers market for homes in hard hit livingston parish east of

this is the only personal genome service with the fda's blessing, and it's revolutionizing the healthdigm by helping you and your family figure out what conditions you might be prone to while still early enough to do something about it. now, earlier today i got a chance to sit down with ann wojcicki. she is the co-founder and ceo of 23andme, to learn more about her company, its science, and how it could potentially change the way we treat all sorts of diseases. take a look. when i think of your company, i think about empowering the patient. what does that do for the whole health care system. >> i think one of the things i'm super proud about is 23andme is really leading the charge of saying that the individual, like you the consumer, actually needs to have a voice in health care. and if you think about the health care system and how it is today, there's this whole world that sort of operates above you. so like how you get your drug, your medications, how decisions are made by your physicians, how they're made by the insurance company. and i think that one of the things i learned is th

and so 1993 we petitioned the fda to require labeling of transfat. and i don't want to go into all the details, but it took fda 10 of transfat. >> you're saying what? what are some of the products that people eat with transfat? >> crisco in everything with vegetable shortening. mcdonald's and every other fast food restaurant, fried chicken. we were drenched our foods in transfat. and the controversy and then the labelling made tremendous progress in getting rid of it. so the 1993 mandate for labelling and right about then, denmark banned partially hydrogenated oil. and so the fda is still talking about labelling denmark as banning. we petitioned -- the evidence had gotten so strong with both the clinical studies and epidimological to cause them to ban partially hydrogenated which the fda didn't do until 2013. but transfat really became a dirty word, and so many companies started labelling their foods, "no transfat." it has been largely whisked out of the food supply. 90% or more of transfat is gone. 7 to 7.5 billion pounds a year. it really shows the

the fda inspects manufacturers to make sure they're meeting requirem for good manug practices and also conducts label reviews during these inspections. and the usda tells us it, quote, ensures that meat, poultry and processe egg products entering commerce are safe, wholesome and correctly so what can you do? well, omahasted tries to avoid heavily process food, because they can hide a lot of fake ingredient when you can buy food in their most whole form. like coffee beans, whole fish and cheese. so y always know exactly what you're get i'm andrea day for "nightl >>> finally tonight, two professors one from harvard, the other from m.i.t., awarded the nobel prize in economics for their work on contract theory. according to the royal cad believe sciences, their work has helped shape business, finance and publ >>> and that will do it for "nightly b for tonight. th for joining us, i'm sue herera. and i'm tyler mathisen. thanks from me, as well. have a great evening, everybody. we'll see you back here tomor ♪ announcer: a kqed television production. sbrocco: and everybody say "opa!" together:

kybella® is an fda-approved non-surgical treatment for adults with a moderate amount of fullness... orit more. don't receive kybella® if you have an infection in the treatment area. kybella® can cause nerve injury in the jaw resulting in an uneven smile or facial muscle weakness, and trouble swallowing. tell your doctor about all medical conditions, including if you: have had or plan to have surgery or cosmetic treatments on your face, neck or chin; have had or have medical conditions in or near your neck or have bleeding problems. tell your doctor about all medicines you take. the most common side effects are swelling, bruising, pain, numbness, redness, and areas of hardness in the treatment area. find a doctor at mykybella.com

if it doesn't make landfall on friday, it's gonna be a rough day, basically right up and down 95 in fda daytona beach and st. augustine in jacksonville. on the other side tampa as well as fort myers, not anticipating significant weather conditions on that side of the state. so to be basically along and east of interstate 95. from there it parallels the georgia coastline as well as the south carolina coastline and loops back to the south. more of a threat for south carolina as opposed to north carolina, and no threat to new england, back to you guys. matthew already causing problems for those preparing to go on vacation. we'll have more on that in the next few minutes. you can keep up to date by using our mobile tablet apps or go to our web site at whdh.com. >> protests at harvard started this morning after workers failed to reach a contract with

tonight, the fda as a warning for all of you using home homeopathic tab lits. >> reporter: one of the ingredients in this cab is okay in small doses is okay, but in large doses it is how macbeth month old jocelyn tapper having a surgery. >> it was really brightening. really frightening to see your baby doing something like this. >> reporter: her parents pinned it down to these. teething tabs. >> it is supposed to be a safer way to keep the baby in less pain. >> reporter: instead, jocelyn got so sick, she was taken to the emergency room. now, the food and drug administration is looking into whether these teething tablets have caused the death of ten other babies. >> it is what we expect to see from that substance. >> reporter: it is belladonna. in a high enough dose, it becomes a poison. because rules are not quite as strict for homeopathic medicines, that is what may have happened. >> when you get a bottle of something, it is not an exact the fda is warning parents not to use them. >> see? >> the scary part was we thought our girl might have some kind of permanent neurological problem

a year ago 23andme started offeringme ones that meet fda reporting standards, include whether you're a carrier for certain genetic disorders, which is very important if you're thinking about having kids. they've also started using the gigantic pool of data they've gathered to help with medical research. i think this is a very exciting story that is at the forefront of personalized medicine because they're empowering patients like you to learn more about themselves in order to prevent illness, to save lives, and help mine data for cures. this is the only personal genome and it's revolutionizing the health care paradigm by helping you and your family figure out what conditions you might be prone to while still early enough to do something about it. now, earlier today i got a chance to sit down with ann wojcicki. she is the co-founder and ceo of 23andme, to learn more about her company, its science, and how it could potentially change the way we treat all sorts of diseases. take a look. when i think of your company, i think about empowering the patient. health care system. >> i think on

>>reporter: angela also peers without some movement on the part of the fda the drugmaker may give up, denying jack the medication that seems to be helping him. so while jack and amber march on the field, his mother is pushing for a cure, hoping washington uses some common sense to extend the life for young men like jack. >>> a little kindness is something we could all use, that is why here at denver7 we have shared up with rachel's challenge to help spread the message of kindness and compassion to schools around the world. some of the messages are simple, like this billboard. a reference to rachel scott writings that she wanted to see a change of kindness. many of the bulletin boards and even posted notes are creattd by friends of rachel. now, f you or someone you know is doing something to spread kindness we want to hear from you. send us a note and you can also learn more in the spot ike section of thedenverchannel.com. >>> next, a look at today's top stories, plus more states could legalize pot in november. >>> now to tonight's top stories, by people are dead after a crash on the e

erika: three massachusetts doctors suing the fda. what they want the fence to do regarding cigarettes. >> the 10:00 news on metv boston with maria stephanos and ben simmoneau, on comcast channel 942, verizon 461 and over the the outside corporate interests bankrolling question two are trying to deceive you. here's the truth: every time a new charter school opens, it drains money from the existing public schools. that's 400 million just last year - according to the state's own data. which means real cuts to our kids - in arts, technology, ap classes, pre-school, bus service and more. join them in voting no on question two. kelly: you know me. nfalse, negative ads- but as your first female attorney general- equal pay and against workplace discrimination, to expand access to birth control, strengthen and preserve medicare, and i reached across the aisle to protect access to mammograms. i approve this message because after all the false, negative ads, i'm still the kelly ayotte you know- and i'm still fighting for you. erika: it is back

has to have approved that manufacturing plant--- if the fda hasn't approved it it can't be sold in the u.s." overall tyler believes that generics are safe and just as effective as their brand name counterparts.(sot: timothy tyler/ pharmacy director)"i do think that brand drugs offer us a great opportunity, they're new drugs, that treat new indications... however, once a generic becomes available, i have no doubt that a generic will serve your needs almost as well."and especially if you're on a budget.(sot: timothy tyler/ pharmacy director)"if i'm a senior and i have a chance at paying 4 dollars vs 50 or 60 bottom line, according to the pharmacist, generics are just fine unless your doctor is specific about the need of a brand name drug. about half of american adults take some type of dietary supplement. researchers tracked the use of vitamins and supplements by 38-thousand people from 19-99 to 20-12. although supplement use remained stable at about 52- percent, the use of multi- vitamins decreased during this time. the survey also showed greater use of vitamin-d and fish oil supplement

homeopathic tablets and gels haven't been approved by the fda. if you do have these products, them away..and talk to your doctor about safer treatments. this morning yahoo is under fire, after a new report claims the company scanned all incoming emails for the nsa. after a new report claims the company scanned all incoming emails for the nsa. abc's kendis gibson and diane macedo have the details in today's tech bytes. < ((diane oc)) in today's there's word yahoo secretly scanned customers' incoming messages last year. ((kendis vo)) according to reuters, the scans came after a request from either the f-b- i or the national security agency. it's not known what information intelligence officials wanted or what data yahoo may have handed over. ((diane/vo)) google goes hard core into hardware, introducing its pixel and pixel x-l smartphones. the company is selling the first phone with 'google assistant' built in. ((kendis)) the pixels are also compatible with google's new daydream virtual reality headset. both are available for pre- ordering. and ulti

so we petitioned the fda again. and we got the institute of medicine to do a report on what should be done about excess sodium. not whether or not it's harmful. that had been settled, but what should be done. and the institute of medicine basically endorsed that 1978 petition saying the fda should limit sodium levels in cheeses, in breads, and different levels for these different categories of food. the fda immediately said it wouldn't limit the levels, but it might set voluntary targets. so it took another six years, earlier this year, well, for five years the fda didn't do anything. we sued the fda for inaction, public citizen represented us. and that got the fda to get off the dime and propose voluntary targets. so if we're lucky, those voluntary targets will be adopted as final voluntary targets, with two-year and ten-year goals. the ten-year goals would bring sodium down to safe levels. >> mike, i wanted to ask you, you have been pretty critical of the food and drug administration and u.s. department of agricul

there is not an exact link just yet but the fda is investigating. there has not been a recall of some drugstores have pulled them from their shelves. >>> a new wave of zika infections in florida. health officials say mosquitoes are spreading the virus at a new neighborhood in miami. five people are infected in a one square-mile area. that meets the federal criteria for a new transition zone. there have been 155 cases of the zika virus in florida that are not related to travel. >>> we have a recall alert. honda is recalling civic coupe then sedans because the parking brake may not function properly. the electric parking brake may not work if it is applied immediately after turning the ignition off. if that happens in the driver does it put the car in park the car could just roll away. >>> more precautions to avoid major fires sparked by phones are laptops. at least three us airlines are putting fire suppression equipment on their planes in case one of those devices burst into flames. surrounding the samsung galaxy note 7 phones catching fire. just to

the fda is investigating reports of adverse reactions, caused by the products. including seizures, breathing problems, and lethargy. no recall has been ordered. but drug store giant cvs has already pulled all homeopathic teething products from its shelves. a big change to how you and your kids play at chuck e. cheese. the chain is getting rid of its tokens. and switching to cards, loaded it's similar to cards used at dave and buster's. you'll still get the strips of tickets, after you a play a game, to exchange for toys. for those who collect tokens, they could soon become more valuable. if you look on ebay, people have rare tokens. and tokens that changed looks through the years. in sports, a new era of hockey in madison is set to begin this weekend. plus, one aspect of the packer'' defense is the best in the nfl right now. how they can improve on the other areas. and how hosting a pga championship differs from hosting a ryder cup for dan needles returns with sports. before we go to break, here are tonight's winning lottery numbers. workers: he campaigned as a

they're fda approved and activated by the acid in your stomach. >> the bandage is recording your rest, testimony and heart rate and is listening taken. >> now the company that developed the device is conducting a trial on it for pediatric patients at a dallas hospital. it involves young patients recovering from an organ transplant who generally have to be on a very regimented medication schedule. >>> as 9news reporter maya difference in the lives of some coloradans. >> reporter: 87-year-old donna tadlock is on a special journey at st. anthony hospital in lakewood. >> i've never heard anyone come out of it like i did. >> reporter: the fact that she's even walking now is a huge feat considering that earlier this week she had a potentially deadly stroke. >> my hand was very stiff. i couldn't move my right side of my body. i mean i felt like maybe i died >> reporter: strokes are the fifth leading cause of death in america, but donna's daughter recognized something was wrong and brought her to st. anthony, a hospital with something extra. >> did you ever think you'd be ab to e inside of yo

. >> reporter: after calling more than 50 places the manufacturer and fda, melissa got nowhere. >> i don't understand and 2016 when we have great health insurance other could be a shortage of a key component of a leukemia drug. >> reporter: the type of erwinia. >> anytime a drug is on shortage in a has to be omitted from the regimen as a physician you can't counsel families about the curate because the studies incorporate that.>> reporter: a helpless feeling for melissa.>> this hinders her chances for success and that's her chance for survival. >> reporter: and frustration for doctors. >> there's nothing i can do about it. i can't make it or order more. >> reporter: doctors and melissa said the shortage came after a shortage at a warehouse where the drug was made but luckily she got a call this mog treatment but ava needs more than three doses. >> it won't be the last. i talked to the manufacturer and the fda and both said it isn't the first issue. >> reporter: doctors say they have been communicating with the manufacturer about the shortage and in the meantime looking for other ways

after calling more than 50 place -- places, the manufacturer, and the fda, they got nowhere. rate but that is when this drug is used. >> you are not able as a physician to counsel families about what to expect about the cure rate because all of the studies incorporate disparaging ace. >> reporter: luckily she got a call this morning saying there is enough days of treatment but ava needs more than three doses. >> i have talked to the manufacturer and have been in close contact with them and at the fda and they tell me this is not the first issue. >> reporter: doctors have been communicating with the manufacturer about the shortage problem and said in the meantime, they are looking for other ways to treat their patients. reporting in st. petersburg, jana jones, news channel 8. >> we understand the hospital received a shaman of the drug today but it was only half of what was actually ordered. >>> before long, when you crack open a pepsi, what's inside >>> plus , flying home for the holidays? it could be a bit cheaper this year, we have the tips for finding the most affordable fl

i just feel better the fda has on people. it used for wound hearing, it's used for carpal tunnel acute and chronic neck pain. you have to be skeptical for something like this. bertha sandoval had reasons to be acceptable, but i've been in and outs of a hospital because of infections. so she tried something different. i was kind of like oh, now i'm a dog, what are they going to do to me. that feeling was so good that i didn't there's no pain involved at all. reporters. finally closed and now she returned for pain relief. my doctor is kind of in shock he didn't believe it would work either. low-level lasers are gaining more acceptance, but not for most health insurance. the insurance especially new insurance doesn't really cover a lot of what i do because it is classified as preventative. >> but for keeley sept and she says it's money well spent. sit still when i wake up and am so happy he's still here. i couldn't be happier. >> out to you, the price of all this his sessions can cost anywhere from 25-$75. most are sold as part

so we have a whole team that's making research discoveries and giving that back to you. >> and the fda understands the idea that the clients should be empowered and has been helpful in trying to figure out what the priorities are. >> one of the most revolutionary things i think that the fda did is they actually gave us a label that is direct to consumer. so they're saying, you have the like cystic fibrosis results, through 23andme without a genetic counselor and without a physician. to me that was a real sign that the fda is actually embracing this idea that there is a whole world of consumer-driven health, that consumers want this information and they have to provide a safe path for them to get it. >> once they get it, what do you advise them to do? >> frequently it's following up with their physician. if you are a carrier for cystic fibrosis, it doesn't mean you have the disease but you could have a cha we try to make it really clear to people what do you do with this information, and then if there is a medical reason to follow up with your physician, then you should actually follow

to be honest, the issue there is the fda. of course we have to stay in friendship with fda. a lot of these wearable sensors are trying to avoid being diagnostic. as soon as you become diagnostic you have to walk down the 510-k medical device pathway. as long as you're just telling someone about the aspect of their health, you know, here is some information about your sleep. here is some information about heart health. we're just telling you your ekg looks like this. as soon as -- as long as there's no diagnosis, they don't have to walk down fda pathway. the 510-k process takes a little bit of time. as long as the fda keeps progressing on the digital health side of things, which they really are. they are coming out with more and more guidance documents, that will hopefully be reduced. that hurdle will be reduced. for someone to say, okay, you've got the sensor on. can you check your heart health. come out with ecg, but they don't want to say, this is what you need to do next. that becomes diagnostic and goes down fda pathway. the challenge is the balance with fda and whether

it is a type of electric shock this and the fda has tried to ban this their -- therapy. this is the only center that does it. you can see signs that say "stop the toor tour." we -- "stop the torture." no doubt there is a lot of rubbernecking to see what is going on. >> ben: now to commitment 2016. after debate, attack ads, twitter wars and can i say thankfully the 2016 election jc: i don't think anybody will argue with you there. now more on the next commander-in-chief. reporter: donald trump and hillary clinton talk about bringing americans together. >> i will be a president for all of our people. >> if you don't vote for me i will still want to be your president. reporter: how difficult will that be after a bitter presidential campaign? >> donald thengs be -- thinking belittling women makes him bigger. >> she liar. >> this one feels nastier than other races. reporter: analysts say political decisiveness is part of a fabric of a democracy and sometimes compromise does not payoff. jay if you are a politician and you reach out to the other side, guess what can happen. you

and the bill i just mentioned with the fda. the companies developing these new drugs are all private companies. the problems they faced across the country was that they could not raise enter capital anymore in the united states, it was all going to europe and asia because of the regulatory uncertainty caused by the fda. i worked with the republican from north carolina to change the way the approval process works. 1-2 drugs perthat year would be approved, 50 drugs have been approved. i can't remember the number of bioscience companies, that i companies, we0 have thriving bioscience come -- companies here we need to protect. moderator: mr. glenn, to specific bills you advance the private sector to create more jobs. when you're out there talking a small business owners, it is crushing them to have to deal with the affordable care act. we need to repeal the affordable care act and have a replacement in place that is extremely important, the other thing i am hearing when i go and talk to , they need regulatory reform. the war on coa

the fda says there could be as many as 10 deaths, the parents are being advised not to purchase certain tablets and jails -- gels being marketed as homeopathic teething to prevent pain. >>> workers on strike at the jim beam distilleries in kentucky, being forced to work long hours to keep up with the demand, some saying they work up to 80 hours a week, and they have not been able to reach an agreement with the company but negotiations are expected to continue today. jim beam says they have plan in place to prevent the shortage during the talks. >>> and we are watching the roads, along with the maccarthur maze. >> slow along the berkeley curve, and earlier crash at the bay bridge not causing much of a backup because he was already backed up at the toll plaza. here it is coming around the corner to the bay bridge, and when you look at the bay bridge, backed up this morning. a lot of slow traffic in the area, and we go to 880 into east bay, southbound slow from hayward down to milpitas with earlier issues being blamed. 680 slow out of pleasanton, and looking at the silicon valley commute,

is an fda-approved non-surgical treatment for adults with a moderate amount of fullness... or a bit more. don't receive kybella? if you have an infection in the treatment area. kybella? can cause nerve injury in the jaw resulting in an uneven smile or facial muscle weakness, and trouble swallowing. tell your doctor about all medical conditions, including if you: have had or plan to have or have bleeding problems. tell your doctor about all medicines you take. the most common side effects are swelling, bruising, pain, numbness, redness, and areas of hardness in the treatment area. find a doctor at mykybella.com attention! did you or anyone in your household work around asbestos-containing gaskets, packing, or equipment? if you or a loved one have an asbestos-related disease, you may have a right to vote on a plan to reorganize and pay claims in y. garlock's and coltec's products were used in industrial and maritime settings, including where steam, hot liquid or acid moved in pipes. votes must be filed by december 9, 2016 call 844-garlock or go to garlocknotice.com it's the little things i

i think the important thing, as you point out, is that fda is rolling out expectations for cyber securit being built into medical devices as well as prepar when. unanticid fashion so i think manufacts w improving, t it's not going to be an overnigh wt other types of medi devices are vulnerable to these attacks? >> well, pretty much every device that has had a computer in it is breakable. there is unhackable device, so i think the more interesting questi is not whether you can hack into a device but how well do the devices tolerate the kind of threats that are endemic to computg today and endemic t devices ranging from the insulin pumps to infusion pumps that are bedside devices and hospitals and then you also have on the extreme things like pase-makers and defibrillators and in between all sorts of other things, patient monitors, radiatn therapy and all sorts of devices are in the hospital. and in meg's report she discusd how one researcher thit of curiosity and concern out of his own safety. what do you think the motive hospits or individuals? >> well, to be honest i'm less concerd a ta

as long as there's no diagnosis they don't have to walk down the fda path way.a little bit of time but as long as the fda keeps progressing on the digital health side of things which they are. and you can can can check your heart health and come out with an ecg but they don't want to say this is what you need to do next because that becomes diagnostic and then goes down the fta pathway so the challenge is the balance with fda and whether these products want to stay as a consumer product. >> from all of your research and looking at this where non-obvious things have become so an example is i was talking to a company a couple of years ago and people that filled out forms in pencils were higher credit risk. it was not something that was obvious or intuitive so are you seeing anything like that coming out of all of this aggregation. >> interesting weight loss a couple of research studies out now showing that weight loss when people are wearing multiple different trackers, weight loss have more to do with the people you spend time with versus your own food intact. wh

lyrica is fda approved to treat this pain, from moderate to even severe diabetic nerve pain. tell your doctor right away if you have these, new or worsening depression, or unusual changes in mood or behavior. or swelling, trouble breathing, rash, hives, blisters, muscle pain with fever, tired feeling or blurry vision. common side effects are dizziness, sleepiness, weight gain and swelling of hands, legs, and feet. don't drink alcohol while taking lyrica. don't drive or use machinery until you know how lyrica affects you. those who have had a drug or alcohol problem may be more likely to misuse lyrica. now i have less diabetic nerve pain. and these feet o keep the beat going. i'm terrible at golf. he is. but i'd like to keep being terrible at golf for as long as i can. new patented ensure enlive has hmb plus 20 grams of protein to help rebuild muscle. for the strength and energy to do what you love. new ensure enlive. always be you. feel secure in your dentures... feel free to be yourself all day. just switch from denture paste to sea-bond denture adhesive seals. holds stronge

. >>> the fda warn this is morning that at least ten deaths are associated with teething products, the fda says they also is more than 400 bad reactions on file, in connection with these products including seizures. earlier this month the fda warned two also stop using homeopathic teething tablets and jells, they can pose a risk to children as well. they may not be closely regulated making it easy for doses to be toxic. for former pharmaceutical ceo, martin, that top it is stories that we're following right now. >> he was arrested in december of 2015 on allegations of securities fraud. retro pen that he was then heading you have 11 million has to pay off investigators. he was suspect of previously ran. he will ask first degree separate trials. the trial debt is set for june of 2017. >>> say six week old baby girl was killed when she and her mother plunged down an elevator shaft the 21-year-old mother was pushing her baby in her stroll never apartment building the elevator doorings opened and the mother pushed it stroller in side but the elevator wasn't there the mother and baby both fe

this drug was approved a couple of weeks ago by the fda and that was a controversial decision peopleeing saying there wasn't enough efficacy data saying this worked. it is a very small population. anthem coming out, second largest insurer saying its investigational and not medically necessary saying in the statement in reviewing medical literature determined that this drug failed to show it improves health outcomes and therefore is not a covered benefit for the members. a lot of people are reacting and you can see the stock is down because the fda has approved this drug and taking this to mean that this insurer is going back to the fda and saying you may have approved it and we don't see a benefit here. people are saying this isn't going to be a huge financial thing for anthem because there are so few patients so it does seem like take ag stand on the issue. >> this is the whole puzzling part. the point of an insurance company is to ensure because it is going to be so expensive to help somebody afford this drug. so where do they come off trying to make a comment about the efficacy of