Sentences with phrase «drug administration about»

Huang says the team has also been in discussions with the US Food and Drug Administration about allowing the procedure to be done there, but progress has been «very minimal» so far.

Adding to the hit on sales, Whole Foods has been contending with some negative bad publicity, including a warning in June from the U.S. Food and Drug Administration about food safety at a Massachusetts plant that makes prepared foods and other products.

Not exact matches

The endorsement came despite lingering questions about safety and effectiveness, but also followed a high - stakes pressure campaign in which the manufacturer accused the Food and Drug Administration of gender bias, since several pills were already approved for men with sexual problems.

The Food and Drug Administration (FDA) is investigating patient deaths following an obesity - fighting procedure which involves the use of balloons that fill up inside the stomach and remain for about six months.

Meanwhile, despite much talk about change, Congress and the Trump administration have done little to control drug prices or threaten drug - company profits.

Cannabis sales are still illegal on the federal level, and the Trump administration has played coy about its plans for the burgeoning marijuana industry, even as the man the president hand - picked to be the country's law enforcement officer has made it no secret that he despises the drug.

«Our policies from the last Administration — and quite frankly the Democrat policies of today — of an open border and sanctuary cities allow and enables these drug smugglers who don't care about human life to put people in this horrific situation,» Patrick said.

Meanwhile, the U.S. Food and Drug Administration says it is looking into the vulnerability claims (Muddy Waters told the agency about the claims before going public with them).

That's because consumers have becoming increasingly skeptical of artificial sweeteners, most recently fretting about the health implications of consuming aspartame, which is still deemed safe by the Food and Drug Administration.

Food and Drug Administration (FDA) Commissioner Dr. Scott Gottlieb isn't mincing words about kratom, the increasingly popular herbal substance that's been hawked as an alternative to painkillers and anti-depressants by companies promoting its ostensible curative properties (and supposedly innate safety as a «natural,» plant - based product).

In 2013, after 23andMe had acquired about half a million customers, the U.S. Food and Drug Administration shut down the genetic - testing part of 23andMe (customers could still get information about their ancestry).

Spicer's comments during a press briefing predictably put a damper on biotech stocks — but it wasn't nearly the plunge the Trump administration's other statements about drug price regulations have wrought.

Sprout's controversial pink libido pill was approved on Tuesday by the U.S. Food and Drug Administration for pre-menopausal women, after being rejected twice over concerns about its effectiveness and side - effects.

She said Janssen has acted responsibly regarding its opioid pain medications, which are approved by the U.S. Food and Drug Administration and carry FDA - mandated warnings on their labels about the drugs» known risks.

Its claims about some of its products, the company says on its website, have not been evaluated by the Food and Drug Administration.

We do this by conducting clinical trials in which we collect safety and efficacy data about our experimental drugs with the goal of submitting those data to regulatory authorities, like the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA), so that these experimental drugs can be approved for use by patients.

SRSE accounts for about 25,000 to 41,000 cases each year in the United States and there are currently no treatments approved by the U.S. Food and Drug Administration for the disorder, Sage said.

This summer, the Drug Enforcement Administration will consider a move that may turn the tide of how people think about marijuana.

You can read about the U.S. Food and Drug Administration's proposed gluten - free labeling rule.

Rogers serves as a subject matter expert to various regulatory and industry organizations such as the Food and Drug Administration, Grocery Manufacturers Association and the Packaging Machinery Manufacturers Institute, and writes articles and blogs about this critical industry issue.

First approved by the Food and Drug Administration in 1988, Acesulfame K is a calorie - free sweetener that is about 200 times sweeter than regular old table sugar.

Ocean's Flavor Natural Sea Salts has urged the Food and Drug Administration to be clear about the distinction between salt and sodium, as it considers how to react to a recent report from the Institute of Medicine.

Alarmed by DMSO's sudden popularity and worried about misuse of it, the U.S. Food and Drug Administration banned the substance for medical use in 1965, citing a study that suggested it caused eye damage in laboratory rats.

You know I let the FDA, Food and Drug Administration, worry about whether something is really dangerous in my food and I pay attention to this a lot.

Earlier this year, the Food and Drug Administration released a report raising concerns about the possible adverse effects of BPA (Bisphenol - A).

While the US Food and Drug Administration (FDA) had earlier stated that BPA — the chemical that hardens plastics in products like bottles and cups, and is used in linings of metal cans — is safe; the agency announced last month that a few new studies have underlined «some concerns» about BPA's possibility of potentially damaging the brain of fetuses, infants and children.

I spoke with Dr. Danielle Aparecida da Silva of Brazil's Oswaldo Cruz Foundation (equivalent to the Food and Drug Administration in the USA) to learn more about the upcoming «World Day of Human Milk Donation» which will be celebrated on May 19, 2013.

State Rep. Elaine Nekritz kept waiting for the Food and Drug Administration to do something about bisphenol A, a plastic chemical additive used in many products, from baby bottles to metal canned food linings.

Although the American Academy of Pediatrics, the Food and Drug Administration, and the drug manufacturer have raised concern about the use of fluoxetine by women while breastfeeding and the drug manufacturer recommends against its use, these guidelines are based on little information.Drug Administration, and the drug manufacturer have raised concern about the use of fluoxetine by women while breastfeeding and the drug manufacturer recommends against its use, these guidelines are based on little information.drug manufacturer have raised concern about the use of fluoxetine by women while breastfeeding and the drug manufacturer recommends against its use, these guidelines are based on little information.drug manufacturer recommends against its use, these guidelines are based on little information.1, 2

Information about my products or recipes haven't been evaluated by the Food and Drug Administration.

The Food and Drug Administration has long permitted its use, but in recent years concerns about the chemical have grown as studies have indicated low doses of the substance can disrupt hormone systems in laboratory animals and possibly increase the risk of cancer or other serious illness.

The U.S. Food and Drug Administration, based in Silver Spring, Md., places few restrictions on the claims that food manufacturers can make about how ingredients affect the body's function (e.g. «this product contains ARA for visual acuity»).

Citing concerns about the possibility of a link between this toxin and impaired language, memory, cognitive thinking and fine - motor and visual - spatial skills among children who were exposed to it in utero, the U.S. Food and Drug Administration (FDA) and the Environmental Protection Agency (EPA) have established fish - intake guidelines for women who are pregnant or might become pregnant (and, later, when nursing).

Consumer - grade pumps have the potential for cross contamination which is why everyone from La Leche League to the Food and Drug Administration cautions women about sharing.

To assist consumers in making informed choices about what is sweetening the products they purchase, the Sugar Association petitioned the Food and Drug Administration (FDA) requesting changes to labeling regulations on sugar and alternative sweeteners.

Erie County leaders expressed alarm and outrage over a report by National Public Radio on Friday that the Trump administration is thinking about gutting several federal programs aimed at fighting the opioid drug crisis.

Plateau State NDLEA commander, Ibrahim Braji, who paraded them, also handed over counterfeit and expired drugs of about 5, 580 kg seized from a suspect named Jude Okoye Okeke, aka Zuma to National Agency for Food and Drug Administration and Control (NAFDAC).

A number of new, highly effective therapies to treat both Hepatitis C and HIV / AIDS have been approved by the Food and Drug Administration in recent years, but their extraordinary costs have raised questions about states» ability to pay the sticker price.

He also expressed reservations about the 18 - month timeline for the program's implementation, saying he hopes the administration finds a way to deliver the drug to patients who need it during the interim.

ESD chief operating officer Kevin Younis said the decision about Athenex was made because of its experience dealing with the federal Food and Drug Administration, and was not a sign of a blanket policy shift.

Some lawmakers were concerned about a potential tax reduction for «reduced harm tobacco products» that have not been approved by the federal Food and Drug Administration and are not yet on the market.

Erie County leaders expressed alarm and outrage Saturday over a report by National Public Radio on Friday that the Trump administration is thinking about gutting several federal programs aimed at fighting the opioid drug crisis.

The U.S. Food and Drug Administration originally approved the drug in 1999, but subsequent case reports of abnormal behavior in adolescents who used the medication led the agency in 2006 to require that all packaging of the drug include a warning label about potential neuropsychiatric side effects, such as hallucinations, delirium, self - harm and even suicDrug Administration originally approved the drug in 1999, but subsequent case reports of abnormal behavior in adolescents who used the medication led the agency in 2006 to require that all packaging of the drug include a warning label about potential neuropsychiatric side effects, such as hallucinations, delirium, self - harm and even suicdrug in 1999, but subsequent case reports of abnormal behavior in adolescents who used the medication led the agency in 2006 to require that all packaging of the drug include a warning label about potential neuropsychiatric side effects, such as hallucinations, delirium, self - harm and even suicdrug include a warning label about potential neuropsychiatric side effects, such as hallucinations, delirium, self - harm and even suicide.

The U.S. Food and Drug Administration recently banned TCC from soaps because of questions about its safety and efficacy.

Recalls of Cox - 2 inhibitor drugs during the past year have raised questions about the credibility of the U.S. Food and Drug Administration's (FDA's) regulation of new drugs and suspicions that pharmaceutical companies have been overly eager to put fresh remedies on the market.

The Food and Drug Administration recommends that Americans eat about 25 grams of dietary fiber per day.

True, the CDC, the Food and Drug Administration, and other governmental organizations feature accurate and up - to - date information about vaccine risks on their Web sites.

In science news around the world, NASA's Cassini mission is about to take its final plunge into the atmosphere of Saturn after 13 years providing an unprecedented view of the planet and its moons, a fight over whether to preserve or develop of one Europe's oldest gold mining sites heats up again, the U.S. Food and Drug Administration approves the first cancer gene therapy for people, a U.S. court gives a green light to a $ 1 billion lawsuit brought by the Guatemalan victims and survivors of mid — 20th century syphilis experiments by research institutions including Johns Hopkins University, and more.

That question is about to test the jurisdiction of the US Food and Drug Administration (FDA) in a landmark legal battle — and is fuelling a war of words between doctors marketing such therapies and academics who urge caution.

A study of Food and Drug Administration data for several million pacemakers and defibrillators implanted in 1990 - 2002 found that about one in 150 failed, about one quarter of these failures were battery / capacitor abnormalities, and 61 people died due to device malfunctions.