Sentences with phrase «after food and drug»

Reuters reports that Cetero's Chapter 11 filing comes only months after the Food and Drug Administration put the company on notice for «instances of misconduct and violations» involving fake documents and manipulated drug samples.

Problems with food from Diamond Pet Foods may be more widespread than originally thought after the Food and Drug Administration (FDA) announced contaminated dog food had been found at a second Diamond manufacturing facility.

A new population - based study has found that patients with glioblastoma who died in 2010, after the Food and Drug Administration (FDA) approval of bevacizumab, had lived significantly longer than patients who died of the disease in 2008, prior to the conditional approval of the drug for the treatment of the deadly brain cancer.

New York doctors are in desperate need of high - speed flu tests after the Food and Drug Administration banned two top brands at the height of a deadly flu season.

Last year, after the Food and Drug Administration and Federal Trade Commission told the four biggest manufacturers of alcoholic energy drinks the caffeine in their beverages was... Continue Reading

The announcement from Juul (JOO - «uhl) Labs comes one day after the Food and Drug Administration questioned the design and marketing of the company's small, sleek vaping devices.

Cholesterol busters Demos didn't originally see this group as a big target market but changed his mind after the Food and Drug Administration certified in 1999 that soy protein can help fight coronary heart disease.

Shares of biotech Spark Therapeutics rose 4.5 % in early Monday trading after the Food and Drug Administration (FDA) agreed to review its gene therapy for vision loss patients who have vision loss due to a rare genetic condition called biallelic RPE65 - mediated inherited retinal disease (IRD).

Not exact matches

And the Food and Drug Administration has ordered the makers of several supplements to recall their products after scientists found traces of illegal and potentially dangerous molecules in their formulAnd the Food and Drug Administration has ordered the makers of several supplements to recall their products after scientists found traces of illegal and potentially dangerous molecules in their formuland Drug Administration has ordered the makers of several supplements to recall their products after scientists found traces of illegal and potentially dangerous molecules in their formuland potentially dangerous molecules in their formulas.

Several major biotech stocks fell after the U.S. Food and Drug Administration made it easier for the public to search for drug side effects through a databDrug Administration made it easier for the public to search for drug side effects through a databdrug side effects through a database.

Fremanezumab had been expected to receive the nod from the U.S. Food and Drug Administration in June, which would have likely made it the second to the crucial American market after Aimovig, which is expected to be approved next month.

After Health Canada demanded a recall of Apotex's mispackaged birth control pills (they contained too many placebos and not enough medication), the U.S. Food and Drug Administration threatened to block Apotex products for «repeated deficiencies,» including bacterial contamination.

Speaking of checkpoint inhibitor drugs... Merck's star cancer immunotherapy treatment Keytruda is facing some troubling clinical trial incidents which have now compelled the Food and Drug Administration (FDA) to halt three studies of the drug in multiple myeloma, a rare blood cancer, after a number of patient deaDrug Administration (FDA) to halt three studies of the drug in multiple myeloma, a rare blood cancer, after a number of patient deadrug in multiple myeloma, a rare blood cancer, after a number of patient deaths.

The Food and Drug Administration is alerting people to a voluntary recall of 465,000 pacemakers after security vulnerabilities were discovered that could let hackers reprogram the devices, potentially putting patient lives at risk.

After a preliminary review, the U.S. Food and Drug Administration determined it had insufficient evidence for the drug's effectiveness and is «unable to complete a substantive review,» according to a release from AlkerDrug Administration determined it had insufficient evidence for the drug's effectiveness and is «unable to complete a substantive review,» according to a release from Alkerdrug's effectiveness and is «unable to complete a substantive review,» according to a release from Alkermes.

April 15 - Nearly 207 million eggs from a farm in North Carolina are being recalled from nine U.S. states after 22 people fell ill, the federal Food and Drug Administration has said.

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).

The Food and Drug Administration (FDA) has given Alnylam Pharmaceuticals the green light to relaunch clinical trials of its treatment for the bleeding disorder hemophilia after pausing the studies after a patient death.

Nearly 207 million eggs from a farm in North Carolina are being recalled from nine U.S. states after 22 people fell ill, the federal Food and Drug Administration has said.

The Food and Drug Administration has given Bayer's experimental blood cancer treatment copanlisib a priority review designation after the drug showed promise in fighting back follicular lymphoma in 60 % of participants in a mid-stage clinical trDrug Administration has given Bayer's experimental blood cancer treatment copanlisib a priority review designation after the drug showed promise in fighting back follicular lymphoma in 60 % of participants in a mid-stage clinical trdrug showed promise in fighting back follicular lymphoma in 60 % of participants in a mid-stage clinical trial.

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.

Nearly a year after it clashed with the Food and Drug Administration over labeling on its dried fruit and nut bars, KIND has received approval to use the word «healthy» as part of its marketing.

In early March, the J.M. Smucker Co. recalled more than 107 million cans of dog food — sold under popular brands like Gravy Train and Kibbles»n' Bits — after determining it had used ingredients containing toxic euthanasia drugs.

An expert panel for the U.S. Food and Drug Administration voted today to approve a drug that has been dubbed the «female Viagra» after two previous attempts failed to gain approDrug Administration voted today to approve a drug that has been dubbed the «female Viagra» after two previous attempts failed to gain approdrug that has been dubbed the «female Viagra» after two previous attempts failed to gain approval.

After concerns are raised by the Food and Drug Administration, Theranos temporarily halts its trademark practice of collecting tiny blood samples from finger pricks.

Fresenius had warned in February that it could terminate the deal after starting an investigating into alleged breaches of U.S. Food and Drug Administration (FDA) data integrity requirements.

A federal appeals court ruled in 2015 that the notice can't take place until after biosimilar makers gain approval from the Food and Drug Administration.

Lilly outlined in July a likely multi-year delay for its experimental rheumatoid arthritis drug baricitinib, after the U.S. Food and Drug Administration declined to approve the drug, calling for an additional clinical stdrug baricitinib, after the U.S. Food and Drug Administration declined to approve the drug, calling for an additional clinical stDrug Administration declined to approve the drug, calling for an additional clinical stdrug, calling for an additional clinical study.

Court documents made public late on Tuesday show that Fresenius (NYSE: FMS) dropped its acquisition of Akorn after uncovering evidence that the generic drug developer submitted fraudulent data to the U.S. Food and Drug Administration for at least six different drugs dating back to 2drug developer submitted fraudulent data to the U.S. Food and Drug Administration for at least six different drugs dating back to 2Drug Administration for at least six different drugs dating back to 2012.

Bulls have emerged in defense of Celgene Corporation (NASDAQ: CELG) as the sell - off continues after unfavorable news from the U.S. Food and Drug Administration.

Celgene Corporation (NASDAQ: CELG) shares plummeted 10 percent Tuesday evening after the U.S. Food and Drug Administration rejected its New Drug Application for ozanimod in the treatment of relapsing multiple sclerosis.

Celgene Corporation (NASDAQ: CELG) is under continued stock pressure Wednesday after the U.S. Food and Drug Administration rejected its New Drug Application for ozanimod in the treatment of relapsing multiple sclerosis.

Analysts at Cantor Fitzgerald continue to hold a bullish stance on Spark Therapeutics Inc (NASDAQ: ONCE) after the U.S. Food and Drug Administration gave the company a critical recommendation for its therapy called Luxturna.

AstraZeneca PLC (LON: AZN) ticked higher even as it went ex-dividend after the US Food and Drug Administration granted orphan drug designation for Selumetinib, a drug used to treat incurable genetic condition Neurofibromatosis TypDrug Administration granted orphan drug designation for Selumetinib, a drug used to treat incurable genetic condition Neurofibromatosis Typdrug designation for Selumetinib, a drug used to treat incurable genetic condition Neurofibromatosis Typdrug used to treat incurable genetic condition Neurofibromatosis Type 1.

After one particularly offensive show on Aug 19, 2010 where he and his cohost, Crank, spent the morning railing against the «mentally diseased perverts» everyone else calls gay, preaching that women aren't equal to men and should be home raising the kids and making dinner, and Blacks need to kick their drug habits and get a job instead of freeloading off his hard earned tax dollars by trading in their food stamps for drug money, we started a blog documenting his abuses on the air waves.

That case began after Washington State adopted regulations in 2007, requiring pharmacies to make available «in a timely manner» to consumers drugs that the Food and Drug Administration has approved.

The presentation also didn't mention that the U.S. Food and Drug Administration told Impossible Foods that the company hadn't demonstrated the safety of heme after it applied to the FDA seeking GRAS (generally recognized as safe) status.

The U.S. Food and Drug Administration (FDA), the nation's chief food safety regulator, plans to start testing certain foods for residues of the world's most widely used weed killer after the World Health Organization's cancer experts last year declared the chemical a probable human carcinoFood and Drug Administration (FDA), the nation's chief food safety regulator, plans to start testing certain foods for residues of the world's most widely used weed killer after the World Health Organization's cancer experts last year declared the chemical a probable human carcinofood safety regulator, plans to start testing certain foods for residues of the world's most widely used weed killer after the World Health Organization's cancer experts last year declared the chemical a probable human carcinogen.

Last week, the parents of two young men who died earlier this year after ingesting caffeine powder met with Food and Drug Administration officials to deliver a citizen petition urging the agency to ban the sale of powdered caffeine.

After suffering from the terrible side effects of steroids, antibiotics, and immunosuppressant drug therapy, I decided to do some research of my own and I soon discovered that my symptoms could be controlled simply by the food I put in my body.

She would feel tired and drugged after she ate food with gluten in it.

Philips AVENT recommends that moms boil or sanitize (that is, use a Philips AVENT sanitization product after each use), but the U.S. Food and Drug Administration (FDA) states that sterilization is not necessary.

After much petitioning by the Center for Science in the Public Interest (CSPI), The Food and Drug Administration (FDA) has announced plans to form an advisory committee meeting which will review clinical studies conducted on common food dyes including Yellow 5 and Red 40 and the link connecting them to adverse behavior issues in childFood and Drug Administration (FDA) has announced plans to form an advisory committee meeting which will review clinical studies conducted on common food dyes including Yellow 5 and Red 40 and the link connecting them to adverse behavior issues in childfood dyes including Yellow 5 and Red 40 and the link connecting them to adverse behavior issues in children.

Since then an advisory committee to the US Food and Drug Administration has been studying whether the process is safe, after a Portland researcher said he had conducted the technique successfully on monkeys - and now wanted to begin trying it on humans.

The Brong Ahafo Regional Director of the Food and Drugs Authority (FDA), Mr. Matthew Gyang Nkum, in an interview with journalists after the exercise, said the exercise which took place at the Sunyani East and West Municipalities is in line with a market surveillance mounted in the region.

But a Cuomo official said allowing people to smoke the drug while there are other options like vaporization, pills and food form would send the wrong message after the state has spent big money on anti-smoking measures over the years.

And just this month, the federal Food and Drug Administration requested Endo Pharmaceuticals, an international pharmaceutical manufacturer, remove Opana ER — a semi-synthetic opioid painkiller — from the market after concluding the drug's potential for abuse outweighed its therapeutic valAnd just this month, the federal Food and Drug Administration requested Endo Pharmaceuticals, an international pharmaceutical manufacturer, remove Opana ER — a semi-synthetic opioid painkiller — from the market after concluding the drug's potential for abuse outweighed its therapeutic valand Drug Administration requested Endo Pharmaceuticals, an international pharmaceutical manufacturer, remove Opana ER — a semi-synthetic opioid painkiller — from the market after concluding the drug's potential for abuse outweighed its therapeutic vaDrug Administration requested Endo Pharmaceuticals, an international pharmaceutical manufacturer, remove Opana ER — a semi-synthetic opioid painkiller — from the market after concluding the drug's potential for abuse outweighed its therapeutic vadrug's potential for abuse outweighed its therapeutic value.

The Food and Drugs Authority (FDA) has explained what might have killed three siblings from Abavana Down in Accra, after...

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.

The decision was made after a scientific review by the Food and Drug Administration (FDA) concluded that the evidence for the medical benefits of marijuana did not meet their standards for new drug approDrug Administration (FDA) concluded that the evidence for the medical benefits of marijuana did not meet their standards for new drug approdrug approval.