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How To Use Food and drug administration In A Sentence

  • No drug is approved by the U.S. Food and Drug Administration for use in mesotherapy.
  • The vaccine has been licensed by the US Food and Drug Administration.
  • Last week, the US Food and Drug Administration said it will re-evaluate the safety of triclosan, which is added to plastics, soaps and toothpastes to kill bacteria and fungi. New Scientist - Online News
  • But before you stock up, consider this: The Food and Drug Administration in 2009 warned consumers not to use any intranasal zinc products because of concerns that it can make people lose their sense of smell. No cure in sight for fighting the common cold
  • The Food and Drug Administration said all lots of the supplement had been recalled because it contained the weight loss drug, sibutramine (Meridia), and phenolphthalein, a chemical that may cause cancer. FDA recalls Pai You Guo weight loss supplement
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  • The National Childhood Vaccine Injury Act of 1986 "reflects a sensible choice to leave complex epidemiological judgments about vaccine design to the FDA and the National Vaccine Program rather than juries," Justice Antonin Scalia wrote, referring to the Food and Drug Administration. Supreme Court rules vaccine makers protected from lawsuits
  • Traders had thought the Food and Drug Administration, which is testing imports for a fungicide not approved for use on oranges domestically, might prohibit shipments. FDA Says No Ban on Orange-Juice Imports
  • On Sept. 5, the State Food and Drug Administration banned the use of Hualian's injectable methotrexate, in addition to another drug made by Hualian called cytarabine hydrochloride, across the country. China Drugs: A Cautionary Tale
  • The Food and Drug Administration on Tuesday approved the first drug test available without a prescription.
  • WASHINGTON -- The Food and Drug Administration said it is reviewing additional information submitted by Amgen Inc. and Johnson & Johnson involving risks associated with the antianemia drugs Aranesp, Epogen and Procrit and "may take" additional regulatory action. FDA Reviews New Amgen, J&J Data
  • Like brand-name drugs, generics must be approved by the U.S. Food and Drug Administration and have an excellent safety record.
  • The Food and Drug Administration will meet this week to discuss the public health impact of tobacco products known as dissolvable tobacco, which some say resemble candy, including their use by children. Yahoo! News: Business - Opinion
  • The company just received U.S. approval in late May for a new drug for Pompe disease, and its experimental biologic drug for multiple sclerosis is getting expedited review by the Food and Drug Administration. Sanofi Launches Genzyme Takeover Battle
  • VATICAN CITY (RNS) A top Vatican official has criticized a decision by the Food and Drug Administration to allow the world's first clinical trials using stem cells derived from human embryos. Vatican Blasts FDA Over Stem Cell Ruling
  • Generics can produce blood levels as much as 20% below or 25% above that of the original drug and still be considered "bioequivalent," according to Food and Drug Administration guidelines. Inexact Copies: How Generics
  • The system used in the trial -- the Gateway-Wingspan intracranial angioplasty and stenting system, made by Stryker Corp. -- is the only system approved by the U.S. Food and Drug Administration FDA for certain high-risk stroke patients. Study: 'Brain stents' for stroke patients do more harm than good
  • The company has completed trials on a lymphoma drug and is awaiting approval from the Food and Drug Administration.
  • In the 1970s the Food and Drug Administration responded to public concerns by dramatically cutting back on the quantity of nitrates and nitrites that could be added to foods.
  • And the Food and Drug Administration has asserted that it has the right to limiting tobacco advertising.
  • The Food and Drug Administration has approved deep-brain stimulation to treat Parkinson's and a movement disorder known as dystonia, and it is used to treat chronic pain and severe depression. Memory Gets Jolt in Brain Research
  • The hawk-eyed Food and Drug Administration deems lung - a common ingredient in haggis - to be unfit for human consumption.
  • Some manufacturers use toxic chemicals like hexane or acetone and are not required by the Food and Drug Administration to list them on the label if they account for less than 2 percent of ingredients.
  • But the Consumer Product Safety Commission and the Food and Drug Administration said they've received 12 reports of deaths over the past 13 years involving babies who have suffocated in a sleep positioner or became trapped and suffocated between a sleep positioner and the side of a crib or bassinet. FDA Issues Warning on Infant Sleep Aids
  • The Food and Drug Administration said all lots of the supplement had been recalled because it contained the weight loss drug, sibutramine Meridia, and phenolphthalein, a chemical that may cause cancer. FDA recalls Pai You Guo weight loss supplement
  • (In an unrelated development, Baxter is recalling heparin vials amid a Food and Drug Administration investigation of reports of allergic reactions and deaths that appear to be linked to manufacturing problems.) Hospitals Tackle
  • Hamming It Up A press release from the Food and Drug Administration reports that Vita Food Products is recalling lox possibly contaminated with Listeria monocytogenes bacteria: Potemkin Prayer
  • Called Stratis ACL , the system has been cleared by the U.S. Food and Drug Administration ( FDA ).
  • The drug, once prescribed for losing weight and known as fen-phen when used with phentermine, was withdrawn by the Food and Drug Administration after reports of cardiac complications.
  • The U.S. Food and Drug Administration said it granted Ranbaxy Laboratories Ltd. approval to sell a generic verson of Pfizer Inc.'s Lipitor, called atorvastatin calcium. The Seattle Times
  • In a letter to the Food and Drug Administration, Consumers Union wrote that Bechler's death "should remind all consumers about the dangers" of ephedra and "should serve as a clarion call to the [FDA] to immediately ban dietary supplements containing ephedra from the marketplace. USATODAY.com - Consumers Union calls for baseball to ban ephedra
  • The flavorist asked whether the Food and Drug Administration would even allow nanoingredients. Signs of the Times
  • And the Food and Drug Administration has asserted that it has the right to limiting tobacco advertising.
  • A year ago, the Corn Refiners Association asked the Food and Drug Administration if it could start using the term "corn sugar" as an alternative to high fructose corn syrup. Bitter battle over high fructose corn syrup claims
  • The Food and Drug Administration will ban some uses of antibiotics in cattle, pigs, chickens and turkeys out of concern that food-borne bacteria that can sicken humans are becoming resistant to the drugs. FDA Moves to Restrict Use of Antibiotics in Livestock
  • The Food and Drug Administration has a name review process that's supposed to prevent pharmaceutical companies from using a name that's too close to another one already on the market. NPR Topics: News
  • In fact, the Food and Drug Administration recently made it easier for companies to make health and nutrition claims on food.
  • The Food and Drug Administration Tuesday announced a program aimed at providing consumers with better information about prescription drugs.
  • One drug that is effective for eliminating gapeworms is fenbendazole, however, its use is not presently approved for use in birds by the Food and Drug Administration.
  • WASHINGTON—Food and Drug Administration staff recommended against an immediate approval for Johnson & Johnson and Bayer AG's anticlotting drug Xarelto as a treatment to prevent strokes in patients with atrial fibrillation. Bayer, J&J Suffer FDA Setback
  • Until recently, one form of this substance, alpha-interferon (also called interferon A) was the only treatment for HCV infection approved by the U.S. Food and Drug Administration (FDA). DR. SANJIV CHOPRA’S LIVER BOOK
  • The drug industry has very substantially captured the Food and Drug Administration, which is far too quick to approve new "me-too" drugs of dubious clinical value and far too slow to remove dangerous or ineffective drugs from the market -- or at least condition them with clear limitations and warnings. Robert Kuttner: A Depressing Story You Need to Read
  • Almost unbelievably, the federal government may block one of the disease's more promising therapies for no other reason than the Food and Drug Administration's obsolete, even antimodern, regulations and approval models. A Moral Test for the FDA
  • The popular outrage generated by Upton Sinclair's devastating, fact-based novel about the meatpacking industry in Chicago, The Jungle, had helped to create the Food and Drug Administration in 1906.
  • The doctor managed to stop the bleeding by using a coagulant, still unapproved by the American Food and Drug Administration, which he has since used to treat several other bomb-blast victims.
  • The popular outrage generated by Upton Sinclair's devastating, fact-based novel about the meatpacking industry in Chicago, The Jungle, had helped to create the Food and Drug Administration in 1906.
  • Now the Food and Drug Administration has ordered makers of fluoroquinolone drugs — like Cipro, Levaquin, and Floxin — to add a “black box” warning that they can cause tendon ruptures. FDA issues warning on Cipro, similar antibiotics « Isegoria
  • Recently, the US Food and Drug Administration approved the use of liposomal daunorubicin and liposomal doxorubicin for treatment of AIDS-related KS.
  • Cinryze was approved by the Food and Drug Administration in 2008 to treat hereditary angioedema, or HAE, a rare genetic disease involving potentially deadly swelling of various parts of the body. FDA Rejects Expansion Of ViroPharma Drug
  • In particular, early in her term Hagan fought efforts to raise the federal excise tax on tobacco and voted against a bill to allow the Food and Drug Administration to regulate tobacco products. News & Record Article Feed
  • Further, the US Food and Drug Administration has called for a ban on the use of the fluoroquinolone class of antibiotics in poultry. Sunil Chacko: Time for Antibiotics-Free Animal Industry Practices
  • Laurens Dorsey, of Syracuse, N.Y., sentenced in 1998 to five years of probation and $71, 000 in restitution for conspiracy to defraud by making false statements to the Food and Drug Administration.
  • In fact, only a small fraction of such treatments have been approved by the Food and Drug Administration, and virtually all the diseases that can be treated with such cells are blood diseases, while diseases of virtually every other organ remain unresponsive to adult stem cells. Stem-Cell Bill Passes...Again
  • The U.S. Food and Drug Administration says that women should be discouraged from having so many so-called keepsake ultrasounds. CNN Transcript Oct 21, 2002
  • Mannkind on Friday affirmed its commitment to its inhaler, which is in Phase III studies and which the company expects to submit for Food and Drug Administration approval by the end of the year. Eli Lilly Drops Inhalable-Insulin Product
  • With biopharmaceutical company MannKind awaiting word from the Food and Drug Administration on its key product candidate, an inhalable form of insulin, Chairman and Chief Executive Alfred Mann has spent more than $22 million in recent months to add to his already considerable holdings of company shares. Mann With Plan: MannKind Chairman Bets on Success
  • Food and Drug Administration said antianemia drugs from Johnson & Johnson and Amgen should continue to be marketed for cancer patients, but recommended current use be restricted amid concerns the drugs could increase the risk of tumor growth and death. It's Here
  • The U.S. Food and Drug Administration considers genetically modified foods equivalent to unmodified foods.
  • Makers of branded drugs must prove to the Food and Drug Administration that their product is "safe and effective," and its label "accurate and adequate," Justice Thomas wrote. Drug Firms Score High Court Victories
  • We recently heard that absorbable hemostatic agents intended to be left in patients have been recalled by the US Food and Drug Administration.
  • The studies aren't anywhere near conclusive - they describe only 24 long-term fen-phen users, and the Food and Drug Administration has found nine others. Weighty Problems
  • The discovery has the potential to revolutionise pre-clinical cancer research and clinical diagnostic practice, and it makes use of compounds that have already been approved for treating patients: the anti-cancer drug bevacizumab (Avastin) and Copper-64, a radioactive copper nuclide, which is approved by the US Food and Drug Administration (FDA) for some clinical trials. Health News from Medical News Today
  • Food and Drug Administration, has announced a voluntary recall of approximately 12,000 units of Infants' Mylicon Gas Relief Dye Free simethicone-antigas non-staining drops, which were sold in 1 oz. plastic bottles that were distributed nationwide after October 5, 2008 in retail stores and pharmacies. Recall: Infants' Mylicon Gas Relief Dye Free Drops
  • Three trials studied acetazolamide, marketed as Diamox and approved by the Food and Drug Administration to prevent acute mountain sickness. Reuters: Press Release
  • The Food and Drug Administration Tuesday announced a program aimed at providing consumers with better information about prescription drugs.
  • Since being approved by the Food and Drug Administration in 1981, aspartame has been repeatedly panned in the media, for different reasons.
  • Food and Drug Administration or in the European Union for the treatment of Dupuytren's contracture, which is treated primarily by an open surgical procedure. BioSpace.com Featured News
  • The drug industry has also very substantially captured the Food and Drug Administration, which is far too quick to approve new, "me-too" drugs of dubious clinical value and far too slow to remove dangerous or ineffective drugs from the market or at least condition them with clear limitations and warnings. Robert Kuttner: A Depressing Story You Need to Read
  • Food and Drug Administration was warning consumers to avoid using Zicam's nasal spray and swabs because it had 130 reported cases where users suffered from anosmia, which is a loss of smell. Investopedia.com Headlines
  • In 1998, the Food and Drug Administration inspected manufacturers who made drugs that relied on time-release beads.
  • But because the Food and Drug Administration approved the patch, the company is arguing in court that it cannot be sued by women who claim that they were injured by the product — even though its old label inaccurately described the amount of estrogen it released. Mislabeling Drug OK by FDA even if it hurts people...
  • Actavis have recalled fentanyl patches from US shelves after the Food and Drug Administration (FDA) identified problems with manufacture that could result in overdose. In-PharmaTechnologist RSS
  • Food and Drug Administration, often is used as an alternative to other antihypertensive drugs in people who cannot tolerate other blood pressure medicines.
  • Exhibit A is the US Food and Drug Administration.
  • S. Food and Drug Administration ( FDA ) recognizing that soy protein lowers cholesterol 3 andpercent.
  • United States approves contraceptive skin patch: The Food and Drug Administration has approved the first transdermal skin patch contraceptive.
  • David Kessler, a former commissioner of the Food and Drug Administration, has written a book, The End of Overeating, that accuses the food industry of manipulating the levels of sugar, salt, and fats in food in order to create a neurochemical addiction. Beating Obesity
  • Incyte Corp.'s Jakafi pill obtained U.S. Food and Drug Administration approval Wednesday, making it the first drug approved specifically for myelofibrosis, a rare bone-marrow disease, according to the government agency. FDA Approves Incyte's Drug for Bone-Marrow Disease
  • The U.S. Food and Drug Administration warns that taking stimulants such as dextroamphetamine can aggravate psychotic symptoms. The News Tribune - Tacoma - - HOMEPAGE
  • Lanthanum Carbonate tablets, indicated for the treatment of kidney failure and would facilitate phosphate absorption, are currently sold under the 'Fosrenol' brand by its innovator Shire Plc. Natco had filed an abbreviated new drug application (ANDA) seeking the US Food and Drug Administration's (USFDA) approval for marketing generic versions of Fosrenol in 500mg, 750mg and 1gm dosages. Top Stories - Google News
  • After a two-year investigation, the Food and Drug Administration asserted control over tobacco products by deeming them drugdelivery devices.
  • The Food and Drug Administration this week approved the over-the-counter sale of Allegra fexofenadine, an antihistamine often used for hay fever. Allergy drug Allegra goes OTC
  • The Food and Drug Administration has announced a warning on electronic cigarettes, also known as “e-cigarettes,” after a lab analysis found that they contain carcinogens and toxic chemicals such as diethylene glycol, an ingredient used in antifreeze that may be harmful to humans. FDA warns e-cigarettes contain toxins and cancer-causing agents
  • In 1997, the U.S. Food and Drug Administration reviewed nearly 60 studies about mercury exposure and dental fillings.
  • The Food and Drug Administration is reviewing the safety of a widely used chemical called triclosan found in antibacterial soap, toothpaste and other consumer goods. Breaking News: CBS News
  • The U.S. Food and Drug Administration recently approved the labeling of a new conjugate heptavalent pneumococcal vaccine for use in infants and children.
  • They fired off a no-holds-barred letter to the Food and Drug Administration, announcing an investigation into what they call the adequacy of the efforts of the FDA to protect the safety of the nation's food supply. CNN Transcript Aug 29, 2007
  • The vaccine has been licensed by the US Food and Drug Administration.
  • Food and Drug Administration next week for a clearance to market its Illumigene molecular test for C. difficile, which is currently undergoing a clinical trial. Los Angeles Business News - Local Los Angeles News | Los Angeles Business from bizjournals
  • Before tests can begin, the Food and Drug Administration must decide if the potatoes are likely to pose major safety hazards.
  • For more than 15 years military officials sought the Food and Drug Administration's approval of a drug that combats the deadly nerve agent soman.
  • Last year, Dr. Lawrence Deyton, the director of the Food and Drug Administration's tobacco division, sent letters to both Reynolds and smaller rival Star Scientific Inc. in which he expressed concern that their dissolvable tobacco lozenges are candy-like in appearance and may appeal to the youth market. Altria Plans To Test-Market Smokeless 'Tobacco Sticks'
  • FALCPA also requires the US Food and Drug Administration to develop and finalize rules for the use of the term gluten free on product labels. WN.com - Business News
  • The U.S. Food and Drug administration tries to regulate consumerism.
  • The Food and Drug Administration Tuesday announced a program aimed at providing consumers with better information about prescription drugs.
  • But the U.S. Food and Drug Administration (FDA) recently announced that these drugs will now require a black box warning label-the strongest in the industry-because they can cause a rare, and sometimes fatal, condition known as nephrogenic fibrosing dermopathy (NFD). Republic Broadcasting Network
  • Food and Drug Administration's approval to make and sell fexofenadine hydrochloride 180 milligram and pseudoephedrine hydrochloride 240 mg tablets, the generic version of Allegra D-24, in March 2010. U.S. Court Approves Dr. Reddy's Drug
  • It calls for increased government inspections of food processors. And it lets the Food and Drug Administration order the recall of unsafe foods.
  • Food and Drug Administration, it is possible to suffer lead poisoning if you consume food or beverages that have been stored or served in improperly glazed ceramic ware. Mexico - travelers tips
  • By the spring of 1999, 2,000 suicides by Prozac users had been reported to the Food and Drug Administration, at least a quarter of which appeared to be linked to agitation and akathisia.
  • The US Food and Drug Administration announced rules today that will enhance the security of the US food supply.
  • The Food and Drug Administration warned against eating lobster tomalley in the summer of 2008 due to high levels of a naturally occurring toxin likely stemming from red tides, or dangerous algal bloom. Q&A: Is it safe to eat fish skins and guts?
  • These cruelty-free products have not been certified by the Federal Food and Drug Administration authorities.
  • In 2002, the Food and Drug Administration warned that kava root had been linked to 'severe liver injury,' including liver failure and the need for a transplant.
  • WASHINGTON —The Food and Drug Administration has decided to ban some uses of a class of antibiotics on livestock out of concern that bacteria that sicken humans are becoming resistant to the drugs. FDA to Ban Some Antibiotics for Livestock
  • The Food and Drug Administration in 2009 warned consumers not to use any intranasal zinc products because of concerns that it can make people lose their sense of smell. The cure for the common cold? There is none
  • The Food and Drug Administration said late Monday that a food distributor in Moore, Okla., is recalling romaine lettuce that came from the same farm in Yuma, Ariz., that grew lettuce that sickened students in Michigan, Ohio and New York. E. Coli Outbreak: Middle, High Schoolers Sickened In New York
  • RACKAUCKAS: Well, we just learned yesterday that -- from the Food and Drug -- from the Food and Drug Administration that the baby food was contaminated with this castor oil that contains ricin, which is a-- which is a poison. CNN Transcript Jul 29, 2004
  • WASHINGTON—The Food and Drug Administration is recommending limits on the use of cholesterol-lowering medication simvastatin, commonly known as Zocor, marketed by Merck & Co., because the drug is associated with a risk of muscle injury. FDA Urges Limits on Dosages of Zocor
  • Syngenta's corn was cleared in 2007 for human consumption by the Food and Drug Administration, which is responsible for ensuring the safety of food. USDA Clears Syngenta Biotech Corn Opposed by Grain Millers
  • One, Pradaxa, a so-called direct thrombin inhibitor, was approved late last year by the U.S. Food and Drug Administration. Merck Returns Betrixaban Rights Amid Pipeline Review
  • The label says it has 0 calories and 0 grams of fat because the Food and Drug Administration allows companies to put zero on the label if a product has less than 5 calories and 0.5 grams of fat per servings. Leslie Goldman: 8 'Foods' I'm Glad I No Longer Eat
  • The U.S. Food and Drug Administration questioned the impact of the company's drug that would treat a condition caused by the buildup of toxic substances that impairs brain function known as hepatic encephalopathy. Penford Ends Higher; Salix Shares Drop
  • The only U.S. Food and Drug Administration approved therapy is interferon and ribavirin, which is very toxic, requires 48 weeks of treatment and works in less than half of patients. Health News from Medical News Today
  • In a complaint to the Food and Drug Administration, we pointed out that hydrogenated oils, corn syrup, and alkalized cocoa powder are clearly not natural. Michael F. Jacobson: Ben & Jerry's No Longer Fudging the Truth
  • The Food and Drug Administration on Tuesday approved the first drug test available without a prescription.
  • The vaccine has been licensed by the US Food and Drug Administration.
  • Lawsuits and investigations from the Food and Drug Administration into the health hazards of mixing alcohol and caffeine have prompted many manufacturers of alcoholic energy drinks to discontinue product lines or remove the addition of caffeine to their drinks, as has been the case with Sparks, one of the first alcoholic energy drinks on the market. At Vassar, Caffeinated Alcohol Leds To Concern Over Student Drinking Habits
  • The company said late yesterday that the US Food and Drug Administration approved antiplatelet medication Brilinta to reduce the rate of heart arrack and cardiovascular death in adults with acute coronary syndrome. Pharma News: Eli Lilly Earnings, AstraZeneca Receives Drug Approval
  • The Food and Drug Administration suggested that manufacturers consider taking zinc out of denture cream, following reports of neurological problems that might be associated with zinc poisoning. Zinc in Denture Creams Poses Risk
  • A Biogen spokeswoman said the company worked with the Food and Drug Administration on the change, which includes a table that details the incidence of progressive multifocal leukoencephalopathy, or PML. Biogen, Elan's Tysabri Label Updated
  • CLAIMED VINDICATION 17 MONTHS AGO, when the Food and Drug Administration decided not to pursue charges that the firm had concealed the hazards of its controversial sleeping pill, Halcion. Halcion: A Damaging Report
  • Valerie Jensen, associate director of the Food and Drug Administration's drug shortage program, said her team is working with the three makers of preservative-free methotrexate, which is used to treat the most common childhood cancer, acute lymphoblastic leukemia, or ALL. Msnbc.com: Top msnbc.com headlines
  • Food and Drug Administration has issued a "complete response letter" with respect to the company's Biologics License Application for its KRYSTEXXA (TM) (pegloticase) product candidate (the "BLA"), then the exercise price shall, from and after the eleventh trading day following the first such public announcement by the company, be changed to be the weighted average price for the common stock for the five trading days immediately preceding the tenth trading day following the date that the company publicly announced that the FDA issued its complete response letter. Undefined
  • Most conventional whitening toothpastes use sodium or potassium hydroxides, also known as lye, which is considered a poison by the Food and Drug Administration.
  • KEILAR: The Food and Drug Administration has just finished inspecting a drug factory in China that makes the active ingredient in heparin, that is the blood thinner that is under recall, linked to four deaths and hundreds of sick patients. CNN Transcript Feb 29, 2008
  • America's Food and Drug Administration has already published draft guidelines for xenotransplantation.
  • In addition to the Similac recall, Abbott earlier this month withdrew the diet drug Meridia from the market at the request of the Food and Drug Administration, after it was linked to increased risk for heart attacks and strokes. Abbott Profit Falls 40% on Acquisition, Recall Costs
  • The Food and Drug Administration approved anastrozole for cancer treatment in 1996, and another drug letrozole in 1997.
  • Food and Drug Administration (FDA) does not allow vitamin K to be sold as a dietary supplement in its menadione form. The World's Healthiest Foods

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