Sentences with phrase «only food and drug»

It is the only Food and Drug Administration conditionally approved drug to treat squamous cell carcinoma and mammary carcinoma in animals.

At the present time, hydroxyurea is the only Food and Drug Administration - approved medication that decreases the number of pain crises and episodes of acute chest syndrome.

«Hormone therapy is the only Food and Drug Administration - approved treatment for hot flashes and night sweats,» Dr. Newton said, «and fewer women are opting for hormone therapy these days.»

Not exact matches

Separately, a Food and Drug Administration panel recommended that an experimental rheumatoid arthritis drug developed by Lilly and Incyte should only be approved at a lower dDrug Administration panel recommended that an experimental rheumatoid arthritis drug developed by Lilly and Incyte should only be approved at a lower ddrug developed by Lilly and Incyte should only be approved at a lower dose.

And only one of the three new therapies (Pradaxa) has a Food and Drug Administration (FDA) approved antidoAnd only one of the three new therapies (Pradaxa) has a Food and Drug Administration (FDA) approved antidoand Drug Administration (FDA) approved antidote.

The only way to get around the ban is to receive approval from the U.S. Food and Drug Administration (FDA).

According to the Federal Food, Drug, and Cosmetic Act, the FDA can only require foods to be labeled as GMO if there is a material difference between the GM product and its non-GM counterpart.

The Biojector 2000 is the only needle - free device to have earned Food and Drug Administration clearance to deliver drugs into the muscle.

The amoeba is rare in the US, but just to be safe, the Food and Drug Administration says you should only rinse your sinuses with tap water that's been boiled and cooled, or distilled water purchased from a store.

Tylenol was buffeted by a series of quality - related product recalls and shortages in recent years as it overhauled manufacturing under a consent decree from the Food and Drug Administration, with full production in the U.S. only resuming within the past year.

Ionis only has a small handful of Food and Drug Administration (FDA)- approved therapies, but it has a clinical - stage portfolio that's 25 experimental therapies deep, and spanning a number of indications.

The Food and Drug Administration (FDA) has only set standards of enrichment for four nutrients lost during grain processing (vitamins B1, B2, B3 and the mineral iron).

There are two things, safety and efficacy — you do not talk about safety and efficacy in food, you only talk about these in terms of drugs.

Glass is the only widely - used packaging considered by the U.S. Food and Drug Administration as «generally recognized as safe» or «GRAS,» the agency's broadest standard for food - contact materiFood and Drug Administration as «generally recognized as safe» or «GRAS,» the agency's broadest standard for food - contact materifood - contact materials.

Glass containers are endlessly recyclable, made from all - natural ingredients (sand, soda ash, limestone, and recycled glass), and glass is the only packaging material accepted by the U.S. Food and Drug Administration (FDA) as «GRAS» or «generally recognized as safe» for food and beverage contFood and Drug Administration (FDA) as «GRAS» or «generally recognized as safe» for food and beverage contfood and beverage contact.

It is the only one of its kind recognized by the Food and Drug Administration (FDA) as a Category I skin protectant.

The U.S. Food and Drug Administration notes that ultrasounds should only be performed per the request of a healthcare provider and by a trained professional, such as a sonographer, radiologist, or obstetrician.

Instead, the program is intended to serve the millions of impoverished American children whose parents can not send them to school with a home - packed lunch for a whole host of possible reasons that never seem to cross Parker's mind: the family's SNAP benefits fail to cover a month's worth of healthful food, in light of today's rising food costs; there is only one parent in the household and he or she works one or more jobs and is not home to pack a lunch; one or both caretakers are drug - addicted, mentally ill, physically disabled or otherwise unable to adequately provide for their children; the family lives in a homeless shelter and lacks access to kitchen facilities; the family lives in a food desert where healthful groceries are scarce, etc. etc..

Arsenic (As) exposure from rice is of particular concern for infants and children.1 - 4 Infant rice cereal, a common first food, 5,6 may contain inorganic As concentrations exceeding the recommendation from the Codex Alimentarius Commission of the World Health Organization and the Food and Agriculture Organization of the United Nations of 200 ng / g for polished (white) rice, 4 the new European Union regulations of 100 ng / g for products aimed at infants7 (eTable 1 in the Supplement), and the proposed US Food and Drug Administration limit.8 Infants consuming only a few servings of rice cereal or other products (eg, rice snacks) per day may exceed the now - withdrawn provisional weekly tolerable intakes for As set by the Joint Food and Agriculture Organization of the United Nations and the World Health Organization Expert Committee on Food Additives.9food, 5,6 may contain inorganic As concentrations exceeding the recommendation from the Codex Alimentarius Commission of the World Health Organization and the Food and Agriculture Organization of the United Nations of 200 ng / g for polished (white) rice, 4 the new European Union regulations of 100 ng / g for products aimed at infants7 (eTable 1 in the Supplement), and the proposed US Food and Drug Administration limit.8 Infants consuming only a few servings of rice cereal or other products (eg, rice snacks) per day may exceed the now - withdrawn provisional weekly tolerable intakes for As set by the Joint Food and Agriculture Organization of the United Nations and the World Health Organization Expert Committee on Food Additives.9Food and Agriculture Organization of the United Nations of 200 ng / g for polished (white) rice, 4 the new European Union regulations of 100 ng / g for products aimed at infants7 (eTable 1 in the Supplement), and the proposed US Food and Drug Administration limit.8 Infants consuming only a few servings of rice cereal or other products (eg, rice snacks) per day may exceed the now - withdrawn provisional weekly tolerable intakes for As set by the Joint Food and Agriculture Organization of the United Nations and the World Health Organization Expert Committee on Food Additives.9Food and Drug Administration limit.8 Infants consuming only a few servings of rice cereal or other products (eg, rice snacks) per day may exceed the now - withdrawn provisional weekly tolerable intakes for As set by the Joint Food and Agriculture Organization of the United Nations and the World Health Organization Expert Committee on Food Additives.9Food and Agriculture Organization of the United Nations and the World Health Organization Expert Committee on Food Additives.9Food Additives.9, 10

The Food and Drugs Authority (FDA) in the Ashanti region says it has confiscated over 4,000 tablets of controlled prescription only medicine from 21 chemical shops in the Ashanti region.

Epidemiology studies have linked low sperm counts not only to aging but also to being too fat, being too thin, lack of exercise, excessive exercise, junk food, soda, exposure to toxins in food and air, and use of both prescription and nonprescription drugs, including tobacco and alcohol.

The U.S. Food and Drug Administration regulates all dietary supplements as food products under the 1994 Dietary Supplement Health and Education Act, which says that the manufacturers are only responsible for making sure a supplement is safe and meets efficacy claFood and Drug Administration regulates all dietary supplements as food products under the 1994 Dietary Supplement Health and Education Act, which says that the manufacturers are only responsible for making sure a supplement is safe and meets efficacy clafood products under the 1994 Dietary Supplement Health and Education Act, which says that the manufacturers are only responsible for making sure a supplement is safe and meets efficacy claims.

While CA 19 - 9 is the only biomarker approved for use by the U.S. Food and Drug Administration, and only for monitoring treatment for the disease, according to first author Seetharaman Balasenthil, Ph.D., instructor in Translational Molecular Pathology.

But the U.S. Food and Drug Administration's decision, announced August 5, covers only a specific, preliminary test release of GM mosquitoes on Key Haven in the Florida Keys, where no locally transmitted Zika cases have been reported.

The only «noninvasive» glucose meter to have received U.S. Food and Drug Administration (FDA) approval is no longer on the market.

None of the consumer kits have officially undergone the rigorous testing process that a drug or medical device must undergo for approval by the U.S. Food and Drug Administration, and the purchaser has only the manufacturer's claim that it works for its intended drug or medical device must undergo for approval by the U.S. Food and Drug Administration, and the purchaser has only the manufacturer's claim that it works for its intended Drug Administration, and the purchaser has only the manufacturer's claim that it works for its intended use.

Manufacturers and the U.S. Food and Drug Administration say such drugs are only for short - term use.

At the heart of this interest in rTMS treatment is the only such device cleared by the U.S. Food and Drug Administration (FDA).

He also tried naltrexone and acamprosate, the only two drugs approved by the U.S. Food & Drug Administration to treat alcohol dependency, without success.

Then, the Food and Drug Administration only has to ensure the product's safety for patients, not for the general public as potential terror targets.

The U.S. Food and Drug Administration (FDA) recommends eating up to 12 ounces of fish and shellfish per week, but only if they are «lower in mercury.»

Only one such treatment has so far received Food and Drug Administration approval (a therapy to treat bladder cancer), though others are in the pipeline.

The Food and Drug Administration - approved yellow fever vaccine, YF - VAX, is currently unavailable in the US because of manufacturing difficulties, and the alternative yellow fever vaccine, Stamaril, is only available through a limited number of US yellow fever vaccination clinics.

In the United States, Medical Maggots are regulated by the Food and Drug Administration as a prescription only medical device.

The Food and Drug Administration has approved the drug only for the treatment of children with pituitary dwarfism, who do not produce enough of the hormone themselves, but some paediatricians are giving the drug to children who are simply shDrug Administration has approved the drug only for the treatment of children with pituitary dwarfism, who do not produce enough of the hormone themselves, but some paediatricians are giving the drug to children who are simply shdrug only for the treatment of children with pituitary dwarfism, who do not produce enough of the hormone themselves, but some paediatricians are giving the drug to children who are simply shdrug to children who are simply short.

Presently there's only one Food and Drug Administration - approved laboratory test for Lyme disease: a blood test that relies on detecting antibodies, proteins the body's immune system makes in response to the disease.

They are currently the only drugs approved by the Food and Drug Administration to treat PTSD.

Fifty days after the mice were born, one group was injected three times a week with Hsp70 and another received Riluzole, the only drug approved by the Food and Drug Administration to combat drug approved by the Food and Drug Administration to combat Drug Administration to combat ALS.

It has been a few years since the «personal genomics» industry took off, and the US Food and Drug Administration is only now warning firms that genome scans are «medical devices» that require approval.

This technique, known as «responsive neurostimulation» (RNS), has proved effective for epilepsy and an existing system has been approved by the U.S. Food and Drug Administration for treating partial onset seizures (which affect only part of the brain).

More than 7,500 metabolites have been detected in humans, and only about 2,500 of them come directly from the person; the others come from other sources, including foods and drugs that the person ingested.

Previous clinical studies showed that Truvada, the only prophylactic drug approved by the Food and Drug Administration to help prevent the spread of HIV, was more effective at reducing infection rates in men than in women, despite similar rates of drug adheredrug approved by the Food and Drug Administration to help prevent the spread of HIV, was more effective at reducing infection rates in men than in women, despite similar rates of drug adhereDrug Administration to help prevent the spread of HIV, was more effective at reducing infection rates in men than in women, despite similar rates of drug adheredrug adherence.

Currently, immunotherapy is approved by the Food and Drug Administration (FDA) to treat kidney cancer patients only after they've tried more traditional therapies, such as targeted therapies killing the cancer's blood supply.

At the moment, the only influenza antivirals approved by the U.S. Food & Drug Administration are the neuraminidase inhibitors, compounds that include Roche's Tamiflu (oseltamivir) and GlaxoSmithKline's Relenza (zanamivir).

In an April 6 statement announcing the decision, the Food and Drug Administration said that the tests only assess the genetic risks for the conditions.

For only the second time, the Food and Drug Administration approved a company's request to test an embryonic stem cell - based therapy on human patients.

Dr. Mark Mattar, a gastroenterologist at MedStar Georgetown University Hospital, explained to Newsweek the Food and Drug Administration (FDA) only allows fecal transplants to be performed in patients with a C. difficile infection.

However, despite the increasingly important role of companion diagnostics in the realization of personalized medicine, in the United States, there are only twenty - three Food and Drug Administration (FDA) approved companion diagnostics on the market for eleven unique indications.

In addition to children, all women of childbearing age are, therefore, advised by the United States Food and Drug Administration (FDA) to eat only up to twelve ounces per week of a variety of fish and shellfish known to be lower in mercury.

«Its a big issue because there is only one real Botox cosmetic currently approved by the Food and Drug Administration (FDA), but there are lots of cheaper fake and foreign products,» says Julius Few, MD, spokesman for the American Society for Aesthetic Plastic Surgery and director of the Few Institute for Aesthetic Plastic Surgery in Chicago.