Sentences with phrase «label use of a drug»

Federal law prohibits the extra label use of this drug in food - producing animals.

Off label prescription drugs — coverage for off - label use of drugs - for individual and group plans

Off label prescription drugs — coverage for off - label use of drugs --- for individual and group plans including HMOs

Not exact matches

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.

Doctors often use a combination of off - label drugs to try to manage patients» nightmares, flashbacks and depression, but the drugs do nothing to treat the underlying condition, and can have negative side effects.

Sales of the prostate cancer drug jumped 61.6 % to $ 845 million in Q1 following a label expansion in February that allows its use for patients with metastatic high - risk castration sensitive prostate cancer.

In its proposed gluten - free label rules, The U.S. Food and Drug Administration, has said that wheat grass and barley grass could be used to make foods labeled gluten - free, as long as they do not contain 20 parts per million or more of gluten.

In a long - awaited step toward accurate gluten - free food labeling, the Food and Drug Administration (FDA) has released its definition of «gluten free» to be used by food manufacturers.

In comments submitted to the U.S. Food & Drug Administration (FDA), the Grocery Manufacturers Association (GMA) called on the agency to more clearly define the use of the term «natural» in food labeling.

is that off - label uses for medications are supported by medical trials / testing, but lack of FDA - approval means the drug manufacturers can not * advertise * the off - label uses?

So, it softens their cervix - that just supports what has been said about it being used when it comes to medical abortion (another «off label» use of the drug).

However, the U.S. Food and Drug Administration has not approved Sudafed for the purpose of ending milk production, which is considered an «off - label» use of the medication.

The U.S. Food and Drug Administration has strengthened the label warning to state that breastfeeding is not recommended while using medicines containing codeine or tramadol because of the potential for serious adverse effects in the infant due to opioid overdose (76).

Subsequently, by virtue of defining that an adult and infant are unable to safely sleep on the same surface together, such as what occurs during bedsharing, even when all known adverse bedsharing risk factors are absent and safe bedsharing practices involving breastfeeding mothers are followed, an infant that dies while sharing a sleeping surface with his / her mother is labeled a SUID, and not SIDS.26 In this way the infant death statistics increasingly supplement the idea that bedsharing is inherently and always hazardous and lend credence, artificially, to the belief that under no circumstance can a mother, breastfeeding or not, safely care for, or protect her infant if asleep together in a bed.27 The legitimacy of such a sweeping inference is highly problematic, we argue, in light of the fact that when careful and complete examination of death scenes, the results revealed that 99 % of bedsharing deaths could be explained by the presence of at least one and usually multiple independent risk factors for SIDS such as maternal smoking, prone infant sleep, use of alcohol and / or drugs by the bedsharing adults.28 Moreover, this new ideology is especially troubling because it leads to condemnations of bedsharing parents that border on charges of being neglectful and / or abusive.

Doctors say that for babies with extreme reflux, off - label use of heartburn drugs can sometimes help.

ALBANY — Labeling it «structural racism» and the «new Jim Crow,» activist Alice Green released a stinging report Tuesday that condemned recent local sweeps against suspected drug dealers and gang members using a federal racketeering statute for continuing a historical conspiracy of fearful whites to repress young black men who intimidate them.

At the same time the papers supported unvetted «off - label» uses for HRT that were not approved by drug regulators, including healthier skin, protection against Alzheimer's and Parkinson's diseases, and a generally higher quality of life.

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.

These antianxiety drugs «are known to be safe, and we are using them at very low levels here,» study author Scheuer notes, adding he is not concerned about human patients receiving low doses of antianxiety drugs off - label.

It was a subject - oriented adjective that was used to label the harmful, injurious, unpleasant or undesirable reactions (or responses) that a subject manifested - thus, nocebo reactions (or nocebo responses)- as a consequence of the administration of an inert, dummy drug, in cases where these responses had not been chemically generated, and were entirely due to the subject's pessimistic belief and expectation that the inert drug in question would produce harmful, injurious, unpleasant or undesirable consequences.

The bill would've given the U.S. Food and Drug Administration (FDA) the authority to prohibit the use of certain ingredients, including carcinogens and reproductive and developmental toxins, to recall products that fail to meet safety standards, and to require product labels to name each ingredient.

In early 2006 new Food and Drug Administration rules went into effect requiring food labels to show trans fat content; in September the city of New York proposed severely limiting the use of trans fats in local restaurants.

Antipsychotics were originally developed for use in patients with schizophrenia or psychosis, but the study shows that «off - label» prescribing of these drugs to treat the behavioural and psychological symptoms of dementia is a common practice in care homes.

«Research challenges use of off - label drug to treat osteoarthritis.»

Last May, a group of advisers to the Food and Drug Administration concluded that Halcion was safe and effective when used correctly, but that the warning on the label should be strengthened.

You report on the difficulties of finding replacement drugs for executions and hence the off - label and experimental use of fentanyl...

Two days later, the FDA, which had already been assessing the health risks of Avandia, imposed its toughest warning label, the «black box,» on the drug, as well as on Actos, another drug used to treat diabetes.

In this webinar, a panel of experts will discuss their research and describe the use of real - time, label - free cell monitoring in their investigation of novel cancer targets and the impact of their work on translational research and drug development.

Varying strengths of risperidone tablets, manufactured by TEVA Pharmaceuticals USA, have been approved, although the labeling of the generic risperidone might differ from that of Risperdal because some uses of the drug are protected by patents and exclusivity, the agency said.

In academic contexts, some universities are already trying to curb the off - label use of prescription drugs to enhance academic performance, with Duke University explicitly considering such use as «cheating.»

Written by world - class experts in clinical cancer therapeutics, this essential reference provides a complete, easy - to - use catalogue of over 100 drugs and commonly used drug regimens — both on - and off - label — for the treatment of all the major cancers.

They hypothesized that, if they labeled the parent cell population using the library, propagated it, separated it into roughly identical replicate groups, and treated these groups with the same drug regimen, they would find one of two outcomes (see schematic depiction below):

According to the researchers, more research is needed to determine if off - label use of antipsychotic medications yields substantial clinical benefit and to identify how doctors decide to prescribe these drugs for non-FDA approved conditions.

Label the FDA approved label is the official description of a drug product which includes indication (what the drug is used for); who should take it; adverse events (side effects); instructions for uses in pregnancy, children, and other populations; and safety information for the patLabel the FDA approved label is the official description of a drug product which includes indication (what the drug is used for); who should take it; adverse events (side effects); instructions for uses in pregnancy, children, and other populations; and safety information for the patlabel is the official description of a drug product which includes indication (what the drug is used for); who should take it; adverse events (side effects); instructions for uses in pregnancy, children, and other populations; and safety information for the patient.

Drug Labels FDA drug labels contain the name of the particular symptom, disease, or subset of patients within a disease that the drug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingredieDrug Labels FDA drug labels contain the name of the particular symptom, disease, or subset of patients within a disease that the drug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingredLabels FDA drug labels contain the name of the particular symptom, disease, or subset of patients within a disease that the drug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug labels contain the name of the particular symptom, disease, or subset of patients within a disease that the drug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingredlabels contain the name of the particular symptom, disease, or subset of patients within a disease that the drug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug is approved to treat, along with instructions for using the drug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug properly (including the dosage and what to do when a patient misses a dose), a description of any special instructions for taking the drug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug (such as with food or water), storage instructions, the symptoms of side effects to the drug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug, the names of any conditions or foods the patient should not have while using the medication, any warnings or precautions, any risk of drug tolerance or dependency, and a list of drug ingrediedrug tolerance or dependency, and a list of drug ingrediedrug ingredients.

«Off - label drugs are used in many different scenarios in cancer care,» said William A. Wood, MD, MPH, a UNC Lineberger member, an associate professor in the UNC School of Medicine Division of Hematology / Oncology and a co-author of the study.

The researchers offer four steps for improving the review process: develop methodological standards for evaluating evidence used to back off - label drug recommendations; combine the findings into one «single, rigorously developed resource» rather than five inconsistent reference guides; assess whether those reviewing and determining off - label drug use policies have potential financial conflicts of interest; and make the compendia listings, which currently are only available by subscription, free to the public.

However, the Food and Drug Administration in 2006 asked the manufacturers of stimulants, including Adderall, to add a warning to their label saying the medications should not be used in children with structural heart abnormalities or other heart problems.

Smart drugs, on the other hand, have potentially dangerous side effects (especially when used off - label or by someone they were not prescribed to) and should generally be avoided, especially without the oversight of a trained doctor or medical professional.

While the cinema perception may be that college students are using illegal drugs recreationally, I never saw this when I was in school and instead saw rampant off - label use of potentially dangerous but legal pharmaceuticals by students to keep up with demanding academic programs.

The Food and Drug Administration is considering changing the «use of the term «healthy» in the labeling of human food products.»

Node Smith, ND A very interesting study on an off - label use of a common diabetes medication for the treatment of cocaine addiction was recently published in the journal Neuropsychopharmacology.1 The research is specifically addressing the tendency for cocaine addicts to relapse on the drug.

Experiment with spices such as, parsley, basil, oregano, ginger, sesame, dill, cilantro, curry, pepper, and thyme to reduce the amount of salt used in cooking • Cut back on sodium, including that in processed foods and in many drugs (check labels for soda, sodium, or salt).

After six years, the Food and Drug Administration (FDA) has finally defined and set standards for the use of the phrasing gluten free on labels...

They are drugs, drugs that were initially developed by and for the military to treat acute mercury, lead and other poisonings of World War II army and navy personnel.2, 3 Their use for the removal of chronic levels of toxic metals is off label and controversial.

In 2010, the Corn Refiners Association (CRA) petitioned the U.S. Food and Drug Administration (FDA) to allow manufacturers the option of using the term «corn sugar» instead of «high fructose corn syrup» (HFCS) on food labels.

BACKGROUND — The diagnosis of non-steroidal anti-inflammatory drug (NSAID) induced enteropathy is difficult, requiring enteroscopy or the use of four day faecal excretion of 111In labelled white cells.

In October 2005, the Non-Prescription Drug Advisory Committee of the US Food and Drug Administration (FDA) was convened to discuss the potential benefits and risks associated with antiseptic products marketed for consumer use, such as soaps labeled as «antibacterial.»

Off Label (Unrated) Prescription drug expose» highlighting the explosion of the use of pharmaceuticals in America as seen through the eyes of eight unique patients.

Doctors say that for babies with extreme reflux, off - label use of heartburn drugs can sometimes help.