Sentences with phrase «what drug labels»

Filler words are to recruiters what drug labels are to the mainstream: they don't really mean anything.

Not exact matches

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).

Be sure to read labels carefully to see what the products contain so that you don't give your child a double dose of the same drug.

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.

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.

[1] The guidelines call on the Food and Drug Administration to clarify what information pharmaceutical companies can share with stakeholders beyond the information now found on FDA labels.

All the subjects of the study are now on what's called an «open label extension» - those on placebo have been moved to drug and will continue to be monitored.

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.

• What the experts say: Though the FDA did not conclude definitively that the events reported were induced by the drugs, the agency in June 2009 requested that the manufacturers of these drugs include a precaution about neuropsychiatric events in their prescribing information and labeling.

Since we can not rely on the U.S. Food and Drug Administration to label GMOs (though many other countries are starting the process), we have to look outside of food labels to know what products have been genetically modified.

Like Lucas» own drug, which he labeled with the brand name of «Blue Magic», it isn't offering a different product; it just gives you more bang for your buck than what anyone else is offering these days.

The film includes a young prostitute, a lesbian wedding, a drugged - out hick party, and what the MPAA would have labeled «male rear nudity» had this been rated PG - 13 instead of R. It's all in good fun, though, and mostly good taste, granting you enjoyment similar to Mike Judge's Office Space.

It's important to read the label and understand what the most common adverse reactions that are associated with the drug.

The term «off label» describes the use of a drug for conditions other than what it was approved for.

«In recent years, with a newfound understanding of artificial ingredients, hormones, and drugs, people have made a very conscious decision to start reading labels to gain a better understanding of what they are purchasing for themselves, families and pets.»

J & J's Janssen unit, however, is adamant that unlike what Pledger's family and other plaintiffs are claiming, the medication's Food and Drug Administration - approved label did properly warn about the possible risks.

Zofran is an anti-nausea drug that was originally approved for patients undergoing surgery or cancer treatment, but has been often prescribed «off - label» (a use other than what was approved by the FDA) to treat morning sickness during pregnancy.

«Comparatively,» the Supreme Court preemption precedent on which the defendant relied (chiefly Mensing / Bartlett) «spoke directly on the FDA's power to regulate what speech appears in a drug's «label» and when that power takes preemptive effect over what is required by state tort law.»