Sentences with phrase «drug administration in»

First of all, The Food & Drug Administration in the USA adopted the technology and later U.S. Department of Defense Transportation Command also shown a recent interest in the blockchain.

The transvaginal mesh patch was approved by the Food and Drug Administration in 2002, but the FDA issued an update in 2011 stating that it was wrong in its initial assessment that the product was safe.

Approved by the Food and Drug Administration in 1993, over-the-counter pain medication Cataflam has been linked to serious birth defects in infants born to women who took the medication while pregnant.

The specific context is an infusion pump system that the Federal Drug Administration in the US thought was insecure and sent a warning about — a warning that sounded like a «defective product» warning.

The Food & Drug Administration in the United States has recently kicked off a review of its official definition of the word «healthy.»

In other instances, products bought online are manufactured in other countries, and do not have the same standards and guidelines set forth by the Food and Drug Administration in the United States.

APOQUEL was approved by the U.S. Food and Drug Administration in May 2013 and is the first and only Janus kinase (JAK) inhibitor approved for veterinary use.

Here's a quote from this article from the U.S. Food and Drug Administration in reference to the fraudulent weight - loss diet pill industry:

«I look forward to productive discussion with the US CDC and Food and Drug Administration in light of this new scientific evidence.»

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.

Approved by the U.S. Food and Drug Administration in December 2016, Eucrisa inhibits an enzyme that promotes inflammation.

They were involved in clinical trials of methylnaltrexone, a drug developed at the University of Chicago and approved by the Food and Drug Administration in 2008.

After decades of additional research, azacitidine (Vidaza) was approved by the Food and Drug Administration in 2004 for treating myelodysplastic syndrome (MDS), a cancer of the blood and bone marrow.

The Investigational New Drug application for the Phase 1/2 trial, called STEP ONE, or Safety, Tolerability, and Efficacy of VC - 01 Combination Product in Type 1, was allowed by the US Food and Drug Administration in August 2014.

Study Selection Randomized placebo - controlled trials of antidepressants approved by the Food and Drug Administration in the treatment of major or minor depressive disorder were selected.

All six patients suffered from end - stage heart disease and were enrolled in this first - in - human (FIH) clinical trial, approved by the U.S. Food and Drug Administration in late 2015.

Therefore, PCSK9 is an excellent target for clinical inhibitors that lower blood LDL concentration and therefore cholesterol levels; in fact, two different drugs were approved for this purpose by the US Food and Drug Administration in 2015.

Thus, PCSK9 is an excellent target for clinical inhibitors that lower blood LDL concentration and therefore cholesterol levels; in fact, two different drugs were approved for this purpose by the US Food and Drug Administration in 2015.

The Food and Drug Administration in November approved the company's plans to test cells created from human embryonic stem cells on 12 patients suffering from each condition.

Second, our current study suggests that after the long - term drug administration in mice, the more rapid recovery may also involve the interplay of ABC efflux transporters and SLC influx transporters in the testes.

In the drafting of the document, «we were careful to include... representatives of the Industry and the Food and Drug Administration in addition to government and non-governmental organizations.

The wheat was cleared by the US Food and Drug Administration in 2004 as safe for human consumption, but Monsanto abandoned commercial development the same year, citing a drop in demand.

Chava Kimchi - Sarfaty of the U.S. Food and Drug Administration in Bethesda, Maryland, and colleagues report online this week in Science that such «silent mutations» can, under certain circumstances, determine how well a final protein performs — an «extremely provocative» result, says cell biologist William Skach of Oregon Health & Science University in Portland.

The U.S. Food & Drug Administration in 2015 approved two prescription versions of naloxone — an auto - injector and a nasal spray formulation.

The finding suggests that the drug — methylnaltrexone, approved for use by the United States Food and Drug Administration in 2008 to treat opioid - induced constipation — could play a role in cancer therapy.

The radioactive dye used, florbetapir (Amyvid), was approved by the U.S. Food and Drug Administration in 2012 for PET imaging of the brain to estimate beta - amyloid plaque density in patients being evaluated for cognitive impairment.

Rituximab, a monoclonal antibody that attacks cancer cells in patients with a certain subtype of B - cell lymphoma, was approved by the Food and Drug Administration in 1997.

The drug, which is being developed in conjunction with Sanofi, should be up for review by the Food and Drug Administration in a couple months, and will be up for European regulatory approval next year.

In light of the growing opioid crisis, the Federal Drug Administration in October 2014 reclassified all hydrocodone products in a way that makes them more carefully controlled, including limiting prescriptions to a 30 - day supply with no refills.

Beletsky — who recently helped the U.S. Department of Justice's Bureau of Justice Assistance design a naloxone toolkit for police — will discuss the paper's findings at a scientific workshop at the Food and Drug Administration in July.

- Geoffrey Heinzl, postdoc in chemistry at the U.S. Food and Drug Administration in Silver Spring, Maryland

The current standard of care for advanced pancreatic cancer — a combination of nab - paclitaxel and gemcitabine — was developed by TGen and the HonorHealth Research Institute, and approved by the U.S. Food and Drug Administration in 2013.

A testosterone patch developed for women was rejected by the US Food and Drug Administration in 2004 because it had little impact on sexual desire, and carried potential cardiovascular risks

Geoffrey Heinzl, Second - year chemistry postdoctoral fellow at the U.S. Food and Drug Administration in Silver Spring, Maryland

«These CAR - T cells are extremely potent,» Mackall said, noting that a therapy that uses CAR - T cells to treat pediatric leukemia was approved by the Food and Drug Administration in 2017.

PreScience Labs, a U.S. company founded by Geschwind, received approval for a phase I study from the U.S. Food and Drug Administration in 2013.

The company has shown in pilot studies that the technology works, and it is on track to begin filing for approval with the U.S. Food and Drug Administration in July.

The drug, trade named Mylotarg, received accelerated approval from the U.S. Food and Drug Administration in 2000 for treatment of AML in adults.

Nusinersen, approved by the U.S. Food and Drug Administration in December 2016, became the first drug approved to treat spinal muscular atrophy, with several other experimental drugs still in clinical trials.

A number of new, highly effective therapies to treat both Hepatitis C and HIV / AIDS have been approved by the Food and Drug Administration in recent years, but their extraordinary costs have raised questions about states» ability to pay the sticker price.

In fact, the group, along with the National Alliance for Breastfeeding Advocacy, went as far as to petition the Food and Drug Administration in 2008 to require warning labels on omega - 3 — fortified infant formulas.

In a draft report released earlier this year, the Environmental Protection Agency estimated that over 5 percent of children consume more than 6 micrograms per day of lead — the maximum daily intake level set by the Food and Drug Administration in 1993 — in their diet.

I spoke with Dr. Danielle Aparecida da Silva of Brazil's Oswaldo Cruz Foundation (equivalent to the Food and Drug Administration in the USA) to learn more about the upcoming «World Day of Human Milk Donation» which will be celebrated on May 19, 2013.

A Freedom of Information request to the Food and Drug Administration in the US by the Cornucopia Institute found similar reactions logged in some babies fed on formula with Long Chain Polyunsaturated Fatty Acids (such as DHA and ARA), which it was suggested may be linked to the production process.

The novelist meant to call attention to the working conditions of the immigrant but instead his work helped pressure the federal government into the Meat Inspection Act and eventually the beginnings of the Food and Drug Administration in 1930.

This has obviously been quite a concern for parents, and although the Food & Drug Administration in 2008 deemed items with BPA to be safe, it's still rightfully a concern for many people.

First approved by the Food and Drug Administration in 1988, Acesulfame K is a calorie - free sweetener that is about 200 times sweeter than regular old table sugar.

GPI Letter to FDA in Response to Petition Related to Bisphenol - A, September 17, 2012 The Glass Packaging Institute filed a letter with the U.S. Food and Drug Administration in support of a petition to ban bisphenol - A in infant formula containers.

Regulatory agencies throughout the world including European Food Safety Authority (EFSA), Food Standards Australia New Zealand (FSANZ), Food and Drug Administration in the US (FDA) and the UK's Food Standards Agency (FSA), consider the appropriate use of caffeine in food to be safe and acceptable.

PCSK9 inhibitors, the main ingredients in Amgen's Repatha and Sanofi and Regeneron's Praluent treatments, were first approved by the Food and Drug Administration in July 2015 for use by patients with a family history of high cholesterol or those who suffered high - cholesterol - induced heart attacks.