Parents need to open a discussion about Adderall and
other study drugs.
Not exact matches
A new government - funded
study suggests that addictive opioid painkillers may not be better than
other, non-opioid kinds of
drugs for treating chronic back pain and arthritis.
Bristol - Myers emphasized Opdivo's
other successes and ongoing
studies evaluating its effectiveness in combination with the company's
other cancer
drugs.
Other charities that have benefited from the organization include healthcare outsourcing platform Watsi; The Water Project; the Electronic Frontier Foundation digital - rights activism group; MAPS, an organization that
studies therapeutic uses of psychedelic
drugs and marijuana; the medical nonprofit SENS Research Foundation; and charity: water.
But according to the Government Accountability Office (GAO) which did a
study in 2013 on the
drug shortage,
other reasons include a lack of materials to make the
drugs, as well as delays in getting government approval for new and experimental
drugs.
The DEA will now conduct its own eight - factor analysis to
study the
drug's potential for abuse, the current state of medical and scientific knowledge, the history and pattern of abuse, and
other considerations.
These risks and uncertainties include: Gilead's ability to achieve its anticipated full year 2018 financial results; Gilead's ability to sustain growth in revenues for its antiviral and
other programs; the risk that private and public payers may be reluctant to provide, or continue to provide, coverage or reimbursement for new products, including Vosevi, Yescarta, Epclusa, Harvoni, Genvoya, Odefsey, Descovy, Biktarvy and Vemlidy ®; austerity measures in European countries that may increase the amount of discount required on Gilead's products; an increase in discounts, chargebacks and rebates due to ongoing contracts and future negotiations with commercial and government payers; a larger than anticipated shift in payer mix to more highly discounted payer segments and geographic regions and decreases in treatment duration; availability of funding for state AIDS
Drug Assistance Programs (ADAPs); continued fluctuations in ADAP purchases driven by federal and state grant cycles which may not mirror patient demand and may cause fluctuations in Gilead's earnings; market share and price erosion caused by the introduction of generic versions of Viread and Truvada, an uncertain global macroeconomic environment; and potential amendments to the Affordable Care Act or other government action that could have the effect of lowering prices or reducing the number of insured patients; the possibility of unfavorable results from clinical trials involving investigational compounds; Gilead's ability to initiate clinical trials in its currently anticipated timeframes; the levels of inventory held by wholesalers and retailers which may cause fluctuations in Gilead's earnings; Kite's ability to develop and commercialize cell therapies utilizing the zinc finger nuclease technology platform and realize the benefits of the Sangamo partnership; Gilead's ability to submit new drug applications for new product candidates in the timelines currently anticipated; Gilead's ability to receive regulatory approvals in a timely manner or at all, for new and current products, including Biktarvy; Gilead's ability to successfully commercialize its products, including Biktarvy; the risk that physicians and patients may not see advantages of these products over other therapies and may therefore be reluctant to prescribe the products; Gilead's ability to successfully develop its hematology / oncology and inflammation / respiratory programs; safety and efficacy data from clinical studies may not warrant further development of Gilead's product candidates, including GS - 9620 and Yescarta in combination with Pfizer's utomilumab; Gilead's ability to pay dividends or complete its share repurchase program due to changes in its stock price, corporate or other market conditions; fluctuations in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead's future revenues and pre-tax earnings; and other risks identified from time to time in Gilead's reports filed with the U.S. Securities and Exchange Commission (the S
Drug Assistance Programs (ADAPs); continued fluctuations in ADAP purchases driven by federal and state grant cycles which may not mirror patient demand and may cause fluctuations in Gilead's earnings; market share and price erosion caused by the introduction of generic versions of Viread and Truvada, an uncertain global macroeconomic environment; and potential amendments to the Affordable Care Act or
other government action that could have the effect of lowering prices or reducing the number of insured patients; the possibility of unfavorable results from clinical trials involving investigational compounds; Gilead's ability to initiate clinical trials in its currently anticipated timeframes; the levels of inventory held by wholesalers and retailers which may cause fluctuations in Gilead's earnings; Kite's ability to develop and commercialize cell therapies utilizing the zinc finger nuclease technology platform and realize the benefits of the Sangamo partnership; Gilead's ability to submit new
drug applications for new product candidates in the timelines currently anticipated; Gilead's ability to receive regulatory approvals in a timely manner or at all, for new and current products, including Biktarvy; Gilead's ability to successfully commercialize its products, including Biktarvy; the risk that physicians and patients may not see advantages of these products over other therapies and may therefore be reluctant to prescribe the products; Gilead's ability to successfully develop its hematology / oncology and inflammation / respiratory programs; safety and efficacy data from clinical studies may not warrant further development of Gilead's product candidates, including GS - 9620 and Yescarta in combination with Pfizer's utomilumab; Gilead's ability to pay dividends or complete its share repurchase program due to changes in its stock price, corporate or other market conditions; fluctuations in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead's future revenues and pre-tax earnings; and other risks identified from time to time in Gilead's reports filed with the U.S. Securities and Exchange Commission (the S
drug applications for new product candidates in the timelines currently anticipated; Gilead's ability to receive regulatory approvals in a timely manner or at all, for new and current products, including Biktarvy; Gilead's ability to successfully commercialize its products, including Biktarvy; the risk that physicians and patients may not see advantages of these products over
other therapies and may therefore be reluctant to prescribe the products; Gilead's ability to successfully develop its hematology / oncology and inflammation / respiratory programs; safety and efficacy data from clinical
studies may not warrant further development of Gilead's product candidates, including GS - 9620 and Yescarta in combination with Pfizer's utomilumab; Gilead's ability to pay dividends or complete its share repurchase program due to changes in its stock price, corporate or
other market conditions; fluctuations in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead's future revenues and pre-tax earnings; and
other risks identified from time to time in Gilead's reports filed with the U.S. Securities and Exchange Commission (the SEC).
According to Living Goods, clients may also be reluctant to buy
drugs from
other private providers because of the risk of getting a counterfeit medicine.63 Living Goods sent us a
study conducted at the midline of its RCT that claims that both availability of counterfeit
drugs and
drug prices decreased at private retailers in areas where CHPs worked.64 According to the
study, about 37 % of private
drug shops in the areas it
studied sold fake ACT
drugs, 65 and availabilty of fake ACTs was about 50 % lower among non-Living Goods sellers in the areas where Living Goods worked.66 Additional results on these potential effects will be made available when the full RCT is published.
Potential subjects were accepted into the
study if they had none of the following conditions: severe or symptomatic cardiac disease or hypertension; history of bleeding disorders; chronic history of gastric, intestinal, liver, pancreatic, or renal disease; any portion of the stomach or the intestine removed (
other than an appendectomy); history of intestinal obstruction, malabsorption, or use of antacid
drugs; cancer (active or use of medications for a history of cancer treatment within the past 5 y); history of chronic alcoholism; a convulsive disorder; or abnormal results in screening blood or urine samples.
Students would buy the attention - deficit
drugs from
other students with an ADHD diagnosis before AP Exams, research papers or SAT / ACT tests, in hope of increased concentration and a greater ability to stay awake during
studying.
Other studies show children who have limits and rules enforced reasonably, are less likely to get involved in
drugs and juvenile crime, whereas children raised by authoritarian, harsh parenting or overly permissive parenting, had a higher risk.
ACEs usually refers to the 10 types of childhood adversity that were measured in the U.S. Centers for Disease Control and Prevention's Adverse Childhood Experiences (ACE)
Study: physical abuse, emotional abuse, sexual abuse, physical neglect, emotional neglect, a family member who's an alcoholic or addicted to
other drugs, a family member diagnosed with a mental illness, witnessing a mother being abused, a family member in prison, and loss of a parent through separation or divorce.
Many
studies have shown that weed is often laced with
other drugs.
If however many MDs aren't practicing evidence - based medicine, then why not don't MDs * police their own * before going off on
other professions for their lack of evidence - base... or attacking what evidence - base there is even if it isn't multiple double - blind placebo controlled
studies funded by wealthy
drug manufacturers?
Other studies have shown that children with involved fathers are less likely to do
drugs or drink alcohol, will be more emotionally secure, and have better social interaction with their peers.
The Journal of the American Academy of Pediatrics released a
study in April of 2010 detailing just what that one medicine / vitamin / herbal supplement is... and the «miracle
drug» is none
other than BREASTFEEDING.
They also took into account mother's age, the baby's birth weight, the position the baby was last left in and
other important factors, but they only had the data on the mother's alcohol and illegal
drug usage for two of the five
studies — a pretty significant limitation to the overall analysis.
For the purposes of this economic evaluation, the forms were initially used in a related
study funded by the National Institute of Health Research (NIHR) research for patient benefit programme «assessing the impact of a new birth centre on choice and outcome of maternity care in an inner city area,» which will be reported in full elsewhere, comparing the costs of care in a free standing midwifery unit with care in an obstetric unit in the same trust.16 The data collected included details of staffing levels, treatments, surgeries, diagnostic imaging tests, scans,
drugs, and
other resource inputs associated with each stage of the pathway through intrapartum and after birth care.
The Food and
Drug Administration has long permitted its use, but in recent years concerns about the chemical have grown as
studies have indicated low doses of the substance can disrupt hormone systems in laboratory animals and possibly increase the risk of cancer or
other serious illness.
And while the science may be disputed, depending on who is funding the
study, as to whether commonly used food dyes such as Yellow 5, Red 40 and 6
others made from petroleum pose a «rainbow of risks» that include hyperactivity in children, cancer (in animal
studies), and allergic reactions, because of the problem of hyperactivity, the Center for Science in the Public Interest petitioned the Food and
Drug Administration to ban the use of these dyes given that the British government and European Unionhave taken actions that are virtually ending their use of dyes throughout Europe.
In controlled
drug studies, some
study participants receive the
drug under testing;
others get a placebo, which is like a sugar pill that has none of the
drug being texted.
For all women included in the
study, we collected data on their age, height, weight before pregnancy, body mass index, income quintile,
drug and alcohol use (v. no use) during pregnancy, smoking status, status of parenthood (single v.
other), parity, gestational age at first prenatal visit, number of antenatal visits and history of ultrasonography before 20 weeks» gestation.
And I only used the word «
drugs» as a general term in my post, avoiding the reference to marijuana in particular because as many
studies have found recently, it may very well have
other valid medical uses.
«We could apply the strategy used in this
study to quickly identify and design small molecule
drugs for
other RNA - associated diseases,» explained
study first author Sai Velagapudi, a research associate in the Disney lab.
«
Study debunks fears of increased teen suicide risk from popular flu
drug:
Other side effects remain a concern.»
Moreover, the findings, if replicated in his and
others» ongoing
studies, could spur development of
drugs that target HDL subclasses, working to raise HDL without apoC - III and lower HDL with it.
Two recent large
studies reflect growing evidence that ADHD increases children's risk for abusing tobacco, alcohol and
other drugs when they are older.
The FDA recently okayed the first therapeutic cancer vaccine, and
other drugs that enlist the immune system against tumors are under
study
With this kind of review process, if 20
studies of the effectiveness of a truly ineffective
drug are conducted, and one of them shows a significant effect with a p - value of 0.05 because of chance alone, investigators for the
other 19
studies not showing any effect would presumably not be inhibited from writing up and submitting reports of these for publication out of fear that they'll be denied publication because of their nonsignificant results.
For this
study the researchers targeted very specific types of GABA receptors to improve social behaviors with clonazepam, but the team also found that by using a different
drug, they could target
other GABA receptors and actually reduce the ability to socially interact in normal mice — underscoring that future medications would need to target very specific receptors so as not to diminish the
drug's impacts.
People with
drug addictions who started opioid abuse later in life use injections for their
drugs, or increased their use of downers before starting
drug treatment, are more likely to relapse from treatment than
others, says a new
study from McMaster University.
Studies of the
drug abroad have shown that it is effective and has fewer side effects compared to
other corticosteroids, namely less associated weight gain.
In the heady postwar years, hundreds of promising
studies were conducted in the United States, Canada, and Europe on the use of LSD and
other psychedelics, like peyote, to treat such psychiatric maladies as schizophrenia, autism,
drug addiction, alcoholism, and chronic depression.
«Some
drug addicts more likely to relapse than
others:
Study.»
After controlling for
other factors, a generic
drug in the highest marketing competition group was expected to see a decrease of 32 percent in price over the
study period, while a generic
drug in the lowest market competition was expected to see a price increase of 47 percent over the same period.
Two major
studies published within about a week of each
other suggest that the
drugs do not work for these conditions.
Dr. McCabe said nanoparticles are a leading - edge technology also being
studied for delivery of
drugs for
other conditions, such as cancer, heart disease, and bacterial infections, in order to target specific cells to reduce toxicity and side effects of those medications and to make them more effective.
Preliminary results of the
study were presented at a World Health Organization (WHO) evidence review group meeting, while UNITAID has issued a call for further research into the use of endectocide class
drugs, of which ivermectin is currently the only one registered for human use, as new vector control tools in the fight against malaria and
other mosquito borne disease.
SapC - DOPS (saposin - C dioleoylphosphatidylserine), is a nanovesicle
drug that has shown activity in glioblastoma, pancreatic cancer and
other solid tumors in preclinical
studies.
Some methods may be good at providing positive evidence that a
drug works, for example, but
other types of
studies may be better at finding evidence that it doesn't — or that it also causes unacceptable side effects.
Other studies found no benefit from taking the
drug.
The
drug was not associated with severe toxicity in this or
other recent
studies.
In the current
study, Frank Longo, MD, PhD, and
others at Stanford University, tested LM22A - 4, a
drug that specifically binds to and activates the BDNF receptor TrkB on nerve cells, in mice that model the disorder.
In animal
studies this sharply reduces cravings and halts addicted animals» tendency to self - administer cocaine and
other habit - forming
drugs.
Other studies suggest that nicotine may be as effective at enhancing attention as methylphenidate (Ritalin) and the wakefulness - promoting
drug modafinil (Provigil).
The findings support
other recent rodent
studies that showed
drugs that enhance the action of BDNF can reduce brain changes and symptoms of Huntington's disease.
During imaging
studies probing the causes of addiction, the insula often was activated when
drug abusers were shown movies of
others taking
drugs or shown pictures of cocaine, heroin or nicotine.
The new
drugs offer the hope of treatment to perhaps thousands of HIV patients who have stopped responding to
other medications, says William Towner, medical director of the Kaiser Permanente HIV / AIDS research trials program and member of the
study team, which reported its findings online today in The Lancet.
Currently, Deng's laboratory is conducting additional preclinical
studies using the human - derived stem cells from Down syndrome patients and mouse models to determine whether cellular and behavioral abnormalities can be improved with minocycline therapy and
other candidate
drugs.
Currently there are no registries of egg donors in the UK or in the US, and there are only a few long - term follow up
studies on egg donors who have received fertility
drugs to help
others.