New weight loss drug at gnc,what can i eat on the atkins diet uk,burn belly fat 10 days,best weight loss programs in denver - 2016 Feature

Contrave, which won its official stamp of approval this week from the Food and Drug Administration (FDA), is being trumpeted as the latest wonder treatment in America's seemingly endless quest to shed weight.
Produced by Orexigen Therapeutic Inc, the weight loss medication is a cocktail of two drugs, naltrexone, which is used in the treatment of alcohol and narcotic addiction, and bupropion, an antidepressant, also prescribed to people who want to quit smoking.
The FDA said the drug is approved for treatment of individuals who are considered to be clinically obese.
However, because the pill contains an antidepressant, the FDA said Contrave would carry a warning about the "risk of suicidal thoughts" when taking the medication. It was precisely due to the potential health risks associated with Orexigen's new drug that the FDA, citing cardiovascular complications, rejected approval of the pill back in 2011. Contrave will be distributed in the United States by Takeda Pharmaceuticals, a Japanese company, which will give Orexigen royalties on sales, AP reported.
Comment: Naltrexone is an opiate-blocking drug that can cause mental depression, or other mood and cognitive changes. A better way to lose weight and improve your mood is to ditch the carbs and increase the fat. Be a long time before he hits someone, spits on someone, or runs around the bus loop trying to get run over. Called Contrave, the medicine is a combination of two approved drugs: naltrexone, which treats alcohol and drug addiction, and bupropion, which treats depression and seasonal affective disorder and is used to help smokers quit. The agency said in a news release that Contrave can be used by obese adults and by overweight adults who have at least one other weight-related condition or illness, such as high blood pressure or type 2 diabetes. Two years ago, the FDA approved two other prescription obesity drugs, the first such drugs endorsed in more than a decade. Disappointing sales may reflect the common belief that obesity is a problem of willpower, not a medical condition that requires pharmaceutical treatment, experts told the newspaper. Contrave was developed for people unable to lose weight through diet and exercise alone who aren’t ready for weight-loss surgery, according to the newspaper.
The drug’s approval was based on the results of multiple trials involving 4,500 people.

Because Contrave contains bupropion, the label will include a boxed warning about the increased risk of suicidal thoughts and behaviors associated with antidepressants. Contrave can also increase blood pressure, and should not be used in people with uncontrolled high blood pressure, according to the FDA.
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Experts point to the potentially hazardous drug combinations for users who may be taking other pharmaceutical drugs in addition to the new pill. Users of Contrave may also experience seizures, increased blood pressure and accelerated heart rates. Orexigen resubmitted its application to regulators in December, saying that the drug fared well in an early analysis of a study designed to rule out excessive cardiovascular risk. It also can have an amphetamine effect on the body which will certainly curb your appetite.
Wellbutrin has been shown to cause seizures, hallucinations, hostility, thrill-seeking behavior, unexplained fear and anxiety. Carbs, once metabolized by the body, are essentially sugar and sugar is what makes you fat.
Food and Drug Administration, a new obesity drug, Belviq, will be available to certain patients by prescription, starting Tuesday. Food and Drug Administration, a new obesity drug will be available to certain patients by prescription, starting Tuesday. Centers for Disease Control and Prevention, more than one-third of adults in the United States are obese, the FDA said in its news release. One trial found that 42 percent of people who took Contrave lost 5 percent of their body weight, compared to 17 percent who took a placebo. See the Terms of Service and Privacy Policy (Your California Privacy Rights) for more information. An FDA advisory committee is scheduled to meet Thursday and vote on whether to recommend approval of the drug, lorcaserin.

Food and Drug Administration’s approval of a new weight-loss drug on Wednesday marks the third time the agency has given its blessing to a new diet medication since 2012. A second trial found 36 percent of people with type 2 diabetes who took Contrave lost 5 percent of their body weight, while only 18 percent of those on a placebo did.
But in documents released Tuesday in advance of the meeting, the FDA noted that studies on lorcaserin showed the average weight loss while taking the drug was not significantly different than the average weight loss among people taking a placebo. The delay in availability was in part because the Drug Enforcement Administration needed to review the drug. An FDA advisory committee already voted earlier this year against approval of another obesity drug under development, Qnexa, and will vote Wednesday on whether to recommend removing the weight-loss medication Meridia from the market due to an increased risk of heart attacks and strokes among people who have a history of cardiovascular disease. Belviq, as the FDA pointed out in its statement announcing approval last year, is intended "as an addition to a reduced-calorie diet and exercise." Belviq, or lorcaserin hydrochloride, works by activating a serotonin receptor in the brain, which may help a person eat less and feel full after eating smaller amounts of food, according to the FDA. Belviq received approval about the same time as another weight-loss pill, Qsymia, which hit the market in September. Patients in clinical trials went from an average 227 pounds to 204 pounds on Qsymia; on Belviq, the average weight dropped from 220 to 207. In trials, 47% of patients without Type 2 diabetes lost at least 5% of their body weight on Belviq, according to the FDA. In people with Type 2 diabetes, 38% of patients on Belviq lost at least 5% of their body weight, compared with 16% on a placebo.
At the time of approval, the FDA said Belviq's manufacturer, Arena Pharmaceuticals, would be required to conduct six post-marketing studies, including a long-term cardiovascular trial to assess the risk of heart attack and stroke. The most common side effects of Belviq in nondiabetic patients included headache, dizziness and fatigue, according to the FDA. In addition, some people taking medicines such as Belviq have reported heart valve problems, according to Eisai Inc., which markets the drug.

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