Prescription Weight Loss / Diet Pills: What Are the Options? Prescription weight loss pills, also called anti-obesity drugs or “diet pills”, are sometimes prescribed to a patient as an additional tool in the treatment for weight loss . Weight loss drugs should not be used as a substitute for healthful eating and a regular exercise program. Most weight loss drugs that suppress the appetite are known as anorexiants . Common "Diet Pills" or Weight Loss Drugs. How Effective are Weight Loss Drugs? Weight loss drugs may not work for everyone. Who are Candidates for Weight Loss Drugs? However, prescription weight loss drugs should be used in addition to diet and exercise. Weight loss drugs should not be used during pregnancy. All weight loss drugs fall under pregnancy category X and are contraindicated in pregnancy.
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Oz Show touted a “revolutionary” weight-loss supplement derived from an Indonesian plant call garcinia cambogia. But a new report shows that the majority of garcinia cambogia pills sold online or in stores contain only a fraction of the key plant compound listed on their labels. Consumer Lab.com—an independent company that tests the quality and safety of health products—examined 11 of the most popular garcinia cambogia supplements, including several whose packaging untruthfully claimed endorsements from the The Dr.
11, 2014 - The FDA's approval on Wednesday of a new prescription weight loss pill offers yet another option for the more than one-third of American adults who are obese. Called Contrave, the new drug is the third prescription weight loss drug to be approved by the FDA since 2012. Contrave combines two drugs already on the market: bupropion ( Wellbutrin ), an antidepressant , and naltrexone , an anti- addiction drug. Weight loss experts say all three drugs work in similar ways, but they welcome Contrave as yet another option, especially since not all weight loss drugs work the same for everyone. The FDA approval came after the agency looked at new information it requested from the drug's maker in 2011 to be sure the drug was safe for the heart . How the combination works for weight loss is not entirely understood, even by experts.
FDA Approves New Weight-Loss Drug Contrave. Regulators are greenlighting a new weight-loss drug called Contrave, the third in a string of approvals for anti-obesity treatments. The Food and Drug Administration said Thursday that it is approved for use by people who have a body mass index of 30 or higher, which is considered to be obese, and for people with a BMI of 27 or higher who also have a weight-related medical condition such as diabetes. Contrave is a combination of two drugs that are already approved, naltrexone and bupropion. The combination pill joins two similar drugs from Arena Pharmaceuticals and Vivus Inc., which FDA approved in 2012 after a 13-year drought of new prescription weight-loss medicines. Patients on Contrave for a year lost 4.2 percent more weight than patients taking a dummy pill.
The Food and Drug Administration has approved Belviq, the first new prescription drug for long-term weight loss to enter the U. WASHINGTON (AP) — The Food and Drug Administration has approved Arena Pharmaceutical's anti-obesity pill Belviq, the first new prescription drug for long-term weight loss to enter the U. The drug should be used in combination with a healthy diet and exercise. The company resubmitted the drug with additional data earlier this year, and the FDA said there was little risk of tumors in humans. Obesity rates nearing 35 percent of the adult population, many doctors have called on the FDA to approve new weight loss treatments. The cocktail of phentermine and fenfluramine was a popular weight loss combination prescribed by doctors, though it was never approved by the FDA. The FDA said patients should stop taking Belviq after three months if they fail to lose 5 percent of their body weight. Patients are unlikely to see any significant weight loss by staying with the drug. Side effects with the drug include depression, migraine and memory lapses. Belviq is the first new prescription drug approved to treat obesity since Xenical's approval 13 years ago.
A new diet pill called the Obalon inflates inside your stomach to mimic the results of weight loss surgery. Once you swallow the pill, the device can stay in your stomach up to three months before it is removed. You can swallow up to three balloons in a 12-week period to speed up weight loss, according to the company. Though not all experts are convinced that the Obalon is effective, the idea is part of a growing trend to find alternatives to weight loss surgery, which can be expensive and risky. The American Society for Metabolic and Bariatric Surgery tracks alternative weight loss procedures that may one day provide a viable alternative to going under the knife. They found that the patients lost an average of 20 percent of their body weight after six months. Related: Super Dieters Share Weight Loss Secrets Pryor said the balloons can be easily removed and the biggest risk seems to be unintentional deflation. They are available in many parts of the world but the Food and Drug Administration has not yet approved them for use in the U. The device attaches to the bottom of the stomach and snakes through the first two feet of the small intestine so that food does not come into contact with the intestine itself. The Endo Barrier was approved in Europe, South America and Australia in 2006 and is expected to be approved for use in the U. He added that in foreign clinical trials, average weight loss was 20 percent of body weight in 12 months or less and many patients were also able to reach healthy blood sugar levels and reduce or eliminate the use of anti-diabetes medications. Pryor pointed out that the most current Centers for Disease Control and Prevention statistics put the percentage of Americans who are overweight or obese at nearly 70 percent, so new and novel approaches to weight loss are certainly needed. She said it's unlikely any one procedure will work for everyone and that any and all of these devises may eventually find their place in the arsenal in the fight against obesity.
To find out more about Facebook commenting please read the Conversation Guidelines and FAQs. For the third time in about two years, the Food and Drug Administration has approved a new weight-loss pill. All of the new drugs work by decreasing appetite and all have some side effects and drawbacks, though they differ. In Belviq’s studies for the FDA, average losses were 3% to 3.7% over placebo; for Qsymia, average losses were 6.7% to 8.9% over placebo. “The ideal candidate for a drug to treat obesity is someone who uses the drug as a tool, along with diet and exercise,” says Tsai, who has no ties with drug makers. So far, the other new pills have not been big sellers – considering that more than a third of U. Adults, 78.6 million, are obese, according the federal Centers for Disease Control and Prevention. Patients filled about 138,000 prescriptions for Qsymia in the second quarter of 2014, according to drug maker Vivus Inc. Prescription numbers for Belviq were about 110,000 in the same period, according to Arena Pharmaceuticals Inc., which makes the drug. That’s a lot of room for growth, he says, and having a third drug approved just “gets more voices out there” talking about the pharmaceutical options. In the past, some obesity drugs have been linked to serious heart problems and pulled from the market. The makers of Contrave, Belviq and Qsymia have all agreed to conduct long-term heart safety studies and report the results to FDA.
Clip 1 of 7. A New Silver Bullet for Weight Loss? Is this the magic bullet youve been waiting for? Get the facts to see if this medication could be right for you. Clip 2 of 7. Clip 4 of 7. Clip 5 of 7. Clip 6 of 7. The New Silver Bullet for Weight Loss. Oz reveals the new super weight loss pill you have been waiting for!
And finally, there are herbal supplements for weight loss that you'll find in many vitamin shops and drug stores. The best resource for information regarding the use of any supplement or weight loss pill is your healthcare provider. The diet pill is prescribed along with a reduced-calorie diet and exercise program to help people lose weight. Non-Prescription Weight Loss Pills and Supplements. This is the only over-the-counter weight loss pill approved by the FDA. Lipozene for weight loss is the most popular product that contains glucomannan. Unfortunately, the studies have been inconclusive and have not been able to confirm that the fiber substance can help you lose weight. However, the NIH found that chromium has no significant benefits for weight loss. There is little evidence to support the use of bee pollen for weight loss. If the weight loss pill that you are interested in is not listed above, visit the National Institutes of Health Dietary Supplement Fact Sheets website. And remember to talk to your doctor about any diet pill or weight loss supplement that you are considering.
New Weight Loss Pill Burns More Calories, Uses Fat For Fuel — Compare To Low-Carb Diet [Video] Now the Food and Drug Administration (FDA) has approved three new prescription diet drugs as well as a weight loss injectable medication. But it’s a fledgling weight loss pill that has everyone’s attention by providing a way to turn up the body’s fat-burning furnace to burn additional calories without exercise, reported the Los Angeles Times. When the researchers studied its effects on mice, they found that it caused the mice to use fat for fuel and burn more calories. How do the actions of Fex compare to a diet known for shifting the body into fat-burning mode? As the Inquisitr reported, a high-fat low-carb ketogenic diet has become the new gold standard for many weight loss gurus. They view it as the answer both for endurance athletes, such as marathon runners, and for dieters. Low-carb eating allows the body to burn fat for fuel.” But for those who want to talk with their physicians about using a medical booster such as a diet drug, there are three currently approved FDA weight loss pills , as reported by the Inquisitr. But Fex is different than the other weight loss drugs, according to io9. “And the reality is that the very first responder for all this is the intestine.”
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Scientists develop a weight-loss pill that fools the stomach. A protein that activates the gut's natural response to food may be the next thing in weight loss. Enter fexaramine, billed as a new approach in the treatment of obesity and metabolic syndrome — the cluster of cardiovascular risk factors that often precedes the development of full-blown Type 2 diabetes in the obese. Fexaramine — known affectionately as Fex by drug developers at the Salk Institute — isn't a drug candidate yet. Fex appeared to turn up the thermostats on mice that got it, so they burned more calories and made better use of fats for fuel. The fexaramine compound mimics the farnesoid X receptor, or FXR, a protein that responds to an influx of food by triggering the release of bile acids for digestion, changing blood sugar levels and prompting the body to burn some fats in preparation for an incoming meal. The FXR protein is active in the liver, kidneys and adrenal glands, as well as the intestines. The Salk team wondered whether an FXR activator that acted only in the intestines might work as well, with fewer unwanted side effects. By building a once-a-day pill that acts only in the intestines and never reaches the blood stream, they found, Fex set off a cascade of events, each occurring in its natural order, to create a more adaptive response to incoming calories. Administration of Fex even changed the mix of microbiota in the guts of mice, although the researchers acknowledged that they were uncertain whether or how such changes might have promoted weight loss. The Salk researchers believe that because Fex does not act directly on systems beyond the intestines, it will probably have fewer of the safety issues that have dogged the development of weight-loss drugs that act more systemically.
While most side effects of prescription medications for obesity are mild, serious complications have been reported (see below.) The use of weight-loss medications should be combined with physical activity and improved diet to lose and maintain weight successfully over the long term . Using prescription drugs to treat obesity should be used as an option for the following individuals: What Prescription Medicines Are Used to Treat Obesity? Currently, most available weight-loss medications approved by the FDA are for short-term use, meaning a few weeks or months.
Compared with a placebo the new drug increased weight loss and also offered greater improvements in the other outcomes measured, including blood pressure. This study will form part of the manufacturer’s submission to have the drug approved by the US Food and Drug Administration, and the drug company may then submit a similar application for marketing authorisation of this treatment in Europe. The study compared this drug in two different doses to a placebo. The treatments (placebo and the study drug at different doses) were once-daily oral medications that were intended to be taken for 56 weeks alongside standardised counselling for diet and lifestyle modification. Participants were also asked about the use of any other drugs, adverse events and how compliant they had been with their treatments. Both doses of the study drug were more effective than the placebo, resulting in greater weight loss: 6.5kg and 8.8kg more than placebo for the low and high dose treatments, respectively. The drug also improved other outcomes measured, including blood pressure, waist circumference, blood fats and inflammatory markers. The researchers note that the psychiatric adverse events were mainly during the early phase of treatment and they disappeared when the drug was discontinued. The researchers conclude that their drug combining topiramate and phentermine, when given along with lifestyle interventions, could be “added to the limited number of available treatments for obesity”. This large randomised controlled trial describes a study assessing the effects of a new treatment for weight loss in overweight and obese individuals. The manufacturer’s website for this new drug, Qnexa, says that there are three large studies investigating its effects and that together they demonstrate that the drug is effective. If the drug is approved for use in the US, an application to the EU may then follow for consideration of the treatment under European regulations and systems.
Louis Aronne, director of the weight loss program at Weill-Cornell Medical College. Vivus Inc.'s Qnexa is thought to be the most promising of the drugs, achieving the most weight loss. Arena's studies showed that patients taking Belviq, known generically as lorcaserin, had modest weight loss. By comparison, average weight loss with Qnexa is 11 percent, with more than 83 percent of patients losing 5 percent of their weight or more. The FDA said patients should stop taking Belviq after three months if they fail to lose 5 percent of their body weight. Patients are unlikely to see any significant weight loss by staying with the drug. Side effects with the drug include depression, migraine and memory lapses. Experts say the challenge of weight loss drug development lies in safely turning off one of the body's fundamental directives: to eat enough food to maintain its current weight. Belviq is the first new prescription drug approved to treat obesity since Xenical's approval 13 years ago.
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Belviq, the first new prescription drug in years to help people lose weight, is expected to be available in four to six months. For the first time in 13 years, the Food and Drug Administration has approved a new drug to help people lose weight. "The approval of this drug, used responsibly in combination with a healthy diet and lifestyle, provides a treatment option for Americans who are obese or are overweight and have at least one weight-related comorbid condition." The drug was approved for obese people (those with a body mass index of 30 or more) and overweight people with a BMI of 27 or more who also have at least one weight-related health condition, such as high blood pressure, Type 2 diabetes or high cholesterol. The FDA had rejected the drug in 2010 after a panel of experts advised the agency to give it a thumbs down because of safety concerns. Early studies indicated the drug might cause tumors in rats and possibly heart problems in people. But the company submitted new data aimed at alleviating those concerns, and the same panel endorsed approval in May. The FDA hasn't approved a new weight-loss drug since Orlistat came on the market in 1999. The once-popular weight-loss drug Meridia was pulled from the market in 2010 because of concerns about heart attacks and strokes. The FDA had rejected Qnexa in 2010 because of concerns about heart problems and birth defects. Qnexa is a combination of two drugs that are already on the market: phentermine, a stimulant used for short periods to help control weight, and topiramate, which is used for migraines and seizures.
FDA delays decision on latest weight loss pill. Consumers awaiting the latest weight loss pill will have to wait at least another three months. The FDA has delayed a decision that was expected today on the prescription medication Contrave. FDA delays decision on latest weight loss pill Consumers awaiting the latest weight loss pill will have to wait at least another three months. FDA is delaying a decision on the latest prescription weight loss pill, a drugmaker announced Wednesday. Consumers awaiting the latest weight loss pill will have to wait at least three more months. The Food and Drug Administration has delayed a decision that was expected Wednesday on the prescription medication Contrave, drugmaker Orexigen Therapeutics Inc. If approved in September, the drug will be the third new prescription weight loss aid in about two years, joining Qsymia, from Vivus Inc. The company already has submitted interim cardiovascular data from an ongoing study of 8,900 patients — which the FDA requested after it rejected Contrave in 2011. Reasons include costs, low levels of insurance coverage and lingering concerns about the safety of any weight loss drug. Ryan, who has consulted for companies including Vivus, Eisai and Takeda, says the delay from FDA on the latest contender "is not a negative signal, it's a sign that officials at the FDA are taking the review seriously — as they should."
15 photos: Weight loss through history: The good, bad and scary. Weight loss drug Saxenda was approved in December, the latest in the pack of obesity treatments. The most effective weight loss drugs are typically associated with only 5% to 10% loss in body weight. The latest medication to join the pack is Saxenda, the name for liraglutide, which the Food and Drug Administration approved in December. "Some people are more worried about the cosmetics of being obese and they may not be as happy as one could be," Siraj said. Experts consider Qsymia, an oral medication, to be one of the most effective drugs, but it's only associated with between 5% and 10% weight loss among most patients. A recent study found that 33% of participants taking the injectable medication lost more than 10% of their body weight and 63% lost at least 5%. Among the control group, which only received advice about diet and exercise, 11% of participants lost more than 10% of their body weight, and 27% of participants lost at least 5%. Angela Fitch, director of medical weight management at the University of Cincinnati and a diplomat of the American Board of Obesity Medicine. Saxenda is the first in a class of diabetes medications called glucagon-like peptide-1 mimetics to be approved for weight loss. The current study found that the most common side effects of Saxenda were nausea and vomiting. The most serious side effects were pancreatitis and breast cancer, which affected less than 1% of participants in the Saxenda group.
November 25, 2013 10:04 PM By Mary Kay Kleist. Filed Under: Carcinia , diet pill , Georgetown University , Mary Kay Kleist. CBS 2’s Mary Kay Kleist checks out garcinia cambogia. “Everybody’s looking for the magic pill,” says Mike Carlucci, who tried the product. Harry Preuss from Georgetown University studied the extract and says it has “great metabolic effects” that prevents conversion of carbohydrates into fat. “It was very rewarding to see the difference, and I think in moms that’s a big deal when you can lose some of that belly fat,” she says. Because supplements are not all created equal, here’s what to look for: the words garcinia cambogia; at least 50 percent HCA (hydroxycitric acid); potassium (for absorption); and zero fillers, binders or artificial ingredients. Mary Kay Kleist facebook Follow. Mary Kay Kleist is a meteorologist for CBS 2 Chicago.
Once the pill has made its way to your stomach, doctors use the tube to inflate the balloon with gas; the tube is then disconnected and pulled out. The balloon can stay in for up to three months, and you can have up to three balloons in place at a time. The idea is that the balloon(s) simply make you feel full. And while the Obalon is not FDA approved for use in the U. S., since 2012, patients abroad have been swallowing the pill, which has a price tag of up to $4,000 a pop. Resident Helene Fleckney, 45, the Obalon has ended a long struggle with her weight. "It's quick and painless," says Fleckney, who notes that she has lost an additional six pounds since then. Aronne, director of the Center for Weight Management and Metabolic Clinical Research at New York's Weill Cornell Medical College, who is helping to oversee the U. Endo Barrier has been used overseas since 2010 for the treatment of obesity and type II diabetes, conditions that often go hand in hand. For Hale, the procedure was easy, and the only side effect has been a transient tummy-ache. Other possible but unlikely hazards are bleeding, infection, and migration of the device.
Patients and doctors eagerly awaiting FDA approval of the new weight-loss drug Qnexa will have to wait at least another three months. Expected to approve the drug on April 17, the FDA now says it will take another three months to evaluate the risk-reduction plan offered by Vivus in return for approval. And that’s not the only stumbling block to Qnexa approval. But an FDA advisory panel last February voted 20-2 to recommend Qnexa approval before the study is completed, or even under way. A bit tends to get gained back in the second year, but people who stayed on the drug for a second year tended to maintain most of their weight loss. And the FDA may not be particularly worried about Qnexa safety, given the advisory panel’s strong opinion that the drug’s weight-loss benefit appears to outweigh its known risks. The opinions expressed in Web MD Second Opinion are solely those of the User, who may or may not have medical or scientific training. These opinions do not represent the opinions of Web MD. These opinions do not represent the opinions of Web MD Second Opinion are not reviewed by a Web MD physician or any member of the Web MD editorial staff for accuracy, balance, objectivity, or any other reason except for compliance with our Terms and Conditions. Some of these opinions may contain information about treatments or uses of drug products that have not been approved by the U.
The pill was approved Tuesday, July 17, 2012 by the Food and Drug Administration for patients who are overweight or obese and also have at least one weight-related condition such as high blood pressure, diabetes or high cholesterol. WASHINGTON (AP) — A new weight-loss pill that many doctors consider the most effective of a new generation of anti-obesity drugs got the approval of the Food and Drug Administration on Tuesday. The pill, called Qsymia, was approved for patients who are overweight or obese and also have at least one weight-related condition such as high blood pressure, diabetes or high cholesterol. The drug's maker, Vivus Inc., said it plans to bring the drug to market in the fourth quarter of this year. In testing, the drug made led patients to lose more weight than two other weight-loss pills recently review by the FDA. Patients taking Qsymia for a year lost 6.7 percent of their body weight in one study and 8.9 percent in another study, the FDA said. The drug is actually a combination of two older drugs long known to help with weight loss: phentermine and topirimate. Qsymia is the second weight-loss drug approved by the FDA in less than a month, following Arena Pharmaceutical's pill Belviq in late June. Previously the agency had not approved a new drug for long-term weight loss since 1999. Vivus has to do studies of the heart effects of Qsymia, the FDA said.
With more than 36 percent of American adults now classified as obese according to the Centers for Disease Control and Prevention, and the numbers still climbing, doctors are clamoring for more pharmaceuticals to treat their patients. But even as doctors have begun scribbling prescriptions for these new weight loss medications, many dieters remember the long and checkered past of diet drugs in this country. Some drugs that were originally viewed as rock stars for weight loss and appetite control were ultimately pulled off the market after it was found they posed serious health risks. "Once people stopped losing weight they would take more and more of the pills, and this left some feeling racy and agitated with a rapid pulse and high blood pressure," said Dr. By the 1970s, the FDA limited its use for weight loss to short-term treatment only. Riding the wave of the supplement's popularity a similar drug named dexfenfluramine and marketed as Redux was quickly approved by the FDA in 1996. Approved in 1997, the drug was found during clinical trials to increase heart rate and blood pressure. The drug's risks proved not to be worth the benefits: Studies found a 16 percent increase of major cardiac events in patients taking Meridia compared with those who weren't taking the drug, with a negligible difference in weight loss. Done often enough, the drug is not as effective and weight loss is minimal. Belviq is approved for the obese and those who are overweight and have other serious health risks. In clinical trials, the average person lost 3 percent to 3.7 percent of his weight after taking Belviq for a year compared to those taking a placebo. The FDA said patients should stop taking Belviq if they fail to lose 5 percent of their body weight after three months of use. Patients are unlikely to see any significant weight loss by staying on the drug, the agency said. About half of the 4,430 overweight and obese patients in the Qsymia studies on the recommended dosage lost an average of 10 percent of their weight in the first year of taking the drug. We are talking about taking a pill to fix what's busted - the circuitry of the brain that misreads the signals of appetite, fat storage and other factors.
For the third time in about two years, the Food and Drug Administration has approved a new weight loss pill. FDA approves a third new weight-loss pill For the third time in about two years, the Food and Drug Administration has approved a new weight loss pill. To find out more about Facebook commenting please read the Conversation Guidelines and FAQs. FDA has approved a new weight loss pill, the third in about two years. For the third time in about two years, the Food and Drug Administration has approved a new weight-loss pill. All of the new drugs work by decreasing appetite and all have some side effects and drawbacks, though they differ. In Belviq's studies for the FDA, average losses were 3% to 3.7% over placebo; for Qsymia, average losses were 6.7% to 8.9% over placebo. "The ideal candidate for a drug to treat obesity is someone who uses the drug as a tool, along with diet and exercise," says Tsai, who has no ties with drug makers. Adults, 78.6 million, are obese, according the federal Centers for Disease Control and Prevention. Patients filled about 138,000 prescriptions for Qsymia in the second quarter of 2014, according to drug maker Vivus Inc. Prescription numbers for Belviq were about 110,000 in the same period, according to Arena Pharmaceuticals Inc., which makes the drug. That's a lot of room for growth, he says, and having a third drug approved just "gets more voices out there" talking about the pharmaceutical options. In the past, some obesity drugs have been linked to serious heart problems and pulled from the market. The makers of Contrave, Belviq and Qsymia have all agreed to conduct long-term heart safety studies and report the results to FDA.
“Any time you put a foreign object into the gastrointestinal tract, the two big worries are obstruction and rupture,” he says. Then as far as rupture goes, the balloon could push against the wall of your stomach and stretch it or stretch the esophagus. The better option, says Katz, is to skip out on the pill entirely. The first is that it only helps you not each as much—it doesn’t help you eat well. “It’s more important to focus on eating the right foods in the first place to fuel your body, and this balloon pill does not teach you how to do that,” he says. “The lining of the stomach contains regulators that help you feel full .
★ Increases your energy levels. Firstly by suppressing your appetite, it is going to help you feel less hungry and reduce the amount of calories you eat. It will also help to reduce your cravings for foods you know should be avoiding (the ones we all like best – full of sugar and fat!), and because you are less hungry it will be easier for you to make sensible food choices and stick to your diet plan. Next it helps your body to burn fat. It also contains Dendrobium Nobile extract, a natural stimulant, which helps to boost your metabolism and so burn off calories from your food faster. Phen375 will boost your energy to help you make good diet choices, feel better and be able to work out for longer – giving your body the kick start it needs before your weight loss helps your energy levels increase naturally.
On Tuesday, the Food and Drug Administration ( FDA ) approved Qsymia, the second new diet drug in a month, and the most effective of the weight-loss pills that the agency has considered in recent years. (MORE: A Brief History of Diet Pills and the FDA ) The drug is approved for obese adults with a body mass index, or BMI, of 30 or higher. Some doctors have already been prescribing the two drugs together for weight loss. In clinical trials, overweight and obese patients taking Qsymia for a year lost differing amounts of weight: on average, patients taking a middle dose of the drug lost 8.4% of their body weight; on a higher dose, patients lost 10.6%. Most of the weight came off in the first three months, so doctors should monitor patients at that point to see if the drug is working. The FDA notes that people who don’t lose at least 3% of their body weight by three months are unlikely to go on to lose any significant weight, so they should either be counseled to discontinue the drug or to try a higher dose (Qsymia will be available in two doses). If patients still don’t lose at least 5% of their weight after three additional months on the higher dose, they should quit taking Qsymia. The drug is designed to be used in conjunction with traditional weight-management strategies like diet and exercise. Doctors stress that because of the potential risks of the drug, dieters should not use the drug for cosmetic weight loss. It will also be available in specialized pharmacies that register for the right to sell the drug, where pharmacists have been educated about Qsymia’s risks and can pass that information along to patients and doctors. Safety concerns led the FDA to reject Qsymia’s first bid for approval in 2010, but the agency and Vivus have now put in place strategies to reduce risk: for example, women of child-bearing age who want to take Qsymia must test negative for pregnancy before starting the drug and are expected to use contraception and take a pregnancy test once a month while on the drug. People with recent or unstable heart disease or stroke are not recommended to take the drug because of the potential heart risks. Vivus has also agreed to continue monitoring Qsymia users for side effects after the drug reaches market; in particular, it will conduct a long-term cardiovascular outcomes trial to assess the effect of Qsymia on major events like heart attack and stroke. The FDA’s approval of Qsymia, after such a long diet-drug drought and despite the potential safety problems that plague weight-loss pills, marks a willingness to make new solutions available.
Weight-loss drug Belviq is now available by prescription for overweight or obese patients. A new drug, Belviq, is available to overweight and obese patients. The drug received FDA approval nearly a year ago. The FDA approved Belviq, an oral medication, in June 2012. 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." 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. The most common side effects of Belviq in nondiabetic patients included headache, dizziness and fatigue, according to the FDA.