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A new weight-loss drug which has anti-addiction drug naltrexone has become approved by the U.S. Food and Drug Administration today, the company said in the statement. Using two separate drugs to shed pounds can be very effective you can find combinations while watching FDA now awaiting approval. When dealing with weight reduction and the people who go through it you need to err along the side of caution and permit the FDA do its job and demand some research be done in order that the public is aware of the side effects and risks of the medications before we drive them. Keep in mind that drug companies will be in business to generate income and that they would say anything to keep people on their medications. Researchers found that participants investing in this drug for the year, lost weight within a month and have kept the extra weight off through the entire 56 weeks of the study. Contrave is often a combination in the drugs naltrexone and bupropion, which seems to reflect a new trend of weight-loss drugs which are made up of multiple active ingredient, which may make them more effective and safer. Combo-pilling will be the newest fad or also the newest to come under scrutiny and for that reason it is just more publicly known in recent months, comb-pilling for weight loss has been around since the eighties. The biggest reason that utilizing a combination of pills is now popular is the fact that at the time of right now there aren't long term prescription slimming capsules that have been licensed by the FDA other than orlistat. The truly disturbing part is always that doctors are prescribing these combinations of medications and some of the combinations are actually rejected or have yet to be licensed by the FDA. Seizures certainly are a side effect with Contrave and mustn't be taken in those with seizure disorders. The drug could also raise blood pressure level and heartrate, and must not be used in people with a history of heart attack or stroke in the last six months. Blood pressure and pulse should also be measured before starting the drug and throughout therapy with all the drug. The FDA also warned that Contrave can raise hypertension and pulse rate and must stop used in patients with uncontrolled high blood pressure level, and also by you aren't heart-related and cerebrovascular (circulation dysfunction impacting the brain) disease. Patients with a history of cardiac event or stroke in the earlier six months, life-threatening arrhythmias, or congestive heart failure were excluded from the clinical trials. Those taking Contrave really should have their heart-rate and pulse monitored regularly. In addition, since compound includes bupropion, Contrave comes with a boxed warning to alert physicians and patients to the increased probability of suicidal thoughts and behaviors associated with antidepressant drugs. The warning also notes that serious neuropsychiatric events happen to be reported in patients taking bupropion for quitting smoking. Approving a drug with this particular many potentially lethal unwanted effects is inconsistent with the mission statement with the FDA. The power of the drug manufacturing lobby is blatantly evident in the approval of many drugs requiring 'post-marketing' studies which might be clearly significant to overall drug safety in the US.