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  • The Food and Drug Administration, FDA, has approved the drug Vivitrol for the treatment of opioid dependence as outlined by a news release by them on 10-12-2010.

    Using two separate drugs to lose weight naturally can be very effective you'll find combinations before the FDA now awaiting approval. When dealing with fat loss and the people who go through it you should err to the side of caution and allow the FDA do its job and demand some study be done so that the public knows the side effects and hazards of the medications before we bring them. Keep in mind that drug companies are in business to earn money and that they would say almost anything to keep people on their medications.

    Researchers discovered that participants taking this drug for any year, lost excess weight within four weeks and have kept the extra weight off through the entire 56 weeks of the study. Contrave is a combination from the drugs naltrexone and bupropion, which seems to reflect a whole new trend of weight-loss drugs which can be made up of multiple active ingredient, which might make them more efficient and safer.

    Combo-pilling may be the newest fad or also the newest into the future under scrutiny and for that reason it is just more publicly known although in the past, comb-pilling for weight reduction has been around since the eighties. The biggest reason that utilizing a combination of pills is becoming popular could be the fact that at the time of right now there are not any long term prescription weight loss supplements that have been approved by the FDA apart from orlistat. The truly disturbing part is doctors are prescribing these combinations of medications however some of the combinations have been rejected or have yet to be approved by the FDA.

    Seizures certainly are a side effect with Contrave and really should not be taken in those with seizure disorders. The drug could also raise blood pressure level and pulse rate, and shouldn't be used in people who have a history of cardiac event or stroke in the earlier six months. Blood pressure and pulse should also be measured before commencing the drug and throughout therapy with all the drug.

    The FDA also warned that Contrave can raise blood pressure level and heartbeat and must not be used in patients with uncontrolled high blood pressure levels, in addition to by anyone with heart-related and cerebrovascular (circulation system dysfunction impacting the brain) disease. Patients having a history of cardiac arrest or stroke in the last six months, life-threatening arrhythmias, or congestive heart failure were excluded in the clinical trials. Those taking Contrave really should have their heart-rate and pulse monitored regularly. In addition, because the compound includes bupropion, Contrave comes having a boxed warning to alert medical professionals and patients on the increased probability of suicidal thoughts and behaviors related to antidepressant drugs. The warning also notes that serious neuropsychiatric events are actually reported in patients taking bupropion for stopping smoking.

    Approving a drug using this type of many potentially lethal unwanted effects is inconsistent using the mission statement of the FDA. The power of the drug manufacturing lobby is blatantly evident within the approval of several drugs requiring 'post-marketing' studies which might be clearly significant to overall drug safety within the US.

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