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The FDA announced the approval of a new fat loss drug on Sept. 11, 2014. The drug name is Contrave.

Using two separate drugs to shed weight can be very effective you'll find combinations as you're watching FDA now awaiting approval. When dealing with fat loss and the individuals who go through it you need to err along the side of caution and permit the FDA do its job and demand some investigation be done so the public is aware of the side effects and risks of the medications before we take them. Keep in mind that drug companies will be in business to earn money and that they would say almost anything to keep people on the medications.

Researchers discovered that participants using this drug to get a year, lost weight within a month and have kept the extra weight off through the entire 56 weeks of the study. Contrave is really a combination in the drugs naltrexone and bupropion, which seems to reflect a fresh trend of weight-loss drugs which might be made up of many active ingredient, which can make them more effective and safer.

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

Seizures really are a side effect with Contrave and really should not be taken in people 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 last six months. Blood pressure and pulse should also be measured before starting the drug and throughout therapy using the drug.

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

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