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A new weight-loss drug which contains anti-addiction drug naltrexone has been approved by the U.S. Food and Drug Administration today, the agency said inside a statement.

Using two separate drugs to shed pounds can be very effective there are combinations before the FDA now awaiting approval. When dealing with fat loss and the those who go through it you should err assisting caution and permit the FDA do its job and demand some study be done so that the public understands the side effects and dangers of the medications before we take them. Keep in mind that drug companies are in business to generate income and that they would say anything to keep people on their own medications.

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

Combo-pilling will be the newest fad or better yet the newest ahead under scrutiny and thus it is just more publicly known recently, comb-pilling for losing weight has been around since the eighties. The biggest reason that utilizing a combination of pills has become popular could be the fact that at the time of right now there are no long term prescription weight loss supplements that have been approved by the FDA other than orlistat. The truly disturbing part is always that doctors are prescribing these combinations of medications although some people might of the combinations happen to be rejected or have yet to be authorized by the FDA.

Seizures can be a side effect with Contrave and must not be taken in individuals with seizure disorders. The drug also can raise blood pressure levels and heartrate, and must not be used in those with a history of heart attack or stroke in the earlier six months. Blood pressure and pulse should also be measured before beginning the drug and throughout therapy using the drug.

The FDA also warned that Contrave can raise blood pressure and heartbeat and must not be used in patients with uncontrolled high blood pressure levels, along with by anyone with heart-related and cerebrovascular (circulation system dysfunction impacting the mind) disease. Patients with a history of cardiac arrest or stroke in the previous 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, since compound includes bupropion, Contrave comes having a boxed warning to alert physicians and patients on the increased chance of suicidal thoughts and behaviors connected with antidepressant drugs. The warning also notes that serious neuropsychiatric events are already reported in patients taking bupropion for quitting smoking.

Approving a drug using this many potentially lethal unwanted side effects is inconsistent with the mission statement of the FDA. The power with the drug manufacturing lobby is blatantly evident inside approval of countless drugs requiring 'post-marketing' studies which are clearly significant to overall drug safety inside the US.
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