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A new weight-loss drug that contains anti-addiction drug naltrexone may be approved by the U.S. Food and Drug Administration today, the agency said in the statement.
Using two separate drugs to shed pounds can be very effective there are combinations in front of the FDA now awaiting approval. When dealing with weight loss and the individuals who go through it you ought to err assisting caution and permit the FDA do its job and demand some research be done so that the public knows the side effects and perils associated with the medications before we bring them. Keep in mind that drug companies are in business to generate money and that they would say everything to keep people on their own medications.
Researchers found that participants taking this drug for a year, dropped a few pounds within one month and have kept the body weight off during the entire 56 weeks with the study. Contrave can be a combination in the drugs naltrexone and bupropion, which generally seems to reflect a brand new trend of weight-loss drugs that are made up of many active ingredient, which may make them more potent and safer.
Combo-pilling is the newest fad or better yet the newest in the future under scrutiny and therefore it is just more publicly known although in the past, comb-pilling to lose weight has been around since the eighties. The biggest reason that employing a combination of pills is starting to become popular will be the fact that since right now there aren't any long term prescription weight loss supplements that have been approved by the FDA apart from orlistat. The truly disturbing part is that doctors are prescribing these combinations of medications although some people might of the combinations happen to be rejected or have yet to be licensed by the FDA.
Seizures really are a side effect with Contrave and must not be taken in people who have seizure disorders. The drug could also raise blood pressure level and heartbeat, and really should not be used in individuals with 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 and heart rate and must 't be used in patients with uncontrolled high blood pressure levels, and also by anyone with heart-related and cerebrovascular (circulation system dysfunction impacting the mind) disease. Patients which has a history of cardiac event or stroke in the earlier six months, life-threatening arrhythmias, or congestive heart failure were excluded in the clinical trials. Those taking Contrave needs to have their heart-rate and pulse monitored regularly. In addition, considering that the compound includes bupropion, Contrave comes with a boxed warning to alert medical researchers and patients for the increased chance of suicidal thoughts and behaviors connected with antidepressant drugs. The warning also notes that serious neuropsychiatric events have been reported in patients taking bupropion for smoking cessation.
Approving a drug with this many potentially lethal unwanted side effects is inconsistent with the mission statement in the FDA. The power in the drug manufacturing lobby is blatantly evident in the approval of numerous drugs requiring 'post-marketing' studies that are clearly significant to overall drug safety inside US.
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