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A new weight-loss drug made up of anti-addiction drug naltrexone has been approved by the U.S. Food and Drug Administration today, the company said inside a statement.
Using two separate drugs to shed weight can be very effective there are combinations as you're watching FDA now awaiting approval. When dealing with fat loss and the people who go through it you should err on the side of caution and allow FDA do its job and demand some study be done so that the public knows the side effects and risks of the medications before we bring them. Keep in mind that drug companies come in business to earn money and that they would say everything to keep people on the medications.
Researchers found that participants investing in this drug to get a year, dropped excess weight within one month and have kept the weight off through the 56 weeks with the study. Contrave is a combination from the drugs naltrexone and bupropion, which generally seems to reflect a new trend of weight-loss drugs that are made up of more than one active ingredient, which can make them more effective and safer.
Combo-pilling will be the newest fad or better yet the newest in the future under scrutiny and thus it is just more publicly known in recent months, comb-pilling for losing weight has been around since the eighties. The biggest reason that employing a combination of pills is becoming popular will be the fact that since right now there aren't any long term prescription diet pills that have been authorized by the FDA aside from orlistat. The truly disturbing part is that doctors are prescribing these combinations of medications although some people might of the combinations are actually rejected or have yet to be authorized by the FDA.
Seizures can be a side effect with Contrave and must not be taken in those with seizure disorders. The drug also can raise blood pressure and heartbeat, and mustn't be used in individuals with a history of cardiac arrest 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 hypertension and heart rate and must not used in patients with uncontrolled high hypertension, and also by a person with heart-related and cerebrovascular (blood vessel dysfunction impacting your brain) disease. Patients which has a history of heart attack or stroke in the last six months, life-threatening arrhythmias, or congestive heart failure were excluded from the clinical trials. Those taking Contrave must have their heart-rate and pulse monitored regularly. In addition, because the compound includes bupropion, Contrave comes having a boxed warning to alert medical researchers and patients for the increased likelihood of suicidal thoughts and behaviors associated with antidepressant drugs. The warning also notes that serious neuropsychiatric events are already reported in patients taking bupropion for smoking cessation.
Approving a drug with this particular many potentially lethal unwanted effects is inconsistent with the mission statement in the FDA. The power of the drug manufacturing lobby is blatantly evident in the approval of several drugs requiring 'post-marketing' studies which might be clearly significant to overall drug safety in the US.