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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 in the statement.
Using two separate drugs to shed pounds can be very effective there are combinations as you're watching FDA now awaiting approval. When dealing with weight loss and the those who go through it you need to err along the side of caution and allow the FDA do its job and demand some study be done so the public is aware of the side effects and dangers of the medications before we take them. Keep in mind that drug companies are in business to earn money and that they would say everything to keep people on their medications.
Researchers found that participants taking this drug for any year, dropped a few pounds within four weeks and have kept the load off through the entire 56 weeks of the study. Contrave can be a combination with the drugs naltrexone and bupropion, which seems to reflect a whole new trend of weight-loss drugs which are made up of more than one active ingredient, which may make them more efficient and safer.
Combo-pilling will be the newest fad or better yet the newest ahead under scrutiny and therefore 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 by using a combination of pills is now popular is the fact that as of right now there aren't long term prescription diet pills that have been approved by the FDA other than orlistat. The truly disturbing part is always that doctors are prescribing these combinations of medications however some of the combinations happen to be rejected or have yet to be licensed by the FDA.
Seizures certainly are a side effect with Contrave and shouldn't be taken in those with seizure disorders. The drug may also raise blood pressure levels and heartrate, and shouldn't be used in people with a history of heart attack or stroke in the last six months. Blood pressure and pulse should also be measured before starting the drug and throughout therapy with all the drug.
The FDA also warned that Contrave can raise blood pressure level and heartbeat and must stop used in patients with uncontrolled high blood pressure levels, in addition to by you are not heart-related and cerebrovascular (circulation dysfunction impacting mental performance) disease. Patients with a history of cardiac arrest or stroke in the earlier six months, life-threatening arrhythmias, or congestive heart failure were excluded from your clinical trials. Those taking Contrave must have their heart-rate and pulse monitored regularly. In addition, since compound includes bupropion, Contrave comes using a boxed warning to alert medical professionals and patients to the increased chance 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 stop smoking.
Approving a drug using this type of many potentially lethal unwanted effects is inconsistent using the mission statement with the FDA. The power of the drug manufacturing lobby is blatantly evident within the approval of several drugs requiring 'post-marketing' studies that are clearly significant to overall drug safety in the US.