If you are ill or coping with a protracted illness, odds are that you will be prescribed drugs by your physician to aid in your recovery. To get more info about tasigna lawsuit you may head to http://www.tasignalawsuit.com/tasigna-lawsuits.aspx.
Prescription drugs in the USA are regulated by the Food and Drug Administration, and in almost all instances, a prescription medication can't be sold until it's been thoroughly researched by the Administration. Regrettably, some prescription medications are found to do more harm than good, even after being accepted by the FDA.
Why Does This Happen?
There are a number of motives that prescription medication might wind up causing more damage than good, such as rivalry within the biotech sector. Since drug makers are usually in a rush to rush their latest medication to market, researchers and doctors may cut corners when testing and developing their drugs.
This may then result in unforeseen side effects and much more. Additionally, deceptive marketing and advertising practices may result in over-prescribing and over-use of particular drugs.
In the end, supervision on the part of the Food and Drug Administration may result in medication not being properly screened before individuals start taking them.
Bad Drugs and the Law
As a consequence of poor drugs, drug companies are now seeing more suits than related to problems with prescription medication.
By way of instance, there are medications which are supposed to decrease the chance of stroke and blood clots which have been in the information recently because of their potential dangers of causing internal bleeding.