When your doctor prescribes a prescription drug, you assume that it will improve your overall level of health.
Unfortunately, there are times when dangerous prescription drugs make their way to market. If this happens, a large number of patients are put in a risky position.
Generally speaking, the FDA and manufacturers make recall decisions based on a number of factors. Of course, the health of the public is always the most important thing.
Here are some of the most common reasons for issuing a prescription drug recall:
-- Potential for health problems to develop. It goes without saying that a prescription drug is supposed to improve a person's health. If this isn't the case, if the drug could cause more harm than good, it's taken off the market.
-- Previously unknown drug interactions. In short, this means that the drug can cause a health problem when taken with another.
-- Manufacturing errors. This has nothing to do with the safety of the actual drug. Instead, it's all about mistakes made during the manufacturing process. For example, a particular batch of the drug could be contaminated, thus making it unsafe.
There are times when prescription drugs are recalled before anyone is harmed. Conversely, there are times when the FDA and manufacturer don't act in a timely manner, thus harming a large group of people.
If you think you've become ill due to a dangerous prescription drug, it's important to receive immediate medical treatment. Along with this, you'll want to learn more about your legal rights, as someone, such as the manufacturer, may be responsible for your illness and other damages.
Source: FindLaw, "Why Drugs Get Pulled from the Market," accessed Nov. 28, 2016