Patients worldwide who rely on medications and drugs to help relieve symptoms and control health conditions expect that the products they use will be relatively safe and free of danger. Should a drug have the potential to cause complications, manufacturers are obligated to inform consumers of these risks. However, some drug makers fail to do so, and many have designed and marketed products that have been linked to several severe health conditions and life-threatening side effects.
FDA Drug Approval Process
The U.S. Food and Drug Administration (FDA) exists to ensure that safe products are placed on the market, but the agency has been scrutinized for allegedly allowing several bad drugs to be released without prior testing or investigation into potential side effects. Whether the drug is available by prescription or for sale over the counter, the same rules apply, and manufacturers are often held responsible for the injuries or complications that are allegedly caused by their products.
Although the FDA takes the necessary steps to ensure that safe products are released to the public, it is not always possible to catch every single side effect or complication prior to the drug’s introduction on the market. For this reason, the FDA put the Adverse Event Reporting System into place so that patients could have a way to let the agency know of any adverse effects that they experienced while taking a drug. If the FDA receives an increasing number of reports about one particular medication, it may require a recall or request that the manufacturer further investigate the safety of the product.
Individuals may wish to work with a Colorado bad drug lawyer to pursue claims against manufacturers if they believe they have a case. It is often beneficial to have an experienced Colorado bad drug lawyer in your corner, as most pharmaceutical companies have their own legal teams ready to defend them against claims. A Colorado dangerous drug attorney can fight for you and help to protect your rights.