What Are FDA Warnings Supposed to Warn About?

The Food and Drug Administration is the federal agency in charge of monitoring any food or medications that are sold in the United States. This agency has the power to issue warnings for certain drugs that may pose a threat to the safety of American consumers. However, some patients may not be sure why these warnings are produced or why their physicians haven’t taken action to follow the warnings.

If you’ve suffered because of a dangerous prescription, you may be entitled to pursue compensation for your injuries. For more information about how we may be able to help you with these claims, contact the Philadelphia medical malpractice lawyers of Lowenthal & Abrams, P.C., today by calling 215-238-1130.

The Purpose Behind FDA Warnings

A doctor should pay close attention to the warning labels and literature provided by the FDA. Ignoring this information or delaying action on changing a prescription can have serious consequences for a patient’s health. These warnings are provided in the following instances to better inform doctors and patients about what health risks certain drugs may include:

• If a drug can lead to severe side effects
• If a patient taking a drug should be monitored more closely
• If a drug becomes dangerous when taken with other drugs or chemicals
• If a drug particularly affects certain types of patients

If a physician ignores these warnings or takes too long to move a patient off of a dangerous drug, that patient may develop serious health conditions as a result.

Contact Us

If a doctor’s mistakes when prescribing a potentially dangerous medication have cost you your good health, we may be able to help you file for financial compensation. To learn more about your legal options, contact the Philadelphia medical malpractice attorneys of Lowenthal & Abrams, P.C., at 215-238-1130 today.