Drugs with deadly or dangerous side effects often make it to the market because their potential dangers were not anticipated during clinical trials. These drugs are classified as defective drugs and have been identified by the FDA as having dangerous side effects that may outweigh whatever benefits they may have. Such an FDA classification often leads to drug recalls, personal injuries and lawsuits against drug companies.
Heninger Garrison Davis has successfully represented over 8,000 individuals who have been injured by defective drugs and devices over the past 5 years, resulting in settlements of over $190 million. Our attorneys are on the cutting edge of investigating and litigating these types of cases, the result of which is that we routinely get premium values for our cases.