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Karl Truman: Trusted Dangerous or Defective Drugs Lawyer Serving Kentucky and Indiana
Offices in Louisville, KY and Jeffersonville, IN
Pharmaceutical companies have a legal and ethical obligation to ensure that the drugs they bring to market are safe and that patients are fully informed of the risks. When they fail, and patients suffer serious harm as a result, the manufacturer can be held liable. A drug that causes heart failure, organ damage, cancer, or birth defects when those risks were known or should have been known is not just a tragedy. It is a legal claim.
Attorney Karl Truman brings the discipline and leadership of a retired Lieutenant Colonel in the U.S. Army to every dangerous drug case. We work with a network of attorneys who have the experience and resources to take on large pharmaceutical companies and their legal teams.
Our network of legal teams handles:
- Prescription drugs with undisclosed or inadequately warned risks of serious side effects
- Drugs pulled from the market after causing widespread patient harm
- Off-label marketing of drugs for uses not approved by the FDA
- Generic drug defects including contamination and manufacturing failures
- Over-the-counter drugs causing serious harm when used as directed
- Drugs causing birth defects when taken during pregnancy without adequate warning
No fees unless we win. Available 24/7 throughout Louisville, Southern Indiana, and all of Kentucky and Indiana.
Count on the Colonel
Retired Lt. Colonel, U.S. Army
Karl Truman: Trusted Dangerous or Defective Drugs Lawyer Serving Kentucky and Indiana
Understanding Dangerous or Defective Drugs
Dangerous drug cases fall into three categories. Design defect cases argue the drug’s formula or composition is inherently dangerous even when manufactured correctly. Manufacturing defect cases involve contamination or deviation from the approved formula in the production process. Failure to warn cases, the most common, argue that the manufacturer knew of serious risks and failed to adequately disclose them in the labeling or prescribing information.
The FDA approval process does not protect manufacturers from liability. Pharmaceutical companies have an ongoing duty to update their drug labeling when new safety information emerges. When they delay those updates, suppress adverse study results, or aggressively market drugs while downplaying known risks, they become liable for the harm that follows.
Many dangerous drug cases become mass tort litigation when large numbers of patients are harmed by the same drug. The firm’s Mass Tort Trial Lawyers Top 25 credential reflects Karl Truman’s experience in this specific area of high-complexity litigation.
Why Dangerous or Defective Drugs Cases Are Different
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Failure to Warn
Drug labeling must accurately reflect known risks. When a manufacturer knows a drug causes serious side effects and buries that information or fails to update the label, failure to warn liability attaches.
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Suppressed Research
Pharmaceutical companies sometimes conduct or commission studies that reveal dangerous effects and then suppress or selectively publish the results. Discovery in litigation can expose this conduct.
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Off-Label Promotion
Marketing a drug for unapproved uses while suppressing safety data related to those uses is a distinct basis for product liability and, in some cases, fraud claims.
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4
Mass Tort Experience
Karl Truman holds a Mass Tort Trial Lawyers Top 25 credential. Our firm understands how to navigate both individual dangerous drug claims and large-scale mass tort litigation.
How We Handle Dangerous or Defective Drugs Cases
From the moment you call, we take over the legal fight. You focus on recovery. We handle everything else.
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Thorough Investigation
We move immediately to build the strongest possible case: gathering records, securing evidence, consulting experts, and documenting every aspect of your situation before anything is lost or altered.
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Handle All Paperwork
From insurance claims to medical records, legal filings, and demand letters, we manage every detail so you can focus on healing. You will never be left wondering what is happening with your case.
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Fight for What You Deserve
The party on the other side of your claim has professionals working to minimize what they pay you. We deal with them directly and protect you from every tactic designed to undervalue your claim.
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Trial-Ready Representation
While most cases settle, we prepare every case for trial. The other side knows we will not back down, and that gives us the leverage to secure maximum compensation.
Frequently Asked Questions
Comprehensive answers about personal injury law in Kentucky and Indiana. Find the information you need to make informed decisions about your case.
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Can I sue a drug company if my doctor prescribed the drug?
Yes. Pharmaceutical companies have an independent duty to warn physicians and patients of known drug risks through accurate labeling and prescribing information. If the manufacturer failed to adequately disclose known risks, you may have a claim against the manufacturer regardless of your prescribing physician’s role.
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What if the drug was FDA approved?
FDA approval does not eliminate manufacturer liability. The manufacturer has an ongoing obligation to update labeling as new safety data emerges. Approval based on incomplete or manipulated clinical data, failure to update labels when new risks are identified, and off-label promotion are all bases for claims against approved drugs.
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How do I prove my injury was caused by the drug?
This requires expert testimony from pharmacologists and physicians who can establish the drug’s known effects, the patient’s exposure history, and the causal link to the specific harm suffered. We handle this entirely.
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How long do I have to file a dangerous drug claim?
In Kentucky, generally one year from injury or discovery. In Indiana, generally two years. Drug cases involving ongoing harm or latent injuries may have discovery rule extensions. Contact us immediately to know how these deadlines affect your claim.
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Should I join a class action or file individually?
It depends on your specific injuries and the litigation landscape for the drug at issue. Class action settlements distribute fixed amounts among large groups of plaintiffs, which often results in lower individual recoveries. Individual claims can produce higher compensation but require more resources. We evaluate both and give you an honest assessment.
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How much does a dangerous drug attorney cost?
Nothing upfront. We work on contingency and advance all expert and litigation costs. You pay nothing unless we win.
Still Have Questions About Your Dangerous or Defective Drug Case?
Get personalized answers from Colonel Karl Truman and our experienced legal team during your free consultation.
Serving Personal Injury Victims Across Kentucky & Indiana
Karl Truman Injury Law represents clients in Louisville, Jeffersonville, Lexington, Bowling Green, Owensboro, Covington, and throughout Kentucky and Indiana. We handle car accidents, truck accidents, motorcycle accidents, slip and fall cases, medical malpractice, workers’ compensation, wrongful death, dog bites, premises liability, and all types of personal injury claims. Available 24/7 for free consultations.
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Count on the Colonel
Take the first step toward justice. Contact The Colonel today for a no-obligation case review and experience the difference disciplined authority makes.