Dangerous Drug Lawyer in Los Angeles: Former Insurance Defense Attorneys
Legal help for people injured by a prescription drug, over-the-counter medication or medical device that was defective or sold without adequate warnings.
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At a Glance
- What it is: an injury claim over a drug or medical device, which may involve a manufacturing defect, inadequate warnings or negligence.
- Where we help: Los Angeles, Santa Monica, Beverly Hills, Culver City, Pasadena and the rest of Los Angeles County.
- Why us: David Lederer and John Nojima spent years defending insurers and know how these defenses are built.
- Proof: rated 4.5 stars from 41 Google reviews, with verified results on our case results page.
- Next step: call (310) 312-1860 for a free consultation. No fee unless we win.
Quick Answer
A drug or medical device claim can arise from a manufacturing defect, from inadequate warnings about risks the manufacturer knew or could reasonably have known, or from negligence. In California the duty to warn about a prescription drug usually runs to the prescribing doctor (the learned intermediary rule). Most claims have a two-year deadline, but the clock can depend on when you discovered or should have discovered the connection, so a recall or news report does not mean time is unlimited.
Dangerous drug lawyer in Los Angeles from Lederer & Nojima is for patients who developed a serious injury after taking a prescription drug or using a medical device and want to know whether the product or its warnings were to blame, so you can decide on a claim before the deadline passes.
Drug and device injury claims are product liability claims. The usual theories are a manufacturing defect (this batch or unit was made wrong), a failure to warn (the risks were not disclosed to doctors and patients in time) and negligence. California limits design defect claims against prescription drug makers, and federal law can restrict some claims, so the theory has to fit the product. A claim can reach the manufacturer, and in some situations a distributor or other company in the chain.
These cases are document-heavy and technical. They turn on clinical trial data, adverse event reports, FDA submissions and label changes, the medical records showing when the medication was taken and what happened next, and sometimes on whether a brand-name or generic manufacturer is involved, because different legal rules apply to each. Some injuries are part of larger consolidated litigation. Which path fits depends on the product and your facts.
David Lederer and John Nojima spent years defending insurers. They know how a defendant's lawyers approach a case that depends on expert testimony and large volumes of records, and they decide early whether a claim is worth bringing.
Former Insurance Defense
David Lederer and John Nojima used to defend insurers. Now they use that knowledge to pressure carriers that try to delay, discount, or deny injury claims.
No Fee Unless We Win
You pay no upfront attorney fee. Our attorney fee comes from the recovery. If we do not recover, there is no attorney fee, and the written agreement explains how case costs are handled.
Free Consultation 24/7
Call any time after an injury. We can protect evidence, deal with insurers, and explain your next move before deadlines pass.
What do we look for first in a dangerous drug case?
Keep the evidence
Hold on to pill bottles, packaging, lot numbers, pharmacy receipts, instructions and any device itself. Do not throw away a device that was removed.
Medical timeline
We reconstruct when the drug was prescribed, the dose, when symptoms began and what your doctors knew. That timeline ties the injury to the product.
What the label said
Whether the manufacturer warned doctors of the risk, and when, is often the center of the case. We compare the label history with what was known.
Deadlines
The discovery rule can start the clock when you knew, or reasonably should have suspected, that the drug caused the harm, but how it applies depends on the claim and the facts. We calculate it early so a good claim is not lost.
What does California law say about defective drug claims?
California recognizes several product liability theories, but a prescription drug maker is generally not strictly liable for a design defect, so manufacturing defects, warnings and negligence are analyzed separately. For prescription drugs and devices, courts apply the learned intermediary doctrine, so the manufacturer's duty to warn generally runs to the physician rather than directly to the patient. Federal law also affects what a manufacturer must do, especially for generic drugs, so the type of product matters.
Most personal injury and wrongful death lawsuits have a two year filing period under Code of Civil Procedure section 335.1, but accrual rules, exceptions and claims against public entities can change the applicable deadline. When the injury or its cause was not reasonably discoverable, the discovery rule can change when the clock starts. Because that analysis is fact-specific, speak with a lawyer rather than assuming you have time.
What can a dangerous drug claim recover?
- Medical bills and the cost of treating the injury
- Future medical care and monitoring
- Lost income and lost earning capacity
- Pain, suffering and loss of enjoyment of life
- Wrongful death damages when a drug injury is fatal
- In some cases, punitive damages where a company knowingly hid a risk
What should I do if I think a drug or device hurt me?
- 1
Talk to your doctor before you stop a prescribed medication
Some medications are dangerous to stop suddenly. Get medical advice first, and get the injury documented.
- 2
Keep the product and the paperwork
Save the medication, packaging, lot numbers, receipts, patient information sheets and any recall or safety notices.
- 3
Get your records
Request medical records and pharmacy records that show prescriptions, doses and dates.
- 4
Report it
You can report an adverse reaction to the FDA through its MedWatch program. A report does not replace a legal claim.
- 5
Call Lederer & Nojima
We can review your records, explain whether a claim looks viable and protect the deadlines. The consultation is free.
Frequently Asked Questions
How much does it cost to hire Lederer & Nojima?
What is a dangerous drug claim?
Do I need a recall to have a claim?
Can I sue if my drug was a generic?
Where is the Lederer & Nojima office?
Our office is at 12100 Wilshire Boulevard, Suite 480, Los Angeles, CA 90025. Call (310) 312-1860 to schedule a free consultation, or see our Google Business Profile for directions and reviews.
Legal references
General information, not legal advice. Primary sources for the rules described on this page:
- California Supreme Court: Brown v. Superior Court
- Judicial Council of California: CACI civil jury instructions (PDF)
- California Code of Civil Procedure section 335.1
- California Supreme Court: T.H. v. Novartis Pharmaceuticals Corp.
- California Civil Code section 1431.2
- California Code of Civil Procedure section 377.60
- California Civil Code section 3294
- fda.gov: medwatch fda safety information and adverse event reporting program
Related Practice Areas
Lederer & Nojima, LLP
12100 Wilshire Boulevard, Suite 480, Los Angeles, CA 90025
(310) 312-1860
Results may vary. Every case is unique. This page is general information, not legal advice.
Hurt by a drug or device? Call Lederer & Nojima.
Former insurance defense attorneys. No fee unless we win.