Posted on April 11, 2024 in Defective Products

As a consumer, you trust that your products are safe and will function as intended. Unfortunately, defective products can cause serious injuries, property damage, and financial losses. If a defective product has harmed you, it is essential to understand your legal options and the steps you can take to protect your rights with an Illinois lawyer with decades of experience.

What You Should Know About the Product Liability Law

Product liability law in Illinois allows consumers to hold manufacturers, distributors, and retailers accountable for defective products that cause harm. There are three main types of product defects recognized under Illinois law:

• Design defects: This happens when the design of a product is fundamentally defective, making it excessively hazardous even when utilized as directed.

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 Posted on April 04, 2024 in Personal Injury

Suppose you have taken the prescription medication Elmiron for interstitial cystitis and suffered vision problems or retinal damage. As a result, you may be considering filing a lawsuit against the drug manufacturer. An Illinois lawyer can help guide you on what to expect during the litigation process.

Filing a Complaint

The first step is filing a complaint in the appropriate Illinois court. Your lawyer will draft the complaint, outlining the facts of your case, the legal claims being made (such as failure to warn, design defect, breach of warranty under the Illinois Product Liability Act), and the damages you seek. The complaint is then served on the defendants.

The Discovery Phase

Once the complaint is filed, the discovery phase begins. This involves exchanging relevant information and documents between the plaintiffs and defendants. Your lawyer will request records from the drug manufacturer and may also subpoena third parties. You can expect to answer written interrogatories about your Elmiron usage and injuries. Depositions will also be conducted, where lawyers question parties and witnesses under oath.

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 Posted on March 27, 2024 in Personal Injury

The prescription drug Elmiron, used to treat interstitial cystitis, has recently been the subject of intense legal scrutiny. Numerous plaintiffs have filed lawsuits alleging that long-term use of Elmiron led to vision-related injuries, including a rare and potentially irreversible eye disorder. An Illinois lawyer can help you through your case to ensure you are taking the proper steps.

What the Elmiron Litigation is All About

In the ongoing litigation surrounding the prescription medication Elmiron, it has been revealed that the drug has led to pigmentary maculopathy, a rare and potentially irreversible eye disorder. Manufactured by Janssen Pharmaceuticals, a subsidiary of Johnson & Johnson, Elmiron (pentosan polysulfate sodium) was approved by the FDA in 1996 to treat interstitial cystitis, a chronic bladder condition.

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 Posted on March 25, 2024 in FDA

Interstitial cystitis, a chronic bladder condition, impacts millions of Americans. For years, the prescription medication Elmiron provided relief for many IC patients. However, recent studies have linked the long-term use of Elmiron to serious vision complications like pigmentary maculopathy. This has prompted numerous lawsuits against the drug's manufacturer, Janssen Pharmaceuticals, with the adequacy of Elmiron's safety warnings emerging as a critical issue. An Illinois lawyer can help you understand the role of FDA warnings in Elmiron litigation.

FDA Warnings and Drug Liability

When the U.S. Food and Drug Administration (FDA) approves a drug for consumer use, pharmaceutical companies have a duty to provide proper warnings about potential risks and side effects. Failure to adequately warn patients and doctors can expose drug makers to legal liability under Illinois product liability law.

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 Posted on March 19, 2024 in Medical Malpractice

If you or a loved one has been prescribed the medication Elmiron (pentosan polysulfate sodium) for the treatment of interstitial cystitis and have experienced vision problems or injuries, it is crucial to document your case meticulously. Proper documentation can strengthen your potential legal claim against the drug manufacturers and help you secure the compensation you deserve for your injuries. An Illinois lawyer can make sure you do this properly.

At Newland & Newland, LLP, we have nearly 30 years of experience in injury cases. As a result, our firm is especially qualified to assist clients in even the most complex matters. Clients can feel confident knowing our team of attorneys will always protect their rights.

Gather Medical Records

The foundation of your case lies in your medical records, which serve as objective evidence of your condition and the treatment you have received. Request copies of your complete medical records from all healthcare providers involved in your care, including ophthalmologists, optometrists, primary care physicians, and specialists. These records should detail your diagnosis, prescribed medications (including Elmiron), treatment plans, test results, and any noted vision problems or eye-related injuries.

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 Posted on March 14, 2024 in Acetaminophen

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 Posted on March 14, 2024 in Acetaminophen

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 Posted on March 05, 2024 in Medical Malpractice

As a consumer, you trust that the medications prescribed by healthcare professionals are safe and effective. However, there are instances when pharmaceutical companies release defective drugs that cause serious harm to patients. If this happened to you, an Illinois lawyer can help determine if you have potential grounds to take legal action.

Failure to Warn

A prevalent basis for initiating a defective medication lawsuit is the failure to provide adequate warnings. Pharmaceutical companies bear a legal obligation to furnish comprehensive information regarding the potential risks and adverse effects associated with their medications. This crucial information must be conveyed to healthcare professionals and patients through various means, including labeling, packaging inserts, and other relevant documentation.

The company may be liable if a drug manufacturer neglects to provide sufficient warnings and a patient suffers harm. For example, consider a scenario in which a medication is known to cause severe liver damage, yet the manufacturer fails to include this vital information in the warning label. In such a case, the manufacturer could face legal action in the form of a lawsuit, as their failure to disclose the potential risk directly contributed to the patient’s injuries.

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 Posted on October 16, 2023 in Uncategorized

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 Posted on October 12, 2023 in Acetaminophen

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