Leading Justice is a full-service marketing company working with law firms on a cash-buy basis to sign up fully qualified, fraud-free Paragard-related injury cases. Here at Leading Justice, we can customize your firm’s Paragard IUD advertising needs and help you sign up cases via internal cash buys. Our clients only pay an agency fee to cover the cost of Paragard advertising, plus a fee for each case we sign, and any data we generate for your firm belongs to you. We also cross-qualify all of our contacts, which means any data we generate that doesn’t qualify for the target campaign is evaluated to determine whether it qualifies for another type of claim. By using advanced approaches to target contacts specifically related to the Paragard IUD and side effects like device fracture, organ perforation, device migration and device expulsion, Leading Justice will increase your firm’s Paragard caseload. If you are interested in helping victims of Paragard IUD side effects and complications, our direct advertising strategies and extensive consumer reach at Leading Justice give you the competitive edge and confidence you need to allocate your full budget, knowing that your money is being used in the best way possible.
Each law firm we work with at Leading Justice plays a crucial role in determining how we categorize claims as qualified or not. And while our experience working with plaintiff law firms allows us to recognize a great case when we see one, we will tailor our Paragard IUD intake specifications to the exact criteria you are seeking. So, if your firm has specific Paragard qualifying case criteria you want us to use, we can train our intake specialists to apply the criteria to each phone call and email they receive. By getting rid of the middle man, Leading Justice offers clients an opportunity for internal cash buys of Paragard IUD injury data with zero chance of fraud.
Paragard IUD Litigation
Paragard is a small, T-shaped copper intrauterine device (IUD) marketed by Teva Pharmaceuticals and The Cooper Companies as a safe and effective form of long-term birth control that is hormone-free, more than 99% effective and completely reversible. Unlike hormonal contraceptive methods, which interfere with the body’s natural cyclical hormones to prevent pregnancy, the copper component of the Paragard IUD is what prevents pregnancy in women who choose this method of birth control. It does so by triggering an inflammatory reaction in the uterus, which in turn inhibits the mobility of sperm and prevents fertilization from occurring. Paragard must be implanted and removed by a healthcare provider and while the device is meant to provide continuous pregnancy prevention for up to 10 years, it can be removed at any time. However, many women have experienced serious side effects and complications after being implanted with the Paragard IUD or during the removal process.
Paragard has been on the market in the United States since 1984, and the contraceptive device is used by more than 200 million women worldwide as an alternative to hormonal contraception. Sadly, many of these women remain completely unaware of the serious and potentially life-threatening injuries they could face if their Paragard IUD migrates out of position, becomes embedded in their uterus, perforates their internal organs or fractures upon removal, among any number of other possible complications. Dozens of women have already filed lawsuits against Teva Pharmaceuticals and The Cooper Companies, alleging that the drug manufacturers misrepresented Paragard as a safe and effective form of birth control and failed to provide patients and healthcare providers with adequate warnings about the potential health risks associated with the Paragard IUD. Most Paragard IUD claims involve women whose birth control devices fractured during removal and left IUD fragments inside their bodies, some requiring a hysterectomy. Other potential plaintiffs in the Paragard IUD litigation include women who experienced allergic reactions, irregular bleeding, infection, chronic pain, ectopic pregnancy, infertility or permanent internal injuries from the Paragard IUD.