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Actemra

Leading Justice is offering limited Actemra advertising and virtual secretarial services for mass tort law firms pursuing an increased case docket of Actemra heart attack and pancreatitis claims. With more than 15 years of experience helping people wronged by Big Pharma, and the staying power of an honest, 100% fraudulent-free business history, Leading Justice has the transparency in advertising to be your partner in building a large Actemra docket. Leading Justice will create and place Actemra media for your buy, screen all Actemra-related contacts according to your case criteria, single sign the client’s claim to your retainer/medical release using the most rigorous security industry certification standards, and send the signed Actemra claim to your intake team for the final screen and medical record retrieval.

If your firm is interested in pursuing Actemra heart attack, stroke, lung disease and pancreatitis claims, Leading Justice can build your docket via our effective advertising and virtual secretarial services. Law firms partnered with Leading Justice know they are working with an honest, transparent advertising shop that will build their Actemra docket with best marketing practices and bar opinions in mind.

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Actemra Contacts

(800) 426-1207

Categories: Actemra, Dangerous Drugs. Tags: actemra, Heart Attack, heart failure, interstitial lung disease, pancreatitis, rheumatoid arthritis, stroke.
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  • Description
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Product Description

Leading Justice is a full-service marketing company working with law firms on a cash buy basis to sign up fully-qualified, fraud-free Actemra cases. Here at Leading Justice, we can customize your firm’s Actemra advertising needs and help you sign up cases via internal cash buys. Our clients simply pay an agency fee to cover the cost of Actemra 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 reviewed to determine whether it is eligible for another type of claim. By using advanced approaches to target contacts specifically related to Actemra use and side effects like heart attack, heart disease and pancreatitis, Leading Justice will increase your firm’s Actemra caseload. If you are interested in helping victims of alleged Actemra side effects, our direct advertising strategies and extensive consumer reach give you the competitive edge and confidence to allocate your full budget, knowing your money is being used in the best way possible.

Each and every law firm we work with at Leading Justice plays an important role in determining how we classify claims as qualified or not. While our experience working with plaintiff law firms helps us recognize a great case when we see one, we will tailor our Actemra case intake specifications to the exact criteria you are seeking. So, if your firm has specific Actemra qualifying case criteria you would like us to use, we can train our intake specialists to apply the criteria to each email and phone call they receive. By eliminating the middle man, Leading Justice offers clients an opportunity for internal cash buys of Actemra data with zero chance of fraud.

Actemra Side Effect Litigation

Actemra (tocilizumab) is a blockbuster prescription medication that relieves joint pain associated with rheumatoid arthritis (RA). Taken intravenously or by injection, Actemra works by inhibiting parts of the immune system that cause inflammation, a hallmark of the autoimmune disease. When Actemra first entered the market in 2010, it was touted by Roche Holding AG as a superior alternative to other rheumatoid arthritis medications, like Humira, Enbrel and Remicade, many of which carry warnings regarding their potential for causing serious cardiovascular problems and other side effects in users. According to a growing body of research, Roche’s Actemra treatment may actually pose a risk of heart-related complications and other adverse events that is as high or even higher than its competitors.

A number of studies and adverse event reports submitted to the FDA by Actemra users have identified a risk of serious side effects potentially linked to the rheumatoid arthritis drug, which has been associated with at least 13,500 reports of health problems and at least 1,128 deaths since 2010. Yet, federal regulators have failed to require new warnings on the Actemra label notifying users about the potential for the rheumatoid arthritis treatment to cause heart attack, heart failure, interstitial lung disease and other side effects that may be life-threatening. As more information comes to light about the serious health risks associated with Actemra, which is prescribed to treat RA and, off-label, up to 60 other conditions, Actemra injury lawsuits are expected to be filed against Roche in the coming months and years.

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