Levaquin and Cipro Lawsuit

Levaquin and Cipro Lawsuit

A Levaquin and Cipro lawsuit can claim that a particular drug caused serious health problems in its patients. Cipro and Levaquin were prescribed without warning. In addition, the lawsuit alleges that the manufacturers ignored MedWatch reports, pharmacovigilance reviews, hundreds of reports from patients and other sources, and the Cipro and Levaquin labels. This negligence led to prescriptions without warning.

Stevens-Johnson syndrome

Several lawsuits have been filed against drug companies, alleging that generic drugs can cause the onset of SJS. In one of these cases, a family filed a lawsuit against Johnson & Johnson for failing to warn about the risk of SJS after their daughter began taking Children’s Motrin. The US Supreme Court denied Johnson & Johnson’s appeal. Despite the lawsuit’s success, however, other lawsuits have been filed against pharmaceutical companies for failing to warn their customers about the dangers of generic drugs.

The onset of SJS symptoms typically occurs between four and 28 days after the drug is taken. The symptoms include flu-like symptoms, fever, rash, and severe peeling of the skin. In severe cases, a person may experience a life-threatening infection or lose part of his or her skin. Some people have even suffered scarring to major organ systems. As the number of cases rises, so too do the lawsuits against these manufacturers.


In an Aneurism lawsuit against Levaquin or Cipro, patients can seek compensation for the side effects they experienced from taking the drug. These antibiotics have been linked to aneurysms, a potentially life-threatening condition. While the drug manufacturers were aware of the potential side effects, they failed to warn doctors and patients of them. Further, they failed to provide reasonable warnings about their products.

This type of case is known as a bellwether case because it allows lawyers to test legal arguments and set the stage for future litigation. The drug manufacturer, Ortho-McNeil-Janssen Pharmaceuticals Inc., failed to properly warn consumers of the risks of Levaquin. The drug manufacturer, Janssen Pharmaceuticals, has since stopped selling the drug. However, some unexpired tablets may remain on the market until September 30, 2020.


The Levaquin and Cipro manufacturers, Johnson & Johnson, Vistakon Pharmaceuticals, and Bayer/Schering, are facing a growing number of tendon injuries related to their antibiotics. The two brands are used to treat a wide variety of infections, including respiratory, skin, and urinary tract infections. Despite their widespread use and popularity, they have been linked to serious health risks, including tendons and neuropathy. The lawsuits allege that the makers of the drugs knew of the dangers of their products by 1996, but failed to warn consumers. This is one of the most recent instances of a mass tort docket involving Levaquin and Cipro.

Several organizations have taken action against the companies in response to these cases, including Public Citizen. The public advocate group filed a lawsuit in January 2008, which prompted the FDA to issue a black box warning for fluoroquinolone antibiotics. The FDA has since made it clear that Levaquin can lead to tendon rupture, which is considered an unnecessary side effect. Additionally, the drug may worsen symptoms of myasthenia gravis, which can be life-threatening and require ventilator support.

Gross negligence

Many patients have filed legal claims against the manufacturers of Cipro and Levaquin alleging misconduct and defective testing methods. Pharmaceutical companies must develop safe and effective drugs, and these manufacturers failed to do so in the case of fluoroquinolone medications. Hundreds of lawsuits have been settled, and several proposed class actions have been filed. One case has been settled out of court by a former FDA commissioner.

The lawsuits are based on the fact that both Levaquin and Cipro fail to warn patients of the risk of an aortic aneurysm. The drug companies knew that the drugs carried the risk of aortic dissection, but failed to warn patients and physicians about it. They also failed to give reasonable warnings to physicians and patients. Because of these failures, patients are suffering as a result.


If you are suffering from side effects caused by the use of the antibiotics Levaquin and Cipro, you may be entitled to file a legal claim for monetary damages. The pharmaceutical companies responsible for the creation of these drugs, Bayer, Johnson & Johnson, and Merck & Co, have agreed to settle the lawsuits. These companies also manufacture the antibiotic Avelox, which is marketed under the brand name Cipro.

Despite these risks, drug manufacturers failed to adequately warn patients and healthcare providers about the side effects of these drugs. According to these lawsuits, Cipro and Levaquin manufacturers knew the risks but failed to disclose them to the public, causing thousands of patients to develop serious side effects. In addition to the failure to warn, the drug manufacturers also failed to comply with their laws and regulations. Even though these two types of medications have been approved by the FDA, the companies ignored the numerous reports and safety warnings.

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