Prescription & Over-The-Counter Drug Lawsuits

Some patients who have taken Ozempic^® injections, or Wegovy^®, Rybelsus^®, Mounjaro^™, or Saxenda^®, or Trulicity^®, or Zepbound^™ have experienced gastroparesis, persistent vomiting (more than 4 weeks) stomach paralyzed/not working, persistent nausea or diarrhea (more than 4 weeks), and even death.

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Women who developed brain and/or spinal tumors or lesions (called meningiomas) after receiving Depo-Provera or Depo-SubQ Provera 104 injections are filing lawsuits.

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The FDA has warned women that use of Veozah^® (fezolinetant) to treat menopausal hot flashes can cause rare but serious liver injury.

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Pfizer recalled Oxbryta^®, a drug prescribed to treat sickle cell disease, because studies show a higher rate of vaso-occlusion crisis and more deaths among patients taking Oxbryta than those taking a placebo.

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Xeljanz and Xeljanz XR may be prescribed to treat rheumatoid arthritis, psoriatic arthritis, or ulcerative colitis. People who take Xeljanz may be at increased risk for developing cancer or a pulmonary embolism (PE) or deep vein thrombosis (DVT) or experiencing a major cardiac event.

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Testing has shown that generic valsartan manufactured in recent years may be contaminated with two dangerous, cancer-causing chemicals (NDMA or NDEA) due to changes in the manufacturing process.

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Gardasil is an HPV vaccine manufactured by Merck and Co. HPV, or the human papillomavirus, is the most common sexually transmitted infection. People vaccinated with the Gardasil vaccine for HPV who have experienced severe health issues are filing lawsuits.

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Recent testing has shown that Zantac may be contaminated with unsafe levels of the cancer-causing chemical NDMA. Some scientific evidence suggests that the ranitidine molecules in Zantac may decompose into NDMA while in storage or inside the human body after ingestion.

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