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Prescription & Over-The-Counter Drug Lawsuits

Gastroparesis and stomach issues Ozempic.

Some patients who have taken Ozempic® injections, or Wegovy®, Rybelsus®, Mounjaro, Saxenda®, Trulicity®, Zepbound® or Victoza® 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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Hearing loss and tinnitus Tepezza.

Numerous studies link Tepezza, the thyroid eye disease treatment, to hearing loss and tinnitus (ringing in the ears).

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Depo-Provera brain and spinal tumors.

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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Veozah liver injury.

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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Oxbryta vaso-occlusive crisis events.

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 lawsuit information

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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Valsartan high blood pressure medication and potential cancer risks.

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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Side effects of Gardasil vaccination.

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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Woman with heartburn.

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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