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Zantac Lawsuit

Class action lawsuits have been filed against drug manufacturers Sanofi-Aventis and Boehringer Ingelheim Pharmaceuticals. The lawsuits claim the companies knew or had reason to know that Zantac exposes users to harmful quantities of NDMA when ingested. Patients who have taken Zantac will be filing more lawsuits against the manufacturers. Those who may be eligible to file a Zantac lawsuit include people who regularly took Zantac OTC or prescription for at least 60 days and were diagnosed with a form of cancer.

The removal of Zantac and other ranitidine products from the market will encourage more patients and consumers to take legal action against ranitidine drug manufacturers.

FREE CLAIM REVIEW

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Did you ingest Zantac (Ranitidine)?

Did you take the brand or generic form of Zantac (Ranitidine)?

Were you diagnosed with cancer?

If so, which type of cancer were you diagnosed with? (Please check all that apply.)

Please provide details.

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Last Name

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ZANTAC HEALTH ISSUES

Serious Side Effects

NDMA exposure

Coughing up green or yellow mucus

Easy bruising or bleeding

Fast or slow heartbeat

Vision problems

Yellowing of the eyes or skin

Dark urine

Clay-colored stools

Zantac Linked to These Cancers

Bladder Cancer

Colorectal Cancer

Esophageal Cancer

Lung Cancer

Liver Cancer

Pancreatic Cancer

Stomach Cancer

WHAT PATIENTS SHOULD KNOW

All ranitidine medications are being removed from the market.

Consumers should stop taking any type of ranitidine medication and should not buy any of these medications

Consumers who need heartburn medications should look into alternative OTC drugs approved to treat their condition.

Patients who need prescription ranitidine medication should consult with their doctor to determine the best course of action before stopping ranitidine usage.

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