Zantac, a popular heartburn medication, has been used for indigestion problems for many decades. Zantac (also known as ranitidine) is an H2 receptor blocker. Zantac is used to treat stomach acid excess. Zantac can also be used to treat symptoms such as gastroesophageal acid reflux disease (GERD), and esophagitis. It is also used to prevent stomach or intestinal ulcers from reappearing after they have healed.
Victims of different forms of cancer have been given a reason for their current medical conditions by the discovery of NDMA within Zantac. Consumers claim that Zantac's manufacturers knew about possible NDMA side effects and recalled the medication after the FDA announcements.
To give consumers a better understanding of the possible side effects, manufacturers should have informed the public about potential side effects prior to them taking the medication. However, there are so many New Jersey Zantac reimbursement lawyers available in the market that helps people in getting better help for their cases.
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To better inform potential customers, medication labels must include all side effects. Consumers have the right of knowing what possible dangers may be associated with certain medications. The manufacturer made the decision for consumers, possibly violating their rights.
Instead of allowing them to weigh the Zantac benefits and risks, they had the ability to do so. Zantac's manufacturers have a responsibility for safe drug manufacturing. Many lives could have been endangered if the drug's dangers were not disclosed.