Ranitidine - Causes Of Zantac Recall, Overview

The Zantac recall involves both over-the-counter and prescription Zantac products. The recalled product, the Zantac Punch, was manufactured by Zantac Pharmaceuticals. The recall is a part of the pharmaceutical company's efforts to respond to recent new safety issues regarding the composition and strength of Zantac, particularly its main ingredient, methylene blue (MBC). Methylene blue is used in Zantac to help reduce eye inflammation and pain caused by dryness and inflammation of the eye. Check out these info sources for pharma recals now. 

Zantac also produced an ulcer medication called Talstar. A voluntary recall was issued for this medication due to evidence that some people have been experiencing severe symptoms after taking this medication. It was determined that a patient of the Zantac product, which was administered to a woman who was pregnant, may have been suffering from a possible birth defect. This case is currently being reviewed by the FDA. Research more about medical lawsuits today. 

The other item that was recalled was Lofexidine, an ulcer medication. No one has reported any health problems as a result of using Lofexidine. However, the FDA received reports from consumers saying that patients of Lofexidine have suffered from occasional heartburn and peptic ulcers, which could be associated with the use of Zantac, a Zantac Product. Zantac is not the only manufacturer of ulcer medications that has recently faced a Zantac recall.
Ranitidine is also manufactured by Zantac. A number of Ranitidine deaths were reported in 2020, when patients started using this drug without proper supervision and at higher doses. Ranitidine is not the only Zantac product that has been linked to adverse side effects, including heartburn and peptic ulcers. There are no known safe levels of Ranitidine in either pregnant or non-pregnant women.

In addition to both of these products, the FDA has also issued a Zantac voluntary recall on three other generic ranitidine OTC products, including Metadate, Mylanta, and Norpramin. The FDA says that all three products are associated with a number of serious side effects, including severe stomach pain, allergic skin rash, nausea, vomiting, dizziness, and changes in vision, along with increased risk of cancer. In addition to these symptoms, patients using Ranitidine should avoid driving or operating machinery under any circumstances, and they should immediately contact a doctor if they notice symptoms that they believe are related to this heartburn medication. No one should take a ranitidine without first consulting their doctor. Ranitidine is not the only heartburn medication that could cause this type of situation, but it is the strongest one that are available over the counter.

As you can see, these Zantac recalled results are caused by the combination of a number of different ingredients, and unfortunately, none of them are related to ranitidine at all. In order to understand how to avoid these types of situations in the future, you need to be aware of the different warning signs of possible Zantac side effects, and keep tabs on your prescription records. It will also help you remember the number of Zantac coupons you currently have on hand in case your insurance company ever offers you a coupon for this product. With these resources, you should be able to quickly track down the source of your Ranitidine problem and avoid the potentially deadly consequences.