Can you take zantac 150 while pregnant

Make it closer to lime, further from battery. But what makes the acid the part of your body that makes the acid, they stop it, interfere with it, making the acid in your stomach, to reduce the acid in your stomach. Now, the problem with Zantac and ranitidine is that they were already known to be nitrosatable drugs. And part of it can become something else. And that something else that a nitrosatable drug can become is called a N-Nitros compound. NDMA is known to be highly carcinogenic.

It actually mutates the cells in your body. All cancer is, is a mutated cell that then replicates itself again and again. Now, as I said, the makers of these drugs have known for a long time that this was possible that these drugs would convert in your stomach acid. The very first thing that struck me about this litigation, what I started looking at the science behind it was that of the other nitrosatable drugs, drugs that could convert to NDMA, none of them were created specifically for people who had very acidic, closer to battery acid, stomach acid.

Well, why is that relevant? Because acid, the more acidic your stomach is, the more breakdown of the drug into the carcinogenic NDMA occurs. And they tested them just to see how much… see if it was converting to NDMA before you swallowed it and it went into your stomach, and found massive amounts of NDMA in many of the products.

The allowable amount in drinking water of NDMA is. But what they found in these products was thousands and thousands of times that. So essentially, not only was the drug turning into this carcinogenic mutagenic substance when you swallowed it, when it was sitting at room temperature in your home, on a truck, anywhere else, it was already beginning to convert.

So the longer it sat, the more it was no longer what it started out as, but nothing but a cancer pill. And and women who took it during pregnancy, which many women have stomach problems obviously during pregnancy, it meant it could cause birth defects and stillbirths.

The child to be born dead. One of the best selling drugs of all time, and also sold over the counter. And had the makers of these products cared to do what they obviously needed to do is far as adequately testing them.

OK, and John, you mentioned ranitidine and that is the generic version? Can we talk a little bit about those types of cancers and other side effects? I know you mentioned birth defects and stillbirths. Can you talk a bit about those side effects?

Then it went, as many drugs do, to a generic form. And from there, it went to many over-the-counter forms. Almost every major retailer in the country had an over-the-counter version of Zantac. It was basically the same product. Recently, very recently, the FDA asked the manufacturers of Zantac to please voluntarily pull it from the shelves. Because as of recent, most of the drugs being sold was over the counter.

In fact, the prescription form of the drug, as soon as the generic form was made, they stopped making the brand. Well the sales dropped. So please understand that this has been going on for upward of 25 years or more.

You could have started on the prescription, moved to the generic and then move to the over the counter. So I just want you… I want to make a real distinction between prescription, generic, and over-the-counter.

But regardless, the FDA recently asked the manufacturers to pull all the product off the market, which they did, which then began our litigation, because when something that drastic, the FDA rarely takes an action like that. They have to take them to court. And the manufacturers all complied because they knew the gig was up. Well, what are those ailments that they really could potentially have a claim for? Well, let me start with the three broad categories. First and foremost, cancer in adults.

Now, obviously, that can mean many, many different types of cancers. But most importantly and in the forefront: esophageal cancer, bladder cancer, liver cancer, stomach cancer, and pancreatic cancer.

We also, sadly, have a category of cancer in children. Now, I just want to say with the adults, you have to have three years of use. And what do we mean by use? So cancer in adults, cancer in children because there are pediatric Zantac products, obviously. That means that they have to have taken it for at least six months during their pregnancy. And again, the minimum is three hundred milligrams per week for an adult.

So those are our three baskets of injury. In other words, you take them and they affect the anatomical structure that produces acid. It produces more than it normally would. You need to take it again because it stops your problem, the pain you were having from your stomach acid. But then as soon as the drug was no longer affecting those receptors, they tried to make up for lost time and produced even more.

In April , the FDA confirmed a study published by an independent lab that Zantac contains elevated levels of NDMA — a dangerous, potentially cancer-causing chemical that occurs naturally in certain foods and water, but can cause cancer at higher levels.

The FDA announced that it had requested all Zantac and ranitidine manufacturers to immediately stop selling the popular drugs. While it is unknown exactly which cancers Zantac may potentially cause, these cancers are thought to be associated:. In addition to the dangers presented by Zantac to the general population, it may be especially dangerous to take Zantac while pregnant. Because pregnant women and fetuses can be particularly sensitive to environmental and chemical changes, it is especially important that women not take Zantac while pregnant.

For those women who have been taking Zantac while pregnant, Dr. It is recommended that you talk with your prescribing doctor immediately and stop taking Zantac or generic ranitidine immediately if you are taking the medication in its over-the-counter formulations.

Zantac class action lawsuits are being filed in order to hold manufacturers accountable for potential cancers linked to Zantac. Gathering compelling evidence is key in a dangerous drug case. If you or a loved one has been injured by Zantac or any other defective drug, you can quickly find yourself facing various complications. If you retain the help of a defective drug attorney on our team, we can help you with the most challenging cases.

We have recovered millions for injury victims and we will seek the best possible results for you. For a free legal consultation, call Elmiron Linked with Dangerous Vision Disorder In the last several months, mass tort litigation involving the Elmiron brand name medication has commenced in United States federal court.

Before the. Please leave this field empty. Phone: Text Us. Many people who have taken ranitidine or Zantac have been diagnosed with several types of cancer, including: Bladder cancer Breast cancer Colorectal cancer Esophageal cancer Kidney cancer Liver cancer Ovarian cancer Pancreatic cancer Small intestine cancer Stomach cancer Testicular cancer Uterine cancer What is NDMA?

Zantac also breaks down into NDMA after a person has taken the medication. Prolonged usage of either ranitidine or Zantac can lead to elevated levels of NDMA in the body, which can lead to cancer in pregnant women as well as birth defects in unborn children. The Treatment of Heartburn in Babies Some babies produce too much stomach acid. Birth Defects Versus Birth Injuries Birth defects involve harm to a child that occurred before birth such as exposure to a harmful drug or something that happened during the pregnancy.

Possible Birth Defects Associated with Zantac Usage Several types of birth defects are associated with prolonged usage of ranitidine or Zantac during pregnancy. While there are many potential defects, some of the most common birth defects associated with exposure to NDMA include: Cleft palate Heart murmurs Neonatal deaths Postnatal cancer Stillbirths Qualifying Factors for Zantac or Ranitidine Compensation If your pregnancy resulted in a birth defect after taking ranitidine or Zantac or you or your child developed cancer after prolonged usage of these medications, you might be able to pursue compensation.

If you satisfy the following criteria, you will likely be able to seek compensation: You have taken ranitidine or Zantac for a minimum of six months during pregnancy. You experienced a birth defect.