Zantac Cancer Webinar


November 12, 2019

Zantac Plaintiff Information

A New Webinar has been scheduled for November 19 at 2 pm EST for your law firm to learn more about the Zantac litigation. The webinar is put on by CAMG and your host will be Steve Nober. The leading attorneys on the Zantac litigation will be debunking the recent FDA statement on Zantac Link here.

Neil D. Overholtz and R. Jason Richard from Aylstock, Witkin, Kreis & Overholtz will be presenting  together with Robert C. Hilliard from Hilliard Martinez Gonzales LLP. This will be the attorneys moving this litigation forward. They have already done all the research on the Zantac and if you are interested in the Zantac litigation you want to be on this call.

Please click on the image on the bottom bellow to sign up.

X Social Media always has up-to-date lead information on our website for the first full month of running Zantac with no dis-qualifiers.The information is located here on our website; for people looking only for qualified cancers for Zantac that is coming in right around $200 per lead.

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Zantac Cancer Risk

At one point it was the top selling drug in the world, now the FDA is investigating whether the popular OTC and prescription heartburn drug Zantac causes carcinogens to form in its users. The issue stems from Zantac causing levels of the probable carcinogen N-nitrosodimethylamine (NDMA) to rise in the users’ bodies.
Valisure’s research, along with that of Stanford University and others, found that NDMA was the result of the “inherent instability” of the ranitidine molecule. This means that all manufacturers, brand or generic, and all lots of ranitidine-containing medications are affected and could generate very high levels of NDMA in the human body.
Its important to first understand that the problem Zantac is having is way different than the problems with the blood pressure medication Valsartan. In the case of Valsartan we had a contamination problem caused by a change in manufacturing practices. In the case of Zantac though, we have a root product problem where Ranitidine has been shown to form thousands of nanograms of NDMA in the human stomach. These discoveries are not new if you look at the image below you will see that this was discovered in the 1980’s.
In 2004 Ranitidine (Zantac) was linked to Bladder Cancer in a National Cancer Institute study. Study Link.
A 2016 study at Stanford University gave 10 healthy volunteers 150 milligrams of Zantac and found that subsequent NDMA levels in their urine exceeded 47,000 nanograms  Study Link
Another 2017 study shows how Urination of ranitidine into wastewater suspected as source of NDMA in municipal drinking water. Study link

So what the hell right ? 35 years on the market and now they tell us that its cancer causing?
Ranitidine likely generates millions of nanograms of NDMA in humans where the FDA maximum permissible daily exposure of the probable human carcinogen, NDMA, in pharmaceuticals is 96 ng.

How do we move Forward?
There are a few ways of looking at this developing MDL as we see it. First, you have exposure of millions of people to a cancer causing substance NDMA for 35+ years. Many will end up with different cancers over their lifetime and a known source of this cancer will be Zantac. This would mean you sign up everybody that has taken Zantac and you guys make an MDL that has two tracks one being exposure and one being cancer.Another way of looking at it would be signing up people that have already developed a cancer that Zantac could have caused. Like Bladder Cancer, Stomach cancers and a total of 8 different cancers can be tied to this. We can then use the landing page to Disqualify people that have not developed a qualifying cancer and only send the qualifying cancers though to an intake center for signing-up.For the advertising attorneys- we already have a few big names that cases can be referred to just ask us for introductions to ref. firms.

What do we know so far about prices per lead?
In the last 3 weeks we have been running about a million dollars in advertising spend towards this target market and here is what we know.If you are just looking for anybody that took Zantac with a qualifying cancer or not we see prices of $30-40 per lead and we see huge volume even on big spends.If you want to disqualify people so only people diagnosed with the correct cancer is coming though we see prices of $175-$200 per lead.

Our current spend on Zantac is around $75,000 per day and increasing fast.
Our new Managing Director, Lucas Gerler can also be reached with any questions you have on running new projects at


Intake For Zantac Sign Up
Signing Up Zantac Cases
There will be a ton of leads and to do it with the best economics in mind here is our suggestion:
We have a Texas intake center with 80 agents that will do screening and sign-up of clients that meet your criteria at $35 per lead you send over there no matter if client sign or not but they will chase the leads and try and sign them up.

We are using the Texas call center Legal Conversion Center (LCC) for the sign up because they are the only legal intake center that is fully integrated with X Social Media in respect to the feedback loop where we can see what ad produced the lead that converted into a case on your campaign. This way we can spend your advertising money on the most productive ads. This is a huge advantage for the clients that we have the ability to follow each lead though sign-up.

We can provide introductions to LCC for law firms that are not already clients of theirs or below is their website and main contact is Scott Blackburn 817-991-8915 or via email at

A Great Read To Learn Facebook Advertising For Law Firms

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