Ranitidine is sold under the brand name Zantac. As a generic drug, ranitidine is made by a variety of drug companies to decrease production of stomach acid. Ranitidine is most commonly used to treat gastroesophageal reflux disease (GERD), heartburn, peptic ulcer disease, and Zollinger-Ellison syndrome. The medication is included in a class of drugs called histamine-2 receptor blockers (also known as H2 blockers).
Ranitidine works by inhibiting histamine action at the histamine H2 receptors in the gastric parietal cells. Patients most commonly take ranitidine by mouth, in tablet, capsule, or liquid form, before their first meal and/or last meal of the day. The medication is available without a prescription as an over-the-counter treatment.
IMPORTANT RANITIDINE UPDATE: The United States Food and Drug Administration (FDA) issued a press release on April 1, 2020 requesting manufacturers to immediately withdraw all Zantac and generic Zantac OTC drugs from the market. The FDA has found that N-Nitrosodimethylamine (NDMA) in some ranitidine drugs “increases over time and when stored at higher than room temperatures and may result in consumer exposure to unacceptable levels…” The FDA, the World Health Organization (WHO), and the Environmental Protection Agency (EPA) classify NDMA as a cancer-causing substance.
GlaxoSmithKline (at the time, Glaxo Group Research) first introduced ranitidine on the market as Zantac in 1981. By 1987, it was the world’s best-selling prescription drug. Zantac ownership has changed hands several times over the past 38 years since GSK first brought it to market. Companies such as Boehringer Ingelheim, Johnson & Johnson and Pfizer have also manufactured the drug. Ranitidine is now made by Sanofi and sold in a variety of forms, with trade names that include Zantac, Zantac 75, Zantac Efferdose, Zantac injection, and Zantac Syrup.
Ranitidine is used to decrease stomach acid production and treat, prevent or relieve:
Prescription ranitidine is also available as a syrup for infants whose lower esophageal sphincter is not fully developed. In such cases, stomach acid can flow into the infant’s esophagus, causing acid reflux, sores, and ulcers. Ranitidine for infants is used to prevent:
Infants and children should not be given over-the-counter Zantac (Zantac OTC).
Ranitidine can enter the breast milk and be ingested by a feeding infant. Health care professionals are advised to exercise caution when prescribing Zantac to women who are breastfeeding.
Medications that decrease stomach acid production have been linked to an increased risk of acute gastroenteritis and community-acquired pneumonia in children.
Use of ranitidine may potentially mask stomach cancer. Furthermore, patients who have kidney or liver impairment should exercise caution when using ranitidine.
Ranitidine Side Effects in Adults
Ranitidine Side Effects in Severely Ill, Elderly Patients
Ranitidine Side Effects in Children
Since the FDA approved Zantac in the 1980s, numerous studies have shown a link between ranitidine and cancer. One study published in the journal Chemosphere in 2017 showed that ranitidine forms N-Nitrosodimethylamine (NDMA) when placed in drinking water.
NDMA is a semi-volatile organic chemical that belongs to a family of chemicals known as N-nitrosamines. According to the EPA, N-nitrosamines are part of “a family of potent carcinogens.”
An earlier study published in the journal Carcinogenesis showed that a person who consumes ranitidine has a 400-fold increase of NDMA concentration in their urine. Also noteworthy, researchers in the study found that NDMA excretion rates after ranitidine intake equaled or exceeded those observed in patients with schistosomiasis, a disease in which N-nitrosamines are implicated as the cause of bladder cancer.
In 2004, researchers from the National Cancer Institute found a link between ranitidine and bladder cancer. The study noted that “N-Nitrosamines are known carcinogens, and nitrate ingestion has been related to bladder cancer risk.”
The Zantac cancer attorneys at Wisner Baum have extensive experience aggressively fighting against pharmaceutical companies that manufacture and market unsafe drugs. We are using our formidable resources and in-depth experience to investigate ranitidine cancer claims and possible ranitidine lawsuits.
The judge overseeing the federal Zantac multi-district litigation (MDL) appointed Wisner Baum attorney R. Brent Wisner to the Practices and Procedures team to help establish the protocols and methodology for litigating the tens of thousands of cases to be filed in the months and years to come.
Brent also serves as Co-Chair of the Zantac Litigation Group for the American Association for Justice and has been invited to deliver numerous Zantac presentations at prestigious national lawyer conferences across the nation.
We are accepting generic Zantac (ranitidine) cancer cases in every state, including California. Our cancer attorneys have handled many cancer cases in California and across the US, including the three cases against a major corporation that resulted in record-breaking verdicts for our clients. Among those are a $2.055 billion verdict and a $289.2 million verdict for the plaintiffs.
Among our highly skilled and extensively knowledgeable cancer attorneys:
"Wisner Baum gave exceptional attention to all aspects of the case, detailed inquiry, and tenacious overview of all the information submitted. The paralegals are efficient and diligent. I was completely surprised to find an empathic personal message to take care of my own health during the challenging time of being a full-time caretaker.*"
In May of 2019, the jury in the case of Pilliod et al. v, Monsanto Company ordered the agrochemical giant to pay $2.055 billion in damages to the plaintiffs, Alva and Alberta Pilliod, a Bay Area couple in their 70s. R. Brent Wisner served as co-lead trial attorney for the Pilliods, delivering the opening and closing statements and cross-examining several of Monsanto’s experts. Wisner Baum managing shareholder, Michael Baum and attorney Pedram Esfandiary also served on the trial team in the Pilliod case.
The judge later reduced their award to $87M. Monsanto appealed the Pilliod’s verdict which the California Court of Appeal for the First Appellate District denied on August 9, 2021. Monsanto then requested the California Supreme Court review the appeal’s court decision, which the court denied on Nov. 17, 2021. Monsanto (Bayer) then submitted a petition for a writ of certiorari with the U.S. Supreme Court which SCOTUS denied on June 27, 2022, allowing the final judgment of $87M to remain intact.
$289.2 million jury verdict in Monsanto Roundup trial
Wisner Baum co-represented Dewayne “Lee” Johnson in the first Roundup cancer lawsuit to proceed to trial. On Aug. 10, 2018, a San Francisco jury ordered Monsanto to pay $39.25 million in compensatory damages and $250 million in punitive damages to Mr. Johnson, a former groundskeeper who alleged exposure to Monsanto’s herbicides caused him to develop terminal non-Hodgkin lymphoma.
Months after the jury verdict, the judge overseeing the trial reduced the punitive damages to $39.25 million. Mr. Johnson decided to accept the remittitur, bringing the adjusted amount awarded to Mr. Johnson $78.5 million.
Monsanto (Bayer) appealed the verdict and Johnson cross appealed. On July 20, 2020, the First Circuit Court of Appeals upheld the verdict against Monsanto but reduced Mr. Johnson’s award to $20.5 million. The company chose not to take the case to the U.S. Supreme Court, ending the litigation.
In 2016, Wisner Baum attorney Timothy A. Loranger and six other attorneys in the Plaintiffs’ Management Committee were able to secure a $265 million settlement for victims of the 2015 Amtrak 188 derailment in Philadelphia, one of the largest in the U.S. for 2016.