Heartburn Drug Side Effects And Safety Recommendations Highlighted in Medical Letter

A recent safety analysis highlights the numerous side effects of heartburn drugs, such as Nexium, Prilosec, Prevacid and other popular medications, but concludes that for individuals with a clear indication for long-term use, the benefits probably still outweigh the known risks at this time. 

The report was published last week in the Journal of the American Medical Association (JAMA), from information outlined by The Medical Letter, Inc., a non-profit organization that publishes critical appraisals of prescription drugs and therapeutics.

An increasing number of serious health risks have been linked to a widely used class of drugs, known as proton pump inhibitors (PPI), which are used by millions of Americans for long-term treatment of heartburn, gastroesophageal reflux disease (GERD) and prevention of upper gastrointestinal effects from certain pain medications.

Did You Know?

Ticketmaster Data Breach Impacts Millions of Customers

A massive Ticketmaster data breach exposed the names, addresses, phone numbers, credit card numbers and other personal information of more than 560 million customers, which have now been released on the dark web. Lawsuits are being pursued to obtain financial compensation.

Learn More

According to the analysis, various clinical studies have linked PPI heartburn medications to side effects like kidney disease, bone fractures, vitamin B12 deficiency, iron deficiency, community-acquired pneumonia, clostridium difficile (c-diff) infections, hypmoagnesemia and QT prolongation.

“Long-term PPI use has been associated with an increasing number of safety concerns,” the analysis concludes. “Few of these concerns are supported by a causal relationship or consistent data. For patients with a clear indication for long-term treatment with a PPI, the benefits of probably outweigh the risks.”

Perhaps the most serious proton pump inhibitor risk to surface in recent years has been evidence that the drugs may cause a condition known as acute interstitial nephritis (AIN), which may progress to chronic kidney disease (CKD). The analysis points out that the mechanism of action by which PPIs cause kidney disease remains unknown, but outlines the findings of several studies published in recent years that have identified this serious safety signal.

In December 2014, the FDA required new warnings for the first time about a the risk of acute interstitial nephritis from the heartburn drugs.

According to a study published in the medical journal CMAJ Open in April 2015, users of Nexium, Prilosec or other PPI may face a more than 3 times higher risk of developing acute interstitial nephritis, and 2.5 greater risk of experiencing acute kidney injury.

In January 2016, another study published in the medical journal JAMA Internal Medicine found that the heartburn drugs may also increase the risk of chronic kidney disease by 50%.

Those findings were supported by another study published in April 2016, which found that PPI medications may increase the risk of kidney failure, as well as chronic kidney disease.

As a result of these independent studies, a growing number of former users of the heartburn medications are now pursuing Nexium lawsuitsPrilosec lawsuitsPrevacid lawsuitsProtonix lawsuits and other claims over drug makers’ failure to adequately disclose the kidney risks on the warning labels.

Since the drugs have been aggressively promoted without indication that users may experience serious kidney damage, many users with mild heartburn symptoms continue on the medications for long periods of time without any effort to reduce or stop the need for the medications. Many prominent experts have expressed concern that many users continue to take the drugs even though there may be no real medical need any longer.

As heartburn drug injury lawyers continue to review and file cases, it is ultimately expected that thousands of kidney injury cases may be filed in the coming months and years.

0 Comments

Share Your Comments

I authorize the above comments be posted on this page*

Want your comments reviewed by a lawyer?

To have an attorney review your comments and contact you about a potential case, provide your contact information below. This will not be published.

NOTE: Providing information for review by an attorney does not form an attorney-client relationship.

This field is for validation purposes and should be left unchanged.

More Top Stories

Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits
Ozempic MDL Court To Evaluate Need for Gastroparesis Diagnostic Testing in GLP-1 Lawsuits (Posted 2 days ago)

A federal judge has agreed to divide lawsuits over gastroparesis injuries linked to drugs like Ozempic and Mounjaro into multiple phases, examining how the condition is diagnosed and whether plaintiffs' claims are preempted by federal laws.

Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn
Adult Woman Files Similac Lawsuit Over NEC Injuries Experienced as a Newborn (Posted 3 days ago)

Lawsuit alleges that Abbott Laboratories failed to provide families and the medical community with adequate warnings about the risks associated with it’s cow’s milk-based Similac formula, which a now adult woman indicates has left her with life-long NEC injuries.

Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects
Amended Lawsuit Over BioZorb Implant Side Effects Outlines Problems Caused By Tissue Marker Design Defects (Posted 4 days ago)

Six breast cancer patients have asked a federal judge for permission to amend a complaint filed in March 2024, which describes problems linked to the device and painful side effects experienced when the tissue marker migrated out of position or shattered inside their bodies.