Clarithromycin Side Effects Linked to Heart Problems For Those with COPD

Side effects of the antibiotic clarithromycin, which is most commonly known as Biaxin, could be linked to a risk of serious and potentially life-threatening heart problems, according to researchers from Australia and the United Kingdom. 

In a study published last week by the British Medical Journal, researchers found that patients given Biaxin or other antibiotics containing clarithomycin were 50% more likely to suffer a cardiovascular event or cardiovascular death.

Researchers looked at data on about 3,000 patients admitted to one of a dozen hospitals in the United Kingdom between 2009 and 2011. They found a 50% increased risk of cardiovascular events and acute coronary syndrome among patients given clarithromycin. They also found a 52% increase in the risk of cardiovascular mortality when given to patients suffering from chronic obstructive pulmonary disease (COPD), but not with patients given the antibiotic for the treatment of pneumonia.

Did You Know?

Change Healthcare Data Breach Impacts Millions of Customers

A massive Change Healthcare data breach exposed the names, social security numbers, medical and personal information of potentially 100 million Americans, which have now been released on the dark web. Lawsuits are being pursued to obtain financial compensation.

Learn More

The drug belongs to a class of antibiotics known as macrolides. Zithromax (azithromycin) is another antibiotic in the same class, which has also recently been linked to a risk of heart problems.

“Evidence is accumulating for long term cardiovascular risks associated with macrolides,” the researchers concluded. “Our data would support the need for a high quality randomized controlled trial of macrolides with long term follow-up.”

Earlier this month the FDA issued a warning about the potential side effects of Zithromax, indicating that the antibiotic may disrupt the electrical activity of the heart. Zithromax is also known as the Z-Pak or Zmax.

A May 2012 study published in the New England Journal of Medicine first warned about the potential heart risks with Zithromax. Researchers found patients were 2.5 times more likely to die due to heart related problems on a five day Zithromax treatment when they compared it to treatment with other antibiotics or no antibiotic therapy.

The FDA review found that certain patients were more at risk, including those with existing QT interval prolongation, patients with low blood levels of potassium or magnesium, patients with slower than normal heart rates, and those taking certain drugs used to treat abnormal heart rhythms.

1 Comments

  • TheresaMarch 20, 2017 at 8:57 pm

    After first dose of Clarithromycin developed myalgia and tendinitis in my shoulders more sever on left. severe pain in left shoulder with movement. constant burning pain at rest. now going to physical therapy and have been referred to an orthopedic dr for futther eval and treatment. Pain worsining over the last 2 months. Wondering if I will ever be the same again.

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

Generic Depo-Provera Manufacturers Call for Birth Control Shot MDL to Be Created in NY, Not California
Generic Depo-Provera Manufacturers Call for Birth Control Shot MDL to Be Created in NY, Not California (Posted yesterday)

A growing number of lawsuits against generic Depo-Provera manufacturers have been filed throughout the federal court system, each alleging that women were not adequately warned about the risk of meningioma brain tumors from the birth control shot.

Oxbryta Class Action Lawsuit Filed by Former Users of Sickle Cell Disease Drug Recalled in 2024
Oxbryta Class Action Lawsuit Filed by Former Users of Sickle Cell Disease Drug Recalled in 2024 (Posted 2 days ago)

Former users of the recalled sickle cell disease drug Oxbryta have filed a class action lawsuit, claiming the manufacturer failed to warn consumers about risks associated with the medication, which can result in stroke and death.

Group of 20 Uber Driver Sexual Assault Lawsuits Will Be Prepared for Bellwether Trials in Dec. 2025
Group of 20 Uber Driver Sexual Assault Lawsuits Will Be Prepared for Bellwether Trials in Dec. 2025 (Posted 2 days ago)

Plaintiffs and defendants have each been directed to select 10 Uber driver sexual assault lawsuits to serve as potential bellwether trials by February 14, 2025, which will then go through case-specific discovery to prepare for early test trials.