Abnormal Heart Rhythms Associated With High Doses of Celexa

What are you looking for?

Washington, DC: The Food and Drug Administration (FDA) has notified healthcare professionals and patients that the antidepressant Celexa (citalopram hydrobromide) should no longer be used at doses greater than 40 mg per day because it can cause abnormal changes in the electrical activity of the heart. Celexa is in a class of antidepressants called selective serotonin reuptake inhibitors (SSRIs).

Changes in the electrical activity of the heart (prolongation of the QT interval of the electrocardiogram [ECG]) can lead to an abnormal heart rhythm (including Torsade de Pointes), which can be fatal. Patients at particular risk for developing prolongation of the QT interval include those with underlying heart conditions and those who are predisposed to low levels of potassium and magnesium in the blood.

Legal Help

If you or a loved one has suffered illness or an adverse health event in this case, please click the link below and your complaint will be sent to a lawyer who may evaluate your claim at no cost or obligation.

Please click here for a free evaluation of your case

Last updated on Aug-25-11

LEGAL HELP NOW!

Please complete this form to request a review of your complaint by an attorney.

First name:

Last name:

Email address:

Phone number(s):

State:

Zip Code:

Defendant:

Describe your complaint:

Subscribe to our free newsletter

There is absolutely no cost to you to submit this form. Doing so places you under no obligations and does not establish an attorney-client relationship.

Legal Help Now!

CLICK HERE

Related Lawsuits

Legal Services: