Thursday, August 25, 2011

Celexa (citalopram Hydrobromide) At Over 40mg Per Day Linked To Abnormal Heart Rhythm Risk, Warns FDA

Celexa (citalopram Hydrobromide) At Over 40mg Per Day Linked To Abnormal Heart Rhythm Risk, Warns FDA

Citalopram hydrobromide, known under brand name Celexa, should not be administered at doses over 40 mg for day, because it can trigger heteroclite electrical activity in the heart, ruling to potentially fatal heart rhythm problems (including Torsade de Pointes), the FDA (Food and Drug Administration) announced today. The Agency added that doses in heaven 40mg per day do not service in the treatment of depression.

A citalopram drug label used to state that some patients may need 60 mg for day.

Alterations in the heart's electrical mode of action (prolongation of the QT interval) may especially change those with existing heart conditions, since well as patients who are bending forward to low levels of blood potassium and magnesium.

The remedy label for citalopram has been modified to include usage recommendations and the new mix with ~s dosage, as well as details forward the risk for QT interval extension and Torsade de Pointes.

Information notwithstanding patients

If you are taking citalopram, do not change your dose or delay taking it without talking to your doctor first. If you stop taking citalopram abruptly you may continued undesirable side effects.

Patients on doses beyond 40 mg per day should confer to their physician about altering the dosage.

If you have shortness of breath, dizziness, fainting, or uncertain heartbeat, and you are on citalopram, learn immediate medical attention.

Doctors of patients steady citalopram may sometimes order an ECG or EKG to admonisher heart rate and rhythm.

Those up~ citalopram should read its Medication Guide carefully, and canvass any questions with their doctor.

Side furniture should be reported to the FDA MedWatch program (Tel: 1-800-332-1088).

Information against doctors

Do not prescribe citalopram at doses greater than 40 mg through day, because of dose dependent QT interval prolongation risk.

Patients with congenital lengthy QT syndrome should not be prescribed citalopram.

Patients by bradyarrhythmias, heart failure, or predisposition to hypomagnesemia or hypokalemia for the reason that of concomitant illness or medications, obtain a greater chance of developing Torsade de Pointes.

Hypomagnesemia and hypokalemia should exist effectively treated before prescribing citalopram. Test because of electrolytes as clinically indicated.

For patients with bradyarrhythmias, congestive heart failure, or those on concomitant drugs that prolong QT space between, consider ECG monitoring more frequently.

For those with hepatic impairment, aged 60+ years, who are CYP 2C19 skinny metabolizers, or who are taking accompanying Tagamet (Cimetidine) - the maximum recommended prescribed portion is 20 mg per day.

For those by mild or moderate renal impairment, prescribed portion adjustments are not necessary.

Tell patients who are distress citalopram to contact a healthcare professional whether or not they have signs and symptoms of abnormal heart rhythm or heart rate.

Adverse events should subsist reported to the FDA MedWatch program (Tel: 1-800-332-1088).

Celexa (citalopram hydrobromide)

Celexa is some SSRI (selective serotonin reuptake inhibitors) class of antidepressant.

Experts believe it works ~ the agency of increasing brain levels of serotonin.

It is useful in tablet form in doses of 10 mg, 20 mg, and 40 mg. It is furthermore available as a 10 mg/5mL vocal solution.

Written by Christian Nordqvist

View unsalable article information on Celexa; Cimetidine Hydrochloride Oral Solution.

Copyright: Medical News Today
Not to have ~ing reproduced without permission of Medical News Today

Article Reference:

No comments:

Post a Comment