Questions about Atrial Fibrillation? Get answers from our expert.

Flecainide Pregnancy and Breastfeeding Warnings

Flecainide is also known as: Tambocor

Flecainide Pregnancy Warnings

A series of 14 women who were given flecainide 300 to 400 mg per day to treat fetal supraventricular tachycardias complicated by fetal hydrops and ascites has been reported. The drug was given at a mean gestational age of 31 weeks, and was continued for up to five days. The mean umbilical cord to maternal plasma ratio was 0.80, with fetal concentrations ranging from 400 to 800 mcg per liter. One intrauterine death was observed three days after flecainide was begun, that may have been due to a proarrhythmic effect of flecainide. A second infant died later of sudden infant death syndrome. No adverse effects or problems were noted in the remaining 12 infants. There have been several cases in which flecainide was used safely during human pregnancy. This drug has been used safely and successfully to treat refractory (to digoxin) fetal tachycardia. Average umbilical cord blood to maternal serum flecainide concentration ratios ranging from 0.63 to 0.97 have been reported. However, at least one case of neonatal cardiotoxicity related to maternal use of flecainide for fetal supraventricular tachycardia has been reported.

Flecainide has been assigned to pregnancy category C by the FDA. Animal studies have revealed teratogenicity and embryotoxicity in rabbits that were given doses 30 to 35 mg/kg/day. No data from controlled studies in human pregnancy are available. Flecainide should only be given during pregnancy when there are no alternatives and benefit outweighs risk.

Flecainide Breastfeeding Warnings

Flecainide is excreted into human milk. Adverse effects on the nursing infant are unlikely. Flecainide is considered compatible with breast-feeding by the American Academy of Pediatrics.

Flecainide concentration in human milk averages 2.5 times that found in maternal plasma. Some experts have calculated that, assuming an infant consumes 700 mL of milk every 24 hours and the maternal plasma concentration is 1 mcg/mL, a suckling infant would be exposed to about 3 mg of flecainide per day. The calculated resultant infant plasma flecainide level would be 62 ng per mL. This represents a negligible amount of drug to the nursing infant.

See Also...

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Wolters Kluwer Health and Drugs.com is accurate, up-to-date and complete, but no guarantee is made to that effect. In addition, the drug information contained herein may be time sensitive and should not be utilized as a reference resource beyond the date hereof. This material does not endorse drugs, diagnose patients, or recommend therapy. This drug information is a reference resource designed as supplement to, and not a substitute for, the expertise, skill , knowledge, and judgement of healthcare practitioners in patient care. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective, or appropriate for any given patient. Multum Information Services, Inc. does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. Copyright 2000-2008 Multum Information Services, Inc. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse, or pharmacist.

Hide
(web2)