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Date of issue: December 2023, Version: 3.0

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A corresponding patient information leaflet on USE OF AMITRIPTYLINE IN PREGNANCY is available.

Amitriptyline is a tricyclic antidepressant (TCA) licensed for use in the management of depression, anxiety disorders and neuropathic pain. However, UK guidelines currently do not recommend the use of amitriptyline in the management of psychiatric disorders due to the risk of toxicity in overdose.

Although amitriptyline has been widely used in pregnancy, few studies have quantified pregnancy outcomes in women taking this medication. Whilst the currently available data do not raise concerns that amitriptyline is a teratogen, further studies are required for confirmation. Other adverse fetal effects following amitriptyline exposure have not been assessed.

There is no strong evidence of any association between TCAs as a therapeutic class and congenital malformation overall, or any specific malformations. Other findings are conflicting, with possible associations with miscarriage, preterm delivery, and autism spectrum disorder identified in some (but not all) studies. While most of the studies investigating TCAs as a therapeutic class include (often a minority of) women exposed to amitriptyline, no separate assessment of their pregnancy outcomes was carried out and these data do not therefore provide information about specific amitriptyline exposure.

An increased incidence of neonatal complications has been reported in the offspring of women with psychiatric illnesses; however, the relative contributions of the underlying maternal condition and specific drug treatments have not been clearly defined. While there are no specific data on amitriptyline exposure, use of TCAs throughout pregnancy or near delivery has been associated with withdrawal symptoms in the neonate and/or poor neonatal adaptation syndrome (PNAS). These symptoms are likely to be more severe in infants exposed in utero to more than one CNS acting drug.

No studies have assessed fetal/neonatal outcomes following amitriptyline overdose in pregnancy. However, overdose around the time of delivery, particularly overlaying chronic use, may increase the risk of neonatal withdrawal.

It is important to ensure that maternal chronic pain and/or mental health disorders are treated appropriately during pregnancy. Where a patient is stabilised on a TCA, either prior to conception or during pregnancy, the risk of discontinuing or changing medication, or reducing the dose, should be carefully weighed against the risk of relapse of the maternal condition.

The currently available data do not support the need for any additional fetal monitoring following in utero therapeutic exposure to TCAs; however, other risk factors may be present in individual cases which may independently increase the risk of adverse pregnancy outcome and the need for additional monitoring should therefore be determined on a case-by-case basis. Clinicians are reminded of the importance of consideration of such factors when performing case-specific risk assessments.

Treatment of maternal amitriptyline overdose should be as for the non-pregnant patient and should not be withheld on account of the pregnancy. For current guidelines regarding treatment of amitriptyline overdose please refer to TOXBASE®.

This is a summary of the full UKTIS monograph for health care professionals and should not be used in isolation. The full UKTIS monograph and access to any hyperlinked related documents is available to NHS health care professionals who are logged in.

If you have a patient with exposure to a drug or chemical and require assistance in making a patient-specific risk assessment, please telephone UKTIS on 0344 892 0909 to discuss the case with a teratology specialist.

If you would like to report a pregnancy to UKTIS please click here to download our pregnancy reporting form. Please encourage all women to complete an online reporting form.

Disclaimer: Every effort has been made to ensure that this monograph was accurate and up-to-date at the time of writing, however it cannot cover every eventuality and the information providers cannot be held responsible for any adverse outcomes of the measures recommended. The final decision regarding which treatment is used for an individual patient remains the clinical responsibility of the prescriber. This material may be freely reproduced for education and not for profit purposes within the UK National Health Service, however no linking to this website or reproduction by or for commercial organisations is permitted without the express written permission of this service. This document is regularly reviewed and updated. Only use UKTIS monographs downloaded directly from to ensure you are using the most up-to-date version.