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Date of issue: July 2021, Version: 3

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

Morphine is an opioid analgesic most commonly administered orally, intravenously or rectally for the treatment of severe or intractable pain.

Data relating specifically to morphine exposure in human pregnancy are extremely limited. It is not currently possible to exclude a teratogenic effect.

There are no controlled studies of the effect of morphine exposure on the incidence of miscarriage and no robust evidence of an increased malformation risk. Increased rates of specific malformations have been observed in some studies analysing opioids as a class, but the data are conflicting and the studies confounded. Data are extremely limited in relation to low birth weight, preterm delivery, stillbirth and neurodevelopmental outcomes, but a possible association with altered fetal growth in utero and visual defects (strabismus) have been reported, the clinical significance of which is unclear. Codeine, another opioid analgesic, is metabolised to morphine. Data are similarly limited and are reviewed in a separate UKTIS monograph. 

Owing to the lack of data regarding malformation risks, women who have been exposed to morphine in the first trimester are particularly encouraged to attend their routine detailed fetal anomaly scan, which is generally conducted at around 18 to 20 weeks of pregnancy. Use of any opioid during pregnancy, particularly around the time of delivery, confers a risk of neonatal respiratory depression and neonatal withdrawal. Delivery in a hospital setting is therefore advisable.

Where morphine poisoning or overdose occurs in pregnancy, maternal toxicity is likely to be a major factor in determining risk to the fetus. If use of an antidote (e.g. naloxone) is required in the management of maternal toxicity, it should not be withheld on account of pregnancy.

Exposure to morphine at any stage in pregnancy would not usually be regarded as medical grounds for termination of pregnancy. However, other risk factors may be present in individual cases which may independently increase the risk of adverse pregnancy outcome. Clinicians are reminded of the importance of consideration of such factors when performing case-specific risk assessments.

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.