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Wiley InterScience | ||
![]() British Journal of Clinical PharmacologyVolume 49 Issue 3, Pages 264 - 268 Published Online: 24 Dec 2001 Journal compilation © 2010 The British Pharmacological Society The Journal of The British Pharmacological Society
Abstract | References | Full Text: HTML, PDF (Size: 68K) | Related Articles | Citation Tracking Birth outcome following maternal use of metoclopramide *EUROMAP: Project management group: Henrik Toft Sørensen, Jørn Olsen, Andrew Czeizel, Gunnar Lauge Nielsen, Lolkje De Jong van den Berg, Lorentz Irgens, Ulf Bergman. Other members of the study group: Charlotte Olesen, Flemming Hald Steffensen, Lars Pedersen, Rolv T. Lie, Corrine de Vries, Patrick Leurquin. Copyright Blackwell Science, 2000 KEYWORDS metoclopramide • birth outcome • pregnancy ABSTRACTAims Metoclopramide is an antiemetic drug used widely during pregnancy for nausea and vomiting. Because of its frequent use any adverse effects on infant health would have major public health implications. We therefore examined the safety of metoclopramide during pregnancy. Methods Using the Pharmaco‐Epidemiological Prescription Database of North Jutland County, we identified 309 women with singleton pregnancies who had prescriptions for metoclopramide fom 1 January 1991 to 31 December 1996. Information on malformations, birth weight, preterm deliveries and stillbirth were compared with 13 327 references who did not receive prescriptions of any kind during pregnancy. Results Mean birth weight among exposed women was 3480 g compared with 3470 g among nonexposed. Based on logistic regression models no major differences in the risk were found concerning malformations (OR= 1.11; 95% confidence interval (CI): 0.6–2.1); low birth weight (OR= 1.79; 95% CI: 0.8–3.9) or preterm delivery (OR= 1.02; 95 CI: 0.6–1.7). Conclusions We could not document any association between the use of metoclopramide during pregnancy and adverse pregnancy outcome. Because of the limited power of our study further research is required. Received 31 March 1999, accepted 16 November 1999. |