1-877-327-4636 Alcohol and Substance
1-800-436-8477 Morning Sickness
1-888-246-5840 HIV and HIV Treatment
1-877-439-2744 Motherisk Helpline
416-813-6780 Motherisk Helpline
Pregnancy & Breastfeeding Resources
Current Studies at Motherisk
Study seeks women between 4 and 12 weeks in their pregnancy with morning sickness (NVP)
Pregnancy in Women with Multiple Sclerosis
Environmental Exposures and Children's Health
Alcohol Use during Pregnancy
Control of Hypertension in Pregnancy Study
Folic Acid Before and During Pregnancy
Lamisil in Pregnancy
Meridia in Pregnancy
Autoimmune Diseases in Pregnancy Project
Safety of antihistamines during pregnancy and lactation
Miranda So, RPh, Pina Bozzo, Miho Inoue, MD and Adrienne Einarson, RN
Many of my pregnant and breastfeeding patients suffer from allergies and frequently ask me about the safety of antihistamines during pregnancy and breastfeeding. Should I advise them to use the older sedating medications? I have heard that they might be safer than the newer nonsedating class of drugs. Or have the newer ones been studied as well?
First-generation antihistamines are considered safe to use during pregnancy. There are relatively fewer data on the non sedating second-generation antihistamines; however, published studies are reassuring. All antihistamines are considered safe to use during breastfeeding, as minimal amounts are excreted in the breast milk and would not cause any adverse effects on a breastfeeding infant.
Beaucoup de mes patientes enceintes ou qui allaitent souffrent dallergies et me demandent souvent des questions à propos de linnocuité des antihistaminiques durant la grossesse et lallaitement. Devrais-je leur conseiller dutiliser les plus anciens sédatifs? Jai entendu dire quils étaient peut-être plus sécuritaires que les plus récentes classes de médicaments non sédatifs, à moins que les plus récents produits aient aussi fait lobjet détudes.
Lutilisation des antihistaminiques de la première génération est considéréesécuritaire pendant la grossesse. Il y a relativement moins de données sur les antihistaminiques non sédatifs de la deuxième génération; par ailleurs, les études publiées sont rassurantes. Tous les antihistaminiques sont considérés sécuritaires durant lallaitement, étant donné les quantités minimes passant dans le lait maternel, qui ne devraient pas causer deffets indésirables chez le nourrisson allaité.
Common symptoms of allergic rhinitis include nasal congestion, discharge, and itching, as well as eye involvement such as conjunctival redness, swelling, and excessive lacrimation. The symptoms are typically triggered by airborne allergens (eg, pollens from trees, grasses, weeds); however, household allergens such as dust mites or animal dander are also common triggers.1 Allergic diseases are estimated to affect 20% to 30% of women of childbearing age, making them the most common medical conditions to complicate pregnancy.2 Furthermore, during pregnancy, up to 10% to 30% of women with pre-existing allergic rhinitis have reported increased symptoms.1 Possible explanations include increased circulating blood volume, nasal vascular engorgement, and increased secretions from nasal mucosa due to hormonal influences.1
Antihistamines targeting histamine–type 1 (H1) receptors are commonly used to treat allergic rhinitis. Examples of first-generation antihistamines are brompheniramine, chlorpheniramine, dimenhydrinate,diphenhydramine, doxylamine, hydroxyzine, and pheniramine. Most— with the exception of doxylamine and dimenhydrinate, both used for the treatment of nausea and vomiting, and hydroxyzine (prescription-only)—are commonly found in over-the-counter allergy and cold medications. None of the medications in this class of drugs has been reported to increase fetal risk when used at any time during pregnancy.2 Epidemiologic data support safety in early pregnancy,3 witha meta-analysis involving more than 200 000 participants concluding that there was no increase in any type of congenital malformation.4
At present, medications from this class of drugs are preferred because they do not cause central nervous system adverse effects (eg, drowsiness) and because they are available without prescription. Examples of second-generation antihistamines are cetirizine,desloratadine, fexofenadine, and loratadine.
Cetirizine is the active metabolite of hydroxyzine. A small prospective, comparative study conducted by Motherisk following 120 women exposed to hydroxyzine and 39 to cetirizine (37 in first trimester) did not find differences in pregnancy outcomes between the exposed and comparison groups.5 Pregnancy outcomes from the Swedish Medical Birth Registry (1995 to 1999) of 17766 women exposed to antihistamine drugs, 917 of whom used cetirizine, did not show increased risk of malformations or adverse delivery outcomes compared with the general population.6 In 2004 another study examining 144 first-trimester exposures to cetirizine confirmed the previous results, with no adverse pregnancy outcomes attributed to the drug.7 The most recent data were from the Berlin teratogen information service, with 196 women exposed in any trimester (11% in the first trimester), also showing no increased risk of birth defects or other adverse outcomes.8
Fexofenadine is an active metabolite of terfenadine,9 a second-generation H1 blocker that is no longer available on the Canadian market owing to clinically significant QT prolongation. Although animal studies failed to show teratogenicity, decreases in pup weight and survival were observed. There are no human data on fexofenadine9; however, limited data from terfenadine did not find an increased risk of major malformations.3
Loratadine and desloratadine
Desloratadine is a major metabolite of loratadine; therefore, data pertaining to safety of loratadine might be extrapolated to desloratadine.10 A Swedish registry study involving 292 loratadine-exposed women did not suggest an increased risk of major malformations.6 A Motherisk study prospectively following 161 loratadine-exposed women and an equal number of unexposed controls confirmed the safety of loratadine use in pregnancy.11 Another study comparing 210 pregnant women exposed to loratadine and 267 women exposed to other antihistamines with 929 women in a control group also failed to show an association with loratadine.12 However, a further analysis from the Swedish registry reported an increased risk of hypospadias,13 although this association has not been confirmed by the other studies.3,14 Furthermore, a recent meta-analysis conducted by Motherisk comparing 2694 male infants exposed toloratadine in utero with 450 413 unexposed controls also failed to confirm such an association.15
Antihistamines and breastfeeding
Although the data regarding the use of first-generation antihistamines and breastfeeding is limited, only minimal amounts of these drugs have been reported to be secreted in breast milk.16,17In a telephone follow-up study conducted by Motherisk, 10% of mothers reported irritability and colicky symptoms in their infants exposed to various antihistamines, and drowsiness was reported in 1.6% of infants. None of the reactions required medical attention.18 Therefore, short-term or occasional use of the older generation antihistamines would not be expected to be a concern during breastfeeding.
Among the second-generation H1 blockers, data on drug concentrationin breast milk are available for loratadine, desloratadine,and fexofenadine. The pharmacokinetics of loratadine and its metabolite desloratadine in breast milk were studied in 6 lactating women after a single oral dose of 40 mg of loratadine,19 which is 4 times the current standard therapeutic dose. Assuming the breast milk intake by an infant is 150 mL/kg daily, the maximum infant loratadine-equivalent dose based on the highest concentration of loratadine and desloratadine in breast milk was estimated to be 7.3 µg/kg daily (ie, 1.1% of the daily dose given to the mother in mg/kg). The pharmacokinetics of fexofenadinein breast milk were studied in 4 lactating women taking 60 mgof terfenadine every 12 hours.20 The maximum infant dose of fexofenadine based on the highest concentration of fexofenadinein breast milk would be 9 µg/kg daily (ie, 0.45% of the daily dose given to the mother in mg/kg). Considering the minimal exposure of a nursing infant to the drugs through breast milk, maternal use of loratadine, desloratadine, or fexofenadine in a standard therapeutic dose is unlikely to result in adverse effects in nursing infants and is considered to be compatible with breastfeeding.
Although seasonal allergy is not a life-threatening medical condition, it can be extremely troublesome for pregnant women and breast feeding mothers. Based on the current body of evidence, which is large, first-generation H1 blockers are not associated with an increased risk of major malformations or any other adverse fetal effects. Although there is less evidence on second-generation H1 blockers, they have also not been associated with an increased risk of adverse pregnancy outcomes. In addition, none of the antihistamines is excreted in the breast milk in an appreciable amount so as to have any adverse effects on the breastfeeding infant. Therefore, pregnant and breastfeeding women can be reassured that they can alleviate their symptoms without posing an increased risk to their fetuses or infants.
Can Fam Physician
Vol. 56, No. 5, May 2010, pp.427 - 429
Copyright © 2010 by The College of Family Physicians of Canada
- Incaudo GA, Takach P. The diagnosis and treatment of allergic rhinitis during pregnancy and lactation. Immunol Allergy Clin North Am 2006;26(1):137–54. [Medline]
- Buhimschi CS, Weiner CP. Medications in pregnancy and lactation: part 2. Drugs with minimal or unknown human teratogenic effect. Obstet Gynecol 2009;113(2 Pt 1):417–32.[Medline]
- Gilbert C, Mazzotta P, Loebstein R, Koren G. Fetal safety of drugs used in the treatment of allergic rhinitis: a critical review. Drug Saf 2005;28(8):707–19. [Medline]
- Seto A, Einarson T, Koren G. Pregnancy outcome following first trimester exposure to antihistamines: meta-analysis. Am J Perinatol 1997;14(3):119–24. [Medline]
- Einarson A, Bailey B, Jung G, Spizzirri D, Baillie M, Koren G. Prospective controlled study of hydroxyzine and cetirizine in pregnancy. Ann Allergy Asthma Immunol 1997;78(2):183–6. [Medline]
- Källén B. Use of antihistamine drugs in early pregnancy and delivery outcome. J Matern Fetal Neonatal Med 2002;11(3):146–52. [Medline]
- NATO Advanced Research Workshop on "Drugs in pregnancy: consensus conference on teratogen information services," Prague, 16–18 April 2004 [Abstract]. Reprod Toxicol 2004;19(2):258.
- Weber-Schoendorfer C, Schaefer C. The safety of cetirizine during pregnancy. A prospective observational cohort study. Reprod Toxicol 2008;26(1):19–23. Epub 2008 May 13. [Medline]
- Allegra [product monograph]. Laval, QC: Sanofi-Aventis Canada Inc; 2006.
- Aerius [product monograph]. Montreal, QC: Schering-Plough Canada Inc; 2006.
- Moretti ME, Caprara D, Coutinho CJ, Bar-Oz B, Berkovitch M, Addis A, et al. Fetal safety of loratadine use in the first trimester of pregnancy: a multicentre study. J Allergy Clin Immunol 2003;111(3):479–83. [Medline]
- Diav-Citrin O, Shechtman S, Aharonovich A, Moerman L, Arnon J, Wajnberg R, et al. Pregnancy outcome after gestational exposure to loratadine or antihistamines: a prospective controlled study. J Allergy Clin Immunol 2003;111(6):1239–43. [Medline]
- Kallen B, Olausson PO. Monitoring of maternal drug use and infant congenital malformations. Does loratadine cause hypospadias? Int J Risk Saf Med 2001;14:115–9.
- Gilboa SM, Strickland MJ, Olshan AF, Werler MM, Correa A, National Birth Defects Prevention Study. Use of antihistamine medications during early pregnancy and isolated major malformations. Birth Defects Res A Clin Mol Teratol 2009;85(2):137–50. [Medline]
- Schwarz EB, Moretti ME, Nayak S, Koren G. Risk of hypospadias in offspring of women using loratadine during pregnancy: a systematic review and meta-analysis. Drug Saf 2008;31(9):775–88. [Medline]
- Rindi V. La eliminazione degli antistaminici di sintesi con il latte e lazione latto-goga de questi. Riv Ital Ginecol 1951;34:147–57.
- Findlay JW, Butz RF, Sailstad JM, Warren JT, Welch RM. Pseudoephedrine and triprolidine in plasma and breast milk of nursing mothers. Br J Clin Pharmacol 1984;18(6):901–6. [Medline]
- Ito S, Blajchman A, Stephenson M, Eliopoulos C, Koren G. Prospective follow-up of adverse reactions in breast-fed infants exposed to maternal medication. Am J Obstet Gynecol 1993;168(5):1393–9. [Medline]
- Hilbert J, Radwanski E, Affrime MB, Perentesis G, Symchowicz S, Zampaglione N. Excretion of loratadine in human breast milk. J Clin Pharmacol 1988;28(3):234–9. [Abstract]
- Lucas BD Jr, Purdy CY, Scarim SK, Benjamin S, Abel SR, Hilleman DE. Terfenadine pharmacokinetics in breast milk in lactating women. Clin Pharmacol Ther 1995;57(4):398–402. [Medline]