Transfer of cetirizine/levocetirizine into human breast milk and estimation of drug exposure to infants through breastfeeding: A human lactation study from the ConcePTION project

Author:

Nordeng Hedvig1ORCID,Wegler Christine2ORCID,Lindqvist Annika23ORCID,Melander Erik2ORCID,Magnusson Mikaela4ORCID,Gandia Peggy56ORCID,Panchaud Alice78ORCID,Baranczewski Pawel23ORCID,Spigset Olav910ORCID

Affiliation:

1. Pharmacoepidemiology and Drug Safety Research Group, Department of Pharmacy University of Oslo Oslo Norway

2. Department of Pharmacy, Uppsala Drug Optimization and Pharmaceutical Profiling (UDOPP) Uppsala University Uppsala Sweden

3. Department of Pharmacy, SciLifeLab Drug Discovery and Development Platform Uppsala University Uppsala Sweden

4. Uppsala Biobank Uppsala Sweden

5. Pharmacokinetics and Toxicology laboratory Toulouse University Hospital Toulouse France

6. UMR1436‐INTHERES, Toulouse National Veterinary School Toulouse France

7. Institute of Primary Health Care (BIHAM) University of Bern Bern Switzerland

8. Service of Pharmacy Lausanne University Hospital and University of Lausanne Lausanne Switzerland

9. Department of Clinical Pharmacology St. Olav University Hospital Trondheim Norway

10. Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences Norwegian University of Science and Technology Trondheim Norway

Abstract

AbstractData on drug transfer into human breast milk are sparse. This study aimed to quantify concentrations of cetirizine and levocetirizine in breast milk and to estimate drug exposure to infants. Breastfeeding women at least 8 weeks postpartum and using cetirizine or its pure (R)‐enantiomer levocetirizine were eligible to participate. Breast milk samples were collected at six predefined times during a dose interval (0, 2, 4, 8, 12 and 24 h after drug intake) at steady state. Infant drug exposure was estimated by calculating the absolute infant dose (AID) and the weight‐adjusted relative infant dose (RID). In total, 32 women were eligible for final inclusion, 31 women using cetirizine and one woman using levocetirizine. Means of the individual maximum and average cetirizine milk concentrations were 41.0 and 16.8 μg/L, respectively. Maximum concentrations occurred on average 2.4 h after intake, and the mean half‐life in milk was 7.0 h. Estimated AID and RID for cetirizine in a day were 2.5 μg/kg and 1.9%, respectively. The corresponding values for levocetirizine were 1.1 μg/kg and 1.9%. No severe adverse events were reported. Our findings demonstrate that the transfer of cetirizine and levocetirizine into breast milk is low and compatible with breastfeeding.

Publisher

Wiley

Subject

Pharmacology,Toxicology,General Medicine

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