Drugs in Pregnancy and Lactation: Tenth Edition

GRANISETRON

Antiemetic

PREGNANCY RECOMMENDATION: Limited Human Data—Animal Data Suggest Low Risk

BREASTFEEDING RECOMMENDATION: No Human Data—Probably Compatible

PREGNANCY SUMMARY

Three reports describing the use of granisetron during human gestation have been located. Because of the indication for this drug, the opportunity for fetal exposure appears to be minimal.

FETAL RISK SUMMARY

Granisetron is an antiemetic used for the prevention of nausea and vomiting in patients receiving cancer chemotherapy. The drug is a selective 5-hydroxytryptamine3 (5-HT3)-receptor antagonist with little or no affinity for other serotonin receptors (1). No evidence of an effect on plasma prolactin concentrations has been found in clinical studies.

Reproductive studies at doses up to 146 and 96 times, respectively, the recommended human dose based on BSA in pregnant rats and rabbits found no evidence of impaired fertility or harm to the fetus (1). Shepard reviewed three studies conducted in rats and rabbits before and after conception or in the perinatal and postnatal periods that found no adverse fetal effects or drug-related effects on behavior (2).

It is not known whether granisetron crosses the placenta to the fetus. The molecular weight (about 349) is low enough that passage to the fetus should be expected.

Granisetron has been used to prevent vomiting during cesarean section (3) and with chemotherapy in the 3rd trimester (4,5). No fetal or newborn complications related to the antiemetic were reported.

BREASTFEEDING SUMMARY

No reports describing the use of granisetron during lactation have been located. The indication for granisetron therapy, however, suggests that the opportunities for use of the drug during lactation are minimal. Because of its low molecular weight (about 349), transfer into breast milk should be expected.

References

1.Product information. Kytril. SmithKline Beecham Pharmaceuticals, 1997.

2.Shepard TH. Catalog of Teratogenic Agents. 8th ed. Baltimore, MD: The Johns Hopkins University Press, 1995:204–5.

3.Fujii Y. Prevention of emetic episodes during cesarean delivery performed under regional anesthesia in parturients. Curr Drug Saf 2007;2:25–32.

4.Merimsky O, Le Cesne A. Soft tissue and bone sarcomas in association with pregnancy. Acta Oncol 1998;37:721–7.

5.Merimsky O, Le Chevalier T, Missenard G, Lepechoux C, Cojean-Zelek I, Mesurolle B, Le Cesne A. Management of cancer in pregnancy: a case of Ewing’s sarcoma of the pelvis in the third trimester. Ann Oncol 1999;10:345–50.



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