Actoplus met xr Pregnancy Warnings
Benefit should outweigh risk
US FDA pregnancy category: Not Assigned
Risk summary: Abnormal blood glucose concentrations during pregnancy are associated with a higher incidence of congenital anomalies, increased neonatal morbidity, and mortality. Most experts recommend insulin use during pregnancy to maintain blood glucose concentrations as close to normal as possible.
Comment: Premenopausal anovulatory women may be at risk for pregnancy with use of pioglitazone; these women should be informed of pregnancy risk.
Published studies with metformin use during pregnancy have not reported a risk of major birth defects or miscarriage risk. Animal studies using pioglitazone at 10 to 40 times the maximum recommended human dose have shown increased rates of postimplantation loss, delayed development, reduced fetal weights, and delayed parturition. There are no adequate and well-controlled studies in pregnant women.
US FDA pregnancy category Not Assigned: The US FDA has amended the pregnancy labeling rule for prescription drug products to require labeling that includes a summary of risk, a discussion of the data supporting that summary, and relevant information to help health care providers make prescribing decisions and counsel women about the use of drugs during pregnancy. Pregnancy categories A, B, C, D, and X are being phased out.
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Actoplus met xr Breastfeeding Warnings
UK: Use is contraindicated.
US: A decision should be made to discontinue breastfeeding or discontinue the drug, taking into account the importance of the drug to the mother.
Excreted into human milk: Yes, in small amounts (metformin); Unknown (pioglitazone)
Excreted into animal milk: Yes (metformin); Yes (pioglitazone)
Comments: The effects in the nursing infant are unknown.
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