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Aknederm Ery Gel Pregnancy |
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Aknederm Ery Gel crosses the placenta in small amounts. In one study of 11 patients who had detectable Aknederm Ery Gel levels in the serum, 4 infants did not have detectable cord concentrations. The cord concentrations in the remaining 7 infants generally ranged from 1% to 6% of that found in maternal serum. A case of left absence-of-tibia syndrome was reported in an infant whose mother had received Aknederm Ery Gel, ethisterone, and ethinyl estradiol at approximately 4 weeks gestation. Aknederm Ery Gel has been used prior to delivery in women colonized with group B beta-hemolytic streptococcus to reduce infant colonization. No adverse events in the infants have been reported. Aknederm Ery Gel has also been used to treat genital Mycoplasma infection during the first trimester without evidence of fetal adverse effects. Pregnant women receiving Aknederm Ery Gel estolate may be more prone to hepatotoxicity. In one study of women receiving Aknederm Ery Gel estolate between the 22nd and 32nd week of pregnancy, 10% showed abnormal levels of SGOT.
Aknederm Ery Gel has been assigned to pregnancy category B by the FDA. Animal studies failed to reveal evidence of teratogenicity. There are no controlled data in human pregnancy. The Centers for Disease Control and Prevention considers Aknederm Ery Gel the drug of choice for treatment of Chlamydia infections in pregnant women. However, Aknederm Ery Gel estolate is considered contraindicated because of drug-related hepatotoxicity. Aknederm Ery Gel should only be given during pregnancy when need has been clearly established.
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Aknederm Ery Gel is excreted into human milk in small amounts. Aknederm Ery Gel is considered compatible with breast-feeding by the American Academy of Pediatrics.
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Information checked by Dr. Sachin Kumar, MD Pharmacology
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