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Acnet Pregnancy |
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Acnet crosses the placenta in small amounts. In one study of 11 patients who had detectable Acnet 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 Acnet, ethisterone, and ethinyl estradiol at approximately 4 weeks gestation. Acnet 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. Acnet has also been used to treat genital Mycoplasma infection during the first trimester without evidence of fetal adverse effects. Pregnant women receiving Acnet estolate may be more prone to hepatotoxicity. In one study of women receiving Acnet estolate between the 22nd and 32nd week of pregnancy, 10% showed abnormal levels of SGOT.
Acnet 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 Acnet the drug of choice for treatment of Chlamydia infections in pregnant women. However, Acnet estolate is considered contraindicated because of drug-related hepatotoxicity. Acnet should only be given during pregnancy when need has been clearly established.
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Acnet is excreted into human milk in small amounts. Acnet 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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