“…This does not appear to be associated with clinically important problems and is not a contraindication to breast feeding. There is insufficient information on the teratogenic potential of pyrazinamide, but it should be avoided in the first trimester of pregnancy unless absolutely necessary) 136] Neonates with glucose-6-phosphate dehydrogenase (G6PD) deficiency may have significant sensitivity to isoniazid, resulting in haemolysis during the neonatal period) 137] Shneerson and Francis [138] showed that the placenta was not a significant physiological barrier to the transfer of ethambutol to the fetus. Teratogenic effects of ethambutol or other antituberculosis drugs, can arise up to 23 weeks of pregnancy.…”
Potent antibiotics are required to cure tuberculosis and reduce the burden of illness in the community. Minor adverse effects are commonly encountered and can be managed by reassurance and explanation. Significant hypersensitivity reactions require cessation of all antituberculosis drugs. Adverse effects should be treated appropriately. An effective antituberculosis regimen should be reestablished as soon as possible. Desensitisation may be necessary if suitable alternative drugs cannot be used. In the event of drug-induced hepatitis, all hepatotoxic drugs should be ceased until symptoms resolve and liver function tests return to normal. Other significant direct toxic effects should be promptly detected and appropriately treated. A thorough knowledge of potential adverse reactions and pharmacokinetics is essential for any physician using antituberculosis drugs.
“…This does not appear to be associated with clinically important problems and is not a contraindication to breast feeding. There is insufficient information on the teratogenic potential of pyrazinamide, but it should be avoided in the first trimester of pregnancy unless absolutely necessary) 136] Neonates with glucose-6-phosphate dehydrogenase (G6PD) deficiency may have significant sensitivity to isoniazid, resulting in haemolysis during the neonatal period) 137] Shneerson and Francis [138] showed that the placenta was not a significant physiological barrier to the transfer of ethambutol to the fetus. Teratogenic effects of ethambutol or other antituberculosis drugs, can arise up to 23 weeks of pregnancy.…”
Potent antibiotics are required to cure tuberculosis and reduce the burden of illness in the community. Minor adverse effects are commonly encountered and can be managed by reassurance and explanation. Significant hypersensitivity reactions require cessation of all antituberculosis drugs. Adverse effects should be treated appropriately. An effective antituberculosis regimen should be reestablished as soon as possible. Desensitisation may be necessary if suitable alternative drugs cannot be used. In the event of drug-induced hepatitis, all hepatotoxic drugs should be ceased until symptoms resolve and liver function tests return to normal. Other significant direct toxic effects should be promptly detected and appropriately treated. A thorough knowledge of potential adverse reactions and pharmacokinetics is essential for any physician using antituberculosis drugs.
“…Regimens that include ethambutol are recommended for use in pregnancy 37. One case report that measured ethambutol concentrations in amniotic fluid, maternal, placental, and cord blood specimens suggests that the placenta is not a significant physiological barrier to the transfer of ethambutol to the fetus 38. We have found two reports of ocular malformations in newborn infants of mothers receiving ethambutol in the first trimester 39…”
Section: Ethambutol Toxicity In Childrenmentioning
In the wake of the worsening tuberculosis (TB) situation in young African adults, the number of clinically diagnosed cases of childhood TB is also steadily increasing.
“…Transplacental transfer of ethambutol has been documented to be at least 74.5% of that of maternal serum concentrations (Shneerson & Frances 1979). This pregnancy terminated at 38 weeks with the delivery of a normal female infant.…”
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