TABLE 8.
Drug | Comment |
---|---|
Tenofovir (TDF) | High placental transfer. No evidence of human teratogenicity. All have anti-HBV activity, therefore risk of hepatitis flare if stopped. |
Emtricitabine (FTC) | |
Lamivudine (3TC) | |
Stavudine (d4T) | High placental transfer. No evidence of human teratogenicity. |
Do not use with ddI (risk of lactic acidosis) or AZT (both thymidine analogues). | |
Zidovudine (AZT) | High placental transfer. No evidence of human teratogenicity. |
Do not use with d4T (both thymidine analogues). | |
Raltegravir (RAL) | High placental transfer. Insufficient data to assess human teratogenicity. |
Case report of markedly elevated liver transaminases in late pregnancy. | |
Dolutegravir (DTG) | Unknown placental transfer. Insufficient data to assess human teratogenicity. |
No data on use in pregnancy. | |
Atazanavir (ATV) | Low placental transfer. No evidence of human teratogenicity. |
Increased dosing in T2/3? | |
Non-pathologic neonatal hyperbilirubinaemia. | |
Lopinavir (LPV) | Low placental transfer. No evidence of human teratogenicity. |
Once daily dosing not advised during pregnancy. | |
Avoid oral solution owing to alcohol and propylene glycol content. | |
Darunavir (DRV) | Low placental transfer. Insufficient data to assess human teratogenicity. |
Less experience in pregnancy than LPV/r and ATV/r. | |
Ritonavir (RTV) | Low placental transfer. No evidence of human teratogenicity. |
Not used for antiretroviral effect, but in lower doses as PI booster in combination with other PIs. | |
Avoid oral solution owing to alcohol content. | |
Efavirenz (EFV) | Moderate placental transfer. |
Potential foetal safety concerns. No increase in overall birth defects with T1 exposure in humans. |
HBV, hepatitis B virus; ddI, didanosine; T2/3, trimester 2/3; PI, protease inhibitor.