Clinical Study
Safety and Tolerability of Antiretrovirals during Pregnancy
Table 3
Drug substitutions or discontinuations during pregnancy.
| Class | Drug | events/ pregnancies | Percent (95% confidence interval) |
| NRTI | | 11/114 | 10 (5–17) |
| | AZT | 10/99 | 10 (5–18) | | 3TC | 0/109 | 0 (0–3) | | d4T | 0/23 | 0 (0–15) | | ABC | 1/8 | 13 (0–53) | | ddI | 0/6 | 0 (0–46) | | TDF | 0/2 | 0 (0–84) | | FTC | 0/1 | 0 (0–98) |
| NNRTI | | 3/20 | 15 (3–38) |
| | NVP | 3/19 | 16 (1–33) | | DLV | 0/1 | 0 (0–98) | | EFV | 2/2 | n.a. |
| PI | | 8/97 | 8 (4–16) |
| | NFV | 6/64 | 9 (4–19) | | LPV/RTV | 2/28 | 1 (1–24) | | IDV | 0/5 | 0 (0–60) | | IDV/RTV | 0/1 | 0 (0–98) | | SQV | 0/2 | 0 (0–84) | | SQV/RTV | 2/9 | 22 (3–60) |
|
|
Excludes EFV substitutions. In the drug class summary, a pregnancy in which ≥2 drugs from the same class were substituted was counted only once.
|