TABLE 3.
Safety of anti-thrombotic drugs during pregnancy and breastfeeding.
| Drugs | Risk category | Placenta permeable | Transfer to breast milk | Safety data |
| Antiplatelet drugs | ||||
| Abciximab | C | Unknown | Unknown | Inadequate human studies |
| Acetylsalicylic acid (low dose) | B | Yes | Yes (no adverse effects reported) | No teratogenic effects (inadequate human studies regarding the use of doses between 100–500 mg/day) |
| Cangrelor | C | Unknown | Unknown | No human data |
| Clopidogrel | B | Unknown | Yes | No adequate human data |
| Prasugrel | – | Unknown | Yes | Inadequate human data |
| Ticagrelor | – | Unknown | Yes | Inadequate human data; not recommended |
| Ticlopidine | C | Unknown | Yes | Inadequate human data |
| Vorapaxar | – | Unknown | Yes | Inadequate human data |
| Anticoagulants | ||||
| Acenocoumarol | D | Yes | Yes (no adverse effects reported) | Embryopathy (mainly first trimester), |
| Apixaban | – | Yes | Yes | No human data: not recommended |
| Dabigatran | – | Yes | Unknown | No human data; not recommended |
| Edoxaban | – | Unknown | Yes (contraindicated in breastfeeding) | Contraindicated; Hokusai-VTE study: 10 cases with exposure in first trimester, for up to 6 weeks. Results: six live births (four full term and two pre-term), one first trimester spontaneous abortion, and three elective terminations |
| Fondaparinux | – | Yes | Yes | Inadequate human data |
| Heparin (low molecular weight) | B | No | No | Retrospective cohort study with 693 live births: no increased risk of major developmental abnormalities |
| Heparin (unfractionated) | B | No | No | Human data: no fetus abnormalities |
| Phenprocoumon | D | Yes | Yes | Coumarin embryopathy |
| Rivaroxaban | – | Yes | Yes | Inadequate human data (contraindicated) |
| Warfarin | D | Yes | Yes | Coumarin embryopathy |