Medications, diabetes, and pregnancy
Medicationsa | Pregnancy categoryb | Lactation | Fetal exposure |
---|---|---|---|
Insulins | |||
Insulin lispro | B | Safe | Unlikely |
Insulin aspart | B | Safe | Unlikely |
Insulin glulisine | C | Probably safe | Unlikely |
Regular | B | Safe | Unlikely |
Neutral protamine Hagedorn | B | Safe | Unlikely |
Insulin detemir | B | Safe | Unlikely |
Insulin glargine | C | Probably safe | Unlikely |
Oral antiglycemics | |||
Metformin | B | Unsafe, but not contraindicated | Crosses placenta |
Second-generation sulfonylurea: glyburide | B | Unsafe, but not contraindicated | Crosses placenta |
First-generation sulfonylureas | Not recommended | ||
Antihypertensives | |||
Labetalol | C | Probably safe | Crosses placenta, but acceptable safety profile |
Nifedipine (long-acting) | C | Probably safe | Crosses placenta, but acceptable safety profile |
Methyldopa | B | Probably safe | Crosses placenta, but acceptable safety profile |
Diltiazem | C | Probably safe | Crosses placenta |
Hydralazine | C | Probably safe | Crosses placenta |
Angiotensin-converting enzyme inhibitors | Not recommended | ||
Angiotensin II receptor blockers | Not recommended | ||
Others | |||
Low-dose aspirin | Not classified | ||
Statins | X | ||
Folate supplementation | A |
↵a Other classes of diabetes drugs not listed here, such as thiazolidinediones, alpha glucosidase inhibitors, glucagon-like peptide 1 receptor agonists, and dipeptidyl peptidase 4 inhibitors, have not been studied, and as there are very few data on their effects during pregnancy, should probably be avoided.
↵b Category A: Adequate and well-controlled studies have failed to demonstrate a risk to the fetus in the first trimester of pregnancy (and there is no evidence of risk in later trimesters). Category B: Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women. Category C: Animal reproduction studies have shown an adverse effect on the fetus and there are no adequate and well-controlled studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks. Category D: There is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience or studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks. Category X: Studies in animals or humans have demonstrated fetal abnormalities and/or there is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience, and the risks involved in use of the drug in pregnant women clearly outweigh potential benefits.
Adapted from information in references 9, 16, and 18.