Lidocaine ophthalmic Pregnancy and Breastfeeding Warnings
Lidocaine ophthalmic is also known as: Akten
Lidocaine ophthalmic Pregnancy Warnings
This drug should be used during pregnancy only if clearly needed.
US FDA pregnancy category: B
Animal studies failed to reveal evidence of fetal harm when this drug was administered subcutaneously at doses more than 800-fold greater than the human dose, based on body weight. There are no controlled data in human pregnancy.
US FDA pregnancy 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.
Lidocaine ophthalmic Breastfeeding Warnings
Caution is recommended.
Excreted into human milk: Unknown
Excreted into animal milk: Data not available
Comments:
-This drug is secreted in human milk following systemic use; while no systemic exposure is expected with the ophthalmic formulation, caution is advised.
-The effects in the nursing infant are unknown.
References for pregnancy information
- "Product Information. Akten (lidocaine ophthalmic)." Akorn Inc, Buffalo Grove, IL.
References for breastfeeding information
- "Product Information. Akten (lidocaine ophthalmic)." Akorn Inc, Buffalo Grove, IL.
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Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.