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Conestat alfa Pregnancy and Breastfeeding Warnings

Conestat alfa is also known as: Ruconest

Conestat alfa Pregnancy Warnings

Use is recommended only if clearly needed and the benefit outweighs the risk.

US FDA pregnancy category: B

One animal study revealed evidence of reproductive toxicity. 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.

See references

Conestat alfa Breastfeeding Warnings

The amount of C1 esterase inhibitor excreted into breast milk is expected to be small due to its large molecular weight. Any C1 esterase inhibitor present in breast milk is likely destroyed in the infant's gastrointestinal tract and not absorbed (neonates may be an exception).

UK: Use is not recommended unless benefit outweighs risk.
US: Caution is recommended.

Excreted into human milk: Unknown
Excreted into animal milk: Data not available

Comments: Human plasma-derived C1 esterase inhibitor is considered first-line by an international consensus panel for prophylaxis and treatment of maternal hereditary angioedema during lactation.

See references

References for pregnancy information

  1. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
  2. "Product Information. Ruconest (conestat alfa)." Valeant Pharmaceuticals, Costa Mesa, CA.

References for breastfeeding information

  1. United States National Library of Medicine "Toxnet. Toxicology Data Network. Available from: URL: http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?LACT." ([cited 2013 -]):
  2. Cerner Multum, Inc. "UK Summary of Product Characteristics." O 0
  3. "Product Information. Ruconest (conestat alfa)." Valeant Pharmaceuticals, Costa Mesa, CA.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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