Chlorpheniramine / dihydrocodeine / phenylephrine Pregnancy and Breastfeeding Warnings
Chlorpheniramine / dihydrocodeine / phenylephrine Pregnancy Warnings
The Collaborative Perinatal Project monitored 1,070 first trimester exposures and 3,931 exposures which occurred anytime during pregnancy. No evidence was found to suggest a relationship to large categories of malformations. Antihistamine exposure in the first trimester in general was not associated with an increased risk of malformations. Babies born to mothers who have been taking opioids regularly prior to delivery are likely to be physically dependent. Withdrawal signs have included irritability and excessive crying, tremors, hyperactive reflexes, increased respiratory rate, increased stools, sneezing, yawning, vomiting, and fever. The intensity of the syndrome does not always correlate with the duration of maternal opioid use or dose. To treat opioid withdrawal symptoms in infants, chlorpromazine 0.7 to 1.0 mg/kg every six hours, phenobarbital 2 mg/kg every six hours, or paregoric 2 to 4 drops/kg every four hours have been used. The duration of therapy is 4 to 28 days, with the dosages decreased as tolerated.
Chlorpheniramine/dihydrocodeine/phenylephrine has been assigned to pregnancy category C by the FDA. Animal studies have not been conducted with this combination product. There are no controlled data in human pregnancy. In the pregnancy section of the product labeling for Pancof-PD, the manufacturer states "This combination product should be given to pregnant women only if clearly needed, especially during the first trimester." However, in the contraindications section of the product labeling, the manufacturer of Pancof-PD states that "This product is contraindicated in women who are pregnant." (This may be due to the fact that with conservative use, dihydrocodeine is relatively safe for use in pregnancy. However, if used for prolonged periods or in high doses at term, dihydrocodeine represents a significantly greater risk when used in pregnancy.) The manufacturer further states that the product is "... not recommended for use by women during and immediately before labor and delivery because oral opioids may cause respiratory depression in the newborn."
Chlorpheniramine / dihydrocodeine / phenylephrine Breastfeeding Warnings
There are no data on the excretion of the combination product chlorpheniramine/dihydrocodeine/phenylephrine into human milk.
There are no data on the excretion of chlorpheniramine into human milk. However, because other antihistamines are excreted into human milk in low concentrations, the manufacturer of chlorpheniramine recommends that caution be used when administering chlorpheniramine to nursing women. There are no data on the excretion of dihydrocodeine into human milk. However, because other opioids (e.g. morphine) are excreted into human milk and because the molecular weight of dihydrocodeine bitartrate is low enough, the presence of dihydrocodeine in the milk would be expected. Small amounts of phenylephrine are secreted in breast milk. The manufacturer of phenylephrine recommends that due to the potential for serious adverse reactions in nursing infants, a decision should be made to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother.
- chlorpheniramine/dihydrocodeine/phenylephrine liquid Consumer Information
- Pregnancy Support Group
- FDA Pregnancy Categories
- Medicine use during Pregnancy
- Medicine use while Breastfeeding
- Safe Medications during Breastfeeding
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