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Chlorpheniramine / hydrocodone / pseudoephedrine Pregnancy and Breastfeeding Warnings

Chlorpheniramine / hydrocodone / pseudoephedrine is also known as: A-G Tussin, Atuss HD, Atuss HS, Cordron-HC, Cordron-HC NR, Detuss, Hexatussin, Histinex PV, Hydrocof-HC, Hydron PCS, Hydrotuss HC, Hyphed, JayCof-HC, KG-Tussin, Notuss, Notuss-Forte, P-V-Tussin Syrup, Pediatex HC, Q-V Tussin, Tussend, Tussin-V, Welltuss HC, Zutripro

Chlorpheniramine / hydrocodone / pseudoephedrine Pregnancy Warnings

Use is not recommended, including during or immediately prior to labor

US FDA pregnancy category: Not assigned

-Prolonged use of opioids during pregnancy may cause neonatal withdrawal syndrome and physical dependence in the neonate.
-Neonatal withdrawal syndrome presents as irritability, hyperactivity and abnormal sleep pattern, high pitched cry, tremor, vomiting, diarrhea, and failure to gain weight.
-The onset, duration, and severity of neonatal withdrawal syndrome vary with the specific opioid used, duration of use, timing and amount of last maternal use, and the newborn's rate of drug elimination.
-Observe newborns for symptoms of neonatal withdrawal syndrome and manage appropriately.
-An opioid antagonist (e.g. naloxone) should be available for reversal of opioid-induced respiratory depression in the neonate.
-Monitor neonates exposed to opioids during labor for excess sedation and respiratory depression.
-Advise women of the risk of neonatal withdrawal syndrome and ensure that appropriate treatment will be available.

Animal studies have not been conducted with this combination product, and there are no adequate and well-controlled studies in pregnant women.

Animal studies with subcutaneous hydrocodone have shown teratogenicity when given during organogenesis at doses approximately 70 times the maximum recommended human dose (MRHD). Opioids cross the placenta and may produce respiratory depression and psycho-physiologic effects in neonates. Babies born to mothers taking opioids regularly during pregnancy may become physically dependent. Opioids can prolong labor by temporarily reducing the strength, duration, and frequency of uterine contractions, however this effect is not consistent and may be offset by an increased rate of cervical dilation, which tends to shorten labor. Opioids given to mothers shortly before delivery may produce some degree of respiratory depression in the newborn, especially if high doses are used. Chronic use of opioids may reduce fertility in males and females of reproductive potential; it is unknown if these effects are reversible.

Animal studies administering 35 and 45 times the MRHD of chlorpheniramine during organogenesis showed no adverse developmental effects, however another animal study in mice doses throughout pregnancy, embryolethality was seen at approximately 9 times the MRHD, and decreased postnatal survival when dosing was continued after parturition. The majority of studies using chlorpheniramine during pregnancy did not see an increased risk of fetal abnormalities, and in the few studies reporting an association, there was no consistent pattern of malformations noted.

Animal studies with pseudoephedrine are not available. The majority of studies using chlorpheniramine during pregnancy did not see an increased risk of fetal abnormalities, although some studies showed an increased risk of gastroschisis, however similar studies did not find a statistically significant association.

US FDA pregnancy category Not Assigned: The US FDA has amended the pregnancy labeling rule for prescription drug products to require labeling that includes a summary of risk, a discussion of the data supporting that summary, and relevant information to help health care providers make prescribing decisions and counsel women about the use of drugs during pregnancy. Pregnancy categories A, B, C, D, and X are being phased out.

See references

Chlorpheniramine / hydrocodone / pseudoephedrine Breastfeeding Warnings

Hydrocodone, chlorpheniramine, and pseudoephedrine are excreted in human milk.

Hydrocodone: Case reports have shown variable hydrocodone and hydromorphone (an active metabolite) levels in breast milk with use of immediate release hydrocodone to nursing mothers in the early postpartum period with relative infant doses of hydrocodone ranging between 1.4 and 3.7%. There are case reports of excessive sedation and respiratory depression in breastfed infants exposed to hydrocodone.

Chlorpheniramine has not been reported to have effects on the breastfed infant, but published literature suggests it may decrease milk production due to anticholinergic effects.

Pseudoephedrine: Pseudoephedrine has been reported to cause irritability in breastfed infants. A study of 8 lactating women, between 8 to 76 weeks postpartum, who received a single 60 mg dose of pseudoephedrine, showed a mean reduction in 24 hour milk production of 24%, and an estimated mean relative infant dose from breast milk (assuming mean milk consumption of 150 mL/kg/day and a maternal dosing regimen of 60 mg pseudoephedrine 4 times daily) was calculated to be 4.3% of the weight adjusted maternal dose.

Use is not recommended.

Excreted into human milk: Yes

-Breastfed infants should be closely monitored for excess sedation, respiratory depression, and irritability.
-Withdrawal symptoms can occur in breastfed infants when maternal opioids are stopped or breastfeeding is stopped.

See references

References for pregnancy information

  1. "Product Information. Zutripro (chlorpheniramine/hydrocodone/PSE)." Hawthorn Pharmaceuticals (2022):

References for breastfeeding information

  1. "Product Information. Zutripro (chlorpheniramine/hydrocodone/PSE)." Hawthorn Pharmaceuticals (2022):
  2. United States National Library of Medicine "Toxnet. Toxicology Data Network." (2013):

Further information

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