Can you take emtricitabine while breastfeeding?

What LactMed would consider instead

LactMed ends this record by naming the drugs it would consider in place of emtricitabine. Whether any of them fits depends on what you are treating — this is the database’s list, not a recommendation from us.

• Lamivudine
• Tenofovir

How much emtricitabine gets into breastmilk

Maternal Levels. Five exclusively breastfeeding mothers received oral emtricitabine 200 mg plus tenofovir 300 mg and nevirapine 200 mg at the start of labor, then oral emtricitabine 200 mg and tenofovir 300 mg daily for 7 days postpartum. A total of 16 concurrent maternal blood and milk samples were collected on days 1, 2, 3, and 7 postpartum between 10 minutes and 21 hours after the mothers' doses. Median peak and trough emtricitabine concentrations in breastmilk were 679 mcg/L and 177 mcg/L, respectively. The authors estimated that an exclusively breastfed infant would receive about 2% of the proposed infant dose for emtricitabine and achieve infant serum concentrations that might result in the emergence of viral resistance to emtricitabine.

Fifty HIV-negative women who were nursing their infants were given pre-exposure prophylaxis daily with the combination of tenofovir disoproxil fumarate 300 mg and emtricitabine 200 mg by directly observed therapy for 10 days. On days 7 and 10 of therapy, peak milk samples were obtained 1 to 2 hours after a dose and trough samples were obtained 23 to 24 hours after the previous dose. The median peak milk emtricitabine concentration was 212.5 mcg/L and the trough concentration was 183 mcg/L. These values represent an estimated daily dosage of 27.5 to 31.5 mcg/kg, which is approximately 0.5% of the proposed infant therapeutic dosage.

Emtricitabine was measured in 6 HIV-positive nursing mothers after a 300 mg dose during ongoing therapy. The peak breastmilk level was 872 mcg/L (range 696 to 1063 mcg/L) at a median of 3 hours.

Sixteen Nigerian women took emtricitabine 200 mg once daily as part of a combination therapy for HIV. Expressed milk samples were taken before the dose and at 0.5, 1, 2, 4, 8 and 12 hours after the dose. The median peak breastmilk concentration from dried breastmilk spots was 843 mcg/L (IQR 702 to 1132 mcg/L) at a median of 4 hours after the dose (IQR 2 to 8 hours).

Sixteen mothers taking emtricitabine 200 mg once daily provided 29 milk samples at a median of 15.5 hours after a dose. The median drug concentration in milk was 803 mcg/L, which resulted in an estimated infant dosage of 120 mcg/kg daily and a relative infant dose of 4% of the maternal weight-adjusted dosage.

A clinical trial compared the dapivirine vaginal ring 25 mg monthly to PrEP consisting of 200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate daily as prophylaxis against HIV infection. In women randomized to PrEP (n = 48), emtricitabine concentrations in breastmilk averaged 656 ng/L during the first week of use and trended downward to 558.5 ng/L in the third month of use. At 2 weeks after discontinuation, the milk emtricitabine concentration was below the level of quantification (<5 mcg/L) in all women.

Infant Levels. Fifty HIV-negative women who were nursing their infants were given pre-exposure prophylaxis daily with the combination of tenofovir disoproxil fumarate 300 mg and emtricitabine 200 mg by directly observed therapy for 10 days. A single infant blood sample was obtained after the mother's 7th dose. Of 49 infant blood samples collected, 47 had detectable concentrations of emtricitabine, with a median plasma concentration of 13.2 mcg/L. Infants under 13 weeks of age had a statistically significant lower plasma concentration than those who were 13 weeks of age or older, 16.6 mcg/L and 10.5 mcg/L, respectively.

Emtricitabine 300 mg daily was given to 6 HIV-positive nursing mothers. One breastfed infant had a detectable emtricitabine serum level of 17.5 mcg/L.

Sixteen Nigerian women took emtricitabine 200 mg once daily as part of a combination therapy for HIV. Their exclusively breastfed infants were fed on demand and had blood samples taken at 2 and 8 hours after the dose. Dried blood spots were analyzed and only 3 samples contained quantifiable (>16.6 mcg/L) blood levels of 17.5, 18.8, and 19.4 mcg/L.

Eleven serum concentrations were obtained from breastfed infants whose mothers were taking emtricitabine 200 mg daily, although the extent of breastfeeding was not sated. Infant serum concentrations taken 2 to 20 hours after maternal drug intake at 1 month of age ranged from 0 to 49 mcg/L.

A clinical trial compared the dapivirine vaginal ring 25 mg monthly to PrEP consisting of 200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate daily as prophylaxis against HIV infection. In the infants of mothers randomized to PrEP (n = 48), there were nine detectable concentrations of the emtricitabine triphosphate active metabolite in dried blood spots from five infants, with one infant having four timepoints above the lower level of quantification (<0.125 pmol/punch).

What has been seen in breastfed infants

In a study of 50 infants breastfed by HIV-negative women who were given pre-exposure prophylaxis daily with the combination of tenofovir disoproxil fumarate 300 mg and emtricitabine 200 mg by directly observed therapy for 10 days, 2 infants reportedly had diarrhea lasting 2 to 3 days. No other side effects were reported.

A clinical trial compared the dapivirine vaginal ring 25 mg monthly to PrEP consisting of 200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate daily as prophylaxis against HIV infection. In the infants of mothers randomized to PrEP (n = 48), no infants had reports of adverse events attributable to maternal therapy.

Effects on milk supply

Relevant published information was not found as of the revision date.