Is F 2695 Safe in Breastfeeding

I am a breastfeeding mother and i want to know if it is safe to use F 2695? Is F 2695 safe for nursing mother and child? Does F 2695 extracts into breast milk? Does F 2695 has any long term or short term side effects on infants? Can F 2695 influence milk supply or can F 2695 decrease milk supply in lactating mothers?

• DrLact safety Score for F 2695 is 5 out of 8 which is considered Unsafe as per our analyses.
• A safety Score of 5 indicates that usage of F 2695 may cause serious side effects in breastfed baby.
• Our study of different scientific research indicates that F 2695 may cause moderate to high side effects or may affect milk supply in lactating mother.
• Our suggestion is to use safer alternate options rather than using F 2695 .
• It is recommended to evaluate the advantage of not breastfeeding while using F 2695 Vs not using F 2695 And continue breastfeeding.
• While using F 2695 Its must to monitor child for possible reactions. It is also important to understand that side effects vary largely based on age of breastfed child and time of medication in addition to dosage.
• Score calculated using the DrLact safety Version 1.2 model, this score ranges from 0 to 8 and measures overall safety of drug in lactation. Scores are primarily calculated using publicly available case studies, research papers, other scientific journals and publically available data.

Milnacipran active enantiomer. Serotonin and Norepinephrine selective re-uptake inhibitor antidepressant drug. Frequent and potential severe side effects have been found. Latest update failed to find relevant data on breastfeeding. Pharmacokinetic data (low serum protein binding and high bioavailability) indicates that drug excretion into breast milk in significant amount is highly probable. Absorption by the infant is likely to be high as well. A known alternative would be preferred until more information on the drug is available.

F 2695 has not been studied in nursing mothers and the manufacturer recommends that nursing mothers not take F 2695. Because no information is available on the use of F 2695 during breastfeeding, an alternate drug may be preferred, especially while nursing a newborn or preterm infant.

Relevant published information was not found as of the revision date. However, galactorrhea is reported by the manufacturer to be a side effect of milnacipran, which is the racemic form of the drug.[1] One woman who was being treated for depression took an intentional overdose of 950 mg of milnacipran orally. From day 5 to day 15 after the overdose, the patient noted a flow of milk from her left breast. The galactorrhea resolved without treatment.[2] In a study of cases of hyperprolactinemia and its symptoms (e.g., gynecomastia) reported to a French pharmacovigilance center, milnacipran was not found to have an increased risk of causing hyperprolactinemia compared to other drugs.[3] An observational study looked at outcomes of 2859 women who took an antidepressant during the 2 years prior to pregnancy. Compared to women who did not take an antidepressant during pregnancy, mothers who took an antidepressant during all 3 trimesters of pregnancy were 37% less likely to be breastfeeding upon hospital discharge. Mothers who took an antidepressant only during the third trimester were 75% less likely to be breastfeeding at discharge. Those who took an antidepressant only during the first and second trimesters did not have a reduced likelihood of breastfeeding at discharge.[4] The antidepressants used by the mothers were not specified. A retrospective cohort study of hospital electronic medical records from 2001 to 2008 compared women who had been dispensed an antidepressant during late gestation (n = 575) to those who had a psychiatric illness but did not receive an antidepressant (n = 1552) and mothers who did not have a psychiatric diagnosis (n = 30,535). Women who received an antidepressant were 37% less likely to be breastfeeding at discharge than women without a psychiatric diagnosis, but no less likely to be breastfeeding than untreated mothers with a psychiatric diagnosis.[5] None of the mothers were taking F 2695.