I am a breastfeeding mother and i want to know if it is safe to use RoActemra/Actemra? Is RoActemra/Actemra safe for nursing mother and child? Does RoActemra/Actemra extracts into breast milk? Does RoActemra/Actemra has any long term or short term side effects on infants? Can RoActemra/Actemra influence milk supply or can RoActemra/Actemra decrease milk supply in lactating mothers?
- DrLact safety Score for RoActemra/Actemra is 3 out of 8 which is considered Low Risk as per our analyses.
- A safety Score of 3 indicates that usage of RoActemra/Actemra may cause some minor side effects in breastfed baby.
- Our study of different scientific research indicates that RoActemra/Actemra may cause moderate to no side effects in lactating mother.
- Most of scientific studies and research papers declaring usage of RoActemra/Actemra low risk in breastfeeding are based on normal dosage and may not hold true for higher dosage.
- While using RoActemra/Actemra We suggest monitoring 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.
Monoclonal antibody that inhibits the Interleukin-6 receptor (IL-6r) which is used for treatment of Rheumatoid Arthritis, some types of Juvenile Arthritis and Castleman's disease. At latest update no published data on excretion into breast milk were found. Its high molecular weight makes that excretion into breast milk be very unlikely. Because of a low oral bioavailability it is thought that amount absorbed to the infant's plasma from ingested breast milk would be nil or minimal, except in the immediate newborn period or in case of prematurity who may show an increased intestinal absorption. Until more data on this drug is available, it would be preferred other options that are known to be safer, specially during the neonatal period and prematurity.
Little information is available on the clinical use of RoActemra/Actemra during breastfeeding. Only small amounts of RoActemra/Actemra were detected in breastmilk after intravenous doses in 2 mothers, and a few mothers have breastfed their infants with no reported adverse effects. Because RoActemra/Actemra is a large protein molecule absorption is unlikely because it is probably destroyed in the infant's gastrointestinal tract. If RoActemra/Actemra is required by the mother, it is not a reason to discontinue breastfeeding.[1] Until more data become available, RoActemra/Actemra should be used with caution during breastfeeding, especially while nursing a newborn or preterm infant. RoActemra/Actemra is a human immunoglobulin G1 (IgG1) kappa antibody. Holder pasteurization (62.5 degrees C for 30 minutes) decreases the concentration of endogenous immunoglobulin G by up to 79%.[2][3] A study of 67 colostrum samples that underwent Holder pasteurization found that IgG amounts decreased by 34 to 40%. Specific IgG subclasses decreased by different amounts, with IgG1 activity decreasing by about 37%.[4] None of the studies measured IgG activity.
A pregnancy registry in Japan reported that two mothers resumed RoActemra/Actemra therapy while nursing their infants. No adverse events were reported in the infants, but details regarding extent of nursing, infant age, etc. are lacking.[6] Two women in Japan were treated with intravenous RoActemra/Actemra 400 mg monthly for rheumatoid arthritis while they reportedly breastfed their infants exclusively for 9 and 11 months, respectively. Neither infant experienced any adverse effects from the drugs and received all routine immunizations, including BCG without any adverse consequences.[5] It is possible that these two mothers are the same as those reported above. Three women with rheumatoid arthritis becam pregnant whil taking RoActemra/Actemra. The drug was stopped for the remainder of the pregnancy, but resumed (dose not stated) postpartum. They breastfed their infants (extent not stated). No infants had any adverse effects during the first year.[7]
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Information presented in this database is not meant as a substitute for professional judgment. You should consult your healthcare provider for breastfeeding advice related to your particular situation. We do not warrant or assume any liability or responsibility for the accuracy or completeness of the information on this Site.