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DrugUseduringBreastfeeding
Dateofrevision:December2014
M.S.BrochetBPharmMScS.ItoMDFRCPC
Thefollowingisanoverviewofdruguseduringbreastfeeding.Thisinformationisnotintendedtobea
comprehensivereviewthereaderisthereforeencouragedtoseekadditionalandconfirmatoryinformation.

PrinciplesofDrugUseduringBreastfeeding
Clinicianscanusethefollowinggeneralprinciplestomanagecaseswheredrugexposureinabreastfedinfantis
questioned:
Almostalldrugsareexcretedtosomedegreeinbreastmilk.

Breastmilk/feedinghastangiblemedicalandotherbenefitscomparedtoformula.1,2,3
Evenwhenthebreastmilk:maternalplasmaconcentrationratioapproachesorexceeds1,theamountofdrug
ingestedbytheinfantrarelyattainstherapeuticlevels.
Briefexposuretoadrug,asmightbeexpectedinthecaseofanalgesicsgiventorelievepostpartumpain,is
usuallyoflessconcernthanadruggivenforlongperiodsoftime.Theamountofdrugingestedbytheinfant
can,onoccasion,beminimizedbyfeedingtheinfantjustbeforeoratthetimeofmaternaldosing.
Inthecaseofchronicdrugtherapy,theinfantisusuallyexposedtolowerconcentrationsofthedrugwhile
breastfeedingthanwhilethefetusisinutero.Nevertheless,inmostcasesthelongtermconsequencesof
chronicexposuretosubtherapeuticlevelsofmedicationsarenotknown.
Recommendationsaboutbreastfeedingduringdrugtherapydependonknowingifsmallamountsofthedrug
(subtherapeuticamounts)takenforevenshortperiodsoftimemaybeassociatedwiththefollowing:
idiosyncraticreactions,e.g.,chloramphenicol
interferencewithgeneticallyabnormalmetabolicpathways,e.g.,nitrofurantoininpatientswithG6PD
deficiencies
synergisticeffectswithdrugstheinfantreceivestherapeutically,e.g.,caffeineincoffeeandteamay
enhanceeffectsoftherapeuticcaffeineoraminophyllineintheneonate

Cliniciansrequireareasonableknowledgeofpharmacologyandtherapeuticsinthenewbornaswellasa
knowledgeoftheamountofdrugexcretedinbreastmilk.
TheDrugsandLactationdatabase(LactMed)isareliableandauthoritativewebbasedresourceaboutdrug
excretioninbreastmilkandrecommendationsforbreastfeedingduringmaternaltherapy.5Itisfreeofchargeand
runbytheUSNationalLibraryofMedicine.LactMedishousedwithintheTOXNETWebsite.
Considerseveralimportantquestionswhenabreastfeedingmotherstartsdrugtherapy:4
IsthedrugabsorbedfromtheGItract?
Isthedrugevergivendirectlytoinfantsfortherapeuticreasons?
Doestheestimateddosedeliveredthroughbreastmilkapproachatherapeuticquantity?
Aretheeffectsofthedrugeasilyrecognizedintheinfant?
Arethereidiosyncraticorallergicreactionstothedrugthatarenotdoserelated?
Aretherelesstoxicalternativesformaternaltherapy?
Isthereapotentialfordrugaccumulationduringprolongedtherapy?
Couldsubtherapeuticdosesofthedrugmaskearlysignsofmedicalconditionsintheinfant?
Istheriskposedbythedrugsubstantialenoughtooutweighthesignificantprovenbenefitsofbreastfeeding?

DrugsCompatiblewithBreastfeeding
Drugsconsideredcompatiblewithbreastfeedingfaroutnumberthoseconsideredcontraindicatedduring
breastfeeding.Table1discussessomeexamplesofdrugsconsideredtobecompatiblewithbreastfeeding.
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Table1:DrugsCompatiblewithBreastfeedinga

Therapeutic
Class
Analgesics

Drugs/Drug
Classes
Compatiblewith
Breastfeeding
Acetaminophen,
morphine

Comments
Formostopioidanalgesics,theamountofdrugexcretedin
breastmilkissmall,andshorttermuseshouldbeofnomajor
concern.Ifusedforlongerthan3daysmonitorcloselyfor
drowsiness/sedation,difficultybreathing,difficultybreastfeeding,
decreasedtone,particularlyinprematureinfantsandneonates.6
Meperidineisanexceptioninneonates,thelonghalflivesof
meperidine(13h)andnormeperidine(63h)mayresultin
accumulationinplasma,possiblyleadingtoneurobehavioural
depression.7,8

Inaddition,usecodeinewithcautionatthelowesteffectivedose
fortheshortestperiodoftime.Motherswithultrarapid
metabolizerCYP2D6genotype(Chinese,Japanese,Hispanic0.5
1%Caucasian110%AfricanAmerican3%NorthAfrican,
Ethiopian,SaudiArabian1628%)mayexperienceintensified
effectsfromaregulardosingregimenofcodeineduetoincreased
conversionofcodeinetomorphine,causingmorphinetoxicity.
Resultanthighlevelsofmorphineinmaternalserumcouldcause
relativelyhighmorphinelevelsinbreastmilk.4Mothers

experiencingmorphinetoxicity,whetherduetothisgenotypeor
morphineoverdose,shouldnotbreastfeed.Codeineuseshouldbe
limitedtolessthan34daysinabreastfeedingmother.
OxycodoneandhydrocodonearealsometabolizedbyCYP2D6to
apotentactivemetaboliteseecodeineforinformationregarding
theultrarapidmetabolizerCYP2D6genotype.4Maternal
oxycodoneusehasbeenassociatedwithasimilarincidenceof
neonatalCNSdepressionascodeine 9andlevelsinbreastmilk

stronglycorrelatedwithplasmalevelsinonestudy.10Useof
oxycodoneorhydrocodonewhilebreastfeedingshouldbe
consideredonlyinpatientswhocannottakeotheropioidsand
shouldbelimitedtolessthan34days.
Theamountofmorphineexcretedinbreastmilkcouldreach
7.5%ofthepediatricdose.11Despitewidespreaduseofmorphine
bybreastfeedingmothers,thereisonlyonecasereportofa
nursinginfantwiththerapeuticplasmaconcentrations.12

Limiteddataindicatesthathydromorphoneisexcretedinto
breastmilkinsmallamounts.4

Datafortramadolarelacking.Shorttermusemaybeaconcern
duetoitslonghalflife(7hfortramadoland8.5hfortheactive
metaboliteinnewborns)especiallyinprematureinfants:monitor
forincreasedsleepiness.Excretionintobreastmilkislow,
thereforeitisunlikelytoaffecthealthybabies.Anexclusively
breastfedinfantwouldreceiveabout10%ofthetherapeuticdose
forachild.13

Methadonelevelsinhumanmilkarelow.Anexclusivelybreastfed
infantwouldreceive<5%oftheweightadjustedmaternaldose.b
Buprenorphinelevelsinmilkcouldreach2.5%oftheweight
adjustedmaternaldose binanexclusivelybreastfedinfant.Ithas
poororalbioavailabilityandlowdrugconcentrationsinbreastfed
infant'sserumandurinehavebeendocumented.Onestudy
suggestedthatextraduralbuprenorphineadministrationinthe
mothersuppressedinfantbreastfeedingbut3otherswere
inconclusive.14Levelsofmethadoneorbuprenorphineinbreast
milkareinsufficienttopreventsymptomsofneonatalabstinence
syndrome.4
Datafornaltrexonearelacking.Onecasereportnotedminimal
excretionintomilk.14,15
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Antibiotics

Aminoglycosides,
cephalosporins,
clindamycin,
fluoroquinolones,
macrolides,
metronidazole,
nitrofurantoin,
penicillins,
sulfonamides

Formanyantibiotics,theamountsingestedbyabreastfedinfant
willbebelowtherapeuticlevels(e.g.,penicillins,
cephalosporins),butmightbesufficienttoresultinidiosyncratic
reactions(e.g.,chloramphenicol)orcauseanemiainaninfant
withG6PDdeficiency(e.g.,nitrofurantoin,sulfonamides).Other
potentialproblemsaremodificationstothenormalGIfloraleading
tothrushanddiarrhea.However,clinicalsignificanceoftheserisks
isusuallynothighenoughtojustifydiscontinuationof
breastfeeding.
Aminoglycosidesareexcretedinbreastmilkwhenadministered
imorivtothemotherbecausethedrugsarepoorlyabsorbed
fromtheGItract,itisunlikelythatrenaltoxicityorototoxicity
wouldoccurintheinfant.
Onlysmallamountsoforalclindamycinareexcretedinbreast
milk(26%oftherecommendedpediatricdosage).Itisunlikely
thatthesequantitieswouldbeclinicallyrelevantbutatleastone
caseofbloodystoolshasbeenreportedinthebreastfedinfantofa
motherreceivingclindamycin.Topicalclindamycin(notusedinthe
nipplearea)isgenerallyassociatedwithlowermaternalsystemic
druglevelsandlowerbreastmilkexcretioncomparedtosystemic
use.14
Erythromycinisexcretedinbreastmilkinlowamountsandis
compatiblewithbreastfeeding.Limiteddataregarding
clarithromycinandazithromycindemonstratethatthesedrugs
areexcretedinbreastmilkinsmallamounts,buttheamountof
drugingestedbyabreastfedinfantislikelybelowtherapeutic
pediatriclevels.16,17Nodataareavailableregardingthe

excretionoftelithromycininbreastmilk.
Metronidazoleuseduringbreastfeedinghasraisedsome
concernsbasedonreportsthatitismutagenicinbacteriaand
carcinogenicinrodentsduringlifelongingestion.Specific
untowardeffectsinanursinginfantasaresultofmetronidazole
ingestionhavenotbeenreported.Withoutmoredirectevidenceof
theharmfuleffectsofshorttermuseinhumans,itseemsoverly
conservativetowithholdthedrugordiscontinuebreastfeedingin
patientswithsymptomaticinfections.Forthetreatmentof
trichomoniasiswithasingleoraldoseofmetronidazole2g,some
cliniciansnowrecommendaninterruptionofbreastfeedingfor12
24h,especiallywithyoungbabies.7Topicalmetronidazole(as

longasitisnotusedinthenipplearea)isconsideredcompatible
withbreastfeedingsincebloodlevelsandexcretionintobreastmilk
arelowerthanwithmaternalsystemicmetronidazoleuse.
Fluoroquinoloneshavetraditionallynotbeenusedininfants
becauseofconcernsregardingadverseeffectsonjoint
development.Studiesindicatelittlerisk.Shorttermuseof
ciprofloxacin,levofloxacin,norfloxacinorofloxacinis
acceptableinnursingmothers.Thesequinolonesareexcretedin
breastmilkinsmallamountswhichdonotresultinsignificant
serumconcentrationsinbreastfedinfants.Thecalciuminbreast
milkmayalsodecreasequinoloneabsorptionintheinfant.14
Therearenodataavailableformoxifloxacin.Maternaluseof
gatifloxacineyedropspresentsnegligibleriskforthenursing
infant.14

Thesulfonamidesareexcretedinbreastmilkinsmallamounts.
Thereareconcernsaboutthesedrugscausinganemiainaninfant
withG6PDdeficiencywhichismorecommoninthoseofAfrican,
Greek,middleeasternandsoutheastAsianorigin.Usewith
cautioninmothersbreastfeedingprematureinfantsorneonates
withhyperbilirubinemia.7Usealternativesunlesstheinfectionis
notrespondingtoothertherapy.
Theuseofnitrofurantoininbreastfeedingmothersisgenerally
safe,asonlysmallamountstransferintothebreastmilk.Despite
thelackofdocumentedreports,thereisapotentialriskof
hemolyticanemiainallnewbornsexposedtonitrofurantoinowing
totheirglutathioneinstability,especiallyininfantswithG6PD
deficiency.Althoughsomesuggestthatnitrofurantoinbeavoided
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ininfants<1month,studieshavenotedthatglutathionestability
mightbeestablishedbytheeighthdayoflife.Ininfants<1month,
analternativeantibioticmightbepreferredhowever,ifan
alternativewerenotavailable,theuseofnitrofurantoinwouldnot
beareasontoavoidbreastfeeding.Inanysuchcasethesuckling
infantshouldbemonitoredbyhisorherphysician.18
Somereviewsclassifytetracyclinesascontraindicatedin
breastfeedingbasedonconcernsofstainingofdentalenamelor
bonedeposition.Availabledataindicatethatharmisunlikelywith
shorttermuseoftetracyclines.Milklevelsarelowandcalciumin
breastmilklimitsabsorptionoftetracyclines.However,asa
precautionbasedonthetheoreticalrisk,prolongedorrepeated
coursesshouldbeavoidedduringbreastfeeding.14

Anticoagulants

Heparin
(unfractionatedand
lowmolecular
weight),warfarin

Heparin,administeredparenterallyforacuteshorttermtherapy
ofthrombophlebitis,hasnotbeenshowntobeexcretedinbreast
milk.Heparinisalargepolysaccharidemoleculethatisinactivated
intheGItractwhentakenorally.Itstransferintobreastmilkand
risktoabreastfedinfantareconsiderednegligible.7
Theamountofbenzylalcoholusedaspreservativeinmultidose
vialsofunfractionatedheparinorlowmolecularweightheparinis
toolowtoposeanyrisktoabreastfeedingbaby.11
Fewdataareavailableregardingtheeffectsoflowmolecular
weightheparinsduringbreastfeeding.Thereisacasereportof
12fulltermneonatesbeingbreastfedbymotherstreatedwith20
or40mgofenoxaparininjectedsubcutaneouslydaily.19No

anticoagulanteffects,asmeasuredbyantiXaactivitylevels,were
detectedinthebabies.Itisthoughtthatwiththerelativelyhigh
molecularweightofenoxaparinanditsinactivationintheGItract
iforallyingested,itstransferintobreastmilkandrisktoa
breastfedinfantshouldbeconsiderednegligible.7Nodrugwas
foundinbreastmilkof2patientswhoreceived500010000IUof
dalteparin.20Inastudyof15lactatingmothersafteroncedaily

routinedalteparin2500IUscnoquantitativecorrelationwasnoted
betweenantiXaactivitiesinplasmaandmilk.21Therearenodata
availableonexcretionintomilkofnadroparinortinzaparin
howeverbasedontheirmolecularweightandinactivationbythe
GItract,excretionintobreastmilkisexpectedtobenegligible.
Thereare3casereportsofdanaparoidusebybreastfeeding
mothers.Onereportdescribedtheuseoflepirudinduring
lactation.Theamountoftheselargemoleculesexcretedinto
breastmilkisexpectedtobeverysmall.Additionally,their
deactivationintheGItractafteroralingestionmakesrisktoa
breastfeedinginfantviaingestionfrombreastmilknegligible.22,
23

Theuseoffondaparinuxduringbreastfeedinghasnotbeen
describedinhumans.Althoughanimaldatasuggestthedrugis
excretedintomilk,theeffectonanursinginfantisprobablynot
clinicallysignificantbecauseitisnotabsorbedafteroral
ingestion.11,23

Amongbreastfedinfantswhosemothersweretakingwarfarin,the
drugwasundetectableinplasmaandthebleedingtimewasnot
affected.23

Antidepressants

Desvenlafaxine,
SSRIs,tricyclic
antidepressants,
venlafaxine

Exceptfordoxepintherearenoreportsofuntowardeffectsof
anyofthetricyclicantidepressantsinbreastfedinfants.24

Sertralineistransferredintobreastmilkresultinginanestimated
infantdoseofbetween0.5%and5%oftheweightadjusted
maternaldose b,25,26,27,28Thereisacasereportof

serotonergicsymptomsinaprematureinfantexposedinuteroand
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viabreastmilk,butacausativelinkisuncertain.29Therearealso
reportsofuneventfulbreastfeedingduringmaternalsertraline
use.30

Paroxetineistransferredintobreastmilkresultinginanestimated
infantdoseofbetween0.1%and4.3%oftheweightadjusted
maternaldose b.Inthesestudies,paroxetinewasnotdetectedin
theserumofthemajorityofinfants(inwhomitwasmeasured)
andnoadverseeffectswerereported.30,31,32,33,34

Theamountoffluoxetineexcretedinbreastmilkis218%ofthe
weightadjustedmaternaldose.b,25,26,27,28,30,31,32,
33,34,35Nearlytherapeuticserumconcentrationswere

reportedinsomesymptomaticinfants.36,37,38,39,40,41,
42,43,44Also,infantsbreastfedbymothersonfluoxetinehad
poorerweightgain,althoughthesignificanceisunclear.40Afew
casesofcolichavebeenassociatedwithfluoxetine.37,41

Becauseofthelonghalflivesoffluoxetineanditsactive
metabolites,cautionisadvised,particularlywhenbreastfeedinga
preterminfantorneonate.14

Excretionoffluvoxamineseemstobelowandnoadverseeffects
werereportedinthefewavailablecases.30,45
Theamountofcitalopramexcretedinbreastmilkis

approximately0.79%oftheweightadjustedmaternaldose b.In
onestudy,asingleinfantpresentedanuneasysleeppattern
whichimprovedwhenmaternaldosewasdecreased.46,47,48,
49Theamountofescitalopramexcretedinbreastmilkisless

than8%oftheweightadjustedmaternaldose bandnoadverse
effectswerereportedintheavailablecases.14

Venlafaxineanditsmetabolitesareexcretedinbreastmilkin
approximately59%oftheweightadjustedmaternaldose.b,50,
51Inonestudyof7infantstheactivemetaboliteO

desmethylvenlafaxinewasdetectedintheplasmaof4infants.No
adverseeffectswerereportedintheinfants.52Excretionof

desvenlafaxine(Odesmethylvenlafaxine)intobreastmilkisless
than7%ofthematernalweightadjusteddose bandserumdrug
levelsofbreastfedinfantsarelessthan6%ofsimultaneous
maternallevels.53

Althoughbupropion,moclobemideandmirtazapinehavenot
beenstudiedextensively,foreachofthesedrugstheamount
excretedinbreastmilkislessthan2%oftheweightadjusted
maternaldose.bNoadverseeffectswerereported14,54,55,56
,57,58,59exceptforbupropion(threecasereportsofpossible
seizure)althoughthesignificanceisunclear.60,61,62Limited

dataindicatethatexcretionoftrazodoneintobreastmilkislow,
butdataonitsactivemetabolitesarelacking.63,64,65,66The
amountofduloxetineexcretedintobreastmilkseemstobelow,
lessthan1%oftheweightadjustedmaternaldose bisexcreted
intobreastmilk.67,68
Overall,nosignificantshorttermeffecthasbeenreportedforthe
commonlyusedantidepressantssuchastricyclicsandSSRIs.
Clinicalsignificanceofreportedadverseeventsremainsunclear.
Basethechoiceofantidepressantsonthematernalconditionand
response.Nomatterwhatdrugisused,usecautionuntilmore
experienceisgained.

Antiepileptics

Carbamazepine,
clonazepam,
phenytoin,valproic
acid

Theexcretionintomilkislow:approximately5%and2%ofthe
weightadjustedmaternaldose bforcarbamazepineandits

epoxidemetabolite,lessthan4%forvalproicacid,andlessthan
8%forphenytoin.Noadverseeffectsduetocarbamazepine,
phenytoinorvalproateexposureviabreastmilkwereobservedat

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6yearsinaprospectiveobservationalmulticenterstudy.69Limited
dataforclonazepamindicatethattheweightadjustedmaternal
doseis<3%thereforeriskfortoxicityisexpectedtobelow.14
Howeverthelonghalflifeandlipophilicityofclonazepamcouldbe
aconcern.Despitesporadiccasereportsofadverseeffects,these
antiepilepticsarebelievedtobecompatiblewithbreastfeeding.7,
70

Phenobarbital,ethosuximideandprimidonemaywarrantmore
cautionbecausetheinfant'sexposuremayreachtherapeutic
levels.Theinfantexposurelevelsforphenobarbital,ethosuximide
andprimidoneareestimatedat100%,50%and>10%,
respectively,ofthelevelsexpectedwhenthedrugisgivendirectly
toaninfantinatherapeuticdose.70Whetherthishighlevel
exposureprecludesbreastfeedingornotdependsonvarious
factorsineachindividualcase.Inselectedcases,regular
monitoringofclinicalsigns(e.g.,lethargy,poorfeeding,sedation)
andofdrugconcentrationsinbreastmilkand/orininfant'splasma
mayguidebreastfeeding.
Lamotrigineplasmalevelsashighas50%ofmaternalserum
levelswerefoundinbreastfedinfantswhosemothersweretaking
lamotrigine.Manyinfantshavebeenbreastfedwithoutadverse
reactionsbutthisdrugmaybeofconcern.14
Noadverseeffectsduetolamotrigineexposureviabreastmilk
wereobservedat6yearsinaprospectiveobservational
multicenterstudy.69

Gabapentinexcretionintobreastmilkis1.33.8%oftheweight
adjustedmaternaldose bandserumdruglevelsofbreastfed

infantsare<12%ofsimultaneousmaternallevels.71,72,73
Dataontopiramatearelacking.Thelongeliminationhalflifeand
inadequatelystudiedpossiblelongtermeffectsonneurobehaviour
andcognitivedevelopmentmaybeofconcern.
Clobazam,levetiracetam,oxcarbazepine,pregabalinand
vigabatrinhavenotbeenextensivelystudiedandtheiruseduring
breastfeedingshouldbeevaluatedonanindividualbasis.

Antifungals

AmphotericinB,
caspofungin,
fluconazole,
ketoconazole,
topicalantifungals

DataonamphotericinBarelacking.However,itisvirtually
unabsorbedorallyandiscommonlyusedinpediatrics.74,75

Althoughdataarelackingontopicalfungicidalagentslike
clotrimazole,miconazole,terconazoleandnystatinin
breastfeeding,systemicabsorptioninthemotherisverypoor.Milk
levelsareprobablytoolowtobeclinicallyrelevant.Mostofthese
topicalantifungalsareusedinpediatrics.
Dataoncaspofungininbreastfeedingarelackingbutithaspoor
oralbioavailability.
Fluconazoleexcretionintomilkislowafteroraladministrationof
150mg,amountingto16%oftheweightadjustedmaternaldose b
andlessthan6%ofadailypediatricdose.7Adverseeffectsinthe
infantshavenotbeenreported.Dataonlargerdosesarelacking.
However,breastfeedingmustbecontinuedduringtreatmentfor
yeastmastitiswithfluconazole100200mgdailyfor23weeks.
Thismaternaldoseproducesanamountofdruginmilkthatis
insufficientfortreatmentoforalthrushintheinfant.14
Dataregardingitraconazoleandvoriconazolearelacking
fluconazoleispreferred.7

Lessthan1%oftheweightadjustedmaternaldose bisexcretedin
breastmilkafteranoraldoseofketoconazole200mg.This
amountisalsolessthanthedailypediatricdose.Maternal
systemicabsorptionaftershampooapplicationisconsidered
negligible.14,74,76

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Cetirizine,
desloratadine,
fexofenadine,
loratadine

Loratadineandfexofenadine(basedonterfenadinedata)result
ininfantexposurelevelsof<1%oftheweightadjustedmaternal
dose.b,77,78
Desloratadineistheactivemetaboliteofloratadine.The
calculatedmaximumexpecteddoseofdesloratadineinmilkis
0.46%ofthematernalweightadjusteddose bofloratadine.77

Althoughdataoncetirizinearelacking,useduringbreastfeeding
isconsideredacceptablesincethedrugissafelyusedininfants>6
months.11
Theestimatedamountofdiphenhydramineababyisexposedto
throughbreastmilkislow(approximately0.3%ofapediatric
dose).Occasionaluseisnotexpectedtocauseadverseeffects.
Nonsedatingantihistaminesarepreferredforlongertermuseas
anecdotalreportssuggestapossibledecreaseinmilk
production.14

Otherantihistaminesmaybegiven,butdataontheconcentrations
ofthesedrugsinbreastmilkarelacking.Infantsshouldbe
monitoredforirritabilityordrowsiness.79
Antihistaminesarenotusuallycontraindicatedduring
breastfeeding.Alternativestooralantihistaminesthatmaybe
consideredduringbreastfeedingincludenasallyadministered
corticosteroidsorcromolyn.Cromolynandnedocromileye
dropsareconsideredacceptableduringbreastfeedingbecauseof
theirlowbioavailability.7

Antihypertensives Labetalol,
metoprolol,
propranolol
Benazepril,
captopril,enalapril,
quinapril,ramipril
Methyldopa
Diltiazem,
nifedipine,
verapamil
Hydrochlorothiazide,
furosemide

Betablockersthataresafetouseevenintheneonatalperiodare
labetalol,metoprololandpropranolol.70,80,81

Acebutolol,atenololandsotalol(althoughthelatterisnot
indicatedasanantihypertensiveagent)maycauserelativelyhigh
exposurelevels,10%,25%and20%,respectively,ofthose
expectedwhenthedrugisgivendirectlytoaninfantina
therapeuticdose.Thismaynotbeaprobleminpostneonatal
infants.However,exercisecautionintheearlyneonatalperiod
becausenewbornsmayhavelowclearanceofatenololandsotalol
asaresultofimmaturerenalfunction(lowGFR).Signsofbeta
blockadehavebeenreportedinabreastfedinfantofawoman
takingatenolol(bradycardia,cyanosis,hypotension,hypothermia)
andacebutolol(hypotension,bradycardia,tachypnea,
drowsiness).82,83,84

MethyldopaandsomeACEinhibitors(benazepril,captopril,
enalapril,quinaprilandramipril)arenotexcretedintobreast
milkinclinicallysignificantamountsandareconsideredcompatible
withbreastfeeding.11,14,85,86Dataconcerningtheuseof
angiotensinIIreceptorantagonistsduringlactationare
lacking.Usewithcautioninbreastfeedingmothers.7

Nifedipineisexcretedintobreastmilkinlowamountsandno
adverseeffectshavebeenreportedininfants.Itisconsidered
compatiblewithbreastfeeding.Verylimiteddataindicatesamounts
ofdiltiazemandverapamilinbreastmilkarelowandwouldnot
beexpectedtohaveanyadverseeffectsinbreastfedinfants.14

Dataondiureticsarelacking.Intensediuresismaydecrease
breastmilkproduction.Hydrochlorothiazide50mgdailyis
consideredacceptableduringbreastfeedingbasedonacasereport
whereanexclusivelybreastfedinfantreceived<1%oftheusual
neonataldose.14Althoughthereislittledataavailableregarding
theamountoffurosemideinbreastmilk,itsshorthalflife,high
proteinbindingandextensiveuseinneonatesandpediatrics
indicatethatsmallmaternaldosesmaybeacceptable.11

Antimalarial
agents

Chloroquine,
mefloquine,

Theverysmallamountofchloroquine,mefloquineand
proguanilexcretedinbreastmilkisnotthoughttobeharmfultoa

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proguanil

nursinginfant.7
Thereisnoinformationontheamountofprimaquinethatenters
intohumanbreastmilkbutthedrugmaycauseseverehemolysis
inG6PDdeficientindividuals.Becausedataarenotyetavailable
onthesafetyandefficacyofatovaquone/proguanilininfants
weighing<11kg,themedicationshouldnotbegiventoawoman
whoisbreastfeedinganinfantlessthanthisweightunlessthe
potentialbenefittothewomanoutweighsthepotentialrisktothe
infant.Considermefloquine.
Quantityofantimalarialmedicationtransferredinbreastmilkis
insufficienttoprovideadequateprotectionagainstmalaria.Infants
whorequirechemoprophylaxisshouldreceivetherecommended
dosagesofappropriateantimalarialdrugs.87,88

Antimanicagents

Lithiumshouldbeusedwithcautioninbreastfeedingmothers.
Lithiumisexcretedinbreastmilk,occasionallyinquantities
sufficienttoproduceinfantserumlevelsrangingfrom1050%of
maternalserumlevels.Inaninfantexposedtolithiuminuteroand
throughbreastfeeding,cyanosis,Twaveabnormalitiesand
decreasedmuscletonewerereported.Otherstudieshave
reportednoadverseeffects.7,89
Monitoringofdrugconcentrationsinmilkand/orinfant'sserum
maybejustified.90,91Considerperiodicthyroidevaluationofthe
infantaslithiumcanreducethyroxineproduction.Monitorchanges
ininfanthydrationcarefullyashydrationstatuscangreatlyalter
lithiumserumlevels.7

Antipsychotics

Chlorpromazine,
haloperidol,
olanzapine,
quetiapine,
risperidone

Theamountofolanzapineexcretedintobreastmilkislessthan
4%oftheweightadjustedmaternaldose.bFewadverseeffects
havebeenreportedamongbreastfedinfantsbutmonitoringfor
irritability,tremorandinsomnia(especiallyinthose<2months
old)isrecommended.14,92,93,94,95

Lessthan0.5%oftheweightadjustedmaternaldose bof
quetiapineisexcretedintobreastmilk.Monitorinfants
(particularlythose<2monthsold)forsedation.Nodevelopmental
problemsoradverseeventshavebeennotedininfantsbreastfed
duringmaternaluse.14,96,97,98
Theamountofrisperidoneexcretedintobreastmilkis<5%of
theweightadjustedmaternaldose b.Althoughnoadverseeffects
ininfantshavebeenreported,monitorforsedation,especiallyin
infants<2monthsold.14,99

Chlorpromazineisexcretedintobreastmilkinlowamounts(4%
oftherecommendedpediatricdose)butmilklevelsdonotappear
tocorrelatewellwiththematernaldoseorserumlevel.Monitor
theinfantforexcessivedrowsinessduringbreastfeeding.14,100

Clozapineappearstobeexcretedintobreastmilkinlowamounts
(1.2%oftheweightadjustedmaternaldose b).Useduring
breastfeedingmaybeofconcernduetoitsseriousadverseeffect
profile(agranulocytosisandCNSdepression).Monitorinfantfor
excessivesedation.Periodicmonitoringoftheinfant'swhiteblood
cellcountisadvisable.14,100,101
Theuseofhaloperidolmaybeofconcernduetolackofdata.
Doses<40mg/dayareexcretedinlowamountsinbreastmilk.
Infantsshouldbemonitoredforsedationandextrapyramidal
effects.100

Casereportsforaripiprazole,flupentixol,methotrimeprazine,
paliperidone,perphenazine,trifluoperazine,ziprasidoneand
zuclopenthixolindicatethatthesemedicationsareexcretedinto
breastmilkinlowamounts(<1%oftheweightadjustedmaternal
dose b).11Dataarelackingforloxapineandpimozide.
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Antivirals

Acyclovir,
valacyclovir

Acyclovirandvalacyclovir(whichisalmostentirelytransformed
toacyclovir)excretionintomilkarelow(lessthan1%ofthe
maximaldailypediatricdosage).Noadverseeffectswerereported
inbreastfedinfants.102
Nostudieshavebeenreportedontheexcretionofamantadinein
humanmilk.However,amantadineisadopamineagonist.Clinical
studiesusingamantadineconcurrentlywithneuroleptic
medicationshavedemonstratedadecreaseofprolactinand
galactorrheainducedbyneurolepticdrugs.Thematernalprolactin
levelinamotherwithestablishedlactationmaynotaffecther
abilitytobreastfeed.103,104
Dataonfamciclovirinbreastfeedingandpediatricsarelacking.
Acyclovirandvalacyclovirarepreferred.14

Oseltamivir

Sincetheamountofoseltamivirexcretedinbreastmilkseemsto
below(lessthan1%oftheusualpediatricdosageand0.5%ofthe
weightadjustedmaternaldose bafter75mgtwicedailyfor5days
ina9monthspostpartumnursingmother),itwouldnotbe
expectedtocauseanyadverseeffectsinbreastfedinfants,
especiallyiftheinfantisolderthan2months.105,106

Nodataareavailableregardingtheexcretionofzanamivirin
breastmilk,butduetothepoorinhaledabsorptionandverylow
plasmalevels,itwouldnotbeexpectedtocauseanyadverse
effectsinbreastfedinfants.106

Anxiolyticsand
sedatives

Lorazepam,
oxazepam

Ifusedoccasionallyasasedative,benzodiazepinesarenot
contraindicatedduringbreastfeeding.107Benzodiazepineswith

shorterhalflives,lowerlipophilicityandnoactivemetabolitesare
preferredinbreastfeedingmothers(e.g.,oxazepam,lorazepam).
Benzodiazepinestakenoveralongerperiodoftimetotreat
chronicmaternalconditionsmaybeofconcern.The
benzodiazepinesandtheirmetabolitesareexcretedinbreastmilk,
arepoorlymetabolizedbytheneonate,andhavebeenassociated
withdrowsinessinnursinginfants.Consequently,discouragethe
chronicuseofabenzodiazepineinbreastfeedingmothersunless
theinfant'sconditioniscloselymonitored.

Asthmatherapy

Inhaled
bronchodilators,
inhaled
corticosteroids

Inhaledbronchodilatorsandinhaledcorticosteroidsare
acceptableduringbreastfeedingasbioavailabilityandmaternal
serumlevelsarelow.108

Theaverageamountofterbutalineanexclusivelybreastfedinfant
wouldreceiverangesfrom0.20.7%oftheweightadjusted
maternaldose.bSerumlevelswereundetectableintheinfantin
onecase.109,110
Theamountofinhaledbudesonideinbreastmilkislow(0.3%of
theweightadjustedmaternaldose b).111

Nodataareavailableregardingtheexcretionofomalizumabinto
breastmilk.
Dataonexcretionoftheleukotrienereceptorinhibitor
montelukastintomilkarelacking.However,itdoesnotpenetrate
theCNSormanyothertissuesandishighlyproteinbound,making
theprobabilityofthebabybeingexposedviabreastmilklikely
verylow.7Themanufacturerofzafirlukastindicatesthatitis
excretedintomilkinlowconcentrations(0.5%oftheweight
adjustedmaternaldose b).112Ithasbeenusedinchildrenas
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youngas12months.113

Contraceptives

Progestinonly
formulations

Progestinonlycontraceptivesshouldbeconsideredforpost
partumwomenandmaybeintroducedimmediatelyafterdelivery
(or46weekspostpartuminthecaseoflevonorgestrel
intrauterinedevicetoallowtimeforuterineinvolution).Estrogen
containingcontraceptives(includingpills,patch,vaginalring)
shouldnotbestarteduntilbreastfeedingisfullyestablished
(approximately6weeks)asevenlowdoseformulationscan
decreasemilkyield.114

Corticosteroids

Prednisolone,
prednisone

Prednisoneandprednisoloneareexcretedinbreastmilkinlow
amountsandarenotexpectedtocauseadverseeffectsinthe
baby.Dependingonmaternaldoseadministered,babywillbe
exposedto110%ofaneonataldose.11,115Theoretically,high

dosemethylprednisoloneintravenouspulsetherapymayresult
inbreastmilklevelsthatcouldapproachtherapeuticdosesforthe
nursinginfant.Recommendationsforthetimeperiodduringwhich
toavoidbreastfeedingaftertheinfusionrangefrom448hours.14

Decongestants,
oral

Pseudoephedrine

5.5%oftheweightadjustedmaternaldosage bisexcretedin
breastmilkafterasingleoraldoseof60mgof
pseudoephedrine.Decreasedmilkproductionwasreportedatthe
samedosage.Irritabilitywasreportedininfantsexposedto
pseudoephedrineinonestudyofbreastfeedingmothers.79,116
Useshouldbelimitedtoafewdaysanddiscontinuedifadecrease
inmilkproductionisobserved.Nodataareavailableontheuseof
phenylephrineduringbreastfeeding,thereforeanalternatedrug
maybepreferred,especiallywhilenursinganewbornorpreterm
infant.
Intranasalisotonicsalinesolutionsortopicaldecongestants
(oxymetazoline,xylometazoline)arepreferredoveroral
decongestants.

Diabetestherapy

Insulin,metformin

Humaninsulinisnormallyfoundinbreastmilk.Amountof
syntheticinsulinsecretedintobreastmilkisunknownbut,if
secreted,thispeptidewouldbedestroyedintheinfant'sGItract
withnosignificantabsorption.7

Metforminlevelsinmilkarelowandinfantswouldreceiveless
than0.5%oftheirmother'sweightadjusteddosage.Itis
sometimesdetectableinlowlevelsintheserumofbreastfed
infantsbutnoadverseeffectsinbreastfedinfantswerereportedin
onestudy.Metforminshouldbeusedwithcautionwhilenursing
newbornandprematureinfantsandthosewithrenal
impairment.14
Theamountofglyburideexcretedinbreastmilkseemstobelow
(lessthan1%oftheweightadjustedmaternaldose b):noadverse
effectsonbreastfedinfant'sbloodglucosehavebeenreportedbut
dataarelimited.117
Nodataareavailableregardingtheexcretionofacarboseinto
breastmilk.However,lessthan2%ofadoseofacarboseis
absorbedfromthemother'sGItractmakingitunlikelythatany
drugreachestheinfantthroughbreastmilk.118

Nodataareavailableregardingtheexcretionofgliclazide,
glimepiride,nateglinide,pioglitazone,repaglinideand
rosiglitazoneinbreastmilk.Analternatedrugmaybepreferred,
especiallywhilenursinganewbornorpreterminfant.Some
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expertsrecommendmonitoringthebreastfedinfant'sblood

glucoseduringmaternaltherapywithhypoglycemicagents.118

Gastrointestinal
drugs

Antacids,sucralfate

Aluminum,calciumandmagnesiumantacidsandsucralfate
arepartiallyorpoorlyabsorbedorallyandareconsideredsafeto
use.7

Antidiarrheals

Useofloperamideduringbreastfeedingisunlikelytoaffectthe
infantasitisminimallyabsorbedorally.Basedonitschemicaland
pharmacologicalsimilaritytonarcotics,occasionalsmalldosesof
diphenoxylatemaybeacceptablewhilebreastfeedinganolder
infant,butalternativesarepreferred,especiallywhilenursinga
newborn.7,14

GImotilityagents

Theexcretionintomilkofdomperidoneandmetoclopramide
arelessthan0.05%and6%respectivelyofadailypediatricdose.
Noadverseeventsarereportedfordomperidonebutintestinal
discomfortwasreportedin2breastfedinfantsofmotherstaking
metoclopramide.119,120,121Domperidoneisusedtoincrease
milkproductioninsomewomenwhodonotrespondtoa
nonpharmacologicapproach.

H2antagonists

Thoughconsideredsafeforusebybreastfeedingmothers,
cimetidineandranitidinemayconcentrateinmilkwhereas
famotidineandnizatidinehavethelowestconcentrations,
makingthempreferablechoices.7,23Ranitidinehasbeenwidely
usedinpediatricsprimarilyforgastroesophagealreflux.Adverse
effectshavenotbeenreportedinnursinginfants.

Laxatives

Psylliumisacceptabletouseduringbreastfeedingbecauseitis
notabsorbedfromtheGItract.Therehavebeennocasesofloose
stoolsreportedinbreastfedinfants.14
Docusate,bisacodylandmagnesiumhydroxidearenot
appreciablyabsorbedfromtheGItractandthereforethesedrugs
areunlikelytobefoundinthematernalserumorbreastmilk.7,
14Onepostpartumpatientreceivingalaxativecontaining

docusateinadoseof120mgdailyinadditiontodanthron100mg
dailystatedthatdiarrheaoccurredinherbreastfedinfant.14
Usualdosesofsennaareacceptabletouseduringbreastfeeding.
However,alaxativeeffectwasobservedinafewcasereports.
Cascaraisnotafirstlinechoiceduetocasereportsofalaxative
effectinbreastfedinfantsandunknownoralabsorption.7,14
Nodataareavailableregardingtheexcretionoflactuloseinto
breastmilkhoweverlessthan3%ofadoseoflactuloseis
absorbedfromthemother'sGItract,makingitunlikelythatany
drugreachestheinfantthroughbreastmilk.11
Oralpolyethyleneglycol(e.g.,PEG3350)andrectalglycerin
arenegligiblyabsorbedfromtheGItractandunlikelytohave
significantlevelsinbreastmilk.11

Misoprostol

Misoprostollevelsinbreastmilkarelowamountingestedbythe

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nursinginfantwouldnotbeexpectedtocauseadverseeffects.14

Protonpump
inhibitors

Protonpumpinhibitorsareunstableinanacidmilieuand,when
ingestedviamilk,wouldprobablybedestroyedintheinfant's
stomachpriortoabsorption.7Pantoprazoleandomeprazoleare
excretedinmilkinsmallquantities.122,123Lansoprazoleand
omeprazoleareusedforthetreatmentofgastroesophagealreflux
inneonatesandpediatrics.Esomeprazoleisthesenantiomerof
omeprazoleandthereforewouldalsonotbeexpectedtocause
anyadverseeffectsinbreastfedinfants.123

Migrainetherapy

Eletriptan,
sumatriptan

Occasionaluseofsumatriptanandeletriptanseemstobe
acceptablebecausetheamountofthesedrugsexcretedintomilk
islow(3.5%and0.02%oftheweightadjustedmaternaldosage,b
respectively).Dataonalmotriptan,frovatriptan,naratriptan,
rizatriptanandzolmitriptanarelacking.7

Becausethereislimitedpublishedexperiencewithergotamine,
dihydroergotamineandmethysergideduringbreastfeeding,and
adverseeffectsintheinfantcannotberuledout,mostauthorities
considerthesedrugstobeundesirabletousewhilenursing.7,14

Musclerelaxants

Cyclobenzaprine,
methocarbamol

Theexcretionofcyclobenzaprine,methocarbamoland
orphenadrineintomilkhasnotbeenreported.However,
occasionalcyclobenzaprineandmethocarbamolexposuresare
acceptablebecauseofcyclobenzaprine'sstructuralsimilaritiesto
amitriptyline(seeAntidepressants)andtheveryshorthalflifeof
methocarbamol.Noadverseeventshavebeenpublished,but
infants(especiallythosethatarenewbornorpremature)shouldbe
monitoredforsedationwhilenursing.7

NSAIDs

Diclofenac,
flurbiprofen,
ibuprofen,
indomethacin,
naproxen

MostNSAIDshavebeenshowntobepresentinbreastmilkin
smallamountsandareconsideredsafetouse.Theuseofshort
actingdrugs,suchasibuprofenandflurbiprofen,maybe
preferredoverthosewithalongerhalflifesuchasnaproxen.7

Lessthan1%ofthepediatricdoseofdiclofenacisexcretedinto
breastmilk.Diclofenacalsohasashorthalflife.14,126

Theamountofindomethacinexcretedinbreastmilkislessthan
4%ofatypicalneonataldoseanditisconsideredsafetousewhile
breastfeeding.However,otheragentswithmorepublished
informationonuseduringbreastfeedingmaybepreferable
especiallywhilenursinganewbornorpreterminfant.11
Dataoncelecoxibarelimitedtoafewinfantsbutmilklevelswere
lowandadverseeffectswerenotnotedwhentakenshortterm.7
Moredataareneededtodeterminerisksincethedrughasalong
halflifeandhighoralabsorption.

Scabicides,
pediculicides

Permethrin

Permethrin5%creamisthetreatmentofchoiceforscabies.
Permethrin1%orpyrethrins/piperonylbutoxidemaybeused
forthetreatmentofheadlicewhilebreastfeeding.124Topical
absorptionofpermethrinandpyrethrinsislow.Permethrinis
rapidlymetabolizedtoinactivemetabolitesandexcretedinurine.
Overttoxicityisunlikely.Avoidapplicationonnipples.
Percutaneousabsorptionofpiperonylbutoxideisunknown.7,125

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Lindaneisnotrecommendedbecauseitisabsorbedthroughthe
mother'sskinandexcretedintomilkfat.Directcontactoflindane
withneonatalskinresultsinsignificantabsorption.Directexposure
ispotentiallytoxicininfantswithreportsofelevatedliver
enzymes,seizuredisordersandhypersensitivity.Itmayalsohave
estrogeniceffectsthatcouldinhibitlactation.14,125Lindaneisnot
currentlyavailableinCanada.

Smoking
cessation

Nicotine
replacement
therapy

Dataonnicotinepatchesarelimitedbuttheamountofnicotine
andcotinineexcretedinbreastmilkseemtobelessthan8%of
theweightadjustedmaternaldose b.Witha21mgtransdermal

patch,nicotinepassesintobreastmilkinamountsequivalentto
smoking17cigarettesdaily.Lowerpatchstrengthsof7and14mg
provideproportionatelyloweramountsofnicotinetothebreastfed
infant.Nostudiesonnicotinesprayornicotinegumuseinnursing
mothershavebeenreported.Nicotinegummayproducelarge
variationsinpeaklevelswhengumischewedrapidly:fluctuations
similartosmokingitself.Somecliniciansrecommendtowait23h
afterusingthegumbeforebreastfeeding.127
Dataonvareniclinearelackingbuttransferispossibleandeffect
onCNSisaconcern.7

Forinformationontheuseofbupropionduringbreastfeeding,see
Antidepressants.

Thyroidagents

Antithyroidagents

Theestimatedlevelofexposuretopropylthiouracilin
breastfeedinginfantsislessthan1%ofthetherapeuticdose
standardizedbyweight,andthethyroidfunctionoftheinfantisnot
affected.128Methimazoleindosesupto20mg/dayhasbeen
documentednottoaffecttheinfant'sthyroidfunction.129,130,
131Foreitherdrug,noadverseeffectsinbreastfedinfantshave

beenreportedsofarandmonitoringofinfants'thyroidfunctionis
notnecessaryifdevelopmentisprogressingnormally.131

Thyroidhormones

Levothyroxineiscompatiblewithbreastfeeding.Thyroid
hormonescrossintobreastmilkinlowamounts.Theirpresenceis
notlikelytoaffecttheinfant'sthyroid.23

Vaccines

WomenwhoarebreastfeedingcanbevaccinatedwithTd,Tdap,
pneumococcal,meningococcal,hepatitisA,hepatitisB,HPV,
rabies,typhoid,MMR,varicella,HPVandcholeravaccinesif
indicated.
SafetyoftheJapaneseencephalitisvaccineinbreastfeedingis
unknownanditshouldbeadministeredonlyiftheriskofdisease
outweighstheunknownriskofvaccination.Yellowfevervaccineis
notrecommendedforbreastfeedingwomenandBCGvaccine
shouldbeusedwithcaution.Womenwhoreceivesmallpoxvaccine
aspostexposureprophylaxisshouldavoidbreastfeedingandother
closecontactwiththeirbabyuntilthescabhasseparatedfromthe
vaccinationsite.132

a. Thislistisnotexhaustiveordefinitive.Drugsnotlistedinthetablearenotnecessarilycontraindicated.Individualizedrisk

assessmentisrequiredwhenprescribinganymedicationtoabreastfeedingwoman.
b. Weightadjustedmaternaldoseisamother'sdosebasedonbodyweight(e.g.,mg/kg).Expertsrecommendthatanamountof
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drugreceivedbytheinfantviabreastmilkwhichis>10%oftheweightadjustedmaternaldoseshouldbeatheoreticallevelof
concernwhenconsideringtheacceptabilityofdrugexposure.Theestimatedamountofdrugreceivedbytheinfantviabreastmilk
iscalculatedbymultiplyingthestandardmilkintake(150mL/kg/day)bythedrugconcentrationinbreastmilk.
Abbreviations:G6PD=glucose6phosphatedehydrogenaseGFR=glomerularfiltrationrate

DrugsforNonmedicalUse
Tobaccosmokingandalcoholingestionarethemostcommonsourcesofnonmedicinaldrugexposureinbreastfed
infantsinCanada.Becausetheysooftenoccurinthesameindividual,itisdifficulttostudytheirindependent
effects.Increasingly,thesedrugsareusedtogetherwithillicitdrugssuchasmarijuanaandcocaine.

Table2:BreastfeedingandNonmedicalUseofDrugs
Drug

Comments

Alcohol

Notcompatiblewithbreastfeeding.Thealcoholmetabolizingcapacity(alcoholandaldehyde
dehydrogenase)isprematurethroughouttheneonatalandinfantileperiod.Overall,motor
developmentisslightlyslowerininfantsbreastfedbymotherswhoregularlydrinkalcohol.
Chronicorheavyconsumersofalcoholshouldnotbreastfeed.7

Shorttermalcoholconsumptionbynursingmothersreportedlyhasanimmediateeffectonthe
odourcharacteristicsofthemilkandthefeedingbehaviouroftheirinfants,resultinginless
consumptionofmilk.133Toavoidexposureoftheinfanttoalcohol,breastfeedingmothers
shouldnotconsumealcoholorshouldconsumenomorethanonedrink23hbefore
breastfeeding.7

Caffeine

Hypothetically,anursinginfantingests0.11%ofthematernaldoseafterthemotherdrinks1
2cupsofcoffee.Thisisaninsignificantamountofthedrug,butitmustberememberedthat
thehalflifeofcaffeineis80hinthetermnewbornand97.5hinaprematureinfant(2030
timesthatofanadult).Therefore,repeatedingestionmightleadtoaccumulationofcaffeinein
theinfantduringthefirst2weeksofpostnatallife.Thishasyettobestudied.

Recreational
orstreet
drugs

Nosystematicstudiesofrecreationalorstreetdrug(ordrugmetabolite)excretionexist.

Tobacco

Discourageduringbreastfeedingbecausetherearewelldocumentedhealthriskstothemother
andinfantfromsecondhandsmoke.Infantexposuretonicotineislargelythroughinhalation
ofsecondhandsmoke.Inmothersunwillingtostopsmokingduringbreastfeeding,itshouldbe
notedthatbreastfedbabiesofmotherswhocontinuetosmokehavebetterimmunityandless
respiratoryinfectionsthanbottlefedbabiesofmotherswhocontinuetosmoke.134
Nicotineisconcentratedinhumanbreastmilk.135,136Onestudysuggeststhatcigarette
smokingsignificantlyreducesbreastmilkproduction.137
Encouragenursingmotherstospeaktotheirhealthcareprovidersregardingoptionsfor
smokingcessation.

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