Food drug interaction

Food-Drug InteractionsFood-Drug Interactions

Definition of TermsDefinition of Terms
 Drug-nutrient interaction: the result ofDrug-nutrient interaction: the result of
the action between a drug and athe action between a drug and a
nutrient that would not happen with thenutrient that would not happen with the
nutrient or the drug alonenutrient or the drug alone
 Food-drug interaction: a broad termFood-drug interaction: a broad term
that includes drug-nutrient interactionsthat includes drug-nutrient interactions
and the effect of a medication onand the effect of a medication on
nutritional statusnutritional status

Food-Drug InteractionFood-Drug Interaction
 For example, a drug that causes chronicFor example, a drug that causes chronic
nausea or mouth pain may result in poornausea or mouth pain may result in poor
intake and weight lossintake and weight loss

Key TermsKey Terms
 Bioavailability:Bioavailability: degree to which a drug ordegree to which a drug or
other substance reaches the circulation andother substance reaches the circulation and
becomes available to the target organ orbecomes available to the target organ or
tissuetissue
 Half-life:Half-life: amount of time it takes for theamount of time it takes for the
blood concentration of a drug to decreaseblood concentration of a drug to decrease
by one half of its steady state levelby one half of its steady state level
 Side effect:Side effect: adverse effect/reaction or anyadverse effect/reaction or any
undesirable effect of a drugundesirable effect of a drug

Other TermsOther Terms
 Bioavailability: % free to functionBioavailability: % free to function
 Absorption rate: % absorbed and time forAbsorption rate: % absorbed and time for
absorptionabsorption
 Transported: amount in blood (free or bound)Transported: amount in blood (free or bound)
 Metabolized: altered by enzymes in tissuesMetabolized: altered by enzymes in tissues
 Mixed-function oxidase system (MFOS):Mixed-function oxidase system (MFOS):
enzyme system that metabolizes drugs,enzyme system that metabolizes drugs,
carcinogens, compounds in foods, etc.carcinogens, compounds in foods, etc.

PharmacokineticsPharmacokinetics
Movement of drugs through the body byMovement of drugs through the body by
 AbsorptionAbsorption
 DistributionDistribution
 MetabolismMetabolism
 ExcretionExcretion

AbsorptionAbsorption
 Movement of the drug from the site ofMovement of the drug from the site of
administration to the bloodstream; depends onadministration to the bloodstream; depends on
– The route of administrationThe route of administration
– The chemistry of the drug and its ability to crossThe chemistry of the drug and its ability to cross
membranesmembranes
– The rate of gastric emptying (for oral drugs) and GIThe rate of gastric emptying (for oral drugs) and GI
movementmovement
– The quality of the product formulationThe quality of the product formulation
 Food, food components and nutritionalFood, food components and nutritional
supplements can interfere with absorption,supplements can interfere with absorption,
especially if the drug is taken orallyespecially if the drug is taken orally

DistributionDistribution
When the drug leaves the systemicWhen the drug leaves the systemic
circulation and moves to various partscirculation and moves to various parts
of the bodyof the body
 Drugs in the bloodstream are oftenDrugs in the bloodstream are often
bound to plasma proteins; onlybound to plasma proteins; only
unbound drugs can leave the bloodunbound drugs can leave the blood
and affect target organsand affect target organs
 Low serum albumin can increaseLow serum albumin can increase
availability of drugs and potentiateavailability of drugs and potentiate
their effectstheir effects

MetabolismMetabolism
(biotransformation)(biotransformation)
 Primarily in the liver; cytochrome P-450Primarily in the liver; cytochrome P-450
enzyme system facilitates drugenzyme system facilitates drug
metabolism; metabolism generallymetabolism; metabolism generally
changes fat soluble compounds to waterchanges fat soluble compounds to water
soluble compounds that can be excretedsoluble compounds that can be excreted
 Foods or dietary supplements thatFoods or dietary supplements that
increase or inhibit these enzymeincrease or inhibit these enzyme
systems can change the rate or extentsystems can change the rate or extent
of drug metabolismof drug metabolism

ExcretionExcretion
 Drugs are eliminated from the body asDrugs are eliminated from the body as
an unchanged drug or metabolitean unchanged drug or metabolite
– Renal excretion the major route ofRenal excretion the major route of
elimination; affected by renal function andelimination; affected by renal function and
urinary pHurinary pH
– Some drugs eliminated in bile and otherSome drugs eliminated in bile and other
body fluidsbody fluids

PharmacodynamicsPharmacodynamics
 Physiologic and biochemical effects ofPhysiologic and biochemical effects of
a drug or combination of drugsa drug or combination of drugs
 The mechanism of action, e.g. how aThe mechanism of action, e.g. how a
drug worksdrug works
 Often the drug molecule binds to aOften the drug molecule binds to a
receptor, enzyme, or ion channel,receptor, enzyme, or ion channel,
producing a physiological responseproducing a physiological response

PharmacogenomicsPharmacogenomics
 Genetically determined variations that areGenetically determined variations that are
revealed solely by the effects of drugsrevealed solely by the effects of drugs
 Affect only a subset of peopleAffect only a subset of people
 Examples include G6PD (glucose-6-Examples include G6PD (glucose-6-
phosphate dehydrogenase) enzymephosphate dehydrogenase) enzyme
deficiency, warfarin resistance, and slowdeficiency, warfarin resistance, and slow
inactivation of isoniazid (IHN) or phenelzineinactivation of isoniazid (IHN) or phenelzine

G6PD (glucose-6-phosphateG6PD (glucose-6-phosphate
dehydrogenase) enzymedehydrogenase) enzyme
deficiencydeficiency
 X-chromosome-linkedX-chromosome-linked
 Can lead to neonatal jaundice, hemolyticCan lead to neonatal jaundice, hemolytic
anemia or acute hemolysisanemia or acute hemolysis
 Most common in African, Middle Eastern,Most common in African, Middle Eastern,
and Southeast Asiansand Southeast Asians
 Also called favismAlso called favism
 Fava beans or pollen, Vitamin K or VitaminFava beans or pollen, Vitamin K or Vitamin
C can cause hemolysisC can cause hemolysis

Slow CYP2D6Slow CYP2D6
MetabolizersMetabolizers
 CYP2D6 and CYP2C19 metabolize 25% ofCYP2D6 and CYP2C19 metabolize 25% of
drugs including many antidepressants,drugs including many antidepressants,
antipsychotics, and narcoticsantipsychotics, and narcotics
 Slow metabolizers at risk for toxicity andSlow metabolizers at risk for toxicity and
adverse drug effectsadverse drug effects
 Fast metabolizers have unpredictableFast metabolizers have unpredictable
responseresponse
 Drug genotyping in future will helpDrug genotyping in future will help
determine most effective meds fordetermine most effective meds for
individualsindividuals

Benefits of MinimizingBenefits of Minimizing
Food Drug InteractionsFood Drug Interactions
 Medications achieve their intendedMedications achieve their intended
effectseffects
 Improved compliance with medicationsImproved compliance with medications
 Less need for additional medication orLess need for additional medication or
higher dosageshigher dosages
 Fewer caloric or nutrient supplementsFewer caloric or nutrient supplements
are requiredare required
 Adverse side effects are avoidedAdverse side effects are avoided

Benefits of MinimizingBenefits of Minimizing
Food Drug InteractionsFood Drug Interactions
 Optimal nutritional status is preservedOptimal nutritional status is preserved
 Accidents and injuries are avoidedAccidents and injuries are avoided
 Disease complications are minimizedDisease complications are minimized
 The cost of health care services isThe cost of health care services is
reducedreduced
 There is less professional liabilityThere is less professional liability
 Licensing agency requirements areLicensing agency requirements are
metmet

Therapeutic ImportanceTherapeutic Importance
Therapeutically important interactions areTherapeutically important interactions are
those that:those that:
 Alter the intended response to theAlter the intended response to the
medicationmedication
 Cause drug toxicityCause drug toxicity
 Alter normal nutritional statusAlter normal nutritional status

Patients at Risk for Food-Patients at Risk for Food-
Nutrient InteractionsNutrient Interactions
 Patient with chronic diseasePatient with chronic disease
 ElderlyElderly
 FetusFetus
 InfantInfant
 Pregnant womanPregnant woman
 Malnourished patientMalnourished patient
 Allergies or intolerancesAllergies or intolerances

Food and Drug-RelatedFood and Drug-Related
Risk FactorsRisk Factors
 Special dietsSpecial diets
 Nutritional supplementsNutritional supplements
 Tube feedingTube feeding
 Herbal or phytonutrient productsHerbal or phytonutrient products
 Alcohol intakeAlcohol intake
 PolypharmacyPolypharmacy
 Drugs of abuseDrugs of abuse
 Non-nutrients in foodsNon-nutrients in foods
 Excipients in drugs or foodExcipients in drugs or food

Malnutrition Effect onMalnutrition Effect on
DrugsDrugs
 Low albumin levels can make drugs moreLow albumin levels can make drugs more
potent by increasing availability to tissuespotent by increasing availability to tissues
– Lower doses often recommended for personsLower doses often recommended for persons
with low albuminwith low albumin
– Warfarin and phenytoin are highly protein boundWarfarin and phenytoin are highly protein bound
in blood;in blood; ↓ albumin can result in poor seizure↓ albumin can result in poor seizure
control (phenytoin) or hemorrhage (warfarin)control (phenytoin) or hemorrhage (warfarin)
 Body composition: obese or elderly personsBody composition: obese or elderly persons
have a higher ratio of adipose tissue; fathave a higher ratio of adipose tissue; fat
soluble drugs may accumulate in the bodysoluble drugs may accumulate in the body ↑↑
risk of toxicityrisk of toxicity

Food/Nutrient Effects onFood/Nutrient Effects on
DrugsDrugs
– Presence of food and nutrients inPresence of food and nutrients in
intestinal tract may affect absorption ofintestinal tract may affect absorption of
drugdrug
– Antiosteoporosis drugs Fosamax orAntiosteoporosis drugs Fosamax or
Actonel: absorption negligible if given withActonel: absorption negligible if given with
food;food; ↓ 60% with coffee or orange juice↓ 60% with coffee or orange juice

DrugsDrugs
 Absorption of iron from supplementsAbsorption of iron from supplements ↓↓↓↓
50% when taken with food50% when taken with food
 Best absorbed when taken with 8 oz ofBest absorbed when taken with 8 oz of
water on empty stomachwater on empty stomach
 Food may ↓↓ GI upsetFood may ↓↓ GI upset
 If take with food, avoid bran, eggs, fiberIf take with food, avoid bran, eggs, fiber
supplements, tea, coffee, dairy products,supplements, tea, coffee, dairy products,
calcium supplementscalcium supplements

DrugsDrugs
– Ciprofloxacin and Tetracycline formCiprofloxacin and Tetracycline form
insoluble complexes with calcium in dairyinsoluble complexes with calcium in dairy
products or fortified foods; also zinc,products or fortified foods; also zinc,
calcium, magnesium, zinc or ironcalcium, magnesium, zinc or iron
supplements; aluminum in antacidssupplements; aluminum in antacids
– Stop unnecessary supplements duringStop unnecessary supplements during
drug therapy or give drug 2 hours beforedrug therapy or give drug 2 hours before
or 6 hours after the mineralor 6 hours after the mineral

DrugsDrugs
 AbsorptionAbsorption
– Presence of food enhances thePresence of food enhances the
absorption of some medicationsabsorption of some medications
– Bioavailability of Axetil (Ceftin), anBioavailability of Axetil (Ceftin), an
antibiotic, is 52% after a meal vs 37% inantibiotic, is 52% after a meal vs 37% in
the fasting statethe fasting state
– Absorption of the antiretroviral drugAbsorption of the antiretroviral drug
saquinavir is increased twofold by foodsaquinavir is increased twofold by food

DrugsDrugs
 Adsorption: adhesion to a food or foodAdsorption: adhesion to a food or food
componentcomponent
– High fiber diet may decrease theHigh fiber diet may decrease the
absorption of tricyclic antidepressantsabsorption of tricyclic antidepressants
such as amitriptyline (Elavil)such as amitriptyline (Elavil)
– Digoxin (Lanoxin) should not be takenDigoxin (Lanoxin) should not be taken
with high phytate foods such as wheatwith high phytate foods such as wheat
bran or oatmealbran or oatmeal

DrugsDrugs
 GI pH can affect drug absorptionGI pH can affect drug absorption
 Achlorhydria or hypochlorhydria canAchlorhydria or hypochlorhydria can
reduce absorption of ketoconozolereduce absorption of ketoconozole
and delavirdineand delavirdine
 Antacid medications can result inAntacid medications can result in
reduced acidity in the stomachreduced acidity in the stomach
 Taking these meds with orange orTaking these meds with orange or
cranberry juice can reduce stomachcranberry juice can reduce stomach
pH and increase absorptionpH and increase absorption

DrugsDrugs
MetabolismMetabolism
Changes in diet may alter drug actionChanges in diet may alter drug action
 Theophylline: a high protein, low CHO dietTheophylline: a high protein, low CHO diet
can enhance clearance of this and othercan enhance clearance of this and other
drugsdrugs
 Grapefruit/juice: inhibits the intestinalGrapefruit/juice: inhibits the intestinal
metabolism (cytochrome P-450 3A4metabolism (cytochrome P-450 3A4
enzyme) of numerous drugs (calciumenzyme) of numerous drugs (calcium
channel blockers, HMG CoA inhibitors, anti-channel blockers, HMG CoA inhibitors, anti-
anxiety agents) enhancing their effects andanxiety agents) enhancing their effects and
increasing risk of toxicity; may interfere withincreasing risk of toxicity; may interfere with
the absorption of other drugsthe absorption of other drugs

Grapefruit InhibitsGrapefruit Inhibits
Metabolism of Many DrugsMetabolism of Many Drugs
 Inactivates metabolizing intestinalInactivates metabolizing intestinal
enzyme resulting in enhanced activityenzyme resulting in enhanced activity
and possible toxicityand possible toxicity
 Effect persists for 72 hours so it is notEffect persists for 72 hours so it is not
helpful to separate the drug and thehelpful to separate the drug and the
grapefruitgrapefruit
 Many hospitals and health careMany hospitals and health care
centers have taken grapefruit productscenters have taken grapefruit products
off the menu entirelyoff the menu entirely

Drugs known to interactDrugs known to interact
with grapefruit juicewith grapefruit juice
 Anti-hypertensivesAnti-hypertensives
(filodipine, nifedipine,(filodipine, nifedipine,
nimodipine,nimodipine,
nicardipine, isradipine)nicardipine, isradipine)
 ImmunosuppressantsImmunosuppressants
(cyclosporine,(cyclosporine,
tacrolimus)tacrolimus)
 AntihistaminesAntihistamines
(astemizole)(astemizole)
 Protease inhibitorsProtease inhibitors
(saquinavir)(saquinavir)
 Lipid-Lowering DrugsLipid-Lowering Drugs
(atorvastatin,(atorvastatin,
lovastatin, simvastatin)lovastatin, simvastatin)
 Anti-anxiety, anti-Anti-anxiety, anti-
depressantsdepressants
(buspirone, diazepam,(buspirone, diazepam,
midazolam, triazolam,midazolam, triazolam,
zaleplon,zaleplon,
carbamazepine,carbamazepine,
clomipramine,clomipramine,
trazodonetrazodone

DrugsDrugs
 ExcretionExcretion
——Patients on low sodium diets willPatients on low sodium diets will
reabsorb more lithium along with sodium;reabsorb more lithium along with sodium;
patients on high sodium diets will excretepatients on high sodium diets will excrete
more lithium and need higher dosesmore lithium and need higher doses
——Urinary pH: some diets, particularlyUrinary pH: some diets, particularly
extreme diets, may affect urinary pH,extreme diets, may affect urinary pH,
which affects resorption of acidic andwhich affects resorption of acidic and
basic medicationsbasic medications

Drug Action: MAOIsDrug Action: MAOIs
 Monoamine oxidase inhibitors (MAOI)Monoamine oxidase inhibitors (MAOI)
interact with pressor agents in foodsinteract with pressor agents in foods
(tyramine, dopamine, histamine)(tyramine, dopamine, histamine)
 Pressors are generally deaminated rapidlyPressors are generally deaminated rapidly
by MAO; MAOIs prevent the breakdown ofby MAO; MAOIs prevent the breakdown of
tyramine and other pressorstyramine and other pressors
 Significant intake of high-tyramine foodsSignificant intake of high-tyramine foods
(aged cheeses, cured meats) by pts on(aged cheeses, cured meats) by pts on
MAOIs can precipitate hypertensive crisisMAOIs can precipitate hypertensive crisis

Drug Action: CaffeineDrug Action: Caffeine
 Increases adverse effects ofIncreases adverse effects of
stimulants such as amphetamines,stimulants such as amphetamines,
methylphenidate, theophylline,methylphenidate, theophylline,
causing nervousness, tremor,causing nervousness, tremor,
insomniainsomnia
 Counters the antianxiety effect ofCounters the antianxiety effect of
tranquilizerstranquilizers

Drug Action: WarfarinDrug Action: Warfarin
 Warfarin (anticoagulant) acts by preventingWarfarin (anticoagulant) acts by preventing
the conversion of vitamin K to a usable formthe conversion of vitamin K to a usable form
 Ingestion of vitamin K in usable form willIngestion of vitamin K in usable form will
allow production of more clotting factors,allow production of more clotting factors,
making the drug less effectivemaking the drug less effective
 Pts must achieve a balance or steady statePts must achieve a balance or steady state
between dose of drug and consumption ofbetween dose of drug and consumption of
vitamin K; recommend steady intake of Kvitamin K; recommend steady intake of K
 Other foods with anticlotting qualities mayOther foods with anticlotting qualities may
also have an effect (garlic, onions, vitamin Ealso have an effect (garlic, onions, vitamin E
in large amounts, and ginseng)in large amounts, and ginseng)

Drug Action: AlcoholDrug Action: Alcohol
 In combination with some drugs willIn combination with some drugs will
produce additive toxicityproduce additive toxicity
 With CNS-suppressant drugs mayWith CNS-suppressant drugs may
produce excessive drowsiness,produce excessive drowsiness,
incoordinationincoordination
 Acts as gastric irritant; in combinationActs as gastric irritant; in combination
with other irritants such as NSAIDswith other irritants such as NSAIDs
may increase chance of GI bleedmay increase chance of GI bleed

 Should not be combined with otherShould not be combined with other
hepatotoxic drugs such ashepatotoxic drugs such as
acetominophen, amiodarone,acetominophen, amiodarone,
methotrexatemethotrexate
 Can inhibit gluconeogenesis whenCan inhibit gluconeogenesis when
consumed in a fasting state; canconsumed in a fasting state; can
prolong hypoglycemic episode causedprolong hypoglycemic episode caused
by insulin or other diabetes medsby insulin or other diabetes meds

 Can produce life-threatening reactionCan produce life-threatening reaction
when combined with disulfiramwhen combined with disulfiram
(Antabuse) which prevents the(Antabuse) which prevents the
catabolism of ethanol by the livercatabolism of ethanol by the liver
– Causes nausea, headache, flushing,Causes nausea, headache, flushing,
increased blood pressureincreased blood pressure
 Metronidazole, Cefoperazone,Metronidazole, Cefoperazone,
chlorpropamide (Diabenese) andchlorpropamide (Diabenese) and
procarbacine cause similar symptomsprocarbacine cause similar symptoms

Drug Effects onDrug Effects on
Nutrition: MetabolismNutrition: Metabolism
 Phenobarbital and phenytoin increasePhenobarbital and phenytoin increase
metabolism of vitamin D, vitamin K,metabolism of vitamin D, vitamin K,
and folic acidand folic acid
– Patients on chronic tx may needPatients on chronic tx may need
supplementssupplements
 Carbamazepine may affectCarbamazepine may affect
metabolism of biotin, vitamin D, andmetabolism of biotin, vitamin D, and
folic acid, leading to possible depletionfolic acid, leading to possible depletion

 INH (anti-tuberculosis) blocksINH (anti-tuberculosis) blocks
conversion of pyridoxine to active formconversion of pyridoxine to active form
– Patients with low intake at higher riskPatients with low intake at higher risk
– May cause deficiency and peripheralMay cause deficiency and peripheral
neuropathyneuropathy
– Pts on long term tx may needPts on long term tx may need
supplementssupplements
 Hydralazine, penacillamine, levodopaHydralazine, penacillamine, levodopa
and cycloserine are also pyridoxineand cycloserine are also pyridoxine
antagonistsantagonists

 Methotrexate (cancer and rheumatoidMethotrexate (cancer and rheumatoid
arthritis) and pyrimethamine (malaria,arthritis) and pyrimethamine (malaria,
toxoplasmosis) are folic acidtoxoplasmosis) are folic acid
antagonistsantagonists
– May treat with folinic acid (reduced formMay treat with folinic acid (reduced form
of folic acid, does not need conversion toof folic acid, does not need conversion to
active form) or folic acid supplementsactive form) or folic acid supplements

Nutrition: ExcretionNutrition: Excretion
 Loop diuretics (furosemide,Loop diuretics (furosemide,
bumetanice) increase excretion ofbumetanice) increase excretion of
potassium, magnesium, sodium,potassium, magnesium, sodium,
chloride, calciumchloride, calcium
– Patients may need supplements with longPatients may need supplements with long
term use, high dosages, poor dietsterm use, high dosages, poor diets
– Electrolytes should be monitoredElectrolytes should be monitored

 Thiazide diuretics (hydrochlorthiazide)Thiazide diuretics (hydrochlorthiazide)
increase the excretion of potassium andincrease the excretion of potassium and
magnesium, but reduce excretion of calciummagnesium, but reduce excretion of calcium
– High doses plus calcium supplementation mayHigh doses plus calcium supplementation may
result in hypercalcemiaresult in hypercalcemia
 Potassium-sparing diureticsPotassium-sparing diuretics
(spironolactone) increase excretion of(spironolactone) increase excretion of
sodium, chloride, calciumsodium, chloride, calcium
– Potassium levels can rise to dangerous levels ifPotassium levels can rise to dangerous levels if
pt takes K+ supplements or has renalpt takes K+ supplements or has renal
insufficiencyinsufficiency

 Corticosteroids (prednisone) decreaseCorticosteroids (prednisone) decrease
sodium excretion, resulting in sodiumsodium excretion, resulting in sodium
and water retention; increaseand water retention; increase
excretion of potassium and calciumexcretion of potassium and calcium
– Low sodium, high potassium diet isLow sodium, high potassium diet is
recommendedrecommended
– Calcium and vitamin D supplements areCalcium and vitamin D supplements are
recommended with long term steroid userecommended with long term steroid use
(lupus, RA) to prevent osteoporosis(lupus, RA) to prevent osteoporosis

 Phenothiazine antipsychotic drugs (chlorpromazine)Phenothiazine antipsychotic drugs (chlorpromazine)
increase excretion of riboflavinincrease excretion of riboflavin
– Can lead to riboflavin deficiency in those with poor intakesCan lead to riboflavin deficiency in those with poor intakes
 Cisplatin causes nephrotoxicity and renal magnesiumCisplatin causes nephrotoxicity and renal magnesium
wasting resulting in acute hypomagnesemia in 90% ofwasting resulting in acute hypomagnesemia in 90% of
patients (also hypocalcemia, hypokalemia,patients (also hypocalcemia, hypokalemia,
hypophosphatemia)hypophosphatemia)
– May require intravenous mg supplementation or post-treatmentMay require intravenous mg supplementation or post-treatment
hydration and oral mg supplementationhydration and oral mg supplementation
– May persist for months or years after therapy is finishedMay persist for months or years after therapy is finished

Nutrition: AbsorptionNutrition: Absorption
 Drug-nutrient complexes: example,Drug-nutrient complexes: example,
ciprofloxacin and tetracycline willciprofloxacin and tetracycline will
complex with calcium, supplementalcomplex with calcium, supplemental
magnesium, iron, or zincmagnesium, iron, or zinc
– Take minerals 2 to 6 hours apart from theTake minerals 2 to 6 hours apart from the
drugdrug
 Decreased transit time: catharticDecreased transit time: cathartic
agents, laxatives, drugs containingagents, laxatives, drugs containing
sorbitol, drugs that increase peristalsissorbitol, drugs that increase peristalsis

Nutrition; AbsorptionNutrition; Absorption
 Change GI environmentChange GI environment
– Proton pump inhibitors, H2 receptorProton pump inhibitors, H2 receptor
antagonists inhibit gastric acid secretion,antagonists inhibit gastric acid secretion,
raise gastric pH; cimetidine reduces intrinsicraise gastric pH; cimetidine reduces intrinsic
factor secretion; this impairs B12factor secretion; this impairs B12
absorption;absorption; ↑ pH may impair absorption of↑ pH may impair absorption of
calcium, iron, zinc, folic acid, and B-calcium, iron, zinc, folic acid, and B-
carotenecarotene

Nutrition: AbsorptionNutrition: Absorption
Damage GI MucosaDamage GI Mucosa
 Chemotherapeutic agents, NSAIDs,Chemotherapeutic agents, NSAIDs,
antibiotic therapyantibiotic therapy
 Alters ability to absorb minerals, especiallyAlters ability to absorb minerals, especially
iron and calciumiron and calcium
Affect Intestinal TransportAffect Intestinal Transport
 Cochicine (gout) paraaminosalicylic acidCochicine (gout) paraaminosalicylic acid
(TB) sulfasalazine (ulcerative colitis)(TB) sulfasalazine (ulcerative colitis)
trimethoprim (antibiotic) and pyrimethaminetrimethoprim (antibiotic) and pyrimethamine
(antiprotozoal)(antiprotozoal)
– Impair absorption of B12 or folateImpair absorption of B12 or folate

Nutrition: AdsorptionNutrition: Adsorption
 Cholestyramine (antihyperlipidemicCholestyramine (antihyperlipidemic
bile acid sequestrant) also adsorbs fat-bile acid sequestrant) also adsorbs fat-
soluble vitamins A, D, E, K, possiblysoluble vitamins A, D, E, K, possibly
folic acid; may need supplements forfolic acid; may need supplements for
long term therapy, especially if dosedlong term therapy, especially if dosed
several times a dayseveral times a day
 Mineral oil: (>2 tbsp/day)Mineral oil: (>2 tbsp/day) ↓ absorption↓ absorption
of fat soluble vitaminsof fat soluble vitamins
– take vitamins at least 2 hours aftertake vitamins at least 2 hours after

Drug Side Effects thatDrug Side Effects that
Affect Nutritional StatusAffect Nutritional Status
 Appetite changesAppetite changes
 Oral taste and smellOral taste and smell
 NauseaNausea
 Dry mouthDry mouth
 Gastrointestinal effectsGastrointestinal effects
 Organ system toxicityOrgan system toxicity
 Glucose levelsGlucose levels

Examples of Drug CategoriesExamples of Drug Categories
That May Decrease AppetiteThat May Decrease Appetite
 AntiinfectivesAntiinfectives
 AntineoplasticsAntineoplastics
 BronchodilatorsBronchodilators
 Cardiovascular drugsCardiovascular drugs
 StimulantsStimulants

Drugs That MayDrugs That May
Increase AppetiteIncrease Appetite
 AnticonvulsantsAnticonvulsants
 HormonesHormones
 Psychotropic drugsPsychotropic drugs
——AntipsychoticsAntipsychotics
——Antidepressants, tricyclics, MAOIsAntidepressants, tricyclics, MAOIs

Drugs Affecting OralDrugs Affecting Oral
Cavity, Taste and SmellCavity, Taste and Smell
 Taste changes: cisplatin, captopril (anti-Taste changes: cisplatin, captopril (anti-
hypertensive) amprenavir (antiviral)hypertensive) amprenavir (antiviral)
phenytoin (anti-convulsive), clarithromycinphenytoin (anti-convulsive), clarithromycin
(antibiotic)(antibiotic)
 Mucositis: antineoplastic drugs such asMucositis: antineoplastic drugs such as
interleukin-2, paclitaxel, carboplatininterleukin-2, paclitaxel, carboplatin
 Dry mouth: Anticholinergic drugs (tricyclicDry mouth: Anticholinergic drugs (tricyclic
antidepressants such as amytriptyline,antidepressants such as amytriptyline,
antihistamines such as diphenhydramine,antihistamines such as diphenhydramine,
antispasmodics such as oxybutyninantispasmodics such as oxybutynin

Drugs that Affect the GIDrugs that Affect the GI
TractTract
 Alendronate (Fosamax) anti-osteoporosisAlendronate (Fosamax) anti-osteoporosis
drug—patients must sit upright 30 minutesdrug—patients must sit upright 30 minutes
after taking it to avoid esophagitisafter taking it to avoid esophagitis
 Aspirin or other NASAIDs –can cause GIAspirin or other NASAIDs –can cause GI
bleeding, gastritisbleeding, gastritis
 Orlistat – blocks fat absorption, can causeOrlistat – blocks fat absorption, can cause
oily spotting, fecal urgency, incontinenceoily spotting, fecal urgency, incontinence
 Narcotic agents cause constipationNarcotic agents cause constipation

Examples of DrugExamples of Drug
Classes That CauseClasses That Cause
DiarrheaDiarrhea
 LaxativesLaxatives
 AntiretroviralsAntiretrovirals
 AntibioticsAntibiotics
 AntineoplasticsAntineoplastics
 + liquid medications in elixirs+ liquid medications in elixirs
containing sugar alcoholscontaining sugar alcohols

Drugs That May LowerDrugs That May Lower
Glucose LevelsGlucose Levels
 Antidiabetic drugs (acarbose,Antidiabetic drugs (acarbose,
glimepiride, glipizide, glyburide,glimepiride, glipizide, glyburide,
insulin, metformin, miglitol,insulin, metformin, miglitol,
neteglinide, pioglitizone, repaglinide,neteglinide, pioglitizone, repaglinide,
roiglitizoneroiglitizone
 Drugs that can cause hypoglycemia:Drugs that can cause hypoglycemia:
ethanol, quinine, disopyramideethanol, quinine, disopyramide
(antiarrhythmic) and pentamidine(antiarrhythmic) and pentamidine
isethionate (antiprotozoal)isethionate (antiprotozoal)

Drugs That Raise BloodDrugs That Raise Blood
GlucoseGlucose
 Antiretrovirals, protease inhibitorsAntiretrovirals, protease inhibitors
(amprenavir, nelfinavir, ritonavir, saquinavir)(amprenavir, nelfinavir, ritonavir, saquinavir)
 Diuretics, antihypertensives (furosemide,Diuretics, antihypertensives (furosemide,
hydrochlorothiazide, indapamide)hydrochlorothiazide, indapamide)
 Hormones (corticosteroids, danazol, estrogenHormones (corticosteroids, danazol, estrogen
or estrogen/progesterone replacementor estrogen/progesterone replacement
therapy, megestrol acetate, oraltherapy, megestrol acetate, oral
contraceptives)contraceptives)
 Niacin (antihyperlipidemic) baclofen, caffeine,Niacin (antihyperlipidemic) baclofen, caffeine,
olanzapine, cyclosporine, interferon alfa-2aolanzapine, cyclosporine, interferon alfa-2a

Nutrition Implications ofNutrition Implications of
Excipients in DrugsExcipients in Drugs
 Excipients: are inactive ingredients added toExcipients: are inactive ingredients added to
drugs as fillers, buffers, binders,drugs as fillers, buffers, binders,
disintegrant, flavoring, dye, preservative,disintegrant, flavoring, dye, preservative,
suspending agent, coatingsuspending agent, coating
 Approved by FDA for use inApproved by FDA for use in
pharmaceuticalspharmaceuticals
 Vary widely from brand to brand andVary widely from brand to brand and
formulation strengths of the same drugformulation strengths of the same drug

 Excipients may cause allergic or healthExcipients may cause allergic or health
reactions in persons with celiac disease,reactions in persons with celiac disease,
dye sensitivity, other allergies, inborn errorsdye sensitivity, other allergies, inborn errors
of metabolismof metabolism
 Examples of excipients that might causeExamples of excipients that might cause
reactions are albumin, wheat products,reactions are albumin, wheat products,
alcohol, aspartame, lactose, sugar alcohols,alcohol, aspartame, lactose, sugar alcohols,
starch, sulfites, tartrazine, vegetable oilstarch, sulfites, tartrazine, vegetable oil
 Some meds may contain sufficient CHO orSome meds may contain sufficient CHO or
protein to put a patient on a ketogenic dietprotein to put a patient on a ketogenic diet
out of ketosisout of ketosis

 Some drugs at usual dosages maySome drugs at usual dosages may
contain enough excipients to becontain enough excipients to be
nutritionally significantnutritionally significant
– Agenerase: 1744 IU vitamin EAgenerase: 1744 IU vitamin E
– Accupril: 50-200 mg magnesiumAccupril: 50-200 mg magnesium
– Fibercon/Fiberlax: 600 mg ca+ in 6 tabsFibercon/Fiberlax: 600 mg ca+ in 6 tabs
– Propofol (Diprivan) contains 10%Propofol (Diprivan) contains 10%
soybean emulsion; may provide 1663soybean emulsion; may provide 1663
kcals/day for 70 kg personkcals/day for 70 kg person

Drugs – EnteralDrugs – Enteral
FeedingsFeedings
 Most medications should not be mixedMost medications should not be mixed
with enteral feedings; physicalwith enteral feedings; physical
incompatibilities can occur includingincompatibilities can occur including
granulation, gel formation, separationgranulation, gel formation, separation
of the feeding leading to clogged tubesof the feeding leading to clogged tubes
 Enteral feedings interfere withEnteral feedings interfere with
phenytoin absorption; window thephenytoin absorption; window the
feeding around drug dose (2 hoursfeeding around drug dose (2 hours
before and after)before and after)

Enteral Nutrition andEnteral Nutrition and
DrugsDrugs
 Drugs put in feeding tubes may cause:Drugs put in feeding tubes may cause:
——DiarrheaDiarrhea
——Drug-nutrient bindingDrug-nutrient binding
——Blocked tubeBlocked tube
 If patient does not receive total volumeIf patient does not receive total volume
of enteral feeding, he/she will not receiveof enteral feeding, he/she will not receive
the full dose of the drugthe full dose of the drug

DrugsDrugs
 Avoid adding drug to formulaAvoid adding drug to formula
 When drugs must be given throughWhen drugs must be given through
tube:tube:
– Stop feeding, flush tube, giveStop feeding, flush tube, give
drug, flushdrug, flush
– Use liquid form of drug (but be aware ofUse liquid form of drug (but be aware of
effects of elixirs on bowel function)effects of elixirs on bowel function)
– Avoid crushing tabletsAvoid crushing tablets

DrugsDrugs
 Be aware of potential interactionsBe aware of potential interactions
between enteral feedings and drugsbetween enteral feedings and drugs
– PhenytoinPhenytoin
– CiprofloxacinCiprofloxacin

MNT forMNT for
Food-Drug InteractionsFood-Drug Interactions
 Prospective: MNT offered when theProspective: MNT offered when the
patient first starts a drugpatient first starts a drug
 Retrospective: evaluation of symptomsRetrospective: evaluation of symptoms
to determine if medical problems mightto determine if medical problems might
be the result of food-drug interactionsbe the result of food-drug interactions

TJC 2006 Standards ReTJC 2006 Standards Re
Education onEducation on
MedicationsMedications
Standard PC.6.10Standard PC.6.10 Elements ofElements of
PerformancePerformance
 As appropriate to the patient's conditionAs appropriate to the patient's condition
and assessed needs and the hospital'sand assessed needs and the hospital's
scope of services, the patient is educatedscope of services, the patient is educated
about the following:about the following:
– The safe and effective use of medicationsThe safe and effective use of medications
– Nutrition interventions, modified diets, or oralNutrition interventions, modified diets, or oral
healthhealth
CAMH 2006 online version accessed 1/2007

Avoiding Food-DrugAvoiding Food-Drug
Interactions: ProspectiveInteractions: Prospective
 When medications are initiated, patientsWhen medications are initiated, patients
should be provided with complete writtenshould be provided with complete written
and verbal drug education at an appropriateand verbal drug education at an appropriate
reading level including food-drug interactionreading level including food-drug interaction
informationinformation
 Patients should be encouraged to askPatients should be encouraged to ask
specific questions about their medicationsspecific questions about their medications
and whether they might interact with eachand whether they might interact with each
other or with foodsother or with foods
 Patients should read the drug label andPatients should read the drug label and
accompanying materials provided by theaccompanying materials provided by the
pharmacistpharmacist

 In acute-care settings, patients receivingIn acute-care settings, patients receiving
high risk medications should be identifiedhigh risk medications should be identified
and evaluatedand evaluated
 Nurses should have information regardingNurses should have information regarding
drug-food interactions and drugdrug-food interactions and drug
administration guidelines available at theadministration guidelines available at the
bedsidebedside
 Med pass times should be evaluated in lightMed pass times should be evaluated in light
of potential food-drug interactionsof potential food-drug interactions

 Systems should be established so thatSystems should be established so that
pharmacists can communicate withpharmacists can communicate with
food and nutrition staff regarding highfood and nutrition staff regarding high
risk patientsrisk patients

Interactions: RetrospectiveInteractions: Retrospective
 Clinicians including dietitians should obtainClinicians including dietitians should obtain
a full drug and diet history including the usea full drug and diet history including the use
of OTC and dietary supplements and reviewof OTC and dietary supplements and review
potential drug-food interactionspotential drug-food interactions
 A plan should be developed for dealing withA plan should be developed for dealing with
potential drug-food interactions for short andpotential drug-food interactions for short and
long term drug therapylong term drug therapy
 When therapeutic goals are not met,When therapeutic goals are not met,
clinicians should ask questions about howclinicians should ask questions about how
and when drugs are being taken in relationand when drugs are being taken in relation
to foods and nutritional supplementsto foods and nutritional supplements

Interactions: RetrospectiveInteractions: Retrospective
 Clinicians should evaluate whetherClinicians should evaluate whether
medical problems could be the resultmedical problems could be the result
of drug-food interactionsof drug-food interactions
 Often it may be the dietitian who isOften it may be the dietitian who is
most aware of these issuesmost aware of these issues

Interactions: ExampleInteractions: Example
 A 20-year-old disabled patient who was aA 20-year-old disabled patient who was a
long term resident of a nursing home waslong term resident of a nursing home was
admitted to an acute care hospital for aadmitted to an acute care hospital for a
workup to determine the cause of chronicworkup to determine the cause of chronic
diarrheadiarrhea
 The enteral feeding had been changedThe enteral feeding had been changed
numerous times in an effort to normalize thenumerous times in an effort to normalize the
patient’s bowel functionpatient’s bowel function
 The patient was currently receiving aThe patient was currently receiving a
defined formula feeding at a slow ratedefined formula feeding at a slow rate

Interactions: ExampleInteractions: Example
 The workup revealed no apparent medicalThe workup revealed no apparent medical
reason for the impaired bowel functionreason for the impaired bowel function
 After reviewing the pts medications, theAfter reviewing the pts medications, the
dietitian suggested that the patient’sdietitian suggested that the patient’s
medications (given in liquid elixir formsmedications (given in liquid elixir forms
containing sugar alcohols) might be causingcontaining sugar alcohols) might be causing
the diarrheathe diarrhea
 The patient’s medications were changed,The patient’s medications were changed,
and the diarrhea resolvedand the diarrhea resolved
 The patient returned to the nursing home onThe patient returned to the nursing home on
a standard enteral feeding formulaa standard enteral feeding formula

SummarySummary
 Most drugs have nutritional statusMost drugs have nutritional status
side effects.side effects.
 Always look for therapeuticallyAlways look for therapeutically
significant interactions betweensignificant interactions between
food and drugsfood and drugs
 Identify and monitor high riskIdentify and monitor high risk
patients, those on multiplepatients, those on multiple
medications and marginal dietsmedications and marginal diets

Food drug interaction

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Food drug interaction