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National Institute on Alcohol Abuse and Alcoholism No.
27 PH 355 January 1995
Alcohol-Medication Interactions
Many medications can interact with alcohol, leading
to increased risk of illness, injury, or death. For example, it is estimated
that alcohol-medication interactions may be a factor in at least 25 percent
of all emergency room admissions (1). An unknown number of less serious
interactions may go unrecognized or unrecorded. This Alcohol Alert
notes some of the most significant alcohol-drug interactions. (Although
alcohol can interact with illicit drugs as well, the term "drugs" is used
here to refer exclusively to medications, whether prescription or nonprescription.)
How Common Are Alcohol-Drug Interactions?
More than 2,800 prescription drugs are available in
the United States, and physicians write 14 billion prescriptions annually;
in addition, approximately 2,000 medications are available without prescription
(2).
Ap proximately 70 percent of the adult population
consumes alcohol at least occasionally, and 10 percent drink daily (3).
About 60 percent of men and 30 percent of women have had one or more adverse
alcohol-related life events (4). Together with the data on medication
use, these statistics suggest that some concurrent use of alcohol and
medications
is inevitable.
The elderly may be especially likely to mix drugs
and alcohol and are at particular risk for the adverse consequences of
such combinations. Although persons age 65 and older constitute only 12
percent of the population, they consume 25 to 30 percent of all prescription
medications (5) . The elderly are more likely to suffer medication side
effects compared with younger persons, and these effects tend to be more
severe with advancing age (5). Among persons age 60 or older, 10 percent
of those in the community--and 40 percent of those in nursing homes--fulfill
criteria for alcohol abuse (6).
How Alcohol and Drugs Interact
To exert its desired effect, a drug generally must travel
through the bloodstream to its site of action, where it produces some
change in an organ or tissue. The drug's effects then diminish as it is
processed (metabolized) by enzymes and eliminated from the body. Alcohol
behaves similarly, traveling through the bloodstream, acting upon the
brain to cause intoxication, and finally being metabolized and eliminated,
principally by the liver. The extent to which an administered dose of
a drug reaches its site of action may be termed its availability.
Alcohol can influence the effectiveness of a drug by altering its availability.
Typical alcohol-drug interactions include the following (7): First, an
acute dose of alcohol (a single drink or several drinks over several
hours) may inhibit a drug's metabolism by competing with the drug for
the same set of metabolizing enzymes. This interaction prolongs and enhances
the drug's availability, potentially increasing the patient's risk of
experiencing harmful side effects from the drug. Second, in contrast,
chronic (long-term) alcohol ingestion may activate drug-metabolizing
enzymes, thus decreasing the drug's availability and diminishing its effects.
After these enzymes have been activated, they remain so even in the absence
of alcohol, affecting the metabolism of certain drugs for several weeks
after cessation of drinking (8). Thus, a recently abstinent chronic drinker
may need higher doses of medications than those required by nondrinkers
to achieve therapeutic levels of certain drugs. Third, enzymes activated
by chronic alcohol consumption transform some drugs into toxic chemicals
that can damage the liver or other organs. Fourth, alcohol can magnify
the inhibitory effects of sedative and narcotic drugs at their sites of
action in the brain. To add to the complexity of these interactions, some
drugs affect the metabolism of alcohol, thus altering its potential for
intoxication and the adverse effects associated with alcohol consumption
(7).
Some Specific Interactions
Anesthetics. Anesthetics are administered
prior to surgery to render a patient unconscious and insensitive to pain.
Chronic alcohol consumption increases the dose of propofol (Diprivan)1
required to induce loss of consciousness (9). Chronic alcohol consumption
increases the risk of liver damage that may be caused by the anesthetic
gases enflurane (Ethrane) (10) and halothane (Fluothane) (11).
Antibiotics. Antibiotics are used to treat
infectious diseases. In combination with acute alcohol consumption, some
antibiotics may cause nausea, vomiting, headache, and possibly convulsions;
among these antibiotics are furazolidone (Furoxone), griseofulvin (Grisactin
and others), metronidazole (Flagyl), and the antimalarial quinacrine (Atabrine)
(7). Isoniazid and rifampin are used together to treat tuberculosis, a
disease especially problematic among the elderly (12) and among homeless
alcoholics (13). Acute alcohol consumption decreases the availability
of isoniazid in the bloodstream, whereas chronic alcohol use decreases
the availability of rifampin. In each case, the effectiveness of the medication
may be reduced (7).
Anticoagulants. Warfarin (Coumadin) is
prescribed to retard the blood's ability to clot. Acute alcohol consumption
enhances warfarin's availability, increasing the patient's risk for life-threatening
hemorrhages (7). Chronic alcohol consumption reduces warfarin's availability,
lessening the patient's protection from the consequences of blood-clotting
disorders (7).
Antidepressants. Alcoholism and depression
are frequently associated (14), leading to a high potential for alcohol-antidepressant
interactions. Alcohol increases the sedative effect of tricyclic antidepressants
such as amitriptyline (Elavil and others), impairing mental skills required
for driving (15). Acute alcohol consumption increases the availability
of some tricyclics, potentially increasing their sedative effects (16);
chronic alcohol consumption appears to increase the availability of some
tricyclics and to decrease the availability of others (17,18). The significance
of these interactions is unclear. These chronic effects persist in recovering
alcoholics (17).
A chemical called tyramine, found in some beers
and wine, interacts with some anti-depressants, such as monoamine oxidase
inhibitors, to produce a dangerous rise in blood pressure (7). As little
as one standard drink may create a risk that this interaction will occur.
Antidiabetic medications. Oral hypoglycemic
drugs are prescribed to help lower blood sugar levels in some patients
with diabetes. Acute alcohol consumption prolongs, and chronic alcohol
consumption decreases, the availability of tolbutamide (Orinase). Alcohol
also interacts with some drugs of this class to produce symptoms of nausea
and headache such as those described for metronidazole (see "Antibiotics")
(7).
Antihistamines. Drugs such as diphenhydramine
(Benadryl and others) are available without prescription to treat allergic
symptoms and insomnia. Alcohol may intensify the sedation caused by some
antihistamines (15). These drugs may cause excessive dizziness and sedation
in older persons; the effects of combining alcohol and antihistamines
may therefore be especially significant in this population (19).
Antipsychotic medications. Drugs such as
chlorpromazine (Thorazine) are used to diminish psychotic symptoms such
as delusions and hallucinations. Acute alcohol consumption increases the
sedative effect of these drugs (20), resulting in impaired coordination
and potentially fatal breathing difficulties (7). The combination of chronic
alcohol ingestion and antipsychotic drugs may result in liver damage (21).
Antiseizure medications. These drugs are
prescribed mainly to treat epilepsy. Acute alcohol consumption increases
the availability of phenytoin (Dilantin) and the risk of drug-related
side effects. Chronic drinking may decrease phenytoin availability, significantly
reducing the patient's protection against epileptic seizures, even during
a period of abstinence (8,22).
Antiulcer medications. The commonly prescribed
antiulcer medications cimetidine (Tagamet) and ranitidine (Zantac) increase
the availability of a low dose of alcohol under some circumstances (23,24).
The clinical significance of this finding is uncertain, since other studies
have questioned such interaction at higher doses of alcohol (25-27).
Cardiovascular medications. This class
of drugs includes a wide variety of medications prescribed to treat ailments
of the heart and circulatory system. Acute alcohol consumption interacts
with some of these drugs to cause dizziness or fainting upon standing
up. These drugs include nitroglycerin, used to treat angina, and reserpine,
methyldopa (Aldomet), hydralazine (Apresoline and others), and guanethidine
(Ismelin and others), used to treat high blood pressure. Chronic alcohol
consumption decreases the availability of propranolol (Inderal), used
to treat high blood pressure (7), potentially reducing its therapeutic
effect.
Narcotic pain relievers. These drugs are
prescribed for moderate to severe pain. They include the opiates morphine,
codeine, propoxyphene (Darvon), and meperidine (Demerol). The combination
of opiates and alcohol enhances the sedative effect of both substances,
increasing the risk of death from overdose (28). A single dose of alcohol
can increase the availability of propoxyphene (29), potentially increasing
its sedative side effects.
Nonnarcotic pain relievers. Aspirin and
similar nonprescription pain relievers are most commonly used by the elderly
(5) . Some of these drugs cause stomach bleeding and inhibit blood from
clotting; alcohol can exacerbate these effects (30). Older persons who
mix alcoholic beverages with large doses of aspirin to self-medicate for
pain are therefore at particularly high risk for episodes of gastric bleeding
(19). In addition, aspirin may increase the availability of alcohol (31),
heightening the effects of a given dose of alcohol.
Chronic alcohol ingestion activates enzymes that
transform acetaminophen (Tylenol and others) into chemicals that can cause
liver damage, even when acetaminophen is used in standard therapeutic
amounts (32,33). These effects may occur with as little as 2.6 grams of
acetaminophen in persons consuming widely varying amounts of alcohol (34).
Sedatives and hypnotics ("sleeping pills").
Benzodiazepines such as diazepam (Valium) are generally prescribed to
treat anxiety and insomnia. Because of their greater safety margin, they
have largely replaced the barbiturates, now used mostly in the emergency
treatment of convulsions (2).
Doses of benzodiazepines that are excessively
sedating may cause severe drowsiness in the presence of alcohol (35),
increasing the risk of household and automotive accidents (15,36). This
may be especially true in older people, who demonstrate an increased response
to these drugs (5,19). Low doses of flurazepam (Dalmane) interact with
low doses of alcohol to impair driving ability, even when alcohol is ingested
the morning after taking Dalmane. Since alcoholics often suffer from anxiety
and insomnia, and since many of them take morning drinks, this interaction
may be dangerous (37).
The benzodiazepine lorazepam (Ativan) is being
increasingly used for its antianxiety and sedative effects. The combination
of alcohol and lorazepam may result in depressed heart and breathing functions;
therefore, lorazepam should not be administered to intoxicated patients
(38).
Acute alcohol consumption increases the availability
of barbiturates, prolonging their sedative effect. Chronic alcohol consumption
decreases barbiturate availability through enzyme activation (2). In addition,
acute or chronic alcohol consumption enhances the sedative effect of barbiturates
at their site of action in the brain, sometimes leading to coma or fatal
respiratory depression (39).
Alcohol-Medication Interactions--A Commentary by
NIAAA Director Enoch Gordis, M.D.
Individuals who drink alcoholic beverages should
be aware that simultaneous use of alcohol and medications--both prescribed
and over-the-counter--has the potential to cause problems. For example,
even very small doses of alcohol probably should not be used with antihistamines
and other medications with sedative effects. Individuals who drink larger
amounts of alcohol may run into problems when commonly used medications
(e.g., acetaminophen) are taken at the same time or even shortly after
drinking has stopped. Elderly individuals should be especially careful
of these potential problems due to their generally greater reliance on
multiple medications and age-related changes in physiology.
1The U.S. Government does not endorse or favor any specific
commercial product (or commodity, service, or company). Trade or proprietary
names appearing in this publication are used only because they are considered
essential in the context of the studies reported herein.
References
(1) Holder, H.D. Effects of Alcohol, Alone
and in Combination With Medications. Walnut Creek, CA: Prevention
Research Center, 1992. (2) Sands, B.F.; Knapp, C.M.; & Ciraulo,
D.A. Medical consequences of alcohol-drug interactions. Alcohol Health
& Research World 17(4):316-320, 1993. (3) Midanik, L.T.,
& Room, R. The epidemiology of alcohol consumption. Alcohol Health
& Research World 16(3):183-190, 1992. (4) American Psychiatric
Association. Diagnostic and Statistical Manual of Mental Disorders,
Fourth Edition. Washington, DC: the Association, 1994. (5) Gomberg,
E.S.L. Drugs, alcohol, and aging. In: Kozlowski, L.T.; Annis, H.M.;
Cappell, H.D.; Glaser, F.B.; Goodstadt, M.S.; Israel, Y.; Kalant, H.;
Sellers, E.M.; & Vingilis, E.R. Research Advances in Alcohol and
Drug Problems. Vol. 10. New York: Plenum Press, 1990. pp. 171-213.
(6) Egbert, A.M. The older alcoholic: Recognizing the subtle clinical
clues. Geriatrics 48(7):63-69, 1993. (7) Lieber, C.S. Interaction
of ethanol with other drugs. In: Lieber, C.S., ed. Medical and Nutritional
Complications of Alcoholism: Mechanisms and Management. New York:
Plenum Press, 1992. pp. 165-183. (8) Guram, M.S.; Howden, C.W.;
& Holt, S. Alcohol and drug interactions. Practical Gastroenterology
16(8):47, 50-54, 1992. (9) Fassoulaki, A.; Farinotti, R.; Servin,
F.; & Desmonts, J.M. Chronic alcoholism increases the induction dose
of propofol in humans. Anesthesia and Analgesia 77(3):553-556,
1993. (10) Tsutsumi, R.; Leo, M.A.; Kim, C.-i. ; Tsutsumi, M.;
Lasker, J.; Lowe, N.; & Lieber, C.S. Interaction of ethanol with enflurane
metabolism and toxicity: Role of P450IIE1. Alcoholism: Clinical and
Experimental Research 14(2):174-179, 1990. (11) Ishii, H.;
Takagi, T.; Okuno, F.; Ebihara, Y.; Tashiro, M.; & Tsuchiya, M. Halothane-induced
hepatic necrosis in ethanol-pretreated rats. In: Lieber, C.S., ed. Biological
Approach to Alcoholism. National Institute on Alcohol Abuse and Alcoholism
Research Monograph No. 11. DHHS Pub. No. (ADM)83-1261. Washington, DC:
Supt. of Docs., U.S. Govt. Print. Off., 1983. pp. 152-157. (12) Kelley,
W.N., ed. Textbook of Internal Medicine. Philadelphia: Lippincott,
1989. (13) Jacobson, J.M. Alcoholism and tuberculosis. Alcohol
Health & Research World 16(1):39-45, 1992. (14) Roy, A.
; DeJong, J.; Lamparski, D.; George, T.; & Linnoila, M. Depression
among alcoholics. Archives of General Psychiatry 48(5):428-432,
1991. (15) Seppala, T.; Linnoila, M.; & Mattila, M.J. Drugs,
alcohol and driving. Drugs 17:389-408, 1979. (16) Dorian, P.;
Sellers, E.M.; Reed, K.L.; Warsh, J.J.; Hamilton, C.; Kaplan, H.L.; &
Fan, T. Amitriptyline and ethanol: Pharmacokinetic and pharmacodynamic
interaction. European Journal of Clinical Pharmacology 25(3):325-331,
1983. (17) Balant-Gorgia, A.E.; Gay, M.; Gex-Fabry, M.; & Balant,
L.P. Persistent impairment of clomipramine demethylation in recently detoxified
alcoholic patients. Therapeutic Drug Monitoring 14(2):119-124,
1992. (18) Rudorfer, M.V., & Potter, W.Z. Pharmacokinetics
of antidepressants. In: Meltzer, H.Y.,ed. Psychopharmacology: The Third
Generation of Progress. New York: Raven Press, 1987. pp. 1353-1363.
(19) Dufour, M.C.; Archer, L.; & Gordis, E. Alcohol and the
elderly. Clinics in Geriatric Medicine 8(1):127-141, 1992. (20)
Shoaf, S.E., & Linnoila, M. Interaction of ethanol and smoking
on the pharmacokinetics and pharmacodynamics of psychotropic medications.
Psychopharmacology Bulletin 27(4):577-594, 1991. (21) Teschke,
R. Effect of chronic alcohol pretreatment on the hepatotox-icity elicited
by chlorpromazine, paracetamol, and dimethylnitrosamine. In: Lieber, C.S.,
ed. Biological Approach to Alcoholism. National Institute on Alcohol
Abuse and Alcoholism Research Monograph No. 11. DHHS Pub. No. (ADM)83-1261.
Washington, DC: Supt. of Docs., U.S. Govt. Print. Off., 1983. pp. 170-179.
(22) Greenspan, K., & Smith, T.J. Perspectives on alcohol and
medication interactions. Journal of Alcohol and Drug Education
36(3):103-107, 1991. (23) Caballeria, J.; Baraona, E.; Deulofeu,
R.; Hernandez-Munoz, R.; Rodes, J.; & Lieber, C.S. Effects of H2-receptor
antagonists on gastric alcohol dehydrogenase activity. Digestive Diseases
and Sciences 36(12):1673-1679, 1991. (24) DiPadova, C.; Roine,
R.; Frezza, M.; Gentry, R.T.; Baraona, E.; & Lieber, C.S. Effects
of ranitidine on blood alcohol levels after ethanol ingestion: Comparison
with other H2-receptor antagonists. Journal of the American Medical
Association 267(1):83-86, 1992. (25) Fraser, A.G.; Hudson,
M.; Sawyerr, A.M.; Smith, M.; Rosalki, S.B.; & Pounder, R.E. Ranitidine,
cimetidine, famotidine have no effect on post-prandial absorption of ethanol
0.8 g/kg taken after an evening meal . Alimentary Pharmacology and
Therapeutics 6(6):693-700, 1992. (26) Kendall, M.J.; Spannuth,
F.; Walt, R.P; Gibson, G.J.; Hale, K.A.; Braithwaite, R.; & Langman,
M.J.S. Lack of effect of H2-receptor antagonists on the pharmacokinetics
of alcohol consumed after food at lunchtime. British Journal of Clinical
Pharmacology 37:371-374, 1994. (27) Mallat, A.; Roudot-Thoraval,
F.; Bergmann, J.F.; Trout, H.; Simonneau, G.; Dutreuil, C.; Blanc, L.E.;
Dhumeaux, D.; & Delchier, J.C. Inhibition of gastric alcohol dehydrogenase
activity by histamine H2-receptor antagonists has no influence on the
pharmacokinetics of ethanol after a moderate dose. British Journal
of Clinical Pharmacology 37(2):208-211, 1994. (28) Kissin, B.
Interactions of ethyl alcohol and other drugs. In: Kissin, B., & Begleiter,
H., eds. The Biology of Alcoholism: Volume 3. Clinical Pathology.
New York: Plenum Press, 1974. pp. 109-162. (29) Girre, C.; Hirschhorn,
M.; Bertaux, L.; Palombo, S.; Dellatolas, F.; Ngo, R.; Moreno, M.; &
Fournier, P.E. Enhancement of propoxyphene bioavailability by ethanol:
Relation to psychomotor and cognitive function in healthy volunteers.
European Journal of Clinical Pharmacology 41(2):147-152, 1991.
(30) Rees, W.D.W., & Turnberg, L.A. Reappraisal of the effects
of aspirin on the stomach. Lancet 2:410-413, 1980. (31) Roine,
R.; Gentry, R.T.; Hernandez-Munoz, R.; Baraona, E.; & Lieber,
C.S. Aspirin increases blood alcohol concentrations in humans after ingestion
of ethanol. Journal of the American Medical Association 264(18):2406-2408,
1990. (32) Seeff, L.B.; Cuccherini, B.A.; Zimmerman, H.J.; Adler,
E.; & Benjamin, S.B. Acetaminophen hepatotoxicity in alcoholics: A
therapeutic misadventure. Annals of Internal Medicine 104(3):399-404,
1986. (33) Girre, C.; Hispard, E.; Palombo, S.; N'Guyen, C.; &
Dally, S. Increased metabolism of acetaminophen in chronically alcoholic
patients. Alcoholism: Clinical and Experimental Research 17(1):170-173,
1993. (34) Black, M. Acetaminophen hepatotoxicity. Annual Review
of Medicine 35:577-593, 1984. (35) Girre, C.; Facy, F.; Lagier,
G.; & Dally, S. Detection of blood benzodiazepines in injured people.
Relationship with alcoholism. Drug and Alcohol Dependence 21(1):61-65,
1988. (36) Hollister, L.E. Interactions between alcohol and benzodiazepines.
In: Galanter, M., ed. Recent Developments in Alcoholism: Volume 8.
Combined Alcohol and Other Drug Dependence. New York: Plenum Press,
1990. pp. 233-239. (37) Linnoila, M.; Mattila, M.J.; & Kitchell,
B.S. Drug interactions with alcohol. Drugs 18:299-311, 1979. (38)
Medical Economics Data. Physicians' Desk Reference. Montvale,
NJ: Medical Economics Data, 1993. (39) Forney, R.B., & Hughes,
F.W. Meprobamate, ethanol or meprobamate-ethanol combinations on performance
of human subjects under delayed autofeedback (DAF). Journal of Psychology
57:431-436, 1964.
ACKNOWLEDGMENT: The National Institute on Alcohol
Abuse and Alcoholism wishes to acknowledge the valuable contributions
of Charles S. Lieber, M.D., Director, Alcohol Research Center, Bronx VAMC,
and professor, Mount Sinai School of Medicine, to the development of this
Alcohol Alert.
All material contained in the Alcohol Alert is in
the public domain and may be used or reproduced without permission from
NIAAA. Citation of the source is appreciated.
Copies of the Alcohol Alert are available free of
charge from the Scientific Communications Branch, Office of Scientific
Affairs, NIAAA, Willco Building, Suite 409, 6000 Executive Boulevard,
Bethesda, MD 20892-7003. Telephone: 301-443-3860.
U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES
Public Health Service * National Institutes of Health
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