Interactions between Dextromethorphan / triprolidine and Sodium oxybate
2 drug interactions and 26 additional warnings found for the following 2 drugs:
- dextromethorphan/triprolidine
- sodium oxybate
Drug interactions
Major drug interactions
Major:
triprolidine sodium oxybate
Applies to: dextromethorphan / triprolidine and sodium oxybate
Monitor closely
The central nervous system (CNS) and respiratory depressant effects of sodium oxybate, which is the sodium salt of gamma-hydroxybutyrate (GHB), may be potentiated by concomitant use of other CNS depressants. An increased risk of serious adverse reactions such as respiratory depression, hypotension, profound sedation, syncope, and death should be considered. Controlled interaction data specific to the broad category of CNS depressants are not available. However, supportive sedative-hypnotic interaction data are available. In healthy volunteers, a single 2.25 g dose of sodium oxybate did not alter the pharmacokinetics of lorazepam 2 mg or zolpidem 5 mg. Increased sleepiness occurred with lorazepam; however, zolpidem's pharmacodynamic effect was not assessed. The interaction may also occur with other oxybate salts.
Management
If concomitant use of sodium oxybate and another CNS depressant is necessary, patient response and tolerability should be closely monitored. Reduction or discontinuation of one or more CNS depressants, including sodium oxybate, may be considered as clinically appropriate. All patients treated with sodium oxybate should be advised not to drive, operate machinery, or engage in potentially hazardous activities requiring mental alertness and motor coordination for at least 6 hours after taking a dose of sodium oxybate and until they know how the medication affects them. The same precautions are applicable to other oxybate formulations.
References (8)
- (2022) "Product Information. Xyrem (sodium oxybate)." UCB Pharma Ltd
- (2025) "Product Information. Xywav (calcium/magnesium/potassium/sodium oxybates)." Jazz Pharmaceuticals
- (2025) "Product Information. Xyrem (sodium oxybate)." Innomar Strategies Inc
- (2026) "Product Information. Sodium Oxybate (Reach) (sodium oxybate)." Reach Pharmaceuticals Pty Ltd
- (2024) "Product Information. OXIBATO DE SODIO KALCEKS (oxibato de sodio)." AKCIJU SABIEDRIBA KALCEKS
- (2025) "Product Information. Lumryz (sodium oxybate)." Avadel CNS Pharmaceuticals, LLC, v2
- (2025) "Product Information. Xyrem (sodium oxybate)." Jazz Pharmaceuticals, v1
- (2024) "Product Information. Xywav (calcium/magnesium/potassium/sodium oxybates)." Innomar Strategies Inc
Moderate drug interactions
Moderate:
dextromethorphan triprolidine
Applies to: dextromethorphan / triprolidine and dextromethorphan / triprolidine
Monitor
Central nervous system- and/or respiratory-depressant effects may be additively or synergistically increased in patients taking multiple drugs that cause these effects, especially in elderly or debilitated patients. Sedation and impairment of attention, judgment, thinking, and psychomotor skills may increase.
Management
During concomitant use of these drugs, patients should be monitored for potentially excessive or prolonged CNS and respiratory depression. Cautious dosage titration may be required, particularly at treatment initiation. Ambulatory patients should be counseled to avoid hazardous activities requiring mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
References (36)
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- Sotaniemi EA, Anttila M, Rautio A, et al. (1981) "Propranolol and sotalol metabolism after a drinking party." Clin Pharmacol Ther, 29, p. 705-10
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- Divoll M, Greenblatt DJ, Lacasse Y, Shader RI (1981) "Benzodiazepine overdosage: plasma concentrations and clinical outcome." Psychopharmacology (Berl), 73, p. 381-3
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- Driessen JJ, Vree TB, Booij LH, van der Pol FM, Crul JF (1984) "Effect of some benzodiazepines on peripheral neuromuscular function in the rat in-vitro hemidiaphragm preparation." J Pharm Pharmacol, 36, p. 244-7
- Feldman SA, Crawley BE (1970) "Interaction of diazepam with the muscle-relaxant drugs." Br Med J, 1, p. 336-8
- Ochs HR, Greenblatt DJ, Verburg-Ochs B (1984) "Propranolol interactions with diazepam, lorazepam and alprazolam." Clin Pharmacol Ther, 36, p. 451-5
- Desager JP, Hulhoven R, Harvengt C, Hermann P, Guillet P, Thiercelin JF (1988) "Possible interactions between zolpidem, a new sleep inducer and chlorpromazine, a phenothiazine neuroleptic." Psychopharmacology (Berl), 96, p. 63-6
- Tverskoy M, Fleyshman G, Ezry J, Bradley EL, Jr Kissin I (1989) "Midazolam-morphine sedative interaction in patients." Anesth Analg, 68, p. 282-5
- "Product Information. Iopidine (apraclonidine ophthalmic)." Alcon Laboratories Inc
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- Greb WH, Buscher G, Dierdorf HD, Koster FE, Wolf D, Mellows G (1989) "The effect of liver enzyme inhibition by cimetidine and enzyme induction by phenobarbitone on the pharmacokinetics of paroxetine." Acta Psychiatr Scand, 80 Suppl, p. 95-8
- Markowitz JS, Wells BG, Carson WH (1995) "Interactions between antipsychotic and antihypertensive drugs." Ann Pharmacother, 29, p. 603-9
- (2001) "Product Information. Ultram (tramadol)." McNeil Pharmaceutical
- (2001) "Product Information. Artane (trihexyphenidyl)." Lederle Laboratories
- (2001) "Product Information. Ultiva (remifentanil)." Mylan Institutional (formally Bioniche Pharma USA Inc)
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- Miller LG (1998) "Herbal medicinals: selected clinical considerations focusing on known or potential drug-herb interactions." Arch Intern Med, 158, p. 2200-11
- (2001) "Product Information. Precedex (dexmedetomidine)." Abbott Pharmaceutical
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- Ferslew KE, Hagardorn AN, McCormick WF (1990) "A fatal interaction of methocarbamol and ethanol in an accidental poisoning." J Forensic Sci, 35, p. 477-82
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- (2002) "Product Information. Lexapro (escitalopram)." Forest Pharmaceuticals
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- Cerner Multum, Inc. "Australian Product Information."
- (2012) "Product Information. Fycompa (perampanel)." Eisai Inc
- (2014) "Product Information. Belsomra (suvorexant)." Merck & Co., Inc
- (2015) "Product Information. Rexulti (brexpiprazole)." Otsuka America Pharmaceutical, Inc.
Food/lifestyle interactions
Major food/lifestyle interactions
Major:
sodium oxybate Food/Lifestyle
Applies to: sodium oxybate
Contraindicated
Alcohol may potentiate the central nervous system (CNS)-depressant effects of sodium oxybate, the sodium salt of gamma-hydroxybutyrate (GHB). This may increase the risk of respiratory depression and other serious adverse reactions, including hypotension, profound sedation, syncope, and death. Similar CNS and respiratory depressant effects may occur with other oxybate-containing products. In addition, alcohol may result in more rapid release of sodium oxybate from the extended-release formulation (Lumryz). In an in vitro study with Lumryz, alcohol-induced dose-dumping was demonstrated at 1 hour in the presence of 40% alcohol, and an approximately 60% increase in sodium oxybate release was observed at 2 hours in the presence of 20% alcohol. This dose-dumping finding was specific to Lumryz.
Adjust dosing interval
Food, particularly a high-fat meal, may delay the absorption and decrease the bioavailability of oxybate-containing products. The magnitude of this effect is formulation dependent. Administration of the extended-release sodium oxybate formulation (Lumryz) immediately after a high-fat meal increased the average time to reach peak plasma concentration (Tmax) from 0.5 hours to 1.5 hours and decreased the peak plasma concentration (Cmax) and systemic exposure (AUC) of GHB by 33% and 14%, respectively. With immediate-release sodium oxybate formulations, administration immediately after a high-fat meal increased Tmax from 0.75 hours to 2 hours and decreased Cmax and AUC of GHB by approximately 58% to 59% and 37%, respectively. The combined formulation containing calcium, magnesium, potassium, and sodium oxybates (Xywav) also demonstrated mean reductions in Cmax and AUC of GHB when administered after a high-fat meal, by 33% and 16%, respectively.
Monitor closely
Single-ingredient formulations of sodium oxybate contain significant amounts of sodium. Additional sodium from the diet may increase the total sodium load. This may increase the risk of complications associated with high sodium intake, such as elevated blood pressure, fluid retention, or worsening heart failure, particularly in patients who are sensitive to sodium intake, including those with hypertension, heart failure, or renal impairment.
Management
Concomitant use of oxybate-containing products with alcohol is contraindicated. Oxybate-containing products should be taken on a consistent schedule, at least 2 hours after eating; for twice-nightly regimens, this applies to the first nightly dose. For patients receiving single-ingredient sodium oxybate formulations, consider the total daily sodium intake throughout treatment. Blood pressure should be monitored and dietary sodium restriction considered as clinically appropriate, particularly in patients with hypertension, heart failure, or renal impairment.
References (8)
- (2022) "Product Information. Xyrem (sodium oxybate)." UCB Pharma Ltd
- (2025) "Product Information. Xywav (calcium/magnesium/potassium/sodium oxybates)." Jazz Pharmaceuticals
- (2025) "Product Information. Xyrem (sodium oxybate)." Innomar Strategies Inc
- (2026) "Product Information. Sodium Oxybate (Reach) (sodium oxybate)." Reach Pharmaceuticals Pty Ltd
- (2024) "Product Information. OXIBATO DE SODIO KALCEKS (oxibato de sodio)." AKCIJU SABIEDRIBA KALCEKS
- (2025) "Product Information. Lumryz (sodium oxybate)." Avadel CNS Pharmaceuticals, LLC, v2
- (2025) "Product Information. Xyrem (sodium oxybate)." Jazz Pharmaceuticals, v1
- (2024) "Product Information. Xywav (calcium/magnesium/potassium/sodium oxybates)." Innomar Strategies Inc
Moderate food/lifestyle interactions
Moderate:
dextromethorphan Food/Lifestyle
Applies to: dextromethorphan / triprolidine
Generally avoid
Alcohol may potentiate some of the pharmacologic effects of CNS-active agents. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
Management
Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
References (4)
- Warrington SJ, Ankier SI, Turner P (1986) "Evaluation of possible interactions between ethanol and trazodone or amitriptyline." Neuropsychobiology, 15, p. 31-7
- Gilman AG, eds., Nies AS, Rall TW, Taylor P (1990) "Goodman and Gilman's the Pharmacological Basis of Therapeutics." New York, NY: Pergamon Press Inc.
- (2012) "Product Information. Fycompa (perampanel)." Eisai Inc
- (2015) "Product Information. Rexulti (brexpiprazole)." Otsuka America Pharmaceutical, Inc.
Moderate:
triprolidine Food/Lifestyle
Applies to: dextromethorphan / triprolidine
Generally avoid
Alcohol may potentiate some of the pharmacologic effects of CNS-active agents. Use in combination may result in additive central nervous system depression and/or impairment of judgment, thinking, and psychomotor skills.
Management
Patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
References (4)
- Warrington SJ, Ankier SI, Turner P (1986) "Evaluation of possible interactions between ethanol and trazodone or amitriptyline." Neuropsychobiology, 15, p. 31-7
- Gilman AG, eds., Nies AS, Rall TW, Taylor P (1990) "Goodman and Gilman's the Pharmacological Basis of Therapeutics." New York, NY: Pergamon Press Inc.
- (2012) "Product Information. Fycompa (perampanel)." Eisai Inc
- (2015) "Product Information. Rexulti (brexpiprazole)." Otsuka America Pharmaceutical, Inc.
Disease interactions
23 potential interactions Applies to: 19 conditions, including High Blood Pressure, Depression, Weight Loss, Asthma, and COPD.
Alcoholism
Major:
sodium oxybate
Sodium oxybate has a major potential interaction with Alcoholism.
Sodium oxybate should not be used with alcohol. This drug should be used with caution in patients with history of drug or alcohol abuse. The inappropriate use of this drug alone or in combination with other CNS depressants is associated with CNS adverse reaction including seizures, respiratory depression, decreases in the levels of consciousness, coma and death. Because illicit use and abuse has been reported, physicians should evaluate carefully their patients for history of drug or alcohol abuse and should follow such patients closely, observing them for signs of misuse.
Asthma
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Asthma.
It has been suggested that the anticholinergic effect of antihistamines may reduce the volume and cause thickening of bronchial secretions, resulting in obstruction of respiratory tract. Some manufacturers and clinicians recommend that therapy with antihistamines be administered cautiously in patients with asthma or chronic obstructive pulmonary disease.
Cardiovascular Conditions and Disorders
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Cardiovascular Conditions and Disorders.
Antihistamines may infrequently cause cardiovascular adverse effects related to their anticholinergic and local anesthetic (quinidine-like) activities. Tachycardia, palpitation, ECG changes, arrhythmias, hypotension, and hypertension have been reported. Although these effects are uncommon and usually limited to overdosage situations, the manufacturers and some clinicians recommend that therapy with antihistamines be administered cautiously in patients with cardiovascular disease, hypertension, and/or hyperthyroidism.
COPD
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with COPD.
It has been suggested that the anticholinergic effect of antihistamines may reduce the volume and cause thickening of bronchial secretions, resulting in obstruction of respiratory tract. Some manufacturers and clinicians recommend that therapy with antihistamines be administered cautiously in patients with asthma or chronic obstructive pulmonary disease.
Depression
Major:
sodium oxybate
Sodium oxybate has a major potential interaction with Depression.
A variety of abnormal thinking and behavior changes have been reported to occur in association with the use of most anxiolytics, sedatives and hypnotics. Some of these changes include decreased inhibition, aggressiveness, agitation, and hallucinations. These drugs can cause or exacerbate mental depression and cause suicidal behavior and ideation. Therapy with these drugs should be administered cautiously in patients with a history of depression or other psychiatric disorders. Patients should be monitored for any changes in mood or behavior. It may be prudent to refrain from dispensing large quantities of medication to these patients.
Drug Dependence
Major:
sodium oxybate
Sodium oxybate has a major potential interaction with Drug Dependence.
Sodium oxybate should not be used with alcohol. This drug should be used with caution in patients with history of drug or alcohol abuse. The inappropriate use of this drug alone or in combination with other CNS depressants is associated with CNS adverse reaction including seizures, respiratory depression, decreases in the levels of consciousness, coma and death. Because illicit use and abuse has been reported, physicians should evaluate carefully their patients for history of drug or alcohol abuse and should follow such patients closely, observing them for signs of misuse.
Gastrointestinal Obstruction
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Gastrointestinal Obstruction.
Antihistamines often have anticholinergic activity, to which elderly patients are particularly sensitive. Therapy with antihistamines should be administered cautiously, if at all, in patients with preexisting conditions that are likely to be exacerbated by anticholinergic activity, such as urinary retention or obstruction; angle-closure glaucoma, untreated intraocular hypertension, or uncontrolled primary open-angle glaucoma; and gastrointestinal obstructive disorders. Conventional, first-generation antihistamines such as the ethanolamines (bromodiphenhydramine, carbinoxamine, clemastine, dimenhydrinate, diphenhydramine, doxylamine, phenyltoloxamine) tend to exhibit substantial anticholinergic effects. In contrast, the newer, relatively nonsedating antihistamines (e.g., cetirizine, fexofenadine, loratadine) reportedly have low to minimal anticholinergic activity at normally recommended dosages and may be appropriate alternatives.
Glaucoma/Intraocular Hypertension
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Glaucoma/Intraocular Hypertension.
Antihistamines often have anticholinergic activity, to which elderly patients are particularly sensitive. Therapy with antihistamines should be administered cautiously, if at all, in patients with preexisting conditions that are likely to be exacerbated by anticholinergic activity, such as urinary retention or obstruction; angle-closure glaucoma, untreated intraocular hypertension, or uncontrolled primary open-angle glaucoma; and gastrointestinal obstructive disorders. Conventional, first-generation antihistamines such as the ethanolamines (bromodiphenhydramine, carbinoxamine, clemastine, dimenhydrinate, diphenhydramine, doxylamine, phenyltoloxamine) tend to exhibit substantial anticholinergic effects. In contrast, the newer, relatively nonsedating antihistamines (e.g., cetirizine, fexofenadine, loratadine) reportedly have low to minimal anticholinergic activity at normally recommended dosages and may be appropriate alternatives.
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Glaucoma/Intraocular Hypertension.
Some hypnotic drugs can have an anticholinergic effect and should be used with caution in patients with glaucoma, and trouble urinating due to retention or enlarged prostate.
Heart Disease
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Heart Disease.
Sodium oxybate has a high content of salt, and it should be used with caution in patients sensitive to salt intake such as patients with heart failure, hypertension, or renal impairment.
High Blood Pressure
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with High Blood Pressure.
Sodium oxybate has a high content of salt, and it should be used with caution in patients sensitive to salt intake such as patients with heart failure, hypertension, or renal impairment.
Hypertensive Heart with CHF and Renal Disease
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Hypertensive Heart with CHF and Renal Disease.
Sodium oxybate has a high content of salt, and it should be used with caution in patients sensitive to salt intake such as patients with heart failure, hypertension, or renal impairment.
Hyperthyroidism
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Hyperthyroidism.
Antihistamines may infrequently cause cardiovascular adverse effects related to their anticholinergic and local anesthetic (quinidine-like) activities. Tachycardia, palpitation, ECG changes, arrhythmias, hypotension, and hypertension have been reported. Although these effects are uncommon and usually limited to overdosage situations, the manufacturers and some clinicians recommend that therapy with antihistamines be administered cautiously in patients with cardiovascular disease, hypertension, and/or hyperthyroidism.
Hypotension
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Hypotension.
Antihistamines may infrequently cause cardiovascular adverse effects related to their anticholinergic and local anesthetic (quinidine-like) activities. Tachycardia, palpitation, ECG changes, arrhythmias, hypotension, and hypertension have been reported. Although these effects are uncommon and usually limited to overdosage situations, the manufacturers and some clinicians recommend that therapy with antihistamines be administered cautiously in patients with cardiovascular disease, hypertension, and/or hyperthyroidism.
Liver Disease
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Liver Disease.
Limited pharmacokinetic data are available for the older, first-generation antihistamines. Many appear to be primarily metabolized by the liver, and both parent drugs and metabolites are excreted in the urine. Patients with renal and/or liver disease may be at greater risk for adverse effects from antihistamines due to drug and metabolite accumulation. Therapy with antihistamines should be administered cautiously in such patients. Lower initial dosages may be appropriate.
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Liver Disease.
In general, anxiolytics, sedatives and hypnotics are extensively metabolized by the liver. Their plasma clearance may be decreased and their half-life prolonged in patients with impaired hepatic function. Therapy with these drugs should be administered cautiously in patients with liver disease (some are not recommended in severe liver impairment), and the dosage should be adjusted accordingly. Laboratory testing is recommended prior and during treatment.
Narcolepsy
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Narcolepsy.
The use of sodium oxybate may impair the respiratory drive especially in patients with compromised respiratory function. Sodium oxybate should be used cautiously in patients with sleep apnea and sleep-related breathing disorders as there have been reports of increased central apneas and clinically relevant desaturation. Prescribers should be aware that sleep-related disorders tend to be more prevalent in obese patients, postmenopausal women not receiving hormone replacement therapy and also among patients with narcolepsy.
Renal Dysfunction
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Renal Dysfunction.
Limited pharmacokinetic data are available for the older, first-generation antihistamines. Many appear to be primarily metabolized by the liver, and both parent drugs and metabolites are excreted in the urine. Patients with renal and/or liver disease may be at greater risk for adverse effects from antihistamines due to drug and metabolite accumulation. Therapy with antihistamines should be administered cautiously in such patients. Lower initial dosages may be appropriate.
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Renal Dysfunction.
Sodium oxybate has a high content of salt, and it should be used with caution in patients sensitive to salt intake such as patients with heart failure, hypertension, or renal impairment.
Sleep Apnea
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Sleep Apnea.
The use of sodium oxybate may impair the respiratory drive especially in patients with compromised respiratory function. Sodium oxybate should be used cautiously in patients with sleep apnea and sleep-related breathing disorders as there have been reports of increased central apneas and clinically relevant desaturation. Prescribers should be aware that sleep-related disorders tend to be more prevalent in obese patients, postmenopausal women not receiving hormone replacement therapy and also among patients with narcolepsy.
Urinary Retention
Moderate:
dextromethorphan / triprolidine
The triprolidine in dextromethorphan / triprolidine has a moderate potential interaction with Urinary Retention.
Antihistamines often have anticholinergic activity, to which elderly patients are particularly sensitive. Therapy with antihistamines should be administered cautiously, if at all, in patients with preexisting conditions that are likely to be exacerbated by anticholinergic activity, such as urinary retention or obstruction; angle-closure glaucoma, untreated intraocular hypertension, or uncontrolled primary open-angle glaucoma; and gastrointestinal obstructive disorders. Conventional, first-generation antihistamines such as the ethanolamines (bromodiphenhydramine, carbinoxamine, clemastine, dimenhydrinate, diphenhydramine, doxylamine, phenyltoloxamine) tend to exhibit substantial anticholinergic effects. In contrast, the newer, relatively nonsedating antihistamines (e.g., cetirizine, fexofenadine, loratadine) reportedly have low to minimal anticholinergic activity at normally recommended dosages and may be appropriate alternatives.
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Urinary Retention.
Some hypnotic drugs can have an anticholinergic effect and should be used with caution in patients with glaucoma, and trouble urinating due to retention or enlarged prostate.
Weight Loss
Moderate:
sodium oxybate
Sodium oxybate has a moderate potential interaction with Weight Loss.
The use of sodium oxybate may impair the respiratory drive especially in patients with compromised respiratory function. Sodium oxybate should be used cautiously in patients with sleep apnea and sleep-related breathing disorders as there have been reports of increased central apneas and clinically relevant desaturation. Prescribers should be aware that sleep-related disorders tend to be more prevalent in obese patients, postmenopausal women not receiving hormone replacement therapy and also among patients with narcolepsy.
More resources
dextromethorphan / triprolidine
A total of 443 drugs are known to interact with dextromethorphan / triprolidine.
- Dextromethorphan / triprolidine is in the drug class upper respiratory combinations.
- Dextromethorphan / triprolidine is used to treat Cold Symptoms.
sodium oxybate
A total of 348 drugs are known to interact with sodium oxybate.
- Sodium oxybate is in the drug class miscellaneous anxiolytics, sedatives and hypnotics.
-
Sodium oxybate is used to treat the following conditions:
- Cataplexy
- Fibromyalgia (off-label)
- Idiopathic Hypersomnia
- Narcolepsy
Drug Interaction Classification
| Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
| Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
| Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
| No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.