Central benzodiazepine receptors interact allosterically with GABA receptors, potentiating the effects of GABA and thereby increasing the inhibition of the ascending reticular activating system. (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. Lower doses of one or both agents may be required. Educate patients about the risks and symptoms of respiratory depression and sedation. Type your tag names separated by a space and hit enter. If the extended-release tapentadol tablets are used concurrently with a benzodiazepine, use an initial tapentadol dose of 50 mg PO every 12 hours. Phentermine; Topiramate: (Moderate) Topiramate has the potential to cause CNS depression as well as other cognitive and/or neuropsychiatric adverse reactions. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking a mixed opiate agonist/antagonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. It appears glucuronide conjugation of lorazepam is increased in the presence of combined hormonal oral contraceptives; the clinical significance of this interaction is not determined. Additive CNS depressant effects are possible when ziprasidone is used concurrently with any CNS depressant. Lorazepam is lipophilic; it is widely distributed and crosses the blood-brain barrier. Patients with renal impairment receiving high doses of intravenous lorazepam may be more likely to develop propylene glycol toxicity. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Carbinoxamine; Dextromethorphan; Pseudoephedrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. 0000062954 00000 n Of note, normal therapeutic lorazepam injectable doses contain very small amounts of propylene glycol, polyethylene glycol, and benzyl alcohol. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking an opiate agonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Educate patients about the risks and symptoms of respiratory depression and sedation. Prescribers should re-assess patients for drowsiness or sleepiness regularly throughout treatment, especially since events may occur well after the start of treatment. Educate patients about the risks and symptoms of respiratory depression and sedation. Usual adult dose range is 2 to 4 mg PO at bedtime as needed; use for more than 4 months has not been evaluated. Davis AT Collection. Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. Brompheniramine; Phenylephrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. It appears glucuronide conjugation of lorazepam is increased in the presence of combined hormonal oral contraceptives; the clinical significance of this interaction is not determined. Chlorpheniramine; Pseudoephedrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Diphenoxylate; Atropine: (Moderate) Concomitant administration of benzodiazepines with CNS-depressant drugs, such as diphenoxylate/difenoxin, can potentiate the CNS effects of either agent. If an opiate agonist is initiated in a patient taking a benzodiazepine, use a lower initial dose of the opiate and titrate to clinical response. Concurrent use may result in additive CNS depression. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. 0000002822 00000 n 0000005452 00000 n Use caution with this combination. Maprotiline may lower the seizure threshold, so when benzodiazepines are used for anticonvulsant effects the patient should be monitored for desired clinical outcomes. Alternatively, 1.5 mg/m2 (Usual Max: 3 mg) IV can be given 45 minutes prior to initiation of chemotherapy. Glecaprevir; Pibrentasvir: (Moderate) Monitor for an increase in lorazepam-related adverse reactions and consider reducing the dose of lorazepam if concomitant use of lorazepam and glecaprevir is necessary. Drugs that can cause CNS depression, if used concomitantly with olanzapine, can increase both the frequency and the intensity of adverse effects such as drowsiness, sedation, dizziness, and orthostatic hypotension. Vallerand, April Hazard., et al. Monitor patients for decreased pressor effect if these agents are administered concomitantly. Skilled care residents: The federal Omnibus Budget Reconciliation Act (OBRA) regulates the use of anxiolytics in long-term care facility (LTCF) residents. If an opiate agonist is initiated in a patient taking a benzodiazepine, use a lower initial dose of the opiate and titrate to clinical response. The combination of benzodiazepines and maprotiline is commonly used clinically and is considered to be safe as long as patients are monitored for excessive adverse effects from either agent. Abrupt discontinuation or rapid dosage reduction of benzodiazepines after continued use may precipitate acute withdrawal reactions, which can be life-threatening. Select Try/Buy and follow instructions to begin your free 30-day trial. Even at the recommended concentrations, precipitation has occurred in some situations. Chlorpheniramine; Hydrocodone: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. LORazepam. Educate patients about the risks and symptoms of respiratory depression and sedation. Hydrocodone: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. [41537], Generic:- Discard opened bottle after 90 days- Protect from light- Store between 36 to 46 degrees FAtivan:- Store at controlled room temperature (between 68 and 77 degrees F)Loreev XR:- Store between 68 to 77 degrees F, excursions permitted 59 to 86 degrees F. Lorazepam is contraindicated in any patient with a known lorazepam or benzodiazepine hypersensitivity. Valproic Acid, Divalproex Sodium: (Moderate) Monitor for an increase in lorazepam-related adverse reactions and consider reducing the dose of lorazepam if concomitant use of lorazepam and valproic acid is necessary. Educate patients about the risks and symptoms of respiratory depression and sedation. Extended-release (ER) capsules: Pharmacokinetics of the extended-release capsules are dose proportional over the dose range of 1 to 3 mg. Steady-state is usually achieved following 5 days of administration. Concurrent use of scopolamine and CNS depressants can adversely increase the risk of CNS depression. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking an opiate agonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Attempt periodic tapering of the medication or provide documentation of medical necessity in accordance with OBRA guidelines. DISCONTINUATION: To discontinue, gradually taper the dose. N')].uJr Dose range: 0.02 to 0.1 mg/kg/dose. Aspirin, ASA; Butalbital; Caffeine: (Moderate) Additive CNS and/or respiratory depression may occur with concurrent use. Brexanolone: (Moderate) Concomitant use of brexanolone with CNS depressants like the benzodiazepines may increase the likelihood or severity of adverse reactions related to sedation and additive CNS depression. Fenfluramine: (Moderate) Monitor for excessive sedation and somnolence during coadministration of fenfluramine and benzodiazepines. Lorazepam injection is contraindicated in patients who are hypersensitive to other ingredients in these products (i.e., propylene glycol or polyethylene glycol). Educate patients about the risks and symptoms of respiratory depression and sedation. Cyproheptadine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. Educate patients about the risks and symptoms of respiratory depression and sedation. Follow with water. Monitor patients for decreased pressor effect if these agents are administered concomitantly. 0 Methyldopa: (Moderate) Methyldopa is associated with sedative effects. Caution should be used when iloperidone is given in combination with other centrally-acting medications including anxiolytics, sedatives, and hypnotics. Additive CNS depression may occur. Hydroxychloroquine: (Moderate) Monitor persons with epilepsy for seizure activity during concomitant lorazepam and hydroxychloroquine use. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking a mixed opiate agonist/antagonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Ethinyl Estradiol: (Minor) Ethinyl estradiol may enhance the metabolism of lorazepam. Tapentadol: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. 0.05 mg/kg PO as a single dose (Max: 4 mg) 45 to 90 minutes prior to procedure. If a benzodiazepine must be used in a patient with a history of falls or fractures, consider reducing use of other CNS-active medications that increase the risk of falls and fractures and implement other strategies to reduce fall risk. Patients should be monitored more closely for hypotension if nitroglycerin is used concurrently with benzodiazepines. Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. (Moderate) Drowsiness has been reported during administration of carbetapentane. Dose range: 0.025 to 0.1 mg/kg/dose. Avoid opiate cough medications in patients taking benzodiazepines. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Use caution with this combination. Dextromethorphan; Guaifenesin; Phenylephrine: (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. Monitor patients for decreased pressor effect if these agents are administered concomitantly. Limit the use of mixed opiate agonists/antagonists with benzodiazepines to only patients for whom alternative treatment options are inadequate. Use caution with this combination. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. Levonorgestrel; Ethinyl Estradiol; Ferrous Bisglycinate: (Minor) Ethinyl estradiol may enhance the metabolism of lorazepam. Butalbital; Acetaminophen: (Moderate) Additive CNS and/or respiratory depression may occur with concurrent use. Fentanyl: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. Enter your username below and we'll send you an email explaining how to change your password. Additionally, avoid coadministration with other CNS depressants, especially opioids, when possible, as this significantly increases the risk for profound sedation, respiratory depression, low blood pressure, and death. A published sedation protocol for pediatric mechanically ventilated patients recommends an initial infusion rate of 0.01 mg/kg/hour IV. Educate patients about the risks and symptoms of respiratory depression and sedation. (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. T1 - LORazepam Meperidine; Promethazine: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. Diphenhydramine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. Caution should be used when vigabatrin is given in combination with benzodiazepines. Avoid opiate cough medications in patients taking benzodiazepines. Specifically, sodium oxybate use is contraindicated in patients being treated with sedative hypnotic drugs. coma / Early / 0.1-1.2seizures / Delayed / 0-1.0apnea / Delayed / 1.0muscle paralysis / Delayed / Incidence not knownsuicidal ideation / Delayed / Incidence not knownneuroleptic malignant syndrome-like symptoms / Delayed / Incidence not knownpulmonary edema / Early / Incidence not knownrespiratory arrest / Rapid / Incidence not knownpulmonary hypertension / Delayed / Incidence not knownpneumothorax / Early / Incidence not knownGI bleeding / Delayed / Incidence not knowntissue necrosis / Early / Incidence not knownrenal tubular necrosis / Delayed / Incidence not knownSIADH / Delayed / Incidence not knownlactic acidosis / Delayed / Incidence not knownanaphylactoid reactions / Rapid / Incidence not knownpericardial effusion / Delayed / Incidence not knownheart failure / Delayed / Incidence not knowncardiac arrest / Early / Incidence not knownbradycardia / Rapid / Incidence not knownAV block / Early / Incidence not knownhearing loss / Delayed / Incidence not knownpancytopenia / Delayed / Incidence not knownagranulocytosis / Delayed / Incidence not knowncoagulopathy / Delayed / Incidence not knownneonatal respiratory depression / Rapid / Incidence not knownneonatal abstinence syndrome / Early / Incidence not known, erythema / Early / 2.0-2.4hypotension / Rapid / 0.1-2.4confusion / Early / 0.1-1.3depression / Delayed / 1.3-1.3delirium / Early / 1.3-1.3hypoventilation / Rapid / 0.1-1.2ataxia / Delayed / 0.1-1.0hallucinations / Early / 0.1-1.0elevated hepatic enzymes / Delayed / 0-1.0cystitis / Delayed / 0-1.0metabolic acidosis / Delayed / 0-1.0dysarthria / Delayed / Incidence not knowneuphoria / Early / Incidence not knownamnesia / Delayed / Incidence not knownmemory impairment / Delayed / Incidence not knownpsychosis / Early / Incidence not knownhostility / Early / Incidence not knownmania / Early / Incidence not knownhyperreflexia / Delayed / Incidence not knownrespiratory depression / Rapid / Incidence not knownhypoxia / Early / Incidence not knownmyoclonia / Delayed / Incidence not knownjaundice / Delayed / Incidence not knownhyperbilirubinemia / Delayed / Incidence not knownconstipation / Delayed / Incidence not knownhyponatremia / Delayed / Incidence not knownurinary incontinence / Early / Incidence not knownimpotence (erectile dysfunction) / Delayed / Incidence not knownsinus tachycardia / Rapid / Incidence not knownhypertension / Early / Incidence not knownblurred vision / Early / Incidence not knownleukopenia / Delayed / Incidence not knownthrombocytopenia / Delayed / Incidence not knowntolerance / Delayed / Incidence not knownpsychological dependence / Delayed / Incidence not knownwithdrawal / Early / Incidence not knownphysiological dependence / Delayed / Incidence not known, injection site reaction / Rapid / 0.5-17.0drowsiness / Early / 1.5-15.9dizziness / Early / 6.9-6.9weakness / Early / 4.2-4.2restlessness / Early / 1.3-1.3headache / Early / 0.1-1.2asthenia / Delayed / 0.1-1.0agitation / Early / 0.1-1.0tremor / Early / 0.1-1.0hyperventilation / Early / 0.1-1.0nausea / Early / 0-1.0hypersalivation / Early / 0.1-1.0vomiting / Early / 0-1.0infection / Delayed / 0-1.0chills / Rapid / 0-1.0vertigo / Early / Incidence not knownfatigue / Early / Incidence not knowninsomnia / Early / Incidence not knownanxiety / Delayed / Incidence not knownnightmares / Early / Incidence not knownirritability / Delayed / Incidence not knownhyperactivity / Early / Incidence not knowndiarrhea / Early / Incidence not knownhypothermia / Delayed / Incidence not knownlibido decrease / Delayed / Incidence not knownorgasm dysfunction / Delayed / Incidence not knownrash / Early / Incidence not knownalopecia / Delayed / Incidence not knowndiplopia / Early / Incidence not known. Use caution with this combination. Prasterone, Dehydroepiandrosterone, DHEA (FDA-approved): (Major) Prasterone, dehydroepiandrosterone, DHEA may inhibit the metabolism of benzodiazepines (e.g., alprazolam, estazolam, midazolam) which undergo CYP3A4-mediated metabolism. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking an opiate agonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Patients who are taking barbiturates or other sedative/hypnotic drugs should avoid concomitant administration of valerian. In one study of elderly volunteers, half of the patients received DHEA 200 mg/day PO for 2 weeks, followed by a single dose of triazolam 0.25 mg. Triazolam clearance was reduced by close to 30% in the DHEA-pretreated patients vs. the control group; however, the effect of DHEA on CYP3A4 metabolism appeared to vary widely among subjects. Caution should be used when asenapine is given in combination with other centrally-acting medications including anxiolytics, sedatives, and hypnotics (including barbiturates), buprenorphine, buprenorphine; naloxone, butorphanol, dronabinol, THC, nabilone, nalbuphine, opiate agonists, pentazocine, acetaminophen; pentazocine, aspirin, ASA; pentazocine, and pentazocine; naloxone. Papaverine: (Moderate) Concurrent use of papaverine with potent CNS depressants such as benzodiazepines could lead to enhanced sedation. Melatonin: (Major) Use caution when combining melatonin with the benzodiazepines; when the benzodiazepine is used for sleep, co-use of melatonin should be avoided. Concurrent use may result in additive CNS depression. Send the page "" AU - Vallerand,April Hazard, Caution should be exercised during simultaneous use of these agents due to potential excessive CNS effects or additive hypotension. Skilled care residents: The federal Omnibus Budget Reconciliation Act (OBRA) regulates the use of anxiolytics in long-term care facility (LTCF) residents. Concurrent use may result in additive CNS depression. Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. xb```f``Z @1X T0fk?oZC@jKKU]r3(!( 6A-+dXc If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking an opiate agonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Patients should not abruptly stop taking their prescribed psychoactive medications. Titrate the dose of remimazolam to the desired clinical response and continuously monitor sedated patients for hypotension, airway obstruction, hypoventilation, apnea, and oxygen desaturation. (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. Acetaminophen; Chlorpheniramine; Dextromethorphan; Phenylephrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Monitor patients for decreased pressor effect if these agents are administered concomitantly. Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. Benzodiazepine dependence can occur after administration of therapeutic doses for as few as 1 to 2 weeks and withdrawal symptoms may be seen after the discontinuation of therapy. Pimozide: (Moderate) Due to the effects of pimozide on cognition, it should be used cautiously with other CNS depressants including benzodiazepines. If a benzodiazepine is required during pregnancy, avoid first trimester administration if possible, consider short-acting agents, limit treatment to the lowest effective dosage and duration, and discontinue the drug well before delivery. 0000063370 00000 n Acetaminophen; Aspirin; Diphenhydramine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. Educate patients about the risks and symptoms of respiratory depression and sedation. Codeine; Phenylephrine; Promethazine: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. If a benzodiazepine is prescribed for an indication other than epilepsy in a patient taking an opiate agonist, use a lower initial dose of the benzodiazepine and titrate to clinical response. Vallerand, A. H., Sanoski, C. A., & Quiring, C. (2023). Concurrent use may result in additive CNS depression. Colesevelam: (Moderate) Colesevelam may decrease the absorption of anticonvulsants. Administration of the extended-release capsules by sprinkling the contents in 15 mL of applesauce did not significantly affect overall drug exposure or Tmax. Not a Member? Tizanidine: (Moderate) Concurrent use of tizanidine and CNS depressants like the benzodiazepines can cause additive CNS depression. Methadone: (Major) Concurrent use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. Dose range: 0.02 to 0.09 mg/kg/dose. Avoid prescribing opiate cough medications in patients taking benzodiazepines. Use caution with this combination. As a thank-you for using our site, here's a discounted rate for renewal or upgrade. If an opiate agonist is initiated in a patient taking a benzodiazepine, use a lower initial dose of the opiate and titrate to clinical response. Lorazepam should be used with caution in patients with a neuromuscular disease, such as myasthenia gravis; these patients may be more sensitive to the CNS and respiratory effects of the benzodiazepines. For acetaminophen; oxycodone extended-release tablets, start with 1 tablet PO every 12 hours, and for other oxycodone products, use an initial dose of oxycodone at 1/3 to 1/2 the usual dosage. Both lorazepam oral solution concentrated and injectable lorazepam solutions contain propylene glycol and polyethylene glycol. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. Coadministration of lorazepam with probenecid may cause a more rapid onset or prolonged effect of lorazepam due to increased half-life and decreased total clearance. Attempt periodic tapering of the medication or provide documentation of medical necessity in accordance with OBRA guidelines. Reduce injectable buprenorphine dose by 1/2, and for the buprenorphine transdermal patch, start therapy with the 5 mcg/hour patch. Educate patients about the risks and symptoms of respiratory depression and sedation. Lorazepam is an UGT substrate and valproic acid is an UGT inhibitor. US-based MDs, DOs, NPs and PAs in full-time patient practice can register for free on PDR.net. Reserve concomitant use of these drugs for patients in whom alternative treatment options are inadequate. For extended-release tablets, start with morphine 15 mg PO every 12 hours, and for extended-release capsules, start with 30 mg PO every 24 hours or less. Daviss Drug Guide for Nurses App + Web from F.A. Pharmacokinetic interactions have been observed with the use of zolpidem. When a medication is used to induce sleep, treat a sleep disorder, manage behavior, stabilize mood, or treat a psychiatric disorder, the facility should attempt periodic tapering of the medication or provide documentation of medical necessity in accordance with OBRA guidelines. Even that low dose is difficult to get off of. Carbinoxamine; Pseudoephedrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Observed with the use of mixed opiate agonists/antagonists with benzodiazepines to only patients for decreased pressor effect if these are. Jkku ] r3 ( prolonged effect of phenylephrine may be decreased in patients treated. Oxybate use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired effect... A published sedation protocol for pediatric mechanically ventilated patients recommends an initial tapentadol dose of mg. 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