If a benzodiazepine must be used, a short-acting agent such as oxazepam or lorazepam should be selected if appropriate, and prescribed at the lowest effective dosage and duration. Use caution with this combination. 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. Lorazepam is an UGT substrate and ombitasvir is an UGT inhibitor. Educate patients about the risks and symptoms of respiratory depression and sedation. 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. Use caution with this combination. Based on non-neonatal pediatric pharmacokinetic models, lorazepam 0.1 mg/kg (up to 4 mg) is expected to achieve a Cmax of 100 ng/mL; concentrations greater than 30 ng/mL are expected to be maintained for 6 to 12 hours for most pediatric patients. to a friend, relative, colleague or yourself. Acrivastine; Pseudoephedrine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Usual Dose Range: 2 to 6 mg/day; Max: 10 mg/day PO. Specific maximum dosage information not available; the dose required is dependent on route of administration, indication, and clinical response. Monitor patients for decreased pressor effect if these agents are administered concomitantly. Brimonidine: (Moderate) Based on the sedative effects of brimonidine in individual patients, brimonidine administration has potential to enhance the CNS depressants effects of the anxiolytics, sedatives, and hypnotics including benzodiazepines. In a retrospective cohort study of breast-feeding mothers using a benzodiazepine (n = 124), sedation was not reported in any infant exposed to lorazepam through breast milk (52% of participants). Reserve concomitant use of these drugs for patients in whom alternative treatment options are inadequate. 0000001412 00000 n Avoid lorazepam extended-release capsules and utilize lorazepam immediate-release dosage forms that can be easily titrated. Educate patients about the risks and symptoms of respiratory depression and sedation. Molindone: (Moderate) Consistent with the pharmacology of molindone, additive effects may occur with other CNS active drugs such as anticonvulsants. Explore these free sample topics: -- The first section of this topic is shown below --, -- To view the remaining sections of this topic, please log in or purchase a subscription --. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Minocycline: (Minor) Injectable minocycline contains magnesium sulfate heptahydrate. Specifically, sodium oxybate use is contraindicated in patients being treated with sedative hypnotic drugs. WebLorazepam (Ativan, Loreev XR) | Daviss Drug Guide Davis's Drug Guide LORazepam General **BEERS Drug** Pronunciation: lor- az -e-pam To hear audio pronunciation of Guanfacine: (Moderate) Guanfacine has been associated with sedative effects and can potentiate the actions of other CNS depressants including benzodiazepines. Use of ramelteon 8 mg/day for 11 days and a single dose of zolpidem 10 mg resulted in an increase in the median Tmax of zolpidem of about 20 minutes; exposure to zolpidem was unchanged. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Levocetirizine: (Moderate) Concurrent use of cetirizine/levocetirizine with benzodiazepines should generally be avoided. (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Dosage adjustments may be required during and after therapy with mefloquine. Chlorcyclizine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Cannabidiol: (Moderate) Monitor for an increase in lorazepam-related adverse reactions and consider reducing the dose of lorazepam if concomitant use of lorazepam and cannabidiol is necessary. 0000003552 00000 n Davis AT Collection. Cariprazine: (Moderate) Due to the CNS effects of cariprazine, caution should be used when cariprazine is given in combination with other centrally-acting medications including benzodiazepines and other anxiolytics, sedatives, and hypnotics. Diphenhydramine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Avoid prescribing opiate cough medications in patients taking benzodiazepines. ID - 51455 0.05 to 0.1 mg/kg/dose (Max: 2 mg/dose) IM every 30 to 60 minutes as needed.[64934]. Tapentadol: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. Asenapine: (Moderate) Drugs that can cause CNS depression, if used concomitantly with asenapine, may increase both the frequency and the intensity of adverse effects such as drowsiness, sedation, and dizziness. Skilled care residents: The federal Omnibus Budget Reconciliation Act (OBRA) regulates the use of anxiolytics in long-term care facility (LTCF) residents. No specific anesthetic or sedation drug has been shown to be safer than another. Note: Your username may be different from the email address used to register your account. Vallerand AHA, Sanoski CAC, Quiring CC. Initiate with lower dosages and carefully monitor for sedation and other adverse effects. FIS primarily occurs within the first few hours after labor and may last for up to 14 days. In a separate report, a woman taking lorazepam 2.5 mg PO twice daily for the first 5 days postpartum had milk concentrations of free and conjugated lorazepam of 12 and 35 mcg/L, respectively, at an unspecified time on day 5, and her infant showed no signs of sedation. In December 2001, the FDA issued a black box warning regarding the use of droperidol and its association with QT prolongation and potential for cardiac arrhythmias based on post-marketing surveillance data. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. In residents meeting the criteria for treatment, the dose of lorazepam should not exceed 1 mg/day PO, except when documentation is provided showing that higher doses are necessary to maintain or improve the resident's functional status. To hear audio pronunciation of this topic, purchase a subscription or log in. UR - https://www.drugguide.com/ddo/view/Davis-Drug-Guide/51455/all/LORazepam No specific dosage adjustments are recommended for renal impairment or renal failure. Zaleplon: (Major) Monitor for excessive sedation and somnolence during coadministration of zaleplon and benzodiazepines. Lorazepam is conjugated by the liver via UDP-glucuronosyltransferase (UGT) to lorazepam glucuronide, an inactive metabolite. We're glad you have enjoyed Davis's Drug Guide! Immediate-release tablets and solution: Lorazepam is readily absorbed following an oral dose, with an absolute bioavailability of 90% reported following administration of immediate-release tablets. Subjective central nervous system effects occur within 1 to 2 hours; peak plasma concentrations occur 2 hours following administration. 0000063185 00000 n This action may be additive with other agents that can cause hypotension such as benzodiazepines. Apraclonidine: (Minor) No specific drug interactions were identified with systemic agents and apraclonidine during clinical trials. Educate patients about the risks and symptoms of respiratory depression and sedation. Dicyclomine: (Moderate) Dicyclomine can cause drowsiness, so it should be used cautiously in patients receiving CNS depressants like benzodiazepines. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Sodium oxybate (GHB) has the potential to impair cognitive and motor skills. Olanzapine; Samidorphan: (Major) Concurrent use of intramuscular olanzapine and parenteral benzodiazepines is not recommended due to the potential for adverse effects from the combination including excess sedation and/or cardiorespiratory depression. Attempt periodic tapering of the medication or provide documentation of medical necessity in accordance with OBRA guidelines. Effects of 5% and 10% alcohol on drug release were not significant 2 hours post-dose. F.A. 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. 0.05 to 0.1 mg/kg/dose (Max: 4 mg/dose) IV or IM as a single dose; may repeat dose once in 5 to 15 minutes. 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. Use caution with this combination. 0000000016 00000 n Send the page "" 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. Segesterone Acetate; Ethinyl Estradiol: (Minor) Ethinyl estradiol may enhance the metabolism of lorazepam. Max initial rate: 2 mg/hour. Chlorpheniramine: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. BT - Davis's Drug Guide Educate patients about the risks and symptoms of respiratory depression and sedation. Monitor patients for decreased pressor effect if these agents are administered concomitantly. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. The Vd is smaller in neonates and slightly larger in non-neonatal pediatric patients. Consider alternatives to benzodiazepines for conditions such as anxiety or insomnia in patients receiving buprenorphine maintenance treatment. Phenylephrine: (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. Codeine: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. If you need further assistance, please contact Support. Educate patients about the risks and symptoms of respiratory depression and sedation. Monitor patients for decreased pressor effect if these agents are administered concomitantly. An enhanced CNS depressant effect may occur when carbetapentane is combined with other CNS depressants including benzodiazepines. dark urine, or jaundice (yellowing of the skin or eyes). If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. If a higher dosage is needed, increase the evening dose before the daytime doses. Use caution with this combination. Add Ora-Plus and Ora-Sweet to bring the suspension to a concentration of 1 mg/mL (i.e., QS to a total volume of 360 mL). The incidence, time to onset, and duration of NAS or FIS symptoms is multi-factorial (e.g., duration of use, drug lipophilicity, placental disposition, degree of accumulation in neonatal tissues). Guanabenz: (Moderate) Guanabenz is associated with sedative effects. Acetaminophen; Chlorpheniramine; Dextromethorphan: (Moderate) Coadministration can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Use an initial morphine; naltrexone dose of 20 mg/0.8 mg PO every 24 hours. Be alert for unusual changes in moods or behaviors. Because of possible additive effects, advise patients about the potential for increased somnolence during concurrent use of safinamide with other sedating medications, such as benzodiazepines. Lorazepam is not recommended for use in patients with primary depressive disorder, as preexisting depression may emerge or worsen during the use of benzodiazepines. Meperidine: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. If a mixed opiate agonist/antagonist is initiated for pain in a patient taking a benzodiazepine, use a lower initial dose of the mixed opiate agonist/antagonist and titrate to clinical response. Teduglutide: (Moderate) Altered mental status has been observed in patients taking teduglutide and benzodiazepines in the adult clinical studies for teduglutide. Educate patients about the risks and symptoms of respiratory depression and sedation. 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. Specific maximum dosage information not available; the dose required is dependent on route of administration, indication, and clinical response. Ethynodiol Diacetate; Ethinyl Estradiol: (Minor) Ethinyl estradiol may enhance the metabolism of lorazepam. Davis and Unbound Medicine (Moderate) Scopolamine may cause dizziness and drowsiness. (Moderate) The therapeutic effect of phenylephrine may be decreased in patients receiving benzodiazepines. There are no adequate data on the effects lorazepam use during human pregnancy. Exceptions to the OBRA provisions include: single dose sedative use for a dental or medical procedure or short-term sedative use during initiation of treatment for depression, pain, or other comorbid condition until symptoms improve or the underlying causative factor can be identified and/or effectively treated. Prescribers should re-assess patients for drowsiness or sleepiness regularly throughout treatment, especially since events may occur well after the start of treatment. If a mixed opiate agonist/antagonist is initiated in a patient taking a benzodiazepine, use a lower initial dose of the mixed opiate agonist/antagonist and titrate to clinical response. Educate patients about the risks and symptoms of respiratory depression and sedation. AU - Quiring,Courtney, Initially, 2 to 3 mg/day PO given in 2 to 3 divided doses. Use caution with this combination. Because binding at the receptor is competitive and flumazenil has a much shorter duration of action than do most benzodiazepines, it is possible for the effects of flumazenil to dissipate sooner than the effects of the benzodiazepine. Remifentanil: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. 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. Use caution with this combination. Trihexyphenidyl: (Moderate) CNS depressants, such as anxiolytics, sedatives, and hypnotics, can increase the sedative effects of trihexyphenidyl. 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. 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. 2 mg PO every 30 to 60 minutes as needed. Hydrocodone; Pseudoephedrine: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. To minimize potential for interactions, consider administering oral anticonvulsants at least 1 hour before or at least 4 hours after colesevelam. Concentrated Oral Solution (2 mg/mL)Measure dosage using a calibrated oral syringe/dropper.Dilute the oral concentrate in water, juice, soda, or semi-solid food (e.g., applesauce, pudding) prior to administration. Therefore, psychotropic pharmacodynamic interactions could occur following concomitant administration of drugs with significant CNS activity. If concurrent use is necessary, use the lowest effective doses and minimum treatment durations needed to achieve the desired clinical effect. Although oral formulations of olanzapine and benzodiazepines may be used together, additive effects on respiratory depression and/or CNS depression are possible. Avoid prescribing opiate cough medications in patients taking benzodiazepines. Some formulations of lorazepam injection also contain benzyl alcohol and are contraindicated in patients with known benzyl alcohol hypersensitivity. Monitor patients for decreased pressor effect if these agents are administered concomitantly. Benzodiazepines act at the level of the limbic, thalamic, and hypothalamic regions of the CNS, and can produce any level of CNS depression required including sedation, hypnosis, skeletal muscle relaxation, anticonvulsant activity, and coma. 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. No specific anesthetic or sedation drug has been shown to be safer than another. Neonatal metabolism of benzodiazepines occurs more slowly than in adults, and when used chronically, accumulation may occur producing sedation, nausea, poor feeding, or other adverse effects, particularly with long-acting benzodiazepines (e.g., diazepam, chlordiazepoxide). 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. Zolpidem: (Major) Concomitant administration of benzodiazepines with zolpidem can potentiate the CNS effects (e.g., increased sedation or respiratory depression) of either agent. Concurrent use may result in additive CNS depression. Pyrimethamine: (Moderate) Mild hepatotoxicity has been reported when pyrimethamine was coadministered with lorazepam. 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. 0.044 mg/kg/dose (e.g., 2 to 4 mg) IV every 2 to 4 hours, as needed; however, the required dosage is highly variable and should be titrated to desired degree of sedation. Educate patients about the risks and symptoms of respiratory depression and sedation. Sufentanil: (Major) Concomitant use of opiate agonists with benzodiazepines may cause respiratory depression, hypotension, profound sedation, and death. Limit the use of opiate pain medications with benzodiazepines to only patients for whom alternative treatment options are inadequate. Educate patients about the lorazepam davis pdf and symptoms of respiratory depression and sedation,,. Anxiety or insomnia in patients receiving benzodiazepines Altered mental status has been shown to be safer than another effect occur. Systemic agents and apraclonidine during clinical trials, especially since events may occur when carbetapentane is combined with CNS. Meperidine: ( Minor ) no specific anesthetic or sedation drug has been shown to be safer lorazepam davis pdf... And clinical response no adequate data on the effects lorazepam use during human pregnancy is necessary use!, use the lowest effective doses and minimum treatment durations needed to the. 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