Full Generic Medicine Info
Dosage/Direction for Use

Adult: For short-term treatment: 1-2 mg at bedtime.
Elderly: Initially, 0.5-1 mg at bedtime.

Special Populations: Small or debilitated patients: Initially, 0.5-1 mg at bedtime.
May be taken with or without food.
Pregnancy. Concomitant use w/ ketoconazole and itraconazole.
Special Precautions
Avoid abrupt withdrawal. Hepatic and renal impairment. Elderly, small or debilitated patients. Lactation. Patient Counselling May impair ability to drive or operate machinery. Monitoring Parameters Monitor resp and CV status; CBC and urinalysis periodically during prolonged use.
Adverse Reactions
Somnolence, hypokinesia, dizziness, abnormal coordination; allergic reaction, chills, fever, neck pain, upper extremity pain; flushing palpitation; constipation, dry mouth, decreased/increased appetite, flatulence, gastritis, vomiting; thirst; arthritis, muscle spasm, myalgia; anxiety, agitation, amnesia, apathy, emotional lability, euphoria, hostility, paraesthesia, seizure, sleep disorder, stupor, twitch; asthma, cough, dyspnoea, rhinitis, sinusitis; rash, sweating, urticaria; abnormal vision, ear pain; eye irritation, pain, swelling; perverse taste, photophobia, tinnitus; frequent urination, menstrual cramps, urinary hesitancy/urgency, vag discharge/itching. Rarely, jaw pain, oedema, swollen breast; arrhythmia, syncope; enterocolitis, melaena, mouth ulceration; thyroid nodule; leucopenia, swollen lymph nodes, purpura; increased SGOT, wt gain/loss; arthralgia; ataxia, circumoral paraesthesia, decreased libido and reflexes, hallucinations, neuritis, tremor, nystagmus; epistaxis, hyperventilation, laryngitis; acne, dry skin; decreased hearing, scotomata, diplopia; haematuria, nocturia, oliguria, penile discharge, urinary incontinence.
Potentially Fatal: Anaphylaxis.
Symptoms: Somnolence, resp depression, confusion, impaired coordination, slurred speech, and ultimately, coma. Management: Supportive treatment. Gastric evacuation, either by the induction of emesis, lavage, or both, should be performed immediately. Maintain adequate ventilation. Admin IV fluids to maintain BP and encourage diuresis.
Drug Interactions
Increased plasma concentration w/ CYP3A inhibitors (e.g. nefazodone, fluvoxamine, erythromycin). Decreased plasma concentration w/ CYP3A inducers (e.g. carbamazepine, phenytoin, rifampicin, barbiturates). Additive effect w/ other CNS depressant drugs.
Potentially Fatal: Significantly increased plasma concentration w/ ketoconazole and itraconazole.
Food Interaction
Alcohol may enhance the CNS effect of estazolam. Serum levels and/or toxicity may be increased by grapefruit juice.
Estazolam binds to stereospecific benzodiazepine receptors on the postsynaptic GABA neuron at several sites w/in the CNS, including the limbic system, reticular formation. Enhancement of the inhibitory effect of GABA on neuronal excitability results by increased neuronal membrane permeability to Cl ions, which results in hyperpolarisation (a less excitable state) and stabilisation. Benzodiazepine receptors and effects appear to be linked to the GABA-A receptors.
Absorption: Rapidly and well absorbed from the GI tract. Time to peak plasma concentration: Approx 0.5-1.6 hr after a single 2 mg dose; 1-3 hr after a single 4 mg dose.
Distribution: Widely distributed into most body tissues and fluids. Crosses the blood-brain barrier. Plasma protein-binding: 93%.
Metabolism: Extensively hepatic.
Excretion: Via urine (87% as inactive metabolites and <5% as unchanged drug) and faeces (4% as inactive metabolites).
Oral: Store below 30°C.
CIMS Class
Hypnotics & Sedatives
ATC Classification
N05CD04 - estazolam ; Belongs to the class of benzodiazepine derivatives. Used as hypnotics and sedatives.
Disclaimer: This information is independently developed by CIMS based on estazolam from various references and is provided for your reference only. Therapeutic uses, prescribing information and product availability may vary between countries. Please refer to CIMS Product Monographs for specific and locally approved prescribing information. Although great effort has been made to ensure content accuracy, CIMS shall not be held responsible or liable for any claims or damages arising from the use or misuse of the information contained herein, its contents or omissions, or otherwise. Copyright © 2022 CIMS. All rights reserved. Powered by
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