Adult: For management of anxiety disorders or short-term relief of anxiety symptoms: 400 mg 3 or 4 times daily. Max: 2,400 mg daily. Use the lowest effective dose. Elderly: Use the lowest effective dose. Child: 6-12 years 100-200 mg 2 or 3 times daily. Use the lowest effective dose.
Special Patient Group
Debilitated patients: Use the lowest effective dose.
Contraindications
Hypersensitivity to meprobamate or related compounds (e.g. carisoprodol, carbromal, mebutamate, tybamate). Acute intermittent porphyria.
Special Precautions
Patient with suicidal tendencies or ideation, depression; seizure disorder or history of seizure disorder; history of drug abuse or acute alcoholism; muscle weakness, respiratory disease. Avoid abrupt withdrawal. Debilitated patient. Renal and hepatic impairment. Children and elderly. Pregnancy (avoid use during 1st trimester) and lactation.
Adverse Reactions
Significant: CNS depression; tolerance, physical and psychological dependence (prolonged use); withdrawal symptoms (upon abrupt discontinuation); seizures (particularly in patients with seizure disorder); allergic or idiosyncratic reactions (e.g. erythematous maculopapular rash, urticaria, pruritus), may exacerbate porphyria. Rarely, severe haematologic reactions (e.g. aplastic anaemia, agranulocytosis, thrombocytopenic purpura), severe hypersensitivity reactions (e.g. anaphylaxis, angioedema, bronchospasm, exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, bullous dermatitis). Cardiac disorders: Tachycardia, palpitations, cardiac arrhythmias. Ear and labyrinth disorders: Vertigo. Eye disorders: Visual disturbances. Gastrointestinal disorders: Nausea, vomiting, diarrhoea. General disorders and administration site conditions: Weakness. Investigations: Transient ECG changes; fast EEG activity. Nervous system disorders: Drowsiness, dizziness, headache, paraesthesia, ataxia. Psychiatric disorders: Euphoria, paradoxical excitement. Vascular disorders: Syncope. Potentially Fatal: Hypotensive crisis.
Patient Counseling Information
This drug may cause drowsiness, if affected, do not drive or operate machinery.
Monitoring Parameters
Monitor mental status, potential abuse or overuse, and symptoms of anxiety.
Overdosage
Symptoms: Drowsiness, lethargy, stupor, ataxia, shock, hypotension, respiratory collapse and coma. Management: Symptomatic and supportive treatment. Monitor urine output and avoid overhydration. Induce vomiting in fully conscious patients. Forced diuresis with osmotic diuretics (e.g. mannitol), peritoneal dialysis, or haemodialysis may be used to increase drug elimination. Maintain an adequate airway, employ assisted respiration, and administer vasopressor agents cautiously if necessary. Gastric lavage may be performed in patients in a comatose state, having seizures, or lacking a gag reflex. Consider administering activated charcoal after gastric lavage and/or emesis to adsorb any remaining drug.
Drug Interactions
May result in additive CNS depression with other CNS depressants and psychotropic agents.
Food Interaction
May result in additive CNS depression when used with alcohol.
Lab Interference
May cause false elevation of urinary 17-ketosteroid and 17-ketogenicsteroid concentrations in the Zimmerman reaction and 17-hydroxycorticosteroid concentration in the modified Glenn-Nelson technique.
Action
Description: Mechanism of Action: Meprobamate, a carbamate derivative, is an anxiolytic agent. Its exact mechanism of action is unknown; however, it appears to act at numerous CNS sites, including the thalamus and limbic system, and inhibits multineuronal spinal reflexes. Onset: Sedation: Approx 1 hour. Pharmacokinetics: Absorption: Readily absorbed from the gastrointestinal tract. Time to peak plasma concentration: 1-3 hours. Distribution: Widely distributed in the body. Crosses the placenta and enters breast milk. Plasma protein binding: Approx 20%. Metabolism: Extensively metabolised in the liver into inactive metabolites. Excretion: Via urine (8-20% as unchanged drug); faeces (10% as metabolites). Elimination half-life: Approx 6-17 hours.
Chemical Structure
Meprobamate Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 4064, Meprobamate. https://pubchem.ncbi.nlm.nih.gov/compound/Meprobamate. Accessed July 26, 2024.
N05BC01 - meprobamate ; Belongs to the class of carbamates anxiolytics. Used in the management of anxiety, agitation or tension.
References
Anon. Meprobamate. AHFS Clinical Drug Information [online]. Bethesda, MD. American Society of Health-System Pharmacists, Inc. https://www.ahfscdi.com. Accessed 28/06/2024.Brayfield A, Cadart C (eds). Meprobamate. Martindale: The Complete Drug Reference [online]. London. Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 28/06/2024.Meprobamate Tablet (Alembic Pharmaceuticals Limited). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed. Accessed 28/06/2024.Meprobamate. Gold Standard Drug Database in ClinicalKey [online]. Elsevier Inc. https://www.clinicalkey.com. Accessed 23/07/2024.Meprobamate. UpToDate Lexidrug, Lexi-Drugs Multinational Online. Waltham, MA. UpToDate, Inc. https://online.lexi.com. Accessed 28/06/2024.