BOXED WARNING Concomitant use with opioids can cause profound sedation, respiratory depression, coma and death; benzodiazepines carry risks of abuse, misuse and addiction, and of physical dependence with life-threatening withdrawal on abrupt discontinuation or rapid dose reduction — taper gradually.
FDA dosing
Population
Start
Target
Max
Mild to moderate anxiety disorder / symptoms of anxiety
Adults
5 mg TID–QID
5–10 mg TID–QID
Not stated
Severe anxiety disorder / symptoms of anxiety
Adults
20 mg TID–QID
20–25 mg TID–QID
Not stated
Anxiety
Geriatric patients, or debilitating disease
5 mg BID
5 mg BID–QID
Not stated
Preoperative apprehension and anxiety
Adults
5 mg PO TID–QID on days preceding surgery
5–10 mg PO TID–QID on days preceding surgery; if used as preoperative medication, 50–100 mg IM 1 hour before surgery
Not stated
Withdrawal symptoms of acute alcoholism
Adults
50–100 mg PO initially, repeated as needed until agitation is controlled (parenteral form usually used initially)
Reduce to maintenance level once agitation is controlled
300 mg/day
Anxiety
Children ≥6 y
5 mg BID
5 mg BID–QID; may be increased in some patients to 10 mg BID–TID
Not stated
Renal Undefined
Hepatic Undefined
Acute alcohol withdrawal: repeat the oral dose as needed until agitation is controlled, up to 300 mg/day, then reduce to maintenance.
Instructions
Individualize the dose to the diagnosis and patient response; initiate at the lowest dose and increase as required.
Discontinue by gradual taper to reduce the risk of withdrawal reactions. If withdrawal reactions develop, pause the taper or return to the previous dose level, then decrease more slowly.
Not recommended in children under 6 years of age (limited clinical experience).
With protracted treatment, periodic blood counts and liver function tests are advisable.
Cautions
Concomitant opioid use — profound sedation, respiratory depression, coma and death; reserve for patients without adequate alternatives, limit dose and duration, and monitor for sedation and respiratory depression.
Abuse, misuse and addiction, which can lead to overdose or death — assess risk before prescribing and throughout treatment; risk is increased with concomitant alcohol, other medications or illicit substances.
Physical dependence and withdrawal — risk rises with longer duration and higher daily dose; abrupt discontinuation or rapid reduction may precipitate life-threatening acute withdrawal.
Drowsiness, ataxia and confusion, particularly in elderly and debilitated patients — usually avoidable with dose adjustment but reported even at lower doses.
Blood dyscrasias (including agranulocytosis), jaundice and hepatic dysfunction reported — monitor CBC and liver function with protracted therapy.
Adverse reactions
Drowsiness, ataxia, confusion — especially in elderly and debilitated patients.
Syncope (a few instances).
Skin eruptions, edema, minor menstrual irregularities, nausea, constipation.
Extrapyramidal symptoms; increased or decreased libido.
EEG changes (low-voltage fast activity) during and after treatment.
Blood dyscrasias including agranulocytosis; jaundice and hepatic dysfunction (occasional).
“Liberty Cooler dies of pox” “dies of pox” → just a sound-alike for diazepox; unrelated to medication properties approved for alcohol withdrawal hot pink → benzo theme