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MIDAZOLAM

brandsClassMIDAZOLAM commonly prescribed forHow MIDAZOLAM worksHow long until MIDAZOLAM worksNotable Side EffectsLife Threatening Side Effectsweight gainsedationWhat to do about MIDAZOLAM side effectsusual dosage rangeDosage Formslong term usehabit formingRenal ImpairmentHepatic ImpairmentCardiac ImpairmentElderlyChildren and AdolescentsPregnancyBreast Feeding

THERAPEUTICS

brands

  • Medistat

Class

  • Neuroscience-based Nomenclature: GABA positive allosteric modulator (GABA-PAM)
  • Benzodiazepine (hypnotic)

MIDAZOLAM commonly prescribed for

(Bold for FDA approved)

• Sedation in pediatric patients
• Sedation (adjunct to anesthesia)
• Preoperative anxiolytic
• Drug-induced amnesia

• Catatonia

How MIDAZOLAM works

• Binds to benzodiazepine receptors at the GABA-A ligand-gated chloride channel complex

• Enhances the inhibitory effects of GABA

• Boosts chloride conductance through GABA-regulated channels

• Inhibitory actions in sleep centers may provide sedative hypnotic effects

How long until MIDAZOLAM works

• Intravenous injection: onset 3–5 minutes

• Intramuscular injection: onset 15 minutes, peak 30–60 minutes

SIDE EFFECTS

Notable Side Effects

• Oversedation, impaired recall, agitation, involuntary movements, headache

• Nausea, vomiting

• Hiccups, fluctuation in vital signs, irritation/ pain at site of injection

• Hypotension

Life Threatening Side Effects

• Respiratory depression, apnea, respiratory arrest

• Cardiac arrest

weight gain

unusual

unusual

sedation

common

common

What to do about MIDAZOLAM side effects

• Wait

• Switch to another agent

• Administer flumazenil if side effects are severe or life-threatening

DOSING AND USE

usual dosage range

• Intravenous (adults): 1–2.5 mg

• Liquid (age 16 and under): 0.25–1.0 mg/kg

Dosage Forms

• Syrup 2 mg/mL

• Nasal 5 mg/spray

• Intravenous 1 mg/mL, 5 mg/mL

• Intramuscular solution 50 mg/10 mL (5 mg/mL)

long term use

• Not generally intended for long-term use

habit forming

• Some patients may develop dependence and/or tolerance; risk may be greater with higher doses

• History of drug addiction may increase risk of dependence

SPECIAL POPULATIONS

Renal Impairment

• May have longer elimination half-life, prolonging time to recovery

Hepatic Impairment

• Longer elimination half-life; clearance is reduced

Cardiac Impairment

• Longer elimination half-life; clearance is reduced

Elderly

• Longer elimination half-life; clearance is reduced

• Intravenous: 1–3.5 mg; maximum 1.5 mg within 2 minutes

Children and Adolescents

• In most pediatric populations, pharmacokinetic properties are similar to those in adults

• Seriously ill neonates have reduced clearance and longer elimination half-life

• Hypotension has occurred in neonates given midazolam and fentanyl

• Intravenous dose: dependent on age, weight, route, procedure

Pregnancy

• Effective June 30, 2015, the FDA requires changes to the content and format of pregnancy and lactation information in prescription drug labels, including the elimination of the pregnancy letter categories; the Pregnancy and Lactation Labeling Rule (PLLR or final rule) applies only to prescription drugs and will be phased in gradually for drugs approved on or after June 30, 2001

• Controlled studies have not been conducted in pregnant women

• Midazolam crosses the placenta

• Neonatal flaccidity has been reported in infants whose mother took a benzodiazepine during pregnancy

Breast Feeding

• Some drug is found in mother’s breast milk

• Effects on infant have been observed and include feeding difficulties, sedation, and weight loss

• Midazolam can be used to relieve postoperative pain after cesarean section

Based on data Published online by Cambridge University Press

Compiled by Dr. Jash Ajmera