In addition to medications in this formulary chapter, the following categories of medications can be found in the identified chapters:
Intubation Medications – see chapter 6
Code Medications – see chapter 7
Cardiovascular Medications – see chapter 14
Sedation/Analgesia/Neuromuscular Blockade – see chapter 15
Anti-infective Medications – see chapter 16
Respiratory | |||
Medication | Dose | Mechanism | Comment |
Albuterol | Intermittent 2.5 mg nebulization or | ß2-agonist: bronchodilation via airway smooth muscle relaxation | Frequent re-evaluation needed, especially if tachycardic |
Continuous nebulization from 5–20 mg/hr | Side effects: tremor, tachycardia, agitation, hypokalemia | ||
Acetylcysteine | Infants: 1–2 mL of 20% solution or 2–4 mL of 10% solution (undiluted); three to four times daily | Exerts mucolytic action through its free sulfhydryl group, which opens up the disulfide bonds in the mucoproteins, thus lowering mucous viscosity | |
Children and adolescents: 3–5 mL of 20% solution or 6–10 mL of 10% solution (undiluted); administer three to four times daily | |||
Ipratropium | 125–500 mcg nebulization q6–8 hr | Inhaled anticholinergic (inhibit cGMP) bronchodilator | Systemic SEs rare due to poor absorption from lung |
Saline nebulization 0.9%, 3%, 7% | 3% solution: 4 mL inhaled every 2 hr | Pretreatment with a bronchodilator is recommended to prevent potential bronchospasm | |
≥6 years and adolescents: inhalation: 7% solution: 4 mL inhaled twice daily | |||
Terbutaline | Load: 2–10 mcg/kg IV | Systemic ß2-agonist | SEs same as albuterol |
Infusion: 0.08–1 mcg/kg/min | Stop infusion and obtain ECG for chest pain or ST changes |
Neurologic | |||
Medication | Route | Dose | Mechanism |
Midazolam | IV bolus | Loading dose: 0.15–0.2 mg/kg | Enhances GABA activity |
IV infusion | 0.06–0.5 mg/kg/hr | ||
Intramuscular | 0.2 mg/kg/dose, may repeat every 10–15 min, maximum dose: 6 mg | ||
Buccal | 0.2–0.5 mg/kg once; maximum dose: 10 mg | ||
Intranasal | 0.2 mg/kg once; maximum dose: 10 mg | ||
Lorazepam | IV bolus | 0.1 mg/kg maximum: 4 mg, slow IV over 2–5 min; may repeat in 5–15 min | |
Diazepam | IV bolus | 0.1–0.3 mg/kg/dose given over 3–5 min, every 5–10 min; maximum dose: 10 mg/dose | |
Rectal | 2–5 years: 0.5 mg/kg | ||
6–11 years: 0.3 mg/kg | |||
≥12 years and adolescents: 0.2 mg/kg | |||
Fosphenytoin | IV bolus | 15–20 mg PE/kg; maximum dose: 1500 mg PE | Stabilizes voltage-gated sodium channels |
Administer at 1–3 mg PE/kg/min up to a maximum of 150 mg PE/min | |||
Levetiracetam | IV bolus | 20–60 mg/kg; dose should not exceed adult initial range: 1000–3000 mg | Thought to have multiple sites of action, including calcium channels, glutamate receptors, and GABA modulation |
Pentobarbital | IV bolus | Loading dose: 5 mg/kg | Enhances GABA activity |
IV infusion | Initial: 0.5–1 mg/kg/hr | ||
Phenobarbital | IV bolus | 15–20 mg/kg; maximum dose: 1000 mg |
Miscellaneous | |||
Medication | Dose | Mechanism | Comment |
Albumin | 0.5–1 g/kg/dose IV | Provides increase in intravascular oncotic pressure | Administration rate: |
Use 5% in hypovolemic or intravascularly depleted patients | 5% = 2–4 mL/min | ||
Use 25% in fluid/Na restricted patients | 25% = 1 mL/min (after initial volume replacement) | ||
Diphenhydramine | 0.5 mg/kg/dose IV/PO Maximum dose: 50 mg | Antihistamine | |
Haloperidol | Limited data available | Nonselectively blocks postsynaptic dopaminergic receptors in the brain | Use has been associated with adverse effects, including cardiac effects, circulatory and respiratory insufficiency, extrapyramidal symptoms, and neuroleptic malignant syndrome |
≥3 months, children, and adolescents: IV (lactate, immediate release): loading dose: 0.15–0.25 mg/dose infused slowly over 30–45 min | |||
Mannitol | IV bolus 0.25–1 g/kg/dose infused over 20–30 min | Osmotic diuresis, decrease in ICP through osmosis and reduction in blood viscosity | |
Metoclopramide | 0.1 mg/kg/dose IV/PO | Enhances motility and accelerates gastric emptying | |
Naloxone | Full reversal: | Opioid antagonist | |
0.1 mg/kg/dose IV (2 mg max) | |||
For respiratory depression: 0.001–0.005 mg/kg/dose | |||
Octreotide | Load: 1–2 mcg/kg bolus IV over 2–5 min | Mimics natural somatostatin | Consider tapering dose for discontinuation |
Maintenance: IV: 1–10 mcg/kg/hr continuous infusion | |||
Ondansetron | 0.1 mg/kg/dose IV/PO | Selective 5-HT3-receptor antagonist |
Systemic Steroids | |||
Medication | Dose | Mechanism | Comment |
Prednisolone (PO) | Load: 2 mg/kg | Decrease inflammation, mucus production, and mediator release |
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Max: usually 60 mg | |||
Maintenance: | |||
0.5–1 mg/kg q6 hr | |||
Max: usually 60 mg/dose | |||
Methylprednisolone (IV) | Load: 2 mg/kg | ||
Max: usually 60 mg | |||
Maintenance: | |||
0.5–1mg/kg q6 hr | |||
max: usually 60 mg/dose | |||
Hydrocortisone | Shock: IV 50–100 mg/m2/day divided every 6 hr | Decreases inflammation and reverses increased capillary permeability |
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Physiologic replacement: IV/PO 8–10 mg/m2/day divided every 8 hr | |||
Dexamethasone | Croup: 0.6 mg/kg/dose IV/PO once | Decreases inflammation and mediator release |
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Glucorticoid Equivalency Table | |||||
Glucocorticoid | Equivalent Dose (mg) | Routes | Relative Anti-inflammatory Potency | Relative Mineralo-corticoid Potency | Elimination Half-Life (hr) |
Cortisone | 25 | PO, IM | 0.8 | 0.8 | ∼0.5 |
Hydrocortisone | 20 | IM, IV | 1 | 1 | ∼2 |
MethylPREDNISolone | 4 | PO, IM, IV | 5 | 0 | 1–2 |
PrednisoLONE | 5 | PO | 4 | 0.8 | 2–4 |
PredniSONE | 5 | PO | 4 | 0.8 | 2–3 |
Dexamethasone | 0.75 | PO, IM, IV | 25–30 | 0 | ∼4 |
Fludrocortisone | — | PO | 10 | 125 | ∼3.5 |
Electrolytes | |||
Medication | Dose | Max Dose | Max Rate |
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| 0.5–1 mEq/kg/dose IV over 2–3 hr |
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