Anticholinergic · Antidote

Atropine

Reviewed by Alex G, BSN, RN, CEN, CCRN, CMC, NREMT-P · From the Reference tab of the app

Indications

Dosing

WhereDose
Rhythm controlAtropine: 1 mg IV every 3–5 min, max 3 mg

On the quick cards

Mechanism of action

Atropine competitively and reversibly blocks all five muscarinic receptors (M1–M5), with little nicotinic effect at clinical doses. At the SA and AV nodes, blocking Gi-coupled M2 receptors removes vagal tone: acetylcholine can no longer open IKACh potassium channels or lower cAMP, so the rate rises and AV conduction speeds up. Blocking Gq-coupled M3 receptors dries secretions, relaxes bronchial, gut and bladder smooth muscle and dilates the pupil. The modernized Vaughan Williams scheme (Lei 2018) lists it in class II.

Pharmacology

Pharmacokinetics

OnsetIV about 1 min
PeakHeart-rate effect lags plasma levels, peaking about 7–8 min after IV; IM plasma peak about 30 min (label)
DurationRoughly 1–2 h of vagal block, shorter than glycopyrrolate (2–3 h by its label)
Half-life2–4 h in adults (label); more than doubled under age 2 and over 65
DistributionVd about 1–2 L/kg; crosses the BBB and placenta (label)
Protein binding14–44% (labels differ)
MetabolismLiver hydrolysis to tropine and tropic acid, plus noratropine (label)
EliminationUrine: 13–50% unchanged (label)
RoutesIV, IO, IM, endotracheal; autoinjectors for nerve agents

Chemistry

Adverse effects and cautions

In the one-pagers

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Sources

  1. FDA label: Atropine sulfate injection, Hikma (2023)
  2. FDA label: AtroPen (2022)
  3. PubChem: atropine
  4. Lei 2018, 2025 update (classification)

For education and exam preparation only. Follow your institution’s protocols. Typical adult values for study. Follow the order, the label and your institution's protocols.