Sympathomimetic drugs
The spectrum and severity of a sympathomimetic toxidrome depends on whether the causative drug has predominantly adrenergic, dopaminergic or serotonergic effects. Causative drugs include:
- medications
- beta-adrenergic receptor agonists (eg salbutamol)
- catecholamines (eg adrenaline [epinephrine], dopamine, isoprenaline, noradrenaline [norepinephrine], phenylephrine)
- indirect sympathomimetics (eg dexamfetamine, lisdexamfetamine, methylphenidate, phentermine, pseudoephedrine)
- nonamfetamine psychostimulants (eg armodafinil, modafinil)
- monoamine oxidase inhibitors (MAOIs) (eg phenelzine, tranylcypromine)
- serotonin and noradrenaline reuptake inhibitors (SNRIs) (atomoxetine, desvenlafaxine, duloxetine, reboxetine, venlafaxine)
- xanthines (eg theophylline and caffeine).
- illicit stimulants
- amfetamines and their derivatives (eg metamfetamine [methamphetamine], methylenedioxymetamfetamine [methylenedioxymethamphetamine, MDMA or ‘ecstasy’]) (see Stimulant poisoning)
- beta-adrenergic receptor agonists (eg clenbuterol)
- cocaine
- novel psychoactive substances, including novel stimulant drugs, synthetic cannabinoid-receptor agonists, and novel hallucinogenic drugs.