Drug Guide
Dextroamphetamine and Amphetamine mixture
Classification
Therapeutic: Central Nervous System stimulant for ADHD and Narcolepsy
Pharmacological: Sympathomimetic amines
FDA Approved Indications
- Attention Deficit Hyperactivity Disorder (ADHD)
- Narcolepsy
Mechanism of Action
Increases amount of dopamine and norepinephrine in the brain by promoting their release and inhibiting reuptake, leading to stimulant effects.
Dosage and Administration
Adult: As prescribed, typically 5-30 mg daily in divided doses
Pediatric: Prefixed by age, generally starting at 2.5-10 mg daily, titrated carefully under supervision
Geriatric: Use with caution, lower initial doses recommended due to potential for increased sensitivity and side effects
Renal Impairment: Adjust dose cautiously, monitor for efficacy and adverse effects
Hepatic Impairment: Use with caution; no specific adjustments well-established
Pharmacokinetics
Absorption: Well absorbed orally, peak plasma levels in 3 hours
Distribution: Crosses blood-brain barrier, extensive protein binding (~11-16%)
Metabolism: Partially metabolized in the liver, primarily via conjugation
Excretion: Excreted mainly in urine, with some unchanged drug
Half Life: Dextroamphetamine ~10 hours, Amphetamine ~9-14 hours
Contraindications
- History of hypersensitivity to amphetamines
- In patients with advanced arteriosclerosis, symptomatic cardiovascular disease, hypertension, hyperthyroidism, glaucoma, agitated states, or history of drug abuse
Precautions
- Caution in patients with a history of mental health issues, tics, or tourette's syndrome
- Use with caution in pregnancy and lactation; considered pregnancy category C
Adverse Reactions - Common
- Insomnia (common)
- Dry mouth (common)
- Anorexia (common)
- Headache (common)
Adverse Reactions - Serious
- Cardiovascular events such as hypertension, tachycardia, or arrhythmias (rare)
- Psychiatric effects like psychosis, paranoia, or aggressive behavior (rare)
- Potential for dependency and abuse (serious)
Drug-Drug Interactions
- Monoamine oxidase inhibitors (risk of hypertensive crisis)
- Other central nervous system stimulants
- Antihypertensive agents (may diminish their effects)
Drug-Food Interactions
- May have enhanced effects with caffeine
Drug-Herb Interactions
N/ANursing Implications
Assessment: Monitor cardiovascular status, behavioral changes, BMI, and signs of abuse
Diagnoses:
- Risk for increased blood pressure
- Risk for dependence
Implementation: Administer doses as prescribed, monitor pulse and blood pressure regularly, educate patient on medication adherence and potential side effects
Evaluation: Assess for effectiveness in reducing ADHD symptoms or narcolepsy episodes, monitor for adverse events
Patient/Family Teaching
- Take medication exactly as prescribed, do not double doses
- Report any cardiovascular symptoms, psychiatric changes, or signs of dependency
- Avoid alcohol and other CNS depressants
- Keep medication out of reach of children
Special Considerations
Black Box Warnings:
- Potential for abuse and dependence
- Serious cardiovascular events, including sudden death in patients with pre-existing structural cardiac abnormalities or other serious heart problems
Genetic Factors: Genetic factors may influence metabolism and response
Lab Test Interference: May affect growth in children, monitor height and weight periodically
Overdose Management
Signs/Symptoms: Severe hypertension, agitation, hyperthermia, seizures, coma
Treatment: Supportive care, activated charcoal to reduce absorption, benzodiazepines for seizures, monitoring of cardiac and vital signs, and sedation as needed
Storage and Handling
Storage: Store at room temperature (20-25°C), away from moisture, heat, and light
Stability: Stable for specified periods as per manufacturer instructions