Drug Guide
Dexamethasone Sodium Phosphate
Classification
Therapeutic: Anti-inflammatory, Immunosuppressant
Pharmacological: Glucocorticoid
FDA Approved Indications
- Inflammation and allergic conditions
- Rheumatoid arthritis
- Cerebral edema
- Certain cancers
- Endocrine disorders
Mechanism of Action
Dexamethasone binds to glucocorticoid receptors, modulating gene expression for anti-inflammatory and immunosuppressive effects.
Dosage and Administration
Adult: Dosage varies based on condition; typical doses range from 0.75 mg to 9 mg daily, administered orally, IM, IV, or topical.
Pediatric: Dosing depends on weight and indication; typically 0.02-0.3 mg/kg/day divided into 1-4 doses.
Geriatric: Start at lower doses due to increased sensitivity; monitor closely for adverse effects.
Renal Impairment: Adjust dose based on severity of impairment; consult specific guidelines.
Hepatic Impairment: Use with caution; metabolized hepatically.
Pharmacokinetics
Absorption: Good oral absorption.
Distribution: Widely distributed; crosses blood-brain barrier.
Metabolism: Metabolized in the liver.
Excretion: Eliminated mainly in urine as metabolites.
Half Life: 3-5 hours in plasma.
Contraindications
- Systemic fungal infections
- Hypersensitivity to dexamethasone
Precautions
- Use with caution in infections, diabetes, osteoporosis, psychiatric disorders, or peptic ulcer disease.
- Pregnancy category C; risk-benefit analysis required.
Adverse Reactions - Common
- Insomnia, increased appetite, fluid retention (Common)
- Elevated blood glucose, mood changes (Common)
Adverse Reactions - Serious
- Adrenal suppression, osteoporosis, psychological disturbances (Serious)
- Infections, ocular effects, allergic reactions (Serious)
Drug-Drug Interactions
- NSAIDs (gastric bleeding), CYP3A4 inhibitors (increased levels), vaccines (decreased efficacy)
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor glucose levels, electrolytes, infection signs, bone density, mood changes.
Diagnoses:
- Risk for infection
- Impaired skin integrity
- Potential for altered mood or cognitive function
Implementation: Administer with food or milk to minimize GI upset. Taper doses gradually to prevent adrenal insufficiency.
Evaluation: Assess for reduction of inflammation, stabilization of condition, adverse effects.
Patient/Family Teaching
- Take medication exactly as prescribed.
- Report signs of infection, mood changes, or unusual symptoms.
- Do not stop abruptly.
- Use additional contraception if on long-term therapy.
Special Considerations
Black Box Warnings:
- Potential for immune suppression leading to severe infections
Genetic Factors: Limited specific data.
Lab Test Interference: Can increase blood glucose, may affect electrolyte levels.
Overdose Management
Signs/Symptoms: Cushingoid features, hyperglycemia, hypertension, hypokalemia.
Treatment: Discontinue drug; supportive care; manage symptoms; consider activated charcoal if ingestion recent.
Storage and Handling
Storage: Store at room temperature, away from light and moisture.
Stability: Stable under recommended conditions for the shelf life indicated.