hydrocortisone sodium phosphate: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
hydrocortisone sodium phosphate: clinical details
Prescribing considerations
- Confirm the indication and formulation; oral replacement products, soluble emergency treatment, injection and eye drops are not interchangeable.
- For adrenal insufficiency, provide illness and emergency-management education and ensure eligible patients carry the appropriate steroid card.
- Avoid abrupt withdrawal after clinically significant systemic exposure; assess HPA-axis suppression risk.
- Systemic corticosteroids may mask infection and cause psychiatric, metabolic, cardiovascular, gastrointestinal, musculoskeletal and ocular complications.
- Do not use ocular corticosteroids for an undiagnosed red eye. Exclude infection and corneal disease first.
Contraindications and cautions
- Hypersensitivity to the active substance or formulation excipients.
- Systemic injection in systemic infection without appropriate anti-infective treatment or with live-virus immunisation; do not inject directly into tendons.
- Soluble tablets in systemic fungal infection.
- Eye drops in corticosteroid-induced or other ocular hypertension, acute ulcerative viral corneal infection, ocular tuberculosis or fungal disease, and acute purulent ocular infection.
Monitoring
- With systemic exposure, monitor clinical response and features of excess or inadequate glucocorticoid effect; consider blood pressure, weight, glucose, electrolytes, infection, mood, bone health and growth in children.
- Review interacting medicines whenever treatment starts, stops or changes.
- During prolonged ocular treatment or in susceptible patients, monitor intraocular pressure, cataract formation, infection and corneal integrity.
- Monitor cardiac structure and function in prematurely born infants receiving systemic hydrocortisone because hypertrophic cardiomyopathy has been reported.
Clinical pharmacology
Hydrocortisone is the principal endogenous glucocorticoid and also has mineralocorticoid activity. It modifies glucocorticoid-responsive gene expression, suppressing immune responses and inflammatory-mediator production. Systemic hydrocortisone is extensively protein-bound, metabolised mainly in the liver and tissues, and excreted chiefly as conjugated urinary metabolites.
Formulation and product differences
- Oral solutions are licensed for paediatric adrenal-insufficiency replacement, include oral syringes and can be given through specified gastric feeding tubes.
- The soluble tablet must be dissolved in water and taken immediately; licensed indications include selected replacement and emergency systemic uses.
- Injection can be given intravenously, intramuscularly or into appropriate soft tissues by trained personnel. Transient paraesthesia can occur after intravenous administration and appears related to the phosphate salt.
- Eye drops are preservative-free single-dose containers. Paediatric safety and efficacy have not been established, and damaged corneas may rarely develop calcification with phosphate-containing drops.
hydrocortisone sodium phosphate preparations and strengths
Eye drops
Route: Ophthalmic
Strengths: 3.35 mg/mL
Oral solution
Route: Oral
Strengths: 5 mg/5 mL, 10 mg/5 mL
Tablet
Route: Oral
Strengths: 10 mg
hydrocortisone sodium phosphate interactions
Relevance depends on route, systemic exposure and treatment duration. Check prescribed, over-the-counter and herbal products with a pharmacist or prescriber.
Strong CYP3A inhibitors, including ritonavir, cobicistat, azole antifungals and some macrolide antibiotics
May increase hydrocortisone exposure and systemic corticosteroid adverse effects.
CYP3A inducers, including some antiretroviral medicines
May reduce exposure and increase the risk of inadequate cortisol replacement or adrenal crisis.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.