1. Clinical & Scientific Overview
Deflazacort & Fludrocortisone Acetate (TIP-MED-000098, Reference Code [6.8]) is classified under
Thyroid, Pituitary, Adrenal & Hormonal Medicines (Ch 06) as a Oxazoline Glucocorticoid & Potent Synthetic Mineralocorticoid (Schedule H).
Within the Indian regulatory and compendial framework, it is governed under Schedule H & Schedule G Prescription Drug ('Caution: It is dangerous to take this preparation except under medical supervision' — Drugs Rules 1945).
Representative Indian Market Examples (Edition 2.7 Ch 06 [6.8], p. 75): Deflazacort: Defcort (Macleods), Dezacor, Orthocort, Mahacort-DZ. Fludrocortisone: Florinef, Fludrocort (Samrath) — Strengths & Dosage Forms: Deflazacort Tablets: 6 mg, 12 mg, 24 mg, 30 mg; Suspension: 6 mg/5 mL (Deflazacort 6 mg = Prednisolone 5 mg). Fludrocortisone Tablets: 100 mcg (0.1 mg)
Deflazacort Tablets: 6 mg, 12 mg, 24 mg, 30 mg; Suspension: 6 mg/5 mL (Deflazacort 6 mg = Prednisolone 5 mg). Fludrocortisone Tablets: 100 mcg (0.1 mg)
3. Mechanism of Action & Pharmacodynamics
Oxazoline Glucocorticoid & Potent Synthetic Mineralocorticoid (Schedule H) acting on target receptor/enzyme pathways in Thyroid, Pituitary, Adrenal & Hormonal Medicines (Ch 06): clinical efficacy is mediated via Oxazoline Glucocorticoid & Potent Synthetic Mineralocorticoid (Schedule H) for Deflazacort: Duchenne muscular dystrophy (DMD), rheumatoid arthritis, asthma/allergic disorders, nephrotic syndrome. Fludrocortisone: Primary adrenal insufficiency (Addison's disease) and salt-wasting congenital adrenal hyperplasia (alongside Hydrocortisone), severe neurogenic orthostatic hypotension.
4. Therapeutic Indications & Evidence-Supported Uses
- Deflazacort: Duchenne muscular dystrophy (DMD), rheumatoid arthritis, asthma/allergic disorders, nephrotic syndrome
- Fludrocortisone: Primary adrenal insufficiency (Addison's disease) and salt-wasting congenital adrenal hyperplasia (alongside Hydrocortisone), severe neurogenic orthostatic hypotension
🇮🇳 Jurisdiction & Indication Note: Indications and schedules reflect Indian compendial and regulatory records (CDSCO / Indian Pharmacopoeia & NFI / NLEM 2022). Where international reference labels (US FDA DailyMed / NCBI StatPearls) are cited for pharmacokinetic or mechanistic parameters, international approvals do not automatically imply CDSCO approval in India.
5. Educational Dosage Context, Formulations & Administration
Educational Dosing & Regimen Summary: Deflazacort: 6–36 mg PO OD in the morning (DMD: 0.9 mg/kg/day OD). Fludrocortisone: 50–200 mcg (0.5–2 tablets) PO OD in the morning
Administration & Meal Timing: Take in the morning with breakfast | Morning (8:00 AM)
6. Pharmacokinetics, Metabolism & Renal/Hepatic Adjustment
Absorption, distribution, metabolism, and excretion follow class pharmacokinetic profile; verify patient renal/hepatic function.
Renal & Hepatic: In moderate-to-severe hepatic impairment or CKD, monitor BP and Serum K+/Na+ closely on Fludrocortisone
Renal & Hepatic: In moderate-to-severe hepatic impairment or CKD, monitor BP and Serum K+/Na+ closely on Fludrocortisone
Renal & Hepatic: In moderate-to-severe hepatic impairment or CKD, monitor BP and Serum K+/Na+ closely on Fludrocortisone
7. Contraindications, Precautions & High-Risk Warnings
- Deflazacort is a glucocorticoid prodrug (6 mg = 5 mg Prednisolone) — shares ALL corticosteroid risks (HPA suppression, infection, hyperglycaemia, cataracts)! Fludrocortisone is contraindicated in uncontrolled hypertension, congestive heart failure, and systemic fungal infections
Key Clinical Precautions: Renal & Hepatic: In moderate-to-severe hepatic impairment or CKD, monitor BP and Serum K+/Na+ closely on Fludrocortisone
8. Adverse Effects Profile
- Deflazacort: Weight gain, Cushingoid facies, hyperglycaemia, dyspepsia. Fludrocortisone: Sodium/water retention, ankle oedema, hypertension, hypokalaemia
- Adrenal crisis if stopped abruptly; Fludrocortisone overdose causes severe hypertension, cardiomegaly, congestive heart failure, and profound hypokalaemia
- Monitor for severe hypersensitivity, organ toxicity, or dose-limiting adverse events.
9. Major Drug–Drug, Drug–Food & Drug–Herb Interactions
- CYP3A4 inhibitors (Clarithromycin, Itraconazole, Fluconazole) increase active 21-desacetyldeflazacort 3-fold (reduce Deflazacort to 1/3 of dose!); Rifampicin/Carbamazepine reduce efficacy; Amphotericin B and Loop/Thiazide diuretics worsen hypokalaemia
10. Clinical Monitoring, Patient Counselling & Storage
Clinical & Laboratory Monitoring: Monitor clinical response, baseline renal/hepatic parameters, and relevant serum biomarkers.
Pharmacist Patient Counselling Points:
- Patient Counselling Checklist: Remember that Defcort 6 mg equals Prednisolone 5 mg and must never be stopped suddenly after >2 weeks; for Florinef, store properly and report ankle swelling or high BP
- Meal & Clock Timing Instruction: Take in the morning with breakfast (Morning (8:00 AM))
- Missed Dose Protocol: Take same day as soon as remembered; never miss replacement doses in Addison's disease
- Geriatric Dispensing Pearl: Fludrocortisone >200 mcg/d in older adults carries a high risk of supine hypertension, hypokalaemia, and heart failure (AGS Beers 2023)
Storage, Stability & Dispensing Safeguards: Store below 25°C–30°C in original moisture- and light-resistant packaging out of reach of children. Available forms: Deflazacort Tablets: 6 mg, 12 mg, 24 mg, 30 mg; Suspension: 6 mg/5 mL (Deflazacort 6 mg = Prednisolone 5 mg). Fludrocortisone Tablets: 100 mcg (0.1 mg)
11. Visual Pharmacology & Mechanism Diagram (svg-v339-01-adme-12-step-journey)
12. Authoritative References, Regulatory Sources & Editorial Disclaimer
Primary Compendial & Guideline Reference: Indian Pharmacist Desk Reference — Professional Edition 2.7 (2026–27) • Ch 06 [6.8] (p. 75)
Official Verification Portals: Indian Pharmacopoeia Commission (IPC) & National Formulary of India (NFI) • Central Drugs Standard Control Organization (CDSCO) • Ministry of Health & Family Welfare — NLEM 2022 • NCBI Bookshelf / StatPearls Pharmacology Reference • DailyMed (US FDA Official Prescribing Reference)
Last Medically & Pharmaceutically Reviewed: 2026-11-10 • Verification Status: HANDBOOK_SOURCE_CONTENT
Educational & Clinical Disclaimer: This reference profile is published solely for pharmacy education, academic study, and professional clinical reference. It does not substitute for patient-specific clinical judgement, qualified specialist oncology/medical supervision, or official CDSCO/IP prescribing information. Never self-medicate with prescription, Schedule H/H1/X, NDPS, or oncology medicines.
13. Related Reference Monographs, Educational Guides & Visual Concept
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