Pharmacopeia
HYDROCORTISONE
Core pharmacology
- Class Group
Glucocorticoid
- Legacy Cicm Level
Level 2
- Introduction
Natural
Dose Equivalence 25- Indications Uses
1. as replacement therapy in adrenocortical deficiency states and in the
treatment of
2. allergy and anaphylaxis
3. asthma
4. panoply of autoimmune disorders
5. eczema and contact sensitivity syndromes and
6. in leukaemia chemotherapy regimes and
7. for immunosuppression after organ transplantation- Presentation
10/20mg tablets
White lyophilized power to be mixed in water
Other topical preparations- Main Action
Anti-inflammatory
- Mechanism of action
lipid solubile → crosses cell membranes → bind to steroid receptors via “zinc finger” binding site
→ signal trascribed via second messenger → alters gene transcription and the production of proteins- Onset Peak Duration
Dur: 8-36h
- Physiological effects
1. Metabolic effects
▪ ↑’s gluconeogensis
▪ ↑ protein catabolism and lipolysis → muscle wasting and thin skin and fat redistribution
(cushingoid)
▪ ↑ bone catabolism → osteoporosis
▪ ↑ glucose release but ↓ absorption from the GIT2. Anti inflammatory effects
▪ ↓’d phospholipase A2 → ↓ arachidonic acid → ↓ prostaglandins3. Immunosupression
▪ ↓’d inflammatory mediators
▪ ↓ IL 1-2 → ↓’d lymphocyte prod
▪ altered neutrophil and macrophage function- Adverse Effects Toxicity
▪ Adrenal supression via negative feedback on the HPA
▪ Fluid retention - via weak mineralcorticoid activity
▪ Vascular reactivity - plays a permissive role in the actions of catecholamines on vesselsInhaled: oral candidiasis (poor technique), dysphonia, minor adrenal suppresion
- Absorption
IV
Rapidly given PO or PR
PO BA: 50%- Protein binding
CBG 70%, Alb 20%
- Volume of distribution
0.5 L/kg
- Metabolism
Liver – Tetrahydrocortisone
- Excretion
Urine
- Clearance
167-283 ml/min
- Half-life
0.5-1.5h
- Special Points
100
1
Short
- Route And Dose
PO,TOP, IV, IM, IA