Гидрокортизон

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Гидрокортизон

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Medically reviewed

Rosario Oropesa

Last updated on 22/12/2025

This page provides general, reference-level information compiled from official medical sources. It is not a substitute for professional medical advice, diagnosis, or treatment. For decisions about your health, please consult a qualified healthcare professional.

Overview of Гидрокортизон

What is Hydrocortisone?

Hydrocortisone is a pharmaceutical preparation of cortisol, a steroid hormone naturally produced by the adrenal glands. It belongs to a class of medications known as corticosteroids, which are vital for regulating various physiological processes in the body, including metabolism, immune response, and the body's reaction to stress.

Mechanism of Action

Hydrocortisone works by mimicking the effects of natural hormones produced by the adrenal cortex. When used as a medication, it penetrates cell membranes and binds to specific receptors. This interaction influences the production of proteins that control inflammation and immune activity. By modulating these pathways, hydrocortisone helps reduce swelling, redness, and itching associated with various conditions.

Common Applications

Hydrocortisone is utilized across multiple medical fields due to its versatile properties. Its primary functions include:

  • Anti-inflammatory: It is widely used to manage inflammation in different parts of the body, such as the skin, joints, and internal organs.
  • Immunosuppressive: It can help dampen overactive immune responses, which is particularly useful in treating allergic reactions and autoimmune conditions.
  • Hormonal Replacement: In cases where the body does not produce enough natural cortisol, such as in primary or secondary adrenal insufficiency, hydrocortisone is used to restore hormone levels to a physiological range.

Available Forms

Because it is used to treat a broad spectrum of issues, hydrocortisone is manufactured in several formulations:

  • Topical: Creams, ointments, and lotions for localized skin conditions.
  • Oral: Tablets used for systemic treatment or long-term hormone management.
  • Injectable: Solutions used for acute conditions requiring rapid effect or for localized treatment in joints.
  • Rectal: Suppositories or foams used for inflammatory conditions of the lower gastrointestinal tract.

As a foundational medication in clinical practice, hydrocortisone remains an essential tool for managing both acute inflammatory episodes and chronic hormonal imbalances.

What side effects are possible with Гидрокортизон?

Possible side effects and safety information

Hydrocortisone's safety profile is officially documented by government regulators and reflects its activity as a systemic glucocorticoid. Adverse reactions are formally classified by the organ systems affected (System-Organ Classes), with most significant effects associated with prolonged use of systemic forms.

Commonly Documented Adverse Reactions

Adverse effects such as nausea, headache, insomnia, dizziness, and acne are commonly listed in official patient summaries. Many of the systemic effects listed in prescribing information lack a specific frequency classification, highlighting their grouping by seriousness and physiological system.


Systemic Safety Considerations

Official labels document adverse effects across multiple systems:

  • Endocrine Disorders: Suppression of the hypothalamic-pituitary-adrenal (HPA) axis and the development of a Cushingoid state.
  • Fluid and Electrolyte Disturbances: Sodium and fluid retention, potassium loss, and associated hypertension.
  • Musculoskeletal Disorders: Muscle weakness, loss of muscle mass, and increased risk of osteoporosis and fractures.
  • Psychiatric/Nervous System: Mood swings, severe depression, and elevated intracranial pressure (pseudotumor cerebri).

Serious Adverse Reactions

Officially documented serious risks include acute adrenal insufficiency upon abrupt discontinuation of systemic therapy, peptic ulcer with potential perforation, and congestive heart failure in susceptible patients. The use of systemic hydrocortisone is contraindicated in the presence of systemic fungal infections, as officially stated in the label.

Time and Population-Specific Notes

Prolonged use is officially linked to the development of posterior subcapsular cataracts and glaucoma. For the pediatric population, the regulatory label requires specific monitoring of growth and development due to the documented risk of growth suppression during extended treatment.

Overdose and Emergency Response

Overdose and When to Seek Help

The information in this section is derived strictly from official regulatory labeling and is intended for informational purposes only.

Overdosage with hydrocortisone is typically classified into two main types based on the duration of exposure to excessively high doses.

Acute Overdosage

Acute overdosage, occurring from a single large exposure, is generally managed with supportive and symptomatic therapy by medical professionals. Signs of an acute overdose are often less defined than those of chronic exposure.

Chronic Overdosage

Chronic overdosage results from long-term treatment with high (supra-physiological) dosages of hydrocortisone. This type of exposure can lead to clinical manifestations resembling Cushing's syndrome.

Symptoms of Chronic Overdose May Include:

  • Elevation of blood pressure
  • Fluid and salt (sodium and water) retention
  • Increased excretion of potassium
  • Changes in fat distribution (e.g., increased adiposity)

In cases of chronic overdosage where continuous steroid therapy is required for a severe underlying disease, the official regulatory guidance suggests that the corticosteroid dosage may be reduced only temporarily, or that alternate day treatment may be cautiously introduced under medical supervision. The complexity of these adjustments necessitates professional medical management.

When to Seek Medical Help

Any suspected overdosage with hydrocortisone, whether acute or chronic, requires immediate consultation with a poison control center or healthcare professional. While the official overdose sections focus on managing the physiological effects, any severe, unexplained symptoms following use warrant urgent medical attention.

Therapeutic Uses of Гидрокортизон

Гидрокортизон (Hydrocortisone) is applied in contexts where short-term symptomatic assistance is needed to address periods of heightened distress and noticeable interference with daily stability. The medication is commonly used across therapeutic domains to provide support that helps ease the overall burden of symptoms and assists with maintaining a sense of stability when manifestations become more noticeable.

This medication is utilized for managing symptoms associated with a range of conditions, including various inflammatory and allergic diseases, certain types of rheumatic and skin disorders, and is applied for supportive management of adrenal insufficiency.

It is often used when supportive symptom management is appropriate:

“The medication is used to help address symptom clusters that may become intense or disruptive during acute episodes.”

Гидрокортизон is relevant in clinical settings that involve acute or unstable symptom patterns, such as sudden swelling, redness, and itching, which may signal inflammatory or irritative states. It supports the patient during difficult episodes by easing distress and contributes to improved day-to-day comfort during symptomatic periods.


Quick Fact: Relief for Inflammatory Symptoms

Гидрокортизон is relevant for easing symptoms related to heightened physiological activity, commonly used when supportive symptom management is appropriate.

Regulatory References

  1. NIH DailyMed label overview

Eligibility and Restrictions for Use

Eligibility Map: Official Regulatory Information

The eligibility for systemic Hydrocortisone is defined by official regulatory bodies based on absolute contraindications, patient age, and existing health conditions.

Classification Population Restriction
Contraindicated Patients with systemic fungal infections must not use the medicine, as stated in regulatory labels. Use is also prohibited for individuals with a known hypersensitivity to the drug or its components.
Restricted/Caution Caution is required for patients with pre-existing conditions like diabetes mellitus, hypertension, peptic ulceration, diverticulitis, and ocular herpes simplex. Use in these groups mandates close monitoring as the conditions may alter the drug's effect or increase risk.

Age and Specific Populations:

Pediatric patients require careful use due to the documented risk of growth retardation, necessitating frequent growth assessment. For certain oral formulations, safety and efficacy have not been established in the general pediatric population. For pregnant and breastfeeding women, use requires a documented clinical evaluation where the potential benefits outweigh the possible risks to the fetus or infant, as the drug is known to pass into breast milk and cross the placenta.

What should I know about interactions with other medicines?

Interactions with other medicines and products

Hydrocortisone's interaction profile is significantly influenced by its immunosuppressive and metabolic effects, requiring careful management when combined with other medicines or vaccines.

Key Interactions and Restrictions

Category/Product Interaction Outcome & Management
Live/Live-Attenuated Vaccines Contraindicated when Hydrocortisone is used at immunosuppressive doses due to the risk of infection.
Insulin or Oral Hypoglycemic Agents Hydrocortisone may decrease carbohydrate tolerance, potentially requiring an increase in the dosage of antidiabetic medicines.
Mifepristone Use of Hydrocortisone is generally not recommended as Mifepristone may decrease the corticosteroid effect.
Desmopressin Co-administration is generally not recommended due to increased risks of water retention and hyponatremia.
Killed or Inactivated Vaccines May be administered, but the resulting immune response may be diminished or suppressed.
Antituberculous Chemotherapy Hydrocortisone may be used for specific conditions like tuberculous meningitis, but only in combination with appropriate chemotherapy to address the infection.

Serious restrictions exist regarding certain infections: Hydrocortisone is generally avoided in the presence of systemic fungal infections unless necessary to manage drug reactions. Due to its systemic effects, combining Hydrocortisone with certain serotonergic medicines, particularly opioids, requires close observation for signs of serotonin syndrome. The concurrent use of these product types must be discussed with a healthcare professional.

Mechanism of Action

Genomic and Receptor-Mediated Mechanism

Hydrocortisone (Гидрокортизон) is a non-selective agonist at the intracellular Glucocorticoid Receptor ( GR) and, with lower affinity, the Mineralocorticoid Receptor ( MR). The activated GR complex translocates to the cell nucleus, where it executes two primary genomic actions: Transrepression, which physically blocks the activity of pro-inflammatory transcription factors like NF-kappa B, and Transactivation, which increases the gene expression of anti-inflammatory proteins.

This gene regulation results in the upregulation of inhibitory proteins that block the enzyme Phospholipase A2 ( PLA2). By inhibiting PLA2, the drug halts the metabolic cascade required for the synthesis of eicosanoids, including prostaglandins and leukotrienes. The cellular consequences include decreased expression of adhesion molecules, a reduction in immune cell functionality, and a decrease in capillary permeability, which limits the accumulation of fluid in extravascular spaces. The MR agonism separately modulates sodium and potassium ion transport in the renal tubules, while GR agonism engages a negative feedback loop to suppress the synthesis of endogenous cortisol via the HPA axis.

Dosage and Administration Information

How to Use Injectable Hydrocortisone (Гидрокортизон)

Hydrocortisone (as the sodium succinate form) is a rapid-acting glucocorticoid typically administered via intravenous (IV) injection, intramuscular (IM) injection, or IV infusion for acute or emergency conditions.

Official Administration Procedures

Administration Scope Official Guidelines
Route IV injection, IM injection, IV infusion, Intra-articular, Periarticular, Intrabursal, and Soft-Tissue Injection.
Preparation For IV/IM use, the lyophilized powder vial is aseptically reconstituted by adding not more than 2 mL of Sterile Water for Injection (or Bacteriostatic Water for Injection). Inspect the solution visually; use only if it is clear.
IV Injection Speed The reconstituted dose should be administered by IV injection slowly over a period of at least 30 seconds. For maintenance of high blood levels, injections may need to be repeated every 4 to 6 hours.
IV Infusion The reconstituted solution must be diluted further with 50 mL to 1,000 mL of Dextrose Injection (5%), Isotonic Sodium Chloride Solution, or Dextrose and Sodium Chloride Solution.
Dosage The initial dose for severe conditions is typically 100 mg to 500 mg, which may be repeated at intervals of 2, 4, or 6 hours based on the patient's condition and response. The dose for children should be governed by the severity of the condition, not strictly by age or body weight.

Special Use Conditions

For intra-articular or soft-tissue injections, the drug is administered directly into the joint space or affected tissue. Injection into a tendon should be avoided. For patients discontinuing long-term therapy, the dosage must be reduced gradually to minimize the risk of drug-induced secondary adrenocortical insufficiency. If a dose is missed during routine oral replacement therapy, patients should follow specific, pre-determined instructions provided by their clinician and should not take a double dose.

Recent Clinical Evidence

Research Evidence / Overview of studies for Гидрокортизон

Evidence for Use in Hormone Replacement Therapy

Гидрокортизон was studied for use as replacement therapy in individuals with conditions where their adrenal glands do not produce enough of the natural hormone cortisol, such as adrenal insufficiency. The research exploring this use has primarily involved clinical trials with specific designs, such as randomized comparison studies (cross-over trials), and systematic reviews. These studies examined outcomes related to systemic or functional imbalance, including how patients reported their daily functioning, often measured using Quality of Life (QoL) scores.

Research suggests that while conventional dosing regimens are commonly used, pharmacokinetic studies show patterns related to the variability in plasma cortisol concentrations in individuals throughout the day. What remains uncertain is the long-term impact of various dosing strategies; long-term randomized trials that directly compare different replacement regimens are not widely available.


Evidence for Use in Severe Systemic Inflammation

Research explored the use of Гидрокортизон in critical care settings, specifically for patients experiencing severe systemic inflammation, such as in cases of septic shock. This research base includes several large-scale Randomized Controlled Trials (RCTs) and comprehensive Systematic Reviews. Studies monitored outcomes describing physiological strain or stress, including all-cause mortality at 28 and 90 days, the time required for shock reversal, and the duration of vasopressor support.

Findings were mixed across major clinical trials regarding the measured long-term mortality. The research exploring this use has shown that data related to survival were examined in contexts where there was high variability (heterogeneity) in trial design, making certain conclusions tentative. Data for certain groups remain insufficient.


Evidence for Use in Topical Inflammatory Conditions

The research base for topical Гидрокортизон was studied for conditions characterized by fluctuating or episodic manifestations on the skin, such as eczema and psoriasis. Research examined outcomes related to physical discomfort, including clinical improvement assessed via severity scores and patient-reported outcomes describing perceived discomfort. Findings describe patterns observed in the studies related to changes measured in inflammatory and irritative states, such as redness and itching. However, research describing the long-term effects are not fully established for consistent maintenance use.

Key Studies & References

  1. Adrenal insufficiency: identification and management - NICE Guideline NG243 (2024)

Frequently Asked Questions (FAQ)

Common questions about Hydrocortisone (FAQ)


Q: What is the difference between Hydrocortisone and Prednisolone?

Official sources describe Hydrocortisone as the natural glucocorticoid—cortisol—which also has significant mineralocorticoid activity, meaning it affects water and salt balance. Prednisolone is a synthetic corticosteroid. In equivalent anti-inflammatory doses, Prednisolone is generally described as more potent (stronger) and has less mineralocorticoid effect than Hydrocortisone.


Q: Can Hydrocortisone be taken at the same time as antibiotics?

Taking systemic forms of Hydrocortisone may lower resistance to infection and can potentially mask the signs of an infection. Official instructions state that if an infection is present (such as tuberculosis), Hydrocortisone should be used only in combination with appropriate antimicrobial therapy. Regulatory information indicates that treatment for any co-occurring infection typically requires appropriate antimicrobial therapy.


Q: Should topical Hydrocortisone be used during pregnancy?

The use of topical corticosteroids during pregnancy is generally considered when the potential benefit is determined to outweigh the possible risks to the fetus. This assessment requires clinical evaluation. Official documents from regulatory bodies like the TGA classify Hydrocortisone in Pregnancy Category A, indicating it has been studied in a large number of women without an observed increase in malformations.


Q: Are there scientific studies examining the studied outcomes of Hydrocortisone for certain conditions?

Yes, studies, including Randomized Controlled Trials (RCTs) and systematic reviews, have been conducted to examine Hydrocortisone’s use in hormone replacement, severe systemic inflammation, and topical skin conditions. Research findings report both beneficial outcomes and mixed data, particularly concerning long-term survival in critical care settings, which reflects the variability in trial design.


Q: Is it true that Hydrocortisone can affect blood pressure?

Official sources describe that Hydrocortisone can lead to retention of sodium and fluid, as well as potassium loss, which may be associated with elevated blood pressure (hypertension). This effect is especially noted when systemic Hydrocortisone is administered at higher doses or for prolonged periods due to its inherent mineralocorticoid activity.


Q: What are the common clinical findings when Hydrocortisone starts to take effect?

The onset of effect depends on the form of the drug and the purpose of the treatment. Official patient information describes that for inflammatory conditions, expected signs of action often include a reduction in inflammatory markers, such as redness, itching, and swelling. Improvement is also commonly assessed by objective clinical severity scores or patient-reported outcomes regarding functional status.


Q: What precautions are described for people with diabetes when taking Hydrocortisone?

Regulatory information indicates that patients with diabetes or a predisposition to high blood sugar should use Hydrocortisone cautiously. Official documentation indicates that increased monitoring of blood glucose levels and potential adjustment of antidiabetic medication dosage may be required, as Hydrocortisone is associated with potentially lower carbohydrate tolerance.


Q: Can Hydrocortisone cause mood changes?

Yes, official documents describe that the use of Hydrocortisone may be associated with psychiatric disturbances. These documented effects can include changes in mood, ranging from euphoria and insomnia to severe depression, and potentially worsening existing emotional instability.


Q: Do official sources describe long-term risks associated with Hydrocortisone?

Yes, official documents describe several risks associated with prolonged systemic use of Hydrocortisone. These include suppression of the HPA (Hypothalamic-Pituitary-Adrenal) axis, the development of cataracts and glaucoma, fluid/electrolyte disturbances, and an increased risk of osteoporosis and growth suppression in children.


Q: Why is Hydrocortisone used in different forms (tablets, ointment, injections)?

Hydrocortisone is produced in diverse forms to achieve different treatment goals and administration routes. Topical forms, such as ointment or cream, are used for localized treatment of skin inflammation. Oral tablets are for systemic treatment or replacement therapy, while injection solutions are reserved for rapid systemic action in acute or emergency situations.


Q: What common skin problems is Hydrocortisone ointment typically used for?

Topical Hydrocortisone is officially indicated to reduce redness, swelling, itching, and discomfort caused by various corticosteroid-responsive skin conditions. Examples of conditions for which it is studied and indicated include specific types of eczema (atopic dermatitis), psoriasis, and contact dermatitis.


Q: Can Hydrocortisone cause sleep problems?

Yes, insomnia (difficulty sleeping) is listed in official sources as one of the commonly documented adverse reactions associated with Hydrocortisone. Other documented effects on the central nervous system may also contribute to altered sleep quality.


Q: What is 'withdrawal syndrome' after using Hydrocortisone?

Official documents describe this effect primarily as the risk of acute adrenal insufficiency that can occur after abrupt discontinuation of systemic therapy. Since Hydrocortisone suppresses the body's natural cortisol production, stopping it suddenly can lead to a deficiency, necessitating that the dosage is generally reduced gradually under medical guidance.


Q: Does taking Hydrocortisone affect body weight?

Yes, official sources describe that systemic Hydrocortisone may contribute to changes in body weight. This is attributed to potential effects such as increased appetite, fluid retention, and the potential development of abnormal fat deposition (a Cushingoid state).


Q: Which organs can be affected by long-term use of Hydrocortisone?

Prolonged systemic use of Hydrocortisone can affect multiple organ systems. These include the endocrine system (HPA axis suppression), the eyes (cataracts, glaucoma), the musculoskeletal system (osteoporosis, muscle weakness), the cardiovascular system (hypertension), and the digestive tract (peptic ulceration).


Q: For what adrenal gland diseases is Hydrocortisone prescribed?

Hydrocortisone is officially indicated as a drug of choice for replacement therapy in cases of primary or secondary adrenal insufficiency. It is also prescribed for the management of congenital adrenal hyperplasia, a condition where the adrenal glands do not produce sufficient natural cortisol.


Q: Why might doctors prescribe Hydrocortisone for non-rheumatic inflammations?

Hydrocortisone is prescribed for a variety of non-rheumatic inflammatory conditions due to its powerful anti-inflammatory and immunosuppressive properties. Official indications include management of various dermatologic diseases, severe allergic conditions, and inflammatory ophthalmic (eye) disorders.


Q: What is the difference between Hydrocortisone for injection and tablets?

The main difference is the route of administration and speed of action. Tablets are for oral (systemic) intake or maintenance replacement therapy. The injectable form (intravenous or intramuscular) is reserved for rapid systemic action in acute and urgent situations that require an immediate physiological response.


Q: Can Hydrocortisone affect vision?

Yes, official sources describe that long-term systemic use of Hydrocortisone is associated with the risk of developing posterior subcapsular cataracts and glaucoma. Additionally, blurred vision is listed among the adverse reactions that warrant clinical evaluation.


Q: Are there special dietary guidelines while taking Hydrocortisone?

In some cases, a clinician may recommend that patients on systemic Hydrocortisone adhere to a diet that is low in sodium and high in potassium or calcium. Furthermore, official product information indicates that patients taking Hydrocortisone tablets should avoid consuming grapefruit or grapefruit juice.


Q: Can Hydrocortisone interact with alcohol?

While official recommendations often do not prohibit alcohol consumption, alcohol may exacerbate some Hydrocortisone side effects, such as dizziness or fatigue. In official documents, it is noted that individuals should avoid operating vehicles or machinery if side effects cause impairment.


Q: What is 'topical' Hydrocortisone and how does it differ from 'oral'?

Topical Hydrocortisone (cream, ointment) is applied directly to the skin for localized action, primarily to treat inflammation and itching. Oral (systemic) Hydrocortisone (tablets) is taken by mouth to affect the entire body for systemic diseases or as hormone replacement therapy.


Q: Can Hydrocortisone impair wound healing?

Yes, official documents list impaired wound healing as a possible dermatological adverse effect of systemic Hydrocortisone. Additionally, topical forms are generally advised against being applied to open wounds or damaged skin.


Q: How is the role of Hydrocortisone in replacement therapy described?

Hydrocortisone's role in replacement therapy is derived from the fact that it is chemically identical to the body's natural hormone, cortisol. It is used to substitute this essential hormone when the adrenal glands produce insufficient amounts, helping to sustain critical metabolic and circulatory functions necessary for life.


Q: Can Hydrocortisone affect bone density?

Yes, official sources describe that long-term systemic use of Hydrocortisone may increase the risk of osteoporosis (reduced bone density) and associated fractures. Corticosteroids are known to potentially decrease the formation of new bone tissue and increase the rate at which bone is broken down.


Q: Are there warnings for people with gastrointestinal tract diseases taking Hydrocortisone?

Official sources advise caution when prescribing systemic Hydrocortisone to patients with certain gastrointestinal tract diseases, such as active or latent peptic ulcers, diverticulitis, or nonspecific ulcerative colitis. This caution is due to the potential risk of perforation or other serious complications.


Q: In which cases have studies not confirmed a significant benefit of Hydrocortisone?

Studies examining Hydrocortisone for severe systemic inflammation, such as septic shock, have yielded mixed results, and large-scale clinical trials have not consistently confirmed a reduction in long-term mortality. Furthermore, long-term research directly comparing different replacement therapy regimens remains limited in its scope.


Q: How is Hydrocortisone classified in terms of prescription status?

Systemic forms of Hydrocortisone, such as tablets and injections, are typically classified as prescription-only (Rx) medications. However, topical creams or ointments containing low concentrations may be available over-the-counter (OTC) in certain jurisdictions, depending on specific national regulations and concentration limits.


Q: Why is Hydrocortisone sometimes used to reduce swelling?

Hydrocortisone has a potent anti-inflammatory action. According to its mechanism of action described in official documents, this includes decreasing the permeability of capillaries. This action restricts the accumulation of fluid in the tissues outside of blood vessels, which in turn helps to reduce swelling and puffiness (edema).

How should Гидрокортизон be stored and disposed of?

How to Store and Dispose of Hydrocortisone

Hydrocortisone must be stored according to specific regulatory requirements to maintain its stability and effectiveness.

Official Storage Requirements

Storage Component Requirement
Temperature Store at controlled room temperature, typically 20 C to 25 C (68 F to 77 F).
Protection Must be protected from freezing and stored away from excess heat.
Container Keep the container tightly closed; store away from moisture.
Child Safety Keep this and all drugs out of the reach of children.

Disposal Guidance

Disposal must follow formal regulatory procedures. The safest method is to use a drug take-back program. If a take-back program is unavailable, the unused medication must be removed from its original container, mixed with an undesirable substance like coffee grounds, sealed in a bag or container, and discarded in the household trash. The product must not be flushed down the toilet or sink.

Attention! Always consult to a doctor or pharmacist before using pills or medicines.

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