Clinical and pharmacological group: & nbsp

Glucocorticosteroids

Ophthalmic products

Included in the formulation
  • Hydrocortisone
    ointment externally 
  • Hydrocortisone
    ointment d / eye 
  • Hydrocortisone
    ointment locally 
  • Hydrocortisone
    ointment d / eye 
    SYNTHESIS, OJSC     Russia
  • Hydrocortisone
    suspension w / m in / Sust. 
    FARMAK, JSC     Ukraine
  • Hydrocortisone
    ointment d / eye 
    VALEANT, LLC     Russia
  • Hydrocortisone
    ointment externally 
    AKRIKHIN HFK, JSC     Russia
  • Hydrocortisone
    ointment externally 
    SYNTHESIS, OJSC     Russia
  • Hydrocortisone
    ointment externally 
  • Hydrocortisone
    ointment externally 
  • Hydrocortisone
    ointment externally 
    BIOSINTEZ, PAO     Russia
  • Hydrocortisone
    ointment externally 
    NIZHFARM, JSC     Russia
  • Hydrocortisone
    ointment externally 
    ATOLL, LLC     Russia
  • Hydrocortisone-POS®
    ointment d / eye 
  • Cortef®
    pills inwards 
    Pfizer Inc.     USA
  • Laticort®
    ointment externally 
    VALEANT, LLC     Russia
  • Laticort®
    cream externally 
    VALEANT, LLC     Russia
  • Laticort®
    solution externally 
    VALEANT, LLC     Russia
  • Lokoid®
    cream externally 
    Astellas Farma Europe BV     Netherlands
  • Lokoid®
    ointment externally 
  • Lokoid Creole®
    emulsion externally 
    Astellas Farma Europe BV     Netherlands
  • Lokoid Lipocream®
    cream externally 
    Astellas Farma Europe BV     Netherlands
  • Solu-Cortef®
    lyophilizate w / m in / in 
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    Minimal chemist's assortment

    ONLS

    АТХ:

    S.01.B.A.02   Hydrocortisone

    H.02.A.B.09   Hydrocortisone

    D.07.A.A.02   Hydrocortisone

    Pharmacodynamics:

    By inhibition of phospholipase A activity2 and reducing the release of arachidonic acid from the phospholipids of cell membranes reduces the production of leukotrienes and prostaglandins. Due to this suppresses the development of inflammatory manifestations: pain, swelling, fever and redness in the area of ​​inflammation. It inhibits the expression of the cyclooxygenase-2 gene, which also leads to inhibition of prostaglandin synthesis.

    Reduces the main substance of the connective tissue, weakening the exudative and proliferative processes in the skin. Inhibits cellular kinins, which have proteolytic activity. Prevents the access of macrophages and T-sensitized lymphocytes to the foci of inflammation.

    It has anti-inflammatory, anti-edematous and anti-allergic effect.

    Pharmacokinetics:

    After intravenous administration the maximum concentration in the blood plasma is reached after 1 hour. With intramuscular injection, absorption takes place within 24-48 hours. When intraarticular administration is absorbed slowly, within 6-24 hours. The connection with plasma proteins is 90%.

    Therapeutic effect develops in 6-24 hours. Penetrates through the blood-brain and placental barrier. Metabolism in the liver.

    The half-life is 6-7 days. Elimination by the kidneys.

    When using ophthalmic ointment systemic action on the body does not have.

    Indications:

    It is used for relief of acute allergic reactions, treatment of shock and coma of various genesis, acute leukemia in children, nephrotic syndrome, tuberculous meningitis, acute manifestations of multiple sclerosis.

    It is used to treat osteoarthritis, monoarthrosis, rheumatoid arthritis, bronchial asthma, bursitis, epicondylitis, tendovaginitis. Used for contractures, before surgical treatment of ankylosed joints, as well as in the tuberculostatic therapy.

    In ophthalmology it is used for the treatment of blepharitis, keratitis, iritis, iridocyclitis, in conditions after the operation.

    I.A15-A19.A15   Tuberculosis of respiratory organs, confirmed bacteriologically and histologically

    I.A15-A19.A17.0   Tuberculous meningitis (G01 *)

    I.A15-A19.A18   Tuberculosis of other organs

    I.B65-B83.B75   Trichinosis

    II.C81-C96.C84.0   Mushroom mycosis

    II.C81-C96.C91.0   Acute lymphoblastic leukemia

    II.C81-C96.C92.0   Acute myeloid leukemia

    III.D55-D59.D59   Acquired hemolytic anemia

    III.D60-D64.D60   Acquired pure red cell aplasia (erythroblastopenia)

    III.D65-D69.D69.3   Idiopathic thrombocytopenic purpura

    III.D80-D89.D86   Sarcoidosis

    IV.E00-E07.E06   Thyroiditis

    IV.E20-E35.E27.4   Other and unspecified adrenocortical insufficiency

    VII.H10-H13.H10.1   Acute atopic conjunctivitis

    VII.H10-H13.H10.2   Other acute conjunctivitis

    VII.H10-H13.H10.4   Chronic conjunctivitis

    VII.H10-H13.H10.5   Blepharoconjunctivitis

    VII.H15-H22.H16   Keratite

    VII.H15-H22.H16.2   Keratoconjunctivitis

    VII.H15-H22.H20.0   Acute and subacute iridocyclitis

    VII.H15-H22.H20.1   Chronic iridocyclitis

    X.J40-J47.J45   Asthma

    X.J40-J47.J46   Asthmatic status [status asthmaticus]

    X.J60-J70.J69   Pneumonitis caused by solids and liquids

    X.J80-J84.J82   Pulmonary eosinophilia, not elsewhere classified

    XI.K50-K52.K50   Crohn's disease [regional enteritis]

    XI.K50-K52.K51   Ulcerative colitis

    XII.L10-L14.L10   Pemphigus [pemphigus]

    XII.L10-L14.L13.0   Dermatitis herpetiformis

    XII.L20-L30.L20.8   Other atopic dermatitis

    XII.L20-L30.L21   Seborrheic dermatitis

    XII.L20-L30.L26   Exfoliative dermatitis

    XII.L20-L30.L28.0   Simple chronic lichen

    XII.L20-L30.L28.1   Scabby nodosum

    XII.L20-L30.L30.0   Coin-like eczema

    XII.L40-L45.L40   Psoriasis

    XII.L40-L45.L43   Lichen red flat

    XII.L50-L54.L51.1   Bullous erythema multiforme

    XIII.M30-M36.M30   Nodular polyarteritis and related conditions

    XIII.M30-M36.M32   Systemic lupus erythematosus

    XIII.M30-M36.M33   Dermatopolymiositis

    XIII.M30-M36.M34   Systemic sclerosis

    XIV.N00-N08.N04   Nephrotic syndrome

    XVIII.R50-R69.R57.0   Cardiogenic shock

    XVIII.R50-R69.R57.1   Hypovolemic shock

    XVIII.R50-R69.R57.8   Other types of shock

    XIX.S00-S09.S05   Injury of the eye and orbit

    XIX.T66-T78.T78.2   Anaphylactic shock, unspecified

    XIX.T66-T78.T78.3   Angioedema

    XIX.T79.T79.4   Traumatic shock

    XXI.Z40-Z54.Z51.5   Palliative Care

    Contraindications:

    At rendering of the help under vital indications - hypersensitivity.

    Syndrome Itenko-Cushing, thrombophilia, Achilles tendon lesions, systemic infection, individual intolerance.

    With intraarticular administration: intraarticular fracture of bones, infectious arthritis, infectious osteoporosis, severe deformation and destruction of the joint, aseptic necrosis of the epiphyses of bones.

    Children up to 12 months.

    Carefully:

    Chronic heart failure, osteoporosis, gastric and duodenal ulcer, diabetes mellitus, arterial hypertension, herpetic infection, glaucoma, measles, epilepsy, steroid myelopathy, hypersensitivity.

    Pregnancy and lactation:

    Recommendations for FDA - Category C. Contraindicated in pregnancy and lactation.

    Dosing and Administration:

    Use in children

    In acute, life threatening conditions: intravenously or intramuscularly 1-2 mg / kg every 4 hours. The daily dose is 6-9 mg / kg.

    Periarticular, single dose:

    2-6 years: 25-50 mg;

    7-14 years: 50-75 mg.

    Adults

    Intramuscularly deep, from 50-300 mg to 1-1,5 g per day. In diseases of the respiratory system no more than 3 days. In rheumatology - no more than 6 days.

    According to vital indications: intravenously or deeply intramuscularly, 100-15 mg every 4 hours for 48 hours, then - every 8-12 hours.

    Periarticular, single dose is from 5 to 25 mg.

    The highest daily dose: 1-1.5 g.

    The highest single dose: 300 mg.

    Side effects:

    Central and peripheral nervous system: agitation, headache, dizziness, anxiety, insomnia, irritability, depression, paranoia, hallucinations, pseudotumor cerebellum,edema of the nipple of the optic nerve due to increased intracranial pressure.

    Hemopoietic system: leukocytosis, leukocyturia.

    The cardiovascular system: arterial hypertension, arrhythmia, peripheral vasodilation, cardiac insufficiency, thromboembolism.

    Digestive system: nausea, vomiting, peptic ulcer, pancreatitis, esophagitis, increased appetite, hiccups, flatulence.

    Musculoskeletal system: osteoporosis, rarely - pathological bone fractures, aseptic necrosis of the head of the femoral and humerus, steroid myopathy, arthralgia, decrease in muscle mass, rupture of the tendons of muscles.

    Dermatological reactions: hyperhidrosis, folliculitis, telangiectasia, striae, steroid acne, petechiae, ecchymosis, hypopigmentation.

    Sense organs: glaucoma, exophthalmos, optic nerve damage, posterior capsular cataract, secondary eye infections, trophic corneal changes.

    Endocrine system: a decrease in glucose tolerance, diabetes mellitus, Itenko-Cushing syndrome, suppression of adrenal cortex function, growth retardation in children and adolescents.

    The immune system: exacerbation of chronic infections, exacerbation of tuberculosis, pyoderma and candidiasis.

    Allergic reactions.

    Overdose:

    Arterial hypertension, arthralgia, hypokalemia.

    Treatment is symptomatic.

    Interaction:

    Enhances the effect of anticoagulants.

    Increases the toxicity of cardiac glycosides, barbiturates.

    Enhances the hepatotoxic effect of paracetamol.

    Reduces the effect of somatotropin, oral hypoglycemic drugs, praziquantel.

    Mifepristone, thyroid hormones, estrogens, inhibitors of the adrenal cortex reduce the effect of hydrocortisone.

    When used simultaneously with loop diuretics, carbonic anhydrase inhibitors, amphotericin B, theophylline, the risk of hypokalemia is increased.

    With simultaneous application with salicylates, the risk of developing gastric and duodenal ulcers increases, as well as hemorrhage.

    When used simultaneously with carbonic anhydrase inhibitors, the risk of developing osteoporosis increases.

    The use of tricyclic antidepressants for the treatment of hydrocortisone-induced depression exacerbates mental disorder.

    Special instructions:

    Control of blood pressure, coagulation and the composition of peripheral blood, the concentration of glucose in the blood plasma.

    It is recommended to postpone vaccination for the duration of treatment.

    When treating joints, it is not recommended to administer the drug more than 3 times a year.

    In the treatment it is not recommended to drive vehicles and work with moving mechanisms.

    Instructions
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