Clinical and pharmacological group: & nbsp

Sulfonamides

Included in the formulation
  • Sulfadimezine
    pills inwards 
    IRBITSK HFZ, OJSC     Russia
  • Sulfadimethoxin
    pills inwards 
    BIOCHEMIST, OJSC     Russia
  • Sulfadimethoxin
    pills inwards 
  • Sulfadimethoxin
    pills inwards 
    BIOSINTEZ, PAO     Russia
  • Sulfadimethoxin
    pills inwards 
    IRBITSK HFZ, OJSC     Russia
  • АТХ:

    J.01.E.D.   Sulfonilamides of long duration

    Pharmacodynamics:

    Structural analogue of PABA, necessary for microorganisms for the synthesis of dihydrofolic acid. Competitive blockade of dihydropteroate synthetase of bacteria: disruption of the synthesis of dihydropteroic acid (precursor of tetrahydrofolic acid - cofactor of purine synthesis). Only those microorganisms that are forced to synthesize folic acid themselves are sensitive.

    Pharmacokinetics:

    Absorption is fast. Distribution is good, weakly penetrates the BBB, but increases with meningitis. The connection with plasma proteins is 90-99%. Biotransformation in the liver (glucuronidation, acetylation). Elimination of kidneys in the form of metabolites (20-44% within 24 hours, after 48 hours - up to 56%, after 96 hours - up to 83.3%).

    Indications:

    Infectious-inflammatory diseases caused by microorganisms sensitive to sulfadimethoxin, incl. angina, sinusitis, otitis media, bronchitis, dysentery, inflammatory diseases of the bile and urinary tract, erysipelas, wound infections, trachoma.

    I.A00-A09.A03.9   Shigellosis, unspecified

    I.A30-A49.A46   Erys

    I.A70-A74.A71   Trachoma

    VIII.H65-H75.H66   Purulent and unspecified otitis media

    X.J00-J06.J01   Acute Sinusitis

    X.J00-J06.J02   Acute pharyngitis

    X.J00-J06.J03   Acute tonsillitis

    X.J20-J22.J20   Acute bronchitis

    XI.K80-K87.K81.0   Acute cholecystitis

    XI.K80-K87.K81.1   Chronic cholecystitis

    XI.K80-K87.K83.0   Cholangitis

    XIV.N10-N16.N10   Acute tubulointerstitial nephritis

    XIV.N10-N16.N11   Chronic tubulointerstitial nephritis

    XIV.N30-N39.N30   Cystitis

    XIV.N30-N39.N34   Urethritis and urethral syndrome

    XIV.N40-N51.N41   Inflammatory diseases of the prostate

    XIX.T79.T79.3   Post-traumatic wound infection, not elsewhere classified

    Contraindications:

    Hypersensitivity, oppression of bone marrow hematopoiesis, renal / hepatic insufficiency, CHF, congenital deficiency G-6-PD, porphyria, azotemia, pregnancy.

    Carefully:

    Allergy to other medicines containing a sulfonamide moiety; CRF, hepatic insufficiency, bronchial asthma, systemic lupus erythematosus, G-6-FD deficiency, age up to 2 months, HIV infection, AIDS (systemic use).

    Pregnancy and lactation:

    Adequate and well-controlled studies in humans and animals have not been conducted. Do not apply! There is no information on the penetration into breast milk. Do not apply!

    The category of FDA recommendations is not defined.

    Dosing and Administration:

    Adults on the 1st day of treatment - 1 g, in subsequent days - 500 mg / day. In severe disease, the dose may be increased. Children on the first day of treatment - 25 mg / kg, in the following days - 12.5 mg / kg / day.

    Take 1 time / day after meals. Duration of treatment 7-10 days.

    Side effects:

    From the side of the central nervous system: a headache is possible.

    On the part of the digestive system: dyspeptic symptoms, nausea, vomiting, cholestatic hepatitis.

    Allergic reactions: skin rashes, drug fever.

    From the hemopoietic system: rarely - leukopenia, agranulocytosis.

    Overdose:

    Oppression of bone marrow hematopoiesis: leukopenia, agranulocytosis, infection.

    Treatment is symptomatic.

    Interaction:

    Cimetidine - increases the risk of developing leukopenia.

    Special instructions:

    During treatment, an abundant alkaline drink is recommended, monitoring the blood and urine.

    It is applied externally as a part of combined preparations.

    Parts of the body treated with the drug are recommended to protect from direct sunlight.

    Instructions
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