Wilprafen® (Tablets, Granules) Instructions for Use
ATC Code
J01FA07 (Josamycin)
Active Substance
Josamycin (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Antibiotic of the macrolide group
Pharmacotherapeutic Group
Antibiotic-macrolide
Pharmacological Action
An antibiotic of the macrolide group. It exerts a bacteriostatic effect by inhibiting bacterial protein synthesis. When high concentrations are achieved at the site of inflammation, it exerts a bactericidal effect.
It is highly active against intracellular microorganisms: Chlamydia trachomatis and Chlamydia pneumoniae, Mycoplasma pneumoniae, Mycoplasma hominis, Ureaplasma urealyticum, Legionella pneumophila; against gram-positive aerobic bacteria: Staphylococcus aureus, Streptococcus pyogenes and Streptococcus pneumoniae (pneumococcus), Corynebacterium diphtheriae; gram-negative aerobic bacteria: Neisseria meningitidis, Neisseria gonorrhoeae, Haemophilus influenzae, Bordetella pertussis; against some anaerobic bacteria: Peptococcus, Peptostreptococcus, Clostridium perfringens.
Josamycin is also active against Treponema pallidum.
Pharmacokinetics
After oral administration, Josamycin is rapidly absorbed from the gastrointestinal tract. Cmax is reached 1-2 hours after administration. Forty-five minutes after a 1 g dose, the average plasma concentration of josamycin is 2.41 mg/L.
Binding to plasma proteins does not exceed 15%.
Steady state is achieved after 2-4 days of regular administration.
Josamycin is well distributed in the body and accumulates in various tissues: in the lung tissue, lymphatic tissue of the palatine tonsils, organs of the urinary system, skin, and soft tissues. Particularly high concentrations are found in the lungs, tonsils, saliva, sweat, and tear fluid. The concentration of josamycin in human polymorphonuclear leukocytes, monocytes, and alveolar macrophages is approximately 20 times higher than in other cells of the body.
Josamycin is biotransformed in the liver to less active metabolites.
It is excreted mainly in the bile; excretion in the urine is less than 20%.
Indications
Treatment of infectious and inflammatory diseases caused by microorganisms sensitive to josamycin: infections of the upper respiratory tract and ENT organs (including pharyngitis, tonsillitis, peritonsillitis, otitis media, sinusitis, laryngitis); diphtheria (as an adjunct to treatment with diphtheria antitoxin); scarlet fever (in case of hypersensitivity to penicillin); infections of the lower respiratory tract (including acute bronchitis, bronchopneumonia, pneumonia, including atypical forms, whooping cough, psittacosis); oral infections (including gingivitis and periodontal diseases); skin and soft tissue infections (including pyoderma, furuncles, anthrax, erysipelas /in case of hypersensitivity to penicillin/, acne, lymphangitis, lymphadenitis); infections of the urinary tract and genital organs (including urethritis, prostatitis, gonorrhea; in case of hypersensitivity to penicillin – syphilis, venereal lymphogranuloma); chlamydial, mycoplasmal (including ureaplasmal) and mixed infections of the urinary tract and genital organs.
ICD codes
| ICD-10 code | Indication |
| A22 | Anthrax |
| A36 | Diphtheria |
| A37 | Whooping cough |
| A46 | Erysipelas |
| L70 | Acne |
| A38 | Scarlet fever |
| A48.1 | Legionnaires' disease |
| A50 | Congenital syphilis |
| A51 | Early syphilis |
| A52 | Late syphilis |
| A54 | Gonococcal infection |
| A55 | Chlamydial lymphogranuloma (venereum) |
| A56.0 | Chlamydial infections of lower genitourinary tract |
| A56.1 | Chlamydial infections of pelvic organs and other genitourinary organs |
| A56.4 | Chlamydial pharyngitis |
| A70 | Infection due to Chlamydia psittaci (psittacosis) |
| B96.0 | Mycoplasma pneumoniae [M. pneumoniae] as the cause of diseases classified in other chapters |
| H66 | Suppurative and unspecified otitis media |
| I88 | Nonspecific lymphadenitis |
| I89.1 | Lymphangitis |
| J01 | Acute sinusitis |
| J02 | Acute pharyngitis |
| J03 | Acute tonsillitis |
| J04 | Acute laryngitis and tracheitis |
| J15 | Bacterial pneumonia, not elsewhere classified |
| J15.7 | Pneumonia due to Mycoplasma pneumoniae |
| J16.0 | Pneumonia due to chlamydia |
| J20 | Acute bronchitis |
| J31.2 | Chronic pharyngitis |
| J32 | Chronic sinusitis |
| J35.0 | Chronic tonsillitis |
| J37 | Chronic laryngitis and laryngotracheitis |
| J42 | Unspecified chronic bronchitis |
| K05 | Gingivitis and periodontal diseases |
| K12 | Stomatitis and related lesions |
| L01 | Impetigo |
| L02 | Cutaneous abscess, furuncle and carbuncle |
| L03 | Cellulitis |
| L08.0 | Pyoderma |
| L08.8 | Other specified local infections of skin and subcutaneous tissue |
| N10 | Acute tubulointerstitial nephritis (acute pyelonephritis) |
| N11 | Chronic tubulointerstitial nephritis (chronic pyelonephritis) |
| N30 | Cystitis |
| N34 | Urethritis and urethral syndrome |
| N41 | Inflammatory diseases of prostate |
| N45 | Orchitis and epididymitis |
| N70 | Salpingitis and oophoritis |
| N71 | Inflammatory disease of uterus, excluding cervix (including endometritis, myometritis, metritis, pyometra, uterine abscess) |
| N72 | Inflammatory disease of cervix uteri (including cervicitis, endocervicitis, exocervicitis) |
| T79.3 | Posttraumatic wound infection, not elsewhere classified |
| ICD-11 code | Indication |
| 1A60.Z | Congenital syphilis, unspecified |
| 1A61.Z | Early syphilis, unspecified |
| 1A62.Z | Late syphilis, unspecified |
| 1A7Z | Gonococcal infection, unspecified |
| 1A80 | Chlamydial lymphogranuloma |
| 1A81.0 | Chlamydial infection of lower genitourinary tract |
| 1A81.1 | Chlamydial infection of internal reproductive organs |
| 1A81.Y | Chlamydial infection without ulceration, sexually transmitted, of other specified site |
| 1B50 | Scarlet fever |
| 1B70.0Z | Erysipelas, unspecified |
| 1B70.1 | Streptococcal cellulitis of the skin |
| 1B70.2 | Staphylococcal cellulitis of the skin |
| 1B70.Z | Bacterial cellulitis or lymphangitis caused by unspecified bacterium |
| 1B72.0 | Bullous impetigo |
| 1B72.1 | Nonbullous impetigo |
| 1B72.Z | Impetigo, unspecified |
| 1B75.0 | Furuncle |
| 1B75.1 | Carbuncle |
| 1B75.2 | Furunculosis |
| 1B75.3 | Pyogenic skin abscess |
| 1B7Y | Other specified pyogenic bacterial infections of skin or subcutaneous tissue |
| 1B97 | Anthrax |
| 1C12.Z | Whooping cough, unspecified |
| 1C17.Z | Diphtheria, unspecified |
| 1C19.Z | Legionellosis, unspecified |
| 1C22 | Infection due to Chlamydia psittaci |
| 1C44 | Non-pyogenic bacterial infections of skin |
| AA9Z | Unspecified suppurative otitis media |
| BD90.Z | Lymphadenitis, unspecified |
| BD91 | Lymphangitis |
| CA01 | Acute rhinosinusitis |
| CA02.Z | Acute pharyngitis, unspecified |
| CA03.Z | Acute tonsillitis, unspecified |
| CA05 | Acute laryngitis or tracheitis |
| CA09.2 | Chronic pharyngitis |
| CA0A.Z | Chronic rhinosinusitis, unspecified |
| CA0F.Y | Other specified chronic diseases of the palatine tonsils and adenoids |
| CA0G | Chronic laryngitis or laryngotracheitis |
| CA20.1Z | Chronic bronchitis, unspecified |
| CA40.00 | Pneumonia due to Chlamydophila pneumoniae |
| CA40.04 | Pneumonia due to Mycoplasma pneumoniae |
| CA40.0Z | Bacterial pneumonia, unspecified |
| CA42.Z | Acute bronchitis, unspecified |
| DA01.Z | Diseases of the oral mucosa, unspecified |
| DA0B.Z | Gingival diseases, unspecified |
| DA0C.Z | Periodontal diseases, unspecified |
| DA0Z | Diseases or disorders of the orofacial complex, unspecified |
| EA50.3 | Staphylococcal scarlet fever |
| EB21 | Pyoderma gangrenosum |
| ED80.Z | Acne, unspecified |
| GA01.Z | Inflammatory diseases of uterus, except cervix, unspecified |
| GA07.Z | Salpingitis and oophoritis, unspecified |
| GA91.Z | Inflammatory and other diseases of prostate, unspecified |
| GB02.Z | Orchitis or epididymitis, unspecified |
| GB50 | Acute tubulo-interstitial nephritis |
| GB51 | Acute pyelonephritis |
| GB55.Z | Chronic tubulo-interstitial nephritis, unspecified |
| GB5Z | Renal tubulo-interstitial diseases, unspecified |
| GC00.Z | Cystitis, unspecified |
| GC02.Z | Urethritis and urethral syndrome, unspecified |
| NF0A.3 | Posttraumatic wound infection, not elsewhere classified |
| XN4NV | Mycoplasma pneumoniae |
| GA0Z | Inflammatory diseases of female genital tract, unspecified |
| XA5WW1 | Cervix uteri |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer the drug orally.
For adults and children over 14 years, the total daily dose is 1-2 g.
Divide the total daily dose into 2-3 doses.
For children under 14 years, calculate the dose based on body weight.
The total daily dose for children is 30-50 mg per kg of body weight.
Divide the total daily dose for children into 3 equal doses.
For severe infections, increase the total daily dose for adults to 2-3 g.
In severe infections, divide the higher dose into 2-3 doses.
For the treatment of sexually transmitted infections like urethritis, administer a single dose of 1-2 g.
For gonorrhea, take a single dose of 1 g.
For syphilis, the total daily dose is 1.5-2 g divided into 2-3 doses.
The typical treatment duration for syphilis is 10-15 days.
For chlamydial, mycoplasmal, and ureaplasmal infections, the typical treatment course is 7-14 days.
For streptococcal infections, continue treatment for at least 10 days to prevent complications.
Take the tablets or granules between meals for optimal absorption.
Adhere strictly to the prescribed dosage and duration of therapy.
Do not discontinue treatment prematurely, even if symptoms improve.
In patients with renal impairment, adjust the dosage based on creatinine clearance values.
For patients with severe renal insufficiency, reduce the dosing frequency or the total daily dose.
Adverse Reactions
From the digestive system rarely – loss of appetite, nausea, heartburn, vomiting, diarrhea, pseudomembranous colitis; in some cases – increased activity of liver transaminases, impaired bile flow, and jaundice.
Allergic reactions rarely – urticaria.
Other in some cases – dose-dependent transient hearing impairment.
Contraindications
Severe liver dysfunction, hypersensitivity to josamycin and other antibiotics of the macrolide group.
Use in Pregnancy and Lactation
Use during pregnancy and lactation is only possible in cases where the intended benefit to the mother outweighs the potential risk to the fetus or child.
When treating with macrolides and simultaneously using hormonal contraceptives, non-hormonal contraceptive methods should be additionally used.
Use in Hepatic Impairment
Contraindicated in severe liver dysfunction.
Use in Renal Impairment
In patients with renal insufficiency, dose adjustment is required according to the creatinine clearance values.
Pediatric Use
Josamycin is not prescribed to premature infants. When used in newborns, liver function should be monitored.
Special Precautions
In case of pseudomembranous colitis development, Josamycin should be discontinued and appropriate therapy instituted. Drugs that reduce intestinal motility are contraindicated.
In patients with renal insufficiency, dose adjustment is required according to the creatinine clearance values.
Josamycin is not prescribed to premature infants. When used in newborns, liver function should be monitored.
The possibility of cross-resistance to various antibiotics of the macrolide group should be considered (for example, microorganisms resistant to treatment with chemically related antibiotics may also be resistant to josamycin).
Drug Interactions
Bacteriostatic antibiotics may reduce the bactericidal effect of other antibiotics, such as penicillins and cephalosporins (concomitant use of josamycin with penicillins and cephalosporins should be avoided).
With simultaneous use of josamycin and lincomycin, the effectiveness of both drugs may be reduced.
Josamycin slows the elimination of theophylline to a lesser extent than other macrolide antibiotics.
Josamycin slows the elimination of terfenadine or astemizole, which increases the risk of life-threatening arrhythmias.
There are isolated reports of an increased vasoconstrictor effect with the simultaneous use of macrolide antibiotics and ergot alkaloids. One case of ergotamine intolerance during josamycin administration has been reported.
With simultaneous use of josamycin and cyclosporine, an increase in the plasma concentration of cyclosporine up to nephrotoxic levels is possible.
With simultaneous use of josamycin and digoxin, an increase in the plasma level of the latter is possible.
In rare cases, during treatment with macrolides, the contraceptive effect of hormonal contraceptives may be insufficient.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Granules for the preparation of an oral suspension 125 mg/5 ml: 15 g bottle
Granules for the preparation of an oral suspension 250 mg/5 ml: 15 g bottle
Granules for the preparation of an oral suspension 500 mg/5 ml: bottle
Marketing Authorization Holder
Astellas Pharma Europe B.V. (Netherlands)
Manufactured By
Famar Lyon (France)
Dosage Forms
| Wilprafen® | Granules for the preparation of an oral suspension 125 mg/5 ml: 15 g bottle | |
| Granules for the preparation of an oral suspension 250 mg/5 ml: 15 g bottle | ||
| Granules for the preparation of an oral suspension 500 mg/5 ml: bottle |
Dosage Form, Packaging, and Composition
Granules for the preparation of an oral suspension white, with a strawberry odor; after dissolving in water, it forms a white suspension with a strawberry odor.
| 1 bottle | |
| Josamycin propionate | 1.577 g |
Excipients : sodium citrate – 0.1125 g, methylparahydroxybenzoate – 0.0795 g, propylparahydroxybenzoate – 0.0105 g, simethicone – 0.075 g, hypromellose – 0.18 g, Avicel RC-591[microcrystalline cellulose, sodium carboxymethylcellulose] – 0.57 g, strawberry flavor – 0.0375 g, powdered starch sugar – 10.108 g, mannitol – 2.25 g.
5 ml of the prepared suspension contains 125 mg of josamycin.
15 g – Colorless glass bottles with a capacity of 100 ml (1) (complete with a dosing syringe and syringe holder) – cardboard boxes.
Granules for the preparation of an oral suspension pink, with a strawberry odor; after dissolving in water, it forms a pink suspension with a strawberry odor.
| 1 bottle | |
| Josamycin propionate | 3.1545 g |
Excipients : sodium citrate – 0.1125 g, methylparahydroxybenzoate – 0.0795 g, propylparahydroxybenzoate – 0.0105 g, simethicone – 0.075 g, hypromellose – 0.225 g, Avicel RC-591[microcrystalline cellulose, sodium carboxymethylcellulose] – 1.2 g, strawberry flavor – 0.0375 g, canthaxanthin 10% – 0.0075 g, powdered starch sugar – 7.848 g, mannitol – 2.25 g.
5 ml of the prepared suspension contains 250 mg of josamycin.
15 g – Colorless glass bottles with a capacity of 100 ml (1) (complete with a dosing syringe and syringe holder) – cardboard boxes.
Granules for the preparation of an oral suspension yellow, with a strawberry odor; after dissolving in water, it forms a yellow suspension with a strawberry odor.
| 1 bottle | |
| Josamycin propionate | 6.307 g |
Excipients : sodium citrate – 0.1125 g, methylparahydroxybenzoate – 0.0795 g, propylparahydroxybenzoate – 0.0105 g, simethicone – 0.075 g, hypromellose – 0.3 g, Avicel RC-591[microcrystalline cellulose, sodium carboxymethylcellulose] – 0.6 g, strawberry flavor – 0.05 g, beta-carotene – 0.015 g, powdered starch sugar 3% – 10.2005 g, mannitol – 2.25 g.
5 ml of the prepared suspension contains 500 mg of josamycin.
Colorless glass bottles with a capacity of 100 ml (1) (complete with a dosing syringe and syringe holder) – cardboard boxes.
Film-coated tablets, 500 mg: 10 pcs.
Marketing Authorization Holder
Astellas Pharma Europe B.V. (Netherlands)
Manufactured By
Temmler Werke GmbH (Germany)
Packaging and Quality Control Release
ORTAT, JSC (Russia)
Dosage Form
| Wilprafen® | Film-coated tablets, 500 mg: 10 pcs. |
Dosage Form, Packaging, and Composition
Film-coated tablets white or almost white, oblong, biconvex, with score lines on both sides.
| 1 tab. | |
| Josamycin | 500 mg |
Excipients: microcrystalline cellulose – 101 mg, polysorbate 80 – 5 mg, colloidal silicon dioxide – 14 mg, carmellose sodium – 10 mg, magnesium stearate – 5 mg, methylcellulose – 0.12825 mg, polyethylene glycol 6000 – 0.3846 mg, talc – 2.0513 mg, titanium dioxide – 0.641 mg, aluminum hydroxide – 0.641 mg, methacrylic acid and its esters copolymer – 1.15385 mg.
10 pcs. – aluminum/PVC blisters (1) – cardboard packs.
Dispersible tablets 1000 mg: 10 pcs.
Marketing Authorization Holder
Astellas Pharma Europe B.V. (Netherlands)
Manufactured By
Famar Lyon (France)
Packaging and Quality Control Release
ORTAT, JSC (Russia)
Dosage Form
| Wilprafen® Solutab | Dispersible tablets 1000 mg: 10 pcs. |
Dosage Form, Packaging, and Composition
Dispersible tablets white or white with a yellowish tint, oblong in shape, sweet, with a strawberry smell; with the inscription “IOSA” and a score line on one side of the tablet and the inscription “1000” on the other.
| 1 tab. | |
| Josamycin propionate | 1067.66 mg, |
| Equivalent to josamycin content | 1000 mg |
Excipients: microcrystalline cellulose – 564.53 mg, hypromellose – 199.82 mg, docusate sodium – 10.02 mg, aspartame – 10.09 mg, colloidal silicon dioxide – 2.91 mg, strawberry flavor – 50.05 mg, magnesium stearate – 34.92 mg.
5 pcs. – PVC/PVDC/aluminum foil blisters (2) – cardboard packs.
