Framycetin (Spray) Instructions for Use
ATC Code
R01AX08 (Framycetin)
Active Substance
Framycetin (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Antibacterial drug for topical use in ENT practice
Pharmacotherapeutic Group
Drugs for the treatment of nasal diseases; decongestants and other preparations for topical use; other drugs for the treatment of nasal diseases
Pharmacological Action
An antibiotic from the aminoglycoside group with a broad spectrum of action for topical use in otorhinolaryngology.
It acts bactericidally, damages the cytoplasmic membrane, disrupts the flow of metabolites inside the cell and causes rapid death of microorganisms.
It is active against most Gram-positive and Gram-negative bacteria: Staphylococcus aureus, Staphylococcus spp. (including strains resistant to other antibiotics), some strains of Streptococcus spp., Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Klebsiella spp., Haemophilus influenzae, Salmonella spp., Shigella spp., Enterobacter spp., Proteus spp., Serratia marcescens, Pasteurella spp., Vibrio spp., Borrelia, Leptospira spp., Mycobacterium tuberculosis (including strains resistant to streptomycin), which cause the development of infectious processes in the upper respiratory tract.
Treponema spp., some strains of Streptococcus spp., and anaerobic microorganisms are resistant to framycetin.
Pharmacokinetics
When applied topically, it has low systemic absorption.
Indications
As part of combination therapy for infectious and inflammatory diseases of the upper respiratory tract, including: rhinitis, rhinopharyngitis, sinusitis (in the absence of septal damage).
Prevention and treatment of inflammatory processes after surgical interventions.
ICD codes
| ICD-10 code | Indication |
| J00 | Acute nasopharyngitis (common cold) |
| J01 | Acute sinusitis |
| J02 | Acute pharyngitis |
| J31.0 | Chronic rhinitis (including ozaena, atrophic and hypertrophic rhinitis) |
| J31.2 | Chronic pharyngitis |
| J32 | Chronic sinusitis |
| Z29.2 | Other prophylactic chemotherapy (administration of antibiotics for prophylactic purposes) |
| ICD-11 code | Indication |
| CA00 | Acute nasopharyngitis |
| CA01 | Acute rhinosinusitis |
| CA02.Z | Acute pharyngitis, unspecified |
| CA09.0 | Chronic rhinitis |
| CA09.2 | Chronic pharyngitis |
| CA0A.Z | Chronic rhinosinusitis, unspecified |
| QC05.Y | Other specified prophylactic measures |
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 spray intranasally only. Use 3 to 6 times per day.
Deliver one spray into each nostril per administration.
Before initial use, prime the pump by pressing the actuator several times until a full spray is produced.
Clear the nasal passages prior to application. Tilt the head slightly forward while using the spray.
Do not exceed the recommended frequency or duration of application.
The maximum treatment duration is 7 days. Discontinue use after one week.
Prolonged use beyond 7 days increases the risk of developing superinfection with non-susceptible organisms.
If no clinical improvement is observed within 3-4 days, re-evaluate the diagnosis and treatment strategy.
This regimen is for topical use only. Do not ingest or introduce into the eyes.
After use, wipe the spray tip with a clean tissue and replace the protective cap.
Adverse Reactions
Possible: allergic reactions.
Contraindications
Hypersensitivity to antibiotics of the aminoglycoside group; pregnancy, breastfeeding period.
Framycetin should not be used for washing the paranasal sinuses.
Use in Pregnancy and Lactation
Contraindicated for use during pregnancy and breastfeeding.
Pediatric Use
Can be used in children according to indications, in recommended doses.
Special Precautions
During treatment, the appearance of resistant strains of microorganisms is possible.
Aminoglycoside antibiotics can cause reversible, partial or complete deafness and have a nephrotoxic effect when used systemically and when applied topically to open wounds or damaged skin.
These effects are dose-dependent and are enhanced in cases of impaired liver or kidney function.
The risk of their occurrence should be taken into account in case of topical application of high doses of the drug in children.
Therapy should not be continued after the symptoms disappear.
Framycetin should not be used simultaneously with other antibiotics that have ototoxic and nephrotoxic effects (streptomycin, monomycin, kanamycin, gentamicin).
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
Nasal spray 1.25%
Marketing Authorization Holder
West, LLC (Russia)
Manufactured By
Samaramedprom, OJSC (Russia)
Dosage Form
| Framycetin | Nasal spray 1.25% |
Dosage Form, Packaging, and Composition
Nasal spray
| Framycetin | 1.25% |
10 ml – bottles – for hospitals
10 ml – bottles – cardboard packs – By prescription
15 ml – bottles – for hospitals
15 ml – bottles – cardboard packs – By prescription
20 ml – bottles – for hospitals
20 ml – bottles – cardboard packs – By prescription
25 ml – bottles – for hospitals
25 ml – bottles – cardboard packs – By prescription
Nasal spray 12.5 mg/1 mL: 15 mL bottle
Marketing Authorization Holder
Vita Line, LLC (Russia)
Manufactured By
Pharmtekhnologiya LLC (Republic of Belarus)
Dosage Form
| Framycetin | Nasal spray 12.5 mg/1 mL: 15 mL bottle |
Dosage Form, Packaging, and Composition
Nasal spray in the form of a transparent or slightly opalescent, colorless or yellowish solution.
| 1 ml | |
| Framycetin sulfate | 12.5 mg (8000 IU) |
Excipients : sodium chloride, sodium citrate, methylparahydroxybenzoate (E218), citric acid monohydrate, purified water.
15 ml – polyethylene bottles (1) with a nasal spray nozzle – cardboard packs.
Nasal spray 1.25%
Marketing Authorization Holder
Formula-FR, LLC (Russia)
Manufactured By
YUGPHARM, LLC (Russia)
Dosage Form
| Framycetin | Nasal spray 1.25% |
Dosage Form, Packaging, and Composition
Nasal spray
| 1 ml | |
| Framycetin sulfate | 12.5 mg |
15 ml – bottles – cardboard packs – By prescription
Nasal spray 1.25%
Marketing Authorization Holder
Morelor LLC (Russia)
Manufactured By
YUGPHARM, LLC (Russia)
Dosage Form
| Framycetin Morelor® | Nasal spray 1.25% |
Dosage Form, Packaging, and Composition
Nasal spray
| 1 ml | |
| Framycetin sulfate | 12.5 mg |
15 ml – bottles – cardboard packs – By prescription
Nasal spray 1.25%: 10 mL or 15 mL bottle
Marketing Authorization Holder
Pharmtekhnologiya LLC (Republic of Belarus)
Dosage Form
| Framycetin PhT | Nasal spray 1.25%: 10 mL or 15 mL bottle |
Dosage Form, Packaging, and Composition
Nasal spray in the form of a transparent or slightly opalescent, colorless or yellowish solution.
| 1 ml | |
| Framycetin sulfate | 12.5 mg (8000 IU) |
Excipients : sodium chloride, sodium citrate, methylparahydroxybenzoate (E218), citric acid monohydrate, purified water.
10 ml – polymer bottles (1) with a nasal spray nozzle – cardboard packs.
15 ml – polymer bottles (1) with a nasal spray nozzle – cardboard packs.
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