Alginatol® (Suppositories) Instructions for Use
Marketing Authorization Holder
Nizhpharm JSC (Russia)
ATC Code
B02BC (Local hemostatics)
Active Substance
Sodium alginate (Ph.Eur. European Pharmacopoeia)
Dosage Form
| Alginatol® | Rectal suppositories for children 250 mg: 10 pcs. |
Dosage Form, Packaging, and Composition
| Rectal suppositories for children | 1 supp. |
| Sodium alginate | 250 mg |
5 pcs. – contour cell packs (2) – cardboard packs.
Clinical-Pharmacological Group
Drug with hemostatic, anti-inflammatory, and wound-healing action for topical use in proctology
Pharmacotherapeutic Group
Topical hemostatic agent
Pharmacological Action
A hemostatic drug for topical use. It is a natural polysaccharide obtained from brown seaweed.
It has a pronounced hemostatic effect and possesses anti-inflammatory and reparative properties.
Indications
- Anal fissures in the epithelialization stage
- Chronic bleeding hemorrhoids
- Proctosigmoiditis
- Inflammation of the rectum in the postoperative period
ICD codes
| ICD-10 code | Indication |
| K60 | Fissure and fistula of anus and rectum |
| K62.8 | Other specified diseases of anus and rectum (including proctitis) |
| K64 | Hemorrhoids and perianal venous thrombosis |
| ICD-11 code | Indication |
| DB50.Z | Fissure or fistula of anal region, unspecified |
| DB6Z | Hemorrhoids or perianal venous diseases, unspecified |
| DB70.Z | Infections of anal and rectal regions, unspecified |
| DB72.Z | Some specified diseases of the anal canal, unspecified |
| DE2Z | Diseases of the digestive system, unspecified |
| EG61 | Infections of the anus or perianal skin |
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 one suppository rectally twice daily, typically in the morning and evening.
Continue treatment for a duration of 7 to 14 days, as determined by the prescribing physician based on the severity of the condition and the clinical response observed.
Adverse Reactions
Adverse reactions are infrequent and typically mild in nature.
The most commonly reported adverse reaction is localized allergic reactions, such as skin rash, itching, or redness at the application site. Discontinue use and seek medical advice if any signs of hypersensitivity appear.
Contraindications
- Hypersensitivity to sodium alginate or any of the excipients contained in the suppository formulation.
Use in Pregnancy and Lactation
Rectal use during pregnancy and lactation is possible as indicated.
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 Disclaimer