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KontrDiar (Capsules, Suspension) Instructions for Use

ATC Code

A07AX03 (Nifuroxazide)

Active Substance

Nifuroxazide (Rec.INN registered by WHO)

Clinical-Pharmacological Group

Intestinal antiseptic. Antidiarrheal agent

Pharmacotherapeutic Group

Antidiarrheals, intestinal anti-inflammatory/antimicrobial agents; intestinal antimicrobial agents; other intestinal antimicrobial agents

Pharmacological Action

Antimicrobial agent, a nitrofuran derivative. It blocks the activity of dehydrogenases and inhibits the respiratory chains, the tricarboxylic acid cycle, and a number of other biochemical processes in the microbial cell. It destroys the microbial cell membrane and reduces toxin production by microorganisms.

It is highly active against Campylobacter jejuni, Escherichia coli, Salmonella spp, Shigella spp; Clostridium perfringens, Vibrio cholerae, pathogenic Vibrions and Vibrio parahaemolytique, Staphylococcus spp. Weakly sensitive to nifuroxazide: Citrobacter spp, Enterobacter cloacae and Proteus indologenes. Resistant to nifuroxazide: Klebsiella spp, Proteus mirabilis, Providencia spp., Pseudomonas spp.

It does not disturb the balance of the intestinal microflora. In acute bacterial diarrhea, it restores intestinal eubiosis. When infected with enterotropic viruses, it prevents the development of bacterial superinfection.

Pharmacokinetics

After oral administration, Nifuroxazide is practically not absorbed from the gastrointestinal tract and acts in the intestinal lumen. It is excreted through the intestine: 20% unchanged, the rest is chemically altered.

Indications

Acute bacterial diarrhea occurring without deterioration of general condition, fever, or intoxication.

ICD codes

ICD-10 code Indication
A09 Other and unspecified gastroenteritis and colitis of infectious origin
ICD-11 code Indication
1A40.Z Infectious gastroenteritis or colitis, unspecified

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 orally. Strictly adhere to the dosing schedule based on patient age and selected formulation.

For KontrDiar suspension: shake the bottle vigorously before each use. Use the measuring spoon provided. For children aged 1 month to 2 years, administer 100 mg (5 ml or 1 measuring spoon) two to three times daily. For children aged 2 to 6 years, administer 100 mg (5 ml) four times daily. For children aged 6 to 14 years, administer 200 mg (10 ml or 2 measuring spoons) three to four times daily.

For KontrDiar capsules: For adults and children over 14 years of age, administer 400 mg (2 capsules) four times daily. For children aged 6 to 14 years, administer 200 mg (1 capsule) four times daily.

Maintain an interval of approximately 6 hours between doses. Do not exceed the maximum daily dose.

The duration of treatment should not exceed 7 days. If symptoms persist beyond 3 days of therapy, discontinue use and consult a physician.

Concurrently with nifuroxazide therapy, implement oral rehydration to correct fluid and electrolyte losses.

Adverse Reactions

Allergic reactions skin rash, urticaria, angioedema, anaphylactic shock.

Contraindications

Hypersensitivity to nitrofuran derivatives; pregnancy; childhood – depending on the dosage form.

With caution liver disease, alcoholism, traumatic brain injury, brain diseases; breastfeeding period; childhood.

Use in Pregnancy and Lactation

The use of nifuroxazide during pregnancy is not recommended. During lactation (breastfeeding), it should be used with caution, in a short course.

Pediatric Use

In children, use with caution, according to indications, in doses and dosage forms recommended for the respective age. It is necessary to strictly follow the instructions in the nifuroxazide drug leaflets regarding contraindications for the use of specific nifuroxazide dosage forms in children of different ages.

Special Precautions

When treating diarrhea, rehydration therapy should be carried out simultaneously with nifuroxazide therapy.

In case of bacterial diarrhea occurring with deterioration of general condition, fever, symptoms of intoxication or infection, a doctor should be consulted to decide on the use of systemic antibacterial drugs. If symptoms of hypersensitivity (shortness of breath, rash, itching) appear, nifuroxazide should be discontinued.

Alcohol consumption during nifuroxazide therapy is prohibited.

Drug Interactions

Concomitant use with drugs that cause disulfiram-like reactions and with drugs that depress the function of the central nervous system is not recommended.

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

Over-the-Counter

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

Brand (or Active Substance), Marketing Authorisation Holder, Dosage Form

Marketing Authorization Holder

Krka d.d., Novo mesto (Slovenia)

Dosage Form

Bottle OTC Icon KontrDiar Oral suspension 200 mg/5 ml: 90 ml bottle with a dosing syringe

Dosage Form, Packaging, and Composition

Oral suspension yellow in color, with a banana smell.

5 ml
Nifuroxazide 200 mg

Excipients : carbomers, sucrose, methylparahydroxybenzoate (E218), citric acid (E330), banana flavor*, sodium hydroxide, purified water.

* banana flavor consists of natural flavoring substances, flavorings, propylene glycol (E1520).

90 ml – dark glass bottles (1) complete with a dosing syringe – cardboard boxes.

Marketing Authorization Holder

Krka-Rus, LLC (Russia)

Dosage Form

Bottle OTC Icon KontrDiar Capsules 200 mg: 14 or 28 pcs.

Dosage Form, Packaging, and Composition

Capsules hard gelatin, size 0, body and cap brownish-yellow; capsule contents: bright yellow powder with agglomerates.

1 caps.
Nifuroxazide 200 mg

Excipients : corn starch, sucrose, microcrystalline cellulose type 101; filler: magnesium stearate.

Composition of the empty hard gelatin capsule size 0 gelatin, iron oxide red dye (E172), iron oxide yellow dye (E172), titanium dioxide (E171).

14 pcs. – blister packs (1) – cardboard boxes.
14 pcs. – blister packs (2) – cardboard boxes.

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