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 DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Oral suspension 200 mg/5 ml: 90 ml bottle with a dosing syringe
Marketing Authorization Holder
Krka d.d., Novo mesto (Slovenia)
Dosage Form
| 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.
Capsules 200 mg: 14 or 28 pcs.
Marketing Authorization Holder
Krka-Rus, LLC (Russia)
Dosage Form
| 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.
