Alfa Normix 200mg 12 tablets — Made in Italy — Free Delivery
(Alfa Normix)
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Description Alfa Normix 200mg 12 tablets — Made in Italy — Free Delivery
Indications
Treatment of gastrointestinal infections caused by bacteria sensitive to rifaximin:
- acute gastrointestinal infections (including travelers' diarrhea);
- syndrome of excessive growth of microorganisms in the small intestine;
- hepatic encephalopathy;
- diverticulitis in the acute stage and chronic inflammation of the intestine.
Prevention of infectious complications in colorectal surgery.
Application
Suspension
Adults and children over 12 years of age: 10 ml of oral suspension 3 times a day to 20 ml of oral suspension 2-3 times a day (600-1200 mg of rifaximin).
Children aged 6 to 12 years: 10 ml of oral suspension 2-3 times a day to 20 ml of oral suspension 2 times a day (400-800 mg of rifaximin).
Children aged 2 to 6 years: 5 ml of oral suspension 2-3 times a day to 10 ml of oral suspension 3 times a day (200-600 mg of rifaximin).
For the treatment of adults and children over 6 years of age, instead of oral suspension, Alfa Normix can be used in the form of film-coated tablets, 200 mg each.
Tablets
Adults and children over 12 years of age: 1 tablet 3 times a day to 2 tablets 2-3 times a day (600-1200 mg of rifaximin).
Children aged 6 to 12 years: 1 tablet 2-3 times a day to 2 tablets 2 times a day (400-800 mg of rifaximin).
The duration of treatment should not exceed 7 days and depends on the clinical effect in patients.
If necessary, repeated courses of treatment can be carried out with a break of 20-40 days.
The total duration of therapy depends on the adequacy of the clinical effect in patients.
Doses and frequency of administration may be changed on the advice of a physician.
Suspension preparation
Granules for the preparation of oral suspension are in a hermetically sealed vial. The bottle must be opened, add water to the mark and shake well. Add more water until the slurry reaches the indicated level.
The concentration of rifaximin in the finished suspension is 100 mg per 5 ml. For measuring 5; 10 or 15 ml of suspension is added to the measuring cup.
The suspension is stable for 7 days at room temperature. Shake the vial well before taking the preparation.
Contraindications
Hypersensitivity to rifaximin, or to other rifamycins, or to any of the components of the preparation.
Side effects
Analysis of safety data showed that the risk of side effects when using alpha normix is very low. these events are mainly limited to gastrointestinal disturbances (nausea, dyspepsia, vomiting, abdominal pain and cramps), are mild to moderate, and usually resolve spontaneously without the need to change the dose or stop therapy.
The preparation is practically not absorbed in the gastrointestinal tract, which eliminates the risk of systemic side effects.
In rare cases, skin reactions such as urticaria may occur, which are probably associated with individual intolerance to the treatment. The risk of side effects is 0.7–2% of all cases of preparation use. Post-marketing surveillance data support the above risk assessment and the nature of the observed events.
special instructions
During long-term treatment with high doses or with damage to the intestinal mucosa, absorption of a small amount of the preparation (1%) is possible, which can cause staining of the urine in a reddish color. this is due to the active substance, which, like most antibiotics of this series (rifamycins), has a red-orange color.
Use during pregnancy and lactation. Rifaximin did not cause teratogenic effects in rats and rabbits. There are no adequate data and well-controlled studies in pregnant women.
Since the study of toxicity on reproductive function in animals does not allow to evaluate the possibility of a toxic effect in humans, during pregnancy, the preparation can be taken only in case of urgent need and under the direct supervision of a physician.
The penetration of rifaximin into breast milk has not been studied, but it is presumably insignificant due to very low absorption into the systemic circulation. Therefore, the use of Alfa Normix by women who are breastfeeding is allowed with appropriate medical supervision.
The ability to influence the reaction rate when driving vehicles or operating other mechanisms. Not installed.
Interactions
Not installed.
Overdose
Signs of overdose were not observed when taking alpha normix in doses up to 2400 mg per day for 5 days.
In case of overdose, gastric lavage and symptomatic treatment are recommended.
Storage conditions
Store the prepared suspension at a temperature not exceeding 30 ° C.
Tags: Alfa Normix
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