Cefixime is a medicine intended for the treatment of acute and chronic bronchitis, bacterial bronchitis, middle ear inflammation, pharyngitis and tonsillitis, bacterial infections of the urinary tract, cystitis, urethritis, pyelonephritis, cerivitis.
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Product Description
Semisynthetic Cephalosporin antibiotic of 3rd generation with a broad spectrum of action that is taken orally. Of a bactericidal effect. The mechanism of action is the inhibition of the synthesis of pathogen’s cell membrane.
Safety information
Indications
Infectious-inflammatory diseases caused by sensitive microorganisms: pharyngitis, tonsillitis, sinusitis, acute and chronic bronchitis, otitis media, uncomplicated urinary tract infections, uncomplicated gonorrhea.
Directions
For adults and children over 12 years old with a body weight of more than 50 kg, the daily dose is 400mg (once a day or 200 mg 2 times a day). The duration of treatment course is 7-10 days. With uncomplicated gonorrhea – 400 mg at once.
Children under the age of 12 years – 8 mg/kg of body weight once a day or 4 mg/kg every 12 hours. With infections caused by Streptococcus pyogenes, the course of treatment should last 10 days at least.
In case of renal insufficiency (with CC from 21 to 60 ml/min) or in patients on hemodialysis, the daily dose should be reduced by 25%.
With KK≤20 ml / min or in patients on peritoneal dialysis, the daily dose should be reduced by 2 times.
Contraindications
Hypersensitivity to cephalosporins and penicillins.
Use in pregnancy is possible only if the intended benefit for mother exceeds the potential risk to the fetus.
Side effects
On the level of the digestive system: dry mouth, anorexia, diarrhea, nausea, vomiting, abdominal pain, flatulence, transient increase in hepatic transaminase and alkaline phosphatase, hyperbilirubinemia, jaundice, candidiasis GI, dysbiosis; Rarely - stomatitis, glossitis, pseudomembranous enterocolitis.
On the level of hematopoiesis system: leukopenia, thrombocytopenia, neutropenia, hemolytic anemia.
On the level of CNS: dizziness, headache.
On the level of urinary system: interstitial nephritis.
Allergic reactions: skin itching, hives, skin hyperemia, eosinophilia, fever.
Levitra - the main component - the active agent Vardenafil which promotes strengthening of blood circulation in generative organs of men. It allows to reach a high level erection at sexual stimulation, and also to increase sensitivity of head of a penis and to make sexual intercourse longer and more pleasant. The main feature of a drug Levitra - quickness of effect, duration of impact on an organism up to 12 hours and a very small number of side effects.
Cialis Professional - effective tablets for improvement of erection. They begin to work in 15 minutes from the moment of taking and actions for 36 hours. They can cause not less than 10, but no more than 16 erections. The medicine increases duration of sexual intercourse. The tablets are successfully used for reduction of time for recovery of erection after ejaculation.
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"Loop" diuretic, used for edematous syndrome with CHF II-III st., liver cirrhosis, kidney disease; swelling of the lungs or brain; arterial hypertension, hypercalcemia. Causes a rapidly advancing, strong and short-term diuresis. Has natriuretic and chlororetic effects, increases the excretion of K +, Ca2 +, Mg2 +.
A thiazide diuretic of the average intensity, applied in arterial hypertension, edema syndrome of different origin, gestosis and diabetes insipidus. Reduces reabsorption of Na+ at the level of the Henle loop cortical segment, without affecting its segment lying in the medulla of the kidney that detects a weaker diuretic effect compared with furosemide.
A combined medication used for edema syndrome of various origins and arterial hypertension. The effect is due to the components in its composition; it has diuretic and hypotensive effect. Hydrochlorothiazide is a diuretic of average power action, increases the excretion of Na+, Cl-, K+, Mg2+, bicarbonate; keeps Ca2+, uric acid in the body. Amiloride decreases the excretion of K+ and Mg2+. The combination of the drug components reduces the risk of hypokalemia and hypomagnesemia development.
An antiarrhythmic Ia class drug, a blocker of the "fast" Na+ channels. It has a membrane stabilizing, anti-arrhythmic, hypotensive and m-anticholinergic action. In normally functioning sinus node it causes acceleration of the sinus rhythm due to the antimuscarinic effect.
The drug is used for treatment of infectious diseases such as community acquired pneumonia, exacerbation of chronic bronchitis, acute sinusitis, pharyngitis and skin infections. The active ingredient in Omnicef is cefdinir—a semi-synthetic cephalosporin broad-spectrum antibiotic of the third generation for oral administration. Like other cephalosporin antibiotics, cefdinir has a bactericidal action against susceptible organisms through the inhibition of synthesis of bacteria peptidoglycan cell walls by interfering with the final stage of transamination, required for cross-linking.
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