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Erythromycin Akos Efor 10000g 10g ophthalmic ointment.

$2.50

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Description

The instruction for medical use

of ERITROMITSIN-AKOS medicine

the Trade name

of ERITROMITSIN-AKOS

the International unlicensed

name Erythromycin Dosage Form oculentum of 10.000 PIECES/g 10 g

Structure of 100 g of ointment contains

active agent erythromycin (in terms of active agent) 1,000,000 PIECES,

excipients: anhydrous lanolin, sodium pyrosulphite, vaseline. Description

Ointment yellowish or burovato yellow color.

Pharmacotherapeutic group

Drugs for treatment of diseases of eyes. Antibiotics.

Code of automatic telephone exchange S01AA17

Pharmacological

Pharmacokinetics At properties topical administration system absorption low.

A pharmacodynamics

Erythromycin the antibiotic from group of macroleads produced by Streptomyces erythreus. Drug works bacteriostatically. Reversibly contacts 5OS a subunit of ribosomes that breaks formation of peptide bonds between molecules of amino acids and blocks protein synthesis of microorganisms (does not influence synthesis of nucleic acids).

Chlamydia trachomatis is effective concerning the sensitive microorganisms causing superficial eye infections of a conjunctiva, cornea including concerning Neisseria gonorrhoeae.

Erythromycin has antibacterial effect on gram-positive and gram-negative microorganisms (different types of Streptococcus, Staphylococcus, N. meningitides), including the strains resistant to other antibiotics. Drug is active also concerning Clostridium spp., Corynebacterium diphtheriae, Haemophilus influenzae, Mycoplasma pneumoniae, Actinomyces israelii, Listeria monocytogenes, chlamydias.

Indications

– conjunctivitis (including at newborns)

– an ophthalmia of newborns

– bacterial blepharitis, blefarokonjyunktivit, the keratitis, a meibomitis (barley), clamidiosis, trachoma

– 0.2-0.3 g of ointment put the Route of administration and doses In diseases of eyes for the lower or upper eyelid 3 times a day, in trachoma – 4-5 times a day.

Duration of treatment depends on a form and disease severity, but should not exceed 14 days. In trachoma the treatment should be combined with opening of follicles. When subsiding inflammatory process, drug is used by 2-3 times a day. Duration of a course of treatment of trachoma should not exceed 3 months.

Side effects

Seldom

– allergic reactions, reddening, an itching

At prolonged use the consecutive infection caused by microorganisms, resistant to erythromycin, can develop.

Contraindications

– hypersensitivity to drug components

– heavy abnormal liver functions

Medicinal interactions

It is incompatible with lincomycin, clindamycin and chloramphenicol (antagonism). Reduces bactericidal action beta laktamnykh antibiotics (penicillin, cephalosporins, karbopenema).

At simultaneous use of dosage forms of erythromycin for external use with the abrasive substances leading to excessive irritation of skin and also with the means causing peeling of skin the cumulative irritating or drying-up effect is possible.

Special instructions

With care: in abnormal liver functions and/or kidneys.

Erythromycin can be appointed in an allergy to penicillin.

At prevention of an ophthalmia of newborns it is not necessary to wash away

erythromycin oculentum from an eye.

At children whose mothers have clinically apparent gonorrhea erythromycin as ophthalmologic means is used along with aqueous solution of penicillin G for parenteral use.

Pregnancy and a lactation

Eritromitsin gets through a placenta, is allocated with breast milk. At use of erythromycin at pregnancy it is necessary to estimate expected advantage for mother and potential risk for a fruit. In need of use in the period of a lactation it is necessary to resolve an issue of the breastfeeding termination.

Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms

are not described

to Apply strictly on doctor’s orders.

Overdose

Data on overdose of drug are absent.

A form of release and packing

On 10 g in tubas aluminum.

Each tuba together with the instruction for use in the state and Russian languages is placed in a pack from cardboard.

To Store storage conditions at a temperature from + 15 to + 25 C.

To store out of children’s reach!

3 years

not to apply a period of storage after an expiration date.

Prescription status

According to the prescription

JSC Sintez Producer.

Russian Federation, 640008, Kurgan, Konstitutsii Avenue, 7.

ph./fax (3522) 48-16-89

The address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products

of STOFARM LLP,

000100, Republic of Kazakhstan, Kostanay region, Kostanay, Uralskaya St., 14

ph. 714 228 01 79

Additional information

Ingredient

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