Megapen - Strep Injection

Țară: Irlanda

Limbă: engleză

Sursă: HPRA (Health Products Regulatory Authority)

Cumpara asta acum

Ingredient activ:

Procaine benzylpenicillin; Dihydrostreptomycin sulphate

Disponibil de la:

Franklin Pharmaceuticals Ltd.

Codul ATC:

QJ01RA

INN (nume internaţional):

Procaine benzylpenicillin; Dihydrostreptomycin sulphate

Dozare:

200, 200 milligram(s)/millilitre

Forma farmaceutică:

Suspension for injection

Tip de prescriptie medicala:

POM: Prescription Only Medicine as defined in relevant national legislation

Grupul Terapeutică:

Cattle

Zonă Terapeutică:

Combinations of antibacterials

Indicații terapeutice:

Antibacterial

Statutul autorizaţiei:

Authorised

Data de autorizare:

1987-10-01

Caracteristicilor produsului

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Megapen - Strep Injection.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
3 PHARMACEUTICAL FORM
Suspension for injection.
A white aqueous solution
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Bovine.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For the treatment and control of infections caused by bacteria
sensitive to procaine penicillin or dihydrostreptomycin
sulphate.
4.3 CONTRAINDICATIONS
Do not use in cases of known hypersensitivity to the active
ingredients.
Do not administer by the intravenous route.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
None known.
Each ml contains:
Active substances
Procaine Benzylpenicillin
200 mg
Dihydrostreptomycin Sulphate
200 mg
Excipient
Methyl Parahydroxybenzoate
1.0 mg
Sodium Formaldehyde Sulfoxylate
1.48 mg
For a full list of excipients, see section 6.1
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4.5 SPECIAL PRECAUTIONS FOR USE
SPECIAL PRECAUTIONS FOR USE IN ANIMALS
Use of the product should be based on susceptibility testing of the
bacteria isolated from the animal. If this is not
possible, therapy should be based on local (regional, farm level)
epidemiological information about susceptibility of the
target bacteria.
SPECIAL PRECAUTIONS TO BE TAKEN BY THE PERSON ADMINISTERING THE
VETERINARY MEDICINAL PRODUCT TO ANIMALS
Avoid direct contact with p
                                
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