HYDRODOXX 500 MG/G POWDER FOR USE IN DRINKING WATER FOR CHICKENS AND PIGS.

Nchi: Ayalandi

Lugha: Kiingereza

Chanzo: HPRA (Health Products Regulatory Authority)

Nunua Sasa

Tabia za bidhaa Tabia za bidhaa (SPC)
31-01-2015

Viambatanisho vya kazi:

DOXYCYCLINE HYCLATE

Inapatikana kutoka:

Huvepharma NV

ATC kanuni:

QJ01AA02

INN (Jina la Kimataifa):

DOXYCYCLINE HYCLATE

Kipimo:

500 mg/g

Dawa fomu:

Powder for Oral Solution

Dawa ya aina:

POM

Kundi la matibabu:

Fowl - Chicken, Porcine

Eneo la matibabu:

Doxycycline

Matibabu dalili:

Antibacterial

Idhini hali ya:

Authorised

Idhini ya tarehe:

2009-05-15

Tabia za bidhaa

                                SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
HydroDoxx 500 mg/g Powder for use in drinking water for chickens and pigs.
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
One gram contains:
Active substance:
Doxycycline (as doxycycline hyclate)
500 mg
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Powder for use in drinking water.
Yellow powder.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Chickens (broilers)
Pigs (Fattening pigs)
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
Chickens (broilers) : Prevention and treatment of Chronic Respiratory Disease (CRD) caused by _Mycoplasma_
_gallisepticum _susceptible to doxycycline.
Fattening pigs: prevention and treatment of clinical respiratory infection caused by strains of _Pasteurella multocida_
susceptible to doxycycline.
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.
The presence of the clinical disease in the herd should be established before preventive treatment is started.
4.3 CONTRAINDICATIONS
Do not use in cases of hypersensitivity to the active substance, to other tetracyclines or to any excipient. Do not use in
animals with hepatic disorders.
Do not use in animals with renal disorders
See section 4.7.
4.4 SPECIAL WARNINGS FOR EACH TARGET SPECIES
The uptake of medication by animals can be altered as a consequence of illness. In case of insufficient uptake of
drinking water, animals should be treated parenterally.
HEALTH PRODUCTS REGULATORY AUTHORITY
________________________________________________________________________________________________________________________
_Date Printed 16/01/201
                                
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