Prilocard 2.5 mg tablets for dogs

Nchi: Ayalandi

Lugha: Kiingereza

Chanzo: HPRA (Health Products Regulatory Authority)

Viambatanisho vya kazi:

Ramipril

Inapatikana kutoka:

aniMedica GmbH

ATC kanuni:

QC09AA05

INN (Jina la Kimataifa):

Ramipril

Kipimo:

2.5 mg/tablet

Dawa fomu:

Tablet

Dawa ya aina:

POM: Prescription Only Medicine as defined in relevant national legislation

Kundi la matibabu:

Dogs

Eneo la matibabu:

ramipril

Matibabu dalili:

Cardiovascular

Idhini hali ya:

Authorised

Idhini ya tarehe:

2012-07-13

Tabia za bidhaa

SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE VETERINARY MEDICINAL PRODUCT
Prilocard 2.5 mg tablets for dogs
2 QUALITATIVE AND QUANTITATIVE COMPOSITION
Each tablet contains:
Active substance:
Ramipril 2.5 mg
Excipients:
yellow ferric oxide 0.40 mg (E172)
For the full list of excipients, see section 6.1.
3 PHARMACEUTICAL FORM
Tablets.
Light yellow capsule-shaped biconvex tablets scored on one side of the
tablet and imprinted with 'B'
and '49'
on either
side of the scoring line. The scoreline is only to facilitate breaking
for ease of swallowing and not to divide into equal
doses.
4 CLINICAL PARTICULARS
4.1 TARGET SPECIES
Dogs.
4.2 INDICATIONS FOR USE, SPECIFYING THE TARGET SPECIES
For treatment of congestive heart failure (equivalent to New York
Heart Association [NYHA] classes II,
III and IV)
caused by valvular
insufficiency due to endocardiosis or
cardiomyopathy.
The preparation may if
applicable be
administered concomitantly with furosemide (diuretic) and/or the
cardiac glycosides digoxin or methyl digoxin.
In patients treated concomitantly with ramipril and furosemide, the
diuretic dose may be reduced to achieve the same
diuretic effect as in treatment with furosemide alone.
Class
Clinical symptoms
II
Fatigue, dyspnoea, cough etc. seen in normal activity.
Ascites may occur at this stage.
III
Comfortable at rest, but capacity for activity minimal.
IV
Incapable of any activity.
Clinical symptoms of disablement occur even at rest.
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