Ethambutol 400mg tablets

Country: United Kingdom

Language: English

Source: MHRA (Medicines & Healthcare Products Regulatory Agency)

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Active ingredient:

Ethambutol hydrochloride

Available from:

DE Pharmaceuticals

ATC code:

J04AK02

INN (International Name):

Ethambutol hydrochloride

Dosage:

400mg

Pharmaceutical form:

Oral tablet

Administration route:

Oral

Class:

No Controlled Drug Status

Prescription type:

Valid as a prescribable product

Product summary:

BNF: 05010900

Patient Information leaflet

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Intrapharm Laboratories Ltd., The Courtyard Barns, Choke Lane,
Maidenhead, Berks SL6 6PT, UK
Intrapharm Laboratories Ltd., The Courtyard Barns, Choke Lane,
Maidenhead, Berks SL6 6PT, UK
280.00 mm
150.00 mm
                                
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Summary of Product characteristics

                                SUMMARY OF PRODUCT CHARACTERISTICS
1
NAME OF THE MEDICINAL PRODUCT
Ethambutol 400 mg Tablets
2
QUALITATIVE AND QUANTITATIVE COMPOSITION
Each film coated tablet contains 400mg Ethambutol Hydrochloride.
For a full list of excipients see section 6.1.
3
PHARMACEUTICAL FORM
Film coated tablet.
Smooth, grey, circular, biconvex film coated tablet, plain on both
sides.
4
CLINICAL PARTICULARS
4.1
THERAPEUTIC INDICATIONS
The primary treatment and re-treatment of tuberculosis and for
prophylaxis in cases
of inactive tuberculosis or large-tuberculinpositive reaction.
Ethambutol should only
be used in conjunction with other anti-tuberculous drugs to which the
patient’s
organisms are susceptible.
Consideration
should
be
given
to
official
guidance
on
the
appropriate
use
of
antibacterial agents
4.2
POSOLOGY AND METHOD OF ADMINISTRATION
_Route of administration_:
Oral
_Posology: _
Recommended Dosage
The dosage of ethambutol must be adjusted according to the body weight
of the
patient.
This drug should not be used as a sole anti-tuberculosis agent, but
should be given
with at least one other antituberculosis drug to avoid development of
resistant strains.
The usual daily dosage is 15-25mg/kg body weight given as a single
dose.
_ _
_ADULTS _
For primary treatment and prophylaxis: Ethambutol should be
administered in a
single
daily
dose
of
15mg/kg,
concomitant
drugs
being
maintained
at
their
recommended dosage levels.
For
re-treatment:
For
the
first
60
days
of
treatment,
ethambutol
should
be
administered in a single daily dose of 25mg/kg. Thereafter the dosage
should be
reduced to 15mg/kg, concomitant drugs being maintained at their
recommended
dosage levels.
_ _
_CHILDREN _
For primary treatment and re-treatment: For the first 60 days of
treatment, a single
daily oral dose of 25mg/kg. Thereafter the dosage should be reduced to
15mg/kg,
concomitant drugs being maintained at their recommended dosage
levels._ _
For prophylaxis: A single daily oral dose of 15mg/kg, concomitant
drugs being used
at their recommended dosage levels
As ch
                                
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