KSR potassium Chloride
KSR
Potassium Chloride
Potassium supplement
COMPOSITION
Each film-coated SR tablet contains Potassium Chloride 600
mg
MODE OF ACTION
KSR is a film-coated preparation of potassium chloride
formulated for slow release.
Each tablet contains 600mg of potassium chloride which is
equivalent to 8 mili-equivalent each of Potassium [K+] and Chloride
[Cl-]. The show and sustained release over a period of 6 hours
precludes high concentration of potassium chloride against a localized area of
the gut wall which might irritate or damage the mucosa. The sustained relase
providers conditions of maximum gastric tolerance and effective absorpstion for
the treatment of all types of potassium deficiency, whether hypochloraemic
alkalosis. KSR does not alter normal kidney function; can be used in all age
groups; replaces the essential chloride anion and potassium and so prevents
hypochloraemic alkalosis. During KSR administration, laboratory monitoring of
serum electrolyte level should be done periodically.
INDICATIONS
For treatment and specific prevention of hypokalemia.
DOSAGE and ADMINISTRATION
An average dose is 1 or 2 tablet two or three times daily,
each tablet swallowed whlle with little water, preferably during meals. Where
KSR is administerd routinely with an average daily maintenance dose of an oral
diuretic agent, 1-2 tablet daily may be sufficient.
WARNINGS
If a patien under treatment with KSR develops severe
vomiting, severe abdominal pains or flatulence, or gastoristesinalhaemorrhage,
the preparation should be withdranwn at once. To prevent the risk of
hyperkalemia, potassium supplements should not be administered with potassium
sparing diuretic agent such spironolactone, triamterene or amiloride. In case of
metabolic acidosis, hypokalemia should not be treated with potassium chloride
but with a potassium salt containing an alkalosing anion [e.g potassium
bicarbonate].
PRECAUTIONS
In patien with impaired renal function , special care should
be exercised when prescribing potassium salt because of the risk of
hypokalaemia. The serum electrolytes should be monitored in these patiens and
also in patiens with congestive heart failure, especially if under treatment
with digitalis, in whom hypokalemia should be avoided.
ADVERSE RACTIONS
Oral potassium preparatons can provoke gastrointestinal
disturbance (e.g. nausea vomiting, abdominal pain, diarrhea). In rare cases,
KSR may also cause these side-effect. In this evevnt, reduction in dosage or
withdrawal of drug may be necessary.
CONTRAINDICATION
Advanced ernal failure, untreated Addison;s disease, acute
dehydration, hyperkalemia, in the presence of obstruction in the digestivetract
(e.g. resulting from compression of the oesophagus due to dilation of the left
atrium or from stenosis of the gut). The administration of KSR in such a situation could be conceivably give
rise to ulceration or perforaton.
STORAGE
Store in a dry place below 250C
PRESENTATIONS
Bottle of 100 film coated SR tablets
Box of 10 x 10 film coated SR tablet in strip
PT MERCK
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