POTASSIUM BICARBONATE- potassium bicarbonate tablet, effervescent United States - English - NLM (National Library of Medicine)

potassium bicarbonate- potassium bicarbonate tablet, effervescent

upsher-smith laboratories, inc. - potassium bicarbonate (unii: hm5z15lebn) (potassium cation - unii:295o53k152) - potassium cation 978 mg - - for the treatment of patients with hypokalemia, with or without metabolic alkalosis; in digitalis intoxication; and in patients with hypokalemic familial periodic paralysis. if hypokalemia is the result of diuretic therapy, consideration should be given to the use of a lower dose of diuretic, which may be sufficient without leading to hypokalemia. - for the prevention of hypokalemia in patients who would be at particular risk if hypokalemia were to develop (e.g., digitalized patients or patients with significant cardiac arrhythmias). the use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension is often unnecessary when such patients have a normal dietary pattern and when low doses of the diuretic are used. serum potassium should be checked periodically, however, and if hypokalemia occurs, dietary supplementation with potassium-containing foods may be adequate to control milder cases. in more severe cases, and if dose adjustment of the diuretic is ineffective or unwarra

Potassium (potassium 6.5mmol) effervescent tablets BPC 1968 United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium (potassium 6.5mmol) effervescent tablets bpc 1968

potassium 6.5mmol) effervescent tablets bpc 1968 (actavis uk ltd - potassium bicarbonate; potassium acid tartrate - effervescent tablet - 500mg ; 300mg

EFFER-K UNFLAVORED- potassium bicarbonate tablet, effervescent
EFFER-K ORANGE- potassium bicarbonate tablet, effervescent
EFFE United States - English - NLM (National Library of Medicine)

effer-k unflavored- potassium bicarbonate tablet, effervescent effer-k orange- potassium bicarbonate tablet, effervescent effe

nomax inc. - potassium bicarbonate (unii: hm5z15lebn) (bicarbonate ion - unii:hn1zra3q20) - potassium bicarbonate 977.5 mg - - for therapeutic use in patients with hypokalemia with or without metabolic alkalosis; in chronic digitalis intoxication; and in patients with hypokalemic familial periodic paralysis. - for prevention of potassium depletion when the dietary intake of potassium ion is inadequate in the following conditions; patients receiving digitalis and diuretics for congestive heart failure; hepatic cirrhosis with ascites; states of aldosterone excess with normal renal function; potassiumlosing nephropathy, and certain diarrheal states; long-term corticosteroid therapy. - the use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension or receiving certain antibiotics is often unnecessary when such patients have a normal dietary pattern. serum potassium should be checked periodically, however, and, if hypokalemia occurs, dietary supplementation with potassium-containing foods may be adequate to control milder cases. in more severe cases supplementation with potassium salts may be indicat

POTASSIUM CITRATE EXTENDED RELEASE- potassium citrate tablet United States - English - NLM (National Library of Medicine)

potassium citrate extended release- potassium citrate tablet

strides pharma inc. - potassium citrate (unii: ee90oni6ff) (anhydrous citric acid - unii:xf417d3psl) - potassium citrate 5 meq - potassium citrate is indicated for the management of renal tubular acidosis [see clinical studies (14.1)] . potassium citrate is indicated for the management of hypocitraturic calcium oxalate nephrolithiasis [see clinical studies (14.2)] . potassium citrate is indicated for the management of uric acid lithiasis with or without calcium stones [see clinical studies (14.3)] . potassium citrate extended-release tablets are contraindicated: • in patients with hyperkalemia (or who have conditions predisposing them to hyperkalemia), as a further rise in serum potassium concentration may produce cardiac arrest. such conditions include: chronic renal failure, uncontrolled diabetes mellitus, acute dehydration, strenuous physical exercise in unconditioned individuals, adrenal insufficiency, extensive tissue breakdown or the administration of a potassium-sparing agent (such as triamterene, spironolactone or amiloride). • in patients in whom there is cause for arrest or delay in tablet passage through the gastrointestinal

KLOR-CON/EF- potassium bicarbonate tablet, effervescent United States - English - NLM (National Library of Medicine)

klor-con/ef- potassium bicarbonate tablet, effervescent

sandoz inc. - potassium bicarbonate (unii: hm5z15lebn) (potassium cation - unii:295o53k152) - potassium cation 978 mg - the use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension is often unnecessary when such patients have a normal dietary pattern and when low doses of the diuretic are used. serum potassium should be checked periodically, however, and if hypokalemia occurs, dietary supplementation with potassium-containing foods may be adequate to control milder cases. in more severe cases, and if dose adjustment of the diuretic is ineffective or unwarranted, supplementation with potassium salts may be indicated. potassium supplements are contraindicated in patients with hyperkalemia since a further increase in serum potassium concentration in such patients can produce cardiac arrest. hyperkalemia may complicate any of the following conditions: chronic renal failure, systemic acidosis such as diabetic acidosis, acute dehydration, extensive tissue breakdown as in severe burns, adrenal insufficiency or the administration of a potassium-sparing diuretic (e.g., spironolactone, triamterene

EFFER-K 10 MEQ UNFLAVORED- potassium bicarbonate tablet, effervescent
EFFER-K 10 MEQ CHERRY VANILLA- potassium bicarbonate tabl United States - English - NLM (National Library of Medicine)

effer-k 10 meq unflavored- potassium bicarbonate tablet, effervescent effer-k 10 meq cherry vanilla- potassium bicarbonate tabl

nomax inc. - potassium bicarbonate (unii: hm5z15lebn) (potassium cation - unii:295o53k152) - potassium cation 391 mg - - for therapeutic use in patients with hypokalemia with or without metabolic alkalosis; in chronic digitalis intoxication; and in patients with hypokalemic familial periodic paralysis. - for prevention of potassium depletion when the dietary intake of potassium ion is inadequate in the following conditions; patients receiving digitalis and diuretics for congestive heart failure; hepatic cirrhosis with ascites; states of aldosterone excess with normal renal function; potassium-losing nephropathy, and certain diarrheal states; long-term corticosteroid therapy. - the use of potassium salts in patients receiving diuretics for uncomplicated essential hypertension or receiving certain antibiotics is often unnecessary when such patients have a normal dietary pattern. serum potassium should be checked periodically, however, and, if hypokalemia occurs, dietary supplementation with potassium-containing foods may be adequate to control milder cases. in more severe cases supplementation with potassium salts may be indica

Potassium (potassium 6.5mmol) effervescent tablets BPC 1968 United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium (potassium 6.5mmol) effervescent tablets bpc 1968

potassium 6.5mmol) effervescent tablets bpc 1968 (a a h pharmaceuticals ltd - potassium bicarbonate; potassium acid tartrate - effervescent tablet - 500mg ; 300mg

Potassium (potassium 6.5mmol) effervescent tablets BPC 1968 United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium (potassium 6.5mmol) effervescent tablets bpc 1968

potassium 6.5mmol) effervescent tablets bpc 1968 (the boots company plc - potassium bicarbonate; potassium acid tartrate - effervescent tablet - 500mg ; 300mg

Potassium (potassium 6.5mmol) effervescent tablets BPC 1968 United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium (potassium 6.5mmol) effervescent tablets bpc 1968

potassium 6.5mmol) effervescent tablets bpc 1968 (alliance healthcare (distribution) ltd - potassium bicarbonate; potassium acid tartrate - effervescent tablet - 500mg ; 300mg

Potassium (potassium 6.5mmol) effervescent tablets BPC 1968 United Kingdom - English - MHRA (Medicines & Healthcare Products Regulatory Agency)

potassium (potassium 6.5mmol) effervescent tablets bpc 1968

potassium 6.5mmol) effervescent tablets bpc 1968 (sigma pharmaceuticals plc - potassium bicarbonate; potassium acid tartrate - effervescent tablet - 500mg ; 300mg