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Pronunciation |
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(poe
TASS ee um FOS
fate) |
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U.S. Brand
Names |
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Neutra-Phos®-K |
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Generic
Available |
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Yes |
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Synonyms |
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Phosphate, Potassium |
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Pharmacological Index |
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Electrolyte Supplement, Oral |
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Use |
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Treatment and prevention of hypophosphatemia or
hypokalemia |
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Pregnancy Risk
Factor |
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C |
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Contraindications |
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Hyperphosphatemia, hyperkalemia, hypocalcemia, hypomagnesemia, renal
failure |
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Warnings/Precautions |
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Use with caution in patients with renal insufficiency, cardiac disease,
metabolic alkalosis; admixture of phosphate and calcium in I.V. fluids can
result in calcium phosphate precipitation |
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Adverse
Reactions |
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>10%: Gastrointestinal: Diarrhea, nausea, stomach pain, flatulence,
vomiting
1% to 10%:
Cardiovascular: Bradycardia
Endocrine & metabolic: Hyperkalemia
Neuromuscular & skeletal: Weakness
Respiratory: Dyspnea
<1%: Chest pain, mental confusion, alkalosis, hypocalcemia tetany (with
large doses of phosphate), abdominal pain, throat pain, phlebitis, paresthesias,
paralysis, acute renal failure |
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Overdosage/Toxicology |
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Symptoms of overdose include muscle weakness, paralysis, peaked T waves,
flattened P waves, prolongation of QRS complex, ventricular arrhythmias, tetany,
calcium-phosphate precipitation
Removal of potassium can be accomplished by various means; removal through
the GI tract with Kayexalate® administration; by way of
the kidney through diuresis, mineralocorticoid administration or increased
sodium intake; by hemodialysis or peritoneal dialysis; or by shifting potassium
back into the cells by insulin, glucose infusion, or sodium bicarbonate; calcium
chloride reverses cardiac effects. |
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Drug
Interactions |
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Decreased effect/levels with aluminum and magnesium-containing antacids or
sucralfate which can act as phosphate binders
Increased effect/levels with potassium-sparing diuretics, salt substitutes,
or ACE-inhibitors; increased effect of digitalis |
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Stability |
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Store at room temperature, protect from freezing; use only clear solutions;
up to 10-15 mEq of calcium may be added per liter before precipitate may occur
Phosphate salts may precipitate when mixed with calcium salts; solubility is
improved in amino acid parenteral nutrition solutions; check with a pharmacist
to determine compatibility |
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Usual Dosage |
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I.V. doses should be incorporated into the patient's maintenance I.V. fluids;
intermittent I.V. infusion should be reserved for severe depletion situations in
patients undergoing continuous EKG monitoring. It is difficult to determine
total body phosphorus deficit; the following dosages are empiric guidelines:
0-6 months: 240 mg
6-12 months: 360 mg
1-10 years: 800 mg
>10 years: 1200 mg
Pregnancy lactation: Additional 400 mg/day
Adults: 800 mg
Treatment: It is difficult to provide concrete guidelines for the treatment
of severe hypophosphatemia because the extent of total body deficits and
response to therapy are difficult to predict. Aggressive doses of phosphate may
result in a transient serum elevation followed by redistribution into
intracellular compartments or bone tissue. It is recommended that repletion of
severe hypophosphatemia (<1 mg/dL in adults) be done I.V. because large doses
of oral phosphate may cause diarrhea and intestinal absorption may be unreliable
Pediatric I.V. phosphate repletion:
Children: 0.25-0.5 mmol/kg administer over 4-6 hours and repeat if
symptomatic hypophosphatemia persists; to assess the need for further
phosphate administration, obtain serum inorganic phosphate after administration
of the first dose and base further doses on serum levels and clinical status
Adult I.V. phosphate repletion:
Initial dose: 0.08 mmol/kg if recent uncomplicated hypophosphatemia
Initial dose: 0.16 mmol/kg if prolonged hypophosphatemia with presumed total
body deficits; increase dose by 25% to 50% if patient symptomatic with severe
hypophosphatemia
Do not exceed 0.24 mmol/kg/day; administer over 6 hours by I.V.
infusion
With orders for I.V. phosphate, there is considerable confusion
associated with the use of millimoles (mmol) versus milliequivalents (mEq) to
express the phosphate requirement. Because inorganic phosphate exists as
monobasic and dibasic anions, with the mixture of valences dependent on pH,
ordering by mEq amounts is unreliable and may lead to large dosing errors. In
addition, I.V. phosphate is available in the sodium and potassium salt;
therefore, the content of these cations must be considered when ordering
phosphate. The most reliable method of ordering I.V. phosphate is by millimoles,
then specifying the potassium or sodium salt. For example, an order for 15 mmol
of phosphate as potassium phosphate in one liter of normal saline The dosing of
phosphate should be 0.2-0.3 mmol/kg with a usual daily requirement of 30-60
mmol/day or 15 mmol of phosphate per liter of TPN or 15 mmol phosphate per 1000
calories of dextrose. Would also provide 22 mEq of potassium.
Maintenance:
I.V. solutions:
Children: 0.5-1.5 mmol/kg/24 hours I.V. or 2-3 mmol/kg/24 hours orally in
divided doses
Adults: 15-30 mmol/24 hours I.V. or 50-150 mmol/24 hours orally in divided
doses
Oral:
Children <4 years: 1 capsule (250 mg phosphorus/8 mmol) 4 times/day;
dilute as instructed
Children >4 years and Adults: 1-2 capsules (250-500 mg phosphorus/8-16
mmol) 4 times/day; dilute as instructed |
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Dietary
Considerations |
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Avoid administering with oxalate (berries, nuts, chocolate, beans, celery,
tomato) or phytate (bran, whole wheat) containing foods |
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Administration |
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For intermittent infusion, if peripheral line, dilute to a maximum
concentration of 0.05 mmol/mL; if central line, dilute to a maximum
concentration of 0.12 mmol/mL; maximum rate of infusion: 0.06 mmol/kg/hour; do
not infuse with calcium-containing I.V. fluids (ie,
TPN) |
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Monitoring
Parameters |
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Serum potassium, calcium, phosphate, sodium, cardiac monitor (when
intermittent infusion or high-dose I.V. replacement needed) |
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Test
Interactions |
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ammonia
(B) |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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Do not swallow the capsule; empty contents of capsule into 75 mL (2.5 oz) of
water before taking; take with food to reduce the risk of
diarrhea |
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Nursing
Implications |
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Capsule must be emptied into 3-4 oz of water before
administration |
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Dosage Forms |
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Oral:
Whole cow's milk per mL: Phosphate 0.29 mmol, Na 0.025 mEq, K 0.035 mEq
Neutra-Phos® capsule, powder concentrate: Elemental
phosphorus 250 mg, phosphate 8 mmol, Na 7.1 mEq, K 7.1 mEq
Neutra-Phos®-K capsule, powder: Elemental phosphorus
250 mg, phosphate 8 mmol, K 14.2 mEq
K-Phos® Neutral tablets: Elemental phosphorus 250 mg,
phosphate 8 mmol, Na 13 mEq, K 1.1 mEq
K-Phos® MF tablets: Elemental phosphorus 125.6 mg,
phosphate 4 mmol, Na 2.9 mEq, K 1.1 mEq K-Phos® No. 2:
Elemental phosphorus 250 mg, phosphate 8 mmol, Na 5.8 mEq, K 2.3 mEq
K-Phos® Original tablets: Elemental phosphorus 114 mg,
phosphate 3.6 mmol, K 3.7 mEq
Uro-KP-Neutral® tablets: Elemental phosphorus 250 mg,
phosphate 8 mmol, Na 10.8 mEq, K 1.3 mEq
Intravenous: K phosphate, per mL: Phosphate 3 mmol, K 4.4 mEq
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