What is Phoslo and how is it used?
Phoslo is a prescription medicine used to treat the symptoms of Hyperphosphatemia in End Stage Renal Failure (on Dialysis). Phoslo may be used alone or with other medications.
Phoslo belongs to a class of drugs called Calcium Salts; PO4 Scavengers; Urea Cycle Disorder Treatment Agents.
It is not known if Phoslo is safe and effective in children.
What are the possible side effects of Phoslo?
Phoslo may cause serious side effects including:
- difficulty breathing,
- swelling of your face, lips, tongue, or throat,
- increased thirst or urination,
- muscle weakness,
- bone pain,
- lack of energy, and
Get medical help right away, if you have any of the symptoms listed above.
The most common side effects of Phoslo include:
- increased calcium in the blood,
- diarrhea, and
Tell the doctor if you have any side effect that bothers you or that does not go away.
These are not all the possible side effects of Phoslo. For more information, ask your doctor or pharmacist.
Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
Each white round tablet (stamped "BRA200") contains 667 mg calcium acetate, USP (anhydrous; Ca(CH3COO)2; MW=158.17 grams) equal to 169 mg (8.45 mEq) calcium, and 10 mg of the inert binder, polyethylene glycol 8000 NF. PhosLo Tablets (calcium acetate) are administered orally for the control of hyperphosphatemia in end stage renal failure.
DOSAGE AND ADMINISTRATION
The recommended initial dose of PhosLo (calcium acetate tablet) for the adult dialysis patient is 2 tablets with each meal. The dosage may be increased gradually to bring the serum phosphate value below 6 mg/dl, as long as hypercalcemia does not develop. Most patients require 3-4 tablets with each meal.
In tablet form for oral administration. Each white round tablet contains 667 mg calcium acetate (anhydrous Ca(CH3COO)2; MW=158.17 grams) equal to 169 mg (8.45 mEq) calcium, and 10 mg of the inert binder, polyethylene glycol 8000.
Tablets NDC 59730-6401-1 Bottles of 200
Store at Controlled Room Temperature, 15°-30°C.
Manufactured for Nabi Biopharmaceuticals, Boca Raton, FL 33487. P 8/03
In clinical studies, patients have occasionally experienced nausea during PhosLo (calcium acetate tablet) therapy. Hypercalcemia may occur during treatment with PhosLo (calcium acetate tablet) . Mild hypercalcemia (Ca>10.5mg/dL) may be asymptomatic or manifest itself as constipation, anorexia, nausea and vomiting. More severe hypercalcemia (Ca>12mg/dl) is associated with confusion, delirium, stupor and coma. Mild hypercalcemia is easily controlled by reducing the PhosLo (calcium acetate tablet) dose or temporarily discontinuing therapy. Severe hypercalcemia can be treated by acute hemodialysis and discontinuing PhosLo (calcium acetate tablet) therapy. Decreasing dialysate calcium concentration could reduce the incidence and severity of PhosLo (calcium acetate tablet) induced hypercalcemia. The long-term effect of PhosLo (calcium acetate tablet) on the progression of vascular or soft-tissue calcification has not been determined.
Isolated cases of pruritus have been reported which may represent allergic reactions.
PhosLo (calcium acetate tablet) may decrease the bioavailability of tetracyclines.
Progressive hypercalcemia due to overdose of PhosLo (calcium acetate tablet) may be severe as to require emergency measures. Chronic hypercalcemia may lead to vascular calcification, and other soft-tissue calcification. The serum calcium level should be monitored twice weekly during the early dose adjustment period. The serum calcium times phosphate (CaXP) product should not be allowed to exceed 66. Radiographic evaluation of suspect anatomical region may be helpful in early detection of soft-tissue calcification.
Excessive dosage of PhosLo (calcium acetate tablet) induces hypercalcemia; therefore, early in the treatment during dosage adjustment serum calcium should be determined twice weekly. Should hypercalcemia develop, the dosage should be reduced or the treatment discontinued immediately depending on the severity of hypercalcemia. PhosLo (calcium acetate tablet) should not be given to patients on digitalis, because hypercalcemia may precipitate cardiac arrhythmias. PhosLo (calcium acetate tablet) therapy should always be started at low dose and should not be increased without careful monitoring of serum calcium. An estimate of daily dietary calcium intake should be made initially and the intake adjusted as needed. Serum phosphorus should also be determined periodically. Information for the patient: The patient should be informed about compliance with dosage instructions, adherence to instructions about diet and avoidance of the use of nonprescription antacids. Patients should be informed about the symptoms of hypercalcemia (See ADVERSE REACTIONS section).
Carcinogenesis, Mutagenesis, Impairment of Fertility
Long term animal studies have not been performed to evaluate the carcinogenic potential, mutagenicity, or effect on fertility of PhosLo (calcium acetate tablet) .
Teratogenic Effects: Category C. Animal reproduction studies have not been conducted with PhosLo (calcium acetate tablet) . It is also not known whether PhosLo (calcium acetate tablet) can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. PhosLo (calcium acetate tablet) should be given to a pregnant woman only if clearly needed.
Safety and efficacy of PhosLo (calcium acetate tablet) have not been established. Geriatric Use Of the total number of subjects in clinical studies of PhosLo (calcium acetate tablet) (n=91), 25 percent were 65 and over, while 7 percent were 75 and over. No overall differences in safety or effectiveness were observed between these subjects and younger subjects, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.
Administration of PhosLo (calcium acetate tablet) in excess of the appropriate daily dosage can cause severe hypercalcemia (See ADVERSE REACTIONS).
Patients with hypercalcemia.
Patients with advanced renal insufficiency (creatinine clearance less than 30 mL/min) exhibit phosphate retention and some degree of hyperphosphatemia. The retention of phosphate plays a pivotal role in causing secondary hyperparathyroidism associated with osteodystrophy, and soft-tissue calcification. The mechanism by which phosphate retention leads to hyperparathyroidism is not clearly delineated. Therapeutic efforts directed toward the control of hyperphosphatemia include reduction in the dietary intake of phosphate, inhibition of absorption of phosphate in the intestine with phosphate binders, and removal of phosphate from the body by more efficient methods of dialysis. The rate of removal of phosphate by dietary manipulation or by dialysis is insufficient. Dialysis patients absorb 40% to 80% of dietary phosphorus. Therefore, the fraction of dietary phosphate absorbed from the diet needs to be reduced by using phosphate binders in most renal failure patients on maintenance dialysis. Calcium acetate (PhosLo (calcium acetate tablet) ) when taken with meals, combines with dietary phosphate to form insoluble calcium phosphate which is excreted in the feces. Maintenance of serum phosphorus below 6.0 mg/dl is generally considered as a clinically acceptable outcome of treatment with phosphate binders. PhosLo (calcium acetate tablet) is highly soluble at neutral pH, making the calcium readily available for binding to phosphate in the proximal small intestine. Orally administered calcium acetate from pharmaceutical dosage forms has been demonstrated to be systemically absorbed up to approximately 40% under fasting conditions and up to approximately 30% under nonfasting conditions. This range represents data from both healthy subjects and renal dialysis patients under various conditions.
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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