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Opipramol Brand names, Opipramol Analogs

Opipramol Brand Names Mixture

  • No information avaliable

Opipramol Chemical_Formula


Opipramol RX_link

No information avaliable

Opipramol fda sheet

Opipramol FDA

Opipramol msds (material safety sheet)

Opipramol MSDS

Opipramol Synthesis Reference

No information avaliable

Opipramol Molecular Weight

158.17 g/mol

Opipramol Melting Point

> 160 oC

Opipramol H2O Solubility

No information avaliable

Opipramol State


Opipramol LogP

No information avaliable

Opipramol Dosage Forms

Capsule; Drops; Liquid; Powder for solution; Solution; Tablet

Opipramol Indication

Used to treat hyperphosphatemia (too much phosphate in the blood) in patients with kidney disease.

Opipramol Pharmacology

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 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. Calcium acetate is highly soluble at neutral pH, making the calcium readily available for binding to phosphate in the proximal small intestine.

Opipramol Absorption

40% is absorbed in the fasting state and approximately 30% is absorbed in the nonfasting state following oral administration.

Opipramol side effects and Toxicity

Oral, rat: LD50 = 4280 mg/kg. Symptoms of overdose include mild hypercalcemia (constipation; loss of appetite; nausea and vomiting), and severe hypercalcemia (confusion; full or partial loss of consciousness; incoherent speech).

Opipramol Patient Information

No information avaliable

Opipramol Organisms Affected

Humans and other mammals