section name header

Indications ⬇

REMS


SamscaJynarque

Contraind./Precautions ⬆ ⬇

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects ⬆ ⬇

CV: palpitations

Derm: dry skin, rash

Endo: hyperglycemia

F and E: thirst, hypernatremia, hypovolemia

GI: constipation, diarrhea, dry mouth, ↓appetite, dyspepsia, HEPATOTOXICITY

GU: polyuria

Metab: hyperuricemia

Neuro: dizziness, weakness, osmotic demyelination

Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS)

Interactions ⬆ ⬇

Drug-drug:

Drug-Food:

Availability ⬆ ⬇

(Generic available)

Route/Dosage ⬆ ⬇

Hyponatremia (Samsca)

Autosomal Dominant Polycystic Kidney Disease (Jynarque and Jinarc)

US Brand Names ⬆ ⬇

Jynarque, Samsca

Action ⬆ ⬇

  • Acts as a selective vasopressin V2-receptor antagonist, resulting in increased renal water excretion and increased serum sodium.
Therapeutic effects:
  • Correction of hyponatremia (Samsca).
  • Slowed deterioration of renal function (Jynarque).

Classifications ⬆ ⬇

Therapeutic Classification: electrolyte modifiers

Pharmacologic Classification: vasopressin antagonists

Pharmacokinetics ⬆ ⬇

Absorption: 40% absorbed following oral administration.

Distribution: Well distributed to tissues.

Protein Binding: >99%.

Metabolism/Excretion: Extensively metabolized in the liver via the CYP3A4 isoenzyme; 59% excreted in the feces (19% as unchanged drug), with 40% excreted in the urine (<1% as unchanged drug).

Half-Life: 12 hr.

Canadian Brand Names ⬆ ⬇

Jinarc

Time/Action Profile ⬆ ⬇

ROUTEONSETPEAKDURATION
POwithin 8 hr2–4 hr‡7 days

‡Plasma concentrations.

Patient/Family Teaching ⬆ ⬇

Pronunciation ⬆ ⬇

tol-VAP-tan

Code ⬆

NDC Code