Indications for: TEKTURNA HCT


Adult Dosage:

Take consistently with regard to meals. ≥18yrs: 1 tab once daily. Add-on or initial therapy and not volume-depleted: initially 150mg/12.5mg; may increase after 2–4 weeks up to max 300mg/25mg. Replacement therapy: may be substituted for the titrated components. Maximum effect usually seen at 4 weeks.

Children Dosage:

<18yrs: not established.

TEKTURNA HCT Contraindications:

Concomitant ARBs or ACEIs in diabetes. Anuria. Sulfonamide allergy.

Boxed Warning:

Fetal toxicity.

TEKTURNA HCT Warnings/Precautions:

Fetal toxicity may develop; discontinue if pregnancy is detected. Correct salt/volume depletion before starting therapy or start under close supervision. Discontinue if angioedema or laryngeal edema occurs (have SC epinephrine available). Moderate renal impairment (CrCl <60mL/min): avoid concomitant ARBs or ACEIs. Monitor BP, electrolytes, and renal function periodically. Consider withholding or discontinuing if significant renal dysfunction develops. Renal artery stenosis. Severe HF. Post-MI. Diabetes. Hepatic dysfunction. Asthma. SLE. Gout. Acute myopia. Secondary acute angle-closure glaucoma. Neonates. Pregnancy: avoid. Nursing mothers: not recommended.

TEKTURNA HCT Classification:

Direct renin inhibitor + diuretic (thiazide).

TEKTURNA HCT Interactions:

Avoid concomitant cyclosporine, itraconazole. Caution with NSAIDs, K+ supplements, K+ sparing diuretics, K+ containing salt substitutes; may cause hyperkalemia. Potentiates antihypertensives, possibly non-depolarizing muscle relaxants. May be antagonized by, and renal toxicity potentiated by NSAIDs (including COX-2 inhibitors): monitor renal function in elderly and/or volume-depleted. Dual inhibition of the renin-angiotensin system with ARBs or ACEIs may increase risk of hypotension, hyperkalemia, renal function changes. Concomitant furosemide; monitor. Adjust antidiabetic drugs. Concomitant lithium (risk of toxicity): monitor. Orthostatic hypotension potentiated by alcohol, CNS depressants. Decreased absorption by cholestyramine, colestipol resins (separate dosing by at least 4hrs), high fat meals.

Adverse Reactions:

Dizziness, flu-like symptoms, diarrhea, cough, vertigo, asthenia, arthralgia, elevated BUN/creatinine, ALT, cholesterol, uric acid; rare: angioedema. HCTZ: increased risk for non-melanoma skin cancer.

Generic Drug Availability:


How Supplied:

Tabs—30, 90