Interaksi Lisinopril dan Telmisartan dan hidroklorotiazid

Lisinopril dan Telmisartan dan hidroklorotiazid: kedua label peresepan menandai kombinasi ini dengan bahasa yang paling tegas, seperti kontraindikasi, peringatan kotak hitam, atau instruksi untuk menghindarinya.

Mayor

Jangan dikombinasikan tanpa arahan dokter yang meresepkan. Bahasa label di bawah ini adalah yang paling tegas yang digunakan FDA.

Apa kata label FDA

Dari label Telmisartan dan hidroklorotiazid (Micardis HCT) · berlaku sejak 2024-12-31

Mayor

Patients who received the combination of ARB and ACE inhibitor did not obtain any additional benefit (no additional reduction of risk of cardiovascular death, myocardial infarction, stroke, or hospitalization from heart failure) compared to ARB monotherapy or ACE inhibitor monotherapy, but experienced an increased incidence of renal dysfunction (e.g., acute renal…

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Moderat

…Metabolic Disorders Drugs, including telmisartan, that inhibit the renin-angiotensin system can cause hyperkalemia, particularly in patients with renal insufficiency, diabetes, or combination use with other angiotensin receptor blockers or ACE inhibitors and the concomitant use of other drugs that raise serum potassium levels [see Drug Interactions (7.1 , 7.4) ] .

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Dual Blockade of the Renin-Angiotensin-Aldosterone System and Changes in Renal Function Dual blockade of the renin-angiotensin-aldosterone system (RAS) with angiotensin blockers, ACE inhibitors, or aliskiren is associated with increased risks of hypotension, hyperkalemia, and renal impairment.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Minor

The ONTARGET trial enrolled 25,620 patients ≥55 years old with atherosclerotic disease or diabetes with end-organ damage, randomizing them to telmisartan (ARB) only, ramipril (ACE inhibitor) only, or the combination, and followed them for a median of 56 months.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed

Dari label Lisinopril (Zestril) · berlaku sejak 2025-01-02

Moderat

Patients at risk of excessive hypotension include those with the following conditions or characteristics: heart failure with systolic blood pressure below 100 mmHg, ischemic heart disease, cerebrovascular disease, hyponatremia, high dose diuretic therapy, renal dialysis, or severe volume and/or salt depletion of any etiology.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

In these patients, Zestril should be started under very close medical supervision and such patients should be followed closely for the first two weeks of treatment and whenever the dose of Zestril and/or diuretic is increased.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Risk factors for the development of hyperkalemia include renal insufficiency, diabetes mellitus, and the concomitant use of potassium-sparing diuretics, potassium supplements and/or potassium-containing salt substitutes [see Drug Interactions (7.1) ] .

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Diuretics Initiation of Zestril in patients on diuretics may result in excessive reduction of blood pressure.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Moderat

Potassium-sparing diuretics (spironolactone, amiloride, triamterene, and others) can increase the risk of hyperkalemia.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed

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