Interaksi Perindopril dan Spironolakton

Perindopril dan Spironolakton: kedua label peresepan menguraikan interaksi yang biasanya memerlukan pemantauan, perubahan dosis, atau pemberian jarak antardosis.

Moderat

Biasanya dapat dikelola dengan pemantauan atau perubahan dosis. Beri tahu apoteker Anda bahwa Anda menggunakan keduanya.

Apa kata label FDA

Dari label Spironolakton (SPIRONOLACTONE) · berlaku sejak 2026-08-26

Moderat

This risk is increased by impaired renal function or concomitant potassium supplementation, potassium-containing salt substitutes or drugs that increase potassium, such as angiotensin converting enzyme inhibitors and angiotensin receptor blockers [see Drug Interactions ( 7.1 )] .

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Hypotension and Worsening Renal Function Excessive diuresis may cause symptomatic dehydration, hypotension and worsening renal function, particularly in salt-depleted patients or those taking angiotensin converting enzyme inhibitors and angiotensin II receptor blockers.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Examples of drugs that can increase potassium include: ACE inhibitors angiotensin receptor blockers aldosterone blockers non-steroidal anti-inflammatory drugs (NSAIDs) heparin and low molecular weight heparin trimethoprim 7.2 Lithium Like other diuretics, spironolactone oral suspension reduces the renal clearance of lithium, thus increasing the risk of lithium…

Interaksi obatberdasarkan golongan obatLihat label di DailyMed
Minor

Check serum potassium levels when ACE inhibitor or ARB therapy is altered in patients receiving spironolactone oral suspension.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed

Dari label Perindopril (Perindopril Erbumine) · berlaku sejak 2024-03-13

Moderat

Symptomatic hypotension is most likely to occur in patients who have been volume or salt-depleted as a result of prolonged diuretic therapy, dietary salt restriction, dialysis, diarrhea or vomiting [see Dosage and Administration (2.1) ] .

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Patients should be followed closely for the first two weeks of treatment and whenever the dose of perindopril erbumine and/or diuretic is increased.

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Some perindopril erbumine-treated patients have developed minor and transient increases in blood urea nitrogen and serum creatinine especially in those concomitantly treated with a diuretic.

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 agents such as potassium-sparing diuretics, potassium supplements and/or potassium-containing salt substitutes [see Drug Interactions (7.2) ] .

Peringatan dan perhatianberdasarkan golongan obatLihat label di DailyMed
Moderat

Potassium-Sparing Diuretics/Potassium Supplements: Hyperkalemia.

Interaksi obatberdasarkan golongan obatLihat label di DailyMed

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Bukan nasihat medis. Interaction Checker mengutip teks label FDA dan lembar fakta NIH. Penting atau tidaknya suatu interaksi bagi Anda bergantung pada dosis, waktu penggunaan, fungsi ginjal dan hati, serta kondisi lain. Pastikan dengan apoteker atau dokter yang meresepkan.