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finerenone

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Finelidone can block the effect of aldosterone on the mineralocorticoid receptor (MR) with high selectivity and strong affinity, thereby lowering blood pressure and reducing cardiac burden.

1. Drug name

1. Generic name: Finerenone (Finerenone)

2. Trade name: Kerendia

< h2>2. Indications

It is used to reduce the risk of continued decline in renal function, end-stage renal disease, cardiovascular death, non-fatal myocardial infarction and hospitalization for heart failure in adults with type 2 diabetes (T2D)-related chronic kidney disease (CKD).

3. Specifications and properties

10 mg film-coated tablets

4. Main ingredients

Active ingredient: fenelinone; excipients include lactose, microcrystalline cellulose, etc., and the film coating contains hypromellose, iron oxide red (10mg) or iron oxide yellow (20mg).

5. Usage and Dosage

1. Initial dose : Based on eGFR selection, 20 mg once a day for those with eGFR ≥ 60 mL/min/1.73 m²; 10 mg once a day for those with eGFR 25-<60 mL/min/1.73 m²; not recommended for those with eGFR < 25 mL/min/1.73 m².

2. Target dose : Adjust to 20 mg once daily after 4 weeks (blood potassium and eGFR need to be monitored).

3. How to take : Can be taken with food or on an empty stomach. Swallow the tablet whole or crush it and mix it with water/soft food.

6. Dose adjustment

1. Serum potassium ≤ 4.8mEq/L : can be increased from 10mg to 20mg.

2. Serum potassium >4.8-5.5mEq/L : Maintain the current dose; suspend administration when >5.5mEq/L, restart 10mg after serum potassium ≤5.0mEq/L.

3. How to deal with missed doses : Take the missed dose on the same day, otherwise skip the next day and take the medicine as originally planned.

7. Medication precautions

1. Diet : Avoid grapefruit/grapefruit juice (increases blood drug concentration).

2. Monitor : Monitor serum potassium and eGFR regularly before and during medication.

3. Vomiting/absorption effects : Not clearly stated, it is recommended to consult a physician.

8. Medication for special groups

1. Pregnant women : No human data, animals show fetal toxicity, avoid use.

2. Lactation : Avoid breastfeeding within 1 day after stopping the drug.

3. Elderly : No need to adjust the dose.

4. U200c for patients with liver damage: It is disabled for severe liver damage (Child-PughC); no adjustment is needed for mild to moderate liver damage (A/B), but serum potassium monitoring is required for moderate.

9. Adverse reactions

Common (≥1% and higher than placebo): hyperkalemia (14%), hypotension (4.6%), hyponatremia (1.3%).

10. Contraindications

1. Combined use of strong CYP3A4 inhibitors (such as ketoconazole).

2. Patients with adrenal insufficiency.

11. Drug interactions

1. CYP3A4 inhibitor : Strong (contraindicated), moderately weak (need to monitor serum potassium).

2. CYP3A4 inducer : Strong and moderately effective (avoid combined use).

3. Potassium-raising drugs : Such as potassium supplements and potassium-sparing diuretics, blood potassium needs to be closely monitored.

12. Storage method

Store at room temperature of 20-25℃, allowing short-term fluctuation of 15-30℃.