Empagliflozin

Empagliflozin

Generic Name

Empagliflozin

Mechanism

  • Selective SGLT2 inhibition in the proximal tubule → blocks ~90 % of glucose reabsorption.
  • Glucosuria (≈–60 mg/kg/day) decreases plasma glucose independent of insulin.
  • Secondary effects: mild natriuresis, osmotic diuresis, ↓ preload/afterload → ↓ blood pressure and weight gain.

Pharmacokinetics

ParameterTypical Value
AbsorptionPeak plasma ~1‑2 h post‑dose; high oral bioavailability (~88 %)
DistributionVolume of distribution ~70 L; protein binding ~1 % (so little sequestration)
MetabolismPhase‑I oxidation & glucuronidation (mostly CYP3A4, to a lesser extent CYP2C8)
Elimination80 % excreted unchanged via kidneys; renal clearance ~10 mL/min
Half‑life12–13 h (steady‑state ~24 h)
Renal impairmentDose reduction recommended CKD‑stage 3–5 (CrCl 30–60 mL/min); hold if CrCl <30 mL/min
PregnancyCategory D; avoid in pregnancy due to risk of neonatal hypoglycemia and malformations

Indications

  • Type 2 Diabetes Mellitus (T2DM) – adjunct to diet, exercise, and/or other glucose‑lowering agents (metformin, sulfonylurea, GLP‑1 RA, insulin).
  • Heart Failure with Reduced Ejection Fraction (HFrEF) – 2.5‑mg BID improves morbidity/mortality (EMPEROR‑HF).
  • Chronic Kidney Disease (CKD) – slows GFR decline; recommended for CKD with/without diabetes (EMPEROR‑Renal).

*Note: Not approved for Type 1 diabetes or pediatric patients.*

Contraindications

  • Contraindicated: Severe renal impairment (CrCl <30 mL/min), end‑stage renal disease, active urinary tract infection, diabetic ketoacidosis, hyperosmolar hyperglycemic state.
  • Warnings:
  • Genital/urinary tract infections – ↑ risk of vulvovaginal candidiasis & UTI.
  • Volume depletion – hypotension, dizziness.
  • Acute kidney injury – monitor serum creatinine and BUN.
  • Hypoglycemia – risk increases when combined with insulin or sulfonylureas.
  • Anemia & ketoacidosis – monitor ketones and hemoglobin.
  • Pregnancy – avoid, discontinue before conception.

Dosing

  • Starting dose: 10 mg daily (preferable 10 mg) or 10 mg twice a day (for heart failure/CKD), taken once daily with or without food.
  • Maintenance: 25 mg once daily (or 25 mg BID for heart failure/CKD).
  • Titration: Increase to 25 mg after at least 4 weeks if glycemic control inadequate and renal function acceptable.
  • Renal adjustment:
  • CrCl 30–59 mL/min → 10 mg daily.
  • CrCl <30 mL/min → hold; not advised.

Adverse Effects

  • Common (<10 %):
  • Genital mycotic infections (vulvovaginal candidiasis, balanitis).
  • Urinary tract infections.
  • Polyuria/polydipsia.
  • Mild hypotension, dizziness.
  • Headache, nasopharyngitis.
  • Serious (≤1 %):
  • Ketoacidosis (often normoglycemic).
  • Nephrogenic diabetes insipidus → electrolyte imbalance.
  • Fournier’s gangrene (rare).
  • Hypersensitivity reactions.
  • Acute kidney injury.
  • Anemia (especially in CKD).

Monitoring

  • Baseline & every 3 months:
  • eGFR (or serum creatinine).
  • HbA1c.
  • Serum electrolytes (Na⁺, K⁺).
  • Urinalysis for ketones (if symptoms).
  • During therapy:
  • Blood pressure (especially at initiation).
  • Assess for signs of genital/urinary tract infections.
  • Weight (baseline → every 4 weeks).

Clinical Pearls

  • “Glucose‑insensitive card”: Empagliflozin lowers glucose but remains effective in patients with β‑cell dysfunction; useful when insulin resistance is high.
  • HFrEF synergy: Combining empagliflozin with standard HF therapy (ACEi/ARB, β‑blocker) yields additive mortality benefit—start at 10 mg BID; up‑titrate to 25 mg BID once renal function stable.
  • CKD benefit independent of diabetes: Empagliflozin slows albuminuria progression by ~30 % even when glycemic control not markedly improved.
  • Hypoglycemia mitigation: Use with sulfonylureas cautiously; consider sulfonylurea dose reduction or switch to basal‑bolus insulin titration.
  • Pregnancy‑discontinuation window: Stop at least 3 months before conception due to long‑acting metabolites; counsel on contraception.
  • Genital infection prophylaxis: Educate patients on perineal hygiene; treat early with topical antifungals; switch to systemic therapy if recurrence.
  • Renal dosing nuance: Because 80 % is renal excretion, monitor creatinine within first week after dose change; do not abruptly discontinue if CrCl →30 mL/min—hold therapy, reassess.

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• *All data sourced from FDA prescribing information, EMPA-REG OUTCOME, EMPEROR‑HF & CKD trials, and current KDIGO/ADA guidelines.*

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Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

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