Jardiance

Jardiance

Generic Name

Jardiance

Mechanism

Empagliflozin selectively blocks SGLT‑2 transporters in the proximal renal tubules, reducing glucose reabsorption by ~60 %. This leads to:
Glucosuria and a 30–40 mg/dL decline in post‑prandial glucose.
Caloric loss (~200 kcal/day) → modest weight reduction.
Osmotic diuresis → modest blood‑pressure lowering.

Because it is glucose‑dependent, fasting blood glucose is largely preserved, minimizing *hypoglycaemic* risk when used as monotherapy or with agents lacking this property.

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Pharmacokinetics

ParameterValueNotes
AbsorptionOral; bioavailability ~75 %Wound in 2 h post‑dose.
DistributionCmax ≈ 15 µg/mL; protein binding 85 %Linear kinetics across 10–50 mg.
MetabolismPhase II glucuronidation (UGT1A9), minimal CYP450 involvementAvoid strong CYP1A2 inhibitors.
Elimination50 % renal; 8 % fecalHalf‑life 10–13 h; steady‑state within 3 days.
Renal Dose Adjustments10 mg q.d. if CrCl 30–60 mL/min; 5 mg q.d. if <30No dosing in ESRD (dialysis).

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Indications

  • Type 2 diabetes mellitus – as monotherapy, add‑on to diet and exercise, or add‑on to insulin.
  • Heart failure with reduced ejection fraction – reduces cardiovascular death.
  • Chronic kidney disease – slows eGFR decline (in patients with ACR > 300 mg/g).

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Contraindications

  • Contraindicated: Severe renal impairment (CrCl < 30 mL/min), end‑stage renal disease, severe dehydration.
  • Warnings:
  • *Genitourinary infections* (candidiasis, UTI).
  • *Diabetic ketoacidosis (DKA)* – especially in insulin‑treated patients or low-carb diets.
  • *Euglycaemic DKA*: monitor ketones.
  • *Volume depletion* → hypotension.
  • *Hypotension*, *falls* risk in elderly or post‑dialysis.

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Dosing

RegimenTypical StartTitrationComments
Type 2 DM10 mg q.d.Can increase to 25 mg q.d. after 1–2 weeks*Educate* on glycaemic monitoring.
HF‑REF / CKD10 mg q.d.25 mg q.d. if toleratedKeep eGFR >30 mL/min/1.73 m².

• Take with or without food; avoid alcohol.
• Patients on diuretics: monitor electrolytes & BP.
• OTC: avoid in pregnancy (category B, not well‑studied).

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Adverse Effects

Common (≤ 10 %)
• Genital mycotic infections
• Urinary tract infections
• Polyuria, nocturia
• Dizziness/Hypotension

Serious (> 1 %)
• Diabetic ketoacidosis (rare but serious)
• Fournier’s gangrene (case reports; advise reporting)
• Acute kidney injury (esp. with volume depletion)
• Fractures (in some trials)

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Monitoring

  • Baseline: eGFR, ACR, fasting glucose, ketones (if high-risk).
  • Follow‑up:
  • eGFR every 3–6 months in CKD.
  • HbA1c every 3–6 months.
  • BP, weight for metabolic effects.
  • Ketones if new symptoms (polyuria, nausea, abdominal pain).

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Clinical Pearls

  • SGLT‑2 inhibitors counteract insulin‑induced hypoglycaemia: perfect for patients with sulfonylureas or insulin when tight glycaemic control is needed.
  • Weight loss + BP reduction often seen even before glycaemic benefit—useful in metabolic syndrome.
  • DKA risk: educate patients on “sick day rules”; consider dose reduction or temporary hold if severe illness or low carb intake.
  • Renal protection: evidence from EMPA‑REG OUTCOME indicates slower eGFR decline—think of Jardiance as dual therapy for diabetes + CKD.
  • Travel & dehydration: advise increasing fluid intake or temporary drug pause if traveling to low‑humidity zones.

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• *All information reflects current FDA labeling (2024) and peer‑reviewed studies. For individualized patient care, consult the latest clinical guidelines and pharmacopoeia.*

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

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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