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MD Pharmacology NMC syllabus ~5 min read Recent advances last updated on 2026-06-22

Insulin & Diabetic Emergencies

Insulin preparations, analogues, delivery and basal–bolus regimens, and the stepwise management of DKA, HHS and hypoglycaemia

Past RGUHS + DNB + MPMSU + MUHS + VNSGU · 34 RGUHSSep '25 RGUHSMay '25 MPMSUOct '25 MPMSUOct '25 MPMSUOct '25 MPMSUMay '25 DNBMay '24 DNBOct '24 DNBOct '23 RGUHSMay '22 DNBDec '22 MUHSWinter '22 VNSGUApr '22 RGUHSNov '21 MPMSUAug '21 DNBDec '21 MUHSWinter '21 RGUHSJun '20 MPMSU2020 MUHSSummer '20 RGUHSNov '19 VNSGUMar '19 MPMSU2018 MPMSUMay '18 MUHSWinter '18 MPMSUJun '17 DNBDec '16 MPMSU2014 MUHSWinter '14 DNBDec '12 MPMSU2011 DNBDec '11 MPMSU2009 RGUHSSep '07

Introduction

  • Insulin — A 51-amino-acid two-chain (A 21 + B 30) polypeptide hormone of pancreatic islet β cells, joined by two disulfide bonds; the anchor drug of all type 1 diabetes and of advanced/decompensated type 2, and the only agent that reverses the acute hyperglycaemic emergencies.
  • Biosynthesis — Preproinsulin → proinsulin → insulin + C-peptide (co-secreted equimolar); because C-peptide escapes hepatic first-pass (t½ ~30 min vs insulin ~5 min), peripheral C-peptide is the marker of endogenous β-cell secretion and separates endogenous from factitious hyperinsulinaemia.
  • Unit & strength — 1 IU ≈ 34.7 µg crystalline insulin; most preparations are U-100 (100 U/mL); concentrated U-200/U-300/U-500 forms exist for insulin-resistant patients needing large volumes.
  • Scope of emergencies — Three acute decompensations — diabetic ketoacidosis (DKA) and hyperosmolar hyperglycaemic state (HHS) from insulin lack, and hypoglycaemia as the iatrogenic mirror image from insulin/secretagogue excess. Oral antidiabetics & SGLT2 inhibitors are covered in the sibling LAQ "Newer Oral Antidiabetics & SGLT2 Inhibitors".
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Insulin And Diabetic Emergencies

PharmaNotes Pro · LAQ

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