KEAM cheat sheet
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Pharmacy (KEAM Pharmacy stream)
Zero-order kinetics: elimination rate is constant, t½ = C0/(2k); first-order t½ = 0.693/k (independent of dose).
Bioavailability F = (AUCoral × DoseIV)/(AUCIV × Doseoral); intravenous reference gives F = 1.
Volume of distribution Vd = Dose/C0; clearance CL = k × Vd; half-life t½ = 0.693 × Vd/CL.
First-pass metabolism reduces oral bioavailability; sublingual and intravenous routes avoid it.
Tablet excipients: diluent, binder, disintegrant, lubricant (e.g., magnesium stearate) and glidant.
Sustained release follows Higuchi (√t) or zero-order release; enteric coating resists gastric acid.
Prescription abbreviations: b.d. twice daily, t.d.s. three times daily, q.i.d. four times daily, p.r.n. as needed.
Sterile products are sterilised by autoclave (121 °C, 15 psi, 15–20 min) or dry heat (160 °C, 2 h).