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Success
• Drug
of
• Drug product
Therapy
• Dosage Regimen
Estimation of
initial dosage of
drug
Evaluation of the
patient
Adjustment of
the dosage
regimen
Fixed model
Adaptive model
Empirical
clinical data
Personal
experience
Clinical
observation
In-
patient
out-
patient
Time( in hr)
Plasmaconc.(µg/ml)
MEC
MTC
Therapeutic
range
Plot showing conversion from IV infusion to oral dosing
CSS
IV infusion
Oral
dose
Dosing interval in hr
PlasmaDrugConc.
MEC
MTC
Loading dose
D0 D0 Do Do D0
Maintenance Doses D0
Sub-therapeutic Level
Toxic Level
Therapeutic Range
Plasmadrugconcentration
Time
Drugs Therapeutic range
Digoxin 1-2 ng/mL
Gentamycin 5-10 µg/mL
Pheytoin 10-20 µg/mL
Theophyline 10-20 µg/mL
Amikacin 20-30 µg/mL
51
Selection of Drug
Dosage Regimen Design
Evaluation of Patient’s Response
To Determine need for measuring serum
drug conc.
Assay for drug concentration
Pharmacokinetic evaluation
Dosage Adjustment
Monitoring serum drug concentration
Special Recommendations
Once dailydosing
Multiple daily dosing
FACTORS: DRUG
ADMINISTRATION OR BLOOD
DRAWING
FACTORS: PHARMACOKINETICS
FACTORS: LABORATORY
"Application of pharmacokinetics and bioavailability in clinical situations"
"Application of pharmacokinetics and bioavailability in clinical situations"
"Application of pharmacokinetics and bioavailability in clinical situations"

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"Application of pharmacokinetics and bioavailability in clinical situations"

Editor's Notes

  1. Must be given parenterally for treating systemic infections Demonstrate similar kinetics
  2. Dosing is based on the body weight & renal function. Divided daily dosing Extended interval dosing