# The correct option is B - Decrease.
It takes somewhere between 5 and 6 half-lives for a medication to reach steady state. Thus, medications with short half-lives reach steady state relatively quickly, while those with long half-lives take a long time to reach steady state.
Typical pharmacokinetic parameters of DRUG-A are F-0.02; fex < 0.1; fu 0.3; V- 0.22 L/Kg Half-life...
Drug-A (t1/2° 1 5 hours; V-62 L; fu = 0.1; fe = 0.3) is administered twice a day for 2 weeks. Calculate the accumulation factor at steady state.
QUESTION 12 Typical PK parameters for drug Drug-D are: F-0.01; fexs 0.4; fua 0.2; V 1.5 L/kg; half-life-3 hours. Calculate the amount in (mg) of drug in the body of a 220 pound patient at steady state when the drug is infused at 60mg/hour.
Hepatic Clearance Practice Problems PH4330 1. Normal CL value for this drug is 0.5 L/min and elimination is via the liver. V 100 L a. Is this a low, intermediate, or high E drug? b. In CHF (congestive heart failure) patient, Q is half the normal value of 800 ml/min. What would the hepatic clearance be in the CHF patient? What would be the normal and CHF FFp values? c. 2. Given the following pharmacokinetic information for a drug: .Q...
QUESTION 4 In one patient drug-A (t1/2° 10 hours; v-55L; fu-0.1 ; fe # 0.4; F-09) is administered as two 300 mg day. In another patient, the same drug is administered as one 200 mg tablet three time a day. The two dosing regimen have the same dosing rate. O True tablets once a e False
7. Smokers are known to have about 50% higher CL than nonsmokers for theophylline. If the average observed AUC after administration of 300 mg IV theophylline in nonsmokers is 100 mg.hr/L, what is the expected AUC in smokers after administration of the same 300 mg dose? Theophylline undergoes linear pharmacokinetics 2. After administration of a single 400 mg dose of a drug, a linear plot of the serum concentration-time prorile on a semi-log graph paper showed a y-intercept of 1mg/mL...