腎功能不全時應監測濃度,調整藥物劑量(但常被忽略)之藥物
項次 藥物
ClCr <15 ml/min--2 mg on dailysis day
<3 mg/min: 100 mg at extended intervals
<10 ml/min-- in fast acetylators Q8-16H
ClCr 30-50: 0.25 mg QD or 0.5 mg QOD (treatment-naive)
ClCr <10: 0.05 mg QD or 0.5 Q7D (treatment-naive)
10-50 ml/min Q6-12H; <10 ml/min Q12-18H
Clcr<25 ml/min:dosage adjustments may be necessary
Clcr<25 ml/min:dosage adjustments may be necessary
1# QD in moderate renal impairment and in patients on
10-50 ml/min 75%; <10 ml/min 50% of the usual dose
10-50 ml/min <0.6 mg/day to every other day
ClCr<30 ml/min not on hemodialysis: starting dose should
be 5 milligrams (mg) once daily with titration not to
lower dose and then increased gradually; not
recommended for patients with end-stage renal disease
(requiring dialysis) or severe renal impairment (ClCr<30
GFR 10 to 50 ml/min: 75% of the usual dose
GFR <10 ml/min: 50% of the usual dose
GFR >50 ml/min Q6H; 10-50 ml/min Q12H; <10 ml/min
Clcr 5-29 ml/min: 5 mg ORALLY twice daily
GFR 10 to 50 ml/min: Q24-36H; <10 ml/min Q48H
GFR 10-70 ml/min: 75%; hemodialysis: 50%
GFR 10-70 ml/min: 75%; hemodialysis: 50%
Initial dose should be 50 mg QD in renal impairment
Initial dose should be 50 mg QD in renal impairment
Thiazides should not be used in patients with a serum
creatinine or urea nitrogen level greater than 2.5 mg/Dl
GFR <10 ml/min: 50%; 10-50 ml/min: 75%
GFR 10 to 50 ml/mi: 75% ; <10 ml/min 50%
Clcr<25 ml/min:dosage adjustments may be necessary
Contraindicated in advanced renal impairment
Adjustment for patients with a ClCr< 20 mL/minute
<30 ml/min halved or the dosing interval doubled
GFR 10 to 50 ml/min: 50 to 75%; <10 ml/min: 25 to 50%
Initial dose should be 50 mg QD in renal impairment
GFR 10 to 50 ml/min: 50%; <10 ml/min: 25%
Initial dose should be 50 mg QD in renal impairment
GFR10-50 ml/min: 50%; <10 ml/min: avoided
The lower dose of 7.5 milligrams daily has been suggested
GFR10-50 ml/min: 75%; <10 ml/min: 50%
A reduction in daily dosage should be considered (Clcr<20
A reduction in daily dosage should be considered (Clcr<20
GFR> 50 ml/min: Q6H; 10 to 50 ml/min: Q12-18H;
Potential need for dose adjustments in renal insufficiency
Clcr 10 to 30 mL/min: 5 mg/day; < 10 mL/min: 2.5mg/day
CrCl 20 to 40 ml/min: starting dose 0.5 mg
ClCr>60 ml/min--4 mg/day; 30-60 ml/min--2 mg/day;
15-30 ml/min--2 mg/QOD; <15 ml/min--2 mg on dailysis
GFR <10 ml/min: 50%; 10-50 ml/min: 75%
Clcr<25 ml/min:dosage adjustments may be necessary
< 40 ml/min (>2.5 mg/dL), oral dosing should be reduced
Moderate: < 16 mg/day; severe (creatinine clearance < 9
Patients in renal failure may require higher than usual
Dosage of sulfonamides be adjusted in patients with
Serum creatinine is recommended to be maintained less
ClCr 30 to 49 mL/min: 600 mg QOD; <30 mL/min: 600
mg Q72H; ESRD requiring hemodialysis: 600 mg Q96H,
Clcr<50 ml/min: 50%; Clcr<25 ml/min: 25%
> 50 mL/min Q6-12H; 10 to 50 mL/min Q12-24; <10
112 Superocin(Ciprofloxacin)250 mg 30-50 ml/min 250-500 mg Q12H; 5-29 ml/min 250-500
Slight reduction in the normal dose or by increasing the
Clcr10-30 ml/min:treatment--75 mg/day; prophylaxis--75
> 50 ml/min Q8-12H; 10 to 50 ml/min Q12-24H; < 10
ml/min Q24H, but is best avoided in these patients
One half of the usual adult dose is recommended
Do not use extended-release tramadol in patients with
severe renal impairment (creatinine clearance less than 30
< 30 ml/min: initiated at 300mg/day, one-half the usual
starting dose, and increased at a slower rate than usual
Clcr<30 ml/min: 25 mg (starting dose)
Clcr 10 to 30 mL/min: 5 mg/day; < 10 mL/min: 2.5mg/day
Comparison of methicillin-resistant Staphylococcus aureus (MRSA) carriage rate in the general population with the health-worker population Zena H Fadheel1, BSc, BMLS; Laboratory Technician Holly E Perry2, MApplSc (Hons); Programme Leader Bachelor of Medical Laboratory Science Ross A Henderson1, FRACP, FRCPA, PHD; Clinical Director Laboratory and Consultant Haematologist 1North Shore Hosp
PATIENTS TAKING ORAL BISPHOSPHONATES (FOR EXAMPLE: FOSAMAX, BONIVA, ACTONEL) Because you are taking a type of drug called a bisphosphonate, you may be at risk for developing osteonecrosis of the jaw and certain dental treatments may increase that risk. You should understand that the risk for developing this condition is very small. The following provides you with some additional inf