Tenecteplase
CLINICAL USE
Thrombolytic:Acute myocardial infarction
DOSE IN NORMAL RENAL FUNCTION
30–50 mg depending on patient weight (500–600 micrograms/kg)
PHARMACOKINETICS
Molecular weight                           :70 000 %Protein binding                           :No data %Excreted unchanged in urine     : Minimal Volume of distribution (L/kg)       :6.1–9.1 litres1 (weight and dose related)half-life – normal/ESRD (hrs)      :90–130 minutes/Unchanged DOSE IN RENAL IMPAIRMENT
GFR (mL/MIN)
20 to 50     : Dose as in normal renal function 10 to 20     : Dose as in normal renal function <10           : Dose as in normal renal function DOSE IN PATIENTS UNDERGOING RENAL REPLACEMENT THERAPIES
CAPD                :Unlikely to be dialysed. Dose as in normal renal function HD                     :Unlikely to be dialysed. Dose as in normal renal functionHDF/high flux   :Unknown dialysability. Dose as in normal renal functionCAV/VVHD      :Unknown dialysability. Dose as in normal renal function IMPORTANT DRUG INTERACTIONS
Potentially hazardous interactions with other drugsDrugs that affect coagulation or platelet function: increased risk of bleeding ADMINISTRATION
Reconstition
Water for injection Route
IV Rate of Administration
Over 10 seconds Comments
Incompatible with dextrose OTHER INFORMATION
It has an initial half-life of 20–24 minutes Cleared mainly by hepatic metabolism Re-administration is not recommended due to lack of experience
See how to identify renal failure stages according to GFR calculation
See how to diagnose irreversible renal disease
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