There are errors in Paula's data set.

A discussion of the use of transient (non-SS) doses to continue (extend)
the steady-state pattern of doses can be found in NONMEM Users Guide VI
(PREDPP) Chapter 6,
8.2.8, page 62

Steady state dose event records are not retroactive. They apply only to
event records that follow them in the data set (i.e., have TIME greater
than or equal to the TIME on the SS record.)

On Wed, 14 Feb 2007 14:20:42 -0600, "Schaiquevich, Paula"
<[EMAIL PROTECTED]> said:
>
> Dear all,
>
> I have started working with NONMEM some months ago and I would really
> appreciate some help from the forum.
>
> I am building a monocompartmental model using ADVAN 2 for a drug which
> is administered every 12 h. The morning dose, in some patients, differ
> from the evening dose. The plasma samples have been collected after
> the first dose (i.e. before steady state) and before and after the
> dose given on day 28 (considered at steady state).
>
> I set the data as:
>
> #ID     OCC     EVID    TIME    SS      II      AMT     DV  8       1
> 1       0       0       0       500000 8       1       0       0.52
> 311.0 8       1       0       1.0                     0 1615.0 8
> 1       0       1.5                     0       2966.8 8       1
> 0       2.7                     0       3923.3 8 1       0       5.92
> 0       3355.0 8       1        7.93                    0       2563.7
> 8       2       1 660     1       24      350000  8       2       1
> 672     2 24      500000 8       2       0       671.9 2350  8       2
> 1       684     2       24      333333 8       2        672.6
> 0       2400.0 8       2       0       673.1        2780.1 8       2
> 0       673.67          0       2890.2 8       2       0       675.15
> 0       4110.0 8       2        678.13          0       3440.1 8
> 2       0       680.12        3190.0
>
> I have the following questions:
>
> 1- Is the data file set up to correctly account for both the initial
> (non steady state) dose and concentration time data along with the
> steady state dose and concentration time data?
>
> 2- Does the steady state dosing affect the pre-steady state dose and
> concentration time data?
>
> 3- I can not run the program when just considering the steady-state
> doses and concentrations. Am I missing something?
>
> Thank you very much for your help!!!
>
> Paula Schaiquevich, PhD Postdoctoral Research Associate Pharmaceutical
> Sciences St.Jude Children's Research Hospital 332 North Lauderdale
> street Memphis, TN 38105 Danny Thomas Research Center Room D1034 Mail
> Stop 314 Phone: (901)-495-5938
>
> E-mail: [EMAIL PROTECTED]
>
>
>
-- 
  Alison Boeckmann
  [EMAIL PROTECTED]

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