Well, I have reached a bit of a milestone in my FDA drug import
project, so thought I would write about it here.

I have done the following:

1. Gotten the FDA drug database (in ~5 separate files), and imported
each file into temporary files.
2.  Scanned the existing drug database for pre-existing drugs and
marked these FDA drugs to be ignored.
3. I scan for new ingredients and add those needed.
4. I create new entries in the VA Generic file (a GENERIC name is a
long list of ingredients) if needed, or match to pre-existing entries.
5. For the new drugs, I scan for *similar* pre-existing drug, based on
ingredients and names.
6. For all new drugs, a drug class should be assigned.  I use the drug
class of the similar pre-existing drug as a potential drug
classification.  This isn't assigned, however, until approved by the
user.

I have had to write tools to achieve each of the tasks above.  Its
taken about 4,000 lines of code (expanded format) for this.

So what I am particularily happy is that I have just finished
classifying all the new drugs.  I started out with 12,000 (!) new
drugs to classify and I never thought I would finish.  But with some
added tools, I have been able to finish it in about 4 days.

So all my changes have been to set up a custom file: TMG FDA IMPORT
COMPILED.  From here, new records will be added to the VA PRODUCT
file.

The next step will be to compile the new additions into the DRUG file
(#50), filtering for duplicates etc..

And from there, I hope that I will be able to use Norman Dodd's code
to make the new drugs show up in CPRS.

Since I have started all this, the FDA has released a new installment
of the database (they release every 3 months).  So I will run through
the entire process again with the new data, and hopefully there won't
more than a handful of new drugs.  And then I can do this 4 times a
year to keep current, and will probably be able to automate it.

Anyway, I hope that I am something like 60% done with this project.

Kevin


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