I had a similar conversation with my manager today. They've been looking to cut for awhile, this is the excuse for the public. There is no reason to return all samples in our inventories if most or all of us weren't getting axed. The issue is with Tek/ARB and Tek/ACEI. That is a lable update to contraindications at the most. This in not unheard of and while doctors initially would be a little ticked they'd get over it, and realize that we did the right thing. Yes the Tekturna market would change, but that's what should be investigated by the people making the big $. Besides, there are a lot of doctors that believe in Tek thereapy before and ACE or ARB. I know some of you it's not efficacious but all of the head to head data on file shows it's essentially equal to Diovan dose to dose. Unless, there is something else going on with Tekturna that hasn't gotten out, this whole thing stinks of a conspiracy like another poster suggested. The docs I've spoken to aren't convinced that this really is an issue because they have patients on Valturna, or Tek/ACE for well over a year that are doing awesome, with good results beyond hypertension. How is it that it's Stage 3 and this wasn't picked up on prior. I really believe Novartis is being way to cautious. What I can't figure out is why they added Tek to ARB or ACE. They should have put Tek vs and ARB or ACE, in preventing outcomes. Anyway this company has been a major dissapointment ever since the demise of Galvus. I don't think I've been treated like a human or with an ounce of respect since then.