I'm sorry to have flown off the handle in this discussion. Everywhere I look today, it seems doors are slamming shut. The economy. Newspapers dying. And my beloved e-cigs in imminent danger. It's damn depressing. I'm .. touchy right now! Sorry I took it out on you, Disman.
There may be outside influences that determine the outcome of e-smoking. If there are, we are not privvy to that knowledge. Trog is likely correct with his blunt assertion that if an agency wants to ban e-cigs, they will find a reason. If they don't, we're in.
But I think much hinges on the "what is an e-cig" question. It's an electronic device that looks like a tobacco cigarette and functions as a substitute for one, whether the objective is quitting or simply enjoying an alternative. It was designed to deliver nicotine to those wanting it. The patents say so. So the FDA -- in its own words -- says the e-cig is a drug device.
The drug is nicotine. The formulation used is unapproved, making it a "new drug". But nicotine is used in NRT to treat a medical condition called nicotine addiction. Thus any device that delivers nicotine to addicts is a "medical device" and thus requires testing, review and approval by the FDA.
Just as a company can't dump a new drug on users without following approval guidelines, a company also cannot just start marketing a new medical device.
So that's our problem. Yes, we can say a screwdriver can be used as an ice pick, but that's not its purpose. That's not in its definition. Marketers have done us wrong from the very beginning. They have sold e-cigs as cigarette-like devices to get us off tobacco by delivering us nicotine, sometimes even advocating WHO's step-down practice. The marketing has backfired.
Now let's have discussion on how we get the FDA to see e-cigs as anything other than drug delivery devices. Personal vaporizers? It's a start.
There may be outside influences that determine the outcome of e-smoking. If there are, we are not privvy to that knowledge. Trog is likely correct with his blunt assertion that if an agency wants to ban e-cigs, they will find a reason. If they don't, we're in.
But I think much hinges on the "what is an e-cig" question. It's an electronic device that looks like a tobacco cigarette and functions as a substitute for one, whether the objective is quitting or simply enjoying an alternative. It was designed to deliver nicotine to those wanting it. The patents say so. So the FDA -- in its own words -- says the e-cig is a drug device.
The drug is nicotine. The formulation used is unapproved, making it a "new drug". But nicotine is used in NRT to treat a medical condition called nicotine addiction. Thus any device that delivers nicotine to addicts is a "medical device" and thus requires testing, review and approval by the FDA.
Just as a company can't dump a new drug on users without following approval guidelines, a company also cannot just start marketing a new medical device.
So that's our problem. Yes, we can say a screwdriver can be used as an ice pick, but that's not its purpose. That's not in its definition. Marketers have done us wrong from the very beginning. They have sold e-cigs as cigarette-like devices to get us off tobacco by delivering us nicotine, sometimes even advocating WHO's step-down practice. The marketing has backfired.
Now let's have discussion on how we get the FDA to see e-cigs as anything other than drug delivery devices. Personal vaporizers? It's a start.