I don't think he would intentionally do so either. The problem, I believe, is that doctors are being fed alot of misinformation. He may actually believe what he is saying is true, but where does he get his information about the drugs in question? It's not from an impartial observer, of that I'm certain. The actual drug company in question is the one who provides him the information about the drug in the first place. Are you going to tell me now that there is no conflict of interest there?
Doc did not go to school to learn about every drug that is on the market today. They get visits from various pharmaceutical salesmen whose job it is to sale him on the belief that what they offer helps his patients. They'll run them through all their clinical trials to prove it. Do you believe they are being completely honest when they are trying to sale a doctor on prescribing a drug? Do you believe that these pharmaceutical companies are disclosing every bad result from clinical trials? Do you believe a salesman who likely works on straight commission is acting in your best interest (the patient) or his own?
Therein is the rub. I assure you, I am not trying to be rude or disrespectful to Doc in any way. I respect the effort he put in earning his title. But his title has nothing to do with modern medicine and everything do with how the human body works. On my biology, I defer to him. But what ever info he provides me on drugs being offered today is more than likely second-hand info passed to him from a guy trying to sell him on a drug that will yield the salesman a fat commission check.
The whole system, in my opinion, is flawed. But it's not Doc's fault and I appreciate his effort here to help. It's not so much that I don't trust what he is saying as it is the fact that I can't trust the place where he got his information.
Again, respectfully, misinformation.
The drug reps' job is to represent their product.
Of course they're biased, and of course they're way less educated on these matters than physicians. But we barely listen to their pitch; we just want some starter samples for our patients, so that you can try a medication free of charge.
If they brought no samples, they'd bring no value whatsoever. We get our information from the actual scientific studies; consider our liability if we didn't.
You may not know how the process by which science works.
Any research project has to be objective and legitimate in order to get published, and an old respected scientific journal is the goal. The study should be double-blind and placebo-controlled, and geographically and culturally broad in order to ferret out any variables. Early studies may be small, simply because they represent an emerging discovery or principle. Once published, the study is subject to the critique of other experts in the field, frequently prompting other studies to explore further details or provide additional clarity.
It's highly likely that other researchers will try to duplicate the findings in other objective settings, publishing then their findings which may dispute or verify the original. It doesn't matter if the scientists are employed by a Pharma company or not -- their results must stand the competitive scrutiny of their peers in order to gain any credence.
If a company decides to invest resources in a promising discovery or development, they must submit a plan of action to the FDA, including Phase I, II, and III human clinical trials (animal trials may have been ongoing for decades). These must meet rigorous criteria and be managed by independent 3rd parties who exist simply to manage research projects; they have no connection to the owners of the product, including the absence of stock ownership.
Most drugs fail in this process, which is designed to show both safety and efficacy, with benefits far outweighing risks. In evaluation of R&D expenditures of any random company over ten years, we now find the average cost per approved drug to be near $1 billion. No wonder the retail cost of new drugs is so high.
And there will not be any new drugs approved which are not "new"; the molecule or its method of delivery will need to be different and prove to be beneficial.
Remember, all prescription drugs are regarded as potentially dangerous if not used properly; that's why they're not sold over the counter.
Many are also life-saving or health-maintaining.
That's where your PCP comes in -- he doesn't sell you anything or benefit from your misery.
He's just there to guide you through this complex minefield.
I could have probably seen 3 Medicare patients while I wrote this; after overhead and with much liability, I likely would have netted about $15 each. In case you're wondering, I do get paid for conducting the clinical trials, but I seldom know how the study drug is faring until after the entire trial is completed. (double-blind)