Lol, f*cking capitalists. $1.3b/year means around $100m/month, so if they get an extra couple weeks of exclusivity they get tens of millions! I'm sure they're just looking out for patients, though.Zosyn has been on the U.S. market since 1993 and had 2008 sales totaling $1.3 billion, making it the company's fifth-biggest product line.
Camardo said that Wyeth several years ago filed a "citizen's petition" asking the FDA not to allow generic Zosyn because of the potential for problems. The petition laid out Wyeth's scientific arguments and contained similar statements of support from outside experts on medication errors and drug interactions and effects, he said.
The FDA denied the citizen's petition last Tuesday and then approved Orchid's drug last Wednesday.
who are we looking out for when we substitute 3 generics for 1 monotherapy brand antibiotic to save 3 cents per dose? Are we looking out for the patient? Or the hospital? Our University System is cracking down like crazy on all pharmacy costs and looking for short term gains to get us through these times. For who? We are subjecting patients to 3 or 4 adverse events profiles from multiple generics to save 2 or 3 cents? What is the long term cost to our society?
The data are clear about what it means for the community at large over time.
Do you really think switching out generics a couple times will matter for 99.99% of patients? With few exceptions, it doesn't matter at all what the sticker on the bottle says.
congrats on being small town. I am originally from Prestonsburg although I now live in SC.
Anyway, I am all for generics. 100%.
I'm talking about bolting together 3 medicines(simply because they are available generically) and exposing the patient to potentially 3 different side effect profiles to create a spectrum that equals 1 drug that happens to be branded and costs pennies more than the generic cocktail.
I was taught by Bob Rapp and it was ingrained that monotherapy is almost always preferred to combination therapy. Less chance of medication error, fewer potential missed doses, fewer drug interactions. I am unaware of any combo therapy that prevents resistance with the exception of 5-flucytosine+amphotericin B, rifampin + pyrazinamide or ethambutol maybe, and amino+anti-ps penicillins.
The data are clear that imipenem+ amino, cefepime+cipro, aztreonam+ceftaz or most other combo DO NOT prevent resistance and most likely increase it.
Again, for the simple minded, I am 100% for generics. I like em. I'm just not gonna let the financial dudes fool me. The cost over the long term is what's important.
congrats on being small town. I am originally from Prestonsburg although I now live in SC.
Anyway, I am all for generics. 100%.
I'm talking about bolting together 3 medicines(simply because they are available generically) and exposing the patient to potentially 3 different side effect profiles to create a spectrum that equals 1 drug that happens to be branded and costs pennies more than the generic cocktail.
I was taught by Bob Rapp and it was ingrained that monotherapy is almost always preferred to combination therapy. Less chance of medication error, fewer potential missed doses, fewer drug interactions. I am unaware of any combo therapy that prevents resistance with the exception of 5-flucytosine+amphotericin B, rifampin + pyrazinamide or ethambutol maybe, and amino+anti-ps penicillins.
The data are clear that imipenem+ amino, cefepime+cipro, aztreonam+ceftaz or most other combo DO NOT prevent resistance and most likely increase it.
Again, for the simple minded, I am 100% for generics. I like em. I'm just not gonna let the financial dudes fool me. The cost over the long term is what's important.
Bob Rapp is one of the biggest industry ***** scumbag.
Bob Rapp is one of the biggest industry ***** scumbag.
Thanks,
congrats on being small town. I am originally from Prestonsburg although I now live in SC.
Anyway, I am all for generics. 100%.
I'm talking about bolting together 3 medicines(simply because they are available generically) and exposing the patient to potentially 3 different side effect profiles to create a spectrum that equals 1 drug that happens to be branded and costs pennies more than the generic cocktail.
I was taught by Bob Rapp and it was ingrained that monotherapy is almost always preferred to combination therapy. Less chance of medication error, fewer potential missed doses, fewer drug interactions. I am unaware of any combo therapy that prevents resistance with the exception of 5-flucytosine+amphotericin B, rifampin + pyrazinamide or ethambutol maybe, and amino+anti-ps penicillins.
The data are clear that imipenem+ amino, cefepime+cipro, aztreonam+ceftaz or most other combo DO NOT prevent resistance and most likely increase it.
Again, for the simple minded, I am 100% for generics. I like em. I'm just not gonna let the financial dudes fool me. The cost over the long term is what's important.
shoot the messenger ok, but discuss the content..
For who? We are subjecting patients to 3 or 4 adverse events profiles from multiple generics to save 2 or 3 cents? What is the long term cost to our society?
as I thought, nothing constructive, just attacks
go back to your popcorn
who are we looking out for when we substitute 3 generics for 1 monotherapy brand antibiotic to save 3 cents per dose
F*ck you Wyeth, instead of tying this crap up in court why not spend a small portion of your advertizing budget on developing new antibiotics.
Oh, that's right, you like chronic conditions. Can we have another statin please? Or maybe a combo statin with ezetimibe? Thanks.
I mean, honestly, what would the world be like without desvenlafaxine???
1. Its a blatant patent extender. Effexor XR, which brought in $3.8 billion for Wyeth in 2007, is losing patent protection this year, and Wyeth is introducing desvenlafaxine, which is simply Effexors main metabolite, as a novel antidepressant. Theres nothing novel about it. Every patient who takes Effexor produces Pristiq in their own body, at no additional charge.
2. Its not very effective. In the studies released so far, Pristiq just barely squeaks by placebo on the Hamilton Depression scale. In the U.S. study, Pristiq decreased the HamD by only 2 points (-11.5 vs. -9.5 for placebo), and in the European study, the differences was 2.5 points. And for the higher 100 mg dose, there was no difference between drug and placebo for U.S. patients.
3. Its not very effective. In the studies released so far, Pristiq just barely squeaks by placebo on the Hamilton Depression scale. In the U.S. study, Pristiq decreased the HamD by only 2 points (-11.5 vs. -9.5 for placebo), and in the European study, the differences was 2.5 points. And for the higher 100 mg dose, there was no difference between drug and placebo for U.S. patients.
3. It is not more easily dosed than Effexor XR. The main Wyeth marketing point for Pristiq is that patients can get better by taking the beginning dose of 50 mg, eliminating the need for a complicated upward dose titration process. Sorry, but this is not different from Effexor. If you look at one of the original fixed-dose studies of Effexor, comparing patients taking 75 mg, 225 mg, or 375 mg, youll find that the 75 mg dose separated from placebo as well as Pristiqs 50 mg. Psychiatrists typically begin Effexor at either 37.5 or 75 mg/day. At least with Effexor XR, when you keep increasing the dose, efficacy improves, meaning it actually has an efficacy advantage over Pristiq, because when you increase the dose of Pristiq, you lose efficacy, according to the U.S. study data.
4. It has no meaningful metabolic advantages. Wyeth will highlight the fact that Pristiq is not metabolized by the P-450 system and therefore does not have any drug-drug interactions. Well, guess what, Effexor has no clinically meaningful drug-drug interactions either.
5. Wyeths own lead investigator is unimpressed. I spoke briefly with Dr. Michael Liebowitz, the Columbia University psychiatrist who led the major Pristiq trials. Pristiq, he said, is another SNRI--it is not a revolutionary drug. It may be more tolerable at the starting 50 mg dose, he said, but only time will tell if it truly is clinically useful. If it is useful, then it will make money for the company, and if it is not, it wont.
Wyeth denied order to block rival's generic drug...Booyah!
http://blog.taragana.com/n/judge-de...ht-to-block-rivals-generic-antibiotic-177838/
Right...so a few weeks ago, I told my director that generic Zosyn was coming out the last week of September. He told me it didn't matter because he got a deal from Wyeth that allows him to buy frozen Zosyn from Baxter at the same price as the Apo generic. WTF is that all about? I wonder if he legitimately got that deal or was just making it up to save face because he signed a contract. You heard of Wyeth pushing anything like that?
How can Baxter/Wyeth promise pricing that's not established? Some of the GPO pricing has been published already. If I were you, I'd make sure to demand the price "match" that's been promised..
But, really, should I spend that much time helping someone else's career?