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Does anyone know if there is extreme racism towards blacks/hispanics in either of the above states?
This isn't the 60s, I don't know if you know but they passed laws banning that
I am in NC~ and I think it is the way it is everywhere....I am a minority myself....and I love NC and doubt I will ever live anywhere else......regarding your random ?....if you are thinking about applying to Pharm schools in one of the states I would suggest visiting and getting a "feel" for the schools....to answer your question.
Some of us don't have the financial ability to scope out every university they're interested in.
Does anyone know if there is extreme racism towards blacks/hispanics in either of the above states?
Some of us don't have the financial ability to scope out every university they're interested in.
Well then that is too damn bad (says the middle class american white male). I am racist against idiots, so don't come to Florida if you are one of those.
Then you must be prejudice against yourself because almost all pharmacy residents are idiots...
Then when you're done with the residency, hopefully someone with a clue will deprogram you and learn you the right stuff. 😎
Probably a statement I will agree with in a few years......how many of your hospitals have added doripenem to the formulary for empiric therapy because the guidelines say you can use carbapenems for community acquired pneumonia?
A real question, what do you think about the resurgence of intravenous colistin? I actually think this could be a good move.
Don't ask me a question you don't fully comprehend.Tell me resident.. why should we or shouldn't we add dori?? Why did Ortho release Dori when penem market is saturated with imipenem ready to go generic? Well, at least your question is semi stimulating...
colistin is ok... but we haven't encountered panresistant pseudo and acinetobacter that requires colistin...knock on wood, yet.
Your first question will take me some time to ponder, as I don't think the release time was strategic; on the surface I feel like you are asking me why Merck tried to gain approval of etoricoxib after rofecoxib was removed from the market: the same reason pharmaceutical companies do everything that they do: money. If they can manipulate people to believe doripenem is superior against Pseudomonas with slanted marketing practices, they win. Though there may be something more, my hospital has not considered even evaluating the agent at this point. As for imipenem, I feel it is inferior; 14% of Pseudomonas strains in the institution I work at are resistant, and it clearly has an inferior toxicity profile. The fact it is going generic makes it worth reanalyzing the cost:benefit ratio. However, I would be hard pressed to think doripenem can do anything meropenem cannot.
As for colistin, in a patient with end stage cystic fibrosis, Pseudomonas only sensitive to tobramycin, what do you think?
Likewise, another patient was placed on tigecycline with a strain of Acinetobacter only suscebtible to gentamicin. Would you think colistin may be of use here?
I thought you were an oncology guy! What's with all this boring ID talk?
I thought you were an oncology guy! What's with all this boring ID talk?
Drug rep, stay off our conversation...real pharmacists talking.
Grrrrrrrrrrr....speakin' of that,
I have some kick-ass drugs you have to read up about. Betcha never even heard of them.
Haha, do they all start with levo-, dextro-, des-, etc. Real novel therapies? I'm just kidding, I don't actually know who is a drug rep. or not, just am entertained by the banter.
Your first question will take me some time to ponder, as I don't think the release time was strategic; on the surface I feel like you are asking me why Merck tried to gain approval of etoricoxib after rofecoxib was removed from the market: the same reason pharmaceutical companies do everything that they do: money. If they can manipulate people to believe doripenem is superior against Pseudomonas with slanted marketing practices, they win. Though there may be something more, my hospital has not considered even evaluating the agent at this point. As for imipenem, I feel it is inferior; 14% of Pseudomonas strains in the institution I work at are resistant, and it clearly has an inferior toxicity profile. The fact it is going generic makes it worth reanalyzing the cost:benefit ratio. However, I would be hard pressed to think doripenem can do anything meropenem cannot.
As for colistin, in a patient with end stage cystic fibrosis, Pseudomonas only sensitive to tobramycin, what do you think?
Likewise, another patient was placed on tigecycline with a strain of Acinetobacter only suscebtible to gentamicin. Would you think colistin may be of use here?
Grrrrrrrrrrr....speakin' of that,
I have some kick-ass drugs you have to read up about. Betcha never even heard of them.
As Epic will be quick to tell you, I am currently a lowly PGY-1 resident (and he would be absolutely right). I am pursuing a second year in heme/onc, which consequently includes a lot of ID.
I heard of em all.
Suuuuure you have. You've got no idea what I do...or about the drugs. Said so yourself.![]()
1.Use tobra. 2.use gent. I thought you said you guys had an antibiotic stewardship... doesn't sound like it.
1.Use tobra. 2.use gent. I thought you said you guys had an antibiotic stewardship... doesn't sound like it.
As Epic will be quick to tell you, I am currently a lowly PGY-1 resident (and he would be absolutely right). I am pursuing a second year in heme/onc, which consequently includes a lot of ID.
but you're not a "pharmist"
1. We are, I was just asking; the patient also had synergy studies with another agent that was on board.
2. Patient started complaining of auditory disturbances, was discharged on home tigecycline. Once again, I am just wondering about this from afar. I have not talked with our ID Pharmacists about it. I am hanging on the Bone Marrow Unit, and just happen to be reading some interesting opinions/literature on colistin, and thought I'd run it by you. My whole thing is, our ID Fellows and some Attendings would be much quicker to jump at a carbapenem or tigecycline for a multi-drug resistant gram negative; I am starting to think we should start getting some older drugs back in the mix.
Also, have you seen that a fairly large trial in Israel has begun recruiting patients in a study comparing sulfamethoxazole/trimethoprim versus vancomycin for severe, hospital acquired MRSA infections? This is another area that intrigues me....
Medicare announced their Zevalin reimbursement effective Jan 1st...$16K. Totally sucks. 😡
Also, based on this answer, you believe aminoglycoside monotherapy is adequate for documented pneumonia? Perhaps this is so; is there data to support this?
Medicare announced their Zevalin reimbursement effective Jan 1st...$16K. Totally sucks. 😡
but not everyone has medicare
But all the insurance companies just follow suit. Blind leading the blind...at least when it comes to making clinical decisions.
I resemble that remark...I for one believe CMS did a heckuva job with ESA dosing guideline and monitoring algorithm.. but a drug rep would never understand that..
They've got the FDA on their side, no?
FDA is on the drup company's side.
Which carries some weight...
yeah...but CMS decision didn't weigh Amgen and Ortho biotech very heavily.
True...it's just frustrating to see reimbursement/financial incentives trump appropriate patient care.
Before you blame CMS, look to those drug companies taxing the US by forced subsidization of rest of the world in drug cost.
Who said I was blaming CMS?! You just happened to pick out a rarity 😀
Hush drup rep. I will ban you from my hospitals.
I was talking about Zevalin anyways...not your precious ESAs. Zevalin's much cooler anyways.
Oh...and you don't have the power to do that 😉
Pay attention to scene 7:28 mark.
lol...get back to pickin' the cotton!
what a racist thing to say