casodex price

HI THANKS FOR THE ADVICE.YES MY HUSBAND WAS GIVEN CASODEX WITH THE RADIO THERAPY BUT ONLY FOR A YEAR .THAT WAS IN SPAIN.WE WENT TO LIVE THERE FOR 5 YEARS WHEN WE RETIRED HAVING WORKED ALL OUR LIFES AS I COULD NEVER HAVE CHILDREN BECAUSE OF TERRIBLE ENDREOMETRIOSIS . THE TUMA WAS FOUND JUST A MONTH BEFORE WE WERE TO LEAVE ENGLAND.HIS CONSULTANT AT ST JAMES IN LEEDS YKS WAS QUITE HAPPY FOR HIM TO HAVE THE TREATMENT IN SPAIN AND GAVE US ALL HIS FILE TO GIVE TO THE CONSULTANT IN SPAIN.

My Brother was diagnosed with prostate cancer about 9 months ago, doctors removed his testicles instead of his prostate( tumor was too big), he’s been taking casodex for the past 9 month, but the last couple of days he’s peeing blood, he also has a couple of stents in his kidney which the doctor said he didn’t need to remove because his kidneys were functioning on their own again, I’m concern, any idea what could be going on

The side effects were so bad from the injection that I am not having any more.I am starting casodex 50g daily. The worst was my memory loss. How long can I expect the side effects to wear off.

Terrible side effects with Zoladex so switching to 150 casodex daily.

In 2004 his PSA started to climb and then he was on Lupon intermittently and, a couple of years later, an injection every 4 months. Casodex was also added along the way. The Lupron and Casodex were effective for 5 years as he had no outward symptoms until now and his PSA remained under 30. My husband had the hot flashes also at first, but they did go away. If I recall, the doc gave him something for that, but he didn't take it for very long.

t Have Radiation Again And He Wants Me To Start On Hormone Therapy Immediately.He Even Gave Me A Prescription For Casodex When I Left His Office This Past Monday. Obviously,This Needs To Be Furthered Discussed With My Oncologist Who Feels 2.5 Is Still Within The Safety Zone. I Also Need To Be Educated On Side Effects,Duration Of Treatment,Etc.

my husband is 50 he underwent RP in Feb this year and is currently on anti-androgen Casodex which he is to take for 2 years.

Do you think that maybe she misunderstood you? I'm on Copaxone and it cost about the same price. My copay is $15.00/month, my insurance covers the rest. I would call your insurance company and ask them how much it will be. If your insurance doesn't deal with shared solutions try calling Pression RX.

Question concerns Merkel Cell Carcinoma and CLL. Patient is 63 yo male, dx'd with prostate cancer '95 and treated with seeds. PCa metastatic to bone in '99. PCa controlled with double dose Casodex. Patient dx'd with CLL '99-no treatment given. WBC mostly 35-45K asymptomatic except slow wound healing. Patient dx'd with Merkel Cell Carcinoma '07. Merkel cell treated unsuccessfully with chemo and successfully with radiation.

I am currently doing antiandrogen monotherapy with casodex with a rising PSA. 0.17 to 2.8 in one year. How long does one stay on such treament,and what are the best treatments for hormone refractive prostate cancer. No prostate cells or metastatis has been detected,however possible micrometastasis. Taxatere only has a survival rate of 2 months.I am more interested in QOL and no chemo for me.

Please, anyone could give a hint how to get ENTACAVIR at a good price? This medicine has been very effective to me and I'll have to take it "ad aeternum", BUT it is very expensive. Is there any program or any cooperative group buyer to reach and get some discount? I appreciate any info whoch could help me. Thanks a lot.

Really a good news. I will like to know the possible price for the drugs and which company are going to be given authorize to deliver the drugs.

That was the price with insurance its 450 without..

just called to tell me it went up 5000 dollars this month. Have to get approved again ! Thought price would be dropping or at least hold steady . Heck of a thing once treatment has started . Should be a price freeze or something . Walgreen spec pharm is where my ins . Makes me go and they won't accept coupon from solvadi .

Just thought I'd let everyone know -- I picked up my refill for Tirosint this morning and the price has doubled, from what I've been paying. I've been paying $85.44 for 3 months; that jumped to $170.88 for 3 months. My insurance doesn't cover it, though it does save me a few bucks ($55 on this refill). I've contacted Akrimax, but don't know if they will respond or not.

No, I'm not blame them for everything. But some of them could charge a price less abusive, after all are the same corporations that are profiting here in my country charging the amount I told you ($33). Why do you have to pay 5 times more?

hi..please can anybody tell me how much is the price of baraclude 500 mcg in india?and also tenofovir..thank you very much for your help..

Last time I ordered my three month supply the base price went up about $800. My co-pay stayed the same at $150 for the 90 day supply. I've been interested to see what insurance is charged when I refill again the first week of September.

Well I called tricare and the reason that I had to pay full price is because the doc didn't call the right number for pre authorization. I called my doc and they are going to fix all of it for me so I should be receiving a refund. Thank you so much for the fill in.

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