sensipar study

My doctor wants me to consider Sensipar. After reading up on it am more confused than ever. I do not believe I want to take this drug. Scan was negative but from research am not holding it to be accurate. Suggestions and thoughts greatly appreciated.

Being treated for it all meds are sensipar, metropolal tartrate, famatodine, asprin 325mg, insulin 70/30, Gabapentine, hydroxyzine, reneval, advair 250/250. I may have missed one doing this off the top of my head but this is the bulk of it. She takes dialysis 3 days a week also. Please help this is messing with her breathing and her mood.

oh my parathyroid. Several labs show pth and tsh are normal. I was put on Sensipar for 10 days which barely lowered my calcium. Calcium ranges from 10.3-12.8 depending on the day, and ionized calcium 6.6.... Also, LD-5 elevated, low creatine and proteinuria ....I've seen ent, endo, cardiologist, oncologist....now what? Any ideas?

I was offered a Study on Asthma, Medication Is called, Sinaclar,the Study last 17 Weeks, Is this an Option for me? I do have scoliosis,and asthma, will this Interfere in my Health,?

I'm not sure whether this is the right place to post this but I'm a university student, and I have a really hard time concentrating when it comes to study, and it's not because I'm lazy, whenever I read something it seems to go in one ear and out the other, I just find it really pointless, even when theyre major exams which failing could cost me over a thousand dollars each, I can concentrate perfectly when it comes to other tasks and in a classroom environment, ever since my fir

Since I have not been able to capture the tacky event over years of trying my EP cardiologist has suggested EP study. I guess I would like to know if anyone has experienced this and can help me out with some wisdom/encouragement. I'm worried that they won't be able to identify the problem during the EP study and I will be back to trying to record this by rushing to the ER. I am tired of having my life limited by this problem but also have anxiety about the EP study.

I am a occupational therapy student and have a case study on an 8 year old boy who has developed enuresis at night, he has started to soil himself, as a result is being bullied at school, he is reluctant to go to school and complains of physical symptoms stomach ache and head ache his mother died at the age of five, his dad has recently started a new relationship please can you help, give any suggestions as to why he may being doing these things

It has had (VX 950) a really good track record so far but also is not perfect as their are reports of severe rashes and some evidence of viral mutations in the earlier trials. Being it is in phase 3 with a large group to study the picture will get a little clearer on that drug. I hope that helps and good luck in your decision just think long and hard about it first.

Does anyone know anything about the IDEAL study? This is where I think the info came from regarding my original decision to go with the pegintron.... less relapse rate, less sides, stays in system shorter amt. of time when you come off , etc. My new nurse, said that study had a lot of flaws and she did not put a lot of faith in it and talked me into pegysus... any comments would be appreciated.

I'm considering being a patient in a Remicade Study using a blind study wherin 50% are given the triple therapy: including Riboviron and pegintron, and the other half are given a placebo and the dual therapy. I have type 1, Hep C, my liver biopsy Pathology report showed that I have Cirrhosis>>>>>> Necroinflammatory activity: Grade 2-3 Fibrosis; stage 3.

I was reading today that the LDN study will be for three months and be a double blind study with 80 MS patients from the Univ of California @ San Francisco MS center. It is partially funded by MS patients who have shown improvements in their MS after taking LDN. They raised 25 thousand dollars and gave it to UCSF so they would do the study. The LDN group thought that the drug is so inexpensive that the pharmaceutical companies in the U.S.

One of the things to come out of my hospital stay was an order for a sleep study. Can these be of any help to my diagnosis process (for whatever I have)?? I do sometimes awaken with body parts twitching pretty violently - not all the time though. I sometimes awaken to spasms, but again most of those occur when I am awake. Wake up with a headache almost every day. Just curious. BTW - my borther was released from the hospital today.

hi, i have several heart problems (sick sinus syndrome, MVP, 8 x heart attacks) im from australia & moved to the usa to try to get medical help. ive been told i need an ICD but no doctor is willing to do it due to my lack of insurance and money. i was recently scheduled for an EP Study & the doctor cancelled it because i had a TIA (mini-stroke).

What drugs are you treating with?

I had a sleep study last night in the middle of the nite they put a cpap on does this mean I might have sleep apnea? Or is this just how they do it? I cant see them putting one on that was blasting oxygen with a mask unless I was needing oxygen.

I just did a sleep study, and the doctor told me I awoke up 5-30 times an hour. 5x hour from snoring, and 5.3 times an hour from arousal. I dont get any REM sleep, I know i have PTSD, and this makes the arousal state happen from nightmares. What should be the next step?

The ep study was done for pvc's. I was under the impression they were going to do an ablation but decided not to for some reason. I'll get the results at my follow up in March.

Here is a link to the Roche study: http://www.rocheusa.com/newsroom/current/2007/pr2007110202.html Yes, it does feel great. And I dont want to sound too giddy, because I know its an uphill battle for a lot of folks. But I guess eventually these sudies will benefit everyone.

I m taking ovulution study treatment. Frm 2nd day of period i took good ova 50 and adova tablets for 5 days. Also i m also taking conceva for Month 12th day results: Right ovary:15mm Left Ovary:msf Endometrial echo:6 mm 14th day Right ovary:16mm Left ovary:msf Endo. Echo:7mm 16th day Rt ovary:16mm Lt ovary:msf Endo.echo: 8mm 17th day Doc said that Egg is ruptured early.. And told Us to Keep Relation. My query is why my egg size is not Increasing?

Do any of you with a Chiari Type I gat a Sleep Study done? Is that helpful at all in deciding what pain med to take for the insomnia and migraine type headaches?

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