desmopressin infusion

My father had a brain tumor removed and now has to take a nasal spray called Desmopressin. His endocranologist only wants him to use it one time a day, but the problem is he goes to the bathroom sometimes every 15 minutes!!!! He is also on 1/2 mg of Dexamethasone and that's part of the problem. Sometimes he takes two puffs a day but the doctor doesn't want him to do that daily.

There is a drug called Desmopressin (DDAVP) it reduces urine production at night. But drinking too much liquid with the medication can cause problems, and Desmopressin should be avoided if you have symptoms such as a fever, diarrhea or nausea. Be sure to carefully follow instructions for using this drug. Desmopressin is given orally as a tablet and is only for patients over 5 years old.

t mention in your question what medication you were taking. Commonly central DI is treated with desmopressin. Desmopressin works by limiting the amount of water passed in the urine. I don't know why you would suddenly notice a decrease in your symptoms after 34 years. I would recommend making an appointment with your regular doctor to see what might be causing this. Until you can be seen, it is important that you remain aware of your fluid intake and output.

talk to your doctor about desmopressin, it works.

today the consultant gave me tablets called desmopressin acetate. i understand they reduce urine amounts. will try but cant see them working well. Any new ideas or anyone with same prob please help.

Is there a medication for Diabetes Insipidus other than Desmopressin? The headaches as a side affect are dibilitating. This discussion is related to <a href='/posts/show/557217'>peuatrygland diabetts</a>.

I have phenitone infusion every 5 weeks how does this work i feel ill for a couple of ays after is this normal

DDAVP, Stimate, Minirin) is a synthetic replacement for vasopressin, the hormone that reduces urine production. It may be taken nasally, or as a tablet. Lack of the hormone vasopressin is more common in men than in women. Typically, those that do not produce enough will "correct" by the end of puberty (19-25 years old for men). Check with your urologist about the possibility of this treatment. Best of luck.

s Field Trainers testing the new infusion sets were telling Medtronic that the new infusion sets were of a defective design. The infusion sets would jam inside Insertion Devices, inducer needles would get stuck inside the cannulas, the infusion set adhesives would dry up and allow the Quick-Set Plus to come off the patient, and the infusion sets themselves would interrupt the delivery of insulin.

Mother is in the hospital, the nurse to mother infusion, mother infusion right arm is swollen, nurses decided to use mother left arm infusion, let me help pass the infusion tube, I was taken finger once by infusion tube needles, four weeks later , I catch a cold, have a fever, played a few urticaria, urticaria up immediately after disappear, after eleven days I have a sore throat, then 12 days after again a few urticaria up, until now has more than forty days, appeared the chest, neck, thigh pai

I GET KETAMINE INFUSION EVERY 2 MONTHS FOR TWO THREE HOUR SESSIONS. HAD 6 DAY INPATIENT KETAMINE INFUSION, 6 DAY IVIG INPATIENT INFUSION AND 6 DAY LIDOCAINE INPATIENT INFUSION WHEN IN 4TH DAY I SUFFERED FROM LIDOCAINE TOXICITY & HAD TO BE TAKEN OFF INFUSION. NOTHING HAS HELPED. MY CONDITION IS ONLY GETTING WORSE WITH TIME. SUFFERED SINCE 2009. ANYONE OUT THERE HAVE ANY FEEDBACK. I WOULD GREATLY APPRECIATE ANYTHING YOU HAVE TO OFFER.

I had my second infusion on Wednesday of last week. During my infusion, I was freezing/chilling. I asked for a blanket and a little later, when I was still so cold, they adjusted the A/C. Nothing was said to me that chills could be a reaction. As soon as I left, I felt nausea, dizziness, off balance, jello legs, I fell against the wall outside of the building on my way out.....and I had this internal tremor/vibration shaking feeling inside.

Hi Belle - Are you asking if you can travel with the actual infusion set up or are you asking if you can travel while receiving monthly Tysabri infusions? If it's the first one, I've never heard of home based, self-administered Tysabri. I would imagine that if you needed to be away from home during your infusion window you could get referred to an infusion center near where you'll be. If it;s the second one, yes you can travel in between infusions.

was it much more than doing it at the infusion center? I have BCBS. I think I want to do a round of IVSM....but don't want to have to drive an hour and a half to get it three-five days in a row. There's an urgent care/wellness clinic close by and it says they have an infusion suite. I called them to ask if they could do it I haven't heard anything back.

If still the symptoms persist then medical treatment with desmopressin, imipramine and anticholinergics can be tried. Hope it helps. Take care and please do keep me posted on how you are doing. Kind regards.

alarms so frequently, even after changing sites to places I had never used before (such as sites on my thighs and arms), changing infusion sets (I always use Quick Set with the inserter, never place it manually) and reservoirs. I called Minimed and after a few frustrating days of troubleshooting - the pump would work for a day or half a day and then the no delivery alarm would come on again when priming or when setting a bolus - I finally got a replacement pump.

Hi ladies i m bit stressed. Went to doc yesterday n he asked me to go for iron infusion becoz my iron studies r too low. I m 29 weeks now and not sure if that is safe.

My doctor now is talking about iron infusions. Do they really help with energy? I'm also a diabetic. thanks for any help you can give me.

About 7 years ago, I had my first iron infusion. I was told gastirc by-pass patients often do not absorb iron. I also am B-12 deficient. I had 2 additional infusions within the next few years. In March 2008 my doctor said I was anemic and I went back to the same hematologist. He said I was not anemic and could not help me. In March 2009, I was told my hemoglobin was 10 (not too low), but my ferritin level was 4.

Hi, does anyone know why iron sucrose can't be given as a total dose infusion? Everything I can find on the net says that it has to be given in 100mg doses to a maximum of 3 doses a week. The largest dose I could find is 200mgs at time. I need 1,000 to 1500mgs and would rather have it all at once. I can't have iron dextran due to severe reactions. Has anyone here had larger doses? Any problems?

I was changed to Tysabri and had my first infusion yesterday and everything went great, no reactions or side effects. However, I could swear I have more energy today. I have not been shopping for months and today I was able to go shopping. Is this my imagination? Just a rare good day? Or could the med already be having an effect on my fatigue? FYI, all other symptoms are pretty much the same.

my ferritin has dropped to 44 [15-290]; dr says iron infusion. i'm probably not absorbing iron along the gut. i'm recovering from fatigue and hyperthyroid. have been feeling good the last couple weeks, so wouldn't have suspected low iron, haven't been feeling any worse than last iron level test (which showed low but not this low). this is the drip where i sit for 5 hours and fork out 700 $. apparently i just need the one treatment.

Desmopressin infusion

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