ddavp infusion

How do you wean off the medicine DDAVP? I've been taking this medicine for many years only to find out my tests say I don't need it (I had small injury to pituitary in brain). Unfortunately I find it almost impossible to wean off because it makes you go to the bathroom ALOT after the medicine ware's off! since it's an anti diuretic/water retaining pill! Confusing and tricky.

One of the ways we would try to determine this was by prescribing DDAVP (if there were not any issues that would prevent using it). Desmopressin (trade names: 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).

My question is I have asked her endocrinologist to prescribe DDAVP for her to take during several camps she has this summer. He will not because of a chance she could have a seizure. I can't remember the exact reason but it does have to do with her diabetes and how DDAVP interact in a diabetic's body. He said the chance is very low, but possible. Could you give me your thoughts on a Type 1 diabetic using DDAVP.

We have a 7 year old colllie just diagnosed with Diabetes Insipetes (nephrogenic). Vet recommends treatment with ddavp eye drop. All the information we can find says that this is "very expensive". Can you give us a ballpark of what this actually means for annual cost of care? What are the implications of leaving this untreated if she has on going access to fresh clean water?

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

The tumor was germinoma. Yes u are right it was the optic nerve. I don't know for sure if my pituitary gland still functions I take ddavp, I also took growth hormones in the past and I take l cortef. But I'm not sure. Thanks so much I have a docs visit soon and Ill ask him more about my tumor. Thanks again for your help. And about the scar tissue he wants another MRI and then him and other docs will decide to do a biopsy or something els.

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.

I have used a nasal spray (DDAVP) for three weeks, but the bleeding did not stop. I tried doubling up on the nasal spray since I was prescribed the wrong strength, but it did not help. I had my second Depo Provera shot on December 7. I thought it would help make the bleeding stop, but I am still bleeding. I have also tried a estrogen pill I was prescribed, but it has not helped. I know I will have light bleeding on the Depo Provera, but is it normal to be bleeding for 37 days?

So I have to take DDAVP most of the time now. Before I used to be able to get away with only taking it at night. Maybe this is part of what is going on. I don't really have answer per se, but just an idea on why it might fluctuate more if u have it.

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

ive never went this much during the night..i had to go get on some meds called ddavp to slow it down so i can sleep..

she will have 4 packets of oatmeal and a glass of milk in the am. Another possible symptom is nocturnal enuresis. She is on DDAVP at night .05 mg X approx. 4 months. If I remember to wake her up around 2am she may be dry, before the DDAVP she was going through 2 goodnights diapers a night... if I didn't change it midway she and the bed would be completely soaked. Anyway, her Thyroid was hyperactive, and she is allergic to Milk and Eggs (she did have hives when we were at the Dr).

He also mentioned that she might have a missing hormone but more tests need too be done. In the meantime he has prescribed DDAVP, saying that this might help and if it does she will need this drug support for her entire life.

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.

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.

The medication used for this is called Dessmopressin or DDAVP. It is available in a pill form, nasal spray or injection. There are a few other conditions that can mimic this so it is important to get it ruled in or out. I have this and without medication I am also up every half hour drinking and peeing.i rec that you see a neuro endo to rule this out, your other pituitary hormones, and have a current MRI. It may be as simple as taking a little pill every night to help you to hold onto fluids.

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.

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