Ddavp dosage iv
Common Questions and Answers about Ddavp dosage iv
ddavp
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.
Hello, I'm 26 and I had a non-secreting 3cm by 2cm macro adenoma removed from my pituitary about two years ago. Since then I have had regular MRI scans and Endo appointments. There was a small piece of the tumor left behind but six months ago I had a MRI and it had not grown since the MRI that was done post surgery. I am currently on 50 mcg levothyroxine and my endo told me all my other tests (six months ago also) were normal. Since surgery I have been extremely thirsty and urinating a lot.
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?
hi just a question about steroid use. I dont have MS but was recently diagnosed with Autoimmune Encephalitis after having a brain biopsy 3 weeks ago. Several months ago I was on IVIG which really didn't help my symptoms, so now I'm going to try a trial of prednisone. My neurologist wants to start me on 60mg then slowly taper my dosage. I'm so nervous because I've been reading all the side effects to this large of a dose.
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.
They have more info on dosage now so it is probably more safe now than when you were born. Also through the IV it will help relieve pain in your whole body( but won't take pain away) so they probably won't let you walk around. I will be getting Demerol when I can't take the pain anymore because I want to walk around.
I have been having no lucky in the past year absorbing my thyroid (synthroid) medication. They now want me to go up on my dosage from 900mcg's to 1,800mcg's, and I heard that is a very lethal amount. My TSH level is over 100 and my T4 level is .3 I think. What about other thyroid medications like Armour or cytomel? Need your opinion!
There have been studies that Oral or IV makes little difference, but dosage does. Since the typical IV dose is 500-1000 mg per day. The largest oral tablet I am aware of is a 50 mg dose. The problem is that even in divided doses, trying to get down 10-20 50mg tablets is going to make most people pretty sick. Most neurologist go with the IVSM. Doses under 500 mg/day have had issues with limited effectiveness in many studies.
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.
It went well, except on the third day in the hospital I developed atrial fib which returned to normal rhythm in seven hours with the help of an IV drip of amiodarone. I was released two days later and sent home with orders to take 200mg of amiodarone a day for three months.
My strength is returning and i'm exercising about an hour each day with no ill effects.My blood pressure is good and I have a good appetite, The only other drug I'm currently taking is 80mg of pravachol daily.
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.
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