Ddavp pediatric dosing
Common Questions and Answers about Ddavp pediatric dosing
ddavp
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.
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.
My husband was diagnosed with a condition called neurogenic cough. It has been described as a chronic cough where the nerve that provides sensation to the voicebox and is responsible for triggering the cough reflex has been injured, usually by a virus. When this happens, the nerve's level of sensitivity before it triggers the cough reflex becomes markedly reduced; in other words, it becomes hyper-sensitive.
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).
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?
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.
Call your local pharmacist. We at MedHelp are not allowed to give out dosing instructions. Your pharmacist will be able to tell you exactly how to dose the medications. If your regular pharmacy is closed on Sunday, call any pharmacist availabe at your local grocery store or drug store such as Walgreens, CVS, or RiteAid.
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?
I saw this quote today in an article about a doctor speaking at a pediatric infectious disease conference. The article is at
http://www.familypracticenews.com/news/child-adolescent-medicine/single-article/lyme-disease-avoiding-inappropriate-serologic-testing/841bf9c30e90399a2d239e525b2993d5.html?
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.
Forgive me for adding this second part to the question but --- Could the fact that I didn't experience classic hyperthyroid symptoms after severe over-dosing by my GP on Armour, indicate Peripheral Thyroid Hormone Resistance (myopathy being lack of thyroid hormone in my tissues)?
My neurologist (not the Dr. who is dosing my thyroid) is looking into all possibilities, including referring me to muscle specialist or a thyroid one, etc...
TORADOLORAL (ketorolac tromethamine), a nonsteroidal anti-inflammatory drug (NSAID), is indicated for the short-term (up to 5 days in adults), management of moderately severe acute pain that requires analgesia at the opioid level and only as continuation treatment following IV or IM dosing of ketorolac tromethamine, if necessary. The total combined duration of use of TORADOLORAL and ketorolac tromethamine should not exceed 5 days.
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..
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.
His pupils seem to dilate normally and equally. He seems to close his left eye more easily than his right; as he is dosing the right eye is sometimes very slightly open when the left is fully closed. He can close the right eye fully, however, and does seem to blink normally (both eyyes going from open to closed to open again in unison).
Is this a potential problem, or is this just a case of his head not being completely symetrical, as is the case with most folks?
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.
First 'two' riba? I looked back at a prior post. You said hubby was Geno 3 and weighed 195 lbs. Standard dosing of riba (a flat 800 mg per day) is not as effective as weight-based (in hubby's case about 1200 mg per day). You should talk with the doc one more time. Hubby need to take the best shot at getting rid of this the first time. Good luck.
I was diagnosed with secondary autoimmune adrenal insufficiency in December. I feel lousy most of the time, have chronic abdominal pain and abnormal stools, and feel best flat on my back...which doesn't work well for someone who works 12 hour shifts in a busy ER while selling one house, building another, and has 2 teens and a disabled husband, lol. Here's my question. If a person has say diabetes, their meds are based on their blood sugars.
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