Prednisone dosage all at once

Common Questions and Answers about Prednisone dosage all at once

orapred

when taking the steroid, Prednisone, are you to take the 5-2 pills all at once? What are the side effects if it's done?
My doctor gave it to me to help the swelling in my elbow, and she said it would also help my allergies which have been horrible for several months now. Here in Texas all the trees and flowers or whatever lol are blooming and they hate me, I have suffered somethin awful. She gave me 5 mg. and the bottle says to take one every day, she gave me 60 of them. Do any of you have any experience with this drug?
I'm feeling a little better about the high dose all at once.
The first IV treatment seemed to help, but only for a day. Once I began the prednisone, my symptoms have gotten noticeably worse. I've been taking them for about 18 days (currently on the 30mg dosage). The neuro said he's doubting MS because the predinsone isn't working. My question is this, has anyone ever experienced worse symptoms on prednisone? They symptoms aren't different, just worse. As a side, I really appreciate all the advice and support I've gotten here.
The people I know who have complications with steroids are using it on a daily basis or close to that. Once or twice a year doesn't seem to bother me at all. I also take an asthma controller, Q-Var, which is a steroid. took it throughout tx, twice a day. Also needed steroid skin creams, again throughout tx. I wouldn't worry about it. Asthma is no picnic either.
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. I know many MS patients are also treated with steroids thats why I decided to post my question here. Can some tell me their experiences with prednisone especially if they were on such a high dose? I know this sounds silly, but I really dont want to be puffy, have excess facial hair along with the unpleasant other reactions.
Hi all, I heard some clinics use steroids like prednisone during IVF transfer. Is there anyone who used it in their IVF and had success? If so what was the dosege of prednisone and how long did you take it?
Was very tired, almost zoned out a bit, my body hurt and my eye had been bothering me all day. At about 5am this morning, woke up with an excruciating pain behind my eye and shooting back through my head. I almost called 911. today other than nauseouness, hasn;t been too bad, but still don't have the (bouncing off the walls) energy everyone told me I would have. And my hip and knees have been bothering me. Did anyone else have these sort of effects? Thank you and blessings!!
Prendisone gives you energy, helps you breath better, I was on it after my accident and started last tx with it. I took it for a ruptured adrenal gland and lung issues. Short term it does give you energy and helps with many things, long term my understanding is can cause a lot of other damage. I know it took a long time to be weaned from it, For me it was a long time, Adrenals are little glands that control a lot.
the only way to completely avoid getting these side effects is to not have to take the prednisone at all, which, unfortunately, is not usually an option. Prednisone can be a wonderful drug that can help with many, many illnesses/diseases, but it also can be one of the nastiest drugs when it comes to side effects. The good thing is that once you are off the prednisone, the moon face and weight gain tend to (at least for me) go away pretty quickly.
this is worth than having my 3 babies all at once. Going Monday for a skin biopsy of the hives...have to clue how they do that. I AM MISERABLE, still taking meds, but hives go away for a few hours after taking prednizone, then come right back. I had to quit my job due to all this. I am on complete bed rest and would rather be dead than goin through all this. Appears that there is no END in sight in getting over ths.
I am very worried about giving him the prednisone. He was originally diagnosed with pancreattitis, so all the more reason I am leary about puting him on it. He has been suffering for over two months with nauseau, lethargy, loose stools and constant lip licking and excessive saliva. We nave done numerous blood tests, urinalysis, fecal, tested for addisons, xrays, epi.
I would suggest checking in with your doctor to see what his/her plans are for you getting off the med, whether it will be a taper after the 30 days or if he is just planning on you stopping abruptly. If at all possible, request that he taper you down. Best of luck!
Can anyone tell me what the scaling down dosage is for prednisone. Annie is being treated for possible lymphoma and is receiving 10 mg per day for two weeks. The vet wants to keep her on this dosage but since she isn't sleeping well I feel that I am only prolonging the inevitable. It also takes two people to give her the pills. One to hold her and I pop them in. I am running out of people at this point,, so I need to know how you taper the pred.
HI, My daughter also has a serious autoimmune disease, and has spent the past 5 years on steroids. She has repeatedly done several month courses of 60mg, and it certainly does change her appearance. The bad news is, right now while you are on that dose there is not a thing in this world to make the moon face go away (words straight from the mouth of her immunologist).The good news is it does go away. Many people find 10mg to be the magic number.
Debilitating panic attacks, pounding heartbeat, massive sweats at night, unable to sleep at all for 4-5 days. Almost called an ambulance due to incredibly bad panic attack/feeling of going insane. I immediately stopped the Prednisone but it's been 3 months and I am NOT fully recovered! The recovery has been unbelievably slow. For the first 2 months I couldn't sleep more than 3-5 hours per night, now I am up to 6-7 per night.
I recently got poison ivy, which I normally get once a year really bad and get the little punch pouch of of prednisone (6-5-4-3..). My medical insurance changed and now I need to get generic everything. So when I got the bottle I expected it to look different put the directions was very different. take 6 pills for 3 days then follow doctors instructions. I contacted the doctor who advised to take 6-6-6, 5 1/2-5 1/2- 5 1/2, 5-5-5..etc.).
He weighs only 25 lbs. After the first two 20 MG doses of Prednisone, I cut his dosage in half to 10 MG. today I gave him only 5 MG and will obviously skip his evening dose and that will be the end of it. But his panting and shaking are worse tonight... it is scary to watch.
Hi Lill, I was on prednisone 60 mg for a few months, then slowly reduced my dosage. I think it helped calm down the disease in the beginning. But after some time, especially once I reduced the dosage, I'm not sure it really helped anymore. I think it is your decision what to do, since the doctors don't really know enough about our disease. Have you tried antibiotics first? Is the doctor giving you any other alternatives?
A few doctors I dealt with and got frustrated with give me totally contradictory advice or refuse to comment at all. I have a feeling that if I put them in one room, they would scratch each others' eyes out (and then would bill me for it). I know it's long, but I am bit frustrated in trying to understand it. Thanks.
I hope that I’m wrong and that the whole thing is a coincidence. Ideally, this wouldn’t be happening at all, but I’d feel much more accepting of the situation if I find out that I didn’t directly cause it. Based on the majority of your experience, I have weakened faith that the first doctor I go to will be able to help me. I’m going to give the magnesium and calcium pills a try and seek out testing for Compartment Syndrome. Again, thank you all so much.
At the time I went along with it because I was pregnant so I was fine with the low dose but I thought once I had the baby he would raise the dosage. When I went back after having the baby and asked if he was going to raise the dosage he said no lets just leave it at 5mg and see how it goes for 6 months. I have'nt had a flare up but the large lump, which according to the breast specialist is infammed breast tissue is still the same no changes.
My new neurologist just increased my dosage to 150mg (75mg twice a day) saying that I should not be taking all at once - so half in the morning and half at night. Since I started that I feel like I'm getting migraines daily, putting on weight and had a horrific period (the worst in years!). Has anyone heard of this and if I go back to what I was doing will I go back to my only periodic migraines and back to my weight loss?
I just had a relapse a week ago and was takin 10mg prednisone 2x a day for 4 days. I noticed all I got was massive headaches and still have problems walking when I start off to walk. Prednisone seem to make me feel jittery and not do anything to help. I go to see my dr. this coming Monday. Hope my Dr.
He also should have been gradually increasing my dosage, which he also failed to do - until the injections, when it was increased all at once from 7.5mg/week to 25mg/week. I apologize for the lengthly post.... just trying to give some more background here, as I feel like I have a decision to make, but don't want to make the wrong one.
That being said, used judiciously, and occasionally, it has a place in the management of asthma. At times oral prednisone can mean the difference between life and death. I would use it as little as possible, and only when absolutely positively necessary.
I had to take large amounts of prednisone at that time in order to control the rash (remember, this started at week 7 of tx!). This went on and on for about a month, with doses of prednisone going as high as 80mg a day (that's a lot!). Until finally it got so bad I had to take a shot of IV steroids (a drug called solumedrol), which finally seemed to settle things down (or at least get them on the right path). I was tested with a sensitive PCR all during this phase of my treatment.
It has been one week since his med changes -- to 5 mg Prednisone in morning and fludrocortisone in late afternoon (I think -- I don't know dosage off top of my head). He is feeling better. No symptoms of POTS this week. In fact, he hiked a fairly small mountain in NH with his Dad yesterday and did well. He likes the Prednisone because he only has to take it once per day. Those in this forum may feel i am in denial, or some may have had these same hopes, too.
but which organ is going to shut down first,,,so my recommendations are if at all possible..
Hello, Im having a really hard time with taing my levothyroxine (i take tisorint .25). I understand the need to build it up in the system. At the risk of being bombarded by my mentors on here id like to ask the following questions. I have had really bad symptoms for about 16 months now. The highest my tsh has ever been was about 10.00 and that was about 3 weeks ago. I am only taking .025 of the thyroid.
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