Prednisone vs medrol

Common Questions and Answers about Prednisone vs medrol

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My Eye Dr and Neuro decided it would be best for me to be on Solu-<span style = 'background-color: #dae8f4'>medrol</span>. I started off with a 3 day course, and the Nystagmus (uncontrollled eye movement) caused by ON actually worsened. At this point, my doctors decided that I needed another 3 day treatment.
Does anyone have information about the link if any, between SVR and use of a <span style = 'background-color: #dae8f4'>medrol</span> dose pak?. A dermatologist in the ER prescribed it for my rash and I dont think they consulted my hepatologist. Seems like it could lead to viral breakthrough because it lowers the immune response. Any thoughts??
If this is RSD (which the clinical history sounds like so far), some children benefit from gental physical therapy/stretching, over the counter NSAIDS like motrin, guanethidine, or steroids like <span style = 'background-color: #dae8f4'>prednisone</span> or a <span style = 'background-color: #dae8f4'>medrol</span> dose pack. There is a pain management clinic at the CCF in Weston, but I;m not sure if there is a specialist in RSD. Try calling the general number for pain management there 954 689 5260 and asking. Good luck.
Regarding steroid-related side effects, posttransplant diabetes mellitus occurred in 10% vs. 45%, and wound infection in 6% vs. 31% of steroid-free vs. corticosteroid patients (P=0.003 and 0.01)" Randomized trial of steroid-free induction versus corticosteroid maintenance among orthotopic liver transplant recipients with hepatitis C virus: impact on hepatic fibrosis progression at one year.
I see a lot of people going on solu-<span style = 'background-color: #dae8f4'>medrol</span> lately, some multiple courses within a short period of time. This really concerns me, especially in regards to the potential serious side effects - some which I have experienced personally. My neurologist is very conservative about prescribing solu-medrol He's explained to me that he doesn't give steroids for sensory symptoms like tingling or feeling numb unless it is a new symptom. He orders an MRI to see if there is any change.
A hefty dose of oral steroids is 80 mg or so of <span style = 'background-color: #dae8f4'>prednisone</span> and about 60mg of <span style = 'background-color: #dae8f4'>medrol</span>. The dose used in MS is 1000mg of the <span style = 'background-color: #dae8f4'>medrol</span> equivalent and 1200mg of the prednisone equivalent. It isn't just the overall dose that is important, but how fast you increase the level. With oral administration the pills must dissolve and then be absorbed. By definition the level does not go up very fast. With IV administration the level is instantaneously high.
My first question is what is the likelihood that the meds I have taken for the transplant and follow-up could be carcinogenic - busulfan, cytoxan, methotrexate, <span style = 'background-color: #dae8f4'>medrol</span>, <span style = 'background-color: #dae8f4'>prednisone</span>, voriconazole, cyclosporin, foscarnet, valcite, gancylovir? And my second question is what is the likelihod that this persistently painful area could be cancerous or some complication from the scleroderma? My third, and final, question is should I insist on a follow-up ultrasound and/or biopsy?
I'm a 44 y.o. female physician and athlete who has been experiencing acute onset muscle cramps and fasciculations in my left lower extremity greater than right since September. The cramps in my right shin can get intense and feel like compartment syndrome with pain/paresthesias distally. The left quad is also a site of regular involvement. Also experience fasiculations on occasion in my lats, forearm, and hand.
Corticosteroids for multiple sclerosis Examples Generic Name Brand Name dexamethasone methylprednisolone Depo-<span style = 'background-color: #dae8f4'>medrol</span>, Solu-<span style = 'background-color: #dae8f4'>medrol</span> <span style = 'background-color: #dae8f4'>prednisone</span> How It Works Methylprednisolone, <span style = 'background-color: #dae8f4'>prednisone</span>, and dexamethasone are corticosteroids. These medications shorten multiple sclerosis (MS) attacks by reducing inflammation on the brain and spinal cord. A high dosage of methylprednisolone may be given through a vein (intravenous, or IV) daily for 3 to 5 days during an MS attack.
I was diagonised with autoimmune hepatitis in May 2004. I was started on <span style = 'background-color: #dae8f4'>prednisone</span>, than Imuran was added and now am on Imuran alone. I also am on Fosmax and calicum + D. While on pred I noticed weight gain, bruising , night sweats, tingling across shoulders up neck, and increased blood pressure readings, also broke a rib. Some of the effect went away after weaning off pred.
According to a recent survey of these centres performed by DPIC, it was found that regimens vary from 1250 mg <span style = 'background-color: #dae8f4'>prednisone</span> every 2 days for 5 doses, to 1000 - 1250 mg <span style = 'background-color: #dae8f4'>prednisone</span> daily for 3-5 days. The MS Clinic located at UBC Hospital in Vancouver has used a regimen of oral prednisone 625 mg twice daily at breakfast and lunch for 3 days with no tapering doses.
Neurologists are unsure of diagnosis of current condition. Thoughts are drug induced (steroids, as stated above, vs. botox injection in glabellar area back in early June, vs. benign fasciculations). My question is whether or not this could be related to steroid withdrawal since the onset was so acute and follows the steroid use. I tend to be very sensative to meds and had serious GI problems when on a five-day course of steriods two years ago.
I have read many times that <span style = 'background-color: #dae8f4'>prednisone</span> can completely and totally destroy treatment and cause relapse or something. I know you had pneumonia but did your PCP consult with your hep doc to discuss potential problems of taking them while on treatment?
Now, if your rash takes off and cannot be abated or controlled by the prednisone as described above, try an 125mg IV of Solu-<span style = 'background-color: #dae8f4'>medrol</span>. Solu-<span style = 'background-color: #dae8f4'>medrol</span> is an IV steroid similar to <span style = 'background-color: #dae8f4'>prednisone</span> (i.e. it's in the same class of drugs). It's similar, but it isn't the same thing, so don't let some jive talking doctor try and tell you it is the same thing and won't work any better than prednisone.
Also, when I went to a NP for the horrible headache I thought was a long term migraine (now think it's occipital neuralgia), she rx'ed oral <span style = 'background-color: #dae8f4'>prednisone</span> (helped while I was on it but the pain came back within 2 days of stopping). So it may be that steroids are rx'ed for both MS and migraine.
Just a quick update - saw Neurologist on Monday - she admitted me for 3 day course of Solu-<span style = 'background-color: #dae8f4'>medrol</span> w/oral taper after and gave me meds for the headaches. Feeling better! She ordered MRI of spine - all clear.
I took Solu-<span style = 'background-color: #dae8f4'>medrol</span> for 5 days again, and this time followed it up with <span style = 'background-color: #dae8f4'>prednisone</span> pills for 6 days straight, decreasing the dosage each day by 1 pill. Ok, out of the last three flareups that I've had, this one has been the worst out of them all. It's now the middle of August, and my flareup and treatment was June 18th. I have increasingly been sleeping for 4-5 days straight, won't/can't get out of bed because I'm so weak and tired all of the time.
Both types of autoimmune hepatitis are treated with daily doses of a corticosteroid called <span style = 'background-color: #dae8f4'>prednisone</span>. Your doctor may start you on a high dose (20 to 60 mg per day) and lower the dose to 5 to 15 mg/day as the disease is controlled. The goal is to find the lowest possible dose that will control your disease. Another medicine, azathioprine (Imuran) is also used to treat autoimmune hepatitis. Like prednisone, azathioprine suppresses the immune system, but in a different way.
I am only on the steroids for 10 day and it isn't <span style = 'background-color: #dae8f4'>prednisone</span> because I don't tolerate that very well. I think it is <span style = 'background-color: #dae8f4'>medrol</span>. We'll see how that goes. At least it is only 10 days...and I could actually afford a few pounds right now so that is one thing I am not worried about. Thanks for the virtual chicken soup!
I'm taking five different things which seem to control my pain. A round of <span style = 'background-color: #dae8f4'>prednisone</span>, then antibiotics seemed to take away most of my pain, although the side effects were pretty scary. Thanks for any info. I'm just feeling even more in limbo than when this started. Well. . . better limbo than vertigo.
I was hive free for about @ weeks while on high doses of <span style = 'background-color: #dae8f4'>prednisone</span> but hives returned when weaning off of <span style = 'background-color: #dae8f4'>prednisone</span>. I also have gained 45 lbs. in since June due to prednisone. I have started Plaquenil about 3 weeks ago and am hoping things will get better after being on it for a while. They say it takes couple months to help. Along with the hives I have angioedema in my face, hands and feet. Sometimes I can't find any shoes to fit except crocs or something like that.
Actually, the MRI showed 5 bad discs, but only one is pressing on the nerve. Had phys therapy (no help), oral <span style = 'background-color: #dae8f4'>prednisone</span> (2 rounds) which was great when I was taking it, but all symptoms returned once I got below 20mg/day. Now doing a series of epidural injections (depo-medrol), two down and one to go, which have helped a lot with the pain and weakness, but I still can't sit for very long and still have numbness and tingling in my foot and leg.
One major a 5 day hospital stay in March and starting another round of solu-<span style = 'background-color: #dae8f4'>medrol</span> on monday at home.The last time I was on solu-<span style = 'background-color: #dae8f4'>medrol</span> I had to take insulin.They done the infusions at 250mcgs every 6 hours and now they are doing them at 1000 mcgs at one time.I'm afraid this will send my insulin levels over the edge.Even when I'm on prednisone I have to take glugophage.Any other time my sugar levels are great. Jamie, when they done my EMG/NCS they did the spine area as well as my 4 limbs.
The solu-<span style = 'background-color: #dae8f4'>medrol</span> (<span style = 'background-color: #dae8f4'>prednisone</span>) helps by shrinking inflammation but does absolutely nothing for myelin protection or repair. I'm sure glad Quix isn't around because she would be have a major fit about now. She can dx you on CIS (clinically isolated symptoms) evidenced by your symptoms - you only have to look like MS once to be eligible to use the DMD's for CIS. We've talked about that here before, but at least Rebif and Copaxone are approved by the FDA for use.
Out of all these exams and consultations I was told I have a cyst in my left maxillary sinus, (a year ago I was told I have cervical sinosis in c5-6). I was given <span style = 'background-color: #dae8f4'>prednisone</span> to take for 6 days and meclizine. After taking these medications my symptoms are not going away at all and I am feeling depressed. The endocrinologist said that synthroid would not give me these symptoms. I refused to take synthroid and just started armour today.
It is interesting that you were given <span style = 'background-color: #dae8f4'>prednisone</span> and antihistamines which I also found do not work. <span style = 'background-color: #dae8f4'>prednisone</span> is far more dangerous and has far more side effects than thyroid medication. So it does not make sense not to try thyroid in adequate does for such an awful problem. It is not well know that thyroid is safer than aspirin by far. Both aspirin and desiccated thyroid were discovered in the 1800s.
I also had a flu shot mid October high in the arm. After 3 weeks of agony and a <span style = 'background-color: #dae8f4'>medrol</span> dose pack (steroids), I went to see a doctor. Xrays showed nothing, but an MRI showed inflammation of the bone and a fluid filled pocket between my bone and periosteum. My doctor feels the shot was given between the bone and tissue layer (peristeum) over the bone. The nurse even said to me while giving the injection, I can't get it to inject. I asked her if she was in the bone and she replied no.
Its been 9 months since I have had any <span style = 'background-color: #dae8f4'>prednisone</span>. Still have some hives but a lot less. Doctors said it takes about 10/12 months to get all prednisone out of the body. Waiting to see what happens next. By the way I was also told stress but I baried my father, father n law and brother n law with no hives.
Just wondering if anyone pre or diagnosed with this has had numbness in the areas of the face neck scalp - toungue numbness etc VS pain. <<< CAN anyone help me on that one PLEASE ! Once when having an attack, facial numbness and fast heart beat, I layed on my left side with left side of head on a sofa arm, and almsot EVERYTHING went away instantly. I do have C spine spondylosis (osteophystes), some some other friends, doctors say that what I am experienceing is not likey from this.
Yes, I usually have two really bad attack per year and I have to take the Solu <span style = 'background-color: #dae8f4'>medrol</span> Iv for 2x for 4 days. 2) MRI lesions; Yes, My neuro said I have so many she wouldn't tell me how many I have. 3) LP : Positive in 1995 4.) How many Neuros so far: # 4 - The first Dr. was a jerk, the second Dr. was wonderful. I then moved out of state for my job. The third Dr. canceled 5 appt's in a row while I was in a severe attack. He also miss diagnosed a problem with C2, C3, & C4...
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