Negative responses symptoms and conditions

I'm sorry if someone has covered this already... my grandmother is actually the one on Prednisone because she was diagnosed with peripheral neuropathy about a year and a half ago and I believe they recommended it to help her strengthen her muscles so she could walk. It has really taken a terrible toll as she is now unable to walk, and even using a walker can be stressful and difficult. Once she was put on Prednisone they continued to increase her dosage and because of it she now has terrible tremors. It kills me to watch her go through this and wish that I could fight the illness for her. I just want her to be able to eat without feeling so stressed out because her hands aren't steady. The doctor did say that the medication is causing her tremors, and we were relieved to find out that it wasn't Parkinson's, and now they are beginning to wean her off of the medication but she is still taking it at the moment. If anyone has finally tapered off from the medication, who originally had tremors, did you find that your tremors did go away once you were off the medication? How long before the shaking stopped and you felt better? I just want to give her hope that after she is off the medication there will be some relief. I feel awful knowing there is nothing I can really do but support and be there for her, and do some research. If anyone could help me with my questions it would be greatly appreciated. I'm sad to hear other people's terrible issues with this medication and as far as I know I have only heard negative responses to this drug, so it's unfortunate that in this day and age they haven't found something safer that has the same effect that doctors are looking for in a medication. I wish everyone a safe and happy recovery.

I'm 38 years old and I started Topamax in July of 2008 for severe migraines. I've had an average of 12-15 migraines per month since my early 20's and nothing was working. While initially adjusting to Topamax I had the tingling in my hands and feet during the first month but then it went away. My neurologist increased the dose very slowly from 50mg to 100mg to 150 mg. The migraines have decreased in response to each dose increase. At 100 mg the migraines reduced to 10 per month and at 150mg they reduced to 6 per month. My dose is now being raised to 200 mg which the Dr. says is the maximum recommended for treating migraines. The worst side effects I've experienced are extremely dry mouth (from 150 mg+) and slight hair loss. My starting weight was 138 and I lost 11 pounds very gradually before my weight stabilized at 127. I haven't noticed any problems with food or drinks tasting different. For some reason, I always have insomnia for the first week after a dose increase but then it goes away. I've only had mild concentration problems but nothing notable or problematic. So far, the medication has been remarkable and I can't believe what it's like to live life without so much migraine pain! I hope other people can have the same benefits from this medication.

I have read soo many negative responses in regard to this medication you would think these people are all in the medical profession and could diagnose their symptoms as being avelox triggered.For a few of these people that could be true but unlikely.People have this tendency to read about side affects and believe they are having them.For a minority of people thats true,thats why they are called side effects.I have been taking this drug for 4 days now and I am feeling great!!! I started out with body aches,fever,severe sore throat and sinuses that would not stop.By day 3 only minor sore throat remains.

I had Mirena out in in 2003 and had no problems with it. I had it for the whole 5 years and was completely happy with it. I had light(spotting) during my periods. My sister got the Mirena last year and is also happy with it. I am actually considering having another one, or having the new procedure called essure

I have been taking this pill for almost a year now. Recently in the last few months, I have experienced insane mood swings, irritability, heart palpitations, headaches, and anxiety. I even went to a cardiologist the heart palpitations were so bad. My heart is completely healthy. I have not had a period in like 7 or 8 months which is great but now I am thinking that this pill is doing more damage than good. My poor sweet boyfriend has taken the hit the most and its unfair I dump all my irritability on him. I am calling my doctor in the morning to change. After reading all these negative responses, I think this pill sucks.

I have been taken diovan now for about 4 months and I have no complaints. on last week my doctor switch me to lisinop/hctz but after reading all the negative responses i rather continue paying the high cost medication.

My beautiful 11 year old daughter was on Adderall XR 20 mg per day for 4 years. After about 2 years she started to develop some minor facial tics. After 3 years the facial tics were worse along with severe head shaking and she also started to develop trichotillomania (obsessive compulsive hair pulling). The hair pulling continued until she was almost bald. Her grades began to drop and she withdrew herself from her friends and family. Finally, we took her off the medication in October 2007 at age 12 and she immediately stopped the tics and hair pulling. We have found 3 other families whose daughters have developed these same symptoms after being on this medication for at least 2 years. We have filed a report with the FDA as our own doctor had no idea that this medication was causing the hair pulling. Now 5 months later her hair is growing and the tics are approximately 97% gone. We have taken her to a homeopathic doctor and she is doing absolutely great now. Marks have gone up and she is smiling and socializing. I am so happy we have our daughter back. The side effects of this drug was definitely not work it.