Dalfampridine and Dizziness: What Users Say
Brand names: Ampyra
Reviews for Dalfampridine
- Dit...
- Taken for 5 to 10 years
- August 29, 2016
Dalfampridine for Multiple Sclerosis "20+ years of RR without awareness/disability. When it changed to SD with dizziness, poor balance, many falls, intense fatigue, foot drop, diminished walking, muscle spasms, bladder & bowel issues, MRIs confirmed without argument. I participated in a Canadian study of 'Fampyra' with measurements of ability before and after administration. Improvements were marked, and I certainly couldn't deny the disease. Progression is manageable. When 'Fampyra' was approved for use by Health Canada, I continued on it. My insurer does not cover it. I'm so grateful to be able to continue. The neurologist remains satisfied, and so am I. It's not a cure. Comments from other users encourage physiotherapy to 'keep and improve the ability I have'. Thanks, I needed that!"
- Dia...
- May 16, 2015
Dalfampridine for Multiple Sclerosis "2 days on Ampyra and already noting difference. As I get close to the end of the 12 hours, I do see a lessening of benefits, and I have also experienced vertigo while lying down. But overall, I am looking forward to seeing how much my walking and standing improve."
- Dia...
- Taken for 1 to 6 months
- June 16, 2015
Dalfampridine for Multiple Sclerosis "It has been a month now, vertigo gone after a few days, a couple of nights pain in my upper arms, but not every night. Overall, I seem to be able to do more, but not as much as I want. Hopefully, this will continue to get better."
- Jen...
- Taken for less than 1 month
- November 27, 2018
Dalfampridine for Multiple Sclerosis "I started Ampyra 2x a day. For 3 days, the jittery feeling, insomnia, and loss of balance were too much. They suggested I take it once a day for a week or so to allow my body to get used to it. Tonight is the first night I took it twice after a week of once a day. I’m completely jittery, it’s 11, and I feel my night of non-sleep ahead of me. I’m not sure this drug is for me. Feeling frustrated."
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Your review helps others make informed decisions.- Dee...
- Taken for less than 1 month
- January 20, 2022
Dalfampridine for Multiple Sclerosis "I was diagnosed with MS in 2018. Fatigue, balance, and heavy legs were my major issues. Started Ampyra 2 weeks ago, and it's AMAZING the difference! I have more energy, my balance and walking distance have improved significantly. I experienced dizziness the first week, but it went away in week 2. Highly recommended!!"
- Rea...
- Taken for 2 to 5 years
- September 8, 2022
For Multiple Sclerosis "I have been taking dalfampridine for 4 years. This medication has improved my ability to walk to where I rarely use my cane. I was on the fast track to a walker, but after about a month of this medication, I noticed that I didn't have to use my cane for every step. I have to watch if I miss a dose, for it does affect my balance and back pain."
- Anonymous
- June 14, 2012
Dalfampridine for Multiple Sclerosis "This medicine leaves me feeling exceptionally dizzy and off balance. After seven months, it is doing nothing to help me walk."
- Anonymous
- June 14, 2012
Dalfampridine for Multiple Sclerosis "This medicine leaves me feeling exceptionally dizzy and off balance. After seven months, it is doing nothing to help me walk."
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Dalfampridine for Multiple Sclerosis "20+ years of RR without awareness/disability. When it changed to SD with dizziness, poor balance, many falls, intense fatigue, foot drop, diminished walking, muscle spasms, bladder & bowel issues, MRIs confirmed without argument. I participated in a Canadian study of 'Fampyra' with measurements of ability before and after administration. Improvements were marked, and I certainly couldn't deny the disease. Progression is manageable. When 'Fampyra' was approved for use by Health Canada, I continued on it. My insurer does not cover it. I'm so grateful to be able to continue. The neurologist remains satisfied, and so am I. It's not a cure. Comments from other users encourage physiotherapy to 'keep and improve the ability I have'. Thanks, I needed that!"