May 12th
2009
7:20 PM
been on the patch 50 mg for nine yrs now i don't seem like i get no relive at all its like the patch is not working at all,it fell like i have to take a piss. and then i have to force it out
-- By smokey57 | Reply | (1) replies | Private Message me
March 25th
2009
2:13 PM
Hello again, PLEASE EVERYONE that reads this let me know how long you took DOXYCYCLINE, how long the side affects lasted and what you did to get felling better. Also what your doctor said about you side affects.
I took 100mg twice a day for a month. Stopped in January and I am still having problems!!!!!!!!!!!!!!!!
Thanks for your time and if there is any other webs site to look at let me know!!!!!!!!!!!!!!!!!!!!!
March 11th
2009
7:38 PM
I'm on Wellbutrin since August and I've been loosing lots of hair lately. At the beginning of the loss I didn't give it much importance until about a week ago when pulling my hair back in my usual ponytail I notice that my hairline moved back noticeably, and that my already thin hair was barely covering my scalp...I thought it was stress or something, but I've never seen my hair weak and little like that. Then I thought at the meds I'm taking and googled "wellbutrin and hair loss". A super long list of web pages (including this) were talking about this side effect of Wellbutrin. Now I'm worried not just for my hair loss, but to the process of adaptation of my body to a potential change of medicinal. What should I do? My doctor is in Italy and cannot check on me personally.
Thanks for sharing
M.
March 1th
2009
5:06 PM
First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.
I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.
I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.
I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.
Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.
-- By brbarb | Reply | (10) replies | Private Message me
September 4th
2007
9:58 PM
I have been on methadone for about 4 years. I have gained about 60 pounds within 2 yrs of being on the program. I never had a weight problem in my whole life until now. Dieting and exersize did nothing.Also have severe constipation.Ive tried about 15 diffirent drugs to help the constipation. Most of them helped the issue but still leaving me with 1 or 2 bowl movements within 8 days.If I dident take anything for it Id wind up in the er with no bowl moement at all in severe pain.Also my stomache is huge, at times I look about 5 months pregnant. If anyone has any advice for the problems I am having please let me know.
-- By tm8380 | Reply | (4) replies | Private Message me
Topamax (1) Synthroid (1) Methadone Hydrochloride (1) NovoLog (1) Fentanyl (1) Metformin Hydrochloride (1) Doxycycline Hyclate (1) Singulair (1) Wellbutrin (1)
August 26th
2009
10:58 AM
I have been on Metformin for 6-7 months 500mg 2 x daily, and have puffed up like a balloon with significant weight gain of at least 45lbs., no desire to do anything physical as I have no energy,stomach upset and increased bowel movements, flatulence and absolutely no sex drive. I am going to discuss this with my doctor but before I do in their any other medications other then Glipizide for type 2 diabetes? I keep putting on weight like I am my blood sugar will be way out of control.
-- By ajgiller | Reply | (2) replies | Private Message me