June 19th
2007
8:57 PM
I've taken topamax for approximately five weeks. I had experienced migraines at least twice weekly for more than fifty years, so it's been remarkable that I have been migraine free for more than a month. My biggest side effect has been abdominal pain. I wasn't given any education about side effects, and I was really worried when I began to suffer severe, really severe abdominal cramps about two weeks ago. I didn't have a clue about a connection between the medication and my tum until I went to Patient First one night in terrible pain and was asked if I were on any meds. When I got home, I got online, and realized that the tingling in my feet, and my memory lapses were all side effects. I've been in such a euphoric state because I haven't had a migraine, that I've ignored anything negative that's been happening. Would I stop taking Topamax because of the side effects? Not unless they become much worse - I can live with them - the migaines were far more dibilitating. It wasn't that long ago that I would be lying in a darkened room with my head throbbing, every sound was magnified and even a dim light pierced my eyes with pain. Shots of Demeraol and Imitrex were only temporary and didn't always work so tingles, and memory failiings and even tummy cramps are nothing by comparison!
-- By hiddenkate | Reply | Private Message me
June 14th
2007
6:31 AM
In France I was very fit and active and supple. Just before I left in May 1980 to emigrate to Canada I had a stomach infection that was treated with cipro antibiotic by my Dr in France. I finished them in Canada in my first two days. In France I became very hot and ‘spaced out’ when I began the medication, ached like mad and went to bed for a day (very unusual). I thought it was the infection. On the plane and in Canada I felt like a zombie and ached for some years. 27 year later I find that it was almost certainly a reaction to a drug. Since that time I have often been prescribed cipro for a bad prostate starting in 1985, when I had an operation. It took years of working out and exercsing to get fit - but always ached. Since the 1985 operation my prostate has played up a lot and I have been prescribed cipro many times. I thought that reactions to look out for were a bad tum. I have had progressively worse muscle pains and have had to work out more to keep things under control. I had not realized these drugs can effect the brain and also cause muscles to rupture, as well as causing terrible leg and other body part aches. This year in February in USA I was prescribed Levaquin a member of the same drug family (fluoroquinolones). On way back I was unusually stiff in the car and had headaches and could hardly get out of it or bend my legs. I thought it was old age. Since getting back I have had quite awful leg aches, ‘odd feelings’ and some terrible shooting headaches (never had until Daytona) which have worsened when I have had some Levaquin here in Canada in last few weeks. It has made my legs and knees almost impossibly painful to move and my left leg muscle to seize up behind my knee, so I have to fight to get up off chair or bed. It is best to stand and keep moving. The way these antibiotics work is to kill off a certain enzyme in the chain that the bacteria need to reproduce the cells, so they die. Just lately researchers in the UK have found cipro kills plants, They investigated and are developing a new form of weed killer based on that. Just think about it. The reason is that for 30 years! No one knew that the particular enzyme is present in the ‘DNA’ of ALL plants. Because a very common side effect of these drugs is to permanently destroy the cells of cartilage, muscles, rupture tendons and change the brain and central nervous system of humans, in the same way as it kills plants and bacteria, I have a suspicion that maybe the enzyme or a close relative is present in some humans. If so there could well be a genetic connection. SO if you suffer from thee effects let you family know !
-- By canuck1 | Reply | Private Message me
February 18th
2007
5:58 PM
I've been on Doxycyclene for 2 weeks now. I was trying to get rid of my acne. I've vomited twice. (The likelihood of this increases when there's very little food in the tum)Before I vomited, I'd feel like I was having a heart attack. A sudden tightness in the chest, breathing became difficult, a depression that felt like the end of the world. All eventually leading up to vomiting. My acne hasn't witnessed much improvement either. Either it doesn't suit me or I haven't been taking it properly.
-- By unnamedforever | Reply | Private Message me
March 15th
2008
7:32 PM
Hi All
Don't know what to do.. Been daignosed with Pneumonia, completed 7 days of Amoxicillan 500mg and now on day 4 of Clarithromycin 500mg, and 7 day course of Prednisolone 40mg per day.
-- By diamond4owl | Reply | (1) replies | Private Message meLike everyone else, the most horrific taste in my mouth tried everything to rid of it. It is Sat night and I am NOT going to take my next dose of Clarithromycin as it is upsetting me so much. I will have to wait until Monday am to speak to my doctor and hopefully he can give me something else. I am still struggling with pneumonia however I will take the risk. The bad taste, and upset tum must be the worst side effects ever what do you all think? The companies surely mus be able to something about this and put us patients out of our misery!!