Web search symptoms and conditions

I am in shock and so glad that I came to this website. I have been taking simvastatin for about 5 months now and this morning I decided to do a web search with the words simvastatin and headaches. Everyday I for the last two months I have been asking myself why am I having these terrible headache. My Doctor did a CT scan, I had my eyes tested, I had my hearing tested, my blood tested and everything comes back good. I realized that I have to do something about this problem myself because my doctor prescribed another pill for the headache and that's that. Today I did not take the medication and I will not be taking it again. The symptoms that everyone described are so real to me but the headaches were the worst. I have to thank you all for posting this information. I now feel that I will get my life back.
Thanks verdul1

Hi, about seven years ago I complained to my doctor of noticing a little thinning at the top of my head. They referred me to a dermatologist who thought it was female hair pattern loss. It was minimal and he said that he rarely saw it get much worse in women. He suggested minoxidil. A year later, I relocated and the doctors at the health clinic noticed my blood pressure was slightly elevated. They put me on HCTZ. I am into healthy organic eating and was disturbed by the need to be on medication. They said HCTZ was a mild diuretic and never mentioned that hair loss is associated with it. After five years on HCTZ my hair loss is severe. I have lost half my hair and it is dry and brittle, no matter what styling products I use. I had long beautiful thick glossy natural hair, but the texture of my hair has totally changed. A few days ago, frustrated by the continual hair loss, I began searching for my own answers. In my first web search, I pulled up many connections to HCTZ and hair loss, including this site. As others have said, I am mad at myself for not taking my health care into my own hands sooner. I have stopped HCTZ and my blood pressure is being controlled by diet, exercise, and drinking plenty of water. What I would like to know-- is HCTZ hair loss reversible? Are there any reputable natural solutions to hair regrowth. (And minoxidil has been disappointing.) Thanks for your comments. They have helped immensely. GG.

I am a 49 year old male and took a 14 day course of Cipro for a UTI. By day four the souls of my feet were very sore, especially first thing in the morning but no other side effects. Mentioned sore feet to Dr after 7 days of Cipro but he did not believe it was from Cipro and had me complete the course. After 14 day course of Cipro feet were now so painful that I could barely walk on them especially after resting or getting out of bed. Also burning sensation on skin of feet and hands and some minor tremor. Saw a specialist and he immediately confirmed Cipro as the culprit and advised never to take that drug family again. Have since done the whole web search thing and discovered the whole saga of these drugs. Other symptoms have also appeared, some pain in middle of back, sharp pain in middle of back of both knees, hot and cold flushes, pain in left bicep, fingers that are very susceptible to joint injury and feelings of weakness and anxiety. Has been over three weeks now since I stopped Cipro and condition shows no improvement, may even be slightly worse. About to try a shotgun approach with treatment as there appears little documented evidence of anything conclusive on line. Starting course of anti-inflams (Voltaren) and these have already reduced the pain in my feet. Also magnesium and calcium supplements (theory goes that it may mop up any remaining Cipro and there is plenty of reports from sufferers saying that symptoms continue to appear for some months after stopping Cipro), Vitamin B6 (can apparently help with some types of nerve pain and tingling) and Fish Oil (omega 3's can help reduce inflammation). Not very scientific I know and can't be sure that all these are compatible with each other but am a bit desperate at this stage. Bracing myself for a three to six month recovery (just based on experience of many others). At this stage I am just hoping that damage is not irreversible as this appears to be a real risk. As everyone here will agree it is amazing how this situation is being allowed to continue. I could have stopped my Cipro on day two or three if I had been made fully aware of the risks and what to look out for. I am no expert by any means on this but from what I can gather Cipro and its relatives do nerve damage by the very way they work. It appears that anyone taking these drugs will inflict some nerve damage but for many it will not manifest to a degree that is a problem or at least a noticeable problem. So in some ways we are all sufferers, just to varying degrees. Another point mentioned often is that the symptoms may not appear for some months after the Cipro is stopped and therefore is not always associated with the drug. Also some say there is an accumulative affect with using the drug a second or third time. Symptoms may appear only after multiple use or symptoms may get much worse and more likely irreversible with multiple use. It's all scary reading. At this stage I am just hoping I can make a full recovery. Do damaged nerves repair themselves, does the Cipro eventually leech out of our systems .... I don't know. I will post in this forum again in a few months or sooner if I make a recovery.

I've started experiencing frequent nose bleeds after
taking Prilosec 3-4 times a week for the last 6 months.

After doing a web search for "frequent nose bleeds",
there are a lot of hits for "mold", but I am positive that
that is not the case in my situation.

If anyone else has been experiencing frequent nose
bleeds after using Prilosec, I would appreciate hearing from
them.