Jolts symptoms and conditions

I have been on simvastatin for 2 yrs . The past six months have had foot pain my doctor described as neuroma.By the time I started physical therapy the pain was in my arch + tendons. I went to physical therapy for two months, the therapist became concerned when improvement peaked. Still have burning nerve pain. I think its time for natural supplements . I hear "red Rice Yeast" is effective.
S. M.

I want to know if anyone has experienced severe joint pain while on Doxy. I was prescribed this med on a Monday. I (like an idiot) doubled up on my first dose Monday evening because I know you can do that with other antibiotics to jump start the process. What can I say? I don't like being sick. Well....Tuesday morning, I took my 2nd dose and went to work. Very soon after taking the second dose, I broke out into a very itchy rash all over my back that soon spread to other parts of my body. I called my doctor and was immediately taken off the Doxy and prescribed Augmentin. Later that night, I began aching all over. I woke up in severe pain throughout all of my joints, and was in a terrible mood.....obviously. As the day progressed, the pain continued, but seemed to be moving randomly about my joints. My ankles would hurt for a while, then my arms, the my shoulders, etc. That night, I took a Benadryl (still itching from the rash a little), some ibuprofen, and went to bed. I woke up feeling a lot better. A lot less pain in most of my joints. It was a good day. However, today, Friday, I am still in some pretty bad pain in my hands. Anyone else have a similar experience??????

I share the scare - I developed a bacterial infection after surgery and had an allergic reaction to first two antibiotics so was given Avelox. About an hour after the 1st dose my eyes became bloodshot, my joints ached like I had the flu or severe arthritis and I started having jolts of pain in different places, legs, groin, neck. I became disoriented and developed tiny blisters on bottom of feet, behind knees, on neck they faded, and at base of my fingers. The second dose caused severe joint and neck pain, disoriented feeling and again blisters. My doctor had me break the pills in half to take twice a day with benadryl. I also took large dose of Ibuprofen an hour after taking Avelox. That helped lessen severity of side effects. Final straw was the fifth dose - took before sleeping, woke at 4am and could not move from neck pain. My husband pulled me up so I could use the bathroom with me crying from pain. Sitting on the commode, I threw up and started to pass out. I managed to get downstairs and take an 800 mg. Ibuprofen and passed out for about 30 seconds. We went to ER. The attending physician decided I was having a muscle spasm and dismissed my fear it was the drug. They gave me a muscle relaxer and sent me home. I slept like the dead. My doctor called me that afternoon and told me to stop the Avelox immediately. You can imagine after missing 5 weeks of work for surgery, then having to miss three days last week and who knows this week how bummed I am. I am 46, have a wonderful family (a husband and 4 kids), a job I love, and life is good. I hope my body can recover soon as I am not used to inactivity. I cannot seem to function normally anymore.

I'm aged 36 and have been diagnosed with bronchitis with cough that has lasted for about a month now. My Doctor gave me 'professional samples' of Avelox that I've used for 3 days now.
The very first day, within an hour I could hear my own heart pounding and my left arm started to get numb. I thought I may be having a heart attack. I had joint pain (knees, ankles, wrists) soon after. Though it went away after 5-6 hours, it was quite scary. I started to have diarrhea.
The second day I had pain above my hips (kidney) and even though it went away, I was getting this little jolts like a quick 1-2 second electric shock inside that area. This really freaked me out and I thought this drug would kill me if I continued.
I complained to my Doctor about these and she said they were expected. I took it for the last time, the third day when I developed extreme nausea and giddiness.

The only good that came out of Avelox was it reduced my fever which was almost 103 before starting the dosage.

I am relaying the story of the granddaughter of my boss. She was 15 when she got the first shot of Gardisil in May of 2007. Within hours of the shot, she collapsed and an ambulance was called because she had distressed breathing. She was taken to a hospital and was in intensive care for 2 weeks in and out of consciousness. In the meantime, her mother tried to get the shot records from the doctor's office that gave the shot. They did everything in their power to:
A.Dismiss the correlation between the shot and the girl's collapse, despite the girl being in good health before the shot.
and
B.Keep the parents from getting hold of the vaccination records.
It was like pulling teeth to even get the vaccination batch numbers, and finally the office told the parents that somehow, the girl's health records went "missing". Luckily, the parents still had copies of most of the doctor visits, plus the "aftercare" paper following the shot with vital information on it.

When the girl finally began to be able to sit up again and eat on her own, she experienced mental fuzziness, memory problems, and speech problems. She had perpetual tingling and jolts of pain on the arm that had gotten the shot, in her side and abdomen and down both legs. Three weeks after the shot, she tried to get up out of bed and found she could not walk. She was diagnosed tentatively with Guillain-Barre Syndrome, also with nerve damage. It took her three full months to walk again without help, and even now, a year and a half later when she comes into the office she still has a bit of a limp. She lost over 25 pounds, which is pretty sad as she was not overweight or anything. She now looks very skinny and sickly. She had to quit school and started being home schooled because of the physical and memory problems and depression. I feel so sorry for her and her parents, who thought they were doing the right thing.

Well I posted a couple weeks ago and thought I would update. I intially thought I had no symptoms but lately it seems that in the morning getting out of bed that my muscles are extremly tight in my legs from my calf to my ancles. They seem to stretch out ok after a few minutes but i wondered if the damage has already maybe be not reversable. I just happen to have been seeing a physical therapyst for surgery I recently went thru for another problem altogether. I mentioned this drug to him and he had not heard of it. I told him of the tendon problems people have experienced. I asked him if he knew of any drug that can cause this effect and he stated cortizone can. He says its acks in destroying tissue, cells that act in supporting the tendon and allows them to stretch. . So knowing that a drug can actually cause the same symptoms some of you have experienced I am a believer now. I can see how this drug can possible reak havoc on any part of your body. So since i seem to have been feeling possible symptoms I was wondering if any- one has felt muscle aches and leg stiffness issues and how long after stopping the levaquin were the symptoms felt and what did they progress into if anything and did they subside and or go away all together. To me it seems that if this is about damage then its possible that just simple stretching can cause the tendon to snap. I can also see why some people may have recurring injurys. This would be a sign that one does not heal or the healing process is greatly lenghtened. I do plan on eating better and using some supplements to help.

I have been scheduled for an overnite sleep test at the hospital and was told I'd have to be off of Paxil for 3 weeks prior to the test. I tapered it down myself (now I know better) in what I thought was a reasonable period of 2 weeks. After reading all of the comments here I now know that I should have done this over months not days. I've been experiencing the "brain jolts" accompanied by the rapid distortion of vision for years and just assumed that it was another weird MS related symptom. Now I'm wondering if Paxil may have played a part in this all this time.
This morning I felt so much better about myself after reading all of the comments here. I was saying yes to all of the symptoms I've been having including dizzyness, extremes in emotions, nausea, less appetite, cold sweats, hot flashes, inability to concentrate, some paranoia, slurred speech, tinnitus, disorganized thoughts and disorganized physical space. I had no idea that Paxil was the cause of all of this. Not one clue.
Along with having less appetite I've noticed a change in tastes/flavors. I can taste really salty or really sweet and anything in the middle has almost no flavor. I also get a craving for something and finally make it, eat a bite and throw the rest away. The other thing going along with the LOUD tinnitus is that all sounds seem amplified. I don't know if anyone else has experienced these things. Thanks to all who have written because if not for this I would have continued to think I was losing my sanity.
I am supposed to go back on Paxil after the sleep test but have absolutely no intention of putting myself through this again. I haven't been able to work do to the crying at ever "Kodak moment" and really can't afford to miss this kind of time again. If only the doctor had told me what the withdrawal could be like at the time of prescribing it!

I am on 10 mg. of paxil and have been on it for about 4-5 years. I would like to come off but am worried about all these crazy withdrawal symptoms everyone talks about. I have gone as many as 3 nights without takiing any and never experienced "jolts", maybe a little jittery and confused. I am thinking about doing 7.5 mg. for about a month, then go down to 5 for a month, then 2.5 for a month.

I hear all these stories and wonder if the people who have all these bad withdrawls were on high does and if they weaned themselves off.

PLEASE HELP.

Thanks.

I was on Paxil for 12 years.
The early years I struggled to stay awake then gradually over 4 ti 5yrs I developed a boundless energy, with a constant elated and irritable mood, my thoughts and behaviors leaned towards the aggressive while highly confident. Never used a winter coat with temps well below freezing, I was always warm. Never needed more than 2hrs sleep each night.
Developed muscle aches, rash on both cheeks and along bridge of nose.
I read up on Paxil and discovered that these symptoms were Paxil related. I took myself off of it. I was on 20mgs then one month of 10mgs after that I quit cold turkey. While withdrawing I felt like my head was in a wind tunnel, a constant whooshing sound going round with dizziness, brain jolts, agitation, anger and crying, After 1 month of being off I began to feel better. If you want to quit you just have to tough it out. Once you get passed the withdrawals it is well worth it. I understand the link between school shootings, criminal behavior and serotonin reuptake inhibitors. It is wonderful after quitting to be in control of your thoughts and actions once again. I suggest you never start taking this medicine as it will be a nightmare withdrawing from not to mention the psychotic behavior it is known to cause in some cases.