Retest symptoms and conditions

I was on doxycycline for three weeks because the doctor believed I had Lyme disease due to the slight headache, mild fever, and aching joints that I was experiencing. I was fine for the first few days, but then I began to develop some unusual symptoms. The symptoms fluctuated day to day, but I was never free from one or more of these symptoms: severe headache, chills, night sweats, tingling in my arms, weakness in my legs, ear ache, numbness in my face (especially my eyes and lips), anxiety, depression, insomnia, pain in my eyes, and neck, and stiffness in my jaw. At the end of three weeks, I seemed to have more Lyme symptoms than before I began the medication. My Lyme test was negative, but with my continuing symptoms my doctor recommended that I take the medicine for ten more days, and retest for Lyme. The first day back on the medicine I was sicker than ever. I waited it out because the doctor insisted that it was the best thing to do. I finished the medicine, and the effects were less intense. My second Lyme test was negative. I am being tested for Fifth's disease (my son was ill with it just as I began to experience my swelling joints - a condition that can not be treated, uggh). I seem to get worse if I don't drink all day and night - a lot of water is needed, all the time. The effects also increase when I go to bed, recline on the couch, allow myself to become nervous about my condition, or over work myself through the day. I was at the pediatrician with my son yesterday, and mentioned my problem, wondering how long it could take to get the medicine out of my system. She told me it could be as long as a few months. It's been two weeks since I took my last pill.

Starting taking Lipitor 20mg 3 weeks ago to the day and all of a sudden, over all pain in the muscle and joints to the point I needed to lie down and sleep for 2-3 hours. After I wake up, I feel like a real person again and then within 1 hour, bang right back to pains and a fuzzy feeling in my head!! Dr did some retest and told me that it's not because of the medicine and could be a flu but no flu I ever had felt or acted like this. I have been off it for 4 days now.. does anyone know how long does it take to get this stuff out of your system!!! I want my life back thank you!

Off of Toprol
Re: Nov 26th entry: I visited my primary doctor after my cardiologist said my thryoid med was too high and that was the cause of my high BP. My cardio had put me on Toprol and I had some ugly side effects from it. Well, I gave my primary doc the hospital test results of my thyroid and he said, "But this is in the normal range. There's nothing wrong with your thyroid level." Ugh. Makes me question the cardiologist. I told my primary doc about the Toprol for heart palps, etc., and he took me off of it and onto Triamertine (sp?) which is not a beta blocker but a diurectic for high BP. I took 50 MG for a week, and visited my primary doc again. My BP was down to 100/something small. Can't remember. So he cut my dose of BP med in half. I'm still taking the lower dose of thyroid med until my primary doc can retest and get a handle on my true condition. Thyroid med takes up to 6 weeks to take affect, so it's too soon to test.
So now I don't really know what sent me to the ER with the high BP and arythmia - possibly a panic or anxiety attack. I have Xanax now for that, but have only taken it a couple of times. When I tried it, it pretty much made me sleep great, but don't want to become hooked on it.

So, I'm glad I'm off Toprol. I did not like it. I have a feeling my doc will eventually wean me off BP meds, as I'm losing weight, exercising, etc., to that end.

Oh, you definitely don't want to go off Toprol cold turkey. It can cause a heart attack, etc., is what I've read. I'm not a doctor!

I am a 62 year old healthy male. About two months ago I was prescribed 500 mg. Levaquin by my urologist for a suspected prostate infection. Within the first 24 hours I experienced strange visual effects and extreme fatigue. By the third day on the medication I began to notice motor coordination problems. On the fourth day I awoke with chills, major hand tremors, and extreme motor coordination difficulties in my hands (I was unable to pick up a coffee cup with only one hand). I stopped taking it at this point, of course, and the symptoms gradually declined. It was a terrifying experience.

About one month later I had a relapse of the original symptoms and immediately arranged an appointment with my regular physician, who ordered a brain MRI and a prescription for a beta blocker to relieve the tremors. The MRI was negative. My symptoms improved markedly, almost immediately, and have not returned, even though I am no longer taking the beta blocker (after one month of regular dosage). I have my fingers crossed for the future.

I learned that my sister had similar reactions to Levaqui, suggesting that there might be a genetic predisposition to such an extreme reaction. From now on I will indicate to medical personnel that I cannot tolerate any member of the fluoroquinalone family of antibiotics.

As a side note, it turned out that I did not have a prostate infection after all but rather that a sudden upward jump in a PSA reading led the urologist to suspect the infection. A retest showed that the reading was anomalous, completely out of line with my history of lab tests for PSA. The worrisome part of this experience is the physician's willingness to prescribe such a powerful drug without clear indication of an infection.