Tennis player symptoms and conditions

I started taking Avelox 9 days ago. I was prescribed 14 days of Avelox after a round of Ceftin failed to clear up a sinus infection.
I am an avid tennis player, playing 3-5 times a week. My first bad experience happened yesterday when I went out to play and as soon as I walked outside I had a head to toe tingling feeling. This felt like I had chills but no goosebumps were showing. Over an hour or so later, the goosebumps showed up. This was in 90 degree heat!! I first thought it was dehydration, which it may have been, since I didn't seem to be able to get enough water/Gatorade no matter how much I would drink. This is even at night when I am not in the heat!!
I didn't take the medicine today. Played again this morning. I had the same tingling feeling head to toe, but no chills this time. To explain the tingling, I told a friend my skin felt like it was creepy crawly! It was a horrible feeling again in extreme heat!
I, also, have a hamstring that feels a lil tinge to it. I never have these problems and I am guessing this is due to the medicine, too.
If I walk outside, my body temperature feels like it shoots up! Even though I do not have a fever.
I went to my doctor's office and he is out of town! I asked to see another Dr. and he was "too busy to see me" since he was trying to get to the hospital! I was told to call my family Dr.which I did, only to be told he was also booked and I couldn't be seen. So, I gave up! And, not taking the medicine anymore!! Never again. This will be on my list of 'Allergic to.'
I usually have no side effects from medicines.

Wow, wish I had read this a long time ago. I have been on Vytorin 10/10 for 2+ years. Have many of the same complications as posted by others. Numbness in the hands and arms and severe joint pain in my elbows(I am not a tennis player, or anything remotely close to that) has just started to increase over the last month. Never made the connection until now. And the sleepiness!...I just feel like I could sleep all day everyday!...Now, this is one that I haven't seen in other posts, and am curious if anyone else has noticed capsule shaped things in your stool? They are almost a yellowish color and I would say about the size of a ring finger tip from the top joint to the tip of your finger? Part of me just assumed it was the Vytorin taking the cholesterol out of my system, but now I am worrying it could be something more. Any replies are appreciated, and last night, I took my last dose of Vytorin!

I commenced Lipitor 14 years ago at age 47. At that time I was a regular tennis player, walker and generally fit for my age. No problem with Lipitor for the first couple of years until I began to experience hip and low back pain. My GP diagnosed arthritis. Gradually became worse and I started to gather injuries (over stretched ligament in right knee which refused to heal, plantar fasciitis twice) My back pain became far worse, I persevered with tennis believing that exercise would help. I began to "trip" on the carpet and going up stairs (foot drop). I was sent for a CT scan in 2002 which showed spondylolisthesis and root canal stenosisss. On advice from doctor I stopped tennis. Referred to a neurosurgeon who after several months carried out a laminectomy in July 03. Cleared to recommence exercise in December 03 which is when my nightmare commenced. I developed bursitis in one hip, stopped walking until it settled, then excruciating pain in feet, and then bursitis in the other hip and continuing foot pain. I developed rib/back pain, again diagnosed as arthritis even though I felt the pain was muscular. I had one session of aqua aerobics and woke the next morning with plantar fasciitis which continued for 3 months even with doctor, physio and acupuncture treatment. I was then referred to a Spots Medicine Dr who ordered bone scans/x-rays which revealed a stress fracture in my foot. In 2006 I began to notice that my right arm had a tense feeling all the time, I had a loss of dexterity in my right hand which assumed a claw like appearance and my normally neat handwriting became practically illegible. My physio recommended I see a Rheumatologist who said I had "no more arthritis than I would see in any 62 yo", he sent me to a Neurologist who after 5 mins diagnosed Parkinson's Disease. Within 7 weeks of commencing the PD medication I was experiencing Restless Leg Syndrome every night. The neurologist said that my condition had "progressed" and increased the medication - twice. I was then getting RLS DAY AND NIGHT and getting no relief OR SLEEP!!! Finally after 12 months misery my GP suggested that I try coming off Lipitor to see if that was causing my body pain. Within 6 days I felt better, my muscles became less stiff and relax. I went back to my Neurologist who refused to accept my claims, he insists I still have atypical PD (because I do not have tremors). I told him the cure is worse than the complaint and against his advice I weaned myself off PD medication and Lipitor. It was hard going but I NO LONGER SUFFER FROM RLS AND MY DEXTERITY IS SLOWLY IMPROVING. I still have dexterity problems with my right fingers but the tense feeling in my right arm has gone and my "claw" hand is starting to relax My muscles feel bruised all the time. I am still taking my blood pressure tablets and 150mg of Co-Q10 a day. I have been off Lipitor 9 months. It has been a painful journed for the last 8 years and a nightmare for 12 months. My GP has marked my records as "allergy to statins" but says she just doesn't know if I have Parkinson's. I know that I will never take this awful drug again. My cholesterol has skyrocketed but I will have to try and lower it naturally and take the risk. I constantly feel like I have worked too long and hard in the garden, all my muscles are so sore. I really need to know if this damage is permanent and if this drug has caused Parkinson's Disease itself or just PD like symptoms. I guess I will just have to wait and see. I don't think doctor's believe us when we say Lipitor is doing damage to thousands of people. They love it!! When we are aging we are not surprised to get diagnosed with arthritis and this is why we take this medication unwittingly for so long.

I'm a 50 year old male, very active but plagued with hereditary induced cholesterol. My first experience with Lipitor was that it was a miracle drug for me. Unfortunately after taking continually for 6 months, I keep on developing muscle strains on my legs which forces me to stop playing tennis for a month. I also believe I ruptured my Achilles tendon about two years ago because of taking Lipitor.

Anyway, after stopping taking Lipitor, in just 3 weeks, my legs felt stronger and I'm pretty quick in my game again.

Another side effect is the aging effect it makes on my face. It sags, making me a lot older. Stopping my medication also quickly tightened my facial skin, making me look younger again. In fact , on the street I will know if somebody is on Lipitor even if nobody told me. The skin will be like very soft, double chin will be really sagging.

The problem is doctors don't believe this. When I tell them they dismiss it.

After my father's office was flooded by an AC backup at his workplace in June 2006, and as a result mold grew in the carpeting & walls. He got very, very sick & his doctor put him on Prednisone for almost a year. No local doctor nor specialist told us of the dangers of being on a steroid for more than a few weeks. My father kept getting sicker & sicker until one day in March of 2007 we had to rush him to the ER. There his doctor arrived, put MORE prednisone directly into his veins and as my father grew weaker & sicker we knew we had to get him out of there. We took him to Shands in Gainesville and they immediatly began their magic. It took a good week or so to undo the immediate damage that Prednisone had done to my father. It took until this month (October) until his liver & vital organs started working properly again and reached safe levels. In fact, he's still being carefully monitored by his Shands doctor to ensure his body will continue healing itself. His new doctor told me that if we hadn't taken my dad to Shands that day, he would absolutely be dead. Prednisone is a very lethal, dangerous drug if perscribed for more than a few weeks at most! Please, if your doctor wants you to take this steroid any longer than that, go see another doctor immediatly! It will save your life.

I have been on lipitor for about 2 yrs. Six months ago I developed tendenitis in my right elbow also bicipitel tendenitis in my right shoulder for no reason , I am not a tennis player or a golfer....... I knit. funny but not really. I can hardly lift a dish cloth . Now for the last 2 months I have developed calf pain. Last night woke in the middle of the night with upper thigh pain, thought I should check out more indepth side effects on the internet and am shocked to find all of these entries, but I also feel thankful because as of today I am stopping my lipitor and will go for natural remedies.

Prescribed Levaquin from Nextcare doctor after severe bronchitis with cough and wheezing for 3 weeks was not helped by Azithromycin or Albuterol. 4 days into the 500mg daily dose, I could not walk on rt leg. Knee pain and snapping so severe. Next day lt knee began to go out and snap. I had to scream each time I tried to straighten or bend my rt knee. Concurrently, left index finger swelled 2x normal size with pressure and pain as if it would pop. Rt wrist so sore that if it is touched, feels like all the nerves are exposed and being stabbed. Next my back began to hurt. This all happened before I realized it was toxicity from the antibiotic. I called the pharmacist explaining symptoms and she said mostly women get them and just take the last pill.
I did not, and went back to Nextcare dragging my right leg. The doctor then said he was 80% sure it is a reaction to Levaquin as my chest xray and blood tests came out negative for pneumonia or Valley Fever. So he said just rest a week. My symptoms are getting worse, I am trying to get into an orthopedist and have discontinued all my daily activities for the 9th day now as my rt knee is so horribly painful. It is snapping at least a hundred times a day with movement. I WAS an avid tennis player and have canceled everything due to pain and immobility. I have no support from any doctor so far as the urgent care center just does not care for individuals with a problem that they cannot dx as a cold or some simple thing.
I am in fear for my life after reading www.fqvctims.com site.
Help us all that we are allowed to be given poisons like this.
Ortho-McnNeil knows, so do the doctors, but enough of us have not died yet I guess. I can only hope I will not be one of them.

My daughter was recently put on singulair in october. She has always taken asthma medication since she was two years old.She currently takes advair(500 mg), zyrtec, nasonex.,ventolin . She had a rough fall with her asthma and the allergist put her on singulair and zantac. She is a tennis player who travels around the country playing tournaments and ever since starting the Singulair she has been sick and unable to compete.She has been on four rounds of antibiotics, and she has had a catscan, and all of the numerous bllod tests. We have had her to the DR.S eight times since October. She has also been on prednisone 3 times this fall.Last year she never went on prednisone or had any antibiotics.Her complaints are stuffy nose, sore throat,chronic cough , andno energy. She has symptons for about 12-14 days , then she has about 4 good days and then the cycle starts all over again.If anyone else has suffered from any of the same complaints i would love to know.