Water aerobics symptoms and conditions

Within 5 hours of first dose, I had "severe body aches" like those with the flu. My joints and muscles hurt so much that night that I had to call my parents to help me take care of my kids the next morning. I told the doctor who prescribed it, and he said to try to stick it out for the week...what horrible advice! Thinking it was crazy advice, I reluctantly took doses 2, 3, and 4 and experienced the joint/muscle pain each time, but I guess I just somehow tolerated it as if I had the flu. My hands became rather puffy as well. After the 5th pill, I woke up in the middle of the night with HORRIBLE joint and muscle pain, which was so awful that I could barely move; I was able to move a little bit, with extreme pain all over my body--particularly my knees, wrists/hands/thumbs, feet, and shoulders. I felt and heard unnusual snapping, cracking, and popping all over my body when I would move around at all. I stopped the med immediately, and noticed some improvement over the next several days. It has since been 9 days since the last dose, and I still have considerable pain in my knee, my thumbs/wrists, and arms. Unable to do my regular exercise, I tried gentle swimming and light water aerobics several days ago, but found even that to be too painful to do. I'm still unable to pick up my young children, drive without pain (mostly in right knee and muscles connecting to it, when pushing the brake) and am still somewhat limited in typical daily activities. Also, for the last 5 days or so, I've had a strange nodule present on a tendon in my thumb which has been hurting since taking the antibiotic. This has been a very frightening experience, to say the least.

I was diagnosed with breast cancer in 2003, age 53. I had excellent medical care at NW Cancer Specialists, Dr. D. G., Portland, Oregon. I endured Chemo (8 treatments) I had a lumpectomy and 36 radiation treatments. I also took Arimidex from 2004 - 2009. My doctor suggested exercise would lessen the side-effects and he was right. I followed everything my doctor told me to do, it was very difficult at times, but we are talking about my life and the quality of my days, his suggestions worked. I began a regime of walking, up to 3+ miles a day, water aerobics 3 times a week and I joined Curves. I also took vitamins: Costco multiple vitamin, vitamin E & C, Calcium + D(Viactive), Melatonin (natural sleep aid), probiotics, and fish oil. I also drank up to 6 glasses of water a day. I am now "cancer free" and not taking any RX.

I have been on Simvastatin for several months. I am now experiencing low back pain, stiff neck on the right-hand side, fatigue feelings in back when standing, fatigue, dizziness and generally feeling "awful." My MD cut me back from 40mg daily to 40mg every other day, but I still continue to feel sick.
I read complaints from others on this site and want to share my symptoms. I have a 78% blockage in my right carotid artery and a 58% blockage in my left carotid artery. I am 72 years old but what else can I do to prevent a possible stroke should these blockages increase without the use of a statin drug????

I can't believe that this drug is legal and that it has not been taken off the market. I have been on it for a year and couldn't understand why I was gaining weight, nothing helped to get those pounds off. I started at 160 and now at 195 and growing. Three years ago I had triple bypass, weight 150, some of the meds caused some weight gain, but nothing like this. My joints was so sore in the morning I couldn't hardly walk, I just knew I was going to be using a walker if this kept up. BTW I'm 65 female, always been active and busy, now I just do what I have to or can and that doesn't make me happy. I have recently been having crying spells and sore throat, voice lost, and enlarged tongue. The enlarged tongue caused me to do some searching on side effects.....I am so glad I found this page. I haven't taken any puffs of Advair since., that was 3 days ago. My tongue is starting to shrink, my joints aren't as sore, my crying is stopping. The weight is still with me and might never lose it, time will tell. I don't seem as hungry and eating less so maybe there is hope. This is a drug that should have Big warning all over it. Advair has taken a year of my life at this point. If there is ever a law suit I would be the 1st to sign. I didn't have that many breathing issues and really didn't understand why the Dr. put me on it.
I usually check up on drugs before I take them, this one slipped through the cracks, guess cause it wasn't a pill. At this point I just hope that others find this in time and stop using Advair before it ruins their lives.
God Bless
Barbie Kay

I am a 39 year old white male that had aortic valve replacement surgery five years ago. About three months after the surgery (which went off without a hitch) I had a tremendous spike in my BP that went on for a few days (200/100 - enough so I could see my heartbeat in my eyes!). My Dr started me on Toprol XL 75 and while it brought my BP down some, it didn't bring it down a lot. He moved me to 200 mg a day and now my BP is around 105/55 with a resting pulse around 50.

While I experienced many of the side effects listed here (feeling groggy, confused, etc) they only lasted a few months. I must admit that I did pack on about 20 lbs over six months. However, unlike so many who choose to blame drugs (or lack thereof) for their problems, I took it upon myself to start exercising and guess what?!? The weight comes off! I now weigh less than when I graduated high school, I am in better shape than any time in my life and I believe that exercise helps me sleep better at night. All of this even though I still take 200mg a day. Given that some of you say that you're practically dead at taking 25, I should be 6 feet under or weigh 400 lbs.

I guess what I want to say is that perhaps instead of jumping on the bandwagon here that Toprol causes all of your problems, perhaps you want to take your own health into your hands and begin to eat a little better and exercise (and don't give me "but my ankles are swollen!" excuse - there is something called water aerobics). I don't deny that it can cause some side effects, but it can work wonders with your BP. You just have to DO SOMETHING to help keep the weight off (which then help with the sleep problems, mental clarity, etc).

i am on my last pack of pills for yasmin. my gyn put me on loestrin starting next month. i hope i have a better experience with that than yasmin. at first i didnt notice any side effects at all. then within the past couple of months (ive been on yasmin for about 6 months) i have noticed so many problems.
i am prone to migraines, but i am getting migraines at least twice a week which has severely effected my work and school life.
i had an ear infection.
ive gained close to 20 lbs (!!!!!) when in the past few months my lifestyle has been healthier and more active than it was when i started this pill. it just doesnt make sense to gain so much when i have improved my lifestyle..
i find i am moody and depressed, if something bad happens, even if its something little, i either get so uncontrollably angry or sad and i cry all the time. im not normally this emotional, ive even cried at work. its so embarrassing.
ive also noticed that after any meal i feel like i am extremely bloated and my stomach starts hurting. it doesnt matter what kind of food, it could be healthy, greasy, veggies, or cereal..no matter what my stomach always hurts to much afterwards.
i am also getting night sweats and horrible back pain, especially when i go to bed.
i am gassy, and my cramps last for my whole period. none of those things ever happened before i was on this pill.
my libido went down, however i think this is due to the weight gain. i have never felt so disgusting in my whole life.
i have gone through many pills, and the nuvaring as well. none of them have had side effects on me as yasmin.
does anyone have any suggestions for other pills for me to try? i am willing to give loestrin a chance, especially because it is a lo dose pill..and i know that everyones bodies are different. i just feel so lost..i hope this new pill works out better.

I've been on Prednisone for a couple of months and am now starting to step down on the dosage. After ruling out several different maladies, I was diagnosed with Polymyalgia Rhumatica. Knowing the possible side effects, especially weight gain, I was reluctant to go on it, but my family said they'd love me anyway even if I did look like a chipmunk! Initially, I loved the stuff. Within a few days, my pain went away, my energy level was soaring, and I felt like I was 20 years younger. I started doing things I hadn't done in years like my art work. I felt like I was born again. Then came the time to start cutting back by 2 1/2 mg. every two weeks. I did that twice and now I'm dragging again. I'm up and around for 4 - 6 hours and then I have to go to sleep. I need to get completely off the Prednisone before I can have some much needed knee replacement surgery. Some people with Polymyalgia Rhumatica find it necessary to go on maintenance doses of Prednisone. It looks like that might me me, so I'm going to be some miserable person for a couple of months until I can have my surgery and go back on it. In addition to the possible weight gain, I'm also fearful of the osteoporosis. To offset the negatives of Prednisone, I have signed up for Weight Watchers and take water aerobics twice a week. For the hours that I'm up and about, I try really hard to keep moving like walking the dog, working in the garden, etc. I don't hate the Prednisone, I hate the condition which has necessitated my taking it.