Exercises symptoms and conditions

I just got my Mirena removed today. I am SO excited. I have had it in for 1 year and it has been the worst year of my life. My symptoms were :MIGRAINES!- for which I was admitted to the hospital, they did all kinds of tests, and found nothing-( they even gave me an IV of morphine, and the migraine was so intense, i still felt it with the morphine.), arthritis- (or EXTREME ACHING in all of my joints, especially my hips, knees and lower back area., pain in my chest- like unable to breath, pain in my neck, I was sleeping 9 hrs a day and still exhausted and lately its been severe insomnia, cramping in my lower stomach and bloating really bad. I am 5"3, 21 yrs old, originally 107 pounds, and have two kids. After my daughter I was on Seasonique and although it made me have mood swings it was NOTHING in comparison to this. After my daughter I lost all the baby weight and then some. Even after I had my son in the 6 weeks before I got the Mirena, I lost all of the baby weight and was back down to 107 pounds. Now I weigh 130 pounds- and thats doing the same exercises and eating the same that I have always done. I have also never had ANY UTI's and I have had consistent UTI's since I have had it in, that have NOT gone away with various medications. I have had NO sex drive. Absolutely NONE, and I am 21years old! I felt very fatigued every day and it took all my strength and energy and mostly motivation that I HAVE TO provide for my family, to get up and go to work everyday. I read the brochure for Mirena when I got it inserted, and there were NONE of these side effects. I found some of these side effects on the Canadian website, and found people's horror stories of having Mirena in. I am SO happy to have finally gotten it out and am looking forward to being a normal healthy person again.

Wow, who should I believe? Placebo controlled studies which suggest Avelox is a perfectly safe drug or a bunch of crazy people who like to TYPE every OTHER word IN all CAPS who are probably all middle aged women with psychological problems and/or fibromyalgia, irritable bowel syndrome, or other made up diagnoses.

Here's a hint morons: The reason why every drug in existence now lists every possible side effect is because of crazies like you. This way, the drug company can protect themselves from litigious idiots like the poster below who wants to join a class action lawsuit. This only compounds the problem, though, because then more crazies look at the side effect profile and when they see that "Oh my gosh, it says right here it causes x, y, and z" it just validates in there mind that this is somehow a dangerous drug.

I swear, if all of the pampered babies in this country were put to work in a rice field in Cambodia, there would be a lot less nonsense in the world. You would see what true pain and suffering is about.

I was started on Advair HFA about 35 days ago. A little background about me is that I'm 35 years old, in good physical shape. I'm a competitive cyclists doing road races anywhere from 45-100 miles, I work out 2-4 hours everyday. I've had lifelong chronic asthma, but have fought the disease with my healthy lifestyle. I also play the saxophone.

Since I've been on Advair I've developed a constant sore throat. Been coughing up stuff constantly when I'm out training on my bike. Can't seem to sleep for more than a few hours at a time. The worst side affect has been the leg cramps which are killing my training for up coming races. I have constant leg cramps that force me to get out of bed over and over to work them out. My energy levels have dropped to the point that I can't do even half a workout without being totally wiped out. This is coming from a guy that averages 60miles a day on the bike, the other day I couldn't even do 15 miles and had to stop from the constant cramps and tiredness. This stuff is a nightmare. I've gone back to using nothing but my albuterol inhaler. I'll continue to do lung exercises 4 times a day and completely clean up my diet and basically get this stuff out of my system. Let this be a warning that you can't get something positive without something negative as well.

I feel like I am walking on clouds; I feel light-headed; I can't think straight/logically; I feel drowsy; I see strange images that are not really there; my stomach is bloated and I have severe, disgusting gas; and my vision is blurred. All this to kill my carpal tunnel pain? It's high time I get off of this poison. I suggest all of you do too.

My doc prescribed Avelox for a sinus infection after the first round of antibiotics didn't clear it up. The dosage was for 10 days. After taking pills for 4 days, I started getting a strange shoulder pain. It's like I had worked out my shoulder muscles after a loong time and my muscles were recovering, but I had done no exercises of any sort to cause that. I also did feel some dizziness and unable to focus after the 4th pill. I immediately stopped taking any more pills after that. Would rather face the sinus infection than deal with all this.
I was worried after reading the side-effects of others on taking this med. But luckily enough - it's been one week after stopping the meds and my shoulder pain is now completely gone. So, it does look like the side effects will clear up, but just takes sometime. My prayers to all who are suffering that they recover fast.

I was diagnosed with SLE (lupus) when I was 14, I'm 21 now, and I've had to be on prednisone all this while. The dosages alternate between 60mg (the highest) and 2.5mg (the lowest), I just went for a routine check up today and found out that my protein level in my urine is at an all time high. So the doctor is pushing me back up to 30mg of prednisone. Its 2 am, and I am sitting in bed crying because I don't want to have to go through everything again; the weight gain, the moon-face, everything. I know I may sound shallow, because ultimately, the medicine is keeping me alive, but the side effects are terrible. Very few people understand that its not fat that you're gaining, and the remarks that I know I am going to get are enough to drive me insane.Is there anyway the water retention or the weight gain can be stopped or decreased?

I was diagnosed with asthma as a child. In late teens it seemed to not be problem, however after 50, I started developing symptoms of asthma again as evidenced from COPD tests. I am currently using Advair 250/50 since 55 yo.

One symptom, that I have not seen addressed here is that of "slow healing" after injuries. I injured my back awhile ago, and it seemed like 2 years before most of my symptoms were gone. To this day I still feel lingering effects. Then I scraped my shinbone. It seemed like it took forever to heal, and now there is an ugly red/purple scar where the minor scrape was.

I had never taken so long to heal before, and read that this was a problem with taking Advair. I never figured my asthma was that serious in the first place, so I simply cut back on the Advair to once/day or less as it seems still to keep my breathing OK. Sometimes, after a few days of not taking Advair, I feel some minor difficulty with breathing.

Now that I am 63, and so concerned about "slow healing", which I attribute to Advair, I have asked my Dr. to perhaps take me off Advair and simply take Albuterol when needed. Then I read that Asthma patients should only use Albuterol if that is sufficient to control symptoms and to advance to Advair to control more severe symptoms. Another article says that Albuterol does not heal Asthma, only assists with sudden onset of breathing difficulties and that I may still damage my lungs if I do not take Advair.

I remain at a loss as to what is best: Taking Albuterol when needed (perhaps a few to several times/week) or as I was doing before, contrary to recommended dosage, of 1-2 times/day. Fortunately my Dr. goes along with my changes, but tells me if symptoms get worse, she will put me on Advair 2X's/Day (which I probably will ignore dosage because of healing side effects, and use once/day or less).

I will report back later after trying Albuterol for time without the use of Advair at all.

In addition to the rather common occurrence of the sweats, I have gained 30+ pounds since commencing a Lupron intermittent protocol. The majority of the weight gain has manifested itself in my stomach. My appetite has not increased or if so, not significantly. I exercise regularly and in most cases, aggressive exercises. I have carefully monitored my diet and have been unable to shed any weight or stomach mass.

My father who is going to be 80 on July 15th started taking remeron back in January of 2008 for depression he was in and out hospital and rehab since October. He almost died in October but he fought his way and hes physically doing better now. He was put on remeron cuz his depression was so bad that he just wante to give up, he started on half a pill at bed time..(7.5 i believe) he was doing his exercises and again..he bounced back from a deep depression within days :) February 7th 2008 my dad finally came home after being away for 4months he became very very talkative like hyper, couldn't sleep and got agitated very easily(thats not my dad) on June 18th 2008 the doctor that comes to the house asked what was going on..i told her HES NOT SLEEPING..and hes very like hyper, so she INCREASED HIS REMERON!!! full dose 15mg. well.. July 2nd things changed for the worse, He talked about things that happened years ago, he went as far back as the days of THE DEPRESSION..yeaaaars ago;
just things he never talked bout before...July 3rd he was showing signs of being VERY LOST..VERY DISORIENTED...like he would get up to use his potty(as he calls it) and thats rite next to his bed, and he went rite past it and into my kitchen way. just standing there, NOT KNOWING WHERE HE WAS. and he would repeat himself over and over and over, not remembering what he said, :( very sad )
The 4th of July i had him taken to the HOSPITAL to be checked out cuz he just wasn't acting right, i thought maybe he was on the verge of another stroke his BP was 150/101 HIGH....i think maybe cuz of the agitation,(HE GOT MAD...DIDN'T WANT TO GO TO THE HOSPITAL: )but i needed to know what was going on..they sent him home, they said possible early dymentia, NOT..i don't agree....june 18th -july 2nd IS EXACTLY 2 WEEKS..WHICH IS HOW LONG IT TAKES FOR MEDICATION TO GET INTO THE SYSTEM...i believe its the REMERON causing these problems.i took him to his psych and he asked my what was it increased? i said the doc increased it cuz he wasn't sleeping, well the psych was NOT HAPPY wit this...he was like U CANT DO THAT ITS NOT FOR SLEEP ITS FOR DEPRESSION..U DO THAT AND UR GONNA HAVE BIG PROBLEMS.... Well thats exactly what we are having.So then i was told to decrease him back down to 7.5 and if no change in a week -2 weeks...to stop it...well im stopping it tonight. I am hoping to see him better soon..if anyone agrees with me PLEASE LET ME KNOW...he was perfectly fine b4 the increase in this medication...BESIDE THE EXCESSIVE TALKING..but i am willing to deal that..i just want him back to the way he was. Its soo frustrating and sad to see him this way :(

I'm very curious to read all these side effects! I have some strange symptoms going on and it only occurred to me after weeks of them that they may be caused by the Mirena IUD. Apart from constant annoying spotting and a bit of a dull ache in the pelvis now and then, I thought I had no other symptoms but I can see that my fuzziness in the head, low grade anxiety and stress that I've been feeling lately may be related. I've also been ravenous and am putting on weight but can't seem to stop eating junk. My energy levels are low and I have body aches and fatigue and find it hard to work out. But has anyone had achy joints in the hands and feet? .....tight tendons in the ankles & archilles and sore bones in the feet.......a feeling like swelling/tightness in the joints in the hands? I thought I was getting arthritis but maybe it's related to the IUD. I'd appreciate any feedback. Thanks

I´ve been using Move Free now for almost five months and haven´t felt any side effect. Together with Pilates and static bike exercises, I have really been feeling back to normal. Of course the marks of artrosis are there, but I feel no pain on my left knee and the ankle of my left foot.

I am a healthy woman and love doing sports. My allergies started slowly since I moved from my country Chile to U.S.A . At first it was a mild congestion, second year congestion and conjunctivitis, third year the same plus sore throat. This year almost asthma symptoms. It was right after running a 4 mile race through Central Park here in NYC. My coughing started very dry and by the third day I was coughing phlegm and I worried because I thought I was having bronchitis or something along those lines. Besides I have a 4 months old healthy baby girl. So I went to the doctor and she prescribed singulair once a day and asmanex two hours before starting to do exercises.
Immediately after taking singulair my itchy and watery eyes stopped and the first day was great. I am on the third day and I am so tired and achy almost as if I am ready to have flu. My stuffy nose is permanent now and at night I am anyway coughing but a dry cough. Because I take the medicine at night I wake up nauseous and with a light headache and also feels like if I have sinusitis. These may be mild side effects but it was recommended by the doctor to ease all these symptoms and I feel completely opposite...All these side effects are listed on singulair but I wonder if a medicine is listing more side effects than benefits...Why anyway goes to the market? I do not like taking medicine and I did took singulair for my daughter to protect her and our family as prescribed by the doctor. I could notice the negative difference right away since I haven't taken any kind of medicine since I got pregnant and even before. Maybe is too early to tell but I know my body and I can tell this medicine is not right for me. I have decided to follow up the treatment for 10 days to see if I notice some other improvements but so far it seems that I am taking medicine to get sick instead.

I am 43 yr old woman and have been on simvastatin on and off for the past 3yrs, it's only since coming across this website that I have actually managed to find a connection between this awful drug and a whole heap of medical problems. The most recent course made me so ill that I thought I had an incurable illness that no one could diagnose, at times I have been in so much pain I thought I was going to die. It started with severe knee pain, I have a little arthritis in the knee but doctors were baffled at why it would hurt so much as x-rays on knees and hips were ok. I ended up having an operation to cut a ligament, that was over a year ago and had been in crippling pain ever-since. Also; foggy head, headaches everyday lasting all day, pain in jaw, shoulders, neck, swollen throat, incredible limb swelling, numbness all down right side, kidney problems, weakness in muscles, aching hips and legs, itching, insomnia, to name a few. I complained to my doctor when I was prescribed 50mg of this poison because as soon as I took it, I immediately felt ill and collapsed from terrible weakness, couldn't even lift a feather. They reduced it to 20mg, and I blindly kept taking it, in the meantime, my leg function was worsening, my back was killing me, I couldn't sleep because of the unbelievable burning in my shoulders, hip, neck and legs, everything hurt so much. I have been in tears from the pain and frustration of not knowing what was happening to me, painkillers, even high potency prescriptions just didn't work. I was a healthy gym-going person with a slightly high cholesterol reading, and suddenly, I was almost crippled, unable to function or look after my family, couldn't even handle simple chores that I had done a thousand times before, couldn't think, speak well, do crosswords, it was unbelievable. I have had ECG's, heart stress tests, been to and fro to doctors, hospitals, specialists, even seen an osteopath with these pains, they must have thought I was a hypochondriac! Finally, I insisted on an MRI on my thigh as it had changed shape as there was a lot of muscle wasting in both my right arm and thigh, and so much pain. A lump had also appeared and was really worrying me. The doctor tried to fob me off and said it was a fat lump, I argued that if it was fat it wouldn't hurt so damn much, so the result of the MRI is that I have a tumor which is getting bigger. If I find out that this is a result of the medication, the gates of hell will open.
I took myself off this lethal stuff immediately as soon as I realized there was a connection between it and my debilitating condition, though it's too late to save my 12 yr relationship, that went down the tubes because I just couldn't function well, oh, and my job. and any chance of working after being ill for so long.
I have been off it just a few days but already I feel almost human again. I know it'll be a while before I can see a marked difference and do some of the things I used to be able to do like walk the dog!! but I am furious with my doctor's and have written a letter of complaint, and have told them that I would rather take my chances with god and be a happy person than ever trust them again. I am in no doubt whatsoever that this drug has ruined the last 3 years of my life and probably caused irreversible damage to my leg muscles. Why take a pill because the doctor said so??NEVER AGAIN from now on everything will be checked via websites like this, I am so disgusted that instead of helping me, my own doctor just prescribed other medications I need not have had because of this pill when all he had to do was take me off it. I find it hard to believe that they don't know of these side effects, or pretend not to, how can they not make the connection?? Absolutely furious. I am in worse health now than I ever was, there should be a serious health warning before this is given to anyone, and the first port of call for any complaints should be the doctors who prescribe them instead of offering alternative solutions. This is a time bomb waiting to explode.

Nothing. I just had 2 wisdom teeth and one other tooth exracted. I am taking meprozine at least every 4 hours. Yes I'm a tiny bit off balance and it is making me a little tired AND it is relieving the pain.

Side affects? pain relief and some drowsiness.
Fine with me. I think you'd have to take something else so you can go back to work. Something that doesn't make you drowsy. I hope I don't become addicted by it as someone else stated.
Happy with meprozine.

I am 51 year old female. I have been having similar side effects that everyone is posting. The cough just started. And I am having cramps in my legs and back that I never had before. I also have been a little depressed. I just stopped taking the medicine yesterday. I am at a place called Optimal Health Institute. They put you on raw veggies and juice and fruits and nothing else for a week to 3 weeks or as long as you would like to be here. Also mild exercises to help you cleanse and you juice wheat grass 2 times a day. I decided to go off my meds yesterday (been taking 10mg for about 4 months) and my blood pressure reading just registered 119/78. It has been running 135/85 with medicine average. I just started but after reading all of these posts and my own side effects, I am definitely going off this junk. I hope this cleansing works. I am going to be here for 2 weeks.

VERTIGO!
I've had bouts of it in the past but nothing like this! Falling down, unable to drive, to the point of vomiting. I thought it was from allergies (which are bad but if I'm taking the Zyrtec... as well as Nasonex and psuedofedrine... and I am not getting better... what was I thinking?). Went to the doctor who gave me a 3 more medications and exercises and told me to continue the Zyrtec. Then, after starting the other medication and feeling better, I took Zyrtec before bed and my symptoms got worse again! Thankfully I realized what was provoking it.
I contacted Pfizer to see if they were collecting additional information to fine tune the side effects info they have now.

My 16 year old son took Levaquin 6 months ago and had a bad reaction to it. His symptoms were severe muscle weakness (he would get exhausted walking from the parking lot to a store and back, severe joint pain (in thumbs, wrists, elbows, knees, and ankles), dizziness (he felt like the room was moving away from him and would lose balance), and headaches (a severe pressure in the back of his head that was constant and then shooting pains in his his head that would come and go for no reason). I should say he was in top shape before this and wrestling in the 125 pound category. He took Levaquin to prevent an infection after sinus surgery.

Now 6 months later, his joint pain is completely gone except for his knees. They still hurt when he does squats and they are not good enough for him to go back to wrestling, but he can walk around pain free. His dizziness is also gone as well as his muscle weakness. His headaches are still there and still constant, but not as bad as they once were; however, he has had them 24 hours a day, 7 days a week for 6 months. He is on Lyrica which has helped make the headaches subside.

I have taken him to more than 16 medical doctors of all specialties, had multiple MRIs, CT Scans, blood tests, spinal tap, and an MRA. All come back negative. Thankfully, despite all of this, he still remains happy and positive that he will once again be 100% healthy; it will take lots of time, but he will get better. I know the first three symptoms (joint pain, dizziness, weakness) are clearly Levaquin related, but I haven't heard much about the headaches from people. Anyone else out there that has suffered from a constant headache after Levaquin? I REALLY want to hear about headaches from others!!!!

By the way, we have filed a medwatch already. I also know that Levaquin is not approved for anyone under 18 years old and he never needed such a powerful drug to prevent an infection, but there is nothing I can do about that now except to warn others. One of his UCLA doctors wants to write a case study on him to make this more known to others and I am helping him with that.

If anyone has questions, please feel free to ask. If you have had a headache from Levaquin, please let me know where in the head the pain was, if it is constant, what it feels like (pressure, shooting, throbbing), how long you have had it, and what, if anything, helped. THANKS.

I have been on this for 1 month. The first two weeks was fine then I started feeling bloated big time. I do exercises for my stomach and I know I have good core muscles and I can't hold my stomach in. I'm not working right now need to be looking for work but I have been waiting for the bleeding to stop and the bloating to disappear. I am getting off of this. All of the head problems people are having are due to the extra drug in Yaz that deals with moodiness. I have been on tons of different anti- everything and usually it takes at least 3 to 4 weeks to adjust to your brain. If not it's not for you. I am completely off of meds now because I took the steps to freedom in Christ in a book called Breaking the Bondage by Neil T Anderson. I took ortho tri-cyclene before years ago and it did great compared to this stuff. Taking something to help with moodiness just causes a person to be numb to their feelings. The feelings don't go anywhere the pile up and that's why you find yourself at times crying uncontrollably. The only way to heal these things is to face them and the only one that can take that pain from you is Jesus. I know I tried everything. Exercise and changes in your eating habits will help with period problems. Water water water will help with acne.

42 Year old male; Active, have been on Lipitor 9 months. Started back on the drug last spring, Ride wave runners every weekend, thought I've had whiplash for months, extremely sore/stiff neck, severe muscle pain in shoulders and neck I am convinced its Lipitor not whiplash. Only advice my doctor can give is "see a Chiropractor", no help! I am stopping Lipitor right now and will await changes, Cannot believe after multiple visits to my doctor concerning my shoulder/neck issue he never once considered Lipitor. After doing an internet search for muscle pain, I stumbled across Lipitor's relationship to muscle pain. If my pain stops I will be very grateful.

Where do I begin??? I have been taking Yaz for six months. Migraines! The worst migraines ever, I cannot function for one full day and sometimes more, the pain was so intolerable.

Hives! For the past two months, I keep thinking that I had a food allergy; even my doctor diagnosed it as that. After going to the allergist, I was told that I have developed an allergy to the Yasmin pill. No part of my body has been discriminated with this medication. Hives from the top of my head, in my eyes, right down to the bottom of my feet! This has been the worst experience of my life with this pill.

Fatigue to the extreme! I fall asleep sitting up and never feel rested. Yaz has caused me to go up two cup sizes so far, I went from being a 38C to a 40DD and I can't fit into anything. My boobs are sore a lot.

Weight gain, at least 20 pounds heavier. Nausea; Indigestion; Diarrhea & Constipation; Decreased Sex Drive; and Mood swings; Uncontrollable Rages; Severe body aches; Hot Flashes/Chills; Crying Spells; Blurred Vision; Lack of Concentration; Trouble sleeping; Dizziness; Shaking; Restlessness mainly after 9pm when I should be winding down to go to bed; Terrible night sweats; Never ending cravings for junk food; Inability to cope with stressful situations; Feeling of being inadequate; Can’t concentrate; Gassy; Hate family & partners; Irrational.