Classic case symptoms and conditions

I took Zocor for 9 months after I had a heart attack. After about 8 months I began having sever muscle spasm in my legs. I had a couple of episodes where when walking I couldn't pick up my feet and thought I was having a stroke and had to sit down and rest before walking on. I had to do this several times to get where I was going. I told my cardiologist and he had me stop the Zocor. The spasms stopped but I never regained the strength in my legs. Today I have had to put ramps in at home cannot climb steps. The ramp is difficult because of the incline but it is better than crawling up my steps to get in the house. I can only walk about 50 steps before my legs give out on me. I cannot walk on uneven ground without holding on to something or someone. I have now had 2 back surgeries because I have been told over and over it is my back with no relief for the legs. This last surgery my left foot drags and my big toe hangs down and I cannot pull it up. Now I fall a lot because of that and have to wear an AFO to keep my foot and toe up so it doesn't drag and trip me. The back doctor thinks it another pinched nerve and wants to open back up again. I am so tired of them trying to convenience me it is my back when I know it was the Zocor and the damage apparently is irreversible but no one wants to agree with me. I am sick of it and just wish they would say yes it was the Zocor and get you a scooter and live the best you can. I know I am headed for that road I use a walker and cane when I don't have someone with me to hold on to. Because I am so unstable on my legs.

March 3, 2009
I returned to the doctor today to get a different antibiotic because Avelox made me worse off than the sinus infection I had. I stopped taking it about two weeks ago and still have side effects from the drug. My doctor had given it to me about two other times. The last time I recall was in November. I didn't finish taking my prescription then either.
I thought maybe I was having flu symptoms also, but it was the drug making me more ill. RASH, HIVES, RED HANDS, SWOLLEN TONGUE THRUSH, BUMPS ON MY TONGUE, TINGLING IN MY BACK, VOMITING,HEADACHES, PAIN IN MY STOMACH NOT LONG AFTER TAKING A DOSAGE. FREEZING HANDS, THROAT FEELS LIKE IT'S CLOSING UP AND DIFFICULTY SWALLOWING, COULDN'T GET OUT OF BED, MUSCLE FATIGUE, ACHES WEAKNESS, JOINTS HURT, TINGLING IN HANDS, ANXIETY,CRYING SPELLS, NIGHTMARES, SKIN SENSITIVITY, INSOMNIA, THEN EXTREME FATIGUE, DIZZINESS AND LIGHT HEADED UPON STANDING AND/OR GETTING UP FROM A SITTING OR SQUATING POSITION. EVERYTHING HURTS ALL THE TIME IN EVERY MUSCLE...... I BASICALLY FEEL LIKE I AM DYING.
My fiance thought I was totally losing my mind. I was moody, aggressive, irritable, depressed etc... I felt like like a different person.. My fiance of course got sick also and his doctor prescribed it to him. His side effects included muscle aches and pains and extreme fatigue and mood swings. I looked up some side effects when I was started taking it a few weeks ago, but didn't pursue the research until the side effects got worse. I took it for 7 days this time. My fiance took it for three days. I called him at work after seeing this website and told him to stop taking the medication immediately. I am still sick with a sinus infection, and a whole slew of other crap going on. I called the doctors office and went in right away to get a different medication. To no avail, when I went to my doctors office there was a rep from Avelox there. I said don't give that Avelox to anyone sarcastically. I then saw his tag on his shirt and his bag full of Avelox samples. He asked what type of symptoms I had and I told him.. He said he would report it to the company.... What do you think they will do about it? MOST LIKELY NOTHING. I am an educated person with the capability and time to research anything I need to and I will do my best to dig up the most dirt I possibly can about this horrible medication. They need to stop pushing these meds on doctors to give us and make us more ill than we were to begin with. I JUST HOPE MY AILMENTS AREN'T PERMANENT. People try to make light of the situation because they don't want to be sued. I think the FDA needs to be revamped and the Government should stop letting these pharmaceutical companies poison us. I AM NOT EXAGGERATING EITHER! DO NOT TAKE IT.
I have been going to my doctor for about fifteen years and she never gave me any medication that had made me this ill. I get samples a lot because I have no insurance. Sometimes she gives me scripts. Today I got Zithromax which always worked well for me in the past. Very little side effects. I realize that everyone reacts differently to certain meds, but come on now! It isn't just a coincidence that all of us commenting and complaining here are imagining these horrible side effects! Today I got Zithromax which always worked well for me in the past. (Very little side effects).Then why did I ever have to take Avelox if there are other antibiotics that will make me better not worse. They push these meds on doctors to give to us that's why! I always trusted and admired my doctor. She always treats me well and does right by me. What is going on with these medical companies?! SOMETHING HAS TO BE DONE ABOUT THIS!

memory loss, headaches, tias/mimi strokes, kidney stones, blood clot,vertigo, disorientation, muscle spasms, shaking, trembling could not control , dry eyes, stiffness in neck, back pain, twitching of all muscles , blackout when really sick, cant hold arms up, thought I had Parkinson, ms or Muscular dystrophy, motor skills are no longer great, arms and leg muscles bad, cannot write much at all, no strength in fingers or toes.
chronic fatigue and fibromyalga diagnosed not so sure after reading all these side effects.

started 10 mg in 1998. was controlling everything ok. In 2004 developed weakness in both legs, started slurring words and eye trouble, went to several doctors then in April 2005 had to quit work as I was just to weak. That was at age 54. Finally a neurologist diagnosed me with Myasthenia gravis, and lambert eatons myasthenic syndrome. Had my thymus gland removed, which is supposed to put disease in remission, also had small cell lung cancer surgery at same time. improvement did not come and the drugs for myasthenia only made me sick. started having chest pains and doctors ,.found several blockages in my heart ,still do as to weak for surgery, cardiologist took me off of lipitor and I seem to have stabilized, still have trouble with short term memory, and vision, and really weak

Hi all...I've been taking 25mg. of Topamax at night for 5 days now. Unlike most of you I have not experienced the tingling in the extremities or the weird taste in the mouth or even much tiredness at all other than what has happened as a result of my weird side effect. I was prescribed Topamax by my neurologist for my migraines. I've had them since I was 12 years old. I'm 49 years old. The got worse during peri-menopause which is kinda normal given the hormonal fluctuations, but was told by my neurologist that they would very likely subside significantly when I became menopausal. Well folks, I've been menopausal for 5 years and for the past 2 years my migraines have been the most horrific of my life. I have approx. 15 to 18 migraine days a month, some of the headaches lasting 3 bloody days. So it comes to this...Topamax. In the past I have suffered some pretty rare side effects from some very benign medications so I guess I shouldn't really be surprised that this is happening to me now. The first night I took it I slept like a baby. The second night I was slightly 'hyper' but managed to get to sleep. But for the past 3 nights it's been hell. When I lie down in bed, my body feels as though there are electric currents shooting through it and coming out my right leg. I have to move my right leg or go completely bonkers. Fortunately my daughter is away at university and so I can sleep in her room. So I lie there...on my left side...with my right leg hanging over the side of the bed swinging and swinging and swinging as hard as I can just so that I don't scream. It's awful. Last night was the worst. I saw dawn this morning. I just got off the phone with my pharmacist and he told me that I had described a classic case of RLS - Restless Leg Syndrome. And guess what? Topamax is used to trest RLS!! For bleep's sake! So nice people I am suffering a completely opposite side effect to the one that seems to be the most common one...tiredness. Has anyone else heard of this? Experienced this? It seems to all focus down to my right hip and leg. I have to move it vigourously or go nuts. I am so tired today but that's because I got like 3 hours sleep. I fell asleep from sheer exhaustion after my husband left for work at 7:30am.
A side note...I also take 75mg of Effexor for panic disorder and my neurologist told me that this is a very good mix of meds for migraine prevention. My top dosage for the Topamax will be 75mg taken at night.
I'd really appreciate any feedback on my side effect. Thanks in advance.

D.

I have been off this medication since July 19 and yesterday, a rash began on my stomach again. A few days ago, I developed pain under my rib cage and a tingling feeling on my skin. That still persists. I have read that several people did have the rash return, so that makes me feel better, but what I would like to know is......did anybody take anything that helped get this drug out of their system quicker??? I am tired of feeling terrible.

I have been on Zocor 40mg for many years and doing fine with it, until my doctor thought it was not working that well, hence, switched me to Lipitor 10mg. After a few months I developed severe chest pain along with neck pain. It felt like it might have been a heart attack, but it lasted more than 24 hours. I was admitted to ER for 1 night in the hospital and released the following day. They checked my heart and found it was fine. They ran my blood work, chest x-rays, cat scan and checked my lungs. All O.K.!!! The next morning they told me I had Slight Diabetes and an Under Active Thyroid and thought Esophagus Spasms were the cause of my pain. OH yeah, I also told them it hurt more with each breath of air I took in rather than out. It did not matter to them. They gave me Protonix 40mg because they thought it would reduce acid reflux to the esophagus, thus reducing my pain. Furthermore, they gave me Synthroid 25MCG for my Under Active Thyroid. After about 10 days of these medication plus LIPITOR, I had a recurrence of the same pain. I decided to research and came across this Website. I stopped the Lipitor and the next day my pain was subsiding. By this evening, my pain is almost completely gone. I am scheduled to have an Endoscopy in about a week from now and I am hesitant. Are the pharmaceuticals and physicians in cahoot with each other. I can't believe I was required to take all these tests and even more tests before the pain started (EKG, Heart Monitor, Nuclear Stress Test, Heart Scan and Angiography). Did I forget to mention I was diagnosed with High Blood Pressure and put on X-Forge a few months before all this started, but I was taken off it because of side effects (dizziness, lethargic, and so on). I did research on X-Forge and it said to NEVER use it as a first method of treatment for high blood pressure. I also was having pain under my right armpit. WHY DO WE HAVE TO SUFFER LIKE THIS BEFORE ACTION IS TAKEN TO PREVENT THIS FROM HAPPENING TO SOMEONE ELSE. Well, I guess it's just the price we have to pay before we decide to do things OUR WAY!! GOOD LUCK TO ALL OF YOU! THANKS FOR THE POST! PS. Can't wait to see what my Endocrinologist has to say about me next month $$$$$$$$$$$$$$$$$$$$.

I had 95% occlusion of the major artery in my heart July 2007 with no symptoms except slight shoulder pain on 3 occasions. They did a cath and inserted 2 stents. Started with Lipitor 10 mg. and my LDL dropped from 75 to 112. The MD wanted to double the dose, but I refused because of intermittent nocturnal nausea. MD switched me to another statin and I had immediate muscle involvement and severe nausea at night. She wanted me to try another statin drug and I refused. After a 2 month period of no statins, she put me back on Lipitor 10 mg. daily. I decided to cut the pill in half and take it twice a week, then move to every other day and gradually go to 10 mg. daily. Immediately, the nocturnal nausea started again. Last night I awoke at 2 a.m. with nausea, sweating, sore muscles around my rib cage. Still no sleep at 4:30 a.m., so I got up and tried to eat something. This has been the pattern every night since I went on Lipitor.

I don't know if I can take this any more.

CK

I have been on Lipitor for about 4 years. Now I have an arthritic right knee and the left knee has a little bit of arthritis. My arthritis started getting really bad in both legs my left leg was just as bad as my right leg. Muscle pain was tremendous and getting up and down stairs. furniture, and the car. Then the day before Memorial Day I could hardly move, I thought I was losing both my legs. I could only walk a little bit. No energy. I too had blurred vision with this drug but the doctor said that it probably was just my diabetes. I hurt from the shoulders all the way down to the ankles..It felt like every muscle group was involved. Earlier this year the doctor put my Lipitor up to 40 mg from 20 mg even through my ldl was only 93. My last ldl was 67. The doctors say your cholesterol cannot go to low but I am wondering with all the side affedts I had. I took myself off Lipitor on Memorial Day this year and I feel better. The pain is gone except for the arithritic pain but it is not as bad as what it was on Lipitor. Soo I am done with statins I will lose weight and exercise.

After taking 10 mg of Crestor for a short time, i experienced shortness of breath and was very tired. This continued even thou the doctor said it was not a problem. I finally got in to see him and they had me immediately quit the drug and I was sent for a echo/stress test. My heart rate had dropped so low and my breathing so labored, that I was considering suicide, there was no way I was going to go on living if all that I could do was to wake up and get dressed and be so tired , that I was unable to function at all.