Killer drug symptoms and conditions

Oh I can sympathize with all the others on this killer drug. It has been quoted to me as being the discovery of the century for the treatment of Stroke etc . Well yes it will help with that but it will kill all other parts of your body.
you see when you get to the stage where you need this medication they really do not have much hope for a long future so they do not worry about what affects one will get. They think, 'well you are going to die anyway so it is better to prolong the agony and suffer .
Well I experiences, depression, severe joint and back pain, insomnia, blurred vision, a feeling of flatness of mood . Stomach pain, my hips have never been the same since being on it. I am off it now and take natural Cholesterol support and it is working. It is a nightmare to be on this drug and if you can go to the natural do it and do it now for you life sake.

I am being treated for ulcertive colitis. I have been on prednisone since Sept of 08. I started out on 40 mg. In late Oct. my doctor started tapering me off 5mg per month. Each month following the tapering date, I would get sick. As I look back, all the signs of withdrawal were there. This Jan. I tapered once again, but the window was only 3 weeks. I hit rock bottom. If there was a symptom, I have it. Nausea, burning in my digestive tract, diarrhea every time I eat, muscle ache, numbness in my legs, swollen feet, sore bones and joints. ( The worst was in my feet. I ended up seeing a podiatrist. He thought plantar faciaitis until I told him about being on prednisone. The small bones in my foot were swelling, The muscles in my calf were buning they were so sore. That was last week. Today my other foot started. I can hardly walk. In addition to that, I am lightheaded, have elevated blood pressure, and fatigue. I also had some vision problems that sent me to the doctor. I went through a ton of testing which all were negative. It seems that pseudotumor is another symptom of withdrawal. I have a history of that. It would have been nice to know that. As I look back each month, I had different muscle and joint pain that lasted about a week. I was put on an acid reducer in Dec. to help my stomach, but in all of this time, I was not told that these all may be withdrawal symptoms. I have been off work for two weeks now in addition to the days I missed each month. My physician is now controlling the tapering procedure. They up the dose to 10 mg again. They plan on weaning me by 1mg doses. This has been a terrible experience for me. I have only been severely sick one other time in my life. This pain is awful. It is chronic. This drug may be beneficial, but it is like poison too. Anyone who takes this should really ask a lot of questions, and be careful..

My husband has been taking Omeprazole for about ten years now. About nine months ago he went in for a endoscopy and the doctor said she wanted to increase the omeprazole of 20mg 2xdaily because of the acid reflux. Several weeks after increasing this drug, my husband began getting very depressed. He losted all interest in our business and started having severe mood swings. He couldn't sleep at night, screaming with cramps in his legs, heart palpitations, blurred vision, ringing in ears, hot flashes, headaches behind the eyes. Some night I thought he was having a heart attack. It only got worse, hallucination began and horrible nightmares. He thought I was putting drugs and poison in his food. and felt like the world was against him. He became very violent toward me because of the hallucinations. We went for a follow up at his doctor and she suggested a psychiatry. Of course, my husband refused because he felt nothing was wrong, it was everyone else with the problem. His attacks got so bad, it was happen everyday, all day. We have two small children and we decided to split up for the children sake. My husband left for a week and when he left he refused to take the Omeprazole. He called me during that week and said he has felt great, he was able to sleep, no anxiety. He said to me if you are not putting drugs in my drink and food..it's got to be the omerprazole.
Of course the doctors said it's not possible...he has been off these pills for 8 days and it's unreal how this symptoms has disappeared. He is still having some side effects and withdraws. I don't know how long this will be in his system but I hope it goes away soon. THIS IS A DEVIL DRUG. He almost took his life and my too over OMEPRAZOLE. My doctor recently wrote this drug for me but I will not take it... We would never know about how serious this little pill for heartburn was if we didn't research it. When you get this drug from the pharmacy, they only list some side effects and not the serious one...How many more people out in the world is dealing with this same problem and not aware of these serious side effect. This almost destroyed our lives. WE NEED TO TAKE SOME KIND OF ACTION, SO THESE SERIOUS SIDE EFFECT HAVE TO BE LISTED..

I have posted a few times. My daughter started taking singulair 11-17-2003 and I stopped it 3-28-2008. She is the one that dropped out of dance and cheerleading, withdrew from old friends and family, headaches, stomachaches, missing school with this, depressed, anxiety attacks and CUTTING her self under her clothes. 6 months with a psychiatrist did not help. She is now about 80% back from the darkness. She is so much better and is such a loving child, She is not cutting, has a part time job, and has passed all her classes with 3 A's, 1 B, and 2 C's. BUT there are learned behaviors while in the darkness that still show up. Not every day but they are there. She has been pushed off her life path. I am hanging on to her with all my might and I know that I will get her through college and she will have the tools to be self reliant and happy BUT what could she have been if I never gave her singulair???? I can not help but feel guilty to what I have done to this child

FOR THE LAST 2 YRS OFF & ON I HAVE BEEN TAKING THE KILLER DRUG DIOVAN 160/12.5 MG AND, YES IT'S BEEN TERRIBLE!!!!!!!!! WHERE DO I START ....... CHEST PAIN,HAIR LOSS, LEG CRAMPS, SORE FEET, BACK PAIN, ARM PAIN, KNEE PAIN , SHORTNESS OF BREATH . LAST YR MY LEGS HURT SO BAD MY DOCTOR STARTED TO PUT ME ON MEDICATION FOR RLS ( RESTLESS LEG SYNDROME) ......PLEASE IF YOU JUST STARTED THIS MED STOP RIGHT NOW !! GET YOU SOME APPLE CIDER VINEGAR W/ MOTHER(MOTHER) TAKE 2 TEASPOON W/ 8OZ GLASS OF WATER OR JUICE 3 TIMES A DAY AND, WATCH YOUR BP DROP AFTER ABOUT 2 WEEKS YOUR BP SHOULD BE NORMAL THEN START TAKING IT ONLY IN THE MORNING AND AT NIGHT

I was just placed on Cellecept last week- 500 Mg 4 times a day-
for my autoimmune muscular myopathy- I was a body builder 6 months ago- now I can barely make it across the Target parking lot.
I am sure the myopathy is Statin induced as I was on Lipitor-)rather than Prednisone as my doctor said less side effects.
He said I should see improvement in about 6 weeks- is any body taking Cellcept for autoimmune disease?
Thank you.
PS; So far- side effects seem to be weakness- more shakiness-

Please don't take Yaz if you have any alternative at all!
My 30-year-old, fit, non-smoking daughter is currently in the ICU after just the third pack of this KILLER drug, with a pulmonary embolism (major cause of sudden death in young women) and a clot in her leg. Thank God we got her to the ER in time--don't let it happen to you and your family. If you're taking it and get pains in your legs for no good reason, run, don't walk, to the nearest ER.

I took it for 10 days for a sinus infection. 3 days after I stopped taking it I broke out itching all over my neck, arms, back, stomach and hips. Then it turned into into a red rash with welphs. I could not attribute it to anything else different in my life. I went to the dermatologist who said I was probably allergic to the levaquin and It was possible that the reaction could occur after I stopped taking it.
Has anyone heard of this????