Nancy symptoms and conditions

Please stay away from this drug if you are not already addicted to it. I have tried unsuccessfully to get off of it many times by "Weaning" into another drug, but the side effects are unbearable. I have memory loss too, but what really gets me is how physically sick I feel if I haven't taken it for 2-3 days. I get nauseous and VERY dizzy, to the point where it makes me sick to even turn my head too quickly. I've had to miss work/school until I had a prescription refill.

I didn't realize the memory loss I have been experiencing may be due to Paxil, but it makes sense. I have forgotten the year on numerous occasions, and cannot recall names of people I used to have no problem recalling. It seems to be getting worse. I am only 27 years old, and my friends don't seem to have these issues...

I had been taking this for years and about three-four yrs ago they changed generic. I had horrible stomach and abdominal problems.Not diarrhea or constipation but pain swelling bloating and feeling a lump in ab. Went to cts, ultrasounds, 3 colonoscopies,endoscopy, pill camera,I went through 3 primary care doctors. Had emergency hosp.visits. Doctors.started getting to think I was crazy That made me depressed to the point I didn"t want to see anyone or go any where. Not one Dr. suggested it could be one of my meds. By accident over the Christmas holidays I ran out of my lisinopril hctz. within 3 days I felt normal again Swelling in ab stopped and most of pain.ever gonna get near that poison again.# months later Im doing a lot better I actually feel good .Its amazing I think it caused me a rare reaction called intestinal angioedema .That is basically hives on your insides. Could be dangerous if esophogeous is involved I lucked out.I did have wheezing and shortness in breathing .People Beware Its a dangerous drug.

I started taking 500 mg of Levaquin on Friday. I have a sinus infection, bronchitis and was wheezing. I finished chemo a year ago and have long term effects from it including joint pain. I was improving by working with a trainer, doing basic pilates, etc... My joints are awful and it's not the same pain. My knees hurt all the time, I can't stand for any length of time. My hands, shoulders and hips hurt. My doctor was out today, but the nurse told me to stop taking it and I see her tomorrow.

This is so upsetting, I read the insert from the pharmacy and it mentioned joint pain, so I know it's where the pain is coming from. It took me so long to get to where I am and now this. I am still sick with the sinus infection and bronchitis.

I will post tomorrow after I see my doctor.

N.

I wrote on my side affects on sept. 7th on this site. I have been off topral xl for about 2 months, and my heart beats normal now, my legs are not swollen, no headaches, long story short, most my symptoms gone. I can think so much clearer. My blood pressure now goes from 160/90 to 117/84 which last weekend I did try Diovan hct, a new blood pressure med. and Sat. and Sun. were a nightmare. I do know how dangerous it is to have high bp. for my brother-in-law passed a year ago nov. 2nd and my aunt Bev 3 years ago. But I am happy with my decision to continue the Peptace and Celery seed extract and monitor my bp. closely. My son went to Doctor for his bp. and Doctor said that they get some kind of a kick back from meds. like topral so maybe thats why they push it along with other meds. True or not, I still can't figure out why they kept me on it when I asked them to take me off cause I felt so bad. It sure did take a toll on my whole body. Good luck to ya all and listen and feel what your body is telling you. I know whats good for one is not good for all.

Had Mirena fitted 7th Feb 2008 and having it taken out on 12th June 2008. My stomach is huge despite eating sensibly and exercising. Also suffer from cramps on a daily basis, craved chocolate and have felt down in the dumps!! Can anyone tell me if having it taken out is as painful as insertion and will I bleed as much as when it was fitted. Am very nervous about the whole procedure.

Many thanks

My doctor failed to catch pneumonia in time when I was 13. It cause irreversible lung damage in left lung. I have had to take prednisone for 41 years now. I now have a cortisol insufficiency, hypothyroidism, and IGA, IGG immune deficiency. Although prednisone saved my life; it has now damaged master glands. I have heard it can kill you if taken over a long period of time because of it's immunosuppresive properties. People need to know this and the drug companies still push it as an anti inflammatory.
I use natural cortef for replacement of cortisol insufficiency.
Who makes prednisone? Be knowledgeable about alternatives and don't be afraid to ask the doctor for something that is more natural to what your body makes!!

Sincerely,

Nancy L.
***

I have been on Levoxyl for about 3 years now, maybe more. My mother , father, and I all have Hypothyroidism. Mine was diagnosed at 19 when I started on Levoxyl and now it is around 3 at 75 mcg. I do have alot of these symptoms, including fatigue, depression,insomnia, major migraines, bloating, but my mom and I also have ringing of the ears and I wonder if this is a symptom. I have been to an ear specialist and had my hearing checked, everything is normal he says. Maybe I just have very sensitive hearing and can hear the slightest things? I don't think so, I didn't have this ringing before a year and a half ago!

http://health.groups.yahoo.com/group/Singulair_side_effects_friends/

Doing an article on Yasmin, INFO WANTED on Side Effects that occur after you stop taking the pill

Hey okay so I'm doing an article on Yasmin, the side effects that occur when you stop taking the pill, and would like more information on it. I would like to interview ex users of the pills that have experienced either hair loss, lack of period, severe headaches, and just about anything that resulted. I need to write this article ASAP! All experiences are helpful. I too used to be on the pill, and ever since I stopped taking it my cycle has been out of whack. Please contact me either via email gator924@ufl.edu or through AIM: lipsfullbittin or via phone: 786-239-8751.

While most people know some of the side effects of taking the pill, few know the side effects that occur when you stop taking it. It would be a helpful article to any users or future users of the pill, don't you agree?

I have been on Toprol XL for 4 years - was on 50MG - Dr. tried other meds for a while (bad side effects) - so put me back on 25MG of Toprol until we can figure out something else.

When I was off the Toprol I lost 16 pounds!!!! I have not gained any back being on a lower dosage.

I think it is causing me breathing problems and pain and cramping in my legs - any one else having this? How should you wean off?

Thanks!

I was on Lipitor for either two or three years, maybe more, can't remember, it was around 2003. About a year after starting the meds I started losing my balance, like my feet were heavy and wanting to not lift themselves up when stepping off a curb. I was in fear of falling. After being a professional dancer for many years and still having excellent muscle tone I was shocked by this muscle problem. Then I developed shooting pains in my thighs, and eventually I had an incident where my one leg just gave out and I couldn't walk. It was something in the hip/leg joint. Went to an orthopedic doctor, got x rays and m.r.i., he found nothing. I stopped taking Lipitor because I had spoken with other friends who were having leg pains. My regular doctor would not admit to anything wrong, just kept telling me I needed to stay on the drug, which infuriated me. He also kept blaming the muscle weakness and pain on my weight; which I have never had a problem with before.
The shooting pains in my thighs was all the time, including at night and woke me up at night. This was unreal. Even after walking miles I had these shooting pains, so it wasn't an exercise issue at all, but it certainly did deter me from exercising more often.
Now the pain and swelling is mainly in my knees. I can hardly walk, feel like I am crippled, and have lost my job over not being able to walk around and show apartments! I can't walk steps anymore at all, I am only 55 years old! No matter what I do, the pain and muscle weakness is progressing, I've seen a Chiropractor, a nutritionist, and now I'm going to see a Rheumatologist. I believe I have permanent muscle damage from this drug, no one can tell me otherwise.
Also, I have experienced the gradual increase of brain fog over the last two years. I am scared to death this damage is irreversible.

I am 60 years old female & have been taking Lipitor for about 4 years. I recently went off the drug for 3 months, & in that time much of the muscle pain I was experiencing began to lesson. I have pain in both arms from the below up to my shoulder. Hip pain & leg cramps. I have trouble sleeping & absolutely no sex drive. Of course, my Cholesterol went sky high, over 300. I have only been back on 80 mgs for a month and a half, & all of the aches and pains are back ten fold. I feel a hundred years old.I have to make a big decision...die of high Cholesterol, or live a life of constant pain and sleep deprivation. This is really bad. I f I had to run or crawl to save my life, I'd never make it.

Hi All, I am a 37 year old mother of 4, with a history of severe Hemiplegic migraines (up to 14 a month). I've been on Verapamil and Topamax for 7-8 months with a gradual increase of the Topamax to 150 mg a day. Before I start writing this I have to preface it with two things: First, Before Topamax I was one of those women my friends refer to as a "Supermom", I home school my kids and used to love it, we normally have a lot of fun and I have a successful, happy marriage. Second, on Topamax, I went from 14 migraines a month to 0. It didn't happen over night, they went away as we ramped up the dosage, but for the last few months I have had no migraines, I can feel it occasionally when my head is fighting one off, but nothing an Advil won't stop, and for those of us who've lived with trying to care for kids while having migraines (especially Hemiplegic) you may understand why I initially put up with the following: I started out with the tingling in my hands and feet (that went away in a couple of months), word finding difficulties (which never really went away, I just learned to accept it),occasional blurred vision which never lasts very long but which has been an issue the entire time I've been on the med, and weight loss ...I am 5'4" and was only 118 lbs to start with, and have nearly "disappeared" into a size 0 and 105 lbs, and it doesn't matter how much I eat, I've been trying 3 meals, snacks, cookies, candy, you name it, I can't gain weight. I was never nauseous, no diarrhea, I just don't get hungry... I had to start wearing a watch at one point to remind myself to feed the kids, because if they didn't ask, they weren't getting lunch until 2:00 because I wasn't getting hungry! Soda does taste like metal (fortunately I don't drink it normally anyway), and you do get loopy with one glass of anything alcoholic.
Then to add to the lovely appearance of skin and bones, my hair is falling out. Before Topamax I worked out regularly, I am even on commercials for my gym (recorded a year ago), since Topamax, I was so tired, depressed, and so afraid of losing weight that I stopped working out. Now a woman who has always made it a goal to set a good example for my daughters that a fit body is the goal, not a thin body, has her mother in law telling her that she looks "bulimic"! In August I noticed I was crying a lot, then I thought well, maybe it's the Topamax, so I started drinking more water and it went away... so I've been very careful to drink A LOT of water and only decaf tea while on this med, but apparently that wasn't enough, because a few weeks ago my husband pointed out that I stopped showering every day. I have been crying at the drop of a hat for a couple of months again, and I have never been someone to cry in public, I have even started crying in front of my daughters friends' mothers and near tears in front of her teacher over the littlest things... then last weekend I found myself with four hours to myself in my house for the first time in months and I was thinking about how I might be able to use it for unspeakable things like running away, or worse... if those aren't signs of a pretty severe depression I don't know what are, fortunately I recognized them and put them together with the memory problems, etc. As for the memory loss, there have been problems with that for months as well, my daughter has been telling me I "have a bad rememberer" , This weekend everything culminated and other people were recognizing the memory issues that I had been keeping private until now (including my husband). Before that, I would be in the kitchen cooking and forget what I was doing, I went to drive to a party this weekend and forgot where I was going, so I called a friends husband and he had to tell me four times where to go before I could retain it (at first he thought I was joking) and then I still couldn't remember the name of the place, only the # and street, I haven't been able to remember routes to places I used to drive... I'll find myself sitting at a light not sure where to go, and making mistakes with our money because I forgot whether I did or didn't pay a bill (something I've never done, we have always had excellent credit). On Topamax I went from feeling like an attractive, successful, good mom,with a happy family... to constantly stressed, even by things I had previously enjoyed doing, and a completely depressed failure... but I had no migraines. I have now been weaning off the Topamax for a few days. I was playing phone tag with my neurologist... so due to the urgency of the problem I took myself down to 100 mg a day. I have since spoken with my neurologist and I am going off of it completely... by the way don't ever discontinue this med without ramping off of it, doing so can cause a seizure. I am unbelievably grateful that I put 2 and 2 together the weekend I had time to myself and got lost going to the party and I already feel more awake, less tearful and depressed... I know that things will be ok anyway. I hope that anyone reading this who is having memory or emotional issues on Topamax and just brushing them aside (because they don't want to risk going back to the migraines or whatever), will get off this med. Please realize that this med could have cost me, my kids and my husband a lot more than my migraines ever will. I have never experienced depression before Topamax, and I can't say that I'm completely back to myself yet, but I hope that when I am off this med I will find normal again, and I pray it will be without migraines, but I know that I wouldn't wish these past few months that I've put myself and my family through on anyone. Now, I need to go take a shower :) , then I'm going to my neurologist to pick up some 25 mg samples to continue ramping off! Good luck to you all!

It's hard to describe all the side effects I think I am having from taking 50mg. of toprol 1x a day, at bedtime. Since taking it, I have heart palpitations,flushing, full body pain, sleep all the time. Feel without hope- so I guess that would be described as depression. I have 0 energy, or even motivation. I have become a hermit in my own house, have not gone out anywhere at all- the entire summer. At first I thought it was becuase certain terrible things were happening with my daughter- but now that has abated-BTW she's 47. So I don't think the way I am feeling has to do with that. I feel just ghorrible- worse every day. Don't want to do anything. All I do most of the time, is sleep, or pray that God will let me die- I have nothing to live for- or Please heal me. Finally I have an appointment with my Cardiologist-Internist this Thursday, and I will ask him to take me off the Toprol. Tonight I am not going to take it, nor anymore until I see him. Nancy

I was wondering what was happening to me so decided to get on and pull up this medication and see if it had to do with it. I am on it and slowly working my way up to 150mg a day. I am at 100mg a day and I have tingling in my my arms mainly, but can feel it in my whole body. I thought maybe I was going crazy, but since I just was starting the medicine I wanted to see if it had to do with it and I see that it probably does. Also, I have a lot of energy. Might give the doc a call to see if he wants me to stay on it. Nancy

I want to be Zantac agent in Beijing, China
Dear Sirs,
This is Nancy Y. Zhu (trading office). I am doing import & export and investment consultants business more than 10 years. Have many stable relations with China and overseas factory. I'd like helping you establish Beijing office in China and doing business as your agent if you¡¯re like. If you have any special requirement or suggestion, please let me know no hesitate.
By the way, China is biggest country in the world. Olympic game will be hold in Beijing, China. And China was just taken part in WTO (world trade organization). It is a great opportunity for you and your company. I do believe you know how important chance for both of us. I have more project need financing and I do believe more profit waiting.

My email address is: officedocument@yahoo.com
Hoping hear from you soon.
Cheers,
Nancy

Tel & fax: 8610-63964311
Mobile: 8610-13121145008
Email: officedocument@yahoo.com

lance67@bellsouth.net
I have experienced blurred vision and a shadow of objects and letters that is faint and just below the object or letter. For example, people will appear to have two sets of eyes. My Doctor stopped the Xalatan and assured me that the blurred vision would clear up, but it has been approximately 3 years and it seems to be getting worse. How many others have experienced this problem?? Nancy Dunaway, Oak Ridge, Tenn.