Gradually symptoms and conditions

My six year old daughter started taking Singulair for winter allergies about 1 year ago. After a couple of months she woke up seeing floating bubbles. These were very real hallucinations. We were back and forth with specialists for about 6 months. After she was taken off of the Singulair in the spring, the hallucinations gradually went away. We did not notice the connection. She has been back on the Singulair for one week, and last night she woke up seeing ants crawling on the bed and on her. I am stopping the medication and contacting the doctor. I would really like to know if anyone else has had similar problems.

I am a 48 y/o Caucasian male and am writing to describe the terrible effects Lipitor had on my health. These side effects gradually worsened over years of use. I did not associate my symptoms with Lipitor use until I depleted my supply for about a week...until my mail order prescription was renewed. I began feeling better after just a few days, but the symptoms recurred when I resumed its use. I questioned this link and discontinued its use after a few weeks to determine if the symptoms would subside, and they did. I then conducted another trial, taking Lipitor for a few weeks. The symptoms appeared once again, so I have stopped taking Lipitor and will not use it again.

My symptoms have been well documented over the years by my physician, who did not indicate a relationship between Lipitor and these side effects. Accordingly, you might understand my surprise when I started reading about Lipitor's significant side effects in recent published news articles.

I have suffered from dizziness, confusion, depression, memory loss, painful joints and muscles and severe prostate pain, and I could not determine a cause for these for years. I have been free of all these symptoms since I stopped taking Lipitor about 6 months ago, except for a few recusing leg pains.

You can't imagine the money I have spent on doctors trying to determine the cause of my ailments, confusion and depression, not to mention money lost due to resulting poor work performance.

As far as I am concerned, Lipitor should be totally discontinued. If it isn't, then the side effects, of which there appear to be many, should be fully documented and disclosed to everyone to whom this medication is prescribed.

I'm writing for my mother. She was on 20mg of Lisinopril and her doctor insisted her violent coughs was from her asthma. Being an asthma sufferer her whole life and knowing the difference, she insisted it was not. He told her that this drug does not cause violent coughing as she described (but later admitted otherwise). I saw her in October and then in November for Thanksgiving and it looked as though she aged ten years! She was coughing badly, throwing up from coughing so violently and was white as a ghost and was extremely tired from not getting enough rest (from coughing). Everyone in the family told her to STOP taking the medication. She stopped taking it the day after Thanksgiving. It's been about five days and she is still coughing, although it's not nearly so bad, but she's taking pain medication (Hydrocodone) and I believe this narcotic has helped to subside the coughing, plus allow her to sleep, but masked the effects of the Lisinopril. Please, anyone, that has discontinued this medication, can you tell me how long to expect this drug to be out of her body? This has been an absolute nightmare and I'm so worried about her! Please email at ******

Good grief I just left the Doctor to get my annual pap.. I was curious about
the Mirena.. She said it was great da da da da.. I get the baby in bed and
get on here first thing oh my god is this really all true?
Now, I have a question isn't a lot of these side affects similar to the birth control pill? And with me being a smoker other than surgery what either options do other women have.. I do have really bad periods,I have to change every hour for seven days. And I did miss carry twice before my two children for lack of progesterone. So do you think this might be Okay for me?
Since my lat baby 14 months ago I have had symptoms of acne, weight gain, hair loss so maybe this will reverse it for me? what do you think?
Help from a woman who would like to have sex without wondering if I'm going to get pregnant I am 32 I think I'm way to old to have another baby..

I've been on Topamax for over a year for hormonal migraines, and it's working great for the headaches. I started out at 25mg twice a day and now I'm up to 100mg twice a day. I've lost 40lb (mostly due to the drug -- but my appetite is starting to come back) and have just recently started experiencing the anxiety and tingling in the extremities. I've always felt I've had trouble concentrating and "finding the word", but I attributed it to lack of sleep because I have two small children. My most recent side effect, however, is most worrisome, which is the reason for my visit to this website. I am experiencing severe abdominal pain, almost constant, and it seems to be increasing. I had abdominal pain and diarrhea when I first started Topamax last year, but it stopped after the first month or so. I'm just wondering if maybe long term use can cause ulcers or other stomach problems. Anyone have any experience with this? I know from experience that Topamax dosages have to gradually weaned up and down, so I'm considering decreasing my dosage to see if my stomach problems will stop. I'm just in so much pain, yet my migraines have almost stopped now with 200mg a day, that I'm reluctant to change my dose.

I was taking Danazol for 20years in alow dose for pressitant breast pain. I gradually began to suffer from muscle pains for no apparent reason. My doctor immediately stopped the Danazol, although wouldn't admit they were causing the problem. I ''fell apart at the seams''. None of my muscles worked properly, I had extremely high blood pressure, could barely walk, I was in constant pain and had to have massage for 2 hours per day. My eyes ached, I couldn't control my bladder and bowels very well. I thought I was going to die. My doctor sent me for numerous blood tests, endoscopes etc. But said I was depressed. I was depressed, because I felt so ill !
Its now 4 years since I stopped Danazol and I feel it has caused long term damage to my muscles. I have tried everything from massage to supplements. Things have improved a great deal, but I find it difficult to exercise as I tire very easily and particularly my back muscles seize up even after sitting for any length of time.

Has anyone else been on a low dose of Danazol for this length time. Have you suffered?

I'm having serious side effects currently. The onset of the side effects began after taking Lamictal for over 2 months. I started slowly on 25 mg and gradually increased to 200. I felt a great improvement in Bipolar disorder-mood swings- at 100mg but was told that is not the theraputic dose, so we increased to 200mg.

I had no side effects until the rash began to appear. At first only on legs, then arms, then neck, then face...and surprisingly in private areas. Unbearable itching. Rash continued to rage even after a pack of steroids. Swelling became apparrent in face and entire body. Slight difficulty breathing. Went to the ER and received another dose of steroids intravenously. The rash continues to improve but is still extremely itch. The swelling improved for a couple of days but is back. Had one day of severe headache. It has been 14 days and today I am experiencing blurred vision in the left eye, and new swelling in the tongue.
I sit at home with an Epi Pen next to me waiting to hear back from the doctor.

All of this is so unfortunate because I felt more stable than I have in years while on the medication. I'm feeling very concerned about my continuing side effects. Don't know what to expect.

salt cravings

My Doctor prescribed Vytorin becase my LDL was high (160), about 1 month ago. At the beginning, I didn't feel anything, but gradually I have been feeling stiffness and pain in all my joints and an incredible pain on my left shoulder, extending to the arm giving it a burning sensation. My mood has changed. I'm more irritable, depressed and my memory is worse than ever. I can't enjoy reading anymore because is very difficult to focus. My appetite increased enourmously and I gained 5 pounds since I'm taking Vytorin 10/40 every other day. I just read in this site that many people is experiencing the same side effects, so tomorrow (Monday), I'll notify my doctor I'm going to stop this poison. Iread in other websites that it causes muscle destruction and inhibits the synthesis of cholesterol in the brain, needed for well functioning. Who approved this crazy drug?

I am hoping that this will help at least one person, to get off of lisinopril
There is a big difference between "side effects" and actual symtoms that are happening to most of us that take lisinopril.
Side effects usually occur shortly after taking a certain medication.
i took lisinopril for 2 years and gradually all the symptoms escallated and continued to get worse over time. i tought i was dying, i did so many test to find out what was wrong with me, cost a fortune, eventually i realised that all of these things were being caused by lisinopril.
I had shortness of breath,muscle weakness, joint pain, after every meal i was so bloated and a very heavy feeling at night , i could hardly turn in my bed because of being so weak and felling heavy, and the worse was this lump in my throat that got worse every day until i could not swallow or even breath i decided to do MRI ,found nothing , i ran out of lisinopril medication and this immediately got better, i have stopped taking for 1 month and i feel a lot better but still trying to recover from these "side Effects"

I had been on Cozaar off and on for about three years. Although the medication did bring my blood pressure down, my weight steadily increased, and no matter what I did, I could not lose a pound. I was tired, depressed, and my vision changed for the worse. I had increased urination, and I also developed a strangling type cough, and would have coughing fits every now and then. I experienced light headedness and a loss of concentration. Initially I did not attribute these symptoms to Cozaar, because they came on gradually. I never needed glasses before Cozaar, my appetite was the same, and I was not on any other prescription drug. About 6 months ago, I decided to ween myself off of Cozaar. During that time I have lost about 20 lbs, without dieting--eating the same way I did on Cozaar. My concentration and energy level has increased, and my vision has improved--I don't need reading glasses anymore. My blood pressure fluctuates from normal to medium-high, so I am looking into more natural remedies to control it. Please remember that drugs treat the symptoms, not the disease.

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

Hello,

I read about how YAZ birth control pill affects the body and psych and I am now scared. This is my 2nd day of YAZ (I've never been on birth control pills ever and I am 27 years old), it's all new to me but after reading all these negative posts about Yaz I don't know what to do. Before the birth control pills, I was depressed, annoying, serious weight problems - 210 lbs :~~((, low energy, low libido, always tired, terrible migraines every 2nd day, ridiculously increased appetite and excessive hunger, hair where it shouldn't be, menstrual blood clots, excessive cramping etc
I have all these problems for 3 years now and now that the family doc. put me on YAZ birth control pill I am even more scared - mainly of more weight gain, it would be a tragedy for me, I am fat enough already and what's worse I can't lose the weight, exercise doesn't help, diet doesn't help, NOTHING. Will YAZ birth control pill worsen my already tragic condition? I just don't know what to do and what to believe ... I appreciate any advice or help you can give me ... Thank You to all!

Stomach cramps, night sweats which stopped when I forgot to take them on a long weekend away.

I have been taking Topamax since 2002 for migraines. I started out slow with 25mg at night for a week then 50, 75 then 100mg after one month. The following week I was suppose to start 25mg in the morning. I received headaches from that. I only stick with 100mg at night and have not suffered from a migraine since. Unless I am hung over. I did get the tingling in my hands and now I hate soda. Which to me is a good thing for all the sugar it has in it. However, when my script runs out and it takes me two or more days for a refill, I get extremely sick. Must be a withdrawel thing. So do not miss more than one day.

I have had a severe case of polymyalgia rheumatica and was initially put on 60 mg of prednisone a day. It was wonderful! Within hours my pain level dropped almost in half. From there the pain has gradually improved even more. I went to 40 mg per day to 20 mg per day to 15 mg per day. Have been on the 15 mg for 2 months now and want off as soon as possible. Yes, I too have the moon face, camel hump, slight weight gain, nausea, digestive problems, cramps, depression, etc. Not fun! My question is - does anyone experience burning/stinging in their face, arms and legs from the prednisone? I wonder if it is the polymyalgia rheumatica or if this is a side effect from the steroid. Thanks for your comments.

The first few times taking this drug I had extreme nausea even though I had tolerated most previous antibiotics and pills pretty well up to this point.
I thought it was a little odd, but that it would pass.

The nausea finally did pass, but for the past two weeks I have been taking it I've been doing almost nothing but sleeping, and having extreme spells of tiredness.

Gradually every day has just gotten worse and worse than the next while on these pills. I don't want to get out of bed and lately have looked at the clock to see that I've been in bed for twelve hours at a time.

Now, I'm also in very advanced college courses. I initially attributed my sudden inaccuracy and inability to focus on the fact that I was just nervous about the courses, the material, but each day my concentration got worse, and worse and worse. It feels like I have ADD or something, which I've never had.
I felt like I was going insane when I could not even get through a page of material without wanting to jump up and shake myself around (also because of the numbness I got in my legs and arms). Not like me at all.

I have been dizzy, weak, incredibly tired and cold all the time, and entirely unable to focus all since I've started taken these pills. Unlike many of the other people's symtoms posted here, I've experienced severe chills and cold/ numbness in my whole body rather than heat? Except when I go in the sun, which then feels like I'm burning up.

Today was the last straw when I couldn't even get up out of bed, drive normally I was so dizzy, could not normally read one page of material, and the sun felt like it was burning my eyes out.

And reading some of the even worse symptoms others have had, this drug is not worth all the pain and possible permanent damage just to kill a few of these pimples.

I started taking Wellbutrin three weeks ago. I had been taking Zoloft for four years and it had been working fine except my insurance company tripled the cost and I was beginning to have to take more to get the same results. I thought Wellbutrin might be good alternative after doing some research and my doctor thought it would be good for me to try out. Well, since I have been taking Wellbutrin I have become emotional (wanting to cry at things I would never cry at before), more irritable, my husband says "I am not the same person", dizzy, two sips of a beer gave me a horriable headache which lasted until the next morning, I had to sit down on a bench at the mall because I felt like I was going to faint, and worse of all my brain became very "fuzzy" feeling. It was like my short term memory was damaged. I am taking a Spanish class and was doing well (A's). After I started taking Wellbutrin I could not concentrate enough in class to learn, even saying to my professor, "please skip me, I am not feeling well". It was humiliating. I have maintained a 4.0 in every class I have taken since 1999 and completed a masters degree last year. So, all in all-this was my experience. Maybe if I had taken it longer, it would have been different, but it was like torture for me. One positive note....I felt absolutely no internal depression after a week of taking it (other than being upset about the other symptoms). It worked really well in that area.....so, maybe if others do not have all the symptoms I experienced, it would be a very good drug to take for depression-just not for me!

I had a Kenolog injection in Nov. 2006, for pneumonia. I got better and thought all was fine. After a 2 months i noticed a strange indention on my upper left buttcheek. at that time it was about the size of a quarter. Also at that time, never having heard of any side effects i was stressing Big Time about why I had this "hole" in my cheek. After going to a different doctor and having a sonogram and a bunch of people looking at my behind with No answers. I finally found a Kenolg complaint web site after google-ing indentation in buttcheek. I was shocked as i finally put 2 & 2 together! Now It's Sept. 2007 I still not only have a "hole" in my cheek, it has gotten much bigger, about the size of my fist!!! It's hideous! It also aches. I use to run now that hurts my glute.The doctor has been no help. I keep hoping it gets better, but so far only worse. Does it get better and heal up?? Is anyone currently involved in any lawsuits regarding this situation?
any info would be much appreciated.

I have been on Topamax since June 2007 when RSD was diagnosed after 3 tests that were performed Bone Scan, EMG & VNC after knee surgery. 2 of the 3 tests came back positive) My doseage has been gradually increased to 100mg. Most of the side effects described above I've had, the only one I am experiencing, that I did not see posted here, I have broken out in hives. My skin started off very itchy and then all of a sudden I broke out in hives, and the hives have only appeared on the side of where the RSD was located. I have found that this medication has worked, but the side effects are quite difficult to deal with at times. I find that when the medication is increased it takes 7-10 days for your system to adjust.

I don't know about anyone else, but it took me quite a while to type this email also, it take a while to focus, and to get your thoughts together.

This is to IMISSMYWIFE, I don't know if this is my husband or not, but it sure sounds like it could be, I'm sorry for all the pain I've caused you and Nicole.

I am weaning off Zoloft. I began taking it in Nov. 2001 because I knew I would have post-partum depression since I had it with my first two. Zoloft changed my life so much for the better. That was almost 6 years ago. The past year I have decided that I can do w/o Zoloft. One, because I’ve learned how to choose to be happy. Two, because I don’t like being addicted to a pill. I know I’m addicted (or somewhat addicted to) because if I forgot to take the pill, several hours later, I would get weird feelings, like when I turn my head and move my eyes at the same time, a weird slightly dizzy feeling.
Here’s how I did it. In May and June, I took a whole pill (50 mg) every other day and every other day I took half a pill. That’s 2 months of that. Then, July and August, I took a half a pill EVERY day. Now that it’s Sept., I’m taking a half a pill every other day and NO pill every other day. I must say, this has been the hardest. It’s just 4 days into Sept. and I’m having those weird sensations a lot. My toes and fingers are tingly, too. I was planning on doing this for 2 months but I'm on the 4th day (2nd day of no pill) and I'm having too many tingles and weird dizzy sensations. So, I guess I'll continue taking a half pill every day and take NO pill ONE day a week for this month of Sept. Then, in October, I will take NO pill TWO days a week (but not 2 days in a row). Then, in November, I'll go to THREE days a week of no pill (but not 3 days in a row). And so on. I had hoped to be off by Christmas or Jan. 2008, but I see that it won't work unless I wean to a NO pill gradually. I knew all along that it would have to be gradual, and that's what I've been doing, but I had no idea that just missing a mere 25 mg. for 2 days (but not in a row, mind you) would make such a difference.
Now, if I get too many really sad days, I will consider going back on. But I’ve done really well so far. I know that God is helping me. He can lick it; I can’t. I have had just a handful of occasions where I was told something slightly disturbing or something happened to me that was slightly upsetting and it got me down, but only for the rest of that day. AND, I gave it to God and let Him deal with it. He wants to take care of my problems; He doesn’t want me worrying about it. I know that medicine like Zoloft may be the answer and if that is what I ultimately do, then I’ll just continue leave it to Him. I hope this helps someone.

I started with 25 mgs of topamax about 5 months ago for migraine prevention. I very gradually increased the dosage to 50 mgs and started having the usual side effects of tingling in hands, metal soda taste, concentration problems; but not bad enought to make me stop as my migraines were stopping as well! Then I upped the dosage to 75 mgs, and the side effects were sudsiding. My nurologist had me up the dosage to 100mg, and that very night I awoke from sleep having my first partial conscious siezure. At the time I didn't know what the heck was happening to me and thought I may be having a stroke. I am only 44 years old and I ran across the street at 2:30 in the morning to my neighbors house who is a nurse. Long story short, it took uppin the dosgae two more times and having this happen each time I upped the dose, to finally realize that it was the topamax that was causing the seizures. Now my nurologist is gradually decreasing my dosage to wean me off the topamax, and hopefully the siezures will stop! Has anyone had any experiences like this? Or am I the only one who get s siezures from an anti sewizure medication?

Hi, I'm so sorry about your experience with the mirena, it's such a shame that something that could be potentially brilliant, isn't quite all it's cracked up to be.
I had, and still do have a lot of problems with bleeding. I would say, since I first had mirena fitted in march, I've bleed for two thirds of that time. Th last bleed was 2 weeks ago and it seem to gradually be getting heavier.
The worse thing for me so far is the weight gain. I lost 4 stone last year, put a stone on over christmas - explainable enough. The last month my weight has increased by a good 9lbs. My appetite is uncontrollable.
Has anyone else found that their appetit went haywire?
I am seriously considering having it removed purely for the weight gain as there is no way I'm going back.

I am a fit lady of 67 (now).After taking a mini dose (2.5mg) of Lisinopril daily for 18 months I noticed various odd symptoms, putting them down to what I had eaten, lifestyle etc.
One of these was indigestion which caused a chokey lump sensation in my throat. For this I had an endoscopy which showed a clear result. Had also had an ECG test for palpitations..again no problem. The cough wasn't too bad, but I was always tired and did notice I had lack lustre and thinning hair.
After I came off them (gradually) I started to feel better and best of all am losing the wadge of fat from my stomach and hips.Constipation seems to be a thing of the past too.
Looking at all the comments on this site, can't we get together a petition to
at least get this drug(poison) investigated ?

I have been prescribed Lamictal for seizures, and am currently taking 400mg daily, with my 300mg of Dilantin. Had horrible side effects this weekend-nightmares, exhausted, worsening depression, crying jags, difficulty swallowing. Has anyone else experienced mood changes for the worse while on this drug?