Sentences symptoms and conditions

This is a follow-up to my posting on October 10th regarding my 57 year old husband who began taking Lisinopril in March of 2007. He was NEVER on any other medication prior to taking this drug. He suffered Depression, loss of memory, lack of concentration, can't focus and struggled with small task. We have recently had an MRI done and his brain has shrunk. Deadfred1 replied to my posting and he is a 36 year old male who has been on Lisinopril for 5 years. He has the same side effects as my husband. He had a recent MRI and his brain has shrunk!!! We visited a Neurologist with his MRI results for a second opinion and he is ordering more tests because "it appears to be indictive of Alzeheimers" with the area of the brain that has shrunk. How can this be??? This was a healthy, 57 year old NEVER on a drug in his life and within months of taking this, he is in Depression and having memory issues. Isn't anyone connecting any symptoms here??? Any Doctors out there with an "open mind"? This medication is was developed from the venom of a poisonous Brazilian snake!!! Hello...it's more like a slow death with Arsenic!!! My mother-in-law has been on this drug for years and years and years. She now sits with dementia in an Alzeheimers unit. Is anybody out there listening? Alzeheimers is becoming an epidemic in this country. Have we ever thought the medications we are taking is creating this devastating disease? Millions of people take Ace Inhibitors, millions of people have Alzeheimers. They are getting younger and younger according to the Neurologist. Why, because younger and younger people are being put on Blood pressure medications from poisonous snakes. Are there any open minded Dr.s out there that can "step outside the box"...don't just "think outside the box"...."step out for goodness sake" and start paying closer attention to the symptoms people are having. I am convinced there is a definite connection to my husbands side effects and this drug. Get off people. Get off.

Im only 16 years old and ive been on levaquin for about 3 days now. My doctor told me off the bat that the only thing wrong with the drug were some "theories" on cartilidge damage, how ever, now i see for myself, and for many other people that is not the only side effect. He told me that no one under 18 is supposed to have it but i caught a severe case of sinutitus, and a uti which ive had for 2 months and nothing was working, so he put me on levaquin, once a day for 7 days. Ive now been having the following symptoms and im extremely scared!!
1. Constant fatigue
2. Extreme Migraines
3. Nausea, vomiting
4. Rapid heart beat (and chest pain)
5. Stiffness in joints and horrible pain...
6. Constant anxiousness, to where i cant get to sleep
7. Dizziness

Is there anyone i can talk to who's had these same problems? please email me or something im scared and i don't know what to do my mother doesn't believe me and she says its just a head cold....

******

Please help me!!

I have been taking Yaz for a month and a half. The only medication I have been on in several years.
At work yesterday, my head started getting foggy. And my perception, was all messed up. After about 15 minutes of this not getting better, I started to lose my speech communication. I couldn't finish sentences or words. Stuff was jumbling together. In my right hand, two fingers went numb, then the whole hand. A client ended up driving me to the ER. I tried to call my receptionist, but I couldn't get the words out, my client took the phone and told her I was going to the ER. By the time I got to the ER, feeling started coming back, and I could communicate, in full sentences, if I paused between. By the time I was checked in and saw the doctor, I was able to tell him all that happened. With no problem, then a huge headache came on.
He wanted to rule out stroke, so did the CT scan and MRI. The nurse had some trouble getting blood from me. She kept mentioning that the blood kept clotting. The doctor sent me home saying my brain was perfectly healthy, and to go see my regular doctor.
A friend told me it was the birth control, because she could not take it, as she has lupus, and could have a stroke. She said it causes clotting. All of this was making sense to me. I looked up the side effects I had and found the "stroke symptoms", listed as rare, on Yaz.
My opinion of what happened, I had a blood clot that ended up passing through, and it could have become a stroke.
Another thing I read, besides the clotting. Was that oral contraceptives increase the potassium in your blood. I had been eating a banana for breakfast, 3 mornings in a row (the third on the day of this episode). The added potassium, could have been related to this episode.
How is anyone to know they can't eat something like "bananas" with birth control? I certainly didn't.
I am afraid to try any form of birth control at this point.

I'm taking Wellbutrin and Lamictal (150 mg for both) for at least 5 months now, as a mood stabilizer. Like many people have said on here don't let these bad reviews scare you away from trying it, at the very worst you will take it and not like it so you can stop. But for me it was amazing how it stabilized my moods. I didn't expect it to be so noticeable. I had tried Topamax right before but it was terrible for me- it made me sooo out of it and I had a very hard time talking (finding the right words, pausing in sentences frequently) Lamictal didn't do that to me. I have started to get acne on my jawline like many others have posted, I didn't think it would be related but I've NEVER had acne on my jaw and cheeks they are really tiny bumps of acne, but a lot of them. The reason I started to look at this site for people's side effects was now I have terrible neck soreness and stiffness. I mean BAD. It's slowly working it's way to the middle of my neck as the day goes on and feels like it's going down the middle of my back as well. Very weird, I haven't exercised or done anything in the past 4 or 5 days that would have pulled a muscle, so make what you will out of it but I'm going to stop taking this drug. It's unfortunate because I really did like it and am worried how my moods will be after stopping it. But TRY IT, it has been at least 5 months of me being more stable so that alone is worth the clarity. Also, I'm a woman with usually heavy periods but didn't have that side effect with this drug and I lost weight didn't gain any with this one either, but I'm sure that had a lot to do with the Wellbutrin which is notorious for weight loss rather than weight gain. Also, if you start to feel good at a low dose as I did DON'T INCREASE IT! I hate hearing people say their doctor's wanted to get them to the "therapeutic dose" even when they felt good, your more likely to have neg. side effects if you go higher than you need. Everyone is different in how their body metabolizes the medicines. Do your research and hold your ground, make sure you have a doctor that will listen to you, that's key.

My doctor put me on topamax for daily chronic headaches. I worked my way up to 200mg and had all the symptoms, tingling in my hands and toes, short term memory loss, hard time putting sentences together, etc. I backed myself down to 100mg. and the side effects lessoned up significantly. I stayed on 100mg for almost a year (lost 10 lbs.) One day I decided that I was going to ween myself off and started going down 25mg every week until I stopped altogether. Since I have stopped, I do get headaches, usually 1 or 2 per week, nothing like when I started out on the topamax. I have gained 20lbs since stopping the topamax but no longer have a memory problem or putting together a complete sentence. In my opinion, you should try to take the lowest dose possible that gives you the greatest relieve from your pain.

i heard something on the television about a lawsuit involving advair and came across this site looking for information. i have been on advair for aprox 8 years. when i read some of these comments i began to cry. it so said exately what i have been feeling right down to being diagnosed with rhumetoid arthritis and fibro. i spent 6 hours in the er last week with a heart rate of 112. i went to my doctor as recommended after my visit and he blew me off because he was mad i went to the er and told me to go see a surgeon to cut into my collar bone, go down to my lungs and biopsy them. i see a different doctor next Thursday for a second opinion. i am so tired of being sick and to think, it could all be from this one thing. i am going to talk to the doctor about this on Thursday.

Previously posted 8 year old son w/ suicidal ideation and depression...I'm seeing comments about "inattentive." I've been saying my son is ADD for years....How many of you saw this possible side effect? Off of Singulair for 14 days now....behavior unbelievably improved.

My son is off singulair for two weeks now and is showing improvements. He was on it for 7 years and at the beginning we blamed it on steriods, even though his dose was low. When he went off the steroids, the behavior didn't stop. I questioned the allerist if the singulair could be doing it, but was told no, it doesn't have those side effects. I don't blame the doctors because they weren't given the info. He was extremely emotional, cried for no reason, had no confidence, didn't like himself. We on more than one occasion have told his older sister that when he hits his teenage years we would have to watch him for suicide, as his reaction to problems was sooo out of whack! He was on motrin for headaches 4-5 days a week(blamed it on sinusses). Unexplained stomachaches. These symptoms came on over years, not right away. I have always thought that the steroids had done damage because he took them when he was so young. Until the news reports hit, and I started reading other people's stories and doing the "OMG, that's my kid!", I never put the problems on singulair. I was still skeptical, but took him off. His symptoms immediately got 100x's worse for a week. But funny thing is, his headaches are gone, his stomachaches are gone and he seems much less emotional. The strangest thing is, EVERY night, he comes in to kiss us good night 7 or 8 times, and sometimes by the 7th time he is crying and can't explain why. This has been going on for YEARS, EVERYNIGHT, never a break. It stopped! Just stopped cold 7 days ago. Comes in once, says goodnight, leaves and falls asleep. I know this isn't a coincidence. After years of wondering what's wrong with my kid, now I feel like I've been poisoning my him for 7 years. I'm not skeptical anymore.

Ive only taken the pill 2 times so far. Already looking for the reason why my Dr. Pepper tastes bad, and I haven't slept since I took the very first one. I studder and can not complete sentences after I take it. I have a call in to the Dr. He said it will go away. Im not so sure I believe him. Insomnia I am a single mom, and work in a nursing home how unsafe....

Without repeating what everyone else is already describing all I can say is Thank God!! My step son has been on Singulair as long as I can remember (6 years?)and his anger has been just what everyone describes. Before he could even form sentences he would lay down on the floor and repeatedly bang his head on the floor concrete, carpet, grass it didn't matter. He was diagnosed with ADHD about 4 years ago but his father and I were both desperately against medicating him because we didn't think this was the problem and no one was asking any questions or looking for other answers. He has now been put on 3 different meds for the ADHD and when they don't work they just keep upping the doses. He has since been committed to a hospital 4 or 5 times now for his anger and suicidal threats. HE IS 7!!! He doesn't even know what suicide is he just knows he doesn't want to be here anymore. The other night he pulled a knife on his mom out of the clear blue. They were laughing and playing, he went to the kitchen for jello and came back with a knife!! I don't know if Singulair is the cause but it sure sounds like it and I only PRAY we have finally found an answer and that everyone finally sees what his father and I have been screaming for many years now. Hopefully this will open his mothers eyes as well as the doctors. I PRAY with everything in me this has no long term effects. Also, looking back I realize he has always had problems with bad dreams. From the time they put him on Singulair he has not once slept through the night without wanting to join his daddy and me in bed. He is afraid to even go to bed without daddy. When I think about all the nights I wouldn't let him sleep in bed with us because I thought he was old enough to sleep alone at 7 I literally cry for what he must have been going through. Please let this be the answers to our prayers!!!

Had my Mirena installed in Sept 07 after having a bad experience going back on the pill (LoEstrin 24) for a few months. I am 43, was on the pill for years in my 20s with no issues. After 5 months on the LoEstrin, my blood sugar went through the roof...thought I was having a stroke....never had anything like that happen before, doesn't run in my family. Anyway, decided to try the Mirena. Went through the usual adjustment period....30+ days of spotting, headaches, nausea, dizziness. It got a little better but the bloating remained. Didn't have my first real period until Dec....then another one 3 weeks after that...lighter, but 10+ days long!! Acne has been horrible! Never, ever had that kind of problem before, not even as a teenager. Insomnia almost every night and severe brain fog every day....can't concentrate at work. This past month, the extreme fatigue set in....and to top it all off, the libido is in the toilet....that was enough of that. Went to my OB/GYN for my annual 2 days ago, told him I had enough. I started on my list of side effects and he was finishing my sentences. He said something to the effect of "A year ago, I was really excited about the Mirena, but now, not so much"....he apparently is hearing a lot of this and bless him, he did not try to talk me out of having it removed. After only 48 hours, I feel like that Claritin commercial where the layer of haze is peeled back. Just now starting to spot a little....removal was nothing, just one small cramp. I am happy for those who can use this form of BC without any problems but not all of us can. What's scary about this is that you don't always connect the side effects with the IUD....who would have thought that the stuffy nose had to do with something in that part of your body??? And today I woke up with a clear nose for the first time in months...what a difference. Am expecting the "crash" but maybe I will be lucky and it won't be so bad. It seems that perhaps the longer you have it in, the stronger the crash is. In any event, the difference is already perceptible and everyone around me has noticed. Good luck to all....good health and a good sex life should not have to be this difficult!

For about 6 months I experienced severe cognitive disturbances. I had trouble remembering things, and making basic connections. I also had chronic fatigue, and terrible headaches, severe depression, moodiness, trouble sleeping, and trouble making sentences. I was so out of it that I couldn't make the connection with the medicine. I was 16 at the time, and my doctor thought it was just normal teen issues or something equally absurd My eyesight became worse, and my usual ability to retain information in school was butchered. Once I got off it, I felt much better. I could think again, and no was no longer forgetting important things, like my best friends name. However, it has been a half year since I got off, and some of the symptoms still persist, although in a much less degree. I am afraid of permanent damage, especially with my cognitive ability.

For about 6 months I experienced severe cognitive disturbances. I had trouble remembering things, and making basic connections. I also had chronic fatigue, and terrible headaches, severe depression, moodiness, trouble sleeping, and trouble making sentences. I was so out of it that I couldn't make the connection with the medicine. I was 16 at the time, and my doctor thought it was just normal teen issues or something equally absurd My eyesight became worse, and my usual ability to retain information in school was butchered. Once I got off it, I felt much better. I could think again, and no was no longer forgetting important things, like my best friends name. However, it has been a half year since I got off, and some of the symptoms still persist, although in a much less degree. I am afraid of permanent damage, especially with my cognitive ability.

Firstly I want to mention that I am a simple Turkish guy whose English is not that good; so, sorry for any incorrect or "hard-to-understand" sentences...

I am 20 yard old male who has mild asthma from my 3-4 years old ages...
But since 1.5-2 years, i changed my doctor , a professor, who gave me Singulair...For the first months, it was extremely wonderful...that with this thing taking one pill before sleep everyday, I was just so wonderful and healthy that I even forgot that I had asthma really...

I hardly used Ventolin inhaler once in 1-2 months...

then I wanted to give it up thinking "maybe i got better and my asthma no longer exist as it happens when they age older, so why bother taking more drugs if I have no asthma at all.."
and I tried 3-4 times..to give up Singulair...

however after the 2nd day I have been really bad at breathing every time I tried that...like i needed to 4-5 time of inhaler as i have never needed before...

has anyone experienced this before?..like you are better when you use Singulair, but when you try to give it up, you are much worser then ever before about asthma...?

..and actually the main things is, started after that...like I thought it might be written at prospectus...I looked at the side effects part..(how funny that some pill that I use everyday , that I look at its side effects for the first time!)..
then sooo interestingly, I realized that almost all those psycho logic effects appeared on me...disorder at sleeping, bad and ABNORMAL dreams, restlessness...(but not hallucination or such extremely serious things...)

..and I just can't explain if it's really "there" and if it's caused by that Singulair but...its just always "there"....since I started using Singulair..I just have very weird and unwanted dreams, and especially I REMEMBER them all (which I would almost never remember my dreams before..) ...I am just a bit restless...because of that sleep thing of course...
I don't know, I can't explain exactly...and I am not sure if I am only having this as the psychological effect of reading all these comments here and also at the prospectus of the Singulair...but I am sure that something is wrong about it...and seriously thinking of giving it up no matter what...

Hi My Topamax side effects for the past 4 months have been major confusion, I forget things, such as did I take my pills how many pills do I take this morning when I used to do 4am 3 at night it used to confuse the hell outta me. I am in grad school, I cannot remember a lot of things. I have to read a chapter over and over couple of times, the length of time it might take me to do a 10 page chapter is 4 hours. To get through one set of notes it takes me the whole day or half a day, I am so slow and fatigued from the medicine. My mind works so slow. I have a hard time forming words and sentences. I hate Topamax, decreasing the dose did nothing for me. My eyes burn when I read. Everyday I go on the same road from school to home, I don't drive, someone else takes me, I still don't know how to get from home to school. I know pieces of it. just like my school work, pieces. Everything is a blur.

36 yr old female. Was started on Toprol -XL in Sept 07 during my angiogram to relax my heart and lower my heart rate. Have also been on Lisinopril for several years prior for hypertension. Since starting the Toprol, I have had increasing depression, lethargy, shortness of breath, chest pains that have worsened, my feet are FREEZING all the time, I have gained 17.5 pounds, my fasting blood sugar is now up to 160-170 range, I have had many headaches (like the kind you get when your BP is sky high) and the other thing I have noticed is that my BP is bouncing ALL over the place. Last week it was down to 90/54 and I felt horrible. Then it will go up to 140/99(ISH). Find it really hard to finish my own sentences lately, and if I had nothing else to do, I could easily sleep 12-16 hours a day-everyday. I am down to 12.5 mg a day, and will be speaking to my cardiologist about this asap, had NO idea that Toprol could have been the culprit until I was told about this site. Thank you to everyone for sharing their stories, and good luck and blessings to all.

O an by the way woman who thinks im insensitive, how da ya feel now?.... ya thats what i thought,,,you rellly shouldnt talk when u dont know. i learned that when i was 4, i guess ur just a lil slow

Actually, i have been on the pill for a week and a half and it is perfect!!! I am 17 years old, almost 18 and i think it is amazing, i take it at the same time everyday i mean EXACTLY the same time, 9pm everyday, not 9 :03 0r 8:58, 9 pm my doctor said that taking it at night helps if there are any side effects. Which there are not!!! In fact, my boobs are bigger, i have lost 5 pounds , i was not over weight at all , and am not under weight now. just fyi, anyway all of the postings are like crazy, all these people complaning o im moody my boobs hurt, SUCK IT UP!!!, everyone responds to medicine deiferently and posting what happened to u is fine, but dont complain, anyway, i just wanted to post this for anyone who is getting freaked out by all of the other information. As long as ur not old, fat, a smoker, or a cranky lil Bit*h ur gonna be fine.

I just started taking Topamax about 2 1/2 months ago -- am up to 50 mg now, and had hit 75 when the side effects became so bad that I went online and discovered that my neurologists had been pretty lax with their advice. They told me that Top. was "a great drug for migraines" and that I might "lose a few pounds," and have "some memory issues at first" but that was it. I believed them and so didn't research further.

20 pounds later (I HAD been on a diet, and thought I lost the weight myself) I started experiencing sore throat in the morning and stomach pain (acid from Topamax). I thought I had appendicitus. So I hit the boards. Weight loss was from theTopamax (and my diet coup goes out the window) Appendicitus --probably not. Oh, also I can't be relied on to remember words or sentences or thought structure; or how to move thoughts into words. And it's not like the words are on the tip of my tongue, etiher. They are gone, as if they never existed. The oddest thing! Professional hell. Hair has yet to fall out. I'm going to have to wean myself off, I suppose, and get ready to ream out the neurologists. If I can remember their names or where they practice....

I am so happy to have found this website. I started taking Yasmin 2 months ago and was only on it for 1 month. I began a round of Prednisone at the same time due to hurting my back. Well, while tapering off of the pred (going into my 3rd week of Yasmin) I had one night of NO SLEEP. In the morning my muscles were so tight and painful I could barely walk. My heart was racing, I was so dehydrated I could barely speak, my vision was blurry, I couldn't form sentences clearly my head was in such a fog and I had lost 5lbs literally overnight ( I am already extremely thin naturally, so this is not a good thing for me) I was skin and bones. My normally thick, shiny hair became dry, thin and brittle and my skin broke out horribly and I had painful diarrhea. This is just the physical symptoms. The mental symptoms were out of control. I was crying all the time, yelling at everyone and just being completely irrational. I truly thought I was dying. My doctor thought maybe I was having withdrawal from the pred. This continued for a week until I started researching about Yasmin. I immediately stopped taking it after reading the side effects people were having as they were the same as mine. Strangely, they were also the same as prednisone withdrawal, the only problem was that I was off the pred and still having symptoms. Over the following 2 weeks, they slowly got better. Then, it all started again for my next cycle just to a much lesser degree since I was off the BCP. This makes me certain that my symptoms were absolutely from the BCP and not the Pred. I am reaching the end of my period today and my weight has gone back up and I am again starting to feel better. I just hope next month will be normal again. The thing that makes me the most angry is that my doctor refuses to believe that any of it had to due with the BCP. I have been on plenty of BCP's and NEVER experienced anything like this. This stuff needs to be pulled from the shelves or doctors need to be more aware of it's potential side effects and quit discounting our intelligence. Thank you everyone for your posts.

I am so happy to have found this website. I started taking Yasmin 2 months ago and was only on it for 1 month. I began a round of Prednisone at the same time due to hurting my back. Well, while tapering off of the pred (going into my 3rd week of Yasmin) I had one night of NO SLEEP. In the morning my muscles were so tight and painful I could barely walk. My heart was racing, I was so dehydrated I could barely speak, my vision was blurry, I couldn't form sentences clearly my head was in such a fog and I had lost 5lbs literally overnight ( I am already extremely thin naturally, so this is not a good thing for me) I was skin and bones. My normally thick, shiny hair became dry, thin and brittle and my skin broke out horribly and I had painful diarrhea. This is just the physical symptoms. The mental symptoms were out of control. I was crying all the time, yelling at everyone and just being completely irrational. I truly thought I was dying. My doctor thought maybe I was having withdrawal from the pred. This continued for a week until I started researching about Yasmin. I immediately stopped taking it after reading the side effects people were having as they were the same as mine. Strangely, they were also the same as prednisone withdrawal, the only problem was that I was off the pred and still having symptoms. Over the following 2 weeks, they slowly got better. Then, it all started again for my next cycle just to a much lesser degree since I was off the BCP. This makes me certain that my symptoms were absolutely from the BCP and not the Pred. I am reaching the end of my period today and my weight has gone back up and I am again starting to feel better. I just hope next month will be normal again. The thing that makes me the most angry is that my doctor refuses to believe that any of it had to due with the BCP. I have been on plenty of BCP's and NEVER experienced anything like this. This stuff needs to be pulled from the shelves or doctors need to be more aware of it's potential side effects and quit discounting our intelligence. Thank you everyone for your posts.

I have had migraines for 4 years almost on a daily basis and nothing has worked. Finally started Topamax, the first week iI felt like i had a stroke, my speech was slurred, I couldn't concentrate, I was exhausted couldn't make complete sentences, numbness in hands and feet and every thing tastes bad., I had been on 4 pills a days to start so decreased to one-i believe it it 50 mg. worked well then headaches began again after 2 weeks, so increased to 2 then again in a few weks to 3 now i have had only 3 migraines in 3 months. Still have the numbness and taste aversion but I have never felt better as far as migraines. My new problem is I am having a lot of digestive issues including cramping and constant acidy, bubbly,gassy, bloating feeling and no gas x, pepto or anything works??? Is this a side effect or something unrelated??

LEVAQUIN is a FLURO quinelone. The fluoride replaces the iron in metalloproteases in your tendons. Remodelling to stress thus fails to occur. It is a molecule shapped like a horseshoe. The base is the formula for an INHIBITORY neurotransmmitter: GABA. It also causes cardiac hyperpolarization. If these dangers are not carefully examined before taking the drug, you are playing Russian Roulette.

But don't just be hysterical. Read. America can't survive as a nation of hedge fund BSers with no grasp of science or math. Doctors are drowning in HMO paperwork and 5 mins. per patient. They can't be thorough and don't have time to read other than the BS of drug salesmen. So don't go by the stupid TV ads. READ-->LEARN-->READ--> and contact the FDA and drug company to get their info on your side effects. If they lie, you have a case. Fight for yourselves instead of just panicking over symptoms. That could kill you whether you stop or not the drugs.

I was given this drug Prednisone Last month (JAN 2007) by my new doctor. After one day, I could not concentrate on anything for more than a few minutes, I forget what Iwas doing, ate all the time,and just feeling weak and tired. So I stop taking it. All the the symptoms went away. That was about three weeks ago. So I decided to try it again yesterday,and to my surprise all the above symptoms were back. As one on the guest on post 37008,said "It was often good for a hearty laugh, but sentences and words constantly came out of my mouth backwards or made no sense" how true. I will not take this stuff anymore.

Best Regards

I have been on Tp xl 50 mg for 6 years. I have had several issues through the years that I never thought the Tp was affecting. My throat has been sore for a year, I am tired alllll the time, moody and even worse at that time of the month, my left shouder has hurt for years and I never associated it with my meds, until now. I have NO SEX drive at all, poor hubby. My BP is good however when working out, Cardio my heart rate stays at 95. I have gained a 100 lbs in the 6 years I have been on TP and I am very moody. I never can finish sentence because I am always trying to come up with words to fill my sentences. Still I never thought this was cause of Tp. The only thing I blamed my TP on was weight gain, mood swings. Know I can associate alot more with my meds. Thanks for the reading material.
Cathy