Drugs symptoms and conditions

I'm on Welchol for the second time. I've been having a pain in my left shoulder blade and in the left side of my neck, that seems to be related. I took it for a week, had the pain, then stopped it for two days and the pain went away. I'm trying it again (2nd day) and the pain is back in my shoulder blade. I'm still having the vivid dreams I had the last time I took the drug about a year ago, which cause me to sleep so deeply, it's hard to wake up. It also causes me to grind my teeth harder (sleeping so deep) that causes more jaw pain, and pain in the neck. The first time I took this drug was last year, along with Crestor. Talk about vivid dreaming! With the two drugs together I thought I was hallucinating. The first time I also had horrible headaches and sore throat. I just can't understand why they continue to tell us there are no side effects, when clearly there are. We have all experienced them. I wish there was an easy answer.

can captopril cause itchy ears and erectile dysfunction, i have been taking 25mg for 1 yr now for hpb, i also take atenolol and norvasc, which of these drugs is the culprit

this is not a new side effect ~~~ today is 16 Nov 2009
I never knew of the tendon side effect, neither did my doc

I have literally been bedridden as I cannot walk from these pains,
horrible side effects

this is not my doctors fault - new, old drugs fill tons of books, PDRs - please file against drug companies for these horrible drugs they are
allowing the FDA to approve

THE FDA IS RESPONSIBLE FOR THIS DRUG ON THE MARKET

Where do I begin. I've been on prednisone for about 3 months now, and I feel like it has ruined my life. After having my son in February of this year I went for my 6 week check up and found out that I had high blood pressure and my kidney function was low. Before this I was pretty healthy. So, I was put on 30mg of prednisone in hopes that it would reduce or erase the inflammation. It reduced it for a while, then it went back up. While on the darn drug, Ive experienced moon face, weight gain, Im always hungry, acne, shortness of breath, and paining in my legs and back. The worse side effect has been the mood swings and anxiety, probably because it took something terrible happening to realize that they were really happening. My boyfriend told me that the drugs were making me act different, but I just thought he was picking on me as he did with my weight gain. Turns out, I have read everyone elses post and realized that many people experience what he says I've been going through. As a result of my mood swings and being so mean and demanding, my relationship may be over. I wish that he would understand that it's not me, it's the medication, but I can't convince him. Thats weird, especially since he pointed it out to me months ago. So now, I hate this drug. It's not making me better and it was a contributor in ruining my relationship. I want to just stop taking it, but Im scared I will get even sicker. There is no hope here.

I know that for every woman, the side effects or various medications and hormones are different. I personally had the Mirena IUD inserted a little over 3 years ago on the recommendation of a friend who, at the time, had nothing but positive things to say about it. I went on that recommendation alone, and now wish that I had done more research into the side effects before having one inserted.

The initial insertion was not horrible, but not great either- a pinch at insertion, severe cramping and pain within a few hours, and a dull aching feeling in my abdomen for about a week. After that, though, I couldn't feel the IUD at all.

It was not long after that when I began to experience side effects. Like many of you, I attributed my symptoms to stress and life changes. I figured that my migraines, back pain, fatigue, dizziness, increasing urinary tract infections, and weight gain were a result of a changing metabolism and high-stress job.

When I went to my family physician to have blood work done (because I was declared anemic when trying to give blood), I was told that I wasn't getting enough iron and I went on iron supplements. (The supplements then made me constipated- sorry if that is TMI, but that was a very unwelcome result!) When I took trip after trip to my ob/gyn for antibiotics to treat UTIs, I was told that the UTIs were unrelated to the IUD. When I saw a urologist to have three separate tests done (one for hormone levels, another for uterine function, and yet another to test kidney function), all tests came back within normal range. Even when I went to the ER one Saturday morning, when my back was spasming so badly that I could barely walk or stand, I was told that my back pain was stress-related.

All the while, my friend (the one who recommended the IUD in the first place) was dealing with similar problems- weekly severe migraines, back pain, etc. She was being told the same things by her ob/gyn- none of her symptoms were related to the IUD. Since she and I trusted our doctors completely, we went on about our lives, upped our workout regimens, tried to de-stress as much as possible, took OTC pain meds when it was all too much to bear- and yet for both of us, our symptoms continued.

Then, in July, my husband and I decided to begin trying for a baby. I made my appointment to have the IUD removed (which was a painless process), and it was only then that I began to research the Mirena IUD online. My former ob/gyn had moved, and my new one seemed ill-informed about what to expect once the IUD was removed. I wanted to know how soon I could conceive, and she knew very little about the process- heck, she didn't even know what the hormone was called that she had given me to jump-start my period (it was progestin, by the way- a very common prescription that my paramedic husband knew quite a bit about, but the ob/gyn didn't even know the name of!).

Once I got online and found this site (among many others), I finally began to put two and two together. I am now firmly convinced that my symptoms were directly related to the Mirena IUD. Again, different women are affected in different ways, but I know that for me- nothing good came of messing with Mother Nature like that.

Now that I've had the IUD out for about four months, I feel like a different human being. I did experience the "Mirena Crash," but once that passed, I almost immediately began losing weight, my abdomen was no longer blown up like a balloon, my energy level and sex drive increased, my back pain is now gone, and I haven't had a migraine or UTI since.

I've since switched ob/gyns, but I now have a healthy distrust of anything medically new and experimental. I will never have the Mirena inserted again, and I will definitely research anything and everything regarding my body. Ladies, listen to your bodies- mine was screaming at me loud and clear for over three years, and even though I knew that something was very wrong, I didn't listen. I'm just happy that I "accidentally" figured it out. (Oh, and my friend will be having her IUD removed later this week. She and I now call ourselves the "sister skeptics!")

2 genetic mutations in the gene that encodes for the transporter protein responsible for moving anti cholesterol statin drugs into the liver to be detoxified. have been identified. This gene is "SLCO1B1" (also referred to in the scientific lit as "OATP1B1"). Drugs must be "detoxified" by organs within the body and then eliminated, otherwise the drug stays in the blood stream, building up to toxic levels. With either of the 2 mutations, statins have been found to be (from various studies) anywhere from 122% to 400% ABOVE NORMAL plasma statin levels. How many people have either of these mutations? (Population genetic studies were done in Finland on Caucasian pop--so all the #'s refer to Caucasian population) 25 % to 38% of ALL Caucasian possess one of these 2 mutations. Thus, for however many yrs someone with one of these mutations has taken a statin, the level of the statin in their blood stream conceiveably could have been 400% ABOVE normal statin levels. ALll those pharmacologic effects of statins--decreased coenzyme q10, depressed manufacture of dolichols, depressed manufacture of selnproteins and thus glutathione, interrupted production of GTPases and glycoprotein function, decreased brain cholesterol levels--neuron synapses and new growth of neurons depend upon brain choelsterol--are intensified unrelentingly for the length of time the drug is taken.

Been on coumadin for a year, horrible medication. Have aches all over, legs, shoulders, back, always tired, want to be off this med. Was taking alternative meds previously...nattokinase, bilberry which are blood thinners but are also SAFE. Then I had no leg pain, no muscle pain. I now take vitamin e and fish oil with the coumadin, no interaction since I've been using them for a long time and are more beneficial than the coumadin as far as I'm concerned. What I need is a naturopathic doctor, but they are hard to find, regular mds have no clue about supplements..all they want to do is increase your prescriptions. Doctors try to scare people telling them they'll have a stroke without coumadin, but have no solution on how to prevent stroke, etc. without drugs.

I'm a 70 year old woman, I have taken this drug for 3 1/2 yrs. I was prescribed Spironolactone 25mg for high blood pressure of 140/80. After researching the side effects I chose to stop taking this drug 2 days ago. First off, it's a potassium sparing diuretic and one isn't supposed to eat foods high in potassium, like fruits and vegetables a contradiction to what is needed for both high cholesterol and high blood pressure, does this makes sense no it doesn't. Also I was taking a potassium supplement, maybe I'm lucky to still be alive?
I don't think Dr.'s read about side effects or what one isn't supposed to eat or take along with the drugs they prescribe. They only look at what the drug is supposed to do, then prescribe it to thousands of patients their, victims. This is probably why they're considered, "Practicing Physicians!"
This drug is known to cancer. This drug is known to cause muscle pains. This drug has caused me to go Bald on the top of my head. This drug plays with ones hormonal balance, it can help make someone grow hair, or lose it. This drug should not be prescribed for simple high blood pressure, it is a very dangerous drug!
I have huge rashes on my ankle and now my hands, they say it's eczema or drug induced atopic dermatitis.
Please do yourself a favor and research the many side effects and cancer causing of this drug. If you're taking simply to lower your blood pressure find a safer drug and try to stop taking this one particular diuretic and use supplements and foods to lower it if you can.
I'm taking this and Lipitor which I stopped one week ago and this one two days ago thank God, I thought I was going to be a cripple for the rest of me life from the toxic side effects, all drug induced.

I am a 70 year old woman, I have been on 20mg Lipitor for high cholesterol, 200 total and 25mg of Spironolactone for a not so high blood pressure, for 3 1/2 yrs. Oh, my God, the Spironolactone is a potassium sparing diuretic that is very dangerous and has many uses I didn't know about or the terrible side effects, it causes breast cancer. It's also used to treat women who have an over growth of hairiness, or on a higher dose to treat hair loss and I've gone bald on the top of my head! Plus all of the good foods we're supposed to eat for high cholesterol, fruit & veggies one isn't to eat on this drug, because of lot's of potassium, what a huge contradiction. And muscle pains, and rashes, (eczema, atopic dermatitis) that I've suffered from both.
Anyway, Lipitor, had know idea about the side effects until I looked it up on the internet and read these posts on here.
I stopped taking Lipitor last week and Spironolactone 2 days ago.
I had cholesterol test last week too and saw my dr. Wednesday. He said it was okay that I stopped the Lipitor, but not the other one, why not the other one worse then Lipitor and why am I on this strong drug, geez.
The pain and burning started in my hip for no reason, then my ankles with eczema which started soon after Lipitor, then my fingers, numbness, can't pick things up, tingling, burning. Then my feet, yes, just like all of you I have these same problems. This is not just coincidental, this is from the drug Lipitor. I get severe joint cramps in my legs, feet and fingers.
For now on before I take any drug I've prescribed I will thoroughly check for side effects and not take it if they're seriously impairing like Lipitor. I feel like a cripple and older then I should feel, I almost just felt like why live anymore if this is how it's going to be.
Since I've stopped Lipitor I feel a little better, I read that it causes permanent muscle and nerve damage though, oh I hope not, I can barely walk anymore or get up out of my chair. This is all drug induced toxicity of my system. Thanks so much everyone who posted for sharing and enlightening all of us who are suffering from this drug and others.
It should be banned along with Baycol, (a statin) which was banned a few months ago because of these same side effects. With the studies that it only helps maybe to prevent heart attack, well I'd rather be able to walk again and hopefully all this will go away, the rash, etc.

It has been interesting for me to read this posts. I have been wondering about the long term side affects to singulair- mostly because my 11 year old has been on Singulair for several years now. We spent many of nights in the ER for asthma when he was little and no Dr. did testing. When he was 5 his pediatrician tested him for allergies and put him on Singulair. We have had a great experience with it. I find it interesting that many of the health issues on here- joint pains, bouts of depression, weight gain...I personally experience all of them and i am not on any medication. My 11 year old does not experience any of the mentioned side affects. I wanted to find out long term side affects for my own personal knowledge. Prior to Singulair, he was on Zyrtec which was not a good fit.

Are there any meds that are safe? I was taking 10mg norvasc. I started taking 20/25 mg lisinopril. I was doing ok on the norvasc but the added lisinopril has almost killed me. They had cut my norvasc down to 5 mg then to 2.5 mg when I started the lisinopril. 4 days ago I stopped the lisinopril and added back 2.5 mg norvasc. Back to 5 mg. The side effects seem to be letting up. Now im wondering is all of my meds are killing me. I can't live without them. My BP sores. Im so scared of what I should do. Im afraid of all my meds.

I am looking for any information anyone has about the possibility that Singulair causes colitis or that it can lead to inflamed colon and bleeding colon. My daughter is 4 years old and has never been a sick child. In September, she started bleeding from her colon, and a month later, she was finally diagnosed with colitis after having a colonoscopy. The doctor prescribed Prednisone (steriod) and Phlagyll (antibiotic) (spelling?). I decided to stop giving her the Singulair that she had previously been taking because I didn;t want her to have so many drugs in her system as one time. After a few days of the steriods and antibiotics, she was well, with no signs of problems. Everything was going great for a few weeks, but last week I started giving her the Singulair again, and her colits symptoms have come back. Has anyone else experienced this in relation to Singulair?

Hello everyone! I am a 28 yr old male, and I have now been taking this drug for about 1 1/2 yrs. What is so overwhelming to me is that I have been having some of these side effects, but it never occurred to me that they may have been caused by this medication. My side effects are not major, but they do really affect my self esteem and I think have some what depressed me a bit.

None of us have direct physical evidence that this medication is the cause, but I don't think this is a big coincidence. Below are what I believe may be side effects of this medicine:

Unlike before I now feel:

-Anxiety (im always nerves, and was blaming debt for it)
-Decrease in sexual drive (also blaming my financial problems)
-Joints popping all the time (blaming my gaut)
-Bigger forehead because of minor loss of hair (blaming age)
-Problem falling asleep (blaming financial problems)

and again im always scared, even if everything is ok (ive been holding together because on the other hand, since i was born, I have always been a very strong minded person). This is really depressing because two years ago, nothing would be scare me, I mean nothing, I was afraid of nothing. No matter what time it was, or what situation I found myself in, my buddy down south would be ready for action, now when im going to have sex, im all worried hoping that it works!, (dont get me wrong, it works like 90% of the time) but before it would work 200% of the time, i mean i was turned on by a damn broom, and now its not the same. This really *ux!

I have been blaming everything on my financial ruin that I am currently in, but am having second thoughts on what is causing all of this. This site has really opened my eyes and given me a whole new theory and even hope.

I once asked my doctor that if I went home and got on a diet, exercised and did all that was necessary, would he consider taking me off the pill or lowering my dosage and he immediately said NO. I mean he almost didn't even let me finish asking. He told me that If i wanted to go in a pine box to stop taking it. So he scared the crap out of so I have not stopped taking it. I can afford to go to different doctors because i don't have insurance or money to pay for the visit. I wonder if this doctors has advised me based on his financial convenience. I mean is it possible that a doctor may lie? I never thought doctors would lie. Im afraid of just getting off the pill, im afraid that all the doctors are going to tell me not to get off of it. my bp is usually about 130/85 some times up to 140/90.

I would appreciate peoples thoughts on what I should do?

Thanks everyone that takes part in this blog! it is really helpful for people like me that have no money to get advice.

Hope everyone makes the right decision!

Regards!

I had been on Aciphex for about 4 years because Nexium, Prilosec, and all the other meds did not help my heartburn. I started having problems wtth my bowels, I thought I had IBS but with the diarrhea effects. It was so bad some days that I could not drive to work. I would have strong urges to go to the bathroom which literally gave me less than a minute to find a toilet. I never thought it would be the Aciphex. I recently switched to Zegerid and have not experienced quite the problems I had in the past. Last night I took my 1 remaining Aciphex and this morning the problems returned. I am sure now that the Aciphex has something to do with it. I am wondering if there is any long term damage/effects from it.

I just happened to do some research about lisinopril, and happened to stumble into this website. I am 43 years old, newly diagnosed with type 2 diabetics, i also have a history of hypertension and migraine which is under control. my physician just switch my medication from Norvasc to lisinopril, Im already on my 3rd week of taking it, 20mg a day, however, i noticed that i have more frequent headaches, more of a migraine headache that pulsate in one side of my head, i tried taking some over the counter medicine, but with no relief, i went back to see my doctor, and i was given some sumatriptan for the migraine, but at the back of my mind, i already suspected that the lisinopril might have triggered my migraine headaches, i have a relief when i take the sumatriptan, however the migraines keeps coming back. and its been seven days already, i was not able to work one day, because the migraine made me nauseated and vomit. i was doing well with my other medication, and never had migraine like this that last for 7 days up to now.after reading the comments. i have second thought of taking this medication.it seem like it might be the one that triggers my migraine headache. what do you think?

Although I have asthma, I was in my physician's office for another purpose when the doctor noticed my cough. After listening to my breathing, she offered me samples of Advair Discus 100/50. "This will take care of that cough," she said.

Sure enough, the cough I'd had for 2 weeks disappeared completely after only the second dose. I thought I'd hit the medicinal jackpot!

Then came Advair day 3. I noticed that my heart rate was elevated constantly, even when I was lying down, and my blood pressure was higher than normal. I figured I was coming down with a cold.

On day 4, I awoke to the experience of having all of the muscles in my body feeling stiff 24/7. This is no exaggeration. And of all things, my lats (the muscles running down your sides starting at the armpit) were completely tensed at all times. It was one of the most unnatural and uncomfortable feelings I've ever had.

By day 5, my entire body was completely rigid. I had to chew gum all day just to release excess tension. I was growing more and more agitated by the minute. I wanted to take care of things that needed to be done (dishes, laundry, etc.) but found myself only able to read or watch TV.

On day 6, the fear began to set in. I was terribly anxious about something, but I had no idea what. Since my brain couldn't figure out why my body was literally in flight-or-flight mode 24 hours a day, it began parceling out all the angst to all of the small aspects of my life. I became unable to do anything because I was afraid of everything.

On day 7, my cough returned, and my mind went crazy. Fearing the worst, I told my husband that I was going completely out of my mind, but I had no idea why. We are 35, and have known each other since we were 14, and I have never seen such a look on his face. I told him we were going to have to get some kind of mental help immediately because I was ceasing to function at all.

On day 8, I'm still coughing, and still going out of my mind. I have to get on the computer to look up psychologists on my insurance company's website. I start the search, but then, a thought occurs to me. I opened a new tab and googled Advair and Anxiety. And there was the answer. I called my husband at work, and told him I was going off the Advair and why. He seemed skeptical, but thought I should definitely give the Advair a trial discontinuation.

Day 9, I wake up 24 hours after my last dose, and my cough is gone. I feel more relaxed than I have in days. Perhaps I am not going crazy after all.

It took about 4 days to go completely back to normal. According to my physician, the reaction I had was to the Salmeterol. I therefore should avoid any products containing any long acting beta-adrenoceptor agonist: Formoterol, Bambuterol, and sustained-release oral Salbutamol. I'm just glad I didn't end up institutionalized.

I've been on Advair for 12 years.I'm 27 years old and fed up with all this medications that doctors prescribe.We are so brainwashed into thinking that we misbehave if we don't see a doctor.Let me tell you what: The majority of the doctors, only know to prescribe medication.They get bonuses from the pharma industries every time they prescribe their "new discovered"medicine.
Advair is supposed to be preventive, what you don't know it's for how long.Exactly!!!.....'cause it's not meant to cure Asthma, it's meant to keep you hooked for the rest of your life.
My worse symptom is a very fast heart beating.I'm a martial artist and every time i exert a fast burst of energy(while i'm sparring for example), my heart goes into pumped up mode.It beats very, very fast and i have to stop because it hurts.Sometimes i keep going no matter what and feel like i'm exercising for two people.When i stop, i breath very deeply for 5 minutes and all of a sudden it stops and beats regularly.
It's not fun, and one more thing: I'm from Argentina and my mom sends me the medicine from there cause it's way cheaper, sometimes i run out(i procrastinate sometimes), i'm left off with no medicine for a few days and boy.....I'm a wreck.The time you stop you go right back to where you started.I've been researching about an alternative to this "S***".I'm afraid 'cause i don't want to feel discomfort with my lungs anymore, but i strongly believe that there should be a natural alternative to all this laboratory drugs and i'm on a mission to find it.

My 10 yr old son has been on this medication for 3 months - it helped his symptoms right away. Just in the past week we had a couple days without it when we ran out. He started back up again and has had bad nightmares twice this week and told me that he doesn't sleep well at night. My question is - are their other drugs out there that work as well as this one that do NOT have these side affects? Zyrtec just made him tired.

I stopped taking Aciphex and now try Zegerid because I was experiencing a lot of gas and pain in my stomach along with headaches, anxiety (shaking of the knee), depression, frustration, tight chest pain. The medicine seems to be quite strong.

I have had rheumatoid arthritis for 20 years,controlled reasonably well with a combo of methotrexate, naproxen and enbrel. I do a 10 day course of prednisone several times a year for bad flares. I absolutely hate taking prednisone because it turns me into a crabby, edgy, insomniac who can't stop eating. It makes me bloat and that REALLY makes me nuts because I've done so well at weight watcher's, I don't need that nasty, upset stomach over full bloat feeling. And the "roid head" headache thing ? I'm on the phone all day at work so that's bad, too. The insomnia is the worst, really, because I just lie there awake. When I stop taking it I return to normal within 2 days. I only do it when I am absolutely desperate - I already lost some tendons in my left hand to arthritis related damage so I tend to use the prednisone when the fluid builds up in the right hand or if I'm really too sore. I'm also aware that long term prednisone usage is a one way ticket to osteoporosis / osteoarthritis, so I really have to feel like I cannot deal before I take it. It's a hate/hate relationship.

32 year old male. Admitted to ER with A-Fib. Treated with lovenox and atenolol. Cardioverted 3 days later. The headaches began as soon as I started the coumadin and have persisted everyday since. Worked with doctor to find cause of headaches, tried switching blockers, no avail. The only other med I'm on is warfarin. What else could it be? I love how a quick search shows "coumadin, no known side effects", but here's a room full of people with the same headaches. Now I see, headaches are just the beginning. What kills me, is instead of finding out why I went into A-Fib, and working to fix the real problem, the doctor's would rather thin my blood, so I don't have a stroke when my A-Fib comes back! I refuse to poison myself to death, just to avoid death by stroke. Come get me, I'm done with this qwuap!

In 2002, my doctor prescribe Avalox after two, ten day doses of Levaquin didn't seem to work for a sinus infection. I was very tired, swollen, vomiting and unable to urinate. At the hospital tests determined that my blood sugar was out of control, as was my blood pressure. I had excess potassium and several other nutrients were depleted from my body. It felt as if bugs were inside my skin and my mouth was very dry.

I stayed in the hospital 12 days because my kidneys had shut down. I was put on dialysis. My new doctor says that my kidneys are still sick. I have excess protein. Normal levels are 17 and mine are about ten times higher. I have to take a pill to protect my kidneys every day.

I have learned a lot about natural medicine and have improved my health. It took a several months and painful biopsies before the experts determined the cause. It was a combination of the two drugs.
epbp.....VA

I am so annoyed that this medication is still on the market.
What is it going to take for it to be banned??? It took me almost one year to get my life back together. The side effects from this medication are horrible. Only the people who have gone through them know how severe it is. I had anxiety, insomnia, chills, numbing in the hands and feet, palpitations, vomiting, tremors, twitching, vision problems and the list goes on. My body was out of control. My blood tests were even coming back with all sort of problems thyroid, high blood sugar etc. When retested a few months later, everything was normal.
It took me lots of hard work to get myself back to normal. Thanks to Chinese medicine/acupuncture I now have my life back.
Please don't take Avelox!!!!!

The best drug out there !! No I am not ignorant enough to make these cart blanche statements like some of these posts---Millions of people have used this drug successfully like I have. Just because it works for one individual they should not recommend it to the world nor if it causes you personally some harm YOU SHOULD NOT POST A STATEMENT THAT INFERS IT WILL HARM EVERYONE--IN-OTHER-WORDS GET A LIFE!