Drugs symptoms and conditions

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!

I took lisinopril for 2 months and throughout experienced dizziness and dray cough. Towards the end of the two months I noticed a small itchy rash on my neck. Then I had mirena IUD inserted, immediately my whole body including the head was covered by an itchy rash, have bumps all over my body. Doctor immediately removed the IUD, stopped lisinopril (I was telling her to stop lisinopril before - did not help), and i am still suffering. My fingers are swollen so difficult to type. I am 48 years old and my bp is back. i am taking HCL (water pill for BP) Monday going to see an allergist/immunologist. I am positive the lisinopril and mirena caused these symptoms. I was told it will take a while for this to go off. I had mirena for 7 days and see what a mess. both drugs have given this together. Until then absolute misery!

My whole life 120/70. Two months ago 160/103 wtf. I am on my second month of lisinopril. I am pretty sure it has caused me to be absent minded and grouchy. I was never these before. Worse yet for me is that I am a life long runner. I live to exercise so that I can enjoy the more fun things in life. beer wine and good food. ( I am 47 years old) I ran my first marathon 26.2 miles in January. I now have trouble running three miles with out getting fatigued, dizzy and winded. This sucks!!! any advice would be appreciated.

On Sept. 2, 2009 I had a cortisone shot in my back for L4, L5, C1 disc problems. The shot was painful but brief and I went out of there with no particular symptoms. It was done in a hospital by a neurologist. On Sept. 4th I woke up and the whole room was spinning. I threw up and this continued for awhile. I could hardly stand and went to the hospital emergency room where I spent the next twelve hours getting all kinds of tests. My blood pressure was 185 over 110. Finally, they told me they could find nothing physically wrong and dismissed me with meclizine for dizziness. This is now Oct.27th and I had these vertigo symptoms for seven weeks! I was sent to an ear specialist and underwent vesicular therapy for benign position vertigo several times a week at a rehabilitation center. I had brain MRI and a neck MRA which showed nothing. Last Saturday I passed out for a few seconds. Every medical specialist insists that the Cortisone shot had nothing to do with all this but I am still undiagnosed. Yesterday (Oct. 26th) the dizziness ended (7 weeks). I don't know if it is gone for good. I cannot believe that it is just a coincidence that all this happened two days after the cortizone shot. Does this strike a bell with any of you?

I started taking 400mg yesterday for a sinus infection. Fifteen minutes after my FIRST dose, my stomach started cramping. About five hours later I noticed muscle pain in my thighs all the way down into my toes. It was like I worked out at a gym. This morning I have a metallic taste in my mouth that even lemon water won't cure. I have a VERY HIGH tolerance for medication and usually have to double whatever is prescribed. Fortunately I did not do that with this med since it was new to me. I will not be taking anymore. I will go back to the amox and deal with the infection. I read that apple cider vinegar was good for that - without the side effects. Seriously, beware if you are sensitive to drugs. This one surprised me.

Googled Wellbutrin and hair loss and arrived here. I am female, 54, taking 250 mg per day for about a year now. Just recently, my hairdresser noticed two large bald patches at the top of my head - NO hair! I wonder if the symptom affects more people than the pharmacuticals admit?

I sure hope it grows back! Good luck to all of you.

My Mom started taking Avelox September 28, 2009. She took her first pill at 8:33 P.M. and within 25 minutes could not breathe. Her tongue swelled so much, that it pushed her dentures out of her mouth. Nothing alerts you to this in the side effects. She had no time to call her physician as she died. She had previously taken Cipro and Levoquin, so she had the false security that this drug was safe. It was not. No one should die like this!

i have a friend who went after her husband in a ctalsudden rage after starting the Lamital, she loss huge amounts of hair and it conytinues to fall out , was put out of her house,broke up her family and is a complete mess. She was on adderall, suboxone and the n the dr gave her this,i was trying to figure out what was going on with her and i looked up the newest of her drugs lamital and found out what was going on . Mt advice to all you bipolar people find GOD no one is ever happy all the time and we all go through really hard times . I am sober and take nothing for the last 20 yrs. When i first got sober doctor tried to tell me to take antidepressant, I said ," the difference between us is when all else fails i go to GOD and you go to meds"" YOU wont break. We live in a society run by drug companies that you are not allowed to have emotion, they flat line everyone.and when it doesn't work they give you more drugs till you are a blob of a person. Get off everything{ except if you need it for ceisures } It could take a yr to completely detox, be patient and go to na meetings

I am alarmed to see all of these various side effects posted because I have occasionally taken Avelox-400 for sinus infections during the past five years or so.

Does anyone have any positive results to post?

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.