Reply symptoms and conditions

I cannot disagree with these negative postings more. I absolutely love the nuvaring. I have not gained any weight...of course I diet & exercise about 5 days a week....do those of you who have experienced weight gain exercise regularly? I have also had an INCREASE in my sex drive...I have been with my fiance for 5 years, and for the past 3 of those, I have had no sex drive whatsoever. I got on the ring & bam, it's there with a vengence...the only problem with that is that we're getting married in 2 weeks & I wanted to make it special & stop having sex a couple of months before the wedding...but I just can't get enough of it. I have dealt with depression & anxiety my entire 27 years of life, so if the nuvaring is causing that...it's not any worse than normal. The only side effects I've had is the discharge, (which yes, is very annoying) and tender breasts...but I can deal with that. Although I have noticed that I cry a bit easier...but I was always a crier as well. I cry when I'm mad, sad, happy...always have, so nope...guess that's not from the ring either. ALL birth control effects everyone differently. I'm not saying this for everyone, but sometimes a lot of people like to blame certain actions & physical changes on something & maybe this is the case...for some people. I've been on the pill before & I always got off it b/c of weight gain....well, it was b/c I wasn't eating properly or exercising. I liked to blame my mood swings on the pill as well, but once I thought about it, I still had those before & after taking the pill. The only reason I quit the pill was b/c it did give me acne. Anyway, just my thoughts....& I wanted to post something positive for the ring.

I have been on everything from OrthoCyclen to YAZ and this extra low-dose pill has been the only thing that I can remotely tolerate. I am, however, having some trouble with my cycle. It seems as though every other month, I start this really light period ONE WEEK early. I'm only coming up on my 4th pack, but I can't figure out why it's doing this. This is the only pill I've ever had this happen with. I'd much rather have some light spotting for 2 weeks than to be crazy and psychotic! If anyone else has experienced this, please reply. Was there a pattern????

I've been taking trileptal for a only a couple of days, but I've had an immediate onset of night terrors in addition to having constant joint pain. I've noticed that these are commonly listed side effects.

From reading the posted comments, I noticed that many people reported experiencing losing sensation in their tongue. After taking geodon for five years, I have started experiencing something similar in that I lose feeling in my tongue, but it also appears to swell or otherwise make it difficult or impossible to breathe.

I've taken cogentin (sp?) to help with this, but it hasn't really made a difference. The numb tongue and inability to breathe seem to be brought on by anxiety and although are similar to anxiety attacks, tend to be a little scarier as my tongue literally blocks off my esophogus (sp) making it (sometimes) impossible to breathe.

I started taking trileptal to eventually be weened off the geodon as not being able to breathe isn't really an option. Can somebody p.m. or post a reply to let me know whether the loss of sensation in their tongue is just that, or if it is accompanied by trouble breathing?

Thanks!

my friend has been on geodon for about 3 years and is experiencing some very strange things! She gets cramps, like seizures in her legs and can't walk when this happens. Her doctor says there is nothing wrong. She gets neck and leg twitching and recently, the leg things have come with shortness of breath. Does anyone know anything about these side effects?Please reply! Thank you.

I posted this as a reply in another discussion group, but thought I'd share here too due to the very serious and potentiall deadly side effect (I think may be a result of taking Yasmin):

I suffered a Pulmonary Embolism on 6/4/08 - was not on Yasmin at the time, but had been for about 2 years (was switched about 3 months before my PE). I am 36 years old, otherwise healthy (am very active and have no other underlying risk factors), and have been on other forms of the pill (on & off, but mostly on) since I was 18 - with no side effects. The more I am reading, the more I'm mad about not being appropriately warned! People seem to keep dismissing the risks of this pill. Yes, millions of women are fine on the pill, but from what I'm reading hundreds of thousands are not. PEs are terrifying and potentially deadly. In case anyone needs it, there is a great on-line support group called ***** and there is a PE suport group on there I found last week - they are wonderful people and have saved me from losing my sanity (lots of panic & anxiety). Recovery from PE is a long, painful and bumpy road, and these people are of immense support. Good luck and good health to all!

I have had the Mirena for 1 1/2 yrs now. Within the past six months I have started to develop acne, all the while my period was starting to fade less and less every month. Now, the acne is severe and the periods are completely gone. I'm just wondering if this is all related. I have scheduled a appointment with a skin clinic, and also called my gyno. I am waiting on a reply from the nurse at the gynos office to see if I need to go on to the skin clinic, or if I just need to get this removed. I have never had more then a pimple or two on my face at one time. Now, I have them completely covering my hair line, almost like a rash.

I agree Kenalog has a lot of adverse reactions, being a nurse myself, I suffer from pollen, ragweed, mold, dust mites I can go on and on, and have swollen eyes and wheeze/sob almost on a daily basis from asthma and allergies all yr around, am tired all the time ... I have a heart murmur so I cant take the fast acting inhalers, I also suffer from panic disorder, have 2 benign lung nodules on my left upper lung as of today, still in my 2 yr for the sit back and see if it grows follow up with cat scans every 6 month's, my 19 yr old son passed away from a brain bleed in 06, and am still working in nursing where I want to help out other's, it has changed my thought process to live life to the fullest , try not to dwell on the petty things in life, and yeah every single drug that helps us in one way or another has a side-effect, don't pitty me , just think about this , or at least this is how I get by, I sit and weigh my options, would i rather have sweaty palms, rapid heart rate, tired a lot of the time, mod joint pain, period irr and pit in my butt leg and foot cramps day and night a few, h/a's rather than to, sneeze 24/7, have nasty swollen eyes that burn and hurt to the point I cant see, or not be able to take in one deep breathe and feel like im breathing through a straw, yeah you may not like this post, but to all the people who do not have a whole lot of medical knowledge, I ask you to do your research, don't beg the lawyers to take it off the market, thats what I call petty in my case Kenalog is a godsend!.. have the smarts before you go in, after all they are just Dr's not GOD..we should all re-evaluate what is a priority in our lives, since the death of my son in 06 I have, but please note people , its not the Dr's faults , we need to know what we are taking and have all the info before we take it whether it be the internet, a PDR, they are free to read in the library as well in every doctor office just ask to see one (that might through them into shock making them think your having a part in your health as well), a local pharmacist, because lets face it this world is becoming a fast paced, whirlwind circus and in the end, we all just cant sit back and blame the busy Dr's. I will say one thing though, Kudos to all the Nurses in this world, if it were not for us, now where would the Dr's be :P ..so make the best out of life, we never know whats around the corner, but most of all remember EVERY single drug has a side-effect every one of them, we must realize that we have to take the good with the bad..been there still doing it... take chare of your life, be informed, or get the info, you can do everyone of you! Just food for thought.

I have only been taking singulair for about a month. I have noticed that I have become more irritable, grouchy, hateful and just numb, not really wanting to be around anyone, not caring about anyone else's feelings much. I also noticed I have become extremely lethargic, to the point of falling asleep at work as well as heart palpitations and stomach pains. I just started new birth control pills so at first assumed they were causing these side effects, that is until I looked up the side effects of this drug! I have over half of the side effects so I stopped it immediately and can already tell a difference in my mood. I have to sons age 11 and 14, both who have asthma and allergies. The took this medication for a few years with no side effects but have not taken it for about a year now. My youngest son however, has been diagnosed with ADHA and ODD and possibly BiPolar disorder. As I read the other posts, I realize the description of how their children act while on this drug is exactly how my son acts. I wonder if there can be irreversible permanent damage from taking this medicine? He has been on a number of ADHD drugs, none have helped except to make him stop eating and lose weight and he is small for his age, so I have taken him off everything. Has anyone else out there experienced what could be permanent damage from this drug in their children? Even after being off the drug for a year or so? If it could make me miserable within a month, what can it do when one takes it for years? Its sometimes hard to tell the effects of medicine on small children. My son prob starting taking it around 4 yrs old and took it til he was about 8 or 9. Just wondering if anyone else out there has had this happen to them or their children.

I have been on it for two months due to severe psoriatic arthritis. I'm taking the max infusions every four weeks, methotrexate injections and prednisone. I'm tired, sleepy, sweaty and somewhat nuts a lot. However, after last week infusion, I have some type of rash-little red dots that feel like pin pricks that itch somewhat. I feel like a thousand fleas are attacking me all at one time! Has anyone had this type of feeling? PLEASE reply-it is driving me nuts.

Glad I took the time to read the noncommercial posts! During my thyroid check last year bloodwork showed high cholesterol. I was put on Crestor in addition to having my Synthroid dose adjusted. A few weeks later I was absolutely miserable. Couldn't get out of bed. Everything hurt. My doctor thought I was "depressed" and asked if I wanted anti-depressants. Not needing to add another pill to my daily repertoire - I declined. Six weeks later I am feeling worse and just want to lay down and cry. The doctor had no idea why I would be feeling that way and was convinced it was either depression or thyroid issue. I was getting ready to leave for a trip to Mexico that had been planned a year in advance and was non-refundable - and I didn't have the strength to even pack the stupid suitcase. The trip was a bust - I laid in a pool chair just feeling crappy. What a waste!

Funny thing - nobody stopped to consider I've had a thyroid problem for 20 years and this horrid nightmare just started after I started taking Crestor! A few weeks later I stopped the Crestor entirely and after a couple of months I felt back to normal. Now, three years later - I've been talked into taking Lipitor. In my naivety (because I explained to the doctor that Crestor made me ill) I trusted that it would be different. It's taken three weeks for me to put two and two together - but here I am again - muscle aches - can't get out of bed. Everything just hurts. My knees, arms, mostly shoulders and in between. With all that is an overall lethargic feeling. Lipitor stops today -and if the pattern continues and I feel better in a few weeks - it's no statins for me ever again. I'll just have to eat like I'm supposed to and hope for the best!

My doctor started me on Lipitor over a year ago. I started having muscle pain in my shoulders but didn't equate it to the meds until I was watching television one day and a Lipitor commercial came on. It said that some people experience muscle pain.....I thought HALLELUEH THAT'S WHAT IT IS.....I stopped talking the meds and went to see my doctor who immediately changed my meds to Zocor.....guess what? The same thing happened. Went to see her again and she switched to Crestor.....same thing happened....so I started doing my own research and was amazed at what I learned and bewildered as to why my doctor was acting like I was some whining baby.

No problem, I say to myself and stopped the meds. That was last November, in January I had my yearly physical and blood tests were ordered for me in December......guess what.....my triglycerides were still high so my doctor orders Antara. It didn't say "cor" anything so I'm thinking it's not the same stuff. No, it wasn't the same stuff it was WORSE!! Within three weeks I was crying I was in so much pain. I called her and got her nurse practitioner who says that my doctor said to stop taking the pills and the pain will go away. I call back and say, "you don't understand, I can't sleep, I can't move, I can't function the pain is so bad." After several calls back and forth, and let me tell you I NEVER call my doctor unless something is incredibly wrong and that is less than rarely. Well, my doctors partner tells the nurse practioner that they will not prescribe narcotics for me. WHAT? Who asked for narcotics? I needed relief from this pain.....I would have gone for amputation!!!

So I change docs...more blood work.....high triglycerides, I refuse to take any statins. She says she has something for me that will not cause muscle pain and hands me samples of Welchol.....this one took less than a week for increased muscle pain...again I wanted to trust, but guess what i learned when I went to the Welchol site? The first side effect listed? Muscle pain.

Called the new doctors office to let them know that I was experiencing pain again and was told to stop the Welchol (which I had already done) and take Red Yeast Rice and have bloodwork done in 3 to 6 months and come back to see her. Oh no! Not without research and guess what? A side effect of Red Yeast Rice? Muscle pain.

It has been 4 months since I stopped taking the Antara and took Welchol for a week in that 4 months. Sometimes my shoulders/neck and arms don't hurt too much. Unfortunately most times they do. Both doctors insist that the pain cannot be from the drugs because the drugs have left my body. The new doctor said I probably have myolgia just because I'm 52 and that it's just a coincidence that it happened while taken the drugs but then goes on to agree that I must be "sensitive" to statins. Both doctors treat me like I'm stupid and nuts all balled up in one. I am frustrated and in pain most of the time. I have been trying to find out how long to expect this pain and am dismayed to learn that it can be years or never go away.

Yes I have high triglycerides (so does my mother and she experiences the same kind of pain so refused to take statins) and I've been warned that not taking statins could cause pancreatitis and/or heart problems. My question to that is - "then my choice is chance the heart stuff or live an incredibly painful life?"

I'll take my chances and pray for the best because right now my quality of life stinks!!

I have been taking LIPITOR for about 1.5 years and have been feeling the cotton head but thought it was allergies. for about 8 months or so I have been feeling pain on the left side of my chest and upper back by the shoulder plates. I've told my doctor and had several tests done incl. MRI, C-scan, etc. Once I even had to go to the emergency room thinking I was having a heart attack. But the doc. said the EKG was normal and that it might be muscular. I have not read that anyone else is having the chest symptoms. This is very scary to me. Lately I feel my neck getting stiff and I am also constantly tired and keep waking up at night and have a hard time going back to sleep. I don't seem to have the arm or leg pains that most people here seem to be suffering from but am now convinced it's LIPITOR since it is the only prescription medicine I am taking. I would appreciate hearing from someone who has had the same symptoms I've described above. I stopped taking Lipitor about 4 days ago and do feel already less tired but the upper body pain is still present.

I just started using Singulair a few days ago. I am 54 years old and just started coughing at night only. I would be fine during the day and then never failed, at night I started to cough keeping me awake. I was given antibiotics, narcotic cough syrups but it only helped temporarily and then I went back to coughing nights only again. So as I mentioned, I started taking Singulair a few days ago because my physician thinks I have developed allergies and Singulair is noted to help night coughs. It is helping my night coughs but I still cough a few times at night and now I cough quite a few times in the day when I never use to cough in the daytime. Wondering if Singulair is worth taking as the symptoms are becoming opposite? I hate taking drugs and don't know if I should find a safer alternative? Help, anyone? Thank you

In my previous message I was wondering why the same medication has to have so many different names.

I haven´t had a reply to that, but I found some information on Wikipedia that migth be helpful when looking for more information.

Zocor (=Simvastatin) can have many different names as you can see below.

"Brand names: Zocor, Zocor Heart Pro, marketed by the pharmaceutical company Merck & Co. and Denan (Germany), Liponorm, Sinvacor, Sivastin (Italy), Lipovas (Japan), Lodales (France), Zocord (Austria and Sweden), Zimstat, Simvahexal (Australia), Lipex (Australia and New Zealand), Simvastatin-Teva, Simvacor, Simvaxon, Simovil (Israel), Simvotin (India) and other."

I had posted my case on May 17th on this blog--as I noted, I URGE others to report their adverse event to the FDA--just click on this link and complete the form: http://www.fda.gov/medwatch/. The FDA is responsible for assuring safety of medications. Therefore, it is imperative that the FDA recognize the adverse effects to provide any credibility to a class action suit. Please consider forwarding your case to the FDA to force them into action and begin addressing these atrocities. Such documented cases and recognition by the FDA will provide leverage for attorneys in pursuit of a class action suit. Also wanted to see if anyone has contacted a lawyer on this issue?

-- By slmgator | Reply | (3) replies | Send Private Mail

I took Lipitor for 2 years with all the pain in my shoulder, hand and arm as well as fuzzy memory. I had a friend over for Lunch an have no memory of anything that happened including his arriving and leaving on his Harley and we all know how loud they are. I ended up in the hospital with all kins of tests including an MRI all of which I have no memory of to this date. My hospital bills are still coming in as well as all the Doctors that saw me. I just received my Divorce and then this happened , I was out of work for a week , the Doctors thought I had had a heart attack, stroke or aneurysm.I also had all the foot pain making it impossible to stand up , leg cramps, sleeplessness, sheer exhaustion, depression, headache and nausea. The Doctor at the Hospital took me off of the Lipitor and said to take a 325mg. aspirin daily . This happened on March 23, 2008 . I am felling better but I still pain in my shoulder , neck , stomach , and feet and legs but is nothing like it was. Here I am left with a few thousand dollars of Doctor and Hospital bills. Why can`t something be done about all of this we are all going thru? I called the FDA to report it and got no where. Did I really expect anything to happen ! I hope someone gets something done for us . I would be one of the first to sign up to take Lipitor off the market and get what is due us.

My mother is on Toprol-XL, and she has complained of being so fatigued, she sleeps so much, and this is someone who has always had a tremendous amount of energy. The other thing, and I would love a reply to this - she said she's experienced something at night while sleeping that feels like a seizure. She describes this as follows, "like my brain is shaking or trembling inside my head and my hands are trembling too." Has anyone else experienced this? Please let me know.

Who administers this site? I posted a side effect last night after I registered and then this morning I got an email saying there was a reply to my posting and when I tried to log in, my account was inactive and my posting had been removed, as had the reply to my posting. I don't know if it is because I put a link the an online reporting tool where the FDA is compiling feedback from people/or their children who have experienced terrible side-effects. Here is the link again and I urge you all to report your cases: http://www.fda.gov/cder/drug/early_comm/montelukast.htm

My son is 3.5 and has been on Singular for 2 months and just like all of the other stories about the other young children posted here, he is a different kid after being on Singular. Last night was the first night I took him off of it. All of the side-effects that are mentioned here are the same ones my son is experiencing, nightmares (screaming in the night), hyper, aggressive, reliving injuries from days past, the day care telling me that they now have concerns about how different he has been lately and the even used the term "bad behavior". They said he is hyper, he screams, not listening, aggressive. He is a favorite at day care since he is so loving, polite and kind. I know all parents say that, but pretty much anyone who has met him compliments me on how well behaved he is. I am even nervous to have people over since he seems out of control and I have found myself ensuring people that he isn't normally like this. I have taken him off as of last night and I am hoping he will get back to his old happy-go-lucky self soon. Does anyone know how long it can take to get this poison out of their system? I pray that there are no permanent side-effects.

Has anyone had long term side effects after taking Wellbutrin. I was on ot for two years it helped with my anxiety and energy levels a lot. When the doctor put my dose to 300 mg I had severe muscle pain and swelling in hands, feet, ankles, legs it went down after I went back to 150mg. I tried to up my dose but the same thing happened. After two years of wellbutrin I developed severe headaches feels more like head pressure so I went off wellbutrin. would still have muscle pain and swelling from time to time. started developing severe pain in legs and now everywhere along with muscle twitches and muscle loss. I now am 32 and have severe memory problems and no doctor knows what is going on with me. Has anyone had anything like this or heard of anyone with these problems.

I have had 1 remicade infusion so far for ulcerative colitis. The next day a bunch of spots appeared on my lower legs. There were 30-40 of them, small, roundish, purple/dark red. They looked like blood spots under the skin.
It wasn't a rash and they didn't itch or hurt. My doc had no explanation, and I haven't heard of anyone else having this reaction. They checked my blood for a clotting problem and didn't find anything. The spots faded away over a week or so. My next infusion is in 2 days, so we'll see if they reappear.
I have also been experiencing a weird kind of insomnia where I am so physically antsy I CANNOT keep lying still, I have to shake my body or kick my legs or something. I read up on restless legs syndrome and the symptoms sure sound like what I am experiencing. I don't know if it's connected to the Remicade - I read that iron deficiency can also cause it and I am anemic due to the UC. But since Remicade can disturb the central nervous syndrome, it seems possible. Anyone else experience RLS with Remicade?

I am a 62 yo female who was prescribed Lisinopril in February. Within a week I had such a continuous horrible dry, hacking cough that I trouble communicating with others. This cough was particularly bad during the night. I have had to live with water and cough drops as my constant companions. I can honestly say that I have only slept through the night once from February until last night. My PCP finally decided that I did not have a sinus infection and that a codeine based cough medicine was not the answer and switched me from Lisinopril to Avapro on Monday, June, 2nd. According to my PCP it could take up to a week for the cough to go away.

I am taking my son to our first face to face app tomorrow with the pulmo doctor,although this is our first app since the news broke,i have spoken to him on the phone a couple of times.Of course i am full of questions and fully intend to put him in the hot seat,It has been hard for me but i am sure now i can face him and not punch him in the nose.He is one of the top peds pulmo docs in the country So...........if you have any questions you want me to ask tomorrow just put in reply and i will ask.i will post his response.

I am taking zegerid 40mg around 10 p:m for 2 years. Zegerid used to work well.
Recently I have started to take ditropan-xl 5mg, zocor- 10 mg, a statin drug, and coumadin. I am having frequent bouts of diarrhea with terrible cramps.
I wonder if I am having stomach side effects from my new medications. I have irritable bowel and gerd I have been instructed to take all my meds before I go to bed. Thank you for your reply sw

I took this antibiotic for 2 days. I have no history of mental illness whatsoever and I thought I was losing my mind for 2 days. I had a panic attack 2 nights in a row and stayed up all night starring at front door afraid that someone was going to break into my home and hurt my children. I can not believe that this "antibiotic" is even on the market. This is an extremely dangerous drug. I called the doctor and he sounded like he didn't believe me- maybe I should share some of this stuff with him so he can experience the crazy too!

I received my first shot of Gardasil in January 2007. It could have started sooner, but about a month later my hairdresser noticed a bald spot in the back of my head. I rushed back to my ObGyn and asked her if the Gardasil could be the cause as nothing else had recently changed. She said that she had not heard of this, but she referred me to a dermatologist. I asked him if my hair loss had anything to do with the Gardasil. He replied that I had Alopecia areata and one thing had nothing to do with the other. He advised that I continue with the Gardasil and that he would start treating me for the alopecia. I wish that I would not have listened. I don't know what would have happened if I had stopped then, but I didn't I proceeded with the treatment to the end now over half of my head is bald!!!
I don't know what to do. I keep going back to the dermatologist for treatments for the alopecia, but it just keeps getting worse.
If anyone has had a similar experience and would like to share or has found some other treatments that work, please post a reply.

Melissa