Ordeal symptoms and conditions

I have been on 20 mg Lipitor for years, and as I also have Rheumatoid Arthritis, all my symptoms have been blamed on that. I have been diagnosed with Fibromyalgia and put on Lyrica because of the muscle aches and depression. My lower back, hurt in a car accident when I was 17 years old, had gotten so much worse that I had 12 steroid shots in my lower spine a couple of years ago. They didn't help my back at all, but my blood sugar went from normal to diabetic levels, and I am now on Byetta to try to lower it.
I am a 56 year old woman who was the math specialist in a school district until last December when I had to retire early. My back pain was so severe that I could no longer go from school to school carting materials. I could barely make it from the parking lot to my office. Mentally I was not ready to retire, but physically, I was (and am) a wreck. I have severe muscle pain in my shoulders, sometimes one or the other, but always present. I have tingling in my right hand, especially in my fingertips, and have trouble gripping and drop things easily. In the last few months the pain in my right thigh and calf has gotten unbearable. I thought at first it was sciatica, but I have had sciatica before, and this isn't the same, although there is tingling, burning , but the pins and needles is so deep in the muscles I have just sat and cried, or wanted to scream. I have wished I could just cut my leg off. And...I am on some pretty heavy duty pain killers for the RA: a small dose of prednisone plus Enbrel, Methotrexate, and Vicodin, and this pain is cutting right through all these meds. I get severe headaches, I went off Lipitor for 5 days and seemed a little better, but then went back on, and it came back.
Since I no longer work, I sleep longer, am exhausted ALL the time, have terrible mental fog, am clumsy, cannot stand for more than a minute or so without wanting to scream, cannot walk more than a few yards...just getting to the car is an ordeal. I tell people that I can only shop in shoe stores and furniture stores...the only stores with places to sit down.
I no longer cook or clean, cannot play with my granddaughter, even holding a book to read can be too much, and I love reading. I feel I am just dying bit by bit as I lose parts of myself.
My doctor is really into lowering cholesterol, and has put me on Zetia in the past few months...and it has been in this time that the pain in my leg has gotten unbearable. He wants my cholesterol to be between 50-60, and has said that the Zetia along with the Lipitor will do that. Is this normal or in any way reasonable??? I am having a full blood workup done tomorrow morning, and I want to go off the Lipitor starting the day after.
I came across this web site tonight while looking up Lipitor side effects, and I am shocked. I have so many of these symptoms, and there are so many I had no knowledge of at all. I knew about the muscle aches, but that's all. I hope someone can help me with what supplements and vitamins I should be taking. I started taking CoQ10 a month or so ago. What else should I be taking for my health? I know vitamin C and fish oil, but don't know how much or anything else. Right now I am just stunned with the thought that all of these problems that have left me unhappily retired, exhausted and in constant pain can all be caused from a drug I have been taking to help me be healthier.

As many here many recognize, I had tremendous problems after taking Levaquin. This included: distal bicep tendon rupture, a full range of psychological symptoms, extreme and long lasting fatigue, etc. Even after going through this ordeal and still dealing with the fallout almost 2 yrs. later I am once again in disbelief at the medical community. My 18 yr. old daughter just visited a nurse practitioner and came home with a prescription for Levaquin. This alone was enough to make me angry but the fact that it was prescribed for a cold sore (no, I'm not kidding) is just beyond belief! And we wonder why we have the problems we do. Trust no one!

I just wanna cry.I had mine put in on April 9th 2008. I thought for sure I was crazy and I was making a big deal out of nothing. I have it all the depression, lethargy, extreme irritability, mood swings, cramping, back pain, stabbing pain in my abdomen, bloating, abnormal and irregular bleeding, headaches, nausea, dizziness, lack of motivation, reduced interest in sex, continuous yeast infections, sore breasts, weight gain, itchy flaky oily scalp, joint pain, continuous gotta go feeling, and I so could go on.......... I just wanna give up. I have 4 children and can't afford anymore. I can't deal with the way I feel all the time. I want to get it removed but I don't want to end up pregnant and I'm just at a loss I don't know what to do.

I've been taking Yaz for the past 5, almost 6 months. I was struggling with PMDD symptoms. There were times when, for a week or more, I would become incredibly depressed, full of rage and anger, I craved anything within chomping distance, and felt like the ugliest human being in the world. My periods were so painful, and I would bleed so much, that all of this just began to control my life. I was literally planning my life around this time during each month. The YAZ has really made a difference in helping solve a lot of these problems, but now I've new problems.

My husband and I have always been very sexually active. We try to make time for sex during the week if we can squeeze it in (we work different shifts), but whether we do or not, we always make up for it a lot on the weekends. However, now, I find myself with no interest. I even encourage him to just skip the foreplay and get down to the deed so I can get it over with. I dry up halfway through, become frustrated if he loses his erection (usually due to my personal lack of interest. I can't imagine that's very arousing. lol) because that just means we will have to work harder to get through this ordeal, and I don't want him kissing on me or doing much of anything to me while we are in the act. It's really damaging our relationship. We are 30 and 31 years old...way too young for this nonsense. I dare say I've even thought a time or two, "Why can't he just have an affair like every other husband and leave me alone?" Yeah, I don't mean that at all, but it's crossed my mind.

That's my biggest issue with it, well, that and the monthly cost. The other side affects I had were dry mouth, dry hair (?? - not sure if this is directly related), lower abdominal pain, mild weight gain, and a rash that broke out on my lower legs and left forearm. These are the CONS so far. I'll list my pro's, too, just to be fair.

PROS" Periods, while still very painful, last about 2 to 2.5 days. The painful part only the first day. The food cravings usually only a couple of days instead of a week or more. Mood swings, if any, are not as severe and are shorter in duration. I feel like a normal woman just having normal PMS mood swings now instead of mood swings you see in those crazy women on those Lifetime for Women movies or something. lol I also suffer from migraines, and these pills don't seem to have affected them one way or another. This is actually good enough for me because usually BCPs have caused them to worsen over time.

So there you have it. It's my own long, personal experience with YAZ.

Wow so this really helped me out today. I have been having issues with my bipolar that started acting up this summer. I had become and stayed manic. Im used to not really having major symptoms and dealing with the depressive side. The mania didn't last very long at all. Well I just went through a huge ordeal and just started meds for the bipolar . They put me on Geodon worst mistake ever. Well here I am been reading up on that and bipolar and all that mess. I just so happen to see Nuvaring info and it just dawned on me I have been on this ring oh since the start of summer. Duh. Well come mid to late summer. I am noticing more and more manic symptoms and episodes. Took myself to a doc in the past month or so and said hey i have been manic for a while, lets get to the bottom of this. Put me on Geodon...which am now off. I hadn't taken any meds in almost 2 years previously. I am so glad I just read the little info on here and come to a conclusion that perhaps the Nuvaring is causing or at least increasing the mania. So I went to NuvaRing's web site nothing talking about Bipolar and such with the ring. So if anyone could direct me to any sites that talk about bipolar and the ring and other hormonal bc, please lead me to them. Thank you so much

I recently lost about 25 lbs and decided after about 8 years of 10 mg of lipitor, to go off of it, cold turkey. I consulted both my MD and my pharmacist about whether or not I should wean, and both declined.

I now feel that my sweats, hot flashes are out of control. I am so hot and tired. I feel as though I cannot do the daily functions that I am responsible for.

I truly had NO side effects that I know of ON the drug. I just figured I'd see how I do now that I lost some weight. I wonder if going OFF lipitor is dangerous?

If anyone knows, please reply!

Thank you!

I had the Mirena inserted in July 2008 during my period (as I was told it had to be). I was also told to give my body three months to "get used to" it. Where should I start? I had some cramping, followed by contractions five days later - yes, I said contractions (ladies with babies, we know the difference between cramps and contractions); I had itchiness outside (vulva) and inside which was a yeast infection that was treated twice - once with OTC medication and then with antibiotics. My period ended in July; when I thought I was getting a period in August, it started as that thick brownish gunk. It was like this for 4 days; then I started bleeding, thinking I was gettting a normal period. Well, since August, the bleeding would come and dissipate - not totally go away - until within the last couple of weeks (since the end of August - beginning of September) it has become heavier. This is not normal or natural. I have bled through a pantyliner. I bled through to my pants using a tampon and maxipad. I've had to change the tampon and pad within one hour. I've had bleeding that is bright red followed by small clots and then one huge one (approx. 6 inches long, and 1.5 -2 inches wide). I repeatedly called the OBGYNs office throughout this ordeal; they have told me to give it time, this normal, "well this is better than the alternative - what would you do (re:pregnancy)" and have at times reacted as if I'm overreacting. Last week I went there to express the concerns, to have a checkup, and to express that I want it removed; the PA could find the strings and wrote me a script for a sonogram. But before I left the office, when I mentioned that I wanted this out, she said, "You really don't want to get this out - just give it some time- give it another 3 months - really, you don't want to take this out."
I went for the sono on Saturday and the tech asked when I had my last period. When I mentioned a brief synopsis of what has been happening, she mentioned that my uterine lining is very thick. I questioned, "Shouldn't it be thinning out if I'm having my period?" I also mentioned that it should be thinning out because of the Mirena. She couldn't afford any answers in regards to the Mirena but did confirm that during a period the lining thickens up and then thins out - sheds - but that mine was very thick.
Ok, now I'm totally freaked-out. I hope this isn't anything serious.

Sadly, I am just another case among many it seems. I am a 26 year old female who was prescribed ciprofloxacin for a UTI at my urgent care center. I have health problems to begin with and did not want any more. You know, I’ve had to take all kinds of meds over the years, including harsh ones, but it was never so bad as to prompt me to write comments on the internet about it. What does that say about Cipro? When I got home from the doctor I read the paper before swallowing the pill, which included the description of side effects. Unfortunately, it did not include the truth about what could happen to you while even taking this drug for a short time. If there had been some kind of warning about the strength and potential risk of taking this drug, I most likely would have steered clear from it since I am sensitive to medications and already suffering. The paper led me to believe false information, listing some common antibiotic side effects, and I ended up starting treatment. Some of the negative effects I experienced while on this medication for only 2 days were: severe muscle/overall body weakness, difficulty breathing, fatigue, mental confusion, difficulty concentrating, anxiety/nervousness, restlessness, mild carpal tunnel pain, slight vision change, stiffness, pain, an overall feeling of terrible heaviness, including of the chest, and possible heart palpitations. It felt like the medication was damaging my body; like it was eating away at my muscles or something. I've never had chemotherapy before, but some how that's how I would imagine it. It felt like it was doing damage to every cell in my body. The worst part is the weakness and altered thinking right now. I hope these symptoms go away completely. I felt better after quitting the drug, but not completely. I am just thankful for my hope in Jesus Christ. Even if things don't improve, I am comforted that He cares for me. I am going to be praying for this terrible situation where doctors are just handing this out for common problems without giving proper warning. May fewer and fewer people have to suffer because of Cipro and this class of drugs. I am also going to report this to the FDA and hopefully to my doctor’s office. I would like to see clear and extensive warnings on this drug, if not for it to be taken off the market. My personal advice to any one who is currently on this medicine and experiencing side effects would be to: drink milk or eat other dairy products to lessen the symptoms. It seemed to temporarily help me.

I want to add something to my original post. I only took this med for 10 days (5mg) and was miserable. After 3 weeks I was beginning to feel better (having 1 bad day, then 2 good) when suddenly I experienced pain in my left side, numbness and tingling. My doctor sent me for a kidney scan. Five days after this new pain began, I developed another rash. I realized that I had shingles. So PLEASE be careful if you have any symptoms. This puts a terrible stress on your immune system. Apparently my immune system couldn't handle the stress and the result is shingles. So, I'm miserable again and probably have another 3 weeks to go before I begin to come out from this episode.

Also, for those of you who are switching to another blood pressure medicine that is an ace inhibitor (as lisinopril is), you will not tolerate those either. They are all made from the same ingredient, snake venom.

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

please everyone who is on lisinopril be warned!!!! my mother was on this medication for a month and began having hives. she went to the emergency room and they gave her antihistamines. a few days later she woke up with facial swelling and a sense of not being able to breath. she went back to the emergency room where she was treated as above. twenty minutes after discharge she began swelling and her throat closed. she suffered cardiac arrest due to lack of oxygen from the swelling in her face and throat.she was stabilized, but unfortunately did not survive this ordeal. please, everyone on this medication, if you experience hives, facial swelling, or lip swelling, see your doctor immediately and push to have medication switched!!!!!!!

Hi All - I have been off prednisone for one week and I am not doing as well as I thought I would be at this stage. My symptoms are not flaring, which is a very good thing but I am so tired and feeling very depressed and low energy. I thought I'd feel great once I was off the evil prednisone but so far I am feeling almost as bad as when I was on it. My moon face has not started to go away, which sucks, but I guess I have to be patient. I am so tired of this situation as it feels never ending. Part of the problem is I have continued to work throughout my ordeal, and it's been very hard at times to carry on like a normal person who is not sick. I have been sick since last November (with an autoimmune disorder) and I had really hoped by this time that I'd be on my way to being better :( Prednisone saved my life but the side effects are horrendous, as are the after affects of it. Good luck to all who are taking it. I share your pain and frustration.

I am a 35 yr old male and have been taking lipitor about 7 yrs. I have a genetically high cholesterol and it has been up to 275. On lipitor its around 175. Over the years I have been on this drug I went from being a normal weight and active to pretty much lethargic and sedentary due to lack of energy and gained ~50 lbs. I couldn't sleep. I got random nausea and fogginess in my brain to the point I could not remember how to perform my job. I usually had minor aches and was bloated. the past year everything has gotten much worse. For a year now, I have been getting large rashes on my body that itch severely and no medications have worked to alleviate them. I found out recently from my doctor that I have a genetic marker in my cholesterol that makes me 3 times as likely to have a heart attack. Its a portion of the cholesterol, i think its called LDL-b or something like that. Anyways, My doctor prescribed zetia to help with my cholesterol since the lipitor wasn't doing it alon. I begin feeling very sick when taking the zetia and after a week or two stopped it. The problems didn't end. As long as I remained on the lipitor, the problems seemed to continue. Its like the zetia released a dam of problems. I stopped the lipitor 4 days ago and have noticed that I feel energy coming back to me and the rash is starting to go away, but I ache severely all over. My shoulders, forearms, and legs are so sore and painful that I can't do anything about this except sleep so I don't feel the pain. I am also very weak feeling and I notice stiffness in my fingers and my grip is very weak compared to how it normally is. I have nausea and stomach cramps and constipation. I feel miserable. I notice its worse in the morning and gets a little better towards the afternoon. I typically took my lipitor in the morning. I do not know if there is a relationship here. Please advise on any help you can provide.

KMJ
07-30-08

on may 31 i wrote the symptoms my mother had from 4 doses of levaquin over a 4 day period.....on june 2nd she died from levaquin induced myosistis
it was a horrible ordeal and i hope this website saves a life. luanne

I am a 60 yr old woman, and have been on statins for several years, most recently 40 mg. I have been getting more and more side affects over the years that I kept attributing to age, overweight, lack of exercise. After reading so many of these postings, I stopped the statin in March. Some of the side affects i.e. the aches in my arms, hands went away fairly quickly. But my legs still ache so much and the muscles in them seem to be weak, I have a hard time standing up from a sitting position. Do any of you know if it sometimes takes this long for symptoms to go away or is it possible that they won't???

Hi everyone! I posted on June 27th about the Mother Goose looking doctor and not having sex a week prior to getting your Evil Thing (ET) removed. Well, I just wanted to post once more to say that I did get it out the following Monday, which was almost a week ago. I'll spare you all the details about the incompetencies of my doctor's office not having my appointment on the books and my doctor yet again going off to deliver another baby and the amount of time I had to wait for her to return. The point is that she did come and she did take it out. The other thing I'd like to mention is that unlike Mother Goose, my doc said that of course the ET was causing my cramps and they should certainly go away as soon as it was removed. She then said that as far as my other symptoms were concerned the best she could figure (after she bluntly asked if I was depressed) was that because I had been on the pill so long that I had not had any real PMS symptoms and now I was having them and just didn't recognize that. Ok, again I'm 31 and yes I do look a bit younger than that, but I promise you I'm actually a bit wiser than that. Although that was not the craziest thing I had heard during this ordeal, (please see my Mother Goose post) it was a bit on the ridiculous side because I did in fact have a whole lotta PMS while I was on pills and I certainly know what PMS is and how to recognize it! Also, who has PMS everyday, which is essentially what my doc saying although I doubt if she realized it. I said nothing, but just waited for her to be done with her defense of this piece of crap she recommended I put in my body. She also had no explanation for my bladder issues and offered no concern or way to fix it nor did she address my discomfort and at times pain during sex. She just stood after she was done dismissing the list of symptoms I had written down for her and accusingly told me that she warned me that women who had not given birth often had problems with the Evil Thing. Actually, what she told me was that I was a great candidate for the Evil Thing and that women who had not given birth only experience more pain/discomfort with insertion. I remember this very clearly. Again, I do not care--just get on with it and get it out!! She did and now I have to say I am finally me again. The next day even I could tell a difference--that little black cloud wasn't following me around anymore. Each day that passes I feel a little less like I might impulsively quit my job or beat the crap out of some innocent bystander for no apparent reason. I've even had sex--because I wanted to--and it felt like it used to, not at all uncomfortable or painful. I no longer have any cramps at all--that was an immediate relief and overall I can tell it's just not there anymore, just no longer present in my body. My face is still full of acne, but fewer new breakouts. You can put food in front of me and I eat like a normal person and not like some starved refugee. I still have some bladder issues, but again as time passes I can tell that it is improving. I think with a little more time I'll be back to 100% and I'll just look back on this as a little hitch--a mistake I made when I started going to a new doctor's office. BTW, I don't plan on going back there at all. I've been to that office 5 times and seen 4 different doctors in a four month span. I've also decided that the next time someone asks me if I want a foreign object placed in my body, I think I'll just say No Thanks! Take care everyone and best of luck with your Evil Thing.

Here are some more side effects that I encountered during my ordeal with Lipitor. A week after I started the medication, I started experiencing blurry and decreased vision, this used to go away and come back sometimes, I could swear I always had 20/20 although I never went to eye doctor, but I never needed glasses all my life, if fact any type of glasses will blurry my vision and make me dizzy. I had my first eyes exam a couple days after I discontinued Lipitor, guess what? I have 20/20 vision.
More details about the back and right arm pain, not only the pain was unbearable, I felt my muscles sagging and they did not have any strength, this thing sucked the life out of my muscles, it made me very tired and easily irritable. My fist victim was my little baby ( my beautiful 4 year old), her daddy couldn’t hold her anymore, I even avoided staying close to her, because anyone who touches that right arm will make it feel like another deep stab to the arm deep into the bone. I have never experienced pain like this. I knew about toothache when I had a cavity at 23, but it was fixed and went away, I even experienced the pain of a broken arm at 16, but this thing was something else. The other victim is my wife, I stopped doing stuff, I used to be a very active dude, I do stuff on weekends with family and even every day after work ( you name it, park, boating, swimming pool, malls etc..). It felt like I was dying one piece at a time, going down the tubes fast with no clue of what was wrong with me.

It`s very important to educate yourself when it comes to medications.

When I saw people close to me suffer I had to find out why and I am quite sure that it had to to with side effects.

I started to do my own "research" in 2003 and it continues to this day.

One of the groups of medications that I have looked at is quinolone antibiotics to which group Levaquin belongs.

Most medications in this group have similar side effects. For more information go to:

Please visit www.fqresearch.org and www.fqvictims.org (?).

Also search on Google for "floxed" or "floxies". That´s what people call themselves when they suffer from side effects.

I would also recommend Stephen Frieds interesting book "Bitter Pills".

Medications are needed sometimes, but not to the extent that they are prescribed today!

Update. The count down is on. Next week on Tues my 6yr old son will be having his tonsils removed. Only 5 months after the adenoids were removed. I am hoping once this is over the improvements I have seen will just get better! His sinus drained in April, 9 days after coming off Singulair after battling sinus infections for entire year or more actually. When his sinus drained the infection went right into the tonsils and he has had tonsillitis ever since. One thing I wanted to share is that around the same time he came off singulair we started omega 3 supplement. Both my son and I stopped Singulair the same day. We both started the Omega 3. Last week I had to stop his dose because of the upcoming surgery because it can thin the blood. I noticed this last week his nasal allergies kicked in. He did pretty good through this allergy season and wasn't on any meds a lot of the days. I hardly had to take allergy meds this time around also. Im allergic to trees/grass and this is usually my bad time. I really feel the omega 3 has helped a lot!!! I am also waiting to get the results of his blood tests to see if his cholesterol has gone down. Just wanted to share!

I've been taking Topamax now for about 6 weeks, and my headaches are still just as bad as ever, except now I have headaches with the thrill of numb fingers, confusion, weight loss, memory loss, an absolute horrid taste in my mouth, and now the latest.... my hands feel dirty all the time. Has anyone experienced this?? I just feel like my hands are dirty. I wash them, and a half hour later, it almost feels like there's a film on them, and I have to wash them again. Almost ocd-ish. So 6 weeks in.... Anyone have any advise on how much longer I should give this topamax before I give up on it & try something else? My doc said it should have worked by now if it was gonna - but I have read on here, that it sometimes can take months...? I just don't know if I can take these side effects, AND the headaches for much longer without going NUTS! {grin}
Any advise?

Meprozine worked for my abscessed tooth! I was in severe pain to the point of crawling the walls... I could not tell you which tooth was even hurting on Fri. when I went to the dentist. She had to numb my mouth to give me even a minutes relief. My cheek swelled the size of a baseball! Today it's the size of a plum.... I think I'll make it through this ordeal now, but without this medication I certainly would not have made it.

My son is almost 6 yrs old. He has been taking Singular for approx 3 years, in addition to Claritin and Nasonex. This is all for his allergy to mold. His doctor started him on these meds after a 6 month episode with sinus infections leading to asthma-like symptoms. We have not noticed anything unusual about his behavior until approx 3 months ago. He started waking up every night (2-3 hours after going to bed) with bad dreams. At first he would not fully awaken and fall back asleep immediately. After a month or so of this happening most nights, he had two nights in a row where he woke up screaming and was inconsolable for about 30 minutes. We initially thought it was night terrors, but he was not scared or fearful, he was just upset/angry. He would hit the bed repeatedly and yell. He didn't know what he was upset about but would talk about how he thought we hated him, he was dumb, etc. After about 30 min he would 'snap out of it' and return to his normal self and go back to sleep easily.
At first we thought these were night terror brought on by a recent fever, but he had another episode last night. He has also been falling apart at the littlest things and getting quite violent (for a 6 yr old). He was sent to his room yesterday evening because he was complaining about the dinner his mom made (lots of complaining these days..). He had a total melt down an started throwing things and hitting the door so hard he put a hole in it.
Some of this behavior I would chalk up to normal kid stuff, new baby brother, etc. But I am suspicious about the negative thoughts, bad dreams, and instant melt downs... I stopped giving him Singular today and we will see what happens. God bless you all as we figure these things out...

I'm an 18 year old male and I've been taking Singulair for years; I don't even remember when I started taking it. I've had chronic sinusitis my whole life, and use a Singulair 10mg/ Allegra 180mg combo to control it. I never gave it a second thought. From my adolescent years on, I've been able to sleep (if undisturbed) for 15, 16+ hours a night, and have always felt like I was in a fog during everyday life. Getting out of bed has always been a terrible problem for me.

Throughout high school, I became progressively more depressed and apathetic toward school work, to the point where I dropped a number of classes my junior year. Got put on Prozac for a while, it helped a great deal with the depression, and seemed to give me enough energy to get through the week. I discontinued it after a year or so, everything was going okay (aside from mood swings and tiredness- explained away as symptoms of my age/hormones/going to bed too late), and then I went to college.

I had a mild depression that I think most people get upon leaving home for the first time, but the real problem was anxiety; I had a number of anxiety attacks, and decided to transfer to a school closer to home. I started Celexa and therapy- the celexa seems to take the edge off, but I fear its making me even more tired than before.

I've just heard about the whole Singulair controversy, and I am not taking it from here on out. I really hope that this whole ordeal was brought on primarily by the Singulair. After a month or two, I'll repost to report whether the symptoms went away.

I have been on lisinopril for two years, in that time I became unable to do anything. I would eat, but it would not give me energy, so I would eat more. I gained over 100 lbs from this. Nothing tasted, for all I knew I could of been eating rubber. My head hurt in one spot on my head. I could not remember anything, even how to cook anything, I have cooked all my life. If you can not taste then it is hard to cook. I was told in Aug of last year that I was hypothyroid. Come to find out the body can not make your thyroid work well while taking Lisinopril. I thought good they found out what was wrong with me. . I had the stomach problems they started in the night, I felt like if I went to the bathroom that I was going to die. For a full year I delt with my stomach hurting, before I got really sick. I was so depressed, really depressed. I was taking Norvasc which was doing good for my blood pressure. Before this started my doctor told me to try this wonder drug, it would make everything perfect, it was cheap and my insurance would cover it. It was the start of a two year ordeal that I hope is over. The wonder drug was Lisinopril, the death pill is what I call it. I was in the ER blood pressure 170/110 pulse 130. My day of grace came when I ran out of Lisinopril and started taking HCTZ, a water pill. My blood pressure is perfect, 123/75. I can taste, I can remember, I can clean my house, I can take care of my kids and I am looking forward to getting back to work. I hate that this drug stole two years from me and my kids. It seems like there should be a lawsuit somewhere to repay us for all our pain and suffering.

I was given 100 mg FENTANYL with Versed for anesthesia / colonoscopy. I am a very healthy 50 yr old female (non-smoker, non-drinker, etc...) with no difficulties or any complications from any (5) surgeries my entire life. Prior to surgery, I had a cold/flu and had been on a few antibiotics (Erythromycin), etc.... which I wrote on my pre-op and told the pre-op nurse. When I woke in recovery, I was too dizzy to lift my head and began vomiting. After the nurse gave me a phenergan shot to make me quit vomiting, I got the heck out of there. After more vomiting that night, I called the GI doctor on call for more presc. meds to make it stop. Regardless, the meds didn't help at all and I fainted. It was necessary for me to go to ER as I was getting worse. My status was urgent in the ER with an extremely low blood pressure (I have normal b/p), heart rate was very low, I was extremely dizzy and vomiting. This was like nothing I have ever experienced in my life. The next morning I was in somewhat decent enough shape to return home but it took me weeks to fully recover from that ordeal with periods of dizziness, nausea and vomiting. I consider this experience very unique for me. I've had surgeries since with no complications or aftermath but of course, the anesthesiologist told me that he would have never used FENTANYL (different doctor, different hospital). FENTANYL did nothing but make a very healthy person going through a routine procedure, extremely sick afterwards. All FENTANYL needs to be recalled.