Adverse effects symptoms and conditions

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 ave a friend who has just had a bad case of the flu which has turned into pneumonia. her doctor out her on levaquin! i almost had a heart attack, called her and begged her to stop it. i sent her a bunch of info about it. why not put her on augment, something with less chance of adverse effects.
now i find she had a stroke over the weekend and is in the hospital! has anyone heard of anything like this on levaquin?

I am a few days away from my 19th birthday and i've been taking Yasmin since the age of 11. I was diagnosed with PCOS when i was 11 and Yasmin has been what's keeping my period regular and more or less pain free since then. In May of 2008 i was switched to the generic version of Yasmin called, Ocella and started to notice more and more symptoms and side effects. My stomach pain in the mornings grew greater by the day and when i was on my sugar pill i would gain an unbearable migraine. Thinking it was just part of being a woman i ignored it and went about my life. It wasn't until December of 2008 while out with a group of friends i came into some serious stomach pain. thinking it was just a typical stomach ache that i normally got i ignored it. when i came to be about 4 am and the pain hadn't stopped i started to worry. first thing in the morning i went to the doctor who referred me to get an ultrasound. The ultrasound showed that i had gall stones and that i should have my gall bladder removed before more complications were to occur. Being a college student only a week away from returning to my second semester i opted to wait until spring break to have the surgery. During the 3 month wait i experience extreme diarrhea whenever something was put in my mouth, extreme stomach pain, heartburn, nausea, headaches, sore muscles, the list goes on and on i felt like i had been hit by a truck every day and i still had to go to class. in March of 2009 i had my gall bladder removed thinking that the symptoms would finally stop i returned to school only to find that nothing got better. It's been 7 months since my gall bladder has been removed and i'm still having the same symptoms as before and now i've added depression, stress, lack of energy and interest and many other things to the list. I'm still taking Ocella because i've never been advised otherwise but the symptoms are taking over my life. I am a sophomore majoring in electrical engineering at college and it's just become harder and harder to focus on my work or to enjoy the aspects of college that i should be with the frequent trips to the bathroom or having to opt out of a fun activity because of stomach pain. I was wondering if anyone can help me, maybe point me in a direction where i can get better and get back to enjoying what a 19 should be. Thanks.

I am a generally active and fairly healthy 77 yr old who had been taking 10 mg of Lipitor for over 12 years with no obvious adverse effects. Recently I started having pain in my right leg, severe enough to wake me at night. This was followed by a significant weakness in both legs, and for a while, accompanied by a lightheartedness. The doctor had me take a series of lumbar and leg x-rays which didn't show much of significance. He wrote a prescription for physical therapy, which I did not follow.
I did internet research on my own which made me aware that Lipitor could be the cause, in spite of the fact that I had tolerating the drug for so many years. I told the Doctor of my suspicions and we agree to stop the Lipitor for at least 6 weeks to see. A few days later, all my symptoms were gone. So be cautious, adverse effects from Lipitor can occur anytime.

I have been taking Lipitor for about 6 years suddenly developed a rash on my shoulders and chest. My doctor diagnosed SCABIES!!so I treated myself for that then the rash progressed so I had a biopsy done and after 3 months of agony my slin specialist had taken me off Lipitor as theh test showed a reaction to a drug. I am still itchy prickly and burning on arms legs and hands and cannot tolerate cortisone cream so am on tablets for a week..can anyone relate to this condition? My scalp is also very dry and scaly.

Sorry to keeping annoying y'all with more posts from me, but I have another question. I noticed that my symptoms were worse with Yasmin's generic, Othello, than they were with Yasmin. I am not knowledgeable about generic drugs vs. brand-name drugs, but I wonder if there is something different about Othello that my body doesn't agree with. Just a thought... Any comments???? :)

Hello everyone,
Can I ask if anyone with type 1 diabetes has had any adverse effects wtih the Mirena in regards to blood sugar/ insulin?
Have just had one inserted a week ago and it is still painful and from reading these posts it is worrying that this pain won't go away.. but am wondering about the effect it has on me as a diabetic - doctors say next to no effect as it is a LOCAL hormone and so not circulating... but from these posts listing nausea, depression and weight gain, these are all side effects of hormones circulating the body.... Any one have any answers in regards to this?
Thanks

The Health & disability commissioner in NZ has received my complaint of criminal negligence re my former doctor. They have now asked my former doctor for a please explain his version of events. The police have written to me saying they are seeking medical advice re criminal/negligence/failing to carry out professional duties complaint. Whilst I agree with everyone's feelings on big pharma, it is my very firm opinion that the doctor is the "retailer" and it is the doctor's direct responsibility to us the customer/patient to monitor and inform us of all safety concerns. Big pharma in covering their butts have warned the doctors to warn the patients. Of the 8 doctors including an anesthetist I have spoken with socially and in consultation, not a single doctor could name any adverse effects with statins beyond mild muscle pain. Given the warnings from pharma on the labels that is wholly shameful & negligent. An effective way to help others avoid being maimed like us, is to fight back from the bottom. The FDA and CARM in NZ take no notice, litigation is expensive and drawn out so neither really helps future innocent victims. I encourage everyone where negligence is fairly on the table to take your complaints to your country's police and medical discipline bodies enough of these complaints will soon have the doctor's "reading & obeying instructions" which would go a long way to preventing more tragic victims.

I've had Mirena for almost a year and I'm wondering if there is anyone who's suffered adverse effects that didn't start until much later. I had the usual severe cramping and excessive bleeding for a few months after I got it, but my period has been pretty regular since then. I do have sharp stabbing pains (I'm guessing they're cramps) off and on. Very occasionally they are just terrible, but normally it's just like a quick shock every now and then. I can tell that there are extra hormones being put into my body because I have experienced all the stereotypical period side-effects (moodiness, cramping, cravings) much more than I ever did before I got Mirena. About two months ago I was sure I was pregnant - I had all the symptoms - but three pregnancy tests all came out negative. I'm not experiencing anything bad enough to get it out. So far it has actually been great. I feel terrible for everyone suffering all these severe side-effects. I guess I'm just wondering if these symptoms show up sooner or if they can start a year or more after Mirena has been in. Please let me know if there's anything I should be watching for. Thanks.

As i read some of the news reports on the new FDA comments,i see we are referred to as a handful of reports,the very words handful conjure up a picture of 10 not the thousands that there actually are.Also i noted missing from the news reports was ,that this drug is largely given to children,as young as 6 months,not for 10 days or 2 weeks but everyday,for as long as they need it.i know myself trying to convince my doctor,that my sons depression,insomnia and anxiety,came from this drug was impossible,so i fired him.I am wishing the best to everyone that has suffered,and ask all to please report your adverse effects to the FDA

I have been taking 40mg lipitor for over 9 years now.

I have had back issues since an injury to one disc (L4?), and had microdiscectomy in 2001? Took about two years to actually get close to normal.

The last few years, I have had multiple issues with shoulder pain, wrist pain, elbow pain, lower back pain, Upper rump muscle pain , and now both hips are killing me (the shoulder, upper rump muscles and hips are by far the worst). And I am now so weak in my lower back muscles, that it feels like I will (and do) pull out my back.

I have seen NO many doctors I can't even name them all. I have had operations, multiple injections (cortisone) taken pain meds, etc. Nothing has helped and in the last year and a half, I have gotten steadily worse. To the point where I can't really do much of any activity. Sleeping at night is painful. Can't lie on left shoulder, and can't lie on either hip for more than a few minutes. If I fall asleep on my side, the pain wakes me up. When I try to walk, 80% of the time, I end up with a pain in my upper right rump (sacroiliac area), that I MUST sit down to get the intense pain to go away, which it does. But comes right back when I walk again.

I have had x-rays, MRIs etc, and never reveals all that much. Disc issues, yes. NOt much else.

Recently, I have begun to get a nasty clicking (catching) on my left jaw (joint?). Not really painful, but something definitely wrong. My dentist sent me to his Chiro. I went and liked him right away. I had gone to another chiro for years and I believe in them. But this one is the best I have seen.

Anyway, one of the FIRST things he suggested, was that it was POSSIBLE that the Lipitor is causing all of my problems. Put me on COQ10, and doing multiple adjustments and treatments. I will be seeing my regular doctor 5/26, and my chiro wants me to see if he will take me off lipitor and put me on Niaspan instead.

I guess my question is: Can Lipitor be fine with me for so long, and then in such a short period of time, turn me into a compete wreck from the pain and wasting away of my body/muscles? I've told doctors for over a year now that there is SOME connection as to all these issues and pain. One Doctor, of course, gave me the "you are getting old" bull. Yes, I am 56 yrs old. But I understand the process of getting old, vs the complete failing of ones body.

Also, IF it is the Lipitor, can it possible all go away? Or should I expect some damage forever?

One more thing, the last ortho I went to the other day for a second opinion, wants me to do a EMG, to see if there is muscle damage. I was not planning on doing it, but wonder now, should I? He was not doing it because of lipitor, as he never even talked about that to me. I had shoulder operation and have not had the results I feel I should have had.

Can anyone tell me if you can just stop Lipitor cold turkey or do you have to stop it slowly? I have been taking Lipitor for 5 years now and I have been trying to find out what is causing my leg weakness. I mentioned it to my doctor who said it si just a fact of getting older. The problem is getting worse and I noticed it started about 3 months after taking the Lipitor and has steadily gotten worse. I am 49 years old a little over weight {which I am working on}. I also noticed my asthma which I haven't delt with since a small child has come back. This may or may not have to do with the Lipitor but the pain in my knees and legs I believe do. It really hurts in the joints of my legs and sometimes in my shoulder area.

I never really paid much attention to side effects on pills because I have never experienced any adverse effects, until loestrin 24 fe that is! I couldn't believe how terrible I felt after only taking this for one week. I was tired to the point of not wanting to get off the couch. I felt so sick to my stomach that I couldn't eat more than a few bites of food at a meal. I cried at the drop of a hat and I felt so anxious I couldn't believe it. I decided to stop taking the pills even if it meant some horrible period for a month. I didn't care! The next morning I already felt ten time better. I can't wait to see how I feel tomorrow! I will never take this medicine again. And maybe now I will listen a little closer to possible side effects!

I get these painful cramps in both legs the back of my legs above my
calf muscles. They always come after midnight when I am asleep. i
get up and I have to walk 30 minutes or more until they stop,and for
two days my legs are sore.

I'm on Lisinopril-HCTZ and have been for not even a month and I'm having those coughing spells so desperately, that I almost pass out. I can't stop coughing all day and night, now another doctor says I have asthma, but I don't think I do. I think its the adverse effects of this medication. I can't eat because it feels as though my esophagus is closing up all the time, I've been living on soup mostly since I started these meds, otherwise I can't swallow. I have to get off this medication because its causing decreased lung capacity already and I've only been on it two weeks!

I am 59 and switched to Simvastatin from Lipitor. Much lower in price. My cholesterol is 200 and the doctor was very pleased with the number. So far no side effects but it has been only 5 days. The dose is 20mgs. Now after reading all the BAD side effects I am very scared!
Is there any positive statements about Simvastatin?
S.

My doctor had me on a 10-day course of amoxicillin for a sinus infection. By the last day, I had contracted pneumonia and the sinus infection had rebounded until it was worse than ever. So, like many others who have posted here, my doctor prescribed Avelox. Fortunately I read the entire printout from the pharmacy, including all warnings of potential side-effects, both minor and serious. I grew concerned on day three when I had numbness and tingling all down my right arm, and following the warnings, called my doctor. Fortunately, my doc is a smart guy: he told me to stop the course of Avelox immediately, and if the nerve symptoms returned, I should go to the ER.

Some of the symptoms others here have mentioned -- many far, far more serious than mine -- seem neurological, as if the drug is also messing with brain function rather than just causing an allergic reaction (especially the seriously altered mental states).

A symptom that has occurred occasionally during the past weeks since I stopped the Avelox is an odd tremor in my eyes when I'm tired. My eyeballs shake quickly and sharply from side to side for about 10 seconds at a time. I had a similar reaction many years ago, when my doctor at the time prescribed a high dose of Paxil (anti-anxiety). The difference was that then the eye tremors stopped two days after I stopped the drug; the symptoms now started long after the Avelox was out of my system.

I linked to this webpage specifically because I was wondering how common adverse reactions to Avelox are. God knows we need some new antibiotics to fight the increasingly more resistant strains of bacteria. But if our bad experiences are as common as I fear, even though some people experience wonderful results, this is one drug that should be prescribed with extreme care. Not only that, but both the physician and the pharmacist should be especially diligent in explaining the more dangerous adverse effects so that patients (who don't always have a half hour to read through hundreds of single-spaced lines of instructions on drug sheets) are well-informed enough to participate in our own care. If that just means telling our doctors that the risks outweigh the benefits, please prescribe something else, so be it.

I URGE YOU TO PLEASE SUBMIT ANY ADVERSE EVENTS OF THIS TERRIBLE KENALOG DRUG TO THE FDA--JUST CLICK 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. Here's my case: I am also a victim of having the Kenalog injection administered over a year ago to alleviate poison ivy itching symptoms. Prior to having the injection, I was not informed of any side effects. Not only did the injection not alleviate the symptoms, but has resulted in a discolored and uncomfortable indentation in my left buttock area and psychological anguish because of disfigurement of my body. It is over a year later and the indent remains and continues to cause discomfort. The dermatologist who administered the injection stated that there was nothing I could do to reverse such effects. I reported my case to the FDA (Food and Drug Administration) Med Watch and strongly urge others to report their adverse event to the FDA (see link above).

I must admit I am very surprised by all of the side effects of Advair. I have been taking Advair 250 for years and have NEVER had any problems. I'm 28, healthy, thin, and happy. I exercise several times a week. ALL drugs have side effects. I don't think it's fair for anyone to say "don't take Advair, it's a horrible drug" because it works for some of us. I was taking Flovent before but it didn't work for me. I needed a rescue inhaler several times a week. Since I've been taking Advair I don't even fill my prescription for my rescue inhaler! All drugs have side effects, but they don't effect all people!

My 12 year old daughter completed the 3rd round of the Gardasil shot in late August of 2008. School started the next week. A couple of weeks later, she became ill and I rushed her several times to the doctor and to the emergency room only to have the doctor say she had a virus. After 2 weeks of horrible pain, nausea, and headaches, I took her to the emergency room at Wake Forest Baptist Medical Center. She was referred to a Gastroenterologist where she has been going ever since. The doctor has had her on pain medicine since December to help her cope. I analyzed all of her information and compared it to the 12,000 cases in the VAERS database and I am convinced that the shot made her sick. NO DOUBT! The database is located at http://www.medalerts.org/ and you can run the lot # of the dose given to you through the database to determine if their has been any adverse effects noted. The first dose that Lauren had was listed 78 times. Her second dose was listed 70 times. Her third dose was listed 74. I researched the ingredients contained in the shot and the one that I am concerned with is Aluminum. After researching the effects of aluminum poisoning, I believe that she has all of the signs. I begin treating my daughter at home with sublingual (dissolves under the tongue) Vitamin B12 and Vitamin C tablets available at the local drug store over the counter. My daughter has been sick for 7 months and has missed almost her entire Eighth Grade year. As you can see, since starting the vitamins, she has gone from being sick 97% to only being sick 28% of the time. This is a BIG improvement and this may help other young ladies who are affected. I don’t think it will help all, but as sick as these girls are, I don’t see how it could hurt. Her doctors at Wake Forest are aware of what I am doing and agree.

Month Sick Well
SEPT 93% 7%
OCT 97% 3%
NOV 83% 17%
DEC 87% 13%
JAN 71% 29%
FEB 43% 57%
MAR (WK 1-3) 28% 72%

My daughter has been referred to Duke Medical Center now and will go for her first appointment in about 1 month. The FDA and CDC need to pay attention to what is going on and pull this drug off the market. If you have been affected, please ensure that you report your reaction to the VAERS Database. Your doctor is required to report adverse effects, so demand that they do so.

I hope this helps, and if anyone tries the vitamins and it does help or if you would just like to ask me some questions about my daughters experience, email me at ****** and let me know. I will update the doctors at Wake Forest and Duke. Hopefully, if we band together, we can get to the bottom of this and figure out what to do help these vaccine injured girls.

Hi . I am a 69yr old male. My doctor has recently increased my Lipitor from 20 to 40mg. My cholesterol reading was 3.6 which he considered to high after a quad bypass. I am suffering painful cramps down the front of both lower legs as well as cramps down the back of my lower right leg. I plan to revert to 20mg to see if the cramps stop. I am not sure if I should stop completely.

I posted a short one, would like to add to it. My daughter was taken by ambulance twice last week to the ER, after having violent seizure like episodes. On second visit, she had several while we were waiting to be seen. She spent 5 days in the hospital, having these episodes as few as 10, as many as 30. lasting any where from 4 minutes to 40. She screams out in pain. It's like her entire back, including arms, legs, hands, feet are having a severe muscle spasm at that same time. If you look up dystonia, the definition fits. Dr. said it was too severe for that diagnosis. They ran EEG, EKG, Cat Scan, MRI, X-ray, extensive blood and urine work, video for 24 hours, with EEG. Everything was normal. DR decided it was stress and anxiety. Released from hospital still having episodes. I called a dystonia specialist in Maryland, she asked if she had the GARDASIL shots. Said it sounded like a side effect she had heard of. Well, after reading all these blogs, youtube, I believe it's the GARDASIL causing her problems. I knew it wasn't stress & anxiety. We are currently detoxing with ionizing foot baths, gluten free diet and meds from Health food store, called HMD-Heavy Metal Detox. I feel we are moving in the right direction. My daughter is a cheerleader, dancer and honor student. She just wants her life back. It has been on hold for 2 weeks now. I consider her one of the lucky girls, after reading many blogs. God Bless each and everyone of you. Sign the petition to stop hurting our girls.

My mother, 70 years old, been on Coumadin for 3 years (doctor said best to take since she suspected heart palpitations). Mother developed gradual memory loss, over the 3 year period, we didn't think anything wrong!! just a part of aging process!! Then one night she fell on the floor, stroke, we took her to hospital - done MRI and CTscan - result: severe brain bleeding. From that time - 4 months ago - she is now diagnosed with Dementia. I cant even describe how I feel about god damn Coumadin. Wish they never given it to her in the first place.

UGGG!!!! You all have helped clear up my confusion. I had my mirena put in July 2008. I didn't seem to have any adverse effects...at least not anything big enough to question the mirena. I had acne and a little weight gain, and then my knees started hurting. Then over the last month I started getting this stomach!!! It's huge!! I look 6 months pregnant. I also noticed that I was getting a lot of headaches, and extreme mood swings. Then it got harder and harder for me to read the TV from the couch. I was wondering last night if I should go get my eyes checked. I also find myself wondering who has taken over my body. I get all angry and mean!! I can't believe the stuff that comes out of my mouth, and my husband is looking at me like I've lost my mind. I feel thirsty all the time, and I have dry skin and chapped lips a lot. I've also experienced constipation, chest pain, pain in my right breast, extreme abdominal pain, like when you ovulate. After I got it in I bled for a month straight and I haven't bled since...not one period. I thought it was a perk, but now I feel so strange. It's like an out of body experience. I also struggle to find energy for anything, I'm tired all the time. I feel like I'm falling apart. I had to pay for the mirena out of pocket because it was the beginning of the fiscal year for our insurance, and so I(because of the expense) decided I should leave it in. I appreciate your comments, no amount of money is worth what I'm experiencing!

Having breathing problems since taking yaz?-- I have been reading all the postings on ladies having breathing problems. It has been maybe 7 years ago now, but I feel a necessity to share my story. I had been on Yaz for 2 months. I became short of breath to the point I could not walk across the room without having to sit down. My primary dr did an EKG and immediately had me rushed to the ER for test. I was sent to different specialist and over $10K in test were done within a week. By this time I WAS ON OXYGEN! They ran blood work, test on my heart, lungs and checked my legs for blood clots. I ask my GYN if it could be the Yaz. (the only med I was taking) and he said no- never heard of such. I took it upon myself to stop taking it and guess what!---I immediately was better. I turned my oxygen tanks in, doctor's never diagnosed me and I never heard from them again. I am 34 and have always been healthy with the exception of this incident which praise God was resolved "in time".
However, I would like to share that I now have a Mirena. The first 5 years was great, I had it replaced in May 08 and I believe this second one is not agreeing with me. I bled for 5 months, have a very heavy feeling in the bottom on my stomach, lower back pain, & fatigue. My appt is Jan 29th to have it removed. ******