Plague symptoms and conditions

Hi, I'm a 35 year old, who is now on day 4 without the Mirena. I woke up on Monday morning with what I believe to be the dreaded "Mirena rash". I called my OB immediately and requested it be removed, much to my dismay, he was very rude about my suggesting that I was having these problems because of a silly little IUD. I told him that a friend of mine had led me to this website and he basically told me not to believe everything I read, even after I explained to him that thousands of women, experiencing the same side effects, with only one common denominator could not be wrong. He sarcastically said that he hoped removing my "little" Mirena would solve all of the worlds problems.

So, in response to my complaint about this rash, he prescribed me Hydroxyzine which is an antihistamine. I take it religiously 4x a day. Mind you this was Monday, yesterday I ended up in the ER because I just couldn't stand the itch, and it was spreading. They put me on Prednisone, and still no relief.

Does anyone have any ideas for me? This thing is like the plague. I work in a hospital and cannot go in looking the way I do with this rash all over my face and neck... If anyone has successfully treated this, please email me...******

Thank you ! F.

ok, so I am 28yrs old just had my second lap for endo and my doctor has recommended lupron, after reading this I am soooooooooo scared to even get near this med. Its like you either take this with the hope of saving fertility and no pain..or not and have endo ravage your body and you will live with unbearable pain!!! I have no idea what to do, my post-op surgery appt is this week, and i am so scared after reading this. Is there anyone that did not have weight gain, headaches etc...anyone that can testify that lupron actually worked for them? Cause right now its my health on the line, my ability to have children, my ability to have a normal life free of endo pain or these crazy, horrible side effects...please help me!!!

I met my fiance a little over two years ago. Initially our sex life was hot and heavy as is the case with most new relationships so we decided to look into some sort of birth control. Like most of you, I was attracted to the idea of not having to worry about taking a pill and the potential consequences of forgetting to take one. We started using the NuvaRing and I went from having an absolutely healthy and fulfilling sex life to now avoiding my fiance like the plague... The decreased libido side effect associated with using the NuvaRing is seriously life altering. It has been approximately 1 year now since I discontinued using it and I still have not regained my sex drive. Its definitely ruining my relationship and I don't see a wedding anywhere in the near future. I cannot urge enough women to avoid it at all costs... Find something else to use if you cherish your libido as much as I did. Best of luck ladies!

I was taking sulfamethoxazole for 9 days and woke up on the lasttay with whatr looked like the measels all over my entire body, it is now two days later and I am still covered in hives and really itchy. I, too had a fever of 100.7 at the highest. It's terrible because I work with the public, and everyone I come across looks at me as though I have the plague. Well, I guess there have been more severe allergicreactions. I should count my blessings. It's also nice to know I'm not the only one. You never know when a health professional; is gonna slip up and misdiagnose you.

I've been on in a little over one day. The 6 day treatment. 5mg pills-6 the first, 5 the second, and so on and so forth. I have been SO HOT! I didn't sleep for very long, and woke up a couple times in the middle of night burning up. For me, the mental side effects have been HORRIBLE. I'm a 20 yr old fairly healthy female. 5'3'' 110 lbs. I have had unbelievable depression.... really really irritable and angry. I've just felt like hitting someone 24/7. I don't want to talk to anyone, I just want to sleep, I can barely keep my eyes open. I don't know how I'm going to take 5 more days of this. I also experienced the extra sensitivity to heat that others described. I read online that photo therapy... or sun exposure will help speed up healing and can be used alongside prednisone. I just really want this all to be over with. I look like I have the plague, and I feel worse than I look on the outside. Every little stress or worry just makes me want to end it, though I know that that isn't the answer. I'm a Christian, and I'm just going to pray about it. God will take care of me. I'm BURNING UP AS WE SPEAK! I've also been extra thirsty and my skin feels so dry!

I was in the health food store the other day, and the sales clerk started raving about this Iron Supplement she'd been taking for a while. She said that she never felt better and that she had a ton of energy. I purchased a bottle to see what all the "hype" was about. Unfortunately, ever since I took the recommended dosage yesterday, I have had excruciating abdominal pain, nausea and now I'm just waiting for the diarrhea to kick in. If anyone's in the market for some extra iron, I would avoid this brand like the plague. It's called Floradix Iron + Herbs, manufactured by Salus Haus, a company in Bruckmuhl, Germany. Just a heads up for everybody...

First, I don't really like taking BCPs and have avoided them like the plague in the past. After giving birth to my first child this past December I had some complications. My doctor tried to fix the complication with BCPs, not Yasmin, and apparently they worked. I was recently prescribed Yasmin by my doctor as I am SO not ready to get pregnant again. I only took the pills for 5 days and then stopped, at my husband's request, and for my personal quality of life. I am not sure if the pills are the cause of my symptoms or not as I was only on them for 5 days but here they are. I woke up every morning with a headache, a nagging headache that did not go away. I had terrible nausea and hot flashes. The worst thing happened on the 5th day. I was shopping with my mother at a store that I have frequented when I had a terrible reaction. I had vision problems and felt as if I was going to faint. I have never had this feeling in the past when visiting this store, it was a sensitivity to the lighting, I think?

I quit taking the pills 5 days ago. Yesterday I started my second period for the month which may be my own fault for stopping so abruptly. At least I hope that is the cause and it isn't something more serious.

AVOID YASMIN LIKE THE PLAGUE! I never have got on with contraceptive pills, but this pill is absolutely the worst of all types I've tried. I specifically told my doctor that responded badly to hormones in BC pills such as weight gain and tender and enlarged breasts - well, two days after starting Yasmin, I started to get shooting pains in the sides of my breast and I grew at least a full cup size. I was miserable, having to wear sports bras and unable to move in any way without feeling discomfort.

The discomfort was not only in my breast, I also started to get extremely moody and a bit depressed. My best friend and husband and I were on a weekend seminar and the two of them called me 'punchy' all weekend. This occurred for about two weeks, succinctely during the two months, I was on Yasmin.

Other side-effects were: heavy periods, spotting, weight gain, dizziness and I swear, I could have slept my life away on this pill. I was always feeling tired and like I needed more rest.

I'm now trying Loestrin 20 now - hoping that will be ok for me.

After by-pass heart surgery in 2002, my cardilogist put me on 40mg of zocor.
I was in good health with no physical limitations. I had no heart damage. The restriction of heart arteries were found due to my stress test that was performed each year as a part of my annual Physical. After surgery I was on zocor for three years, during that time I experienced a little tiredness, little weakness, a little muscle aches. some tingling in my right arm and shoulder. I went to my heart doctor Jan. 2006 and he changed me to vytorin (10mg zetia and 40mg zocor). about 6 months all of the about symptoms got worse.
By Jan. 2007, my muscles became so stiff, I could not walk, had balance problems, severe muscle aches and cramps, numbness and tingling in both arms and hands, also stifness and pain in my hands, stiffness and pain in both feet, stifness and pain in my back and weird nerve sensations over my entire body. During Jan. and Feb 2007, I was seen by my family doctor, a neurologist, and a muscle doctor. Thanks to the internet, I found info on zocor and zetia, which is the drug vytorin. Warnings described the same symptoms I am experiencing. I stopped vytorin, I am not taking any statins drugs now. My doctor order a blood test to check for muscle damage, It indicated severe damage, a Creatine level of 770. This level should not be over 200. After being off the drugs for 30 days the creatine level dropped to 645. My condition has improved by 25%. I am walking a little better, but I still having muscle problems, there is improvement. I think there will be a very long recovery. There seems to be some evidence that these Statins affect people of age much more than the young. I am 70 years old. PLEASE PEOPLE, IF YOU ARE TAKING STATINS DRUGS, STOPPED NOW! SLOVE YOUR CHOLESTROL PROBLEMS BY OTHER MEANS. Since I stopped my cholestrol has gone from 157 to 280, but I am not going back taking these drugs. I am trying the natural way now. I have read post after post on many web-sites of people with the same symptoms that were using these drugs. The drug companies and the FDA are responsible for the the degradation of people's health taking these statin drugs.

in regards to quest 02222,,, i too suffr from teh effects of this drug have been off since Jan-07 nad have bee taking some
different supplements to rid my self of this plague and the effects are slowly goign away but my question is do you ever eat anything else?it seems like what you are taking would be a all day task,and no offense but do yousell country life products???? rod..

I was given the 500mg, 10 day prescription as well. I was also given Amoxicyllan, an albuterol, and Hypotuss (syrup) for my return home from a Spontanious Pneumothorax( collapsed lung). I am on my 4th day now, and have immediately discontinued. Last Night I began to sweat relentlessly, heat went crazy, my muscules completely tighten ed and severe mental physco-dileria. I woke up this morning before reading the endless amount of consistent reports about this poison and took another one. Earlier today I called my fiancee home because I was feeling extremely suicidal, and the aches began to plague my lungs, which is really confusing seems Im recovering from a chest tube and have and Upper resp. Infection. I have taken Amoxill for years and never felt a single discomfort. I know without dispute that the levaquin is doing this to us. I absolutey fear long-term effects and hope the best for everyone dealing with this each and everyday. NEVER EAT THIS PILL!!!!NEVER

I have administered Ambien to patients during hospital stays and I have seen more than approximately 90% of instances where very undesirable and dangerous side effects occured. In my patients the usual pattern is complete amnesia once the med has taken effect or after a short course of 1 or 2 hours of "drop dead" sleep. People experience complete disconnection with their immediate reality they have no idea what is going on usually becoming argumentative and at the least very suspicious of what is going on. Disoriented to place, time, situation. Become angry, often uncooperative and occasionally violent. Always with paranoid ideations and dellusions of persecution. Many times these drug induced symptoms take up to 6 hours to abate and then a persistent mild paranoia may plague the person for hours after.

Dear Friends:

I have been off and on prednisone for thirty years. I am a chronic asthmatic, and things flare up easily. This past six months have been difficult, as my symptoms have exacerbated about every month.

Prednisone has taken its toll. My weight has been a problem even though I am careful what I eat. My muscle mass seems to have decreased, and I find that I do not have the strength I used to have. I am 67 years of age and otherwise in good health. I do have peripheral neuropathy in both feet and legs, and polycythemia vera. The Polycythemia is been under control for 7 months, with no phlebotomies required.

The worst side-effect of all is on my libido. I have always been sexually active, but the prednisone has made me dysfunctional. When I ask my doctor(s), the inevitible reply is, "Well, as we age, things are never what they used to be." They avoid the subject like the plague.

I need some information. Is it the prednisone which has caused erectile dysfunction and loss of libido? If so, what can be done about it?

Dave

I was given two days worth of Levaquin, as well as a precription for another seven days, for recurring acute sinusitis. I took one tablet, and within two hours was having cold clammy sweating spells, a headache on one side, and was unable to sleep. The next morning, I had aches and pains all over. Called the doctor and got a different prescription, but the aches and pains continued for two more days.

I later realized that the samples that the doctor gave me had no drug information included, but upon looking at Ortho-McNeil's website, they have no information about the types of side effects I was experiencing.

I have told everyone I know to avoid this drug like the plague. I know it works for some people - but my three-day experience with it was more than I could handle.

Took 28 days of levaquin in summer 2001. Had all the side effects imaginable. Tingling/numbness, tinnitus, vision problems, cold hands and feet, metallic taste, hair loss, sun sensitivity, muscle twitching, and horrible full body pain in tendons, muscles and joints. Two years later, I have seen some recovery--especially the nervous system problems. However, the muscular skeletal problems continue to plague me. They are getting better, but it is VERY SLOW progress. Stay away from this drug, and if you have any type of reaction, please file a report directly with the FDA and the drug company.