All sorts symptoms and conditions

I was only on Yasmin for one month. After 2/3 weeks of being on it I started getting really bad migraines. I've had a severe migraine now ever since I got off of it. Does anyone know how long side effects last? Does anyone have this problem too?
I ended up in the hospital twice for the headaches. After the bloodwork, and CAT scan I was discharged, but to this day (I stopped taking the pills during the second week of October) I am still in constant pain. It feels like something is moving in my brain (as weird as that sounds). I am now debating to call a neurologist.
If anyone has any type of help or advise please help me!!

I have been on Prednisolone about 4 times in recent years. the highest dose was last year when i was on 80mg reducing weekly by 5mg. I have had most of the side affects you all talk about above. I have severe colitis so the side-effects of this drug are something i have to put up with. at the moment i have all the classic side-effects i usually get, rapid hunger, swelling to my face (moon face), neck has layer of fat, swollen back (buffalo hump), bruising easily, horrible taste in my mouth, swollen stomach. the one good side effect is it gives me lovely smooth skin lol. anyway the point of my post isn't to rip this drug appart as i have to say for me its a wonder drug and this time has prevented me from having my bowel removed! from personal experience once you finish the steroid treatment after a few weeks you'll notice the swelling go, my hunger usually fizzles out quite quickly (altho i have a large appetite in the first place!!) none of the side effects are permanent, so please all rest assured you will go back to normal just try not to put on too much weight while on the drug.

I was prescribed Lisinopril by my physician about six months ago. Everything was OK until about two weeks ago when I developed a HORRIBLE skin red, flaky, itching skin rash. This first appeared as heavy dandruff and was confined to my scalp, but letter moved to my neck, chest arms, back and legs. I am so grateful to have found this web site and I will discontinue this medication IMMEDIATELY!!! I will inform my doctor of these side effects and I will refuse to take this or any similar medication in the future. I have tried all sorts of shampoos, skin creams, cortisone ointments and such...it just keeps getting worse. I am hoping that getting off of this medication will improve things. Please let me know if you have had a similar experience with this medication.

By: T

My derm prescribed Doxycycline to me yesterday but after reading all the comments i am afraid to take it. I'm 23 years old and my acne is looking worse and worse as i get older and need to do something about it but do i put myself through this? Can anyone help me make up my mind?

Oh my goodness.....my daughter, age 17, had her first injection in June 2008, started losing her hair w/in a month. We thought it was form straightening, some high lightening etc. She had blood work done which showed she was anemic...strange, as 2yrs prior her blood work was stellar, and she had not changed her diet, or physical activity. She increased her iron and protein intake (along w/ supplements).....three months later, and after her second injection, iron was still anemic....worse actually, and her hair loss significant.I found this website last night....and I am floored......I called MERCK today and spoke to a representative wh o was not aware of the hair loss issue, but said that in their case studies, Autoimmune Hemolytic Anemia was a side effect.....which leads to hair loss itself.....so I am researching now what to do next.....anyone else have this issue??????

Thank goodness it is not all in my head. For the past year, I have been feeling as strange as the comments I have just read. Life is hard in the first place, but since having this IUD, life has been hard and very overwhelming. I have had constant mood swings, at least 3-4 days out of the week. Not only do I feel extremely nauseated 10 days before my period, even after it has come and gone, I feel nauseated again a week later. I had hoped that this new method of birth control would give me new freedom to have relations with my husband without being overly concerned about getting pregnant due to the less likelihood of the device failing. Boy was I wrong. I don't even think about sex. Nothing for the most part that he does turns me on. I can't even concentrate on feeling sexual when we are having sex. I just want to hit him or flip out on everyone. I feel a flush of anger go through my body that makes me think of very dangerous ideas, such as harming myself or others that are not really doing anything to deserve my anger. I have been very paranoid about everything and feel that I can not trust anyone, especially when I am telling them how I feel. I think that they just think that I am crazy. I have had extreme pain in my back near my spine, which I had thought before reading your comments was perhaps a side effect from the epidural I received during my child birth. I also have extreme pain in my sacral and hip areas that I never had before. My stomach is bloated with more stretch marks than I had when I was pregnant, my feet hurt. And I have an uncontrollable hunger at times. My short term memory is passe'. In fact, I took off my engagement and wedding rings in the house and can not for the life of me remember where I might have put my engagement ring. I am going to have this thing removed as soon as I get on my husband's insurance, before I go completely mad and hurt myself or my family. In closing, who cares if our doctor doesn't believe these things are not side effects. The truth is that God created all of us with common sense to know if something is blatantly wrong with us. We need to be wise and take care of our bodies and minds. This is something that God expects us to do. We have to live up to our obligations and commitments to our families like we promised we would when we got married.zfcII.

I had a sinus infection and my doctor handed me samples of Levaquin, 5 doses at 750mg each. I took it for the first 2 days, couldn't sleep, forgot to take it on the 3rd day because I finally was able to catch up on the sleep that I missed from the 1st and 2nd day. Took the third dose and noticed that my shoulder (left shoulder) was starting to hurt, I thought I had slept on it the wrong way, until I started looking at the side effects on the 4th day after I took my 4th dose. After I read the side effects I threw the 5th dose in the trash. I love my doctor and he has always helped by giving out samples, but what the samples don't tell you are the side effects. Needless to say I have been off of it for 2 days now. I am sleeping slightly better, but now have to adjust the way I sleep because I can't raise my arm any higher than level to my shoulder with out horrible pain. I am 28 and very active but now I fear that I may have to worry about rupturing my shoulder. I think I will head back to my doctor to see what I can do.

I am a 49 year old female I took Cymbalta for 3 days and on the 4th morning I woke up with severe blurred vision and roaring in my ears that was April 26,2008. My ears are still ringing. I clenched my teeth so hard in my sleep I traumatized one of my upper molars which resulted in a root canal and crown. I have been to a ENT to have my ears checked, he said I had minimal hearing loss and gave me lipo flavonoid to take for the ringing. I just went to a neurologist today who is requesting an MRI on my brain to rule out a tumor. I don't know if this is a coincidence or not ,I know the clenching caused the damage to my tooth. The neurologist said ringing in the ears is not a side effect of Cymbalta. My life has been a nightmare since I took it.

I went to my primary doctor last Wednesday. He gave me samples for a 5 day regime of Avelox to treat a head/chest cold. Well, the cold does seem a little better, but, I would have never traded that to the side effects I am experiencing now! I took my first daily dose of Avelox last Wednesday. On Friday I thought I had dry skin. By Sunday I was itching so bad that it was almost unbearable. My eyelids are itching, burning and swollen, my forehead looks sunburned from the itching and scratching, my chest, stomach, back and thighs feel tingly and are itching NONSTOP. I am taking an antihistamine, but it doesn't seem to be helping much. I hope this goes away. I cannot imagine what this drug does to people that have allergies and sensitivities to medications. I have never experienced an adverse reaction to medications before this. I would never recommend this drug to anyone.

Hi I am 35 and had the Mirena put in after I had my first baby and it was in for 1 year.....But I had the Mirena taken out about a month ago (there is no pain at all in taking it out)....within days my mood was better, I had numbness in hands and feet and that is almost completely gone....the pain in my side is gone....a month before I had it out I was told after my yearly I had Yeast Infection, Abnormal cells so I would need a biopsy and because of the pain in my side (and having the Mirena in a year) she did an ultrasound. I had a cyst....so I just went back for a recheck...cyst is gone, abnormal cells after biopsy are not abnormal....I did get another yeast infection (prior to Mirena I have never had a yeast infection) and I had 2 vaginal infections when it was in...and have one now....I will be honest it feels like I have toxins coming out of my system...I have had diarrhea once a day for a week and I start sweating even when sitting still...I do not regret for one second having it out....I already feel less bloated...also I had been going to the gym, eating well and gaining weight with the Mirena...I already feel like I have lost some....I will keep you posted....My friend had it in 4 years and she just had it out also....she had cysts, pain, bloating, weight gain, all the same symptoms.....the day before she had it out she was rushed to the ER for severe back and side pain and looking like she was 8 months pregnant....she has gone through all sorts of testing and everything came back normal....so I hate to say...but the Mirena may have a class action suit some day.....If it had worked it would have been great....but when something is too good to be true....there is probably a reason! Hope this helps you and I will post it out on the board for others!!!! Take Care Ladies! Michelle

A lot of people are complaining of the same symptoms, and saying they are going to get the Mirena out.....can more people update us with the results of having it removed? Did all the symptoms go away?
I've recently had a lot of the same symptoms (basically feeling pregnant--headaches, very tired, mild cramping, bloated, pants very tight around the waste, lower back aches, indigestion, and just a general yucky sick feeling like morning sickness--and wasting money on 2 pregnancy tests so far!), which seem now to have been PMS-related (PMS which lasted about 3 weeks before my period), though I've not had PMS like this since having the Mirena put in, and it's been over a year now. And my periods have been very irregular the whole time. I basically had spotting for about a year, then nothing for like 2 months, then this whole thing followed by a light period lasting 8 days.
I'm thinking about getting it removed, but would like to hear others' experiences with having it removed. Did these symptoms go away??

I am on my 3rd NuvaRing, and my last NuvaRing. This thing has cause me more pain and problems than anything I have ever used! The first time around the only problem I had was an increase in UTI's and extreme discomfort in my vagina and urethra, especially during and days after sex. I was told these side effects would go away within the next trial of the NuvaRing. Boy, were they wrong. After Taking out my second NuvaRing my period lasted from JULY 5TH to JULY 18TH! I also had to face the heaviest period of my life. I would go through a super plus absorbency tampon and panty liner in less than an hour. How embarrassing, inconvenient, and uncomfortable! I have had two ultrasounds, and 3 pelvic exams since starting the NuvaRing just 3 months ago. I have also had to face headaches, stomach pains, MOOD SWINGS, IRRITABILITY, and depression. This thing has put a damper on my sex drive and my relationship with everyone around me including my boyfriend of 3 1/2 years. I would not recommend the NuvaRing to anyone!!!!!!!!

I started using Fosamax two years ago and after approximately 18 months of use I noticed some distortion in my right clavicle (which I named my “barnacle) and pain in my upper shoulders and neck. At the time I attributed this to perhaps the heavy luggage I had been pulling around on a trip and that maybe I had strained something. I mentioned this to my doctor who ordered an x-ray which indicated an asymmetrical clavicle. She then ordered an MRI and the result was that perhaps I had a touch of arthritis. I asked her if perhaps this “barnacle” could be a result of the Fosamax I have been taking. She was very doubtful about that. I then googled Fosamax and started reading some of the side effects of this drug – NOT GOOD!! I did not see any mention in the comments by others who have been taking Fosamax about bone growth, but I did read about bone and joint and muscle pains. I had never had a problem and I am certain that the sudden pain in the shoulders and neck is a direct result of this toxic drug. I saw the doctor again and told her that I wanted to stop taking Fosamax and told her about the comments that I had been reading about and I claimed that this distortion in my clavicle and pain in the shoulders, etc. was the result of this drug. She then ordered a bone scan and additional x-rays which indicated again an “asymmetrical” clavicle and the suggestion was that I see an orthopedist. She mentioned that she had once had a patient who had a similar distortion of the clavicle and was sent for all sorts of tests, ending at the orthopedist who did a biopsy which turned out normal. I told her I was not interested in going to see one. I said I would stop taking Fosamax and see what would happen. She did order a blood and urine test checking for cancer, both of which turned our normal. I have not taken Fosamax since the end of June and already I have noticed a lessening of the pain in my shoulders and neck. Hopefully it will stop completely once this toxic drug is out of my system. I am an otherwise healthy 64 year old woman, I exercise, and eat a well balanced diet. I will take my chances with brittle bones, etc. and advise others who are taking this drug to get off it immediately.

Holy crikey. The docs put me on Advair Diskus for my shortness of breath , and although I've had minor anxiety my entire life, this sent it through the roof. When my girlfriend and I thought she might be pregnant, I flipped out and my mind raced for the week or so before we found out it was a false alarm. I've had that scare before, and wondered why I flipped out so much more this time around. Toward the beginning of April, I noticed my heart racing much more than ever, so I stopped taking it abruptly (nobody told me not to do that, and the doctors later on said it was fine to do so!). Later on that week, I had some trouble at work (big but not anything I haven't conquered before), and was in the doctor's office on the EKG because my heart rate was twice what it should've been! They put me on Xanax, which helped (but threw me up and down emotionally and physically), but for the past 4 months I've experienced all sorts of paranoia, psychoses, and phobia. Luckily it's almost gone, so for those of you experiencing it, don't worry, it gets better!

To a small population of people, this drug has an immediate detrimental effect to mood. In my case it caused a strong urge to commit suicide within 5 hours. The doctors all said it was impossible. I was inclined to believe them since these drugs are not meant to be effective for days after treatment initiation. However, my reaction cannot be ignored or dismissed.
The prescribing physician (Robert Moffat, MD in Longmont, Colorado) suggested I try it again because he was so certain it was my problem. I did try it again, and I had the same reaction. And so I filed a complaint against him.

Incidentally, I was not taking this medication for depression. It was for nocturnal panic attacks.

I am not saying people should not try it. I just suggest that FOR THE FIRST 24 HOURS WHEN YOU TAKE THIS MEDICATION YOU SHOULD NOT BE ALONE. It probably works great for some. Also see ******

After reading these posts, I am glad I didn't change my mind about having the MIUD removed. I have had all sorts of problems since that evil piece of plastic was inserted. I didn't think much of it at first and thought maybe I am just tired because I have my period and cramps alllllll the time. The relationship I was in was bad and thought maybe I was tired and moody because of that. After a couple of months - boyfriend free - things didn't change. I had horrible mood swings, my concentration was shot. My work ethic went down the toliet, I felt like a 10 year old kid with ADD. No energy, back hurt on a regular basis, carpal tunnel came back with a vengence and TMJ (I don't know if that's related but I've never had it before), acne, weight gain, no sex drive, and a constant itching around my neck. I am sure the NP was ready to try to talk me out of it and wait the full 6 months for "side effects" to go away. Well, the last 5 sucked, I really didn't want to deal with this crap any longer, besides with the price of gas, I can't afford the money for the regular buying of feminine products. I am only 6 hours free of this and I am already feeling a little better. I don't have that "pressure" you feel in your belly and a have bit more energy. I am so looking forward to the next few weeks when things start to get back to normal!!! If you have any doubts about this thing....get rid of it. Its really not that bad to get it out, 99 times less painful than getting it inserted!!!

I had my mirena fitted in 2000 when I was 40 years old. I have suffered with psoriasis since that time and only recently realized that maybe this could be linked to the hormone. I have spoken to my GP who insists that there could be no link and that it is purely co-incidental, however he can offer no other advise as to the cause of the psoriasis, so how does he know. I have tried all sorts of remedies to alleviate the psoriasis with no luck. I am now practically convinced that the mirena is the cause and am considering having it removed asap. I have also experienced palpitations for the last two years and have had all the tests and have been told I am fine. I also suffer from IBS. Has anyone else experienced similar?

How about MUSCLE SPASMS?? My mom has had right leg and arm muscle spasms for the past 3 weeks, but has been on warfarin since end of March.

I am a 42 male, I have always been healthy and felt healthy as long I can remember, I never went to the doctor. So this year, 3 months ago to be exact, I decided to do “the right thing”, start taking a physical at least once every years, who know something might be wrong with me and I don’t know it.

Anyway, after I took the physical and some blood tests, my doctors office calls me and they told me that the sugar was a little high (124) and that I am at risk for Diabetes, so they started me on a diabetes medication. Although my Cholesterol wasn’t high, they suggested starting Lipitor (20 ML) just in case because I am at risk and I don’t want to take chances.

A month into it, I started having some back pain, but never suspected medication. I was exercising at least 4 times a week, some cardio and free weights, so I thought, I might have made the wrong move while exercising or maybe sleeping without knowing it ( although I never recall such a thing). Usually it takes a few days for the pain to go away when I did the wrong move, but this pain wouldn’t go away. A month after that (last month), a sharp pain started on my right wrist (shooting pain), that goes up my right arm until my shoulder blade and upper right back. The pain was so sharp and wouldn’t let go, all day, all night and every minute in between. Also, I experienced some numbness on some of my right fingers (especially the thumb and index). I never suspected the medication. Of course the doctors wanted me to take all sorts of tests and MRIs etc..you name it. They also wanted me to go on pain pills (strong ones), I never did, and I used Advil instead, which did not help much. This pain ruined my two week vacations to France (I didn’t not want to forgo the airplane ticket and the hotel, they were already paid for).
I started “googling” the web for “sharp back pain”, just to get some clues, which led me to side effect sites, which led me to this site. I decided to stop all medications immediately 3 days ago, the pain went away, I still have s slight numbness on my thumb, although it is much better, I will keep you posted. Thanks to all the people who shared their story with us, I know that everyone of us could be a different case, what worked for me doesn’t necessarily work for someone else, I know that many here are frustrated about these side effects and whether they are permanent or not, I wish I have the answers. One thing is sure, Lipitor could be poison for some people, I felt going down fast for the last 3 months with no way to stop it, glad I found this site.

i started taking yaz a couple months ago and developed a blood clot in my lung, a pulmonary embolism. i was hospitalized for a week in may of this year. i have visited many websites to see if other women have developed blood clots due to yaz and i have found a startling number of women that have developed blood clots, and a couple girls who even lost their lives. the side effects of birth control are explained to us before we start taking them, and it is expected that some women will experience the side effects, and this is normal. however, when a disproportionately large number of women start having serious health problems due to yaz, then something is not wrong with us, something is wrong with yaz. i have seen many women express an interest in starting a class action lawsuit and i am trying to do so. i have worked in a personal injury law office for the past 2 years and know an excellent lawyer looking to take on a case of this nature and magnitude. if you or your loved one has developed a blood clot, lost their life, or have developed another serious health problem due to yaz than please email me at ****** with your name and an email address i can reach you at. A class action lawsuit requires a large number of plaintiffs. I have already gotten a few emails but need many more before we can make this happen. please email me... help me and yourself.

hi, im not sure what to do. my 3 1/2 year old daughter was today given the prescription for singulair. i voiced my concerns to the doctor after my friend telling me its no good due to the side effects.she said that there are risks and side effects with any drug you take but for some reason i don't feel right about this. don't doctors know better than this. anyway Would like to know if all the people who take singulair suffer some sort of side affects or is it minimal? or going by this side it looks like its probably best not to give it to her at all.

Perhaps you should read a little further on the Advair paperwork. I started having all sorts of problems while taking Advair for 4 months, first thing I told Drs. that I was taking Advair, all just ignored that and tried coming up with a reason for problems. I finally did my own research and if you look at the fine print at the end of Advair paperwork you will find your info about heart problems and withdrawal symptoms that you possibly be on another medication while withdrawing from Advair and the Symptoms of withdrawal.
It has been over a year now since I stopped taking Advair and am having lingering heart problems do to Advair, slowly getting over them, but went to the ER two weeks ago due to rapid and irregular heartbeat. Advair has thrown my electrical system out of whack, not to mention the mental stuff.
Ask a Heart Dr. about Advair, I had two pages of problems when I saw the Heart Dr., no surprise, he said all are related to Advair. There are a few of us that are sensitive to this drug and most doctors. have never seen these symptoms and think you are nuts. So be skeptical but don't dismiss these people. Oh by the way after doing a breathing test with the top guy at Pomona Valley Med Center, guess what, I don't have Asthma, so why did My Dr. put me on it in the first place without first getting tested? I am now so sensitive to anything with caffeine or other things that can increase your heart rate that any of them can trigger Palpitations and such. Yes it can help people, but it can also ruin a life, so beware. Oh, My breathing was great while i was on it, but not worth a heart attack or stroke
If I keep having problems I will soon be on Beta Blockers, so you take all the Advair you want, but you've been warned.

I am soooo glad I found this website!! Please read further!!!! I had a horrible experience on the NuvaRing. Can't even begging to explain, but I want to express my knowledge to anyone that is on this site. I think doctors should ask every patient that requests the NR if they have had or have symptoms or have been diagnosed with depression, or at that, any mental illness. With women most mood disorders are somewhat hormonally linked along with some kind of chemical imbalance. The ring has a very strong hormone in it that can cause all sorts of problems for women in this category. However, it is probably great for some people. I was only on it for 2.5 weeks and I was screaming at my fiance for no reason then I would lay in bed and just feel hopeless and cry for hours. I know I have suffered from depression for a great deal of my whole life, but I had it under control until I put that little devil inside my vagina. We, my finance and I, thought it would be great to not have to keep forgetting pills and having a pregnancy scare once a month. We didn't link the two together until I told my therapist that I started the ring and he told me to immediately take it out!!! He said DEPO and NuvaRing are a big "no-no" with mentally frustrated patients. So, to all you ladies out there, the ring is good if you have never been to a psychiatrist!!! If you are on any type of SSRI or Benzo's then you obviously have a mental thing going on....stay away from these type of BC's because they are just simply toooooo strong. I hope this helps doctors and patients.

I am very skeptical of all of the claims I have read here. I am no advocate of GSK or any other drug company for that matter, but I think people are getting carried away with attributing their symptoms to Advair. The known side-effects are readily available, anything else is purely based on assumption. I agree that Advair may in fact have many more possible adverse effects than they let the public know, but let us be careful about making ourselves little scientific researchers and concluding a causal relationship based upon a single case study (and an informal one at that). Talk to your doctor about trying something with less risk, such as Singulair, Azmacort, Intall, Fluticasone Propionate, etc. Please though, be careful not to be so quick to claim generalizable findings based on your specific case. I myself am going to work with my physician to attempt a gluten-free diet and a less invasive medication therapy. Advair is not habit-forming or addictive, so withdrawals are doubtful at best. Read up on the pharmacology of Advair (salmeterol in particular), and you can come to your own conclusions. Best wishes to all of you fellow asthmatics!

I was on Lamictal for 4 years and after the first year I suddenly started having all kinds of teeth and gum problems for no discernible reason. But since Lamictal has the possible side effect of "sores or blisters on the inside of the mouth" I wondered if it could be related.

I did a Google search and am coming up with no experts yet, but lots and lots of posts connecting anticonvulsant meds, particularly Lamictal, Topamax, Neurontin, and Depakote, with dental problems. Dilantin is well known for causing gum disease and breaking down tooth enamel, loosening of teeth, and even breaking down of jawbone tissue.

I don't think the experts have connected the dots yet, but is anyone else having this problem?