Aching muscles symptoms and conditions

i have been on the nuvaring for about five years, at the start before i put it in had sever acne and fluid retention, i started on the NR and i did get nausea and breast/nipple tenderness the week i put it in for about three months then i loved it, skin came good and the weight came off. in the last maybe year or two i have been had these problems, anxiety, heart palpitation, diarrhea like IBS symptoms with cramps and pelvic pain, bladder pain, stomach upsets, dizziness and yeast infections continuously, also the total loss of libido like im a dead fish!
i have since decided to go off it, im a week off it now and i have had spotting and some dark brown bleeding, bloated, aching muscles and pelvic area, nausea, and sleeplessness with a raised heart rate at rest. the main problem at the moment is the tiredness, i just cant do anything! im struggling to get out a bed and even when i do i feel lik im falling asleep and my body and limbs are lik rocks..
i hope this doesn't last long its taken over my life!

I am 19 years old and have never had a health problem in my life. Of course the occasional cold or flu, but nothing serious, until I received my first Gardasil vaccination in August 2008. I was an active girl, running 5 miles a day and in the best shape of my life when I started getting dizzy and light-headed while I was running. At first I didn't think anything of it, perhaps I just didn't eat well enough that day, until it started happening day after day. When I went to my doctor as told her about these symptoms and asked about the possibility of an allergic reaction to Gardasil, she said, "No, absolutely not." So I didn't think about it anymore, and received my second dose in November. The week after I received my 2nd shot, I felt sicker than I have ever felt in my life. Extreme nausea, headache, dizziness, aching muscles, diarrhea, almost anything you can think of, I had it. After being reassured by my doctor that my prior symptoms were not from Gardasil, I didn't connect this week of suffering with it either, until I found this website. Now I wake up every day wondering if I am going to be able to get through my classes. I don't even remember what it feels like to be healthy anymore. I was scheduled to receive my third vaccination this week, but there is no way I am going to risk it. I beg of anyone who is thinking about getting the vaccine, or having their daughter receive the vaccine, please get as much research on it as you can. Gardasil has changed my life, and not for the better.

I had Kenalog injections a few days ago for MyoFacial Pain Syndrome. They are used for Trigger Points in the body that cause severe muscle spasms.
I have experienced these spasms for about three years. The first three times I had the injections I had no side effects. But the relief from the pain only lasted about three weeks.
So the nurse practitioner upped the dosage the other day. Since that evening I have been suffering from chills, sweating, fatigue, lost appetite, anxiety, aching muscles, and insomnia. I wake in the night several times sweating.
The pain in my upper back has subsided now but am not sure it was worth it.
I called their office but have not heard back from them.
Am so tired from suffering already and I hope the side effects subside very soon!

I suffer from chronic fatigue syndrome and fibromyalgia. I have problems with painful joints and have fluid on my knees. I tried Aqua Ban to try to relieve the fluid on my knees. I started by taking 2 tablets x 2 times on the first day, I was fine. The next day I took same dosage. In the afternoon I started feeling unwell. I went to bed as I had terrible tummy pains, felt sick and went downhill quite quickly. The next day I felt worse and had cramping pains all day. I stayed in bed with a hot water bottle. I had no energy at all. This went on for 4 days and eventually I ended up with a pain in my pelvic region. I can only think that the Aqua Ban had such an affect because of the chronic fatigue/fibromyalgia? Has anyone else had an experience like this?

Since I haven't seen it documented, I thought I should not the constant popping of my ears. It's not unbearable, but I question whether the ongoing pressure is affecting my hearing. Also, perhaps related, I have begun to observe soreness in my right jaw. But I have not had any true inner ear problems, such as dizziness or nausea.

On another note, my short-term memory seems to be affected. I'd be very disturbed by this fact, except that I'm taking the Lamictal for bipolar disorder and the net effect is a higher level of functioning.

I'm happy overall, but it's only been two months. I'm concerned about more serious effects setting in later after reading this page. I should note, however, that certain side-effects have already come and gone, including the runny nose, aching muscles, and a brief scare of a serious rash.

One question: does Lamictal affect the immune system? I've taken two rounds of antibiotics now to beat a sinus infection and bronchitis, and I still have a cough....

Do not abuse them,they are very hard to come off of.I heard that it is just like oral heroin.I have a prescription and at first everything was good but then I started liking how good they made me feel and started taking more and more now I am having to recover and I wish that I would of never put that pill in my mouth.At first you are full of energy then after a long period of use your body becomes immune and it has a higher tolerance level so you find yourself taking more and more the the aching muscles begin,muscle that never ached before,you stay tired,ill and lose your sex drive.I really don't recommend them unless you are in severe pain!Trust me everything is good at first but that will in time come to an end and so will your liver.

Oh my god. I can't believe I have just stumbled upon all these women talking about the same problems. Feeling chronic fatigue, depression, listlessness, anxiety and insomnia, bloating and loss of a sex drive! (THATS birth control for ya! Ha!) I also experience aching muscles, headaches, and a brain fog that makes me feel like a fraction of my former self. All of these symptoms, among others, can describe Candida overgrowth.

I have had my Mirena for 2 1/2 years, and I never put together these symptoms and the IUD! Even though they started shortly after my insertion, I also had some serious life circumstances happen to me and assumed I felt crummy from that. Also, I loved not thinking about birth control and was convinced that the small progestin-only tips had to be the most gentle form of hormonal birth control out there. And no period! Sweet. I also worked in the field of sexual health and trusted my doctor completely. I recall in hindsight getting really sick right after it was inserted, and asking my doctor if I could be having bloating and intestinal problems from it, and she said it was unrelated.

I called to make an appointment to have the Mirena removed shortly before finding this site, because since I have discovered I have candida overgrowth, I have learned it can be onset by hormonal birth control. Candidiasis Albicons is the same yeast that causes yeast infections, and when the healthy flora of the digestive tract are compromised, it can spread out of control, becoming systematic. That's what happened to me. If this sounds all to familiar, please check it out and see if you have it too.

I am getting better already, after committing for the last two weeks to the candida diet, where my body is detoxifying and I am coming back to life. (Many western doctors know very little about this, so don't be surprised if they laugh you out of the room and prescribe prosac. Trust your gut, literally ;)

I don't believe the Mirena caused my candida overgrowth, only that its a factor in it, like taking antibiotics or heavy metal poisoning. I felt compelled to share my story, because I am starting to recover, and I can't tell you how good it feels to feel better after 2 1/2 foggy years. Don't give up on your health.

Also, I am writing because removing the IUD won't fix your problem completely, just like it didn't completely cause it, so if you have think you may have systemic candida, find out. You will need to continue treating it after you get the IUD removed, so you get the full recovery you deserve. Hoping for more healthy ladies!

I have had my mirena since April of 2006. For the first two years it was the most wonderful thing in the world ( no cramping, spotting or periods). But lately I have been feeling very horrible. I have no desire to do anything. I am very tired, moody, gained weight (just around stomach area), depressed, joint pain and sik to my stomach. After reading a lot of the posting on this website. I realized that a lot of the women feel just like me. Now I know that I am not crazy. I also scheduled to have mine's removed on August 1, 2008 (yay!!!).

Why do I think I landed here, I have been having very bad mood swings mostly relating to anger and dissatisfaction in everything and everybody. Put the mirena in April 2008, braved it out for 4 months with the
1. spotting and all the time kept thinking that my
2. fatigue and no interest in everything was due the stress of having 2 kids, work and the pregnancy weight that I have to shed.
3. I am hungry always (maybe since I am breast feeding the baby)
I had a copper IUD between my first and second son,
4. I don't remember how that was ( am I in a mental fog?). must have been better than this one. I never wanted anything hormonal. I don't want pills. Dont even know why I went with this then. I know the doctor convinced me saying it has very little hormonal effects

Yesterday, I just lost myself over a silly issue, now I feel I am going to lose my wonderful relationships with people. My 3 yr old asks me If I am not angry any more uh!!!. Why cant I call the doctor to get it removed when I doubt it could be the IUD.
5.I am lazy( another symptom).

Do I have to wait a little longer or take it out and maybe get my self back.?
(What a question to an obvious answer)
Confused!!! lazy!!

I'm 19 and i've had mine since 2006...i've had most of these side effects but i never thought it was my IUD!!! I've always had an anxiety/depression/insomnia problem but it has gotten WAY worse over the past 2 years...i just never put it together.And i have had TERRIBLE cramps for 3 weeks now and i can't take it anymore.I've tried 3 or 4 times to get it removed but my doctors kept talking me out of it and telling me everything was fine,but obviously it's not so i'm getting it removed for real tomorrow @ 12:45!!!!YAY!!!!!!

i want to start off with IM SOOOOO GLAD I FOUND THIS SITE!!!

i though.. well i wasn't actually sure what to think.. i got my mirena at the end of January 2008.. at first things were going good... yes my periods got longer.. 3 times longer then normal actually.. i wasn't too worried because the OB said that might happen at first. then slowly i started loosing my sex drive ( im only 25 that really shouldn't happen) started getting achy, especially in my joints, so i started drinking more water. then my clothes started getting tighter.. i cut out soda all together and started watching what i eat more closely..i have also had some pretty bad anexity attacks lately.. which i never had before i got this thing.. i dint know what to do i though i was going crazy.. i talked to my doctors and basically got nothing out of that.. im now in my 6th month of having mirena and i have gained almost 30 pounds!!!! yes i have been hungry all the time but i either restrain myself fream eating altogether or eat healthy snacks.. i exercise daily and still am unable to lose any weight.. the numbers on the scale just keep creeping up and up.. im am moody and easily worn out.. i have no energy at all.. which isnt good with a 3 year old that has more energy then the sun.. i had no idea that mirena could cause any of these symptoms.. but the more i have been reading about it and the more site like these i find, the more i realize that the most likely culprut of losing myself is mirena.. i have decided that on Monday im calling my OB and demanding she remove it!! i want my old self back again.. i wasn't perfect but at least ill be me.. thank you all for sharing your experiences, you made a world of difference!!!!

Last Christmas (07) I was diagnosed with pneumonia in the the right lung and x rays ordered. Xrays revealed an "unknown mass", or so they thought... they decided to redo - confirmed them and ordered CT scan... mass was gone, but there was PE in both lungs... so started the coumadin. I am type 2 diabetic as of Jan 07... have been managing my diabetes with healthy diet and regular exercise (A1C 7.4 to 5.4 in 9 months) ... no drugs... so the prospect of coumadin for life bothered me. However, my doctors all made a great case about how safe it is compared to other drugs... I lost 35 lbs in 07 after changing my lifestyle... and felt great. I am here today because I gained 20 lbs in 4 months of coumadin therapy (no change in how I was living), have aching muscles, chest pain and shortness of breath, and thinning hair.

After 2 days on the web I find only doctors and pharmacies say no side effects, but the hundreds of testimonials of actual coumadin guinee pigs like myself are finding a lot in common. For me, Im off it tonight.

age 72 had MI angioplasty and stent.On lipitor for 3years but recently noticed increase in muscle and joint pains and then lightheadedness and walking unsteady and tending to go slightly from side to side.Also a tendency to have nasal congestion.I am an MD and will stop the statin and assess the progress.

It saddens me to read all the horrible effects this drug has caused. My husband took Levaquin back in August 2007and after 2 days starting have aching muscles, joints, drenching night sweats, high fever, rash. He took this poison drug for days(for a swollen lymph node in groin) and the side effects would not go away. He too was a very healthy 43 year old who worked out 4-5 times a week and very physically fit. This went on for months. He was tested for TB, AIDS, Lyme disease, I think every infectious disease and lymphoma, all came back negative. In Oct. 2007 he was hospitalized for 6 days and we were told that he had a very rare disease called Still's Disease. (google it and read about it please) I with all my heart and soul feel that LEVAQUIN brought this disease on. There is very little known about Still's but it's scary to think that doctors are giving this poison to patients. My husband has been on daily injections of Kineret, Methotrexate and Predisone since October and thank God these meds have given him relief. PLEASE DO NOT TAKE LEVAQUIN and tell all you family, friends and co-workers about it!

I am 60years and a stroke survivor of ten years.
About 9 years ago started on Lipitor 20mg until about 18months ago prescribed 80mg.
Looking back I have symptoms for quite some time, and thought it must have been from tthe strokes.3 weeks ago had a CPK blood test showed my level was about 300 over recommended ratio. Have been nauseas, light headed as though I am going to fall (even when I turn my head in bed) bloated, very hungry, put on weight,stiffness, sore or aching muscles. Have been on Luvox for depression since the strokes chest pain, back pain, shoulder pain foggy vision again, aching under armpit and groin areas, irritable,and always seem tired and the list goes on, even my speech seems to be worse at times
Have had two weeks of Lipitor and started to feel better, but had to try them again for this week. See doctor Friday and I wish to say never again do I want to take another lipitor. I live in Australia and would like to find more info. Any advice would be appreciated.

Can Statins Cause Chronic Low-Grade Myopathy?
Statins (hydroxymethyl glutaryl coenzyme A reductase
inhibitors) are highly effective drugs for reducing serum
cholesterol and low-density lipoprotein cholesterol levels.
Clinical trials have shown that they also reduce risk for
coronary heart disease events, coronary procedures, and
stroke by about one third (1). Millions of people in the
United States and worldwide are being treated with statins.
In clinical trials and in clinical practice, statins have proved
to be remarkably safe.
The one notable side effect of statin therapy is myopathy.
A small fraction of patients who are treated with
statins will develop severe myopathy (2). In the worst cases,
severe myoglobinuria, acute renal failure, and even death
can occur. The incidence of severe myopathy is low, perhaps
1 in 1000 patients (2). Predisposing factors for severe
myopathy appear to include advanced age, relatively low
body weight, female sex, certain medications, use of multiple
medications, multisystem disease, and acute illnesses
or major surgery (3). If statins were avoided or used in low
doses in these circumstances, it is likely that the incidence
of severe myopathy could be greatly reduced.
Less severe forms of myopathy undoubtedly occur. In
some patients, fatigue and muscle pain and weakness develop
with moderately high serum creatine kinase levels
but not acute renal failure. In these cases, the myopathy
resolves when statin therapy is discontinued.
Still more patients report various muscle symptoms—
fatigue, pain, and muscle weakness—but have normal creatine
kinase levels. These symptoms probably are unrelated
to statin therapy in many patients. In middle-aged and
older people, muscle, joint, and tendon symptoms are very
common. Naturally, if a patient takes a medication that is
believed to produce muscle problems, symptoms are often
attributed to the medication. On the other hand, the major
controlled clinical trials have not detected a higher prevalence
of muscle symptoms during statin therapy versus placebo
(1). This failure of detection has generally led clinical
trialists to conclude that statin-associated myopathy with
normal creatine kinase levels essentially does not exist or
that, if it does exist, it cannot be detected above the “background
noise” of muscle symptoms in the general clinicaltrial
population.
Many physicians in clinical practice nonetheless believe
that they can identify a subset of statin-treated patients
who have a unique set of statin-related muscle symptoms.
Some patients clearly relate the onset of muscle
symptoms to initiation of statin therapy. These symptoms
may abate after discontinuation of therapy, only to reappear
when statin therapy is restarted. The number of such
patients is not large, and thus it may have been impossible
to identify them in large clinical trials.
In this issue, Phillips and colleagues (4) report on a set
of studies in four patients who had muscle symptoms during
statin therapy that resolved during placebo use. Quantitatively
measured muscle weakness also resolved during
placebo use. Muscle biopsies were performed in three patients
during statin therapy and then during placebo use.
Several pathologic changes were seen on biopsy specimens
obtained during statin therapy: increased lipid content of
mitochondria, fibers that did not stain for cytochrome oxidase
activity, and ragged red fibers. The authors suggest
that these patients had statin-associated myopathy with
normal serum creatine kinase levels.
Despite the study’s small size, we cannot dismiss these
observations as random variation in muscle structure.
However, these highly suggestive results are clearly preliminary.
The number of patients was small, and all appropriate
controls were not used. Nonetheless, this study is novel
because it used quantitative measures of muscle strength
and muscle biopsy to address the question of myopathy
with normal creatine kinase levels during statin therapy.
To be confirmed, the current data would have to be
extended to many more patients in whom muscle symptoms
are closely correlated with statin use. Reproducibility
of symptoms during therapy and symptom resolution after
discontinuation of statin therapy would be necessary. A
definitive study would have to be carefully designed and
executed. It would need to be double-blinded and placebocontrolled
and include sufficient numbers of patients to
provide a valid statistical comparison. In addition, investigators
would have to carefully consider the appropriate
selection of patients. The development of a registry of candidate
patients at multiple sites could facilitate a multicenter
study.
Is a carefully controlled, sizable study of this type
worth the investment of time and effort? To date, no evidence
indicates that prolonged statin therapy leads to permanent
muscle damage or progressive myopathy in patients
with normal creatine kinase levels. Controlled
clinical trials attest to the general safety of statins, and
symptomatic side effects appear to be limited to a relatively
small proportion of treated patients. In addition, no therapy
prevents or treats statin-induced myopathy, short of
withholding the drug. On the other hand, statins are being
prescribed to millions of people, and are usually continued
throughout the patient’s lifetime. It is certain that statins
cause myopathy in some patients. For these reasons, a valid
argument can be made for a more extensive study of lowgrade
myopathy in patients treated with statins.
In the meantime, physicians should recognize the great
benefit of statin therapy in high-risk patients and their
documented safety for most patients. For high-risk persons,
the proven efficacy for preventing cardiovascular disease
outweighs the unlikely possibility of permanent muscle
damage. Phillips and colleagues’ preliminary results
certainly do not provide adequate information on the spec-
Editorial
www.annals.org 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 617
trum, scope, or prognosis of myopathy with normal creatine
kinase levels during statin therapy. For these reasons,
prescription of statins for eligible patients should continue
despite the current results. Moreover, before discontinuing
therapy, physicians should carefully evaluate any patient
receiving statins who reports muscle symptoms. In most
cases, the symptoms will be found not to be consistent
with chronic myopathy, and often they will not be related
temporally to statin treatment. High-risk patients in particular
should not be deprived of major cardiovascular risk
reduction just because they display symptoms not clearly
documented to be closely related to statin therapy.
Despite these comments, the actions of statin on muscle
metabolism and structure deserve further investigation
to clarify the confusing area of low-grade myopathy apparently
associated with statin use in a few patients.
Scott M. Grundy, MD, PhD
University of Texas Southwestern Medical Center at Dallas
Dallas, TX 75390-9052
Current Author Address: Scott M. Grundy, MD, PhD, Center for
Human Nutrition and the Departments of Clinical Nutrition and Internal
Medicine, University of Texas Southwestern Medical Center at Dallas,
5323 Harry Hines Boulevard, Y3.206, Dallas, TX 75390-9052.
Potential Financial Conflicts of Interest: Honoraria (from Merck &
Co.; Pfizer, Inc.; Bristol-Myers Squibb; and Bayer); Grants (from Merck
& Co. and Pfizer, Inc.)
Ann Intern Med. 2002;137:617-618.
References
1. Executive Summary of The Third Report of The National Cholesterol Education
Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment
of High Blood Cholesterol In Adults (Adult Treatment Panel III). JAMA. 2001;
285:2486-97.
2. Staffa JA, Chang J, Green L. Cerivastatin and reports of fatal rhabdomyolysis
. N Engl J Med. 2002;346:539-40.
3. Pasternak RC, Smith SC, Bairey-Merz CN, Grundy SM, Cleeman JI, Lenfant
C. ACC/AHA/NHLBI clinical advisory on the use and safety of statins (1)
(2). J Am Coll Cardiol. 2002;40:567-72.
4. Phillips PS, Haas RH, Bannykh S, Hathaway S, Gray NL, Kimura BJ, et al.
Statin-associated myopathy with normal creatine kinase levels. The Scripps Mercy
Clinical Research Center. Ann Intern Med. 2002;137:581-5.
© 2002 American College of Physicians–American Society of Internal
Medicine
Editorial Statins and Low-Grade Myopathy
618 1 October 2002 Annals of Internal Medicine Volume 137 • Number 7 www.annals.org

I have been taking Yasmin for 2 months and suffer the following symptoms for the last 7 weeks, lack of balance and co ordination, problems walking which consist of shaking wobbly legs its like they are made from jelly , shortness of breath, palpitations, panic attacks, clumsiness, stomach cramp, constipation, diarrhea, clots whilst not menstruating, headache, blurred vision, dizziness, seeing spots, light headed, aching muscles, fluid retention, swollen hands and feet, abdominal pain, lack of period, mood swings, nausea, lack of appetite, sore breasts, bloatedness, tiredness, insomnia, pais in my chest, has any one else got these symptoms?

My hubsand took levaquin for a swollen lymph node for 7 days 750 mg each day. After 2 days he started having drenching night sweats, fever, rash and aching muscles and joints. This started in August and he was hospitalized in October for 6 days. Dr.'s have diagnosed him with Still's Disease. He does have all the symptoms of Still's, but none of this started until he took Levaquin. He is now having to take 40 mg of predensoine once a day and is still having some bad days. This drug is dangerous!

I feel so blessed to have found this site tonight!!! I took Lisinopril for a year...June 05' to July 06'. I started experiencing allergic reactions....swollen lip, eye, hives (more like welts) all over. Did not connect to the lisinopril right away though I had just renewed my Rx and the pharmacy was using a different manufacturer for my medication. I then started experiencing indigestion and constipation (never ever had problems with)....actually had to go to the ER one night.....ended up calling 911 the following morning because I was going to pass out....woke up fine, after 10 minutes broke out in a sweat....my BP was apparently dropping....never passed out in my life, but knew it was coming so I opened the front door and called 911. The operator kept me on the phone talking while waiting for help....I started throwing up as they walked in the door, and felt immediately better. They had me sit, took my pressure....I was feeling much better.....I still didn't tie it to the Rx, but after several more allergic reactions and tired of taking Benadril, I asked to have my BP Rx changed. I continued to have allergic reaction on 4 different types of BP Rx over a 6 week period. I decided to stop taking all BP medication Sept.06'. Two weeks ago I decided to try the Lisinopril again as I have not been able to control my BP for the past year. I thought maybe I had experienced a food allergy last year....until I found your website tonight. What caused me to look for info tonight was a hot flash experience today....all day. I am 48 and Perimenopausal, but I have not experienced a hot flash as of yet....after reading all the blogs, I don't think I was experiencing a hot flash! I also have not been sleeping well the past two weeks....and I never have trouble sleeping. I also have been lacking energy and have had tingling in my hands and aching muscles....I'm not taking another pill!!! I'm going search for a natural remedy and start working out!
Kathy

I was initially prescribed 20 mg of Lipitor as my cholesterol was well over 300 (365). However, the same week I started the 20 mg, I was hit my a car as a pedestrian and had so many aches and pains from that, that I felt the 20 mg of Lipitor was aggravating my recovery from the car incident so requested of my Doctor to "start" at 10 mg instead. I am also "medication sensitive". I have only been on the med for 4 1/2 months and initially things were "OK"...I did notice some aching muscles and joints, but this actually seemed to subside. However, in the past 4-6 weeks, many symptoms seemed to get worse...I feared I had Lyme Disease again, but the symptoms felt "different" though similar...aching muscles and joints...especially both my hands and wrists, hips and knees, very bad headaches, constant nasal problems including horrendous post-nasal drip and "face pain" like sinusitus, a feeling like I was getting bronchitis all the time and needing to use my asthma inhaler, even though my asthma is very, very mild, and profound fatigue. I also noticed "some" mental confusion and forgetfulness. I decided to go off the medication just two days ago and already feel better. I plan to get my cholesterol checked within the next week, but doubt seriously that I will go back on this drug...UNLESS it would be something like 5 mg every other day. I also lost weight (on purpose), have tried to get more exercise, and eat better as part of the overall plan to better manage my cholesterol...so, unless this continued health plan does not keep my cholesterol down, I will not take more than that of this drug (5 mg QOD).

I was on Lisinopril for one month and it took 18 months for the side effects to go away. The cough, the inexplicable weight gain, the exhaustion, the bloated tummy, aching muscles and joints, swollen eyelids, etc. Luckily, my doctor did listen to me and got me off it as soon as I could get a call through to him instead of having his nurse block calls and tell me that I could take codeine laced cough syrup. I explained to her very carefully to look at my chart--I am allergic to codeine. My doctor switched me immediately to Cozaar when I was able to talk to him directly. The pharmacist looked at what I had been on and asked why I was being switched. When I explained, he said that the side effects were commonly known and really affected people.

The coughing inflamed my bronchial tubes to where they were going into spasms. I was on an asthma inhaler for a month to heal them. That wasn't pleasant, either, because I didn't tolerate it very well.

I am at the point now that whenever I am put on a new medication, I immediately search the internet for side effects. I don't want to go through 18 months of misery because I wasn't told or the insert wasn't clear about possible side effects.

During the first 4 days of Levoquin for treatment of pneumonia started feeling very tired with some aching muscles. It continued to worsen until it became severe pain in my joints (especially hips, knees, shoulders,elbows and hands). I became unable to rise from a sitting to standing position; someone had to lift me up, still with excruciating pain in knee joints. Also had nightmares and started talking in my sleep. Refused to take any more and MD ordered a Z-pack which I am just starting. What an awful drug Levoquin is!!!!!!!

hi everyone.
i too have some trouble during ovulation/mesnstruation with nervousness,shaking,fear etc. and my agoraphobia flares up. i have been taking the following for the last month and have felt sooom uch better. magnesium 400mg,calcium 800mg, vitamin b complex tablet and an additional dose of b6 of 50mg along with a multivitamin. apparently birth control pills can cause a depletion of the b6 vitamin which causes many of the symptoms experienced by some yasmin users like,anxiety,panic attacks,dizzyness,brain fog,muscle cramps,sickness,bowel problems etc. also magnesium and calcium become depleted,these minerals are essential for a healthy body and mind. b6 is directly involved in converting tryptophan into serotonin so it stands to reason that if you are deficient in this vitamin then you are going to experience problems both physically and mentally,it is worse around the time of ovulation/menstruation as the natural hormone shift can take up more of your b6 reserves. try improving your diet and taking supplements for a while and see if it helps,it won't hurt you to try. i totally sympathise with the hell that is caused by the panic attacks,anxiety,chest pains,aching muscles,headaches and all the other horrible side effects that a lot of use have suffered whilst on yasmin, but have faith that your body is an amazing thing,if you give it the tools it will heal itself,eat well,sleep well and take supplements for a while and i am sure that we will all be able to put this nightmare behind us and live the lives we want!

Hi Hill!!

Don't worry too much about that fact. There will be much more ups and downs until your hormones are completely back in balance again!! I've been off Yasmin for about 1 YEAR now and in my case (I had taken that poison for over 5 YEARS!!) I fear it will take even longer than 1 year to be completely healthy again... I didn't get my period since easter 2005, so my hormones are still totally out of whack.

And every few weeks all of a sudden I feel worse (joints are aching, muscles are aching, I feel nauseous and a little bit dizzy) and then better again. It feels as if my hormones are running like a rollercoaster at the moment!! But I definitely know, that when I'm feeling worse again, it's just the hormones and the withdrawal effects of Yasmin and that's how I pull my self forward, looking forward to better weeks that surely are ahead again!!

But believe me, after reading every little new post on this site every day during the last year I know, that 6 weeks without Yasmin is not really long!! Most of the women felt already better there but then went up the hill again and had bloating and anxiety and so on. There is definitely a connection between your cycle and the symptoms you have mentioned.

I think after watching all the posts here I can say, that those women, who finally got their normal periods every few weeks again, feel better earlier than those like me, who still have problems with that!!

Especially the bloating (my ring, that I've been wearing for about 5 years now doesn't come off my finger since about August 2005, only now I can move it a bit easier, so it seems the bloating finally goes back step by step) is definitely brought on by that hormone imbalance after Yasmin!!

So just try to be patient and wait and see. I promise: Better times are ahead and after every setback there will be less symptoms and every month you will feel a little bit more normal!! Don't worry, I know what I'm talking about!!

All the best to you and every lady out there still in Yasmin recovery!! God bless you!!

Silke

I've been on Lipitor for two weeks and have developed pain in my joints, aching muscles, barely able to walk from the pain in my feet and ankles. I have been awakened the last two nights with pain in my chest, pain in my left shoulder and aching in my left arm. These symptoms were not present prior to taking Lipitor. My fingers have begun to ache and I have developed swollen joints in my hands. Since I began taking Lipitor I have been chilled and feel very cold -- something highly unusual for me since I have always felt very warm, even in cold weather.

My husband recently began taking this drug after heart surgery and complains of severe pain in his legs. Initially, I thought these symptoms were due to surgery -- not so sure. Is there a proven effective alternative, that is safe?