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Wow! I can't believe how many of us suffers from the pill from hell, Yasmin. I stopped taking it September 17 after 5 years and I'm worried as hell as to what's going to happen to my body now. But first things first. I seem to have gotten pretty much every side effect in the book.

About a month after starting it I got gastroparesis- paralyzed stomach- and I also became lactose-intolerant after 30 years of drinking a lot of milk. Go figure! I get a huge bloated belly as soon as I drink a little water even now. I have gained about 6 lbs that I can't shake no matter how much I work out and that has never been a problem before.

I had migraines from hell and headaches nearly every day the last few years.

I got panic attacks and was very nervous, had anxiety and it felt like an elephant was sitting on my chest. And that is SO NOT me or anybody in my family. And I know it was the pill cuz I had no reason to feel that way.

I had blurry vision at times. Fainted once in the mall for no apparent reason, I had never fainted before in my life.

I had no interest in my own life or in doing anything whether that was working, going to school, exercising, going out with friends, traveling, whatever it was I was not interested. Again, so not me. I could have died and I wouldn't have cared. I could have gotten a Ferrari and I wouldn't have cared.

I could sleep 10 hours a night, take 1-2 hour naps in the afternoon and go to sleep again at 10 pm, no problem. And the nightmares! Holy crap. Awful dreams about plane crashes, robberies and murderers EVERY night. Thankfully they seem to have disappeared now.

I have high cholesterol, through the roof actually! -no family history there either- and blood pressure is a little high but not too bad. My thyroid was a little elevated last time and the doctor thought it was due to Yasmin.

I snap at everybody and think that I don't love my husband when I actually do love him a lot. He has put up with me being so unbelievably bitchy for 5 year. Bless his soul!

Since I started Yasmin we have had sex about 1-3 times a year. I'm NOT kidding. I haven't wanted anything to do with sex.

I have heart palpitations at times. Shortness of breath just walking up the stairs in my house.

Dry skin no matter what cream I use. Major hair loss.

I went off Yasmin once before and didn't get my period back for over 6 months so I just started taking it again like an idiot cuz I wasn't planning to have kids then anyway.

I was never happy, never sad. Mostly mad or irritated, no problems there.

What else? How many hours do you girls have to read my post? ;-)

To sum it up. Yasmin has destroyed my life for the past 5 years but I was to blind and scared to get pregnant before that I just didn't care. And not caring about my own health was surely caused by that rotten pill too.

What can I expect now that I'm off the pill since 2 weeks? How long before the hormones are gone from my body? What can I expect and when does it get better? Can I go to the ob/gyn after 2-3 months if I don't get my period and have them give me something to start it? Or would that be bad? What about the weight, should it go up or down? Acne? Hair loss? What else? Have you had any medical problems that you needed medicines for due to Yasmin? How long has it taken you to get your period back? And most importantly; can this pill make me infertile???

If there is a class action lawsuit I want to be in it!

My doctor put me on Topamax for migraines, but I can not handle the effects. I just started the 75 mg dose just as I was moving into a new college apartment with new roommates, and I felt like I was going crazy! I couldn't eat anything without feeling completely ill, I was spacing out, and I couldn't remember words.. for three whole days I couldn't remember the word 'tapestry.' I finally had to look it up in the dictionary.. not a good sign for a college student. The worst, though, was the overwhelming sense of panic that was getting worse by the day. I was no longer myself! The last straw was a panic attack, complete with hypernentilating. I have never felt so scared in my life. I actually had to go the ER to get something to calm myself down.

So, I decided to stop taking it. My parents talked to my pharmacist, and she told them that Topamax IS the type of drug you can stop "cold turkey." But after a week, I feel almost as bad as I did when I was on the drug! I still can't eat anything. Also, I wake up hours before my alarm goes off, completely sick at my stomach. I feel panicky and nervous. I have several bouts of diarrhea and this morning I almost didn't make it. I share a bathroom with three (normal!) girls, and it is getting to be embarrasing and annoying. Please, can anyone tell me.. when do the side effects go away?? I want to be a normal 19 year old again!

About eight to ten years ago i had a violent reaction to lactaid. I had taken it numerous time before with no problems and then I woke up one morning - had a bowl of cereal and a lactaid pill - within the hour I was experiencing severe stomach pain along with vomiting and diarrhea. I thought it might have been due to the fact that i had had very little to eat the day before and only a bowl of cereal that morning with the extra strength pill.

the following weekend i was brave enough to try it again with some ice cream at night (this time i had a full stomach from dinner). BIG mistake - this time it was worse - the stomach pain was out of this world (i have a high pain threshold but this had me in the fetal position) and i couldnt leave the toilet and trash can for a few hours. My girlfriend was scared and called one of those nurse hot lines. they told her to coat my stomach with some kaopectate - which seemed to help. I checked the bottle of lactaid - and the expiration date had passed - so i threw it away and swore off of lactaid pills. fortunately they came out with the lactaid milk!

Fast forward to now - never touched the stuff again. well the other day I was out of lactaid milk and my wife (yes the same girlfriend) had picked up some samples of lactaid pills at a trade show - so I guess with the passage of time - I forgot how painful and miserable the other experiences had been - so i took the pill. Nothing happened!

Last night i decide to take another one because i had a craving for ice cream (had been awhile!). I figured it was ok since i had no reaction a week ago. Well sure enough - within the hour I was on the floor in severe stomach pain - followed by vomiting and diarrhea. This time we had kaopectate in the house - so i started taking it - well i just threw it right back up.

This episode lasted about an hour and a half this time. There was a metallic taste in my mouth about the third time i vomited, and the fifth and final time, there was puddle of yellow liquid that came out at the end.

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 first got a headache, then a tinnitus after 14 days of Omeprazole treatment. The tinnitus is centered, with high frequencies (3 kHz up to about 12kHz). It is so strong that it strongly disturbs my sleep at night. The tinnitus seems not to go away any more.

Gas bloting, acid reflux and irregular bowel movement required me to take Zantac. I also suffer from severe asthma. After about a week of Zantac treatment, I realized that I was unable to get an erection, and lacked any sexual desire, even when stimulated by my female partner. This was devastating. I am in my early 40s, and have always been sexually active. I research the internet for possible ED symptons, and found out that prolonged use of Zantac can adversely affect an erection. I have now resorted to Pantoloc, instead of Zantac and hope to enjoy my relations with my partner once again. No more Zantac for me.

I started taking Yasminelle (its dosage is much lower than Yasmin's) about 5-6 months ago; the side-effects I endured during the first two months keep coming back as soon as I start a new packet. Side effects such as nausea during the first week of taking the pills, continuous breast pain. These side effects are completely making me seem like a total freak when I am out- I am always complaining about how sick I feel and I also can't drink because as a result i feel queasy and I'd have to stop. Does any one else feel the same way on Yasminelle particularly? i have been searching online for discussions regarding Yasminelle but I have found none at all...anyone else on Yasminelle and do you consider it a good form of birth control?

After being injected with lidocaine during a root canal procedure, the vision in one of my eyes was beyond distorted (the side they were working on). I had 3 injections prior to prep the tooth which is located upper right near the wisdom tooth. An hour into the procedure, I began to feel the doctor working on the tooth. So I wouldn't experience major pain, he then injected me one more time in the roof of my mouth. Within seconds, I noticed my vision was in that eye was beyond blurry. It was like I was seeing cross eyed, but my eyes were not physically crossed and my vision was distorted beyond belief. This totally freaked me out and lasted for a few hours until the lidocaine wore off. I have had a few root canals and dental work over the course of the years, but they used carbocaine instead, because I get too jittery with regular novacaine. Therefore no epi. What makes matters worse, is that they were unable to finish the root canal procedure, because it freaked me out so bad and my vision was messed up, that I was sent to the ER. I was told that he must have hit an optic nerve during the injection which most likely caused this situation and they were categorizing it as a possible allergic reaction, but again feel as though it was just the optic nerve that the lidocaine traveled to. Now I have to finish the rest of the root canal a week from now and will be having another dentist perform it. I'm so frightened that this will happen again. I honestly thought that my vision wouldn't be restored back to normal. Has anyone ever experienced anything like this?

Thanks.

I took Yaz for 7 days. In that amount of time, I began experience the most horrific symptoms I have experienced in my life. They included: chest pains, nausea, vomiting, arm pain, and the feeling of imminent death (these caused me to go to the emergency room since they are classic heart attack symptoms for a woman); leg and arm weakness; lethargy; migrane; panic attacks; severe insomnia, diarrhea, and vision problems that caused my contact lens perscription to change and night time vision had profound halos when driving, etc. I was literally unable to stomach any normal food portions I was so nauseous. I normally run 3 miles and could not even make it to the gym for weeks. I was afraid to stay home alone with my 4 year-old and 17 month-old for fear something would happen to me while they were in my care. At the ER they found low potassium levels (which makes no sense given Yaz has a potassium sparring diuretic component). In another blood test, I had elevated iron, which I have never had previously.

I am 35 and have been on bcp's periodically for 12-15 years. I have never had any of these symptoms prior to this experience. I have never had anxiety, depression, or any other underlying health condition. I immediately stopped taking the pills once I made the connection. So far, my recovery has been slow, but at least it is improving. I resent that my ob/gyn and internist both said that the pill would be out of my system in 24 hours. The effects are clearly long lasting (I am approximately 7 weeks off of Yaz).

Finally, my eye doctor, of all people, said that he has seen and heard of people having problems similar to mine and that it was understandable that I would have anxiety when I felt like I was dying from a heart attack. No one perscribing this medication bothered to tell me of the diuretic component or any component that was going to affect depression. I am attorney and have always thrived under pressure, not turned into a panic attack ridden mess like this medication caused.

As for the previous post who stated these are common symptoms described by women, at 35, I know the difference between my normal body function and the hell that began when I started taking Yaz. Unless you have experienced this, then you clearly would not understand. I appreciate that Yaz and Yasmin have worked well for some, but that clearly has not been my personal experience. So, I write this not to discourage someone who has had a positive experience, but to provide support for anyone else who has suffered like I have.

I used Simvasta 40 for over a year. I started to experience awful pains in my back and thought is was due to my hernia in my lower back. When I went to my GP he said the pains were muscular and could be a result of taking Simvasta 40 to lower my cholesterol. I stopped taking them and now I have some days without pain. I hope it will improve gradually.
I also have developed Depuytren in my right hand. I am a woman and it does not run in our family. I'm 58 and all these problems started while taking Simvasta 40.
I see someone else has developed Trigger finger, I wonder if this is the same as Depuytren.

headache,nauseous,leg cramps, pain in my left breast, around heart...now, around each period my breasts hurt, and i have terrible stomach ache, like cramps, which i never had before..i also started having acne on my back and shoulders...but the worst thing is, my room-mate, she was using Yasmin for 9months, died a week ago. she wasn't sick at all.she actually did have a few headaches, and weird stomach ache, but we didn't seem to connect the two...

I had my Mirena for 18 months (12/07-4/3/08). My Doctor urged me to keep it in and when I finally went to get it removed, I had retained the strings and the pain when he dilated my cervix was so painful I had to get anesthesia to get it removed.

After about 6 months of the iud, I started experiencing heart palpitations and shortness of breath. And for the last few months and even two weeks post removal I am experiencing shortness of breath at rest. And tightness in my chest. It's very scary. ALSO, I only have heart palpitations mid-cycle (ovulation) and during my period. And my shortness of breath gets worse during that time also. It is painful to exercise bc I can't breathe, I actually got a bronchial inhaler from my doctor and it's helped SO much during exercise. I would be yawning and have so much extra saliva and after 50 running paces I'd have to stop to rest because my chest would be so tight and burning. I was tested for asthma and do not have asthma. That isn't to say I don't have exercise induced asthma. I never ever had problems before this Mirena.

I haven't had any hair loss or trouble sleeping that I can pinpoint either. Mostly I looked 3 months pregnant and haven't been able to drop 5 lbs. I'm ideal weight for my height and have cut out most sugar and limited carbs and nothing has changed even with exercise. I DO notice that I was soooo nasty and couldn't control my temper. I can't positively contribute that to the Mirena but I'll see as time goes on and this wears away.

I wouldn't advise the Mirena to anyone. Not with all these women and myself having the same effects. The Dr tried to tell me that it couldn't be the Mirena causing heart palpitations but I'm 28 years old and entirely healthy.

I also felt when I was ovulating that I was having contractions. My Dr kept telling me it's not supposed to help cramping but won't make it worse and I must have said 100 times that I NEVER HAD CRAMPS before in my life. My ovulation/periods were always very uneventful and painless. And the pain I had during ovulation and my period wasn't traditional cramping. It was a wave of extreme sharp shooting pain that would shoot down my thigh and I'd actually do careful, controlled breathing during that pain. The pain would be so intense I'd stop in my tracks and grip whatever was nearest to me while standing perfectly still and doing breathing exercises.

Also, I should note I have never been pregnant before and my midwife that I go to now was saying that my body could have been trying to expel the iud bc I had never had anything pass through or in my cervix before and that the pain during ovulation and period could actually have been my uterus contracting because it was trying to get the iud out!

I hope that the chest tightness and shortness of breath go away. It's very alarming.

Can this drug cause a rash on my shin?

Just started today with 40 mg dose of Sortis (Swiss-branded Lipitor).
60-90 minutes later, I am very dizzy, sweating, funny taste in mouth.

I am done... no more. My cholesterol is normal, but recommended as complementary treatment with Glucophage, as I am very slightly diabetic.

I am still spaced out as I write this note. Called the MD to tell him that I the one dose is all that will enter my body.

My gynocologist had to put me on Yaz because I had had a Kenalog Injection for a slipped disk and after being injected with Kenalog I kept having menstrual periods....4 in a month a half! So she gave me Yaz, it seems to work so far, but this drug gives me side effects too. Has anyone experienced extreme tiredness? I seem to be tired non-stop even after having a lot of sleep. This wasn't listed as side effect on my prescription, but I thought this may be causing it. Since I started taking this 3 weeks ago I began to feel real depressed and angry for no reason at all. I just get these weird bouts of depression.

Has anyone suffered severe dandruff and itchy scalp, to the point of distraction like???

Has anyone had extreme heavy bleeding/clots after having the Mirena removed? This is day 3. The last time I had such heavy bleeding I had just had my son. When do you start to worry about the bleeding?

I was giving prednisone for only 5 days (not sure about dose, but it tapered to one pill on the last day) for a bronchitis induced severe asthma attack. I have only had asthma twice in my 50 years, both times associated with a bad case of bronchitis. The "doc in the box" reduced his original dosage due to the 3 corisone injections I recently had in my spine. After reading these posts I feel grateful I wasn't on a higher, longer term dose. I have some of the same side effects listed here including uncontrollable appetite, fat gain around the middle, water weight gain, constantly having to urinate, superhuman energy, heart palpitations, and approximately two weeks after finishing, I began to get a mustache (hairs that were previously white became brown over a two week period). I have read on the internet and been told by my pharmacist that this is temporary. I have also read and been told that the 2mg estradiol I take every day since my hysterectomy causes the body to retain and not rid itself of the steroids as it normally would (estrogen is actually listed as drug interaction with prednisone). The doctor in the box apparently just ignored this interaction and prescribed it anyway. However the main reason I am posting is a very strange possible side effect that occurred approximately 1 week after my final dose. I was awakened in the middle of the night with SEVERE pain (felt like bone pain, not muscle) in my right knee that lasted until morning. By mid morning it was gone. The next night I had the same experience but in both knees. It lasted about 5 more days, gradually tapering in intensity, and then just went away. I do have severe arthritis in my lumbar and cervical spine, having had surgeries to repair injuries from a snowmobiling accident. I have normal arthritis elsewhere for a 50 year old, but have NEVER had issues with my knees. Has anyone had this strange symptom? None of my doctors (internist, rheumatologist, physiatrist - who gave me the injections and prescribed physical therapy for my spine) had any explanation. The only explanation I have is the prednisone because I had taken the Z-pac (antibiotic) with no side effects several times in the past. Weird!

Incidentally, I am off the prednisone for about 5 weeks, am still hungry all the time, still fat, still bloated. Unfortunately the extra energy is gone. Best of luck to everyone on this strange drug. My heart sincerely goes out to all of you on long term therapy. God bless.

I started having problems with my voice cracking and throat aching after singing or talking alot. Went to Dr. and he said he thought it was reflux (of which I had no symptoms). Wtihin days I started experiencing fatique, headache, depression, dizziness, ringing in my ears, and my right leg went numb about 3 weeks into taking it. Then about 2 months into taking, my entire right side went numb (thought I was having a stroke). Since that time I have been through CAT scans, MRI's, lumbar punctures. Been to 2 Neurologists, a Neurosurgeon, Cardiologist, Endocrinologist. 3 different Doctors thought I had Multiple Sclerosis or a stroke. All tests negative for both. After researching Prilosec on my own I found that Prilosec and all like meds block the absorption of and strip vitamins out of your body. 2 1/2 months after stoppping it I had B-12 level checked and it was almost non-existent. Started taking B Complex and B-12 shots. Symptoms have tremendously improved but haven't completely left. I still have numbness even 14 months later. The problem is that B-12 deficiency can cause the numbness and if not treated quickly enough the problems can become permanent. IF YOU TAKE any acid reflux medicine have your vitamin levels checked ... especially B-12.

Adderall has been an excellent drug for the treatment of ADD. It took me from a lethargic, disorganized adult, to a more productive one who finally could finish her work and leave her desk organized at the end of the day. Unfortunately...
...there are many side effects to this drug which has, reluctantly forced me to quit taking it. The weight loss was a welcome side-effect as was getting rid of the lethargy I have experienced on a daily basis since the age of 11 (anti-depressants did nothing). However, my infrequent migraines became daily and excruciating after starting Adderall and its generics. My insurance could not keep up with the coverage of the migraine meds I needed. I began experiencing ear problems (primarily in my left ear) that felt like I constantly had the pressure associated with a cold. After visiting my doctor (who told me nothing was wrong), an ENT doctor, getting a hearing test, and an MRI of my ear canals and Eustachian tubes, I finally found out it was due to the Adderall. The worst side effects, however, was a gradual increase in dermatitis (dry, itchy, scaly, skin). My complexion looked sallow and my back and neck broke out in horrible cyst-like acne (not typical AT ALL for me). My eyes became so dry (not to mention the cotton mouth), that I began trying to reverse this effect with pills from a Lasik eye center (helped, but didn't solve the problem). Perhaps the worst side effect, however, has been the hair loss. Long, beautiful blond hair, has been replaced by very thinning hair (comes out tons at a time in my shower), which is now brittle and breaks all the time. I have finally decided to quit this medication despite its benefits. I only took 15mg 2/day. Once my body recovers, I hope to take on an as-needed basis for important work projects or hectic weeks where productivity is necessary. Other than that, I won't take it any more. The side effects are too severe, even for me.

My four year old son has been on singulair for 6 weeks. He has started complaining about nightmares, wetting the bed and has become irritable and easily agitated. In addition, he seems to go into these wierd episodes of not being able to control his body...like someone high on drugs. Has anyone had a similar experience?

I will be calling his dr. in the am.

statins are poison...bring back oat bran with niacin...the big drug manufacturers killed it...it is more effective than all the statins in the world...the big drug manufacturers are killing us slowly...

Post your symptoms since stopping Yasmin!!!

Hey everyone it's Kay21 here and I just wanted to post my 3 month off Yasmin update. Because stopping the pill is a hard decision, I figured we should all post are updates here to help/support those who are planning to stop or who have recently stopped Yasmin.

I have been off of Yasmin since April 17. As some of you already know, I was experiencing horrible side effects while on Yasmin for 3 years (particularly stomach problems, vaginal dryness, muscle cramps, increased blood pressure and heart rate and anxiety).

The first 1 month off of Yasmin was okay. In fact, I felt the best I had ever felt in a while. My blood pressure and heart rate decreased and the migraines and muscle cramps went away. But when I hit the 2 month (8 week) mark, I felt HORRIBLE. I was severely depressed and anxious. I was crying all the time and felt a severe sense of DOOM! The physical symptoms also started to become problematic. The acne increased and I started growing more facial hair. The worse symptom, however, was that I started losing a ton of hair. I would lose stray hairs all day (probably about 200 a day). Since I have hit the three month mark, the hair loss has gotten MUCH WORSE! Now I am losing CLUMPS of hair all day. I have seen several doctors about this. Some say it's because of stress and a few (a derm, GYN and endo) say that hiar loss is common after stopping bcp. I have already loss about 1/3 of my hair.

I am also really concerned, because I have not had a period since April 22. So my doctor has put me on provera for 10 days to induce a period.

For those who have stopped Yasmin, what have your symptoms been (i.e. increased acne, weight gain, anxiety, etc.). Has anyone experienced hair loss? How long did it take to get a period???

Thanks...

i've been on synthroid for 9 years. started at some low dose and gradually went up to112 mg. get extreme itching all day everyday if i don't take allegra for that.not a rash just itching. that doesn't bother me as much as the fatique. every joint in my body aches all the time. sure there are better days but fo rthe most part it's bad. tried physical therapy and chiripratic care but no avail. they ended my sessions. my legs get sooo weak and my feet burn lower back really aches. sometimes muscle cramps. i'm very negative towards my loving family and it hurts me to do so. can't seem to keep upbeat. soo tired all the time.
is it the syntroid? i used to be very energenic and a doer. now i have spurts of activity in the morning , but then i just can't get motivated. help me any suggestions?

throat tightening, SEVERE thirst, hands swelling, loss of feeling in hands and arms, muscle aches, have a history of severe dehydration but my doctor somehow missed that warning, it is Friday 4 AM, so also have the sleep disturbance. I am only on 5 mg, just started taking this med on Monday-4 days ago.

I've only been on Lamictal for about 3 weeks now. I started taking it the day after Christmas. I take 25MG twice a day, with .5MG of Klonopin 3 times a day. I have been diagnosed as Bi Polar II, with very deep bouts of depression and suicidal thoughts. So far the Lamictal has been working for me. I have noticed that if I don't take it in the morning when I am supposed to, I let little things get to me. But as soon as I remember to take it, I feel better in a short amount of time; but that could also be the Klonopin. Anyway, the only side-effect I've noticed so far is that I started my period a week and a half early, and I have been on it for 2 1/2 weeks now. And it keeps getting heavier and that is very annoying.

Are any other females having period issues? Or is it just me? I can't find any other sides that list heavy bleeding or early periods as a side-effect.

I am having tingling burning sensation in my feet, legs and hands and arms. My blood pressure was not improving on 5 mg so I upped it to 10 and those symptoms are much worse. The tingling sensation goes all the way up my left arm and up above my knees on my legs.

I have tried to take the Lisinipril before and stopped for these same reasons. My doctor does not seem to think that it is due to the Lisinipril. so I tried it again and the burning, burning sensation is driving me crazy and keeping me awake. I have to get up and stand in cold water for a while to get some relief.

I have not read about anyone with the same symptoms. Does anyone out there have these symptoms??

I have itching, pain in the abdominal area, sometimes panic attacks, and sometimes drowsiness.
The pain I took it for has gone away now, but I still keep taking it cuz I feel like crap when I get up in the morning, runny eyes and nose, and an anxious feeling, with no energy. I take a perc and drink some coffee and I'm good to go. Think I'm addicted? I do.

I started having panic attacks while taking Percocet. I am a chronic alcohol user, and I am saying this just in case it rings a bell for anyone. I have since stopped taking Percocet (about 3 days). I was a habitual/recreational user ... meaning that I took them when available, but I did not always have them. Since my last dose, I have been having recurrent panic attacks that are very scary. They include physical symptoms (heart pounding, cold and hot flashes, feeling of difficulty breathing, sweating, shaking) - and the much more scary mental symptoms (fear of death, walls closing in, inability to think or concentrate, vivid dreaming, fear of people, etc.). It appears that some other people have had issues like this, but not everyone. Can someone share their story with me. Has anyone had similar experiences ? Do they go away at some point ? Is it withdraw (I am not sure since they started while I was using them - but continued after I stopped) ? I have heard that it just takes some time, but it is very scary. I get some relief by drinking ... in fact almost complete freedom from most of the symptoms, but I can't just drink all day. Please help.

My wife recently suffered nausea, muscle/joint pain, upset stomach, anxiety, insomnia and other symptoms after taking 250mg x 2 daily for 6 days of Cipro poison (thanks Bayer/FDA, burn in hell). She was always an athletic individual, and at 35 she is applying for disability now since she cannot work anymore (we hope it is temporary).

We all are suffering from it - let's find a remedy!
1. People must sue FDA/Bayer/Doctors who prescribe it. We live in Mass, javaman888@yahoo.com
2. Detoxify - I found a good advice from a sufferer, here is an excerpt:
"...I am glad to report that I am much, much better. I have taken what
most would consider very drastic approaches in my lifestyle. I eat a
pretty strict macrobiotic diet, with lots of grains, veggies, sea
veggies, soy products, and some fish. All organic. I took wheat
grass every morning for 2 months, to detox my liver, and also a few
herbs and some supplements. The diet thing has been a huge
challenge, but when I go off even a little, I start to feel a lot
worse. I also walk every day and do some yoga and swimming. I feel
like crap when I don't exercise. I stopped all medications,
including advil and tylenol, in Feb. I have used homeopathic
medicine to counter some of the ADR's, with some success. I took
Ignatia for anxiety, and that actually helped. Some of the others
not so much..."

I had my IUD removed November 12th after having it for two years. The removal was painless. Within twenty-four hours, the abdominal bloating was noticeably less and within a week, gone. I also noticed an increase in energy level and change in appetite. I am looking forward to getting rid of the gained weight over the past two years and getting back into the clothes I love. More importantly, I want to feel alive and attractive again. The only adverse effect of having the IUD removed was four days after removal, I had a very emotional, crying episode for the better part of the day. A minimal amount of vaginal discharge, similar to the start of a period, has been present for about six days. Otherwise, no problems. Also, my knees, hips and back are no longer hurting like they were. Don't hesitate to have it removed and don't let your doctor talk you out of it! It is your body and your right to make all decisions regarding your healthcare! Good luck to you all. Thank you for sharing your experiences. If you had not, I may have never put two and two together.

hives, redness and severe itching on hands, fingers, and forearms. Pain in shoulder which I can only describe as feeling like I slept on it wrong. Nerve-like pain in lower legs/shins (not muscular) which comes and goes and is not associated with movement or exercise - sort of like if you had a back problem, but intermittent.

Post your symptoms since stopping Yasmin!!!

Hey everyone it's Kay21 here and I just wanted to post my 3 month off Yasmin update. Because stopping the pill is a hard decision, I figured we should all post are updates here to help/support those who are planning to stop or who have recently stopped Yasmin.

I have been off of Yasmin since April 17. As some of you already know, I was experiencing horrible side effects while on Yasmin for 3 years (particularly stomach problems, vaginal dryness, muscle cramps, increased blood pressure and heart rate and anxiety).

The first 1 month off of Yasmin was okay. In fact, I felt the best I had ever felt in a while. My blood pressure and heart rate decreased and the migraines and muscle cramps went away. But when I hit the 2 month (8 week) mark, I felt HORRIBLE. I was severely depressed and anxious. I was crying all the time and felt a severe sense of DOOM! The physical symptoms also started to become problematic. The acne increased and I started growing more facial hair. The worse symptom, however, was that I started losing a ton of hair. I would lose stray hairs all day (probably about 200 a day). Since I have hit the three month mark, the hair loss has gotten MUCH WORSE! Now I am losing CLUMPS of hair all day. I have seen several doctors about this. Some say it's because of stress and a few (a derm, GYN and endo) say that hiar loss is common after stopping bcp. I have already loss about 1/3 of my hair.

I am also really concerned, because I have not had a period since April 22. So my doctor has put me on provera for 10 days to induce a period.

For those who have stopped Yasmin, what have your symptoms been (i.e. increased acne, weight gain, anxiety, etc.). Has anyone experienced hair loss? How long did it take to get a period???

Thanks...

I was cleaning out my expired meds. I had some levquin that luckily had not been taken by my family. I dropped a pill and my 16wk. old puppy ate a 500mg. pill and the very next day she was wobbly, I thought she was just tired. As the day went on she lost control of her back legs and eventually lost control of her front legs. It has been 3 days the only thing she can move is her head. This has been devistating to my family. I can just pray and hope that is wares off with no return or other damaging side effects.
I hope this makes others realize just how poisionous this is and after reading other web sites on this I am blown away that this is still on the market just waiting to destoy someone elses life. The learning lesson here is even if it is perscribed by a doctor do your research on any medication before giving it to your loved ones.

heartburn,chronic nasal problems,sneezing,problems catching breath,even though I take asthma and allergy meds

Not sure if this is side effect. Had Thyroid Cancer, Had radiation. became hypoparathroid. Taking large doses of calcium 7200 mg. daily. Taking 200 mcq Synthroid daily. Still hypocalcemic, just increased calcium to 9000 mg. daily. Having heart palpatations so severely, my head feels full. It lasts approximately 1 minute with each episode, skin is really dry, even peeling, leg and feet cramping, finger, hand and arms have episodes of tingling, and hair texture has changed.Doctor has tried to regulate calcium and synthroid for almost 2 years now. Is this normal??

Hi Everyone,
I have been taking Topamax 25 mg for 1 week. I can't stand it. Today I am to up my dosage to 50 mg.I am not sure if I want to do that. The side effects suck.. I think I would rather just deal with my migraines, at least I know how to do that since I have had them for over 25 years. I have tried everything and nothing has worked so the Dr. and I thought we would give this a try.
I am trying to keep my place of employment happy with trying to cut down on the migraines but nothing works.
Most days I just want to give up.
Hopefully we will be able to figure something out.

I can't stand the pickhands and feet, the stumbling like I am drunk( and I dont' drink) nothing tastes right anymore, I have the shakes and I ache.
And all it does is makes me sleepy and like I am in another world.
I went to work today and made it half an hour before I came home because I stumbled and almost fell over. And when the boss talked to me it was like I wasn't there. So I came home. I don't know but I don't like it at all.

I was a 17 year smoker. I took Chatix and have been quit now since April! You are supposed to stay on the pill for like 6 months, but it only took 2 weeks for me. My only problems with it were nausea and weird dreams. For the nausea I just split my doses up, that seemed to help and the dreams I just had to deal with. All in all, I had tried to stop smoking many times before, this is the longest I have been without a smoke since I was 14 years old!

I have hypothyroid. Have been taking Synthroid for about a year, 0.075MG a day. Had my levels checked 3 times since on the meds and still have never gotten to normal, but a lot closer. I have gained 20 pounds that I can't get rid of, which for me, is crazy. I have never had a problem dropping weight, and for the past month or so, I have started losing my hair. Not just losing it, but the texture and everything has changed. No matter what I do it looks dry and flat, and even when I condition it and also use a leave in conditioner, it still knots up and tangles. I have NEVER had a problem with tangles. It's coming out in handfuls. Im not taking any other meds, so I imagine it has to be the Synthroid. My problem is..What else can I take? I mean, I have Hypothyroid, so I can,t just leave it untreated, But I have no wish to be fat and bald either. Please...anyone know of others meds without these side effects?

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

Hi everyone, I read some of the posts here and thought to share my experience with you.
About 15 years ago I started having heart burns and started taking Tums, Gaviscon and some other antacids and they seemed to work for a little while. But my heart burn slowly got worst and worst until I went to my family doctor. He sent me to a specialist and after sending the scope in my stomach (EsophagoGastroDuodenal (EGD) endoscopy), he said that I have H. Pylori infection in my stomach, as well as LES malfunction (LES = Lower Esophageal Sphincter). He prescribed some antibiotics and 20mg/day of Losec for 8 weeks.
After 8 weeks I ran out of Losec, and my heart burn returned again. I went and saw my doctor again and he said I can continue taking Losec and that I can take it as long as I need it and that Losec has been in the market for over 19 years and no one had any side effect from it and it's one of the safest drugs that they have come up with. So I kept on taking it regularly 20 mg/day for 15 years now. Until about 6 months ago I switched to Omeprazole because my insurance company wouldn't cover the cost for Losec but covered the generic brand Omeprazole. I've had none of the side effects mentioned here, BUT PLEASE READ THE REST OF THIS.
Losec is also called Prilosec and Omeprazole is a generic brand with the same active ingredient but different fillers.
About 2 months ago, I went to a Nature's Source store (here in Canada) and was looking around. An employee of the store offered his help to me and I told him about my case. He said you have totally shot down your digestive system and told me to go and see a Naturopathic Doctor.
I found one and went and saw him. His recommendations were: have 2 tablespoons of an Organic Apple Cider Vinegar (I use Bragg brand) 10 minutes prior to each meal. Also gave me some Probiotics pills as well as some Digestive Enzymes pills.
Prior to this, if I missed taking Losec in the morning, I suffered a great discomfort in my stomach with heart burn (a lot!).
I followed the naturopathic doctor's advice and did what he told me. After about 1 month, today is the second day that I haven't taken Losec. I haven't had discomfort in my stomach yet. I'll have to see how long I can go without it. I will post and update this again. BUT PLEASE READ ON!
Losec, Prilosec, Ranitidine, Omeprazole, Nexxium (the purple pill), and all of this family of drugs are Proton Pump Inhibitors (PPI). Which means, they stop the production of the stomach acid. Therefore, no acid reflux or heart burn....
But when there is no acid in the stomach, the stomach becomes the biggest target organ and a paradise for bacteriums, microbes and other microorganisms, which otherwise can not survive in it's very high acidic environment (H. Pylori is an exception). We can not digest our food properly any more. Our bodies suffer from lack of Calcium (regardless of the amount and type of calcium intake), because it can not be processed any more. Meat can not be digested properly any more. Therefore, lack of Amino Acids which are the building blocks in our bodies. Guess what, NO AMINO ACIDS = JOINT PAIN WHICH LEADS TO ARTHRITIS. And lots of other problems later in life.
NO SIDE EFFECT, MY A*S.
If you're suffering from heart burns, indigestion, reflux, or GERD, stop eating: ANYTHING THAT HAS WHEAT IN IT, TOMATOES OR ANYTHING MADE FROM IT (i.e. ketchup, tomato sauce/paste...), DAIRY FOOD, COFFEE/TEA, ALCOHOL. NO CHEWING GUMS, SUGAR, CHOCOLATE, FRIED/OILY FOOD, STARCHY FOOD. STOP SMOKING AS SOON AS YOU CAN. These are all irritants to the stomach and esophagus.
I'm still educating myself about this. I read this book about stomach acid called: Why Stomach Acid Is Good For You by Jonathan V. Wright, Lane Lenard. Read it and you will be surprised.
I hope this will help some of you.

God bless.
S. AA (Toronto, Canada)

just started taking Adderall, though i am not prescribed. I went to my doctor and asked for it but she said no. I explained that I am often overwhelmed at work, I am a case manager and keeping on task with all of the work is hard. My doctor said when she was in med school, med students used to take it for that purpose.So anyway i bought 5 pills from a coworker. I seem to have super human energy, get all types of work done and stay focused all day. On the down side, in 5 days I have lost 3lbs., I want to lose weight, but not that fast. I have what I consider to be Adderall hangovers the next day, where I am extremely tired. I also have noticed severe headaches, every day that I have taken it, I crash by the end of the day at work and cant wait to get home, because I am so tired. My neck aches, and I had to change to a firmer chair at work, because all of a sudden my back is killing me, I also get insomnia and have to counteract the Aderall with Tylenol pm just to get to sleep. These side effects freak me out, and I don't know if I want to again ask my doctor for a script, but I get so much done at work, and I am heading back for grad school, I just don't know what to do? oh yeah, the pills that I bought were Adderall XR 30 mg.

I was born without a thyroid gland so I can't compare the way I feel now to the way I would've felt with a thyroid. I've been on Synthroid my entire life (22 years), and I'm up to 112 mcg now. I am very skinny (5'5", 104 lbs) and feel constantly fatigued no matter how many hours I sleep, what I eat, and how much exercise I get. I periodically get pain in my hip joints, heart palpitations, and intense mood swings. My thoughts race but I have very little physical energy. I feel restless and gloomy almost all the time for absolutely no good reason. My doctor tells me I'm depressed but I honestly have no reason to be depressed and I wish she would see it as a symptom instead of a diagnosis. I graduated from a good college, I've got a job I like, I have friends, I enjoy life and my hobbies, yet I feel overwhelmingly sad. This does not seem like depression to me.

I find that after I do aerobics I get a tightness in my chest, which makes me worry about my heart, but again my doctor doesn't seem to think this is cause for concern. I have been irritable/fatigued for YEARS and I suspect I'll feel this way for the rest of my life. The worst of it started when I hit 16 years old and started the 112 mcg. My tests are always normal and it frustrates me that my doctor disregards my symptoms. I've tried other doctors, but they always send me away with my 'normal' test results. Can anybody help?

I am sooo relieved that I found this site. OMG. I was on the NR before for about a year and 3 months. I didn't have any side effects whatsoever. I went of the NR because my boyfriend and I broke-up and I wasn't having sex. About 4 months later, I developed 2 ovarian cysts that ended up rupturing in my right ovary. BTW, I turned 30 in the same month. I was in so much abdominal pain, hot flashes, painful menstrual cycle, passing huge blood clots, depression, crying all the time, thoughts of suicide, anxiety attacks, very irritable, easily frustrated, inability to concentrate, and nausea. I had NEVER had any bouts of depression, crying all the time, thoughts of suicide, anxiety attacks in my life before. NEVER! My OB/GYN told me my hormones were all out of wack and that I should go back on the NR to regulate my hormones. So, I went back on the NR, my cysts went away and I felt 100% better immediately. Now it's 2 months later and I'm having all the same symptoms I had before the NR, although, it’s not as bad as it was before. Apparently, I'm still ovulating while on the NR although the NR STOPS ovulation. I have developed more cyst(s), haven't gone for the ultrasound yet, in my right ovary, even though my last ultrasound showed that the last 2 cysts went away. Right now, I am emotionally drained and physically in a lot of pain. I think that if I get off the NR my symptoms would be a lot worst. I’m allergic to the patch because of the adhesive, coming off of depo caused too much pain, and I forget to take the pill. So I don't know what to do.

constant hiccups. Stops for 20 minutes and comes back again for 2 to 3 hours. It is a horrible feeling. The doctor prescribed it for bad allergies. I feel like stopping this horrible drug. I still feel the same way about my allergies. This is totally ridiculous!

My daughter was on Yasmin for just about a year for control of irregular cycles when she went off to college.
I got a call from her one evening and she said she was having back pains and one of her legs was getting fat and wouldn't fit in her jeans. I asked her to go to the doctor asap because she was on birth control and I had heard of the rare instance in which it caused blood clots. The doctor sent her home and told her to put her leg up. Thank God, her roomate was a medical student and started measuring her leg and they found that it had started to gain inches in a very short time...the medical student called her relative that was a doctor and they told her to go to the hospital immediately. What happened next was a nightmare for my daughter and I...she was hospitalized for everal days missing finals for DVT,,,a extremely large blood clot that ran through her major vein starting just under her heart in her chest and running all the way down into her hip. They were unable to perform surgery on the blood clot, so consequently she will take blood thinners to prevent future clots which could kill her. She's now 22 years, still has one leg larger than others has monthly drs visits to have blood taken and has had to alter her life permanetly. She Can never take birth control pills again, will need special care if she decides to have kids and is considered high risk for health care coverage. I was angry and felt it was the yasmin all along and now there are so many other problem cases that I am convinced of it. They did every test possible on her and found no signs of any possible contributor so they determined that in likelyhood it was the yasmin as well.
Please advise your daughters, sisters and friends to stay away from it...it is not worth it!.

I to have a huge dent in my right butt cheek. I would be interested in a class action suit. This is ridiculous! It has been about three months since I received the shot. Has anyone noticed their dents getting better with time?

i've been on synthroid for 9 years. started at some low dose and gradually went up to112 mg. get extreme itching all day everyday if i don't take allegra for that.not a rash just itching. that doesn't bother me as much as the fatique. every joint in my body aches all the time. sure there are better days but fo rthe most part it's bad. tried physical therapy and chiripratic care but no avail. they ended my sessions. my legs get sooo weak and my feet burn lower back really aches. sometimes muscle cramps. i'm very negative towards my loving family and it hurts me to do so. can't seem to keep upbeat. soo tired all the time.
is it the syntroid? i used to be very energenic and a doer. now i have spurts of activity in the morning , but then i just can't get motivated. help me any suggestions?

I had the Mirena IUD inserted on October 10th. I had it switched from the copper IUD because I was spotting dark brown blood prior to my period, so my gyno recommended the switch. I spotted for the rest of the day, then stopped for two days, then began what I would call my period, since I was due for it later that week anyway. I am still bleeding, but I'd like to believe I'm nearing the end, since it seems to be lightening up. I expected my period to be fairly long after insertion.

The day after insertion, I experienced severe itching and swelling down there, and decided that I must have a yeast infection, but both symptoms are listed as side effects on the sheet I got from my pharmacy. I treated the infection, but still itch from time to time... I'm wondering if it's the hormones in the IUD.

On the weekend of October 19th, I lost my appetite, my sex drive, all sense of sexual pleasure and my ability to acheive orgasm. I ate three meals all weekend long, and only because I felt that I should eat, not because I was hungry. Sexually, I felt friction and not much else. Upon trying to climax 4 seperate times over the course of the weekend, I failed at all 4 attempts and all I got from my efforts was sore muscles, frustration and tears from being so upset by it. I have never experienced problems with sex or climaxing in the 14 years I've been with my husband. However, a couple of days before insertion, we had had sex and it was fabulous, as always. I climax every time we have sex, so it's been very upsetting.

I weighed myself today, just out of curiosity, and since the insertion, I've lost 7 lbs. I'm not dieting, not exercising, not even trying to lose any weight.

Upon calling my gyno and discussing my symptoms with her assistant, I was told that it couldn't be the Mirena, because the amount of hormones in it are so minute that they wouldn't affect anything outside of the uterus. I was told that something else in my life must be causing my sexual problems. !!! I don't think so! The IUD is the only thing that has changed in the past 2 weeks! And how do you explain a sudden loss of 7 lbs??? She didn't want to say it straight out, but she was trying to tell me it was all in my head.

I've had sex again since my failed attempts, and it's getting better, as is my appetite, so I'm hoping that my body is simply adjusting to the new IUD and getting used to the hormones. I have not been on any medication or hormones in the past two years, as I've been pregnant and then breastfeeding, so it might be quite a shock to my system.

If my inability to acheive climax continues, I am going ot have the IUD removed and have another copper IUD put in. My sex life isn't worth this.

Sorry I haven't been on in a while- just to answer the question: I had blood work done, that's how they determined that my magesium was low. It's not climbing very quickly either, we'll see after my appointment.
Also: the bronchial stuff... I thought I was developing asthma! I moved to NC and have had issues with a feeling of compression, but only in the winter months. It seems to have passed, I'll keep you posted. It probably is allergies because when I went to MD it completely went away.

Interesting to hear that I'm not the only one with the magnesium deficiency. This is the only site where I've seen it posted.

IPJ

I'm so glad I stumbled on this site...I had my Mirena in for 2 years and after reading most of the comments here, decided to have it removed yesterday.
Recently I have symptoms like bloating, pain at my ovaries, painful sex, stomach cramping, moodswings and also my doctor discovered I had a cyst on my left ovary caused by the mirena. Sometimes it also felt as if I was pregnant because of nausea in the morning and also my stomach that was bloated. I also started to struggle with lower back pain.
I couldn't pinpoint the problem before I saw this site. I spoke to my doctor and ask him why now after 2 years and he said it can happen and I never had problems with the Mirena before.
I'm so glad that I got rid of it especially because of the cyst. Luckily it wasn't sore to remove it.

i personally have had the best experience with my Yasmin birth control. I have been on it for 5 years now. Before Yasmin I was a wreck.Before i ever took any birth control i had my period twice a month, super heavy bleeding,10 days,and cramps so bad I would pass out. I even bled for 5 months straight on the Depoprovera shot. I found all of the tricyclic pills make me crazy and over emotional. I have tried so many different kinds of pills and birth control all with the result of bleeding for months on end and finally my doctor recommended Yasmin and I have been completely happy with it. I have not gained weight, I do not get migraines (and i did with other birth control pills), I am much more emotionally stable (although I will never be a hundred percent sane, but I blame genetics for that one) I have never gotten pregnant, I have not suffered any gastrointestinal side effects, I finally have regular 7 day periods and my cramps are less horrible, my skin has cleared up, i have a perfectly healthy if not over active sex drive, my breast are not particularly tender ever, I don't get any more yeast infections than before, basically it is my saving grace in my opinion. I must also add to this that I did stop taking Yasmin once for 5 months in these 5 years just to see how I am without BC and nothing crazy happened. My periods were heavier, i had worse cramps, my skin broke out. I expected all of that to happen. A month after getting back on Yasmin I was back to my happy ol self again. One last thing is that I did try the Ocello generic version of Yasmin and it was all bad for me. I once again bled for 2 months even though I only took it for two weeks, and i went completely nutso overemotional chick. Long story short, everyone is built differently, not every BC will be the right one for you. Try some different ones out. If you are on a pill and it is not doing the right things for you then switch it instead of taking it for 2 years and then blogging about how miserable it makes you. I will leave you with a wonderful quote from I don't know who but I live for this saying "More orgasms, fewer kids, copulate, don't populate!" HOORAY

closing throat, sweats, swollen glands, no menstrual period, leg pain, severe headaches, chest pain. I have been taking 100 mg for over a month. I have ulcerative colitis and I am using colocort enemas and canasa, but would like to know by when will I get the befits of imuran?

i have started omez a week back . all seems to be ok except sex drive and loss of mood for sex.

Hi,
I have been on Cilift for anxiety and depression for 13 years. I also have hypothyroidism so am on Eltroxin every day. I have been on Urbanol for a while but it was not helping the extreme anxiety. I was prescribed Seroquel and have been on it for 3 weeks. My anxiety seems to be far worse, especially in the mornings but it does help me sleep at night. Stilnox sleeping tablets were not working. I have a pain in my chest, severe headaches, tingling feeling in my hands and a 'funny head'. I am on Yasmin as I have the Mirena but it does not work. The Mirena is still fitted. I have now read on this site (thank goodness I came across it) that both these cause extreme anxiety. I have now stopped the Seroquel and plan to stop the Yasmin and have the Mirena removed. If you have any similar experiences please comment.

MEMORY LOSS, acne, mood swings, fuzzy mind, dizziness, dry hair, low sex drive, insomnia, depression, feeling like a baby was kicking inside my belly.

I had Mirena put in February 2008 and it is now one year later. I have had such extreme memory loss for several months now that I was really starting to feel like I was losing my mind. I am only 32 and have the memory of an 85 year old. My mind was so fuzzy I almost couldn't function some days. I attributed it to lack of sleep because I've also had a lot of insomnia over the past few months. I started drinking more and more coffee to wake my mind up and get rid of the fuzzy feeling, it seemed to help but certainly attributed to my insomnia so it was a vicious cycle. After reading all the other posts, I am getting it taken out ASAP. I also experienced the dry hair, acne, mood swings and low sex drive. I really hope I get my mind back once it's gone!

I started Topamax over a year ago and titrated up slowly, 25 mg a week until I got to 125 mg a day, split dosing. I was started for migraine prophylaxis. Once it kicked in, it did an amazing job of keeping my headaches away. But, here is something really important: if you are going to have surgery, there are contraindications with Topamax and anesthesia. No one either knew this or told me this and I only found out weeks after I went through a really lousy experience. What I believe happened is that the combination threw my body's pH balance off. I felt like my insides were burning and it was only at that point that I started to experience the severe diarrhea and weight loss, fatigue, and general malaise. It lasted for weeks. All I could figure at the time was that it was just taking me a really long time to recover from my surgery (ovarian cyst removal and unilateral oophorectomy), but that didn't make sense. I felt like I had a horrible flu for weeks. I kept seeing my doctor saying something was wrong with the way I was healing (ie, i had an infection or something). Anyway, this eventually stabilized as I back off the Topamax. I was so weak that I didn't even realize the memory issues or word finding problems, but when I started to feel better physically, I did notice those. That REALLY bugged me. I like to be sharp. So, I tapered off. About 1.5 months later, my headaches started coming back. I decided to try Topamax again feeling that now I understood it much better and could watch it more closely. Maybe this time I could ride out the side effects. Well, this time several months passed at the same dose. My headaches were still there and I had no side effects. We upped the dosage. Still having headaches, but no diarrhea, no weight loss (in fact, weight gain of 15 pounds over the last 9 months since last Topamax round), no real problem with word finding, etc. Up to about 200 mg daily by this time. It has been about 6 months and I have started tapering down and about to give up, down to 150 mg daily right now. NOW, here is something interesting: I just have another surgery, but no anesthesia. It was oral surgery. I did, however, have to take a round of antibiotics. It seems that this round of antibiotics has kicked the cycle into gear because I started having gastric problems, perhaps because of the antibiotics (although in the past, I have not had problems with antibiotics before, ALTHOUGH I did have to take them last year with my in-hospital surgery), I don't know, but I have finished the round of antibiotics and I am still having diarrhea. My appetite is suppressed, and I have lost 5 pounds in this last week. Many people say you cannot lose weight if you stop Topamax and restart it later. That is an interesting. I wonder why that is. Topamax is such a strange drug. Why did it not work for me the second time I took it, or at least for 9 months? Is it just now kicking in with its side effects as the result of upsetting my gastric system? Will it start working now for my headaches, too? I think I will continue to taper off or maybe see if I can prevent headaches on a very low dose. Oh, another interesting thing: I found the first time I took Topamax, it made me feel energized. I found that this time, it made me feel the opposite. I sleep a lot more and feel more sleepy during the day.

I took Yasmin for 2 years and about 6 months after starting Yasmin I started getting migraines at least 3 x per week and sometimes 5 x per week (before not even really getting many normal headaches). I thought it might be my birth control and saw my OB who referred me to a Neurologist who put me on a medicine for migraines. About another 5 months later I noticed I had a small bald spot in my hair line. Saw a Dermatologist who diagnosed it is alopecia. I immediately stopped Yasmin and migraine meds and decided to get an IUD (GREAT CHOICE!) My migraines stopped almost immediately, however my hair loss continues to progress. I now have 3 additionally bald spots on my head and areas on my scalp that are very thin. I feel great otherwise, no headaches, no depression (other than losing my hair), no anxiety, appetite is normal. I'm so desperate to find someone else that has had this specific problem as no one believes the hair loss is connected to Yasmin. I just pray after awhile the hair will grow back. Please if anyone has experienced this same situation please post what might have helped you get through it and if it does ease up! One more thing - I have scalp pain, like burning on the front and top and back part of my scalp, wide spread, not only in the bald areas.

I had my Mirena IUD removed on Monday, May 5, 2008. I had it inserted on November 10, 2005. I was having major side effects from the birth control, and every doc I went to said that there is no way that Mirena would cause the side effects I was having because the "progesterone amounts are too low to cause these side effects". I have had the following side effects:
WEIGHT GAIN
JOINT PAIN
LUMPS IN BREASTS
BREAST TENDERNESS
HUNGER (as if i were pregnant)
DEPRESSION
LOSS OF SEX DRIVE
HAIR LOSS
SWOLLEN ABDOMEN (BLOATED?)
HEADACHES
GROUCHY/ON EDGE
ACNE
CYST (had a couple weeks ago... i was on vacation in Vegas and had a cyst burst.. never had these issues... this was the last straw)
STABBING PAINS IN ABDOMEN AND IN AREA OF OVARIES
PMS SYMPTOMS EVERY OTHER WEEK FOR TWO YEARS
BREAST GROWTH D TO DD
VAGINAL BLEEDING AFTER INTERCOURSE
FATIGUE
TENDERNESS OF ABDOMEN
BACK PAIN
HIP PAIN

As of today, Friday, May 9, 2008 (4 days after Mirena has been removed) I have lost 9 pounds. I am sure this is probably water weight? I am feeling a little better every day. The night I got home from having it removed, I had major mood swings... would be happy one minute and crying my eyes out the next!!! I would not recommend this IUD to ANYONE.. not even on my worst enemy (if I had one). This needs to be taken off the market. It is not safe! I have spent thousands of dollars on ultrasounds on my breasts (thinking i could have cancer because the lumps i had in my breast) and on other doctors bills to figure out what was wrong with me.. only to find out that "Mirena is not the cause"!!!!

I'm only on 10mg Simvastatin and 10mg Lisinopril. I have type 1 diabetes and a minor TBI from a heat stroke. If I stop taking these then after a day or two I will start feeling barely controllable fits of rage. Sometimes I still get angry but for some reason the lisinopril and Simvastatin seem to ease it. I also have hypogonadism. I like my combo of simvastatin and lisinopril in the morning with my 20mg adderall. Little bit of redness on face but the benefits seem to outweigh.

I had a cough for a few days, which didn't improve,my wife insisted that I go to the Doctor to have it checked. The Doctor determined that I was either getting over a slight case of pneumonia, or it was just beginning. He prescribed LEVAQUIN 500 MG for 10 days. I took the first pill in the evening of Feb 3rd. When I went to bed, I was not able to sleep, I was short of breath, my heart rate went to 140, I did not sleep the entire night, my heartbeat was also irregular and I have a terrible headache. The next AM, I went to the Doctor and he said that I should continue with the LEVAQIUN - and that the symptoms were not related to the drug. - I have had and irregular heartbeat in the past, but no like this. The Doctor insists that the LEVAQUIN did not cause the problem. Then he put me on Toprol - to slow the heart rate. I took the Toprol and took the 2nd dose of LEVAQUIN last night. My heart rate is down, but still irregular, I didn't sleep, have anxiety, shortness of breath and don't feel right. Went back to the Doctor today and he still insists that the LEVAQUIN didn't cause this. Thank God that I found this website and others, I have stopped taking the LEVAQUIN. I already feel better, and hope that I don't get any other of the side effects.

Post your symptoms since stopping Yasmin!!!

Hey everyone it's Kay21 here and I just wanted to post my 3 month off Yasmin update. Because stopping the pill is a hard decision, I figured we should all post are updates here to help/support those who are planning to stop or who have recently stopped Yasmin.

I have been off of Yasmin since April 17. As some of you already know, I was experiencing horrible side effects while on Yasmin for 3 years (particularly stomach problems, vaginal dryness, muscle cramps, increased blood pressure and heart rate and anxiety).

The first 1 month off of Yasmin was okay. In fact, I felt the best I had ever felt in a while. My blood pressure and heart rate decreased and the migraines and muscle cramps went away. But when I hit the 2 month (8 week) mark, I felt HORRIBLE. I was severely depressed and anxious. I was crying all the time and felt a severe sense of DOOM! The physical symptoms also started to become problematic. The acne increased and I started growing more facial hair. The worse symptom, however, was that I started losing a ton of hair. I would lose stray hairs all day (probably about 200 a day). Since I have hit the three month mark, the hair loss has gotten MUCH WORSE! Now I am losing CLUMPS of hair all day. I have seen several doctors about this. Some say it's because of stress and a few (a derm, GYN and endo) say that hiar loss is common after stopping bcp. I have already loss about 1/3 of my hair.

I am also really concerned, because I have not had a period since April 22. So my doctor has put me on provera for 10 days to induce a period.

For those who have stopped Yasmin, what have your symptoms been (i.e. increased acne, weight gain, anxiety, etc.). Has anyone experienced hair loss? How long did it take to get a period???

Thanks...

Was prescribed prednisone 10mg dose pack. Took my first days worth and by bedtime my heart was beating so fast it felt as if it was going to pop out of my chest and burst. I went to the hospital and per the doctors there, SVT is not a reaction to prednisone. Anyways, left hospital with a clear bill of health, heart was in good condition.
Now, If it wasn't the prednisone that caused this rapid heart beat, what was it? I really think that the prednisone was the cause but as long as I'm not sure, I fear this will happen again out of the blue.

I've been on Yaz for 1 year now. I've been in a deep depression since September ( 6 months on Yaz) for which I've had to seek treatment. It took 4 months to get me straightened out on medications and still daily I struggle with it.

Also I've noticed right shoulder pain, weight gain (60 pounds), no libido, chronic fatigue, bloating with horrible gas.Is all of this from the Yaz or is it my depression or what? I'm having a really hard time sorting thru all of this.

I am a 19-year-old female pre-med student who has been taking this nasty drug for exacly 1 year now.... The amount I am on continues to change, for my disease keeps returning and leaving remission. I finally get down to 10mg from 40mg, and have to go back up when symptoms return!!! This is SO discouraging. The worst part is, no one understands the physical and emotional agony this drug brings on. I'm 19 and feel like I'm 90. My body aches, my weight is constantly fluctuating, I bruise from simply being poked (being a clumsy person, I look like I am beat!!), my bones feel as if they are about to break, and I am SEVERELY despressed. Being in college and taking rigorous classes, this is just too much for me to handle anymore... My 5-year relationship with the love of my life/best friend is falling apart because of my horrible mood swings.. don't blame him for leaving. I feel as if this drug has ruined my life more than the disease itself...Does ANYONE know if one's body and mind returns to "normal" after FINALLY being off this drug??? I pray to God the answer is yes... I would appreciate someone's reply and/or insight, because my Dr. fails to tell me about ANY side effects until I mention something. PLEASE REPLY!!!

numbness in hands, sometimes sooo bad it hurts and wakes me up in the middle of the night. Anyone else have this expierence?

I had the Mirena device inserted about 3 months ago, because I have some large fibroid tumors, and my bleeding each month is ridiculous. While I've always bled HEAVILY for about 5-7 days, then light for about 3-4 days after that, since the age of 14, it wasn't until last year that I was told about the fibroids. My options were either a hysterectomy or Mirena. I decided to try the Mirena.

The first issue I faced was with the "installation". Apparently, I had an "s" shaped cervix, which made it very difficult to insert the IUC into my uterus. The first doctor spent about 45 minutes trying to maneuver it in place, which from my end felt like someone stabbing me with an ice pick repeatedly. It was horrible. After the 45 minutes of trying, she gave up and said she couldn't get it in. Seeing me on the table sobbing, she asked if I wanted to just forget it, or did I want to bring in another doctor and let him try it. I said I can't have gone through all that for nothing. Bring in another doctor and do what you have to do to get it in. Just get it done. The next doctor came in and repeated another 45 minutes of stabbing my insides, before he finally said he had gotten it in. I had to lay on the table for 30 minutes after that to stop shaking and crying. I would have never done it, had I know it was going to be like that. They said I was just a rare, 1 in 1000 case, that this had happened to. Lucky me.

Well, the bleeding that was supposed to have stopped, instead continued on for the next 3 months. I told the doctor, and she said that was normal, and to give it a little more time. Yesterday, I had horrible cramps all day and extreme lower back pain. I've never had cramps with my periods in my life. The only time I'd ever had any cramping or back pain was when I was in labor with each of my kids. That is what this felt like, and it went on all day. Then, last night, I felt a huge gush of blood start pouring out of me. I ran to the bathroom, and it was like my insides had fallen out. It scared me and I considered going to the hospital, but the bleeding seemed to subside after about 30 minutes. When I got up this morning and took a shower, as I was bathing, I felt the strings protruding out of my body, (which by the way feel like wires more than strings, so now I understand why they asked if the device had bothered my boyfriend). I'm afraid to pull it out, in case my uterus is still attached to it, but I will be calling my doctor this morning to schedule my hysterectomy. So just as I thought, I was in labor, only I gave birth to an IUC instead of a baby. Apparently I'm also the 1 in 1000 person, whose body rejects the device and gets rid of it on its own. Enough already!

I've been having ringing in my ears (tinnitus) which started at about the same time I started taking Lisinopril. Has anyone else experienced this side effect?

I was prescribed tramacet which did nothing for me.. Ralivia was useless.. but Tridural, which is a type of Tramadol, is working for me very well. I take 300mg slow-release tablets every 24 hours. It is, however, extremely dehydrating at first, and gives me difficulty urinating. I used to be up 7 times a night to pee, and then sat there and had to concentrate to pee! I just thought I would ask if anyone else had the following problem with Tridural: I had been taking it in the afternoon, and I was extremely lethargic and sluggish midday when it began to wear off. I also had insomnia at nighttime. After suffering like this for a few months, I finally clued in to what was causing this lack of energy, and I decided to experiment with the time I took my pill. When I took it before bed, I was wide awake at 5am ready to clean the house! When I waited till morning to take it, my pain was too severe to get out of bed, and I was sluggish again (from withdrawal). Finally I set my alarm and took it at 4:30am, and by 7:30 am I am feeling terrific and am full of energy all day long. I just thought it was important to share this since the time of day really made a huge difference to my quality of life.
By the way, I am using Tridural for pain from "Enthesopathy" or migratory polyarthropathy. In my own words, all of my tendons in my body are weak and very painful. I have trouble walking and carrying my little kids, and some days I feel like all of my limbs are broken and I can't even function or be around my kids, they find it too upsetting.

bloody nose (running, dripping blood), thick clots of bloody mucus (both from blowing nose & from coughing)

just started taking Adderall, though i am not prescribed. I went to my doctor and asked for it but she said no. I explained that I am often overwhelmed at work, I am a case manager and keeping on task with all of the work is hard. My doctor said when she was in med school, med students used to take it for that purpose.So anyway i bought 5 pills from a coworker. I seem to have super human energy, get all types of work done and stay focused all day. On the down side, in 5 days I have lost 3lbs., I want to lose weight, but not that fast. I have what I consider to be Adderall hangovers the next day, where I am extremely tired. I also have noticed severe headaches, every day that I have taken it, I crash by the end of the day at work and cant wait to get home, because I am so tired. My neck aches, and I had to change to a firmer chair at work, because all of a sudden my back is killing me, I also get insomnia and have to counteract the Aderall with Tylenol pm just to get to sleep. These side effects freak me out, and I don't know if I want to again ask my doctor for a script, but I get so much done at work, and I am heading back for grad school, I just don't know what to do? oh yeah, the pills that I bought were Adderall XR 30 mg.

Wow its crazy, Ive had my mirena for almost five years, and Ive had every single side effect that these woman have stated. Ive had thoughts that, it could be causing my stomach cramps. But not all these other symtoms. Its really scary to think thats whats causing me all these problems and I have alot. No sex drive pain everywhere, Im always itching, headaches, horrible discharge, Sometimes bleed for no reason. Im ill and depressed constanly, and Ive always been a happy person even when I had no birthcontrol and regular periods and cramps. Ive been dealing with these problems for almost five years and am now really scared I have no insurance or medicaid and want this out of me.

I have had heart palpitations, Tachycardia (heart rate over 100), chest pain, shortness of breath, irritability, low back pain, muscle aches, depression, and nausea. I have had the mirena in for 2 years and didn't realize it was the Mirena until recently. I went to the ER one night after getting out of bed to experience dizziness, numbness in face and arms, and tingling hands and feet. They told me nothing was wrong with me. They prescribed me an anxiety medication and then a medication to slow my heart rate. They are not working. I just hope all this goes away once I have the Mirena removed.

I was prescribed augmentin for an infected cut on my ankle. I took it for 5 days before I started getting some seasonal rhinitis pain. Doctor said I had a sinus infection and switched me from augmentin to bactrim, and also prescribed me flonase for the non-allergic rhinitis. I took 2 bactrim before I noticed drug allergy symptoms. I developed a very itchy rash on hands and feet (worst on wrists and back of ankles). The rash appeared on itching, puffed up for a bit and dissipated to pink/red marks (slightly less itchy).
I also noticed welts (skin bumps) in the soft tissue of the web of each hand and on the inside of each foot above the arch. These are slightly tender. I called the a consulting nurse as soon as the rash started and she said to immediately take a benedryl to keep things from getting worse. It helped a little that night. Went to the doctor and was prescibed hydroxyzine which is like benedryl but stronger and helps with itching. Rash lasted almost 3 days, was worst second day, then dissipated. Welts on hands and feet have persisted for the last few days. Having general aches and phantom prickles in hands and feet, must be healing from the rash.

Doctor thinks this was all delayed reaction to augmentin. I think this was immediate reaction to bactrim. Pharmacists seem to think bactrim too.

Whichever caused it, I have stopped both and only continue on the flonase which seems to help with the sinus issues.

I haven't heard of anyone having the same kind of soft tissue welting/swelling between the thumb and forefinger. Has anyone experienced this with a rash caused by allegic reaction to antibiotics?

I got my IUD placed in about april of 07 i have seen than experience crazy skin problems such as ance i've never had a problem with ance and i'm 25 i have very bad mood changes that are unexplainable now that i have reread the side effects of Mirena i now know why all the side effects began around the same time and now i'm figuring out why! I will be getting it removed. Has anyone else experience really bad mood swings i was so ready to get on depression medications now i'm going to get it removed and will take it from there!!! Please let me know if i'm not the only one