Tendency symptoms and conditions

I have been on Diovan for 11 years. Most of those years, I believe the dosage was 80 mg. About 2 years ago my doctor increased my dosage to 160 and again up to 320. I am also on medication for Diabetes and High Cholesterol. I believe my doctor was over medicating me because I started to experience many different side effects. As a result, I never ended up taking the full dosage of Diovan until October 2008. He also had me on two other medications for High Blood Pressure. Within two days, I felt like I was so fatigued I couldn't move. And my blood pressure wasn't all that low either. My wife and I looked at the side effects accompanying the medications and we concluded I should stop taking one of the medications. A few months later, my doctor added another med to the list. I didn't mind this one and the dosage was low.

In any case, between the 320 mg of Diovan and 80 mg of Atenol I was feeling constantly tired. Getting up in the morning, I felt like someone had given me a heavy tranquilizer. Now I have complained about that feeling for a few years now but never thought it was medicine related until the effects worsened. Then, once I was up, I used to feel good all day long but now I was feeling drugged all day long. Driving the car, I felt tired and questioned if I should even be driving a car. But I had to drive to work. At work, I had trouble concentrating, I was so tired.

My memory was gone. It was like I had a full blown case of Autheimers which came on in a period of about 3 months. I couldn't think straight or remember anything.

Finally, the effects got really scary. My wife and I both have a tendency to snore at times. Since we are getting older, we are developing allergies which makes us snore at night. For my wife, her problems are when she wakes up in the middle of the night and I am snoring so bad she can not fall back to sleep. For me, her snoring is a problem when I first go to bed. In the past, I would try shaking the bed hoping she would stir just enough to move and stop snoring. I really didn't want to wake her up fully to get her to stop. This routine of shaking the bed would go on for about 20 minutes or so. Well, on this one particular night, after about 2 minutes, I got this urge or desire to put both of my hands on her back push with Superman strength so she would fly out of the bed and on to the floor. This bothered me because I do not normally think this way or get this violent.

The next day, I was in a meeting at work. I am not sure what happened but I could tell my mind was going some where scary. I was convinced that I was becoming psychotic! That night, I layed in bed deciding that I was going to stop the medications since I believed they were causing these psychotic thoughts. But I also made up my mind, if the thoughts continued, I was going to have myself committed rather than wait until I hurt someone. Stopping the medication meant gradually cutting back on the dosage that I was taking. I cut the Atenol in half and only took half and it worked. The next day I felt better. But gradually the fatigue would come back, just not the psychotic thoughts. To make a long story short, I kept reducing my meds until I was only taking about 80 mg of the Diovan.

There has been concern that I am heading for Kidney failure so I was sent to a Urologist. He is concerned over my high blood pressure and decided to put me on Diovan HCT 320/45 mg. I figured he didn't grasp my concern about that being too much medication. Oh, the HCT I was on then taken off and now put on because I have been experiencing significant swelling of the ankles, feet and legs.

My doctor visit was June 2, 2009 and today is July17, 2009. I have been experiencing many moments of extreme dizziness. My wife and I were in a store when I bent over to pick something up and near fell. I stood up and a few minutes later, I was conscious of myself staggering from dizziness. Last weekend, we went to a store and I didn't feel right as we head inside. We got in and the store got very bright, colors seemed to lighten and it felt like I was passing out. It was like I was standing on a cliff waiting to fall off. The brightness did not go away but I also never passed out. Also, I had been having lots of headaches since going back to this heavy amount of Diovan. Currently, the last couple of days, I am having trouble focusing. It is as if my eyes are good but my head is somehow effecting my eyesight. Yesterday, I kept having these moments where it was like I was being hit in the head. I kept seeing stars. Oh, did I mention I am only 52 years old? Too young in my opinion to be chalking this up to old age.

My next appointment is August 24th. I am hoping I can make it to that appointment. I think this is too much medication and I am afraid if I don't get it cut back soon, it will kill me.

I am not against Diovan but I do think there is a point where one can be prescribed too high a dosage. And I am at that point. Oh and my blood pressure in my opinion isn't that great for all of this medication. I am concerned that something is causing the high blood pressure and rather than OD'ing me on medications, the doctors should be helping me determine why my blood pressure is so high. Also, I am now on this kick to see whether I can lower my blood pressure through certain foods and diet. Where is doctor Oz when you need him?

Hi All, I am here for the first time in desperation trying to ascertain if my problems are Advair related. I have been on it for over 20 years (started as a study patient). I probably would be dead if it hadn't come along - seriously - and I had been on prednisone a lot. But, to add a voice to what others are saying, I can't sleep, and always wake with the most terrible headache, along with other general aches and fatigue. I was coping so so until I was rear-ended and developed some neck issues. Now I live with never ending headaches and fatigue and a tendency towards depression. Pain killers and sleeping pills get me through the winter months and then in the summer with lots of activity outside I rebound so that I can go through another yearly slide downward. What is really a killer is that I can't get going in the early mornings and have been hassled by my employer who has determined by a psychologist that I am a malingerer because there is little proof of physical illness! If I didn't have a history of having been, and still being, a very hardworking and persistent individual I would think I was going nuts (I'm 60). If anyone has a similar story, please comment further. Thanks

I've been taking Celexa for about 10 years now...in beginning it was 40mg and it took a good 3 weeks to totally be free of the horrible depression/panic/anxiety attacks that came on me like a flood. I was in bad shape when I finally found out what was wrong with me and I was a total basket case for a month before and 3 weeks after. When the drug took effect slowly I came out of this horrible funk. The side effects mostly were sleepiness, loss of sex drive and sensation like many here are experiencing. Gradually I tapered down to 20mg and now 10mg. I don't take it everyday but about every other day and just enough to keep some in my system so that if I nose dive again I up my dose and it doesn't take as long to feel normal. I don't handle trauma, stress or confrontations well and they have a tendency to make me switch into these nose dives. Celexa and dosage works for ME...I believe each one of us has different chemical structures which is why one pill doesn't work for all of us. I think high dosages tend to make you more "zombie" too. I've tried other types of anti depressants and always come back to Celexa because the side effects aren't anything like the others to me. So, please keep trying different meds to see whats good for YOU. If a doctor gives you a hard time, FIND ANOTHER! I suggest a Psychiatric one too. GP's and OB/GYN's aren't trained enough in this area to really know how to prescribe and help treat this and have a tendency to prescribe what they've been given freebies of. Not all Psych's are good either. Keep trying to find the right one please! I know, I've been there. Above all, pray....it helps. :)

My girlfriend and I just got off NuvaRing. The final straw symptoms were an intense burning pain in and around her vagina, extremely low mood, and for me, an itching blotchy rash on the head of my penis.
There were problems with the NuvaRing for her from day one. There was the acne and weight gain, as many people have mentioned, as well as a slight but steady rust-colored discharge. One of the main nuisances of the ring was its tendency to trap semen somewhere in the vagina, only to release it sometimes hours later at incredibly inopportune moments. (Sorry if that's disgusting... Anyone else have that happen though?)
During the second month, the symptoms became worse and more numerous: Pain during and after sex, partly caused by unusual dryness, became a frequent problem. Weight gain and acne increased. And then, in the day or two before we took the ring out, both my penis and her vagina took on a smell which I will describe (somewhat esoterically) as being very similar to that of a good brie after the rind turns orange. In a bad way.
There followed lots of burning and irritation, especially for her, and a general itch which she seemed to have all over her body. She said the pain in her vagina was on par with the worst she'd ever had, coupled with an intense low mood. We became 100% convinced at that point that the ring had to go, and immediately after its removal the symptoms began to slowly subside. It's been less than 24 hours so far, and we're both still calling each other to complain about our genitals, but the bright side is: We're off NuvaRing, the symptoms are subsiding, and we'll never have to go through that again.
As a final note, a message to the women on here who were dumped by their boyfriends because of what NuvaRing did to you: Those guys sound pretty much worthless. Good riddance.

45 years old, female, diagnosed bipolar II in 2006. On Lamictal for 2 years. Initially, very positive effects of Lamictal - felt "normal" and stable for the first time in years. Didn't notice any side effects. Gradually increased from 200 to 400 mg per day 6 months ago as I still experienced mood swings with a tendency towards depression. I have been on 400 mg/day since August 2008. It is difficult to say what are the side effects of the medication, and what are "natural causes". Since doubling the dosage, I experience memory loss and increasing cognitive problems (slow thought process, difficulty putting together coherent sentences in discussions, fumbling for words. I have spent more than one hour on this posting!). I sometimes wake up during the night drenched in sweat. It could be that I'm menopausal, but I find it unlikely. Mood swings have perhaps become less pronounced, but I would like to regain my mental capacity. I plan to cut back to 200 mg of Lamictal - and perhaps some day learn to live with bilpolar II without medication and a lot of help from my friends and loved ones.

I have been on 50 mg topiramate for a while now. It is part of a 5 drug mix used to address bipolar, anxiety and adult residual add. I take the topamax in one dose at night. When I first started it, I DID try to titrate up to at least 200 mg, but never made it past 75 mg. I took it in the morning, and, after about a week and a half on 75 mg, somnolence kicked in big-time and I was a zombie.
My Dr. and I kicked it back to 50, and moved it from a daytime drug to a night-time drug, and I have not really have problems since. It certainly still seems to have some mood stabilizing benefits for me, even at the relatively low dose I am taking. It also has helped with the awful headaches that I used to get far more frequently than I do now. I do not think that I ever received a weight benefit from it, but it seems that most people generally do not at this dose. Late last year, I had to switch to a different physician. Sadly, the new practicioner is no replacement for the former.
I have gained weight over the past few years for a variety of reasons. A somewhat sedentary lifestyle, social and emotional eating, too frequent consumption of caloric alcohol, (once a week or so,) as well as weight-gain contributory atypical anti-psychotic or mood stabilizing drugs have all helped put me in an unpleasant location on the BMI chart.
I have been enrolled in a hospital-associated, medically-monitered weight-loss program for several months and have een successfully losing weight. My new psychiatrist felt that an increase in topamax dose might be beneficial. I am going to attempt moving up to 100 mg, provided that I feel the change is warranted, and that the side effects do not kick in as before. The aforementioned practitioner has a tendency to be pixelated with respect to the approach towards a patient. This person does not seem to put much effort into reading, absorbing, integrating and using patient file information very well. For instance, this physician would miss the importance of the fact that topamax can cause an acidosis condition, and that the hospital diet typically intentionally puts patients on a diet that causes ketosis. These two conditions together would be unpleasant, to say the least. The doctor never even asked what type of diet I was on....
This is not the first time such an oversight has been made on the doctor's part, and it is my own educational background and awareness that has kept me from being the victim of the doctor's inattention and carelessness, not to mention probable nasty outcomes had I followed the instruction without question.
I am fortunate to be educated about this stuff, and so I do not have to rely on the practitioner's judgment alone. I am shopping for a new one, actually.
As it is, I am not on the hospital's most common diet, the ketosis-inducing one, and so I am not worried much about the potential acidosis due to topamax.
( I am not on the ketosis diet because I am aware of the problem such a diet can cause for bipolar disorder management, independent of any drug interactions. I read about this, consulted with the dieticians and weight-loss center physician, and chose a non-ketosis diet. I have been losing weight at a regular pace. the speed of loss is slower than with a ketosis diet, but safer for me. All it demands is better behavior on my part, but that is life.)
But I want to communicate a few things here.
First, I see that many people suffer not only from adverse effects, but also from arguably adverse treatment by physicians who either are not aware of a drug's information, are marginally aware of it, are not aware of their patient, or some combination of the above, or perhaps they just don't care.
There is also a clear tendency for many docs to balk when the patient's experience doesn't fit the prescriber's leaflet, resulting in dismissal of the patient's concerns and experiences, and may lead to arguably unnecessary tests and diagnostics rather than discontinuation of an offending drug.
Be aware that such treatment is indicative of a problem with your doctor, and the relationship between the two of you. Don't allow yourself to be tossed off that way, especially with no resolution to your problem; get a second opinion. Second, topamax is a specialty drug, and should be prescribed by, and treatment should be monitored by, a specialist. namely, this specialist should be a psychiatrist or neurologist, depending on what you ar taking the topamax for. Even if topamax had been prescribed for you for migraines or weight loss, the doctors most likely to be most educated about its main and adverse effects are psychiatrists and neurologists. There are a very few internal medicine or family practice docs who might be "with it" enough to be following the literature on this type of medication. A sub-point to this is a suggestion that education and information can only help you, and you should seek it out. Don't just read about a diagnosis, or about adverse effects, though. You'll run the risk of getting "medical students' disease", finding that your symptoms seem to match the disease descriptions for all manner of ailments. A general education is actually more useful. Text books can be a great help. Where you find something in a text is a bit advanced for you, try a more elementary text. Texts are available at libraries, so you don't have to buy them all. But reading up on psychology, understanding a little about metabolism, having some familiarity with medical terms, such things can save you from the results of a doctor's distraction, disinterest or disdain. It can also be immensely comforting just to understand how one's body works, and how drugs work within it, when one must face a disease such as Bipolar, Depression, Anxiety, Diabetes, etc. College intro level classes are thorough enough to demonstrate how a 25 mg pill can cause such disruption or such relief in a person's life. Eating certain things, and at certain times, sleeping well or poorly, ambient temperature, hygiene, reading habits, ALL of these things can have a profound effect on a person's day-to-day life. All of those factors, and more, can effect the physiology of an individual. It is good to know a little about how the system works, the better to maintain it. Some pop-sci books are pretty good, too. "You: The Owner's Manual" for instance. But some may read such books and find themselves wanting more information, and this is where any number of college texts about anatomy and psysiology, neuro-physiology, psychology and physiology, metabolism, diet and nutrition, genetics, etc. will come in handy. For those with insatiable curiosity and a deep desire to understand and manage a given disease or condition, there are usually medical texts available specifically covering THAT condition. For instance, those with Bipolar might wish to read at least parts of the text Manic Depressive Illness:Biolar Disorders and Recurrent Depression by F. Goodwin and K. Jamison. This text covers most of the meds those with bipolar would be interested in, it surveys the research done to date, what is known about combo therapies, adverse effects, including hair loss and weight gain, it covers patient experiences, as well as physician descriptions. One of the co-authors, for those who do not recognize the name, is not only a top researcher of affective disorders, but also suffers from manic-depression. The text is almost a good a friend as a patient could have, especially if your own physician is lacking in knowledge about your condition.
Third, several posts express a desire to report adverse effects, as well as doubt that a given personal physician would do so. If you have suffered from adverse effects, and want to report it, you do not require your doc, family practice, psychiatrist, or whatever type, to do so. There is a government website available for the reporting of adverse effects, and it is available to consumers, too. The report data goes to the FDA, which sorely needs such reports, as the drug companies are less than honest with THEIR submissions of information, and the dissemination of research data leaves much to be desired when it comes to the publication of information that is less than glowing about any given drug. I believe that you can find the reporting website on the FDA's site, or some link there. I wish I could recall it here for you.
Fourth, topamax, like most complex drugs for complex diseases and conditions, will affect each person very differently. Some will have little or no problems with adverse effects, while others will find the drug to be anywhere from uncomfortable, intolerable to damn near, or actually fatal. fatalities have occurred with topamax, as they have occurred with almost all, if not all, drugs. There is always a risk for adverse effect, sudden sensitivities, allergic reactions and other wonders and horrors of medicine. This is the nature of it. You have a bad reaction to anything that your body comes in contact with at any time for reasons we do not undrstand and can not even yet identify. Your typical cough syrup could, without warning, suddenly produce in you a rash that could kill you. But the conditions and diseases that drugs treat can be just as awful, and leave us with no option but to take the drugs to survive. Most experiences are not so extreme. For those that are, the greatest sympathy. But just because one had a bad experience with a drug doesn't mean the drug is wholly bad, evil, toxic, or should be banned, or that the drug company should have a class action lawsuit lobbed at it. Drug companies are NOT, in general, being fully honest with their disclosures. But banning a drug because some people react badly doesn't address this, nor does it do any good for the segment of the population that benefits from the same drug with little trouble. I have had very bad experiences with some drugs, but do not feel that these medications should be banned. i know other people who depend on them, and I would not deny them just because I lots hair, gained weight, experienced akasthesia, etc. The individual reaction to a drug requires, sadly, at this time in history with our very limited unerstanding of pharmacokinetics and pharmacodynamics, individual trials. And those trials will often have their share of troubles, too. That is how we find out what works for us and what does not, and that is where we re right now. Maybe in two or three decades, with better understanding of genetics, genomics, epigenetics and related fields, we will be able to customize our cocktails with less trial and much less error. I would love a day when a blood test will tell us who will benefit the most from which drug while having the least adverse effects. I hate going through trials. right now, what I am taking is working without giving me problems. For that reason alone I may decide to NOT try and increase the topamax as my current psychiatrist would like. After all, she wants to increase it so that it might help me lose more weight. I am already losing weight without the increase, and the increase might bring adverse effects, or the additional topamax could simply destabilize my currently very stable mood. The last would then require me to go through another dreaded drug trial to find a new cocktail, a mess I have not had to endure for nearly two years now. I do not think that, for me, the additional POSSIBLE weight loss benefit is really worth the possible adverse effects. The doctor is rather casually experimenting with my life, probably curious to gather more data about topamax's efficacy as a weight-loss drug. I am not so sure that I want to rock my boat. I get the benefits from topamax that i am interested in, mood-stability and headache prevention, from the 50 mg that I already take. I'd rather not exp-erience what most of the posts here have described for adverse reactions, and I most especially do not want a rather casual, needless sort of medication modification to set off a chain of events that results in mood destabilization. That said, I am glad to have topamax available for me to take, as I am fairly sure that it contributes to my cocktail, turning down the amplitude of my highs and lows at a mere 50 mg per night. I would be sore to lose it, and do not want it banned. But I do not think I would want to take more than I am taking now. The somnolence I experienced in the past at 75 mg was not comfortable, and was the type that prevents any meaningful work from being done, anything from reading to laundry to following a conversation. I would not like "pins and needles." I hate it enough when I hit my elbow or when my foot falls asleep! And I really hated akasthesia that I experienced when I tried ability, a drug that made me right sick, but that I know absolutely saves others from oblivion, like my grandmother. I hate the adverse effects, or the experience of them, but I do not hate the drugs. and while I may dislike the drug companies, it is not just because drug have adverse effects, it is for the more perverse behavior of the companies themselves. One still has to try and be, if not positive, rational about one;s experiences. It is healthier to see experiences with drugs as learning experiences. Not everything in life is fun, but try to make everything have some value in experience.
I wish you all better days, and calmer, too. May you all find good and caring doctors, and develop excellent therapeutic relationships with them. May you know your diseases and conditions, own them, control them and thus conquer them.

I was prescribed Zocor approximately 1 month ago. I began taking the Zocor and immediately on the first night I had slurred speech. It went away after two nights...but I continued to have horrible headaches for about a week. Finally, I thought I was in the clear. After about 3 weeks, I had a little spasms in my left leg...from the foot to the hip. It went away...and a few days later it showed up in my right leg...from my foot to my hip. My right knee is currently on fire...and I can't walk really well. I have a tendency to dray my right leg behind me. It gets better after a period of rest, but as soon as I try to walk...it's back again. I stopped taking Zocor a few days ago, and I see the doctor tomorrow.

I've been on Celexa for a few years now. I have very mixed feelings about the drug. I experience bouts of dizziness, brief periods of blurred vision, a tendency to fog out, I'm tired more often than I should be. I have a feeling of being numbed. However before celexa I had terrible insomnia, to the point where couldn't work. Tears were pretty much a daily experience. I've had a lot of therapy in the last couple of years or so and I think it's time to start weaning myself of the drug and see if I can face life without it. Stay tuned...

I've been on synthroid now for about a year. My dosage is VERY little (0.075). My doctor keeps running blood tests every 3 months and assures me I am within the "lower-end" of the norm, but I still feel tired, sleep deprived, wake up with night-sweats and I keep gaining weight...

I am only 24 and have just been told that I need to take this medication for the rest of my life, it\s pretty depressing. I keep asking if there are other ways to lose weight and feel more energized. He tells me that I need to keep taking this medication and has put me on a "sleep hygeine" routine where I go to bed and wake up at the same time every day.

Does this "disease" mean I will always be overweight and tired for the rest of my life? I would like to know if someone else with more experience with this medication can give any sort of advice? Feeling a little hopeless about it and not really interested in complaining to my doctor anymore.

Thanks:)

I have been on Lamictal for about five months for bipolar II. I has been increased slowly over these months and I am now up to 300 mg a day. I have a tendency to sometimes forget things but remembering numbers has never been a problem for me. In fact I can look at someone's tag number driving down the road and remember it for days. Phone numbers of people I have known for 20 years would stick and I wouldn't even have to call them on a regular basis to know the number. However, recently while trying to use my bank debit card at the store I was asked to enter my PIN number and totally could not remember. I tried it several times but it never came to me. I felt like a fool!. At this time, that was three days ago and I still cannot remember it!

This is very, very distressing to me. I feel like something has been wiped clean and that I will never get it back.

My Lamictal dose has been increased in the last couple of weeks and I thought maybe Lamictal or one of my other meds could be making this happen so I started researching and found this site where other people were complaining of memory loss while on Lamictal.

Headaches are another common side effect for me while on this med. It has really helped me emotionally and I need to know if the memory loss is just going to be a temporary thing and it will get back to normal or if I will be forgetting more and more over time. PLEASE HELP!!!

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

I have a three year old son who has severe allergies. He's been taking singulair for 2 years on & off just in the allergy season. He started taking, singulair again in the beginning of April. One morning he woke up and both eyes were really swollen and red, I called his doctor's office and told them i thought he had pink eye, after 2 different drops and no change I brought him into the doctor's to see if it could be his allergies, and they agreed and started him on Zyrtec. I still was not impressed with the results so i brought him back yet again to see if we could see a specialist. Instead they put him on nasonex to try.
In the beginning of March I started to see a change in my usual happy fun loving son. He was scared to sleep in his bed, waking up in the middle of the night from bad dreams, uncontrollable screaming fits that would last up to an hour, saying he wants a Boo Boo. At first we thought it could be jealously over his new brother, or maybe something at his school.
Then i found this website and everything clicked, how scary it must be for a child to have these horrible thoughts and not be able to understand or stop them. What are the people at merck thinking??
Can any one tell me when the symptoms stop. He's been off for a week and we see some improvements. But he still has these fits with almost an OCD tendency to them (mainly when he's overtired), stomach pains, lack of appetite.

hello all, i've been reading your stories and feel i need to write mine too. i started taking Yasmin about 4 months ago. and i really do not know what to think. i haven't put any weigh on or got acne (which were my worries) and my periods got very light and completely pain-free. i did have constant but mild headaches (which i never have) and my sex drive has gone down (never had any problem before). more importantly, emotionally i am feeling terrible. i cry non-stop and i feel totally unstable. I am going through a lot of changes in my life (change career, country, new relationship, etc) so i thought i could be just that i am feeling stressed. but i think this is more than that. my anxiety has rocketed, I never felt like this before, I have racing thoughts almost constantly, panic attacks, and something that i think it's called 'depersonalization' - has anyone got anything like this? it feels like you're looking from outside yourself, if that makes any sense...not nice at all.
as I have a tendency to feel anxious anyway I really don't know whether the pill is causing this or not, but i feel i am going mad. as i read the postings i became more worried that it might be Yasmin
i went to the doctor who suggested to carry on for a few more months to see if the symptoms go away. i followed his advice (as those days i was feeling surprisingly well, and was optimistic about it) but i am still very concerned.
also, has anyone had a really bad depression/anxiety attack when taking antibiotics + yasmin? i could have killed myself that day. felt better when i stopped taking the antibiotics.
again, is it my mind...? or is it Yasmin...?
any comments would be really great

I felt suicidal and got migraines/nausea/vomiting when I was first started taking Lamictal. Then I was on a steady dose of 100mg and I felt better than I've felt in my life with no other side effects except the tendency toward minor skin irritations. I've just gone up to 150mg just to see if that's better, but I'm having suicidal urges, migraines, nausea, vomiting. I expect that will clear up soon and then I'll know if this is a good dose for me.

My psychiatrist warned me about feelings of suicide as a possible side effect. She also told me that as the dose goes up, mental disorganization increases. So we're trying to find the right balance of anti-depressant effect and spaciness.

Hello everyone! Well I started with Loestrin 24 January 2008. I have previously used the ortho evra patch & the NuvaRing. I decided to try bc in the first place, because I had extreme periods lasting more than 9 days sometimes 13 days every two weeks. I tried to stay away from pills in general mostly because I have a tendency to forget to take them. Once the other methods failed to control my periods, I decided to to try the pill. The first month I got that really weird brownish discharge type period then a couple of weeks later, during the white pills I got very heavy spotting to a light period for almost a week. then the normal period. After that my periods are amazing! a few days, very light & hardly any cramping. that only lasted a couple of months. Now I have very ugly acne on my face, back and chest. I have gained about 10 lbs & I am always crying! I found myself just running home to lay down just to get away from people... I am going to finish this trail & discontinue the pill. Hopefully my heavy irregular periods don't start up again right away.

My son is 8 and he has been on singulair for at least three years, maybe four. When I heard about the side effects a few weeks ago, I stopped his medication right away. I have since learned that it should be tapered off, but won't put him back on to do that. He had so many of the depression, I hate myself, everybody hates me, facial tic, stomach ache symptoms . . . Now he is almost two weeks off of singulair and he is throwing screaming fits, kicking, threatening, uncontrollable for up to two hours and more! Is this a side effect of coming off of the medication? Has anyone else had this experience? Please email me at amy-weaver4@sbcglobal.net - I'd really like to hear if anyone else has experienced these symptoms. Thank you! Amy

This is in answer to concernedcitizen. My son, when he began to have behavior issues, was placed on Tegretol, Wellbutrin, and Abilify. He could not tolerate the Tegretol. So he stopped that. His "depression" seemed better so they took him off the Wellbutrin, he continues to be on the Abilify. We tried to take him off of that once, it wasn't pretty. His anger, frustration, rage, crying, depression, etc all came back....of course he was still taking the Singulair. (little did we know then....) We see his neurologist very soon. I am going to ask about trying again to remove the Abilify. My son is 7. He was started on these meds 4 months after having surgery to remove a cyst in his brain....we thought all the problems were just who he had become after having brain surgery. It was very depressing. I read all of your research with great interest. I had thought it had to be a something in the brain being triggered. My son had a tendency toward these things due to the location of his cyst....we had the "luxury" of knowing he would have behavior problems. So did his doctors.... Now with all the research it would seem someone like my son, who has a cyst in the left temporal lobe (a region that controls behavior) should not have EVER been placed on a medicine like Singulair. At the very least, he should have been taken off that medicine, before being placed on anti-psychotics. Good Grief. Thanks again for all your work. I will be taking some of the literature with me to the Dr. As I am sure others on this board will.
By the way - My son has been off Singulair for 10 days now. He is a very happy boy. Downright giddy. He is annoying his sister to no end. Dad and I are enjoying every blissful minute.

Guys, as an explanation: Birth control pills work by using hormones to basically trick your body into thinking it is pregnant. When your body thinks it is pregnant, it stops releasing eggs. This "trick" prevents you from getting pregnant. The problem with this is.. your body thinks it is pregnant, and you can get some of the side effects.
I've tried a variety of pills over time. I think the different pills just affect each person differently. The doctors usually ask you to wait 3 months to see if the symptoms settle down. If they don't, or if it really bothers you too much to continue, call them up and tell them what's going on! They can switch you to another pill.
I had endometriosis and have to be on the pill. If I didn't have this condition I wouldn't be on any birth control... it has never agreed with me and I have had weight gain every time (more or less depending on which pill). The only one that worked for me for a while was nordette. That said, after waiting through weeks of nausea, I have adjusted to Loestrin, and like it. I am waiting to see if the weight gain tendency goes away, as well..

I take 5 diff. drugs and am trying to figure out which side effect is associated with which drug. I have a really shotty memory now where I have lost perception of time. I thought I had spoken to my friend two weeks ago and I spoke to her two days ago. I read the news all day at work and can't remember any of it. This could be from the Ativan, Ambien, Lamictal or Provigil that I am also taking, but I have no idea which or if its the combo of a few. I am on all of these drugs because i have Bipolar 1 disorder. I take 160 mg of Geodon at night. Also, horrible facial paresthesia and insomnia. Does anyone know if this drug causes memory loss?? Thanks

I barely got off the pill Microgestin, because of the weight gain and water retention, to have Mirena inserted the beginning of July. It has been nrealy 3 months, and I am still experiencing back pain, water retention, and my chin breaks out with acne every once in a while. I also have been experiencing moderate cramping and a constant slight feeling of being bloated. I was told when this was put in that weight gain was not one of the side effects, weight gain being the main reason for getting off the pill. I have not lost the weight, and it could be a combo of the pill slowly dissipating, or the Mirena does cause weight gain. Anyone else have the weight gain or slight increase in tendency towards water retention??

I am a 55 year old male, active and mostly physically fit. I have been taking Singulair for 10 years and my asthma has been reasonably well controlled most of the time. Already after 6 months of taking the drug I noticed a tendency of easy bruising, fragile skin and bleeding but my doctor never thought this had anything to do with Singulair but rather because of my prolonged usage of steroid creams for my eczema. However, the bruising never seemed to coincide with the areas of my body where I had mainly used steroid cream. About three weeks ago I decided to stop taking Singulair and I also discovered that bruising and bleeding are mentioned as possible side effects of the drug.

After I stopped taking Singulair I have not had any further bruises and my skin seems stronger.

I am new taking Lipitor. My doctor recommend me to take 10 g of Lipitor everyday after having some medical exams that reveal a tendency for high colesterol. Really I am on the limits so my colesterol is not so high. I have been taken it for almost a month buy I am now experience a loss of balance, I feel like the floor is moving... So after reading the side effects Lipitor can cause, I have decided not to take it more.

I have a tendency for high blood pressure, and due to several major stress factors, I knew my pressure was high & I was having anxiety attacks & not sleeping & migraines. It was my pressure. It was like 137/100. My heart rate was fast. I'm 41. I started ToprolXL 25 mg & really felt better for a couple months. No more headaches. I did, however, always think I'm hypoglycemic or perhaps diabetic. I feel like I need to eat sugar with this med. My scary problem is that I decided to lose weight & started working out at a much higher intensity than my normal walking. I feel REALLY weird. It's like this med is fighting your heart rate when you work out & I feel like I need major sugar. I feel like my heart is swishy in its beats. I'm calling dr tomorrow to get in. The warnings do say that when you are diabetic or hypoglycemic, this med could mask it, but I feel like my blood sugar feels lower taking this med. I also feel like I still have racing heart, but I was under terrible stress & running around when these symptoms started like 2 or 3 days ago.

I am on Lipantil (Fenofibrate) 267MG and Ezetrol (Ezetimibe) 10MG.
I was on a 20MG statin but changed to the above because it didn't agree with me.
Has anyone noticed a tendency to suntan more easily?
I look like I have been under a sunlamp, my face being noticeably browner than the rest of me yet I have not spent a lot of time in direct sunlight.
I believe the Fenofibrate may be the cause of greater photosensitivity.
Should I worry or just be pleased I look browner?
Anyone else noticed this effect?

i recieved 3 kenalog epidural injections for herniated disc, 2 weeks apart, followed by a decompression nucleoplasty, also with Kenalog injection. after the first epidual. i began having extreme irritablity which i reported to the pain management doc. he said he couldn't prescribe anything but could refer me to a psychologist, which i declined , realizing i was having a reaction to something. after the 3rd epidural, my irritabilty had increased to the point where i was shouting and screaming, and had completely lost my patience. my face had blown up, and cheeks were hard to the touch, and my neck skin was swollen and hanging down. i described my appearance as "looking like a blowfish".

on the day of the nucleoplasty, i agreed that the doc should go ahead and use it again, since it was important for the procedure, and it was not a "true (anaphalctic) type reaction.

after this last injection of Kenalog, i had a terrible terrible reaction. my face became even larger, with big dark circles under my eyes, and my eyes partially closed, appeared like slits. i was frightened by my reflection in the mirror.

my feet, ankles and legs swelled up to the point where it was painful and difficult to walk.

i also i developed insomnia.

at the same time i was "off the wall" with irritability, anger, impatience, and could not stop crying.

during the day i had a general ill and sleepy feeling, and fell asleep driving, without notice.

throughout this period of Kenalog adminstration, i also had flu like symptoms every morning. sore throat, laryngitis, loose cough, muscle pains. i noticed black and blue marks on my extremities as well.

now i have a full blown flu and full blown bronchitis, and i feel so very very ill.

my feet and calves, hands and fingers are experiencing very painful cramping, intermittantly throughout the day and night. it's happening right now in my left hand, so i have to stop typing. i wait for one minute and try to continue typing, but that causes the painful spasm to return. i try again 2 more times, waiting a minute in between spasms. finally it stops and i can continue typing.

there are probably more symptoms, like the irregular heart beat, and these little bumps on the skin of my right cheek, but i need to rest now.

generally, i feel sicker probably than i can ever recall feeling in my life.

would appreciate hearing from anyone with similar symptoms, and especially how long before my face returns to normal. i live with the fear of what will i do if it does not?