Brain symptoms and conditions

My daughter is 11 years old. In Nov 08 she received her first Gardasil shot, she did okay at first just some very mild tenderness at the injection site. Just two days ago, she was just lounging around the house and a substantial chunk of her hair fell out! Of course she was devastated and I immediately called her pediatrician. The on call doctor did not seem concerned and didn't' provide any useful information so I took to the internet. I found photos of Alopecia Areata that looked EXACTLY like the bald spot on my daughters head, same shape and size. I searched for a couple days and racked my brain trying to figure out what caused this to happen to a healthy, athletic 11 year old, then I found this website. Although none of the other sites even mention hair loss as a side effect to Gardasil, I now realize that it has occurred in many. I am connived it was the Gardasil that caused this.

I have been on wellbutrin for about 4-5 years.I thought it was a God send..I was feeling so good and had so much energy at first..then recently Im having a lot of memory loss..thought it was due to getting older,kinda normal..but it has gotten so bad..I cant even remember what I had for dinner,or remember names,or even a conversion,Im having I just forget it in the middle of talking to someone,I cant even read,seems like I read the same sentence over and over...Its gotten to the point my family members,including my own kids are noticing it,I feel like Im dumb,or not even capable of anything anymore.I have gone cold turkey as of Dec.31st..I hope I can have my memory return...I even got so scared,I had an MRI on my brain..thats how bad I am.but it came back normal.....what can I do?..I also suffer form hair loss..I have short hair to begin with,I hurts when people just stare at your thin spots,and know what there thinking.
mgd761

I began taking Lupron after I was diagnosed with endometriosis last November. For the first six months, the side effects were minimal. I never had hot flashes and didn't really notice a change in my body. The last six months on the drug I noticed significant differences. My hair started to fall out in clumps and I had trouble concentrating. This past October I had a total hysterectomy because the Lupron was not working. Today I feel like an 80 year old woman. I can't concentrate, my brain is in a constant fog, and I feel like I have Altzheimers. I can't remember anything and it is a major inconvenience. I have suffered from depression for most of my life. However, I believe this drug has worsened it to some extent. All day long, constantly I am battling negative thoughts. I have constant reminders of every little thing I've ever done wrong in my entire life. Recently I've started hearing whispers like I did when I suffered from post-partum depression. I've also been getting headaches every day but I don't know if these are related or not.
It would appear that I'm going to have to seek out a professional to deal with the voices. This is a side effect that I was not expecting, especially not after several months of not being on the shot anymore. The thing that bothers me is that I took the shot every three months for a year. It did nothing for me and I had a hysterectomy anyway. This is something to consider if you are debating whether or not to have the injection.

I was using every excuse possible for what I have been experiencing. I started NR in May, now it's December, I was scheduled to take it out. Since I started I noticed acne, which I never had even in my teen years. I blamed it on the towels in the gym, stopped using those, then on the sweat from workout... kept trying new acne treatments, but acne magically disappears during the ring out days. I'm not sure if I can call depression, what I felt, it was like I'm never happy with anything and many days in a month my thoughts were very dark, unhappy. I noticed serious decrease in energy, blaming it on 2 children, but my son was a year old when I started NR and I had more energy before with newborn and a toddler daughter. Again I thought, he's so active... I have hard time getting out of bed, sometimes sleep is ok, sometimes no sleep for hours, but this happens to many people. night sweats I was blaming on the blanket, the thinnest one we have(my husband uses 2 at night), I was waking up many days in a month drenched in sweat. No discharge, yeast infection for me, lower sex drive. Even more interesting- I noticed the smell of my partner to be less attractive... Then I read in a magazine that BC messes up with the smell as well. I had horrible headaches, feeling I'm going to pass out< dizzy< especially if I was trying to rush(blamed it on rushing too much). I was growling(like my daughter said) at the kids with the smallest mischief, it's like a little bomb heating up and bursting in my head, I felt rage, not anger, total rage.Life has lost any appeal for me, this is not living, just suffering, I thought all the time. But here I am at home with two little children, hardly ever see friends, always doing work around the house, laundry. Hot flashes during the day are frequent and I feel like I want to tear my clothes off. Recently I started to have a lot of pressure in my chest, like it's hard to breathe. Just last week I almost went to the ER, because I was laying on the couch unable to speak out loud, just whispering, could not move. Then couple of days ago my heart started to ache, it aches now, so last night I looked up the side effects of NR, because I didn't even know where to start with this condition, that has all these symptoms I have been listing. I was planning to go to the doc for all the test. My stomach has been hurting slightly in the last 3-4 weeks(I thought it was food, but no one in our family had any problems). I am 28year old in great shape(I cut back on my food intake to keep th weight the same), I work out 2 times a week and have a very active lifestyle. My relationship with my husband is great, my children are well behaved for their age, So I'm stopping NR before I get divorced like some other women did. If you want to try NR go ahead, it's really convenient, but be aware of all these side effects, so you know, it's not something else, before it's too late.

My three year old daughter was on in as a baby and it was great for her asthma. I stopped it for a year and now she is 3 and has started it again about two weeks. She sleeps at least 12hrs a night and has a nap. This is someone who slept maybe 8hrs a night and never a nap. Actual the sleep is so much its kinda worrying me. I have a hard time even waking her up. What should I do?

My doctor prescribed 25 mg Topamax every evening for headache prevention. I had headache and nausea for several days before starting the Topamax, then after starting the Topamax, the headache pain got worse and I also had pain in my back and ears. I did not get the tingling in extremities but noticed some decreased sense of feeling in my face for a few hours after taking the medicine. The pain got progressively worse then I became depressed and suicidal. I was convinced my life was so bad that I wanted to die. I take 100 mg Zoloft daily for depression and still feel a little depressed and was hoping Topamax would help with this, too. I took Topamax to help with headaches and depression and it made both much worse to the point where I was seriously suicidal. I stopped the Topamax after only 5 days and the pains and nausea have gradually decreased to the point where today I have been virtually pain free most of the day for the first time in 2 weeks. I read on the internet that there is an increased risk of suicide while taking anticonvulsants, but it's rare. I am convinced I am one of the very unlucky people who becomes suicidal on this medication. I have 2 beautiful children, a great job, excellent health other than headaches and depression, and plenty to live for. I still can't believe that less than a week ago I just wanted to die and didn't care about seeing my children and family ever again or ever getting back to my job that I love. It's so hard to believe a drug can cause that kind of thinking. I'm pretty sure my doctor doesn't think the Topamax caused me to be suicidal and has no intentions of reporting my case to anyone. I suspect it's not as rare as they say to become suicidal on this med, it's just not reported enough. I wouldn't be typing this if I were still taking Topamax because I would be lying in bed suffering in pain, sleeping, thinking about how good it would be if I would just die. I went for a CT scan of my brain soon after getting off this med and I remember thinking that I hoped I had a tumor or anurism so I could die. I found out today I don't have a life threatening illness and I am happy about that now and can't believe I was thinking such bad things only a few days ago. I hope doctors take more care in prescribing this medication to people who have a history of major depression because I'm afraid people are going to feel like I felt and kill themselves on this med. I think this drug is great for some people and should be available, but people need to be warned that they may become suicidal and given instructions on what to do if that happens. I had no idea if I should go to the ER or call someone or what, so I just got people to watch my kids and called in sick to work and stayed in bed for a few days. I don't miss work often and am very committed to my job and my children are first in my life, so not being able to care for my kids or go to work made me feel so much more depressed. My doctor referred me to a neurologist and I hope to find some way to get relief from the head, neck, and back pain and the nausea. A few days ago I thought I would kill myself if my doctor couldn't find what was wrong with me and I felt terrible for no reason. Now I have hope. It's just not right that a drug can take away the ability to have hope.

My 3 year old is on 5mg of singular daily for her constant allergy issues and has had NO trouble at all with it. Her personality has not changed.. she's happy, outgoing, friendly and MUCH better than she was before she started the medication. Prior to starting she was constantly dripping from her nose, she had both ears filled with fluid, had bags under her eyes and was tired and grumpy all the time, due to allergies we could not get under control with other over the counter or prescription meds. Since being on Singulair she's been 100% better than she was. I'm sad to hear that others are having so much trouble with it, but I can say that I am happy my little girl is feeling better.

When I got the shot (a large dose rescue) I got terrible otherworldly type pain in my left leg and ankle. My theory was that my tissue there was damaged from a recent car reck and dragging a huge limb up a steep mountain. I think the prednisone helped focus on the tissue damage somehow...make it available to my brain as PAIN LOL....

I had my thyroid out due to cancer on 1/22/08. then because of having to take a high amt of levoxyl (synthetic thyroid hormone) I was put on metoprolol for the palpitations. I recently had more surgery to take out cancerous lymph nodes in neck and my dose of metoprolol was increased from 25 to 50 mgs. I was only on 50 mgs for about 4 weeks when I developed depression, insomnia, swollen belly, acid reflux, swollen legs and anxiety. My mind started to go off on me and I had convinced myself that the cancer was in my brain and that's why I felt like I was dying. I was told by my doc that this med does not usually cause depression. I went over the facts and realized I felt pretty good until I started taking this drug. Even on the 25 mgs my legs which are really skinny, started to look like lumpy cottage cheese but I figured it was due to the thyroid removal. I didn't take it at all today because I just want to be rid of it. I know I need to wean off but how long do I have to?

I got my Mirena fitted 5 weeks ago. After the 1st week I could feel myself starting to become really low, my head began to get ‘foggy’, total lack of motivation and the headache from hell. This peeked at 3 weeks when I became very depressed, snappy, anxious, extreme tiredness, tearful, severe headache and an inability to concentrate – my brain felt it had no depth to focus or absorb anything. I also felt I was standing on the outside, looking in! I had a similar but far milder reaction to the POP so recognized the symptoms immediately.
I went back to the doctor and tearfully explained how I was feeling and how I was convinced it was a reaction to the Mirena. She totally dismissed this and said she felt there was a lot more to it than that and started talking about PN depression. She also said that in the 16 years of fitting the Mirena she had never experienced anyone with these symptoms. I assured her I was not suffering from PND, but in my ‘fragile state’ wasn’t capable of arguing my point and began to wonder if she was actually right, so what a relief to discover this web-site! I also found a great document issued by the New Zealand Medicine and Medical Device Authority, a Government Agency (http://www.medsafe.govt.nz/Consumers/cmi/m/Mirena.htm ) acknowledging that all the side effects I was experiencing were all common occurrences in between 1 and 10 in every 100 patients – it also acknowledges virtually all the other symptoms everyone else is listing and states that ‘These side effects are more common during the first months after insertion’- so why wasn’t my doctor prepared to accept these symptoms when they are officially recognized in other countries? Are the drug company bonuses more important than patient health?

Anyway, 5 weeks on and my mood has lifted, deep down I still feel low, but my normal self is sitting on top of it. I still want to snap at the kids, but I can control the urge to do so! My head is still foggy and I still feel detached from everything, the headache is still there and I still can’t concentrate / absorb anything! My fingers, knees and wrists now get really stiff / sore and the back of my neck aches when I wake every morning. Fortunately, I haven’t had any cramping or much spotting.

I am due to get it checked in 1 weeks time, but have decided to get it out and hopefully get it replaced with a non-hormone coil. Heavy periods seem great compared with how I’m feeling right now!.
I can’t wait to get back to my old self!.

I messed up my own Amoxicilin prescription (I kept missing the third dose since my brain is wired to take meds 2x only). So I took all of the pills but they weren't as effective and of course i relapsed and got put on Avelox.

Now, during the Amoxicilin mess, I was told to increase my prednisone from 2.5 mg to 20 a few days later is when I get the Avelox. The first two doses went on without a hitch but I just took the third one about 3 hours ago and I can all ready feel the tremors throughout my body. My mom says its medication induced low blood sugar and I should be fine if I get a glass of juice and go straight to bed.

But I have an auto-immune condition and am now worried about whether or not all of my meds do in fact go together - and yes there are a lot of them. I've decided to go to bed and see if the symptoms are still there in the morning. So now I'm even more anxious about taking dose number four, especially since I'm supposed to go back to work on the day of the last dose.

And, yes, I asked the pharmacist about why prednisone was on the precaution list and he assured me that the side-effects would be minor if anything at all.

My heart doctor had put me on toprol xl for my heart arrhythmia but I was also having really bad dizzy spells and feeling like I want to pass out before the toprol.I did pretty good on it for a good while.then out of no where the dizzy speels started back up and feeling like I want to pass out.Had all the other tests and nothing abnormal was found.But I'm still having the same problems.I had done an oxymeter test and found that I was only getting 79% oxygen to my brain.Then was put on an oxygen concentrator.It worked for a short time but the symptoms came back.So I called the doctor Friday to see if I could quit taking the toprol.They you can't quit cold turkey cause you could have a heart attack.That's scary..And I'm a 44 year old female.I'm not quite ready to go just yet.Especially from quitting a medicine.

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

im 17 and started Yasmin when i was 14 maybe 15, it made me so sick, id start throwing up about 8 hours after taking the pill, and that would last for about 5 hours, (like having mild food poisoning). I got heart palpitations every minute or so for days on end, and unbearable depression. I was the happiest person until i started taking this pill, and its so bad that i couldn't enjoy my life properly. Now im tiny, like really really thin mums worried i have anorexia, and although my life is perfect (great friend, good grades, nice boyfriend), I cant enjoy any of it properly. I went off it about four months ago and my happiness returns now and then like it used to be three years ago, but my mind feels so fuzzy and sort of disorientated, and i cant seem to convince myself of things properly. I was wondering if these things get better and better or am i stuck like this???
plz help xxx

I took Wellbutrin 300 mg for two years before to quit smoking and for mild depression. After the initial (weeks 2-4) side effects of nausea, dizziness and headaches - I felt great. Not drugged and not overly emotional. I had been crying all the time and felt hopeless. I felt much better (and didn't want to smoke at all). I quit it for about 2 years and now I am back on Wellbutrin for the last 7 months. I started with Cymbalta - but hated the loss of sex drive (not able to orgasm - so who wants to have sex, right?) and felt drugged. So Wellbutrin was a welcome "old friend" I didn't have bad side effects with switching and have been pretty happy. EXCEPT for the one very scary side effect that I have experienced just a handful of times - but I really am curious if anyone else has had this HEAD TRIP WHILE DRIVING: It has happened when I'm on the interstate and/or bridge when I am driving at fast speeds, and my head feels whoozie all of the sudden and my brain seems to shift sideways - like on a roller-coaster, up and down, sideways - and I am amazed that my hands don't go with it and drive me into the wall! It takes intense concentration and wheel gripping to get myself where I can pull off the road. What the?? I don't want to ever experience this again - but it is so OCCASIONAL. The only variable I can think of is that I have not been faithfully taking the WB at the same time everyday (I'm more and more forgetful) and have skipped a day. Has ANYONE ELSE had a similar experience???

I just recently had the mirena iud inserted. Oct 30 2008. 3 months after having my first child under a normal vaginal delivery. When I have asked my doctor regarding any side affects he stated that women may have heavy bleeding the first 6 months/ and that after those 6 months that your periods will actually disappear.

The first week that I had the mirena in, I began bleeding almost instantly. Blood clots the size of my closed fist came out of my body from the uterine wall I suppose. I went through a super tampon/ and a pad in an hour and a half. ( I am one of those women who normally use a super tampon maybe once in a while/ normally a reg. size does the job) This bleeding has not stopped since the mirena was inserted.

Looking at a computer screen is part of my daily routine at work. It seems as though my eyes feel blurry through out the day as I am working. Towards the end of the day I can barely stand to look at it. This has never happened to me before. It is almost like I want to turn all lights off and sit in the dark, with no noise(headaches).

Of course sex drive is at the all time low. Who is in the mood to go for it when you are bleeding with a terrible headache?

The first few nights I had a horrible time falling asleep and staying asleep.

Well... at this point I have had headaches... all day for a week now. My head hurts like someone is pounding it against a wall. I have not had a headache in years. My stomach has been upset/ feeling as though I may have to throw up.

I am afraid that I may start seeing the other symptoms that ladies have talked about.
When you had the symptoms did they all happen at once or one at a time over different time periods?

My son was on a cocktail of Singulair, Zyrtec, Astellin and Nasonex. Like a miracle, his severe allergies cleared up almost immediately. Months later, behavioral changes started to surface. Extreme irritability, major meltdowns over nothing, problems in school and pulling out his facial hair including eyelashes and eyebrows. We stopped the medication in April and he improved. By mid summer, the hair pulling stopped. When his allergies started up again about 10 days ago, I put him back on the Zyrtec, because I was certain the Singulair was causing most of the problems. Within 3-4 days, the emotional outbursts started, panic attacks that never happened before - he said he couldn't breathe. Now the hair pulling is back. Everyone thinks I want to blame medication for his problems, but I am certain that Zyrtec has something to do with these problems in addition to Singulair. We have taken him off Zyrtec 2 days ago. We have a dr. appointment in 2 days and we will discuss all of this with him. In the meantime, his allergies are back and he is miserable. I would rather him be physically sick than mentally at this point.

All I can say is:

1 – for no “explained reason” my neck collapsed and I needed a life saving fusion operation to prevent my spinal chord from going any farther into the brain. I was told that I “should” have died. I did not. It was less than one year from starting FOSAMAX. and I had no other symptoms that would have indicated the neck would collapse. Kind of like DEAD JAW, but in the neck.

Thankfully, vIOXX (which (allegedly…) prevents bones from healing (and spines – do a google on “vioxx bone healing”) was not on the market at the time… and the operation did fuse (else death).

Go forward one year… a later total lumbar operation, (also going to be added to a lawsuit in re to FOSAMAX) causing the collapse of the lumbar spine was needed. Sure, before FOSAMAX (allegedly) did its thing, it was supposed to be an EASY, ‘no sweat” operation that would merely help my body geometry a bit with a simple procedure - sure one more year of FOSAMAX and the spine was now about ten times worse than expected. The surgeon was stuned.

Anyway, that (total lumbar fusion) - failed because (allegedly) along to the market comes vIOXX…. I am pursing the detail, but as FOSAMAX is now known to give many DEAD JAW and it now appears that my neck bones destruct – which are near the jaw decided to destruct. Further, FOSAMAX is showing to have more problems than DEAD JAW. Had FOSAMAX and vIOXX not entered my life, I would have merely had arthritis and had done fine except for some pain. My brother, having exactly the same arthritis, DID NOT have either “poison pill”, and has done just fine, by the way.

2 - They are now finding that FOSAMAX also tends to provide problems with long bones and people are breaking femurs (allegedly) from FOSAMAX. Nice huh? So, now what happens? I simply fell and broke my femur – or I am now realizing that I broke my FEMUR THEN FELL – another thing people are finding out about (allegedly….). It also should not have happened as I DID NOT HAVE OSTEOPOROSIS and had fallen many times before I took the FOSOMAX POISON and it imbedded into my bones (takes about 6-12 months). FOSAMAX took me down big time, vIOXX kept me down. Almost having died 3-4 times from operations that failed and complications - I did not die obviously, and will continue my pursuit of the truth – look for a web site in a month or two…..

3 – So, FOSAMAX caused/contributed (allegedly again I must say….) the broken femur, and vIOXX stopped it from healing. That is called the “double whammy” in recent vernacular. After several operations (and over 6 months of hospitalization; 8 months total) failing without anyone knowing why or expecting that (my overall health was just fine except for arthritis and it was supposed to be a routine operation), they were about ready to amputate the leg. Fortunately, an astute NJ surgeon 150 miles away just realized IT WAS NOT GOING TO HEAL, and patched it together with glue, thus saving the leg and walking for first time in more than ½ year.

4 – I am going to leave alone the issue of “stress fractures” as this is enough to digest for now… but watch out for this issue….

5 – someone mentioned this: -- > “Can Fosamx D 70 mg be the cause of Ecchymosis Petechiae, I have developed what looks like an "under the skin" rash, on the ankles and upward on the leg, sometimes dark and also gets lighter…”

All I can say is that I went from having TEXTBOOK just beautiful circulation in my legs (was sincerely told it should be in a textbook) to a lot of problems, including very similar to the above AFTER taking FOSAMAX for 2 years. That was another quick thing to happen. Readers can interpret if FOSO may have caused that.

6 – I shall not forget, also, the horrible aches and pains I had within a few months of having FOSOMAX. I just thought it was arthritis acting up. NO, now I know it was from FOSAMAX. My whole history fits like a glove…

In fact, FOSAMAX brought me down, and vIOXX kept me down (allegedly). Merck should not sell their wares when they know their bone “science” was not “science” but a fraudeulent, dangerous and even (vIOXX) killing poison(s)…. (allegedly….)….

FOSOMAX and VIOXX were the very worst things to have entered my life. I pity others who had them concurrently. I shall spend 2009 finding others in the same situation with bone – spine problems from either or both concurrently.

If you have have had a bone/spine destruction or healing problem and taking FOSAMAX and/or vIOXX at the time – please feel free to email me at badbonehealing@hvc.rr.com. I will be creating a Web Site to dialogue and share research on. These (bone – spine) are horrible problems from these two poisonous (allegedly…) drugs and the PUBLIC NOW NEEDS TO KNOW. I asked the courts to help, and they have not. So, I cannot be blamed for not being transparent and doing as I said I would do.

Thank You…

bones
badbonehealing@hvc.rr.com

I'm not sure my symptoms are the result of Lipitor, but I sure am going to find out by stopping taking Lipitor for a week. My symptoms - the numbing of my left foot, the reduction of motor skills in the left foot - it comes quickly and stops almost right away. I have been on Lipitor for several years taking 20 mg but recently was increased to 40 mg. I have no other
symptoms. Just touching base. Thanks for the site.

My husband was given this medication to stop any infection as he was having a hernia operation,as the doctors started the operation,my husband complained of chest pains,unfortunately he had a massive heart attack,because os this medication and is now severely brain damaged.
Before this he had never suffered with his heart or anything,the doctors said that he will never recover,I have lost everything through this drug.this happened on the 9th august 2008

Felt great going to doctor Fri. but had had a cold. He did culture and found staph. Took Avelox for sinus infection. The next day felt so out of body, depressed, weak had to cancel vacation (husband, daughter, everyone went :-(... All night had psycho fragmented lines from songs etc going through my head. Woke up dopey and weak, had to stay in bed 3 days. Went off the Avelox after 3 days and switched to Augmentin. I am getting my brain back today. This stuff seems very strong & toxic!!
Ruined vacation and made me feel 10x worse than the sinus infection itself.

If you take lipitor, you will be interested in this.

I have taken it upon myself to do my own studies into cholesterol and heart disease. I painstakingly studied various countries comparing rates of heart disease to cholesterol levels in each country.

From the Data, I can honestly say that I find no relationship between total serum cholesterol and heart disease. More surprising is the data showing higher cholesterol levels associated with less disease and longevity.

I had 2 lupron shots back in April and May and it was the worst decision of my life. I now have SEVERE panic attacks, depression and loss of appetite. I was a very healty 33 year old woman and very active and now all I want to do is stay in bed. I was NEVER informed by my doctor of any side effects other than I MIGHT get a little moodier (angry) easier. That never happened. For 2 months straight all I did was cry. I would wake up crying and go to bed crying. I have never had any past experience with depression and I have already seen a psychiatrist and 4 other doctors. I finally saw a new OBGYN and she informed me that the 2nd shot that I received went straight to my head and it messed with the chemicals in my brain. I am a wreck. I have no energy and it's all I can do to just get out of bed and go to work. Had I known about ANY of these side effects, I would have NEVER taken this drug. This drug needs to be banned completely and thrown in the trash can before any other woman goes thru this. I was on the verge of being suicidal. I am a Christian woman and would never harm myself but the thoughts were always there. I would wake up with a severe panic attack and they would come all during the day. The doctor that originally gave me the shots told me I had psychological issues and HE HIMSELF called and got me an appointment with a psychiatrist. Ladies, we are not crazy. These are real symptoms and it is all because of these shots. It messes with the chemicals in your brain. And had I know that, I would have said HECK NO to them. My endometriosis is much more tolerable than these stupid, insane shots. Please do not take them if at all possible. I do not want one more woman to go thru what I have been through and still going through. I now am on anti depressants to try to get the chemicals in my brain back to where they should be. I just hope and trust in the Lord that I will eventually get through this.

I had a chronic sinus infection and my doctor put me on Levaguin and 80 mg of prednisone. I am 62 and I take only synthroid as a prescribe. drug. I told my doctor I was a borderline diabetic. She told me the side effect were bone weakening in the hip and pelvis and stomach upset. At first I had a lot of energy and sleep a lot less. I just thought I was getting better. I tapered down to 1 1/2 . After taking them for 11 days I was not able to function. My body was under extreme distress, I have very excellent blood pressure and I am in very good health. I have been off the drug for 4 days. I am still experiencing sweating, hypertension, extreme muscle spasms. I am unable to wear my contacts, I am short tempered and I am normally the opposite. I have horrible headaches and I very seldom ever get headaches. I told my doc and she said it would go away in time.
My body is fatigued I am have trouble focusing,sleeplessness. I don't know where to turn at this point. Sometimes I feel like I should go to er because of the hyperventilating and rapid heart beat. I am afraid to exercise. I am eating a lot of high protein foods, I am not gaining weight, I have lost 7 lbs in two weeks. PLEASE EVALUATE THE RISKS OF THIS DRUG IT HAS BEEN A NIGHTMARE FOR ME. DOCTORS DON'T ALWAYS TELL YOU THE WHOLE TRUTH AND THEY NEED TO BE HELD ACCOUNTABLE FOR THIS.