Second opinion symptoms and conditions

I have had the Mirena for five months, I have gained weight and seems like I keep gaining and I have tried everything to loose this pouch. I am always tired and moody. I feel sick to my stomach all the time, especially after I eat something. I feel like I am having another baby. I told my doctor and all she did was prescribe me anti depressants and anti anxiety pills( like I need anything else messing with my system ), and she told me to give it time to work, the symptoms that I am having are normal. I feel like crap everyday and didn't feel like this until I got this thing put in me. Don't get me wrong my life was not peaches and cream before the placement but I was able to deal with my days. Now I just feel like i am about to have a nervous breakdown or panic attack. I literally feel crazy. My husband feels neglected and I am going to get a second opinion from a different doctor because I don't know if I can take it any longer.

This is a follow-up to my posting on October 10th regarding my 57 year old husband who began taking Lisinopril in March of 2007. He was NEVER on any other medication prior to taking this drug. He suffered Depression, loss of memory, lack of concentration, can't focus and struggled with small task. We have recently had an MRI done and his brain has shrunk. Deadfred1 replied to my posting and he is a 36 year old male who has been on Lisinopril for 5 years. He has the same side effects as my husband. He had a recent MRI and his brain has shrunk!!! We visited a Neurologist with his MRI results for a second opinion and he is ordering more tests because "it appears to be indictive of Alzeheimers" with the area of the brain that has shrunk. How can this be??? This was a healthy, 57 year old NEVER on a drug in his life and within months of taking this, he is in Depression and having memory issues. Isn't anyone connecting any symptoms here??? Any Doctors out there with an "open mind"? This medication is was developed from the venom of a poisonous Brazilian snake!!! Hello...it's more like a slow death with Arsenic!!! My mother-in-law has been on this drug for years and years and years. She now sits with dementia in an Alzeheimers unit. Is anybody out there listening? Alzeheimers is becoming an epidemic in this country. Have we ever thought the medications we are taking is creating this devastating disease? Millions of people take Ace Inhibitors, millions of people have Alzeheimers. They are getting younger and younger according to the Neurologist. Why, because younger and younger people are being put on Blood pressure medications from poisonous snakes. Are there any open minded Dr.s out there that can "step outside the box"...don't just "think outside the box"...."step out for goodness sake" and start paying closer attention to the symptoms people are having. I am convinced there is a definite connection to my husbands side effects and this drug. Get off people. Get off.

Hi, I am a 36yr old mother of 2 boys aged 14 & 12yrs. I had the mirena fitted in 1 1/2 years ago.. had all the bleeding at the beginning, but unfortunately it carried on for months. had very heavy bleeding in months 7 & 8, so heavy it left me feeling nauseous and faint. then it went back to 3 weeks of bleeding out of 4. and thats now how long i bleed for all the time. have heaps of discharge (eww), zits, feeling constantly like crying over nothing. Had hard cyst, which went on its own. got referred to a gyno (cause of heavy bleeding) which i saw 3 weeks ago. he has no idea why i had the heavy bleeding, has no idea why i am bleeding 3 weeks out of four (not heavy) but he is now booking me in for a vaginal hysterectomy.!! I still have the mirena in, only because i am told that if they take it out, my periods will be a lot worse than before i had the mirena inserted!! argghhhh. anyone else being put forward for a hysterectomy??

Like many patients, I started out on a low dose of Lamictal. Eventually, I was taking 300 mg. This seemed fine for awhile. Then, I started feeling a bit down, so the doctor increased the dose to 400 mg. Increased dosage does not necessarily mean improvement in mood (bipolar). I began to experience a good number of the adverse side effects reported here, including excessive fatigue, gastrointestinal disturbances, cotton mouth and very bad taste in my mouth, muscle tension (particularly in my legs), forgetfulness and confusion, and sinus and chest congestion. At one point in time, I even had difficulty articulating words.

Though I did not suffer from rash, I have been up in the middle of the night with itching all over my body. I had a few episodes of mouth sores and one pimple on my chin. Many of these have improved since the doctor brought me back to 300 mg. However, they have not entirely disappeared. I continue to suffer from the excessive fatigue many of you have reported here.

I recently had a blood test and learned I have very low levels of Vitamin D and Vitamin B-12. I do not know if there is any relationship between long-term use of Lamical and these test results. However, I do know that low levels of Vitamin D can cause fatigue.

Though I am willing to follow through with further blood tests, I am beginning to understand why some people are tempted to discontinue their medications. I am so tired of being so tired and sleeping so much. When I finally get up, I am still tired and drag through the day.

Sometimes, I think I'd rather have a down day or two than take this medication. I should add, though, that my bipolar is not severe, and that I am only reporting how I feel. I'm certainly not recommending anyone discontinue medications for this or any other condition they may be suffering from. If I were to recommend anything, it would be to get a second opinion if one is concerned about his or her treatment.
If I were to make any suggestion to doctors, it would be this: more is not necessarily better. Send your patients for blood tests (mine were ordered by my M.D. and not by my psychiatrist). Increasing the dosage--at least of Lamictal--might result in a host of negative side effects. Your patients might then become disillusioned with their treatment and give up.

If anyone out there has suffered from B-12 and D deficiencies, let me know. I'll let you know what I find out.

And remember, most doctors are really trying to help us.

My husband (57 years old) started Lisinopril in March of 2007 for High Blood Pressure and he's never been the same. At first, we didn't connect the symptoms but now I am convinced this drug caused his problems. His symptoms include loss of memory, can't concentrate, can't retain anything, short tempered, depression. At times confusion or unable to grasp anything requiring multi-tasking. He had a loss of appetite where in lost 25 pounds in less than 6 months. He described months ago that "his head just doesn't feel right". When asked...do you have a headache...he'd reply.."I can't explain it...it just doesn't feel right. The depression has lead to another drug "Lexapro". This drug interferes with concentration too!
Prior to taking Lisinopril my husband was running his own business and working a full time job he's had for years. Within 6 months, our lives changed drastically. I know 2 other people experiencing the memory loss, can't concentrate, can't retain symptoms around the same age as my husband... all taking Lisinopril.

All of this has been weighing heavily on his mind because his mother has been diagnosed with Dementia/Alzeheimers at age 74. Guess what...she has been taking Lisinopril for years and years and has been treating for depression for years and years....any connection here? This drug has been around for many years and it seems like every elderly person is taking this for High Blood Pressure. Could this be a culprit to Dementia/Alzheimers? A reoccurring theme I see amongst all of these side effects is "depression".

Of course when we discussed these symptoms with his Doctor...we were pooh poohed with "I've never heard of these symptoms in 20 years of practicing". Well, he needs to do some research! My husband quit taking this drug on Sept 12th which takes 2-3 weeks to get out of your system. I noticed recently he didn't struggle at all at the ATM machine. I'm hoping this is the culprit as we are now in the process of getting a second opinion to determine if he may be in the early stages of Alzheimers. We pray that he is not! Get this drug off the market!!!

I have been on Ortho Tri-Cyclen Lo for 9 months. I went through a major depression last spring. I was diagnosed with MAJOR DEPRESSION and went on anti depressants and on sick leave from work. Now looking back it seems there could be a link with the birth control pill. Around the same time I started taking it, I started having such bad MOOD SWINGS, ANGER control problems, ANXIETY and fatigue. I was always getting angry at my boyfriend and picked fights. No more sex drive either. I spoke to my GP, to a psychiatrist and to my pharmacist. I asked them "should there be a link with the pill?". Each and everyone said "no", "highly unlikely". Nobody suggested I try stopping the pill BEFORE starting anti depressants. I got a second opinion from a other doctor. THIS is what he said to me:" you'll be very depressed if you get an unplanned pregnancy." the thing is ladies, they DON'T WANT YOU OFF THE PILL BECAUSE THEY DON'T WANT UNPLANNED PREGNANCY. THEY DON'T WANT YOU OFF THE PILL BECAUSE IT PAYS A LOT MORE TO PUSH PILLS THAN TO RECOMMEND OTHER METHODS (pharmaceutical companies giv big incentives and gifts to doctors). THEY DON'T ENCOURAGE YOU TO LISTEN TO YOUR BODY.
I'm going off the pill at the end of my pack and am giving myself a couple months to see if I feel better. then I am going off the anti depressants.

On July 9, 2008, I was admitted to the hospital for severe anemia, due to a heavy period that was on it's 3rd straight week. Because I had lost so much blood, I had to get a blood transfusion (4 pints). Since my bleeding would not stop, my doctor gave me a shot of Lupron. I was discharged from the hospital the next day because the Lupron stopped the bleeding. A week later I got, what I think was my normal period (which I don't even know what that is anymore) and that lasted 7 days. Almost immediately after receiving the shot, I noticed my hair was falling out in clumps when I washed it. 2 weeks later, I started getting bouts of suddenly feeling hot and sweaty. I didn't think much of it. I just thought my A/C unit needed more freon or something. That was until I went to see another Dr. for a second opinion. I am 38 years old with uterine fibroid tumors and my first doctor wanted me to get a hysterectomy. I have 2 teenagers and do not plan to have anymore children, but I just wanted another opinion. My second doctor informed me that Lupron's side effects are hair loss, loss of bone density, hot flashes, and premature menopause. When he mentioned hair loss and hot flashes, I knew then that I was not going crazy! Anyway, the second doctor explained to me that the loss of bone density and premature menopause would happen if Lupron is taken consistently. I just want to know when is my body going to get back to normal. All I had was one shot of this stupid drug! The hot flashes are not only uncomfortable but also embarrassing! It's been 3 months since I received the Lupron shot and the hot flashes have not vanished nor decreased. I know that every female's body reacts differently to different drugs, but if Lupron causes all these side affects, I suggest that you read up on the drug before taking it. I was told that if my bleeding comes back that I can ask for another Lupron shot. Well the answer to that is thanks but NO THANKS. Seriously, I would rather bleed than go through more hair loss, hot flashes or any other debilitating side effect.

Since I've gotten my Mirena Implant I've been diagnosed with 2 different STD's and an infection which after the blood tests came back negative! So far I have taken meds for HPV, Herpes, and a UTI. Each time I go in for my pap smear and check up to make sure the IUD is still in place I inform the doctors (have visited 6: 3 for the first pap, 3 for the second opinion) that one of the biggest side effects of the implant is abnormal pap smears, even hand them the same pamphlet that the inserting doctor gave me when I first got it (which clearly states abnormal pap smears as a side effect) however I still end up with some horrible disease/infection!

So far, in the one year I have had this thing in me, I have taken 20 different meds for these STD's that I NEVER HAD!!!! These meds have made me horribly sick and the UTI meds almost killed me.

Also, like many women on here, I have bad hair loss, headaches, horrible back pains, and crippling stomach pains. Constantly attempting to get my doctor to give me an ultra sound to make sure that the impant didnt tear me but she refuses! Go to the hospital to ask them for the same and they refuse also "Thats not likely with the implant."

This is my one year check up coming up, I want this thing out! If they do not take it out I'm threatening with a lawsuit. This is NOT a life saving device and they should have NO say in whether or not this stays in!

I have had Mirena since June 2007. Since January 2008 I have had nothing but problems. I have had numerous ovarian cysts that cause excruciating pain from my lower abdomen and back all the way down my legs. My doctor that put it in (a male) swears up and down that my cysts and pain are not related to the Mirena. I got a a second opinion today (a female) who says the Mirena ABSOLUTELY can cause my problems and that she has taken more out than she has put in. I loved the Mirena in the beginning because it did stop my periods. But then I started noticing weight gain and no matter what I cannot get it off. Then the abdominal pain and the lower back pain. I go for another ultrasound next week to see how big my current cyst is and if it is restricting blood flow to my ovary. If there isn't any blood flow I will have to have the cyst, and my ovary, surgically removed. I don't recommend Mirena to ANYONE!

Earlier this summer, I developed a case of shingles. It went away, but about a week ago a similar rash broke out. I thought that it was a second bout of shingles, but my doctor assured me that it would be impossible to contract the disease on different parts of my body. Because I am not home with my ordinary doctor, I had to see another doctor, who was unsure of what the rash could be, but nevertheless prescribed with with 50mg of Prednisone daily. I took my first dose today, and am reluctant to continue. I don't want to be a victim of any of the side effects, but am unsure as to whether there is another way to go about getting rid of the rash. Any advice that could be given so as to not have to continue with the Prednisone would be great. I don't want the rapid weight gain, depression, mood swings, etc.

Hi all, I'm hoping someone here with Seroquel-experience can help us with some information. My wife has been on Seroquel for approximately 5 weeks (ramping up to 200mg per day during the first 10 days, approximately). After 4 weeks, the severe breathing problems started. Physicians have verified the oxygen level in her blood to be excellent, her lungs and heart are in perfect shape, she has no fever and no indication of bacteria-infections. All indications are that this is caused by the Seroquel. She explains the intense sensation as drowning, almost passing out while gasping for air. She's feeling very dizzy, probably due to breathing too much as a result. Occasionally her breathing is not so deep, but more like hyper-ventilation. The problem became unbearable (and my wife endures a lot) after approximately 1 week, so 5 weeks into the Seroquel scheme she quit cold-turkey two days ago. The breathing problems are still the same. We are hoping someone could tell us how much time these breathing problems can be expected to remain, as I've googled my eyes out without finding any information on this. A week? - Two weeks? -Even more? - please respond, and in advance, thank you for your help!

I was on synthroid for 10 years after getting treated with Radio Active Iodine. As the years went by my period was all all over the place. They were heavy the first three days and lasted 9 days or more days. I spotted all the way through the month. Other times I was so late that I thought I was pregnant. I had PMS two weeks before I started and was irritable. I had low grade depression. I had anxiety and heart palpitations. My skin was dry and rough. I went to the doctor and had my blood test. He checked for TSH and T4 and T3 levels. He insisted they were normal and that something else is wrong wth me (he wanted to give me sleeping pills, anxiety pills, depression pills) and that it had nothing to do with my thyroid. He sent me to an endo to get a second opinion and he said my levels were normal too. I ended up going to a holistic doctor (paid over 1000 dollars for two visits plus meds) that checked under my feet (yellow) and my reflexes. She checked my reverse T3 and my free T3 and T4. It turns out that my body was not converting T4 to T3 the way they said synthroid (T4 only med) should. My diagnosis was hypothyroid. I was put on Armour and felt the difference in my skin. It was softer and moist! My teeth felt strong compared to before I felt like my teeth were getting loose. My stamina last longer and can run on the treadmil 45 min at six miles per hour. I am less nervous and my low grade depression seems to be lifting. My days are brighter and less anxious. My hair is falling less. I know I have a long way to recovery because my Adrenal glands need some healing and I am still being optimized. I might still need to be raised on the dose that I am in. I will never go back to synthroid! My period has improved drastically as soon as I started on Armour! I am down to 4 days of period and less heavy. I still spot on day 5 and 7 but it is nothing compared to what I went through when I was on synthroid (T4 med only). My gynecologist wanted to burn my uterus to control the menstrual flow. He said that he could also pull it out. It seems like main stream doctors are more interested in treating the symptoms than looking to see what is the problem that is causing the symptoms.

Hi - I posted a couple of days ago (around the 15th). I had the Mirena taken out yesterday. Yes, still bleeding. Yes, with medium to large-sized clots. Oh, I forgot this side affect also - for some time when I had it in, I had a tinging or numb-like feeling passing through my top lip - I thought I was going crazy at first but I realized it had been happening more and more and it wasn't my imagination. I've had this also since it was removed; not as often though.

Could it be that we are the "3%" that has a problem with this IUD??!! I am following up with a second opinion with another OBGYN because I was concerned that the radiological tech said my uterine lining was "very thick" and my friend's mom (who is a nurse) asked right away if the doctor was doing a D & C...(!) Any suggestions or ideas or comments???

I am a 55 year male and my doctor started me on 20mg of Simvastatin in Sept 2006 and has subsequently increased it to 40mg. I try to keep very fit through lots of exercise. Fortunately I have not experienced any major side effects mentioned here and my cholesterol has decreased from 6.8 to 4.5. However, I am constantly tired to the extent that I often doze off at my desk at work. In addition, I am having extreme difficulty in getting erections. My doctor claims these are not side effects and has prescribed Viagra but even that is not working now. At Easter, whilst on holiday, I stopped the medication for a week, my libido recovered after a few days, and I was able to have normal sex again for about a month. During the summer, I stopped it again and within 72 hours my libido started to pick up. My wife says it is psychological but I am convinced that it is the Simvastatin. I am going to see if I can get a second opinion.

Like so many of you, I Googled "tissue atrophy" and have had the very same experience that you have had with Kenalog. I received a shot in late February of 08, shortly after I noticed severe bruising, which eventually turned into the atrophy I now have. I have taken pictures of it for the past several months...and now, 6 months later it is much worse...deeper and darker in color. Is anyone else having discoloration? Mine is a dark purple-red.
I AM PURSUING a lawsuit against the nurse that injected me because I was absolutely not warned of the side-effects...and now have had to suffer with this hole in my side.

It bothers me...and no one would understand unless this had happened to them I suppose. In addition, I received a second opinion and was told the atrophy was permanent...can anyone else confirm this?

I've also noticed other severe menstrual and emotional side-effects...this stuff can stay in your system for a long time.

I have been reading all of these posts and have another question. I hope that someone can help. My daughter, 8 years old, has been on Singulair since she was 4. She is normally a very happy girl with a wonderful disposition. For the last year or so, she has been having trouble getting herself to sleep at night. She says that she hears things in her head such as ringing or "noises". A few hours before she knows it's bedtime, she cries and when we ask her why she's crying, she can't give us a reason. We initially thought that she was crying for no reason because she didn't want to go to sleep. I remember reading about the side effects of Singulair causing mood swings, etc., but her's are not violent mood swings. Just very emotional and has a hard time coming down from the "episode". I'm at a loss...I have not talked to her doctor yet about it, but have told her that we will make an appointment this week to discuss it with him. My husband suggested that maybe it sounded like she was having a panic attack or anxiety attack. I hate to label her as that at such a young age. My mind now goes back to the side effects of Singulair and maybe this is to blame. Any help or suggestions would be greatly appreciated. Thank you! Concerned Mom

I saw an elderly ENT who prescribed Biaxin XL 1000mg/once per day for a severe sinus infection of the ethmoid, maxillay and frontal sinuses. I was not getting any better, in fact I was getting worse. I decided to go for a second opinion and learned that Biaxin is not as wide spectrum of an antibiotic as Augmentin is for sinus infections. The key strains of bacteria are not being obliterated from the Biaxin. MDs who prescribe Biaxin are not staying on top of current literature as Biaxin was commonly prescribed in the 1980s and 1990s.

My incredible side effects to Biaxin XL (including not wiping out the bacteria) include: lingering bad bitter taste, night sweats, insomnia, extreme stomach cramping, constant stomach churning (which kept me up at night), terrible diarrhea, nausea. The only plus side is that was more mentally alert.

If your doctor prescribes Biaxin for sinusitis, leave that doctor immediately and seek help from another practitioner who is more current on medications of choice for treatment.

I am a 37 year old female that went to the ER 3 days ago for chest tightness & extremely high blood sugar. I have had high blood pressure in the past years but as of a year ago when I was diagnosed as being diabetic my blood pressure has been normal about 117/75 so I go to the ER and they give me 2 EKG's and a heart monitor for 24hrs and put me through a stress test,they also give me this little pill and say it will help me, well not feeling well and wanting to feel good again I take the pill no questions asked. I have never felt so tired in my life. I thought well chest pains will do that to you so I dismissed it. I know they were making sure I do not have a heart attack but, my blood pressure seems to be going lower and lower and I am more tired by the minute, they released me from the hospital and gave me a million RX's including toprol and lisinopril both of whch lower blod pressure ??? do they want me to pass out? so yesterday I took the toprol only and felt like I was sinking , my thinking seemed foggy and my legs felt rubbery. I am sooooo glad I found this site because I will not take this drug ever again I already suffer weight issues being diabetic I don't need anything else. I would prefer to be interested in sex and be able too function this drug seems like it is more negative than it is worth. I think I will stick with the lisinopril, and why would they give me two blood pressure meds when my blood pressure is already normal??? If anyone has a comment please let me know I am very scared about this whole thing

Hello all,
I'm a 45-yr old Air Force Major (Male) recently diagnosed with asymptomatic chronic Atrial Fibrillation (As in I have it and was walking around not knowing it). When I went to see the cardiologist, my B.P. was only 120 / 74 (Which, until they changed the rules, used to be normal)and he puts me on Diovan 80mg once a day plus Coumadin 5mg. Well the Diovan almost made me faint and I had numbness in both arms, plus a funky rash, kind of like chicken pox showing up on my arms and thighs.
I went online and read horror stories of Diovan so I stopped taking it immediately (I had only taken four doses and never had any horrible symptoms until after I took the meds!). Then the Dr. put me on an Event Monitor and it showed I was indeed in A-fib all the time, plus at night, my heart was racing briefly to 200 a minute while I was sound asleep. So he puts me on Toprol XL 100mg once a day.
Immediately I had trouble sleeping (Which I never had before, ever!) with crazy dreams and tossing/turning. My B.P. dropped to 88/65 and my fibrillating heart rate was 64!!! I was so mad because I actually felt better before the meds. I found this site and saw what everyone was posting and immediately took myself off the Toprol XL.
The day after stopping the Toprol I had slight chest pains (Like angina or gas bubble) but they went away on their own. I slept fine the next night.
I'm having an Electro-Cardiversion done on the 21st July to see if I can stop the A-fib and get in normal rhythm. I know the Dr. is going to be mad at me for stopping the Diovan and Toprol, but I'm sorry, I'm convinced there is a better way to beat all this (Namely exercise and eating right). Being in the service means you have to be Mr. Physical and Mental "perfect" all the time. I cannot afford to be diagnosed with depression in my line of work! Thanks to all on this website and I wish you the best.
PS. for those who think I'm being ignorant of my medication, I have a nice fat insurance policy and Power of attorney for my wife and kid in the event I keel over!!! I may be medication intolerant but at least I took care of my family.

34 with a diagnosis of a Hormonal Imbalace which consisted of the following symptoms: Vaginal dryness, acne and mood swings.

First pill was Valette 30mg which made me sick to my stomach. I was on that for a week. Then switched to Loette 20mg, which was good, but the state health care doesn't subsidize the medication. I then switched to Nordette which is the same as Loette, but a stronger form of 30mg and experienced rashes with Nordette and I believe Nordette lowered my immune system in which I caught the Herpes Simplex One on my lips. Since I have contracted the virus on my lips, I have not be able to get the virus to suppress itself as I believe my immune system is being affected by the pill.

I was then advised to switch over to Yasmin because my other doctor, which I have many doctors that I see as having a second opinion is important to me, said that Yasmin was the best pill for my health issues. Since being on Yasmin, I have experienced extreme skin rashes on my face, neck, chest, arms and hands, which itches like crazy.

Since I was on Nordette, wearing makeup causes me to get eczema on my eyes and has been consistent since being on Yasmin. So I cannot wear any makeup unless I am going out for the night and then have to remove it the moment I get home and treat my eyes with Hydrozol.

I am concerned with the side effects of the Yasmin and will be consulting with a different doctor about an alternative hormonal imbalance treatment with less side effects. To summarize my experience, Yasmin is causing me very itchy skin rashes all over my upper body and I will probably stop taking it as soon as I see my doctor.

The only good things that have come out of being on the various pills is my skin acne is gone and my vaginal dryness is gone. My libido is still kicking, but its not worth the rashes.

I thought I had sinuses for years..got test for allergies and was founded to be allergic to nothing! Despite having at least 3 infections a year and on my 3rd nose spray, zyrtec, nyquil at night..ect..because I was contantly congested and had drainage & headaches..3-4 infections a year.. She ordered a cat scan and was told that my sinuses had spurs but was clear; my septum was severely deviated and I needed a ENT to have surgery to correct it...The ENT wanted to do major surgery which included a plastic surgeon... so I went for a second opinion to another ENT that was well known who told me I had rebound headaches..and referred me to a neurologist..my goal was to get off all the meds (nose sprays, nettie pot, antihistamines..nyquil..ect..) ..he was a dinosaur and was convinced that although I had a severe deviated septum~he didnt want to do surgery but wanted me to stop all meds I was on and to go to his neurologist that he liked *(another dinosaur) who put me on Topamax..50mg in the morning and 50 mg at night..I had panic attacks right away so he added 20 mg of klonopin at night to help with that and flexeril to help me relax...he hinted at me going to a pysch doctor which pissed me off right as if I was psychosomatic or something... and stiffled me a few times when I tried to talk to him about my drainage and congestion~he wanted to hear none of that because he already made his mind up what I had and "sinuses" didn't jive with his impression that I had migraines.

All of the sudden within days I really did have migraines..they just hit me! HARD...I had to call him and tell him I was in excruciating pain on the right side...he called in Imitrex inj. and they worked within 5 min. and my Topamax went from 100 mg total > 250 mg/day! I had at least 6 shots since and the side effects of the Topamax have profoundly changed my personality...I have no word recall..like being stoned in the 70's but worse because I have a special needs child and I need to engage her and am like a zombie! I have ALL the same sx that are mentioned but notice one that isnt noted which is my tongue is raw as well as my throat...all the way down into my stomach...I am having to take zantac for acid indigestion~it is like my insides are raw!
I am also having extreme constipation...I lost weight in the first 2 mos. where I couldn't eat nothing..but now I am eating cause it's there but it is not leaving me even when I take multiply doses of my old standby... I am drinking tons of water..at least 64 oz a day but it is not helping. My eyes are burning at times...I need my reading glasses all the time now. Some days my heart is beating out of my chest for no reason..at rest..I just feel ill like something is not right at all! I don't go nowhere & have become a hermit. My headaches are gone but I feel I am just a shell of a person and want to get off...I am slowly weaning off by doing it 25mg at a time for one week at a time....then another 25mg another week......I know I will have migraines but I will just bite the bullet and suffer through it till I am off this poison....I have some injections left..MY main goal was to be off meds and these side effects are horrible! Once I am completely off I am going to a good ENT that can do the surgery to fix my sinuses so that I can hopefully be drug free as I intended. I too wasn't told of these side effects at all. So much time & $$$$ wasted! I think if I stay on this too much longer it will truly do long term harm!

my friend has been on geodon for about 3 years and is experiencing some very strange things! She gets cramps, like seizures in her legs and can't walk when this happens. Her doctor says there is nothing wrong. She gets neck and leg twitching and recently, the leg things have come with shortness of breath. Does anyone know anything about these side effects?Please reply! Thank you.

I am 24 years old and I had a pulmonary embolism last month. I was on the birth control YAZ for only 3 months, and that's what doctors seem to think caused it. My insurance only paid for me to be in the hospital for three daysand I was sent home with lovenox shots and Coumadin pills.

One month later, my INR is still unstable, fluctuating so much that they are checking it twice per week. My dosage is constantly changing. I have a red, painful rash on my buttocks - it hurts of sit for more than a few minutes. I am losing clumps of hair. I have lost my libido. I am very irritable and snap at my husband several times per day. I have a headache almost daily and frequent nausea.

I hate these side effects!

I started Topamax in November of 2007 the usual 25mg and worked my way up to 150mg. I have always had pretty thick hair and now have hair loss in the widows peak and top part of my hair. Needless to say I am devastated. I have cut myself down to 50mg in the am and 50 mg in the pm. My Neurologist states that she has not heard of hair loss but even this web site and the drug company states that it can cause hair loss. I have with the help of a very good massage therapist determined that my migraines are cervical so I am seeking a second opinion and taking myself off this drug. Not worth the hair loss if I don't need to be on this drug.

First let me say, i have taken Avelox twice before and had NO side effects whatsoever! It worked great on my pneumonia the last two times (a yr apart) and i recovered very quickly. However, this time was different. I usually only have pneumonia once a yr Jan or Feb time frame, this time i have gotten it thanks to an unthinking oaf (who knew we have 7 little ones at home) and came to visit with a rip roaring sinus infection. I get pneumonia when everyone else gets sinus infections, who knows why? This time my dr. prescribed the usual Avelox for 10 days and the very first dose i was ok for the first hour and after that, wham i was in the bathroom with diarrhea and almost immediately began to vomit to the point where i could not control it, and then my hands and feet turned red and itchy was gone the next morning. I feel lucky compared to some of these people, and i have many drug allergies so i do understand it can be quite aggravating, but any time you have any type of reaction to any meds you should IMMEDIATELY discontinue and then call the doctor. any doctor who tells you anything else should be FIRED!! My husband and i are both EMTs and let me tell you, if your doctor doesn't discontinue use of a medication that causes reaction of any kind--let alone a severe one needs to go back to school. Anxiety attacks, etc. that some of these people have had are NOT minor, they are not side effects, it is an allergic reaction, to a medication. If it were me, i would be firing that doctor immediately or getting a second opinion. Common Sense is so rare these days, if it doesn't sound right, it probably isn't. Do not be afraid to shop around for a new doctor, YOU are their bread and butter, You are still a customer and there are so many out there these days you can find one that IS what he or she should be, concerned about You and YOUR health,
not one who speaks over you or disregards your concerns or symptoms! If your doctor keeps you on a medication that you are allergic to--FIRE him or her and find a new one!