Valium symptoms and conditions

I have been on Warfarin for three months for a DVT in my femoral vein. I get some headaches, fatigue, feel cold, tired and have gained weight. I am a fit middle aged male, back at the gym now and cycling. I eat a balanced low fat high fiber diet, but still cannot shift the weight. I have been a depressive for most of my life and although manage without drugs have resorted to Valium to help me sleep, as insomnia has also been a significant side effect. I do not sit around, drink excessively or eat like a pig, so where is the weight coming from? My GP's seems ambivalent and it took five weeks to diagnose my DVT after my complaining about Phlebitis and pains in my groin. Not a happy bunny.

In reference to my Sept. 20th posting, I have been asked to describe the
"warning signs" of oncoming seizures that I have. To review, I was struck by lightning while serving in the Marine Corp in 1977 and have had seizure disorder and myoclonic jerks and inner ear problems since that time. As I stated in the post on the 20th, I have been tried on "all" of the seizures control medications and they all make it difficult to function as an educational administrator. The best medical advice I ever received was to keep a diary of everything I could remember leading up to a seizure. This included any activities I had been doing, what I had eaten, what time of day it was, any stress or problems that I was having. We are all different and probable all have different triggers. In my case, I learned that as a seizure approached, I would become more light headed or dizzy (I have inner ear problems all of the time secondary to being struck by lightning, I just recognize when they are getting worse) The ringing in my ears increases, (I also have tinnitus all of the time also from the lightning, and over time you get use to it, but I can notice when it increases) When these signs start, I stop what I am doing regardless of what I am doing, If I am in a meeting, I take a break, if I am driving (I drive locally or with someone with me) I get off the road. (In 30 years, I have never had a seizure while driving and actually have never had a traffic ticket in that period, I try to be very carefully with what driving I do, knowing that one occurrence will cost me my licenses.) I try to rest and be quiet, if the dizziness and tinnitus continue, I take two ten Mg Valium tables and lay down. If I am by myself, I will call some and let them know where I am and how I am doing. The valium probable stops the seizures about half of the time and I believe that it always make them less sevier. I have warning signs once or twice per week, and have to take valium on the average of once per week, and will have a gran mal seizure once or twice per month. With Lamictal, I believe the seizures are less frequent and less sevier as long as I keep the dosage low enough to not block my warning signs. I believe everyone's seizure disorder is different and some may be like mine and be able to learn warning signs by keeping good records of what you can remember leading up to the seizure. Always do everything under the direction of a Dr. that you trust and have faith in. The more information you can give your Dr. the better your individual treatment can be developed. If you can develop warning signs, the seizures are much easier controlled and you can live a much better quality of live.

Gran-Mal Seizures and myoclonic jerks for over 30 years as a result of being struck by lightning while serving in the Marine Corp. Have tried "all" of the medications and most made it difficult to do my civilian job. (School Administrator) The best advice I every received was to keep a diary and record everything I could remember happening to me before a seizure. By doing this I have been able to develop a warning system of oncoming seizures. (Same think as most people saying they can feel a headache coming on,) I can live with the myoclonic jerks as they only occur once or twice per day. The seizures while at work or driving are a different matter. (I have warning signs for seizures on the average of once or twice per week, and around one per month goes into a seizure.) Most of the medications other than Lamictal cover up my warning signs and I simply refuse to take them. I work very close with my family Dr. who understands my case better then most Neurologist I have ever had. Neurologist want to give any drug at a strength that will stop all seizures and that can and often does result in side effects that prevent normal live. Lamictal in low dosage, 25mg twice per day may make my seizures less sevier. Any higher dosages causes many of the side effects others have described on this site, but for me the biggest problem is that it blocks my warning signs of oncoming seizure. I get 20 to 30 minutes warning of oncoming seizures and many times can avoid a seizure by just stop doing what I am working on and taking a break and resting. If that does not work, I take two 10 Mg Valium and find a soft place to lay down, the valium will stop or lessen my seizure and I will sleep for one or two hours, and wake up. Sometimes I will have a seizure after taking the valium, but I am in bed or resting and usually under observation. My key has been to learning the warning signs of an oncoming seizure in time to get to a safe place and by always having the valium with me. We are all different individuals and our medical problems are different. Share everything you can remember with a Dr. you trust and attempt to develop warning signs of an oncoming seizure is the best advice I can give after over 30 years of living with a seizure disorder.

So I've been reading all of your posts here and finally decided to share my experience. When I got the mirena put in about 7 weeks after my son was born back in the beginning of September the procedure went easy. It just felt like a little cramp then it was over. Before it was inserted tho, they gave me 2 Advil. The Dr. also had me quickly read the pamphlet about the mirena. All that I read sounded like it would be all good so I said ok to having it inserted. After the insertion I went home about an hour or 2 later I started cramping and bleeding. I figured it was ok until it only got worse. I cramped really bad like I was in labor again for about a week. I wanted to call, but stubborn me wanted to stick it out. Well after that calmed down a bit I had irregular bleeding for months after that. Each time I bled or had my period it hurt really bad. Each period also lasted for 10 days about. I finally made an appt. with my regular Dr. and she just gave me Tylenol 3's. This was at about the 6 month mark of having it in. Also by then I started suffering severe anxiety and depression. I had terrible mood swings and crying spells. Well about a month after that I went back because I needed something for all that stuff and the pain had gotten worse. My whole body hurt. So she gave me percocets, valium and effexor xr 150 mgs. I also noticed when they took my vitals this time and the last my temp was 99.4 and my blood pressure was in the 130's one time and the 140's another time. My pulse was also 111 once and 118 another time. Well about two weeks after that second appt. I developed a urinary infection and after I went in for the 3rd time and my urine was tested it came back severe infection. My vitals were 99.6 and 156 for pressure and 109 for pulse. Mind you each time my vitals were never mentioned or even a concern to the docs. Just I noticed it seemed. Well after I took the 10 day antibiotics the urinary pain went away but not my fever and I had really bad body aches. I went back to the Dr. and was given vicodin and was ordered blood tests. My vitals were all high again. I did the blood tests, made an appt. for 2 weeks later to get results and went home and suffered still. When I went back for my results the only finding was my B12 level was low. I wasn't told how low or what to do. So I got all my meds refilled and went home. I went and bought B12 vit.s. I decided to look up B12 online. Then I made an appt. to go back and get more details of it. She told me the level was 168 and she decided to get me a shot that lasts for a month and refilled my vicodin. A week later I felt a little better, but still had symptoms going on. That's when I thought about the mirena being the problem and stumbled on this site and other sites about mirena neg. side affects. I have severe acne, a low grade fever for 4 months, high pulse rate, high blood pressure, mood swings, depression, anxiety, bloating that looks like I'm pregnant and have been asked 3 times when is my baby due. I am 5ft 3in and weigh 129 so I am not fat all over just my stomach is so bloated and fat that it makes me look pregnant. I bleed for 10 days, I have NO libido, I feel strange sensations in my stomach like a baby moving, but I am not pregnant, Iove had nausea, loss of appetite, yet I can,t lose any weight, I am tired a lot, body aces, joint pain, nerve pain, tension in my neck and shoulders, headaches and low B12 levels which don't normally happen to anyone until they are over 50. Well 2 days ago after reading on this, I decided I have had it and couldn't take it anymore and took the damn thing out myself. It didn't hurt at all, in fact I couldn't even feel it coming out. It came out so easy. I don't recommend anyone doing this themselves, I am simply telling my story. I started what seems to be a period this morning. It's very normal so far. I plan on going to my new Dr. I'm getting soon and getting a check up and a pap since I'm due for one. I feel pretty good so far. No problems and I'm relieved that piece of plastic is out of me and look forward to getting my life back. Good luck to all of you!!

I am a 38 year old male suffering from a combination of occipital neuralgia and migraines. For 20 years, until a year ago, i would endure pain that was only manageable with narcotic pain relievers (imagine all the gamut of such kind). I would have neck and head aches typically 3-4 times a week, accompanied by vomiting, dizziness which would put me to bed for the entire day. Work and family suffered in magnitude comparable to my own suffering. So then I finally saw my GP for that. The pain meds went up the roof, imitrex, maxalt was added to the equation with only marginal side effect. I saw a neurologist. He had me do an MRI and put me on Topamax starting from 25 mg, which I upped to 200 mg within 6 weeks. Past the initial side effects, the headaches subsided, the frequency reduced and i was able to enjoy weeks at a time with no episodes. Stayed at 200 mg for 5 months. In the meantime, the MRI came back positive for some brain inflammation. False positive they said, does not fit the clinical picture. Second MRI, same positive, this time proceeded with LP, which was negative. Third, MRI still positive; making the neurologist uncomfortable. While dealing with MRI results, the topomax had yielded positive results as far as pain management was concerned. But little by little I noticed that I was becoming more irritable, more impatient and more forgetful. Someone would have to remind me of something several times before it would even register in my mind. I empathize will all the posts that mention feeling like having Alzheimer's. I didn't care in the meantime. As long as I didn't have to deal with the pain it was ok with me. But the situation became worst and worst. I couldn't concentrate on anything, the mere task of remembering to do something was insurmountable. I would wake in the middle of the night and find myself staring at the bathroom mirror for no reason. I would have terrible panic attacks which i control with valium. But yet i continued on with topamax convincing myself and being convinced by other people around me that i just had a "personality disorder". Finally, work begun to suffer. I was loosing track of meetings, deadlines and when this happens someone knocks on your door (boss) telling you that something just doesn't click, something just doesn't feel like a personality quirk. Other people playing doctor would slap on my face that i just had ADD, that I should take something for that and get on with my life. But something was wrong. Pain or dizziness or lack of concentration etc are all electrochemical processes in your brain. It turns out that topamax was helping my headaches but it was not slowly deteriorating other cognitive abilities. Finally, the neurologist decided I should wean of the topamax, stepping down from 200 - 150 and then we go to 100 and so on. I dread the re-occurrence of the headaches. I am waiting for them to happen again at some point as I drop the dosage. But in the end of the day, I'd rather be in pain and in control of my life rather pain free and absent minded.

I Just started NR a week ago on the 1st day of my period, I have already gained 5lbs, have constant cramping (not severe but noticeable) my boobs hurt, and I have constant lethargy. Went for a walk today with my BF and could hardly stand it. Just wanted to lie down...

We then got in a huge fight because I was freaking out about every little thing. I was crying and screaming at him, and we almost broke up. I am normally not like this. So I just took it out. Im sure my OBGYN would say to give my body a chance to adjust but I can't take another day! So Im probably messing up my Menstrual cycle but I'll take that chance especially after reading all the experiences of you other poor ladies.

I had tried to get an IUD after many of my friends recommended it. I chose Mirena although I am usually anti hormone, but my doctor says that the hormones in Mirena do not go into your blood stream but stay locally in your uterus. My friends who have Mirena love it, less periods, no cramping, no side effects. My one friend who had the non hormone one had terrible heavy bleeding, severe cramps etc. So after TWO TERRIBLY painful attempts at inserting the Mirena, ( I had to come back a second time on Valium, Vicodin, and a pill to dilate my cervix) I was told I am not a candidate because my uterus is TOO SMALL! The U.S only has two IUD's. Europe, Canada, even Mexico has smaller sizes available.

Sooooooo, long story short, I either have to fly to one of these countries, (England is farthest but will do it for free) or find another option. My friend just told me about a promising sounding option called Lea's shield- ****** which is like an updated, easy to use, strangely shaped diaphragm. Its available from Planned Parenthood, and due to its unique design is one size fits all so you don't have to get it fitted and can order it online. Hope this helps. Thanks everyone for your frank sharing, hope I have helped someone too!

Hello I am clinically depressed. They doctors said I was "severely depressed." I haven't done these post ever so I apologize if I can't make my side effects clear and easy to understand.

Well to the point I am taking Lamactil and Wellbutrin for over a year now. The side effects I have are acne, laziness, always tired. But the side effect I hate the most is really perverted thoughts. Every waking moment I am always thinking about sex of some sort. I can't enjoy a movie because I am always thinking of sex with the person I am with, be female or male. I am straight but I just can't shake thoughts and hate it to no end. PLEASE let me know if anyone is experiencing these side effects.

I just visited my doctor today, after about a year on celexa he changed me to effexor and within a week I will be up to 75mg 2 times a day, I really hope this works for me, I have been really depressed and am in therapy and have just not been the mother and wife and friend that I used to be. I will be monitored very closely, I also take Valium and amitriptyiline.

I got mirena in January of 08, so I have had it about a year now. I have had constant depression, fatigue and chronic headaches. My eyes are are starting to ache now and I am having abdominal pain as well. I get this very odd tingling sensation through my whole body. I have been to so many doctors and like everyone else, all the sudden thought is it mirena? I called to make an appointment to get it taken out, still waiting for the call back. Please anyone write back and let me know if you experience this weird tingling and eye pain. I have also started to have anxiety and panic attacks as well. They put me on Valium and all sorts of stuff. I have anxiety because no one can explain all of these symptoms. I constantly just feel tired and angry. I hope when I get this out I can be NORMAL again.

I had the mirena inserted on Dec 5 2005, I had bleeding for about two weeks and nothing much, up until 3 weeks ago I "loved" my Mirena, I was happy not two to have a period not that I ever had any problems with mine's. I was not until I found this site that I started to realized that my "chronic fatigue" that started in April 06, the hair falling out, sudden anxiety and panic attacks, blood pressure going off the chart for no reason 175/96, after always having low blood pressure, being put on Lexapro and Valium, feeling sad, gaining 20 pounds, not able to lose them no matter what I did, the horrible headaches, migraines and tension headaches at the same time, the fidgeting, nausea and just a general feeling of not being well, that I decided to have that thing removed. Had it removed on 1-15-09, had to be put on a beta blocker 50 milligrams twice a day to lower my blood pressure. I "cried" when I read some of the entries, I almost got diagnosed with lupus, the doctors could not figure out what was wrong with me, I was given all kind of excuses, "well you are 40 now" maybe it is your family life, etc, etc, my mom whom is 74 has more energy than I do!!! Don't let anyone con you, this thing is evil, and Lord knows what kind of other damage it has done to my health. And like many of you I did have a period occasionally, I did not know when, but it was nasty smelling and brownish. Also as of late I started to feel a burning sensation on top of my vagina, I have not been intimate in over a year and had a full exam last year ;therefore, I know I done have any STDs. The headaches were the worst, I could not even comb my hair, I felt like if someone was cutting it in two. Post removal I have not had more bleeding, but I know it is quite early, either way, not having that thing, and even after taking beta blocker I have more energy than I ever had in three years. My son was born in Dec 2002 and I have never felt as tired as I felt while on Mirena. I had double vision, could not control my thoughts and everything was a major disaster, somehow I lost my ability to take control of my life, never again will I put my body through something like this

EXTREME PSYCHOTIC SIDE EFFECTS

I want to preface this by stating that I have never had any mental problems aside from occasional depression, and I have never taken any anti-depressants, or similar drugs, or even ever done any illegal drugs, nor do I drink.

I never would have thought in a million years that an antibiotic would have given me such extreme mental side effects. I was given Z-Pak after a tooth extraction as I had a bad (and similar) reaction to Clindamycin.

I was on the 250 MG X 3 days. After the first day I started to suffer from depersonalization. Depersonalization, in my opinion, is the worst thing that can happen to anyone. Essentially I felt like I was dead, in limbo. Nothing mattered. I questioned reality. I felt like a ghost. It was so bad that I had to break out the Bible.

I had to take Valium in order to sleep, as I would wake up in the middle of the night and have an utterly terrifying feeling of dread. I would wake up and "realize" that I did not exist and have a panic attack.

It has been since December 2nd and only now am I feeling anything close to normal mentally.

Ever since day 5 after taking the drug, I have a burning sensation in my upper abdomen on both sides and a pain in my right side. I just pray to God that this damned drug has not burned out my liver.

Worse yet, I had to be put on Doxycycline, as the Z-Pak did not work, and my extraction site became reinfected.

Thank God the Doxycycline is apparently working with no side effects.

The only positive thing about my horrific experience with Z-Pak is that I went to confession and communion and have accepted Jesus as my savior again in my life.

I also have realized that hell does not need the fire and brimstone. The depersonalization I suffered was the same as separation from God. It was the worse experience ever, and I have been through some tough stuff.

I realize that each drug affects everyone differently, but I have read too many posts listing mental side effects to think that my experience was an anomaly.

If you must take this antibiotic, be sure you understand that it can knock you on your ass if you are not expecting it.

October 22, 1998 I had resp. failure (with intubation). My new pulmonary doctor put me on Singulair 10 mg once a day, a few weeks after. Within time, I started to have numbing and tingling in my face, arms, and legs. March of 1999 the symptoms worsened and started causing pressure in my face, arms, and legs, and anxiety started to kick in. I was told I had neuropathy and to take mobic. Symptoms getting worse, and went to a rheumatologist in June 1999, and he was suspect of singulair. The doctor thought that what I was experiencing was due to the singulair. He (the rheumatologist) discussed this with the pulmonary doctor and the pulmonary doctor did not believe this to be the case. Not forgetting, in March of 1999, I had a ct of the sinus area, and low and behold 1/3 of the cavity was and probably still is full of polyps.

As time went on, symptoms getting worse, and not one bloody doctor could figure out why I was feeling this way. In addition, at times, I was put on steroids for my asthma (not including my inhalers).

Two years ago, my body went into shock, leaving my left side very different than my right side. Affecting: my head, my face, my eye, my ear, my esophogus, my lungs, my arm, my leg.

I have been depressed and anxious not knowing what the heck was going on with me.

Recently ruled out thyroid, and lupus, and possibly ms.

Last weekend, I reviewed the letter from the rheumatologist (dated 1999) and the ct report from March 1999 (regarding the sinus/ polyps) and made copies to present to a pulmonary doctor that I have recently been seeing.

This past Monday the 10th, I had my appt with him. He knew of my situation from the last few visits (in addition, I had met him this past March for a pulmonary rehab program, and thought he seemed to be knowledgeable and compassionate). While waiting for him to enter the exam room, he had read those reports before entering.

The doctor looked at my hands (red as a beet and swollen) and said "You have Churg-Strauss Syndrome, and get off the singulair."

I had done my homework from a few weeks ago, where I looked up untreated polyps.
Untreated polyps, can turn into vasculitis. There are many types of vasculitis, to include Churg-Strauss Syndrome.

I then cross ref CSS and singulair, and low and behold, BINGO!

I have been suffering for ten years, physically and emotionally because of this drug!

There is also recent updates from the fda (fda.gov) regarding singulair, of which most recently includes anxiety and depression.

I suggest before taking singulair, be aware of the side effects. As soon as a side effect comes up, contact your doctor. Also, be aware of existing conditions (like me, sinus problems and asthma) for this could lead to churg-strauss syndrome.

This info is indicated on the actual disclosure (the paper insert that indicates studies, side effects, etc...) not the handout that is given with the drug.

By the way, I am now working with a new rheumatologist in Los Angeles (Cedar-Sinai affiliated) and a new neurologist.

mdklezmer

I had Mirena put in 6 weeks post pardom with my third child with a c-section. The insertion was the worst thing ever!! And my Doctor didn't warn and I almost pasted out. I have no sex drive, painful intercourse, vaginal dryness, burning during urination, massive head aches, blurry vision, mood swings, emotional distress and serious weight gain problems. I too was coxed into this option by my doctor and he said it was so easy and had almost no side effects. I guess this is what I get for taking a mans word!!! I do however have little to no period, but now I am wondering if that is the problem. I mean our bodies our supposed to go through cycles....maybe this thing really screwed something up. I am calling my doctor tomorrow to schedule having it removed. I am hoping I can get my hands on a valium first though....it hurt like Hell last time. I guess I should have looked up some of this stuff in the first place...with what I see here, I would have never had this thing put in.

I just had Mirena implanted and it was not a pleasant experience. I have a high threshold for pain and delivered my children naturally and without medication. I wish I had been given a valium and prescription strength Motrain for this procedure. I passed out and was weak and dizzy the remainder of the morning.
I have read all the posted comments from everyone and am scared to death to wait and see which bizzare side effects will overcome me. I am a true believer that the medical professionals (doctors) are not keenly aware of the general public's documentation on side effects and in this case Mirena. I took the Chantrix (stop smoking drug) this summer and the worst side effects possible presented themselves to me. I quit the drug after 3 weeks of progressively worse symptoms such as nightmarish dreams, auditory hallucinations, depression and stomach aches.
I am going to have Mirena removed immediately -- Monday next week if possible -- because I do not want to experience anywhere near the degree of suffering the poor ladies have in these examples

I hate Effexor XR. I don't really know how long I have been on this medicine because I have almost no short term memory since I have been taking it. I am so hot all the time it's just unbearable. I am sweating when my house temp is 68 degrees. I freeze everyone out of the house, out of the car, etc., because I am never comfortable. I no longer own a winter coat because I don't need one unless it is below zero. I don't own any long sleeve shirts except for a denim one in which I wear as my jacket. I wear short sleeve I have discussed this with my doctor whom always tells me he doesn't think the medicine is the cause of this. Although every time he increases the strength I'm taking, the sweating intensifies. I also wake up in the middle of the night gasping for breath, with an irregular heartbeat and/or my heart beat soaring. I have also experienced the problem with taste. Many things I used to love to eat or drink are no longer tolerable. Nothing tastes quite right. I too have had the dry mouth/cotton-throat problems. I have noticed my emotions are screwed up also. I can hardly cry about the most saddest things I have faced, but will cry about stupid things that don't truly matter. I worry about everything, and I DO mean EVERYTHING, luckily it doesn't last too long because nothing can hold my train of thought for very long. My doc has had me on Zoloft, Celexa and others and there were problems with those also. But I feel that Effexor XR is the worst one I have been on that has caused so many other problems while helping the depression/anxiety disorder. I think the bad outweighs the good, but my doctor refuses to agree with me on this and I have no health insurance to take my problem elsewhere. I have never taken Xanax, Valium or any other "controlled" substances because my doc is afraid of his patients becoming addicted to these drugs. Although Effexor XR is apparently addicting too since you have to be weened off of it. I wish I had NEVER begun to take Effexor XR, good luck to all of you that do! If I knew then what I know now, I would NEVER take it!

Hi everyone,
I cannot live without xanax and its terrible, I have been on them for 5 months and have tried to stop them and its a nightmare. I suffer memory loss, have blackouts that I do not remember what I have said after a few drinks. It does help ease the social anxiety. But I have become moody, sleepy. . Does anyone else have these problems?

I started Levaquin 500 MG on Thursday Aug. 29, 2008. I did not have any problem the first night. But the second day at about 3:00 PM I was working on my computer when my finger joints started to get stiff and my hands and arms started to shake. I just thought I was tired and forgot about it. At 1:30 AM August 30, I was awakened by someone shouting in my ear , You are going to die. I woke up in a sweat and my heart pounding. My hand were stiff and my knee joints were very tight. I also was in a very bad panic attack.
I went to my desk and wrote my wife a letter telling her how much I loved her and my dog Abby. I then proceeded to give her funeral instructions as to which funeral home church and buriel plot.. This writing was 3 pages long. I called my doctor and they as much told me this could not happen. My blood pressure was 240 over 120 when I took it. I took a valium and this calmed me down in 10 minutes. They gave me a new antibiotic for my Bronchitis. So I thought the nightmares and pain was over. Not so quick last night at 2:20 AM I was awake by the screaming in my ears you are going to die. I tried to call my wife but I could not get the word out for help. I tried to move my hands and fingers they would not move. Finally I rolled off the bed and yelled my wifes name she did not hear me.
This drug has set back my recovery from my panic attacks. This drug should be badded by the FDA. But as usual the government does nothing to help the public only big business.

I have been on 500mg Levaquin for approximately 10 days, and thought I was doing fine. I did notice that I felt a bit hyper, but not enough to bother me. Then, last night, I simply could not sleep. I have had insomnia at times in the past, and I have found that mild sedatives such as Valium and Ativan work quite well in small doses. But last night, even after taking Valium, I was simply wide awake. There was nothing particular on my mind - I just couldn't sleep. I got up at 3am to pay bills out of sheer boredom laying in bed. Ultimately, I got a total of two hours sleep. I decided to research if the insomnia and overall hyper feelings might be a side effect of the Levaquin, and read the insert for the first time. And there it is on the first line of side effects - difficulty sleeping. Then I Googled it, and found this site. Apparently, I am not alone. So today, I will contact my MD, and most likely suspend the Levaquin.

its the second day and i feel sick, but coping well, ive got valium to help which seems to help, ive been getting a dry mouth and headaches and feel really run down. body feels weird but i seem not to be worrying at all already, before i started taking it i had very high anxiety but no depression, i hope the side effects go away soon doc said with in a week or two, im only taking a half a tablet then when the side effects wear off ill go to full

I have had issues with my cycle my entire life (started when i was 12 am now 46). THOUGHT this was a godsend until i started feeling like i was in a continual fog. Dizzy, light-headed. I can't walk without holding on to something, tired all the time. Doctor's prescribed Valium to numb my brain from the dizziness.
I've had CT Scans, MRI's blood work, echocardiograms, EKGs, more blood work and all normal.
I am scheduling to have this thing removed.
I can't wait to see if it all goes away.

I took this medication as a malarial prevention whilst traveling through India.
Never EVER again. My boyfriend had suffered from depression in the past and we had heard bad things about Larium in relation to anxiety and insomnia so we specifically asked our doctor for the malarial tablets with the least amount of side effects associated with that kind of stuff. He reassured us that there was no record of Doxcycline ever having caused those sorts of effects.
So off we went- we followed the instructions exactly and began our trip.
A week or so into India I began to notice shortness of breath and stomach pain- I put it down to typical India travelers upset and thought no more about it. A bit later I began to suffer moments of anxiety that were really out of character ( I've never suffered from anxiety or depression). I'm very well traveled ( I work in the travel industry and have traveled extensively in the Americas, Africa, Australasia and se Asia) and so although this was my first trip to India- i knew my anxiety had nothing to do with India itself. ( people kept telling me this but I loved India)
It came to a head on a overnight bus from Goa to Hampi- I was feeling really anxious, sweating and clammy, I couldn't sleep and my breathing was really tight. Eventually I had a full blown panic attack that was almost like a out of body experience- I couldn't see and I couldn't breath. The whole bus had to stop ( embarrassing!) at 3am in the morning. Eventually I managed to get back on and make it to the next town ( although not as far as Hampi) so we could take stock.
I was petrified and had no idea whatsoever what was going on. It never occurred to me it could be the malaria tablets as we had been so clear and our doctor so confident they didn't have these kinds of side effects.
I was worried about being on buses, trains even planes again since I didn't know what caused the attacks and I was terrified another one would happen. I had no valium or any other sort of thing that might have helped. In the end we had to cut our trip short and make it back to Mumbai - In Mumbai I suffered from another two panic attacks- one where I could see the walls closing in in our cheap hotel room. Shortness of breath, tightness all through my body, hysteria, blurry vision - it was awful! And also this ongoing pain and upset in my stomach.
I ended up cutting short a RTW trip that my boyfriend and I had been saving for for over a year and coming home to Australia 2 months early.
It was devastating and I still had no idea what was causing it. Finally a friend said her doctor had mentioned sleeplessness and anxiety as a rare side effect of this drug when she was taking it for some problems to do with vaginal bleeding and spotting. I started searching on the internet and was amazed to find loads of sights with people experiencing heaps of the side effects that I'd been told were never a problem with this drug!
Obviously Malaria is really serious but if I had been properly informed I could have made the decision to come off the drugs and look at alternate medication. For now - Im taking the risk of no malaria tablets at all for my next couple of trips (to Borneo- so not a major risk anyway) and will actually research much harder before taking anything again!

Thank goodness for this sight. If you are thinking you're crazy and can't figure out what's wrong while you're on Nuva, scroll down, you will feel like you're getting a big hug!

I am 27 and have been on the NuvaRing for coming on 8 months and everything has changed. At first I had severe migraines with nausea, a day after starting, that kept going and still occur. They will last all day long and I can take 8 of my migraine medicine and nothing will help. The headaches ruin days, make work difficult, and ruin weekends.

Second: I gained weight around my middle, so perceptibly, I thought I was pregnant. The bloat and gas is constant, I'm always popping Gas-X extra strength but the gas doesn't quit. It was funny at first (yes, I'm immature) but now I'm so uncomfortable, and my pants are tight around the middle but nowhere else. Boo!

Third: ANXIETY. I've been the most relaxed, calm person until I started on NuvaRing, and now I have a prescription for Valium just to keep me from having nervous butterflies all day. The anxiety goes hand in hand with depression, which sucks because I got engaged literally 2 weeks after starting NuvaRing and am always nervous, anxious and sad, and I'm so in love with my fiance but our home life is strained! I sometimes wonder if it's cold feet, but I know it's not. Which leads me to:

Fourth: NO SEX DRIVE. Gone. Dead. Zilch. Zero. I have been the horniest person I know my whole life. I love sex. But I am almost scared of it now. I have no desire to have sex, recoil when my fiance touches me, and get butterflies when I think he's going to try to have sex with me. I sleep as far away as possible, never masturbate anymore, never feel sexy and the idea of sex just doesn't even pop into my head. So unlike me. This causes anxiety, too.

Fifth: Yeast infections and pain during sex. I've never had either of these before. I'm extremely hygienic, and my underwear are constantly filled with discharge. So gross and painful.

I'm going off of it in 5 days and I cannot wait!

I was wondering if high doses of Lamictal can cause seizures. I am prescribed 200 mg 2x daily. I accidentally took 800 mg for a few days after switching from 2 100 mg tabs 2x daily. What followed was miserable. I had this weird vision-thing like a microfiche on its side, running very fast. I got dizzy, then had trouble walking. By the time I got to the hospital, I was having severe tremors, and the (dumb) hospital did not give Ativan for 45 min.after this started. The doctor said it could not be a seizure, because I was slightly aware at times, and could answer questions. I can't remember almost all of it, nor about 24-48 hours after. They had to administer 10 mg of Valium in the ambulance on the way to a separate hospital. The thing lasted for over an hour, I guess, and my husband (who has seizures from childhood also) says it was terrible- full generalized seizure. What ticks me off is that later they called it an anxiety attack, without knowing about the Lamictal doses. Has anyone ever heard of something like this?

Wow! Can I just say I'm scared to death now after reading about all of your horror stories with the Mirena. I have two friends who have the Mirena and both absolutely love it. No mention of any negative side effects from either of them. I've had mine approximately one week and I will say it was a small form of torture having it inserted. I have a ten year old and was told it would be no problem! The first time they were unsuccessful so they asked that I come back on valium to help me relax. I went back and while I was relaxed it still took three different doctors to get it in. Apparently my cervix went back to pre-baby shape which is why it was so difficult. I will say since I had it inserted I have felt bloated and had slight abdominal discomfort. No bleeding though... thats a plus. Guess I'll keep a watch for the mood swings, weight gain, etc.

I am 26 years old, have a great job, boyfriend, friends and family. Everything was great until Oct. 1st, 2007 - the day I started taking Yaz. The first week, I would get into bad moods for no reason, and by the 4th month my life was spinning out of control. Actually, my mind was - my life was still near perfect. Here were my symptoms during this period: Panic Attacks, nausea, shaking, de-realization and so much more. There was a point where I was scared to live and scared to die. I didn't even want to leave my house. This is when I decided to see a psychiatrist who percribed me Klonopin (a form of Valium to get me through the days.)

I stopped taking YAZ The end of Jan 2008 (after I put 2 and 2 together), so I have been clean of it for approx. 2.5 months now. But the upsetting part for me was I thought the day I stopped taking the pill, was the day I would get my life back. Not so!!! I have been feeling a little better but I cry because I I still do not feel like my old self, which was happy, outgoing and full of energy. Does anyone know how long it takes to feel better? I hear 3 months, but I just want to know how long it took for someone to feel normal again. My anxiety is mostly gone, but now I just feel withdrawn and like my head is in a constant fog w/ extreme fatigue :(:(:(

Girls - I feel your pain. And I also see the other side, with the women that had sucess on this pill. My two closest friends were on Yaz and loved it! But for me, it took many months from my life and I am still not 100%. Thanks for everyone who shared. I think this is the first time I ever blogged on a web-site, and you girls gave me the encouragement to share my story. Please feel free to send me a personal e-mail for support.