Dread symptoms and conditions

I have had my Mirena for 3 yrs. (Oct 2006) For a long time my doctor, nurse and I joked about how I was the poster girl for this product. I didn't have much cramping with insertion, had one slight period a month later, and have been period free since December '06.

A few months later I broke out with the cystic acne and they put me on Yaz. It seemed to help for about 6mths. I then went off the Yaz and was fine for a few months, until I broke out again. This time Yaz didn't work. I've delt with them ever since. In the mean time I started having troubles falling to sleep. It was very sporadic at first until this past Jan. (09) My doctor put me on 10mg of generic Ambien. In July she cut me off. I had a full blown panic attack! The next day I contacted another dr who doesn't have a problem with me being on them. She put me on several anti-depressants until we found one that seems to be helping.

I have always been a people person, full of life and love for everyone! Now, I dread going to the store, or taking my boys (11,9 & 4) to soccer practice/games!

My husband has mentioned from time to time that I complain of a lot of headaches. Come to think of it now, they happen nearly every day to one extent or another!

I've been researching the Mirena the last couple of days because of the acne and sleeplessness. MOST posts talk about the symptoms beginning right away, making me think I was crazy and just looking for a reason to feel this way!

My husband has been my rock and is very supportive of me. He has no problems with me taking it out, but will NOT get the sweet lil V done! ugh If I can get this out and have the acne clear up. I'd be HAPPY!

First symptoms: Acne
Then: Sleeplessness, Headaches, back pain especially lower, mood swings, anxiety/depression, oily hair, uncontrollable crying... I'm sure I could go on. The symptoms don't have to be instant. In my case they came slowly...

GOD BLESS!

I started using Nuvaring about 13 months ago after not having been on any type of hormonal birth control for many years. Other than being a little weird out about having it inside me all the time at first, everything seemed fine.

I am just now realizing that my year from hell could be linked to the ring, especially after reading the other testimonials. The least of my problems have been headaches and vaginal dryness. But it is much worse than that; I'm anxious, nervous and moody all the time. I know I shouldn't be upset about little things (or nothing at all) but I can't help it. And I mean screaming, yelling, tearful, throwing things upset. I have missed a lot of work because I'm just too anxious to be there. I have crazy thoughts about my coworkers being angry with me even though I know they are my friends and it's not true.

My poor boyfriend of 14 months thinks I'm unstable, emotionally unreliable and that I have anger management issues. We have come really close to breaking up multiple times because we just can't handle the stress of my mood swings. I even started seeing a therapist a couple of months ago to see if it would help. I can't figure out why I'm there and it isn't helping. Even when my life seems at it's best and least stressful I still tell her that my anxiety level is a 3 out of 10. When she asks me why, I have no idea what to tell her. I have moments in the day when I feel like I am going certifiably crazy and just want to crawl in bed and stay there but I'm too anxious to relax enough to sleep. I have panic attacks in the grocery store, I get an overwhelming sense of dread if my boyfriend leaves the house without me.

Before the ring I road and mountain biked all the time, typically for 2 or 3 hours at a time 5 days a week. I have a hard time motivating to do it now because I feel nervously distracted, fatigued and emotionally dragged out. I even stopped going to my martial arts class which was my life for years. I have dizzy spells and heart palpitations.

Basically, I'm a wreck. I have a great life-I know that there is absolutely no reason to feel like this all the time. I keep telling my boyfriend that I'm not like this, that this is not me. Poor thing has no idea what I'm talking about and doesn't believe me because he's basically only ever known me since I have been using Nuvaring. After another moody day, another near break-up, and another sleepless night I decided to get online this morning to see if I could find any side effect information. I'm so glad I found this site! I called my gynecologist's office as soon as they opened and told them that I feel like I've turned into a psycho and they told me to take it out right away. I hope this works-I am now feeling a little hopeful that I'm not seriously losing my mind after all. I just want to be the happy, energetic me that I used to be.

I started using Nuvaring about 13 months ago after not having been on any type of hormonal birth control for many years. Other than being a little weirded out about having it inside me all the time at first, everything seemed fine.

I am just now realizing that my year from hell could be linked to the ring, especially after reading the other testimonials. The least of my problems have been headaches and vaginal dryness. But it is much worse than that; I'm anxious, nervous and moody all the time. I know I shouldn't be upset about little things (or nothing at all) but I can't help it. And I mean screaming, yelling, tearful, throwing things upset. I have missed a lot of work because I'm just too anxious to be there. I have crazy thoughts about my coworkers being angry with me even though I know they are my friends and it's not true.

My poor boyfriend of 14 months thinks I'm unstable, emotionally unreliable and that I have anger management issues. We have come really close to breaking up multiple times because we just can't handle the stress of my mood swings. I even started seeing a therapist a couple of months ago to see if it would help. I can't figure out why I'm there and it isn't helping. Even when my life seems at it's best and least stressful I still tell her that my anxiety level is a 3 out of 10. When she asks me why, I have no idea what to tell her. I have moments in the day when I feel like I am going certifiably crazy and just want to crawl in bed and stay there but I'm too anxious to relax enough to sleep. I have panic attacks in the grocery store, I get an overwhelming sense of dread if my boyfriend leaves the house without me.

Before the ring I road and mountain biked all the time, typically for 2 or 3 hours at a time 5 days a week. I have a hard time motivating to do it now because I feel nervously distracted, fatigued and emotionally dragged out. I even stopped going to my martial arts class which was my life for years. I have dizzy spells and heart palpitations.

Basically, I'm a wreck. I keep telling my boyfriend that I'm not like this, that this is not me. Poor thing has no idea what I'm talking about and doesn't believe me because he's basically only ever known me since I have been using Nuvaring. After another moody day, another near break-up, and another sleepless night I decided to get online this morning to see if I could find any side effect information. I'm so glad I found this site! I called my gynecologist's office as soon as they opened and told them that I feel like I've turned into a psycho and they told me to take it out right away. I hope this works-I am now feeling a little hopeful that I'm not seriously losing my mind after all. I just want to be the happy, energetic me that I used to be.

i was told i was hypothyroid,but i felt fine! dr. put me on 88 mcg's of levoxyl and i all of a sudden came down with the worst case of acid reflux,which i did not have b4.also,heart palpitations.i choked down this med for 3 years,experiencing hours of burning after my daily pill.i could not take it any more! i put myself on a trial month without levoxyl ,and the burning and acid feelings are gone! i feel gr8! i dread being scolded by my doctor for going off it,but i could not take that burning anymore.ive been to 2 gastroenterologists,plus my general practitioner,all of whom said it was impossible for levoxyl to cause g.i distress.if that is so,why has the burning gone now that i stopped taking it?if u have experienced burning with levoxyl,could u kindly email me/i want to know-am i crazy,or is heartburn an issue for other levoxyl users also/plus,i never felt/looked ill in the first place,so even tho my thyroid functioning may not be optimal,did i really need medication yet?maybe someday i might,but i feel fine,i have long thick hair,decent fingernails,full of energy and not cold all the time-so why do i need meds at this point?(if i ever have overt hypo symptoms,i will have to take something,but why fix what is not broken?) ps-my b/p and cholesterol all very good too,altho apparently ive been hypo about 5 years.

I have had the Mirena for about 3 years now, I first started having noticeable symptoms about 6 months ago. I started having panic attacks out of left field. I am a very happy person, with a good life so I could not understand what was going on with me. I thought I was going crazy. My daughter had to go with my mother for about 2 weeks as I didn't want her to see me the way I was: having panic attacks, paranoia, depression, crying fits. I was put on celexa to help these problems. It worked for the panic attacks, but I'm still moody and can only sleep if I take a 2.0mg of klonopin. I have never had these problems before. I cannot say it was the mirena, but I doubt I have any other reason for it. I recently started getting really bad cystic acne on my face, chest, back, and even on my scalp. I have gained about 25 pounds and cannot get it off for the world. I only have one daughter and a lot of help from my husband and my mother, so I can't understand the feelings of fatigue that plague me. I have a horrible year. Just the anxiety and panic attacks alone have changed me completely. I thought I was abnormal and sometimes just wanted to die. I do feel better, but as I read, I wonder if taking it out will help with the weight, acne and fatigue as my other problems seem to have just vanished after only 2 weeks on celxa, which I thought strange but was thankful nonetheless. I spoke with my doctor today about removal and she gave me a rx for the acne and said we should think about it.... I think I'm all thought out.....

I am so happy I came across this site! I have been experiencing all these symptoms as well. I am 22 years old and I have been on the ring about a year. I have noticed that I gained weight in the past year, but just attributed it to getting older. I have always been a petite woman, and so are all the women in my family, so the 8 pound weight gain in the first couple months was a huge shock. I have tried working out, and eating right, but the weight always comes back and my cravings are unlike anything I have ever experienced. I have also noticed extreme irritability and I seem to cry a lot more than I used to, over simple, stupid things. I am in the best relationship I have ever, I have a great job and school is going great, but I seem to get extremely sad and irritated sometimes, especially the week before I take it out and the week after I put it in. I have never been like this crazy, emotional person I seem to be now. I also seem to have no energy and being active is at times a lot harder than it should be, especially for me, as an active, on the go type of person. I also have noticed my leg is always numb, my doctor recommended a massage therapist, which helped, but it always comes back. After reading symptoms of leg pains, due to blood clots, I am even more skeptical.
I have read up on side effects on other websites, but like other readers, it says some women experience these signs. Maybe a lot of women are like me, and have never posted anything. I have not put the ring back in after my last period and I am not going to. I dread it every time I put it in, but until now I thought it was just in my head. I am not getting back on the ring, lets see if I can get rid of these horrible, hormonal symptoms.

I'm only 18 and I've been using nuvaring off and on for a while.
I took it out the first time because it was making me gain weight, decrease in sex drive, anxiety attacks, painful sex and i had been crying for no reason. I feel so bad for my boyfriend because I'm just now realizing that my lack of sex drive and painful sex is most likely related to the nuvaring. We've both been confused for so long and he's been feeling so bad about himself thinking its his fault :(.

This is the 2nd week I've had it in since the first time i took it out months ago and I've gotten what seems to be a yeast infection...but like someone mentioned earlier, my yeast infection tests come back negative...as do std and sti tests.
This is my second time with yeast infection symptoms and im only 18...
so, already that seems a little fishy (no pun intended).
Ive also been tested twice for all stds and sti's both times negative.

My doctor and mother don't believe any of this has anything to do with the nuvaring and tell me that i shouldn't believe what i read on the internet because most of what im reading is "rare"..but i believe it and i believe its happening to me.

im taking it out right now.
This website has been very helpful!

I have been getting Kenalog injections on and off since I was a teenager. I am now 38 years old. I get these injections about once a year and depending on how bad my allergies get, sometimes twice a year. It is the ONLY MEDICATION that I have ever been able to take that has completely relieved my allergy symptoms. I to have got the "dents" into my skin at the injection sites, which over time have resolved on their own. My hips ache as well but fortunately only just sometimes. Exercise relieves the pain. I am a nurse and know full well the "adverse" side effects from this medication and am reminded by my physician every time I go for the injection. The misery of dealing with my seasonal allergies when nothing either prescription or over the counter helps makes me incredibly grateful for this medication. Everyone will react differently to every medication. People need to realize that it will not work for everyone and there are serious side effects. That is when YOU need to decide if the risks are worth the potential benefits. For me they are, every year I dread spring and summer and will dread it even more if the FDA pulls this drug.

Hello,

I was on Yasmin for 2 years and the only problem I had was bloatedness, heartburn and nausea to the WORST extent. when i went off Yasmin for a few months I felt perfect! after I started taking it a again the Nausea started to kill me, it was so bad I just could not take it anymore, so now I have switched to Triphasil (recommended by a friend) who also had nausea and stomach problems so bad, caused by Yasmin that she ended up in Hospital. Another friend of mine also suffered from mood swings caused by Yasmin. has anyone else had severe Nausea from this product? its awful.

My teenage daughter was taking generic Wellbutrin (manufactured by Watson pharmaceuticals) 150 mg. daily for about 3 weeks or so and started having serious hair loss on the top of her head. The prescribing psychiatrist told her to stop the medication and after about 2 weeks, the hair loss has stopped almost completely. I have read a number of blogs including this one that indicate that hair loss is a side effect yet the Wellbutrin trials only listed hair loss as a side effect for less than 1% of patients. Given the U.S. Supreme court ruling today that says that even if the FDA has approved a medication, a pharmaceutical company is still responsible for fully reporting side effects and can in fact be sued in individual states if they do not provide sufficient warning, I would be interested in hearing ideas of how we can put more pressure on the manufacturers of Wellbutrin and its generic equivalent so that they give better warning of this side effect.

I am just in tears right now... Finally to know what is wrong with me is so overwhelming. I had Mirena put in Oct of 2008 after my son (third child) was born. No other bc had worked for me and I had miscarriages and two other children at age 24 because of this. My doc pushed Mirena like there was no other option on the planet. He raved about it and was VERY quick to just give it to me without discussing any negative side effects. In fact all I heard were positives, I went home AFTER it was in and looked at the official website to see what the side effects may be.
The hair loss started almost immediately, which like many others I chalked up to hair loss that you get after having a baby. I had pains all over my body, but I had a fall at the hospital (off a broken toilet seat with my numb epidural legs) but I didn't know why I was just...sore everywhere. Achy just all the time almost similar to when you have a fever but not quite. Then the memory loss began. This I thought was because my son had been born with Persistent Pulmonary Hypertension and had to be put on ECMO. I thought the stress of it all was just causing memory loss and confusion. The fatigue was constant, never ending no matter how much sleep I got. And like I've read by so many others, thought I have 3 kids and I'm a full time student, my husband works 70+ hours a week, I'm just busy and exhausted. The mood swings, anxiety, and just overall feeling of being crazed started around Christmas time (I thought it was the holidays!)
So I began to cut down on SO much. Like my cleaning, I tried to make the simplest meals I could (I DREAD cooking something that used to be a passion of mine) just getting done what my body allowed. And week after week my body let me do less and less.
Today after an entire weekend of ocular migraines and getting 10+ hours sleep every night and feeling like I have gotten less than 2, fighting with my husband because I'm such a wreck and have ZERO sex drive, constant pain, and after my shower this morning looking at my hair just bawling seeing how much I have lost, I just googled all my symptoms.
I'm so thankful I did, I'm so glad I know that this stupid piece of plastic is what is sucking the life out of me! Thats what its like! Its like RAPID aging. A part of me is outraged too. Why does it take us having to do our own research to find this out? This is SERIOUS. This stupid thing has practically cost me my marriage, I can no longer do school work because I can't remember ANYTHING, I can barely take care of my kids, I make it through the day by the skin of my teeth and honestly I was thinking today if I can't live like this anymore. I mean that. If this got any worse...I don't want to think about it. This should definitely be told to anyone considering Mirena. Yes, it may be a miracle for some people, but there is the chance and I don't care how slight, we are living proof that it happens, that it will suck the life out of you and consequently destroy it. I'm changing docs and getting this thing out ASAP.

i had the mirena put in approximately three months ago (nov. 08). i have been thrilled with it! (so far.) i have been on antidepressants (zoloft, depakote er) for years, and although i have never really had any physical side effects from my menstrual cycle, the mental ones were total anguish. basically 2 weeks (or more) of the month i was in misery, severe depression (pre-pms, pms, post pms). since i have been using this iud, my moods have been great! none of the outbursts, depression, etc...that goes along with hormonal changes of a cycle. HOWEVER, i am only three months into using this, and unfortunately have not been keeping up with my "cycles" (since i have had little or no bleeding). this month i am a little more aware and am noticing feeling bloated, ab. pain, a little difficulty sleeping, some cravings, etc...i do notice a vaginal itching that seems to happen mostly around a particular time each month (which i am assuming is my "period".) so far as sex, it seems like it may have improved, probably just because i "feel" good. basically, what it seems like is that i am happy (maybe too much so, perhaps from the antidepressants?), when i am not having my "period" and during my period, i'm just pretty much level. unfortunately, i am enjoying the "highs" very much, and am thinking i may put up with my side effects (as long as they don't get too bad) in order to continue having them. (i have had the paragard in for the past 10 years, 2 children before that). it feels good to feel good, and not have to "dread" and schedule my life around my periods, pms, post-pms. i am soon to be entering into menopause (i'm assuming) which is something i have really been dreading, thinking i will not be in the bed (but under it) for years. i am hoping that mirena will make menopause a little more manageable. another HOWEVER, i have gained weight, probably 10 lbs. that again is almost a trade off. although i have never really suffered much physically, i have suffered mentally for years, and though it's hard for me to judge with no experience, i certainly think i would rather have the physical! (at least when i'm in the throes of it!)

I can agree with so many of you who've shared your experiences - for about a year I felt more like 'the old me' on Wellbutrin, but in the last six months I've become progressively more fuzzy-minded. It scares me that there are times that I worry that I won't be able to finish a coherent sentence... like I'm speaking in slow motion waiting for individual words to filter through the fog of my brain so that they can be spoken. OK, it's certainly not always like this - and so far only my husband seems to have noticed, but I dread muttering the wrong thing in a business setting. Perhaps worse than this, in the vanity that is our present reality, I've seen significant hair loss from the top of my head - my squeaking clean pate is SHINY in the mirror and I hate it!!! It's winter now, but I can't wear hats all the time, and I just don't happen to work in a 'fashion forward' industry where I might hope to make hats a trend for all to follow. I will be weaning myself off of Wellbutrin and looking into oral and topical arnica b/c I'm nervous about trying Rogaine and begging stuck with that regimen for the rest of my life. The women in my family all have lovely hair; I'm 40, not 80!!

I am 20 years old and i got the copper IUD fitted on the 24th October '08 after being fed up of taking the pill for 4 years.
It has been nothing but trouble since I had it put in!! It was extremely painful when I had it inserted, I have had bleeding in between periods, migraines before periods which I have never experienced before, cramping before, after and in between periods, rectal pain for some reason, bacterial vaginosis, extreme bloating, pain and bleeding during intercourse and mood swings.
Im sick to death of it already and it makes me dread my period, i cant even go out when im on because i feel that ill.
So my advice to you ladies, if your thinking of having one inserted, is don't do it!! Women have enough to deal with, without having extra symptoms to worry about!!!

I was “poisoned” by Levaquin -- resulting in acute tendinitis in both Achilles tendons.

Background:
I am a healthy, athletic male in his mid-50s who has never had an Achilles tendon problem. In early July 2008, my doctor (general practitioner) prescribed Levaquin for an infection. I took the medication for 14 days, as prescribed.
Sudden onset of acute tendinitis in my Achilles tendons occurred near the end of the medication period. The tendinitis occurred in both Achilles tendons simultaneously. Nothing related to my lifestyle would have caused the tendinitis.

Symptoms:
Symptoms included the following at one time or another:
1. aching
2. sharp pain
3. feeling of heat/burning
4. tightness
5. pins and needles in small areas (micro tears?)
6. weakness at rear/base of each heal.
7. When I woke-up each morning my tendons and the back of my heal pads felt sore, weak and tight.
At the height of the problems, I had extreme difficultly walking and negotiating stairs, and I thought there was a risk that my tendons would detach from my heal bone.

Doctors’ Advice:

My general practitioner’s and my podiatrist’s advice was to: (a) not run, cycle, hike or otherwise exercise my legs in any manner other than easy walking and swimming, (b) gently stretch, (c) take ibuprofen, (d) ice regularly, and (e) use heal lift shoe inserts made by my podiatrist. Their advice was based on the view that the damage that was done is more like damage cause by an injury than damage caused by an insidious drug. My readings on the subject indicate that little is known about the mechanisms behind this fluoroquinolone-specific toxicity. It is believed that the tendon’s collagen fibers become disorganized and infiltrated with small blood vessels -- resulting in weakness. And there are no specific treatment plans for this problem.

After 2 months of living with these symptoms, I decided to change course.

My Approach to Healing:

Because I never believed my pain was the result of inflammation, I stopped icing and taking ibuprofen. Because stretching seemed to further weaken the tendon and set me back, I stopped stretching. Because I believe that the body heals itself best when used, I started cycling at an easy pace. I then worked-my-way-up to cycling more aggressively, and to walking in the neighborhood. That’s where I am today. Two days ago I had my first day without discomfort in 3 months. Yet, I have a long way to go. I am not yet hiking or running. It’s a slow healing process with occasional setbacks when I push my tendons a bit harder than I should, Given the progress I have made, I am hopeful for a full or nearly-full recovery in another few months.

Other things I have done in the past month:

1. Taken L-Lysine (1000mg daily), which is believed to aid collagen formation.

2. Taken Magnesium (250mg daily), which some believe may help leech the fluoroquinolone molecules from the tissues because of the affinity of these antibiotics for minerals.

3. Taken Fish oil pills (3000mg daily), which improves circulation

4. Used a heating pad, which improves circulation

5. Started regular Acupuncture (first time for me), which improves circulation

What you can do:

1, Be easy on your tendons until you get a handle on the problem. Don’t over-use tendons when they are in a weakened state.

2. “Listen” to your body and take steps you think best to help the healing process.

3. Tell your friends to beware of potential side effects from fluoroquinolones.

4. File a MedWatch report with the FDA at fda.gov.

5. Share your findings/advice on this forum.

Good Luck

I'm on my second series of the lupron shot, I am also a very young age of 17 years old tying to conquer endo and it's symptoms.... At age 13 I received my first laparoscopy and have been on birth control since "becoming a woman". I have terrible cramps and creeping lower back pain that makes me feel weak and exhausted all the time. I should be full of energy,but i just have terrible mood swings, lost love interest, severe mood swing, extreme hot flashes, memory loss, I've lost so much weight ..... I have lost from 125 lbs to 111lbs in maybe a month. I get very sick to my stomach and vomit when something doesn't appease me such as the smells of certain things, room temperatures, or even if someone around me is smoking. Lupron does take care of my extreme menstrual pains i did have, but sometimes i just wake up to dread the day.... It just feels like anything can make me feel upset and empty on the inside, no one wants to feel like that. From April 08- July 08

the nausea was immediate, and I assumed that was the only side effect. Mind you my first 24-48 hours I started to feel so depressed about life and at night wanted a black hole to swallow me up. Eventually I was filled with panic and dread, never once questioning where this came from because hey, isn't life difficult sometimes? Eventually I went totally psycho on my boyfriend, who is coincidentally on the verge of ending the relationship because he is suddenly not sure if it was the pill or me. When I realized my misery coincided with the exact time line of taking the pill, I looked up side effects online and felt such a wave of relief. Mind you, when I called my doctor's office on a Saturday morning for a switch they wanted me to go to an ER because they didn't want to be liable if I killed myself (the doctor said she never heard of such a side effect in any of her patients - do not let your doctor talk down to you just because her patient pool doesn't do tea time with her). I haven't taken the pill in two days and the nausea is gone and the only sadness I feel is the deep realization of how awful I felt. It's working its way throughout my body, and now I just hope my boyfriend finds the compassion to not hate me for going nuts on me. So when you all right how wonderful your men have been...I'm a wee bit jealous.

I started taking Yaz for about 3 months and couldn't tolerate the daily spotting and severely itchy skin from my knees to my ankles. I switched to Yasmin and though I don't have as much breakthrough bleeding, it still occurs daily a week BEFORE my real period. I have very little to no sex drive and I have to use Aveeno 24 hour anti itch lotion immediately after showering (I've lived in a desert climate for over 10 years now and have NEVER depended on anti itch lotion much less regular lotion since starting these pills). It was so bad a couple of nights that I took Benadryl to get through the night. After reading the posts from others, I'm thinking that I must have an allergy as I, too, have constant post-nasal drip in addition to the itching. I have also noticed more hair shedding but luckily for me, I have thick hair. The only benefit is I don't seem as moody as with other birth control pills and have kept my weight somewhat normal despite not exercising and overeating on the weekends. I am going to my PCP to change back to Ortho Novum although I dread the moodiness that comes with increased estrogen. Why can the drug companies come up with incredible drugs like Cialis but 30 years later, we still have @$#! for birth control pills?

Side Effects: Yaz -- daily breakthrough bleeding
Yasmin -- breakthrough bleeding 2-3xs a week
Both-- severely itchy lower legs, constant post nasal drip, hair loss, severely decreased libido, occasional leg cramping

Hi. I went on Lamictal April 2007 after being diagnosed w/ BiPolar. The key issue that brought me to the psychiatrist to begin with was acute depression following a divorce, move cross country, losing my job and my only son going off to college. All the big stress factors - short of death in family. Nonetheless, I was nervous that one year after all these crises that I was, if anything, feeling worse. I had been able to handle all the changes during them, but now that they were over all I wanted to do was sleep all day.... Anyway, I had been on Paxil for years re anxiety, and my psychiatrist decided to keep my on the Paxil till I tolerated the Lamictal, then get me off the Paxil..... Well, the 20 mg of Paxil and the 100 mg of Lamictal worked great, I thought; the Lamictal really raised the bottom.... BUT, apparently Paxil fuels mania, so after a few months, I was taken off the Paxil completely and my Lamictal went up to 200 mg. Almost IMMEDIATELY upon going to 200 mg Lamictal my ankles / feet / legs got enormously swollen. Plus, I noticed that my hair started to fall out // thin out.... Plus -- and I don't know if this is the Lamictal or the absence of the Paxil, but I sob uncontrollably almost 24/7. The sobbing and anxiety and sense of dread and sadnessness has persisted even when the Lamictal was dropped to 100 mg and the shrink added first Clonazepam .5 mg, then when that wasn't calming me, changed me to 1mg Xanax -- each as needed. The Xanax isn't helping me either, and now I also feel paranoid. So, in short: Lamictal at 200 mg makes my feet / ankles / legs swell or suffer edema; Lamcital as low as 100 mg makes my hair thin out; and either the Lamictal or the loss of the Paxil or these anti-anxieity meds (Clonazepam or Xanax) are making me paranoid, profoundly sad and depressed, panicked, anxious, stressed out and, most urgently, make me sob uncontrollably 24/7... My shrink says that we should use anti-depressants with bipolar, and that Paxil fuels the mania, but I tell you, I'd rather be manic and screaming at everyone than so depressed that I'm fearful and sobbing constantly.... Any answers out there: Any anti-depressants for your bipolar?

I started taking Levequin before a procedure I was getting (cystoscopy) and was told to take ot for 3 days, 500 mg. The first day i took it I had severe insomnia/heart racing/shortness of breath but I attributed this to nerves due to the proecdure I was getting , the night of the procedure I slept fine but I was also doped up on anesethia. Yesterday was my last night of Levaquin and I once again was up all night. Not only that but I have severe anxiety, feelings of hoplelessness, dread and just worry all day long. I don't knwo what to do. I am 31 years old and 2 weeks ago was feeling fine. I actually took some xanax last night for the anxiety and it really did nothing although it usually does help when I have minor anxiety. I really do not know what to do. I have to go to work every day feeling depressed, achy and lethargic. I just made another dr appt. 3rd dr in 4 days. I have lunesta at home but it rarely works for me. Any suggestions to help me sleep and get rid of the jitters??

I have a 15 yr old son, that has been on Singulair for 4 years. He used to complain to me about not being able to sleep through the night, he couldn't concentrate at school. He was an honor roll student. Then he became short tempered. He also isolated himself, and no motivation. He would not want to do anything. He was depressed. Does not want to shower or anything. He has absolutely no self worth. He would talk about having these problems and I would just say to him that maybe it was just the changes going on. New school, changes to his body, it's just those times where changes and expectations are harder. Some handle it better than others. Than everything just continued to go down hill. My son is very intelligent, so when mom did not listen, he decided to self medicate. Went online to try find out what was going on. Tried to find what would help him. He learned quite alot about pharmacology(spelling???) at any rate he then started experimenting with other drugs. Prescriptions drugs. He just wanted desperately to be happy. I found out about this. He was getting into trouble at school, grades fell. So we then sought counceling and then a psychiatrist. They put him on all kinds of meds. Prozac, Ridilin anti pshychotic drugs. You name it my son has probably done it. Now my son is an addict. I now hear all these things about Singulair don't know what to think.??????? I have had him a drug treatment program of which he was kicked out for overdosing. Then, the hospital of which just put him on more drugs. I don't know what to do. He has asthma, when he does not take his Singulair the asthma really kicks in. I know this we are going to look for something else to treat his asthma. I need input. My thoughts are simple. I believe that it is possible that the problems my have started with Singulair but then my son took a step further. I think to try to survive. But in the mean time he is now an addict and I'm scared of whatever permanent damage that may have occured over the years. Are there any other parents out there, that think their teenager might be going through the same problems? If so PLEASE reply to this message.

I was prescribed Avelox for a sinus infection and bronchitis. I didn't have any problems with the Avelox until after the second dose. By the third dose, my abdomen was extremely distended- to the point that I could barely eat b/c the pressure from my abdomen was pressing into my chest area and caused trouble breathing. I saw my doctor after the 3rd dose and explained how bloated I was. She told me that sometimes antibiotics upset your stomach. I was told that I didn't have to take any more of the Avelox (which I wasn't planning to take anymore anyway). It has now been 8 days since I've taken Avelox. I am still bloated. I think the bloating is slightly better. But I'm still miserable and wondering when I will feel better. I dread eating because I know I'll feel worse when I do. I'm just thankful that I haven't had some of the other reactions I've read about here. I'll never take Avelox again.

I too was taking LIPITOR. After 3 months I became short of breath. At first I put it down to the weight that I had regained.I had lost 18kg.the year before. I had muscle pain, nausea, headaches.The Lipitor reduced the LDL alright,but the shortness of breath became worse and worse. If I was sitting on a chair and dropped a piece of paper on the floor I would be completely out of breath from bending over and picking it up! If I was walking for more than a few minutes I would be out of breath and had to stop. I quickly regained my breath; but the moment I started to walk again I would become breathless again!! My heart specialist decide to do an angiogram, that was o.k. He told me it was my weight that made me short of breath, I disagreed with him. My G.P. did not know what caused it either. I had had problems with Pravachol, severe muscles stiffness and pain. I could not straighten a bend leg or bend a straight leg.It was only after I studied the enclosed leaflet in the box of Lipitor that I noticed the RARE BUT SERIOUS SIDE EFFECT: Shortness of breath, if you suffer from this stop straight away and see your Dr. it said. It turned out that the ALVEOLI are affected. I had a lung function test done which showed my lung capacity was down by 20%.After cortisone treatment it has improved a bit but it is still 10% down and it effects me every day. I tire quickly and get out of breath walking uphill or against the wind.If there is a class action going let me know please! I am so fed up . I am only 63 but feel like an old woman.I will not take anymore cholesterol lowering medication; I rather live 5 years less, if that is the consequence.

I've had Mirena in four approximately 5 months now. It wasn't unbearingly painful to have inserted and I was having mood swings and riding emotional roller coasters months before I had it placed. I spotted for about 6 weeks after it was placed, but my periods now have gone from 4-6 days a month to 2 or none. My only concern is that I now have some vulva fissures that I can't really relate to anything else but this. I talked to a midwife about it and she believes that it's due to a lack of estrogen. She said that breastfeeding can sometimes decrease estrogen to the point of thinning the skin and causing these fissures, but I don't know. I never had this problem with my first child and the only thing different is that I'm using Mirena. I don't know if I should have it removed or wait it out until my son weans and see if there is a change. My insurance paid to have it inserted, but I have no insurance now and I dread seeing the price tag to have it removed.

I have been on Levaquin for close to 4 weeks. 27 days at 500mg and the rest at 750. I have a severe open wound after a foot surgery. I started feeling like my shoulders had been hit by a bat. Slowly every single joint in my body is in pain. I cry with every move I make and dread going to sleep for fear of how painful and stiff my body will be in the morning. I begged the Dr. to remove me and he has agreed. i just pray it leaves quickly.