Bridge symptoms and conditions

I had been on BCP a couple of years ago but was really terrible about remembering to take a pill every day. I went off of those because I was no longer sexually active, and I didn't see any reason for it. When i met the man of my dreams and became active again I wend to my Dr. to go back on Birth Control I told her about my previous lack of ability in the pill-taking department and she prescribed the NuvaRing for me. At first I thought it would be great! I couldn't ever feel it, I never had the problems with slippage that other people seemed to complain about, and it didn't even bother my boyfriend or I during sex. After 2 months on the ring though, last night was my day to put it back in, and I didn't. My libido wained to absolute zilch (in talking with my BF about this last night, we realized that we had only made love 3 times in the past 2 months) I just never wanted it. The times that we had made love, I suffered from extreme dryness, to the point where it really hurt a lot, even using lube. I also suffered through 2 UTIs and a Yeast infection in the last 2 months. (not to mention the 10 lbs I've gained, and the crazy irritabless/depression that the poor guy has had to put up with for the last 2 months... best described by me as "a boat load of crazy")

My BF and I discussed it last night and we decided it was best for me to stop using the NR to see if my libido comes back (it seems to be on its way already) and see if the dryness improves. I think my boyfriend put it best when he said "if it makes it so that you never want sex, and when you do - it hurts, that's one hell of a birth control. Can't make babies if you never make love!"

We decided to just continue using condoms as we have even with the BC. (I know they're not perfect) We realize that there's a risk of getting pregnant, but like he said "We'll cross that bridge if we come to it."

I'll see how this next month or two goes... if I am back to normal, it's got to be the NR.

i have had my mirena for about 1 1/2 months now, and so far i love it, i have had the spotting for the first month which doesn't bother me and now my period is on and i do have very bad diarrhea which im sure is associated with the period more than the mirena itself. haven't had any lack of sex drive in fact i 've wanted to have more sex, and i haven't' been irritable or anything else, so some of the side effects i believe everyone is having may be made up, think about it if you read over and over and over again how bad the mirena is your going to begin to feel that way i know if i tell myself that my arm hurts all day long then eventually it feels like it hurts..neways all im saying is relax stop reading these scary ass posts and do something to take your mind off of it, i know 3 other people who have the mirena that live down the road from me and NONE of them have had any of these problems...ladies i think you are just trying to find something to blame it on...

Im 22 yrs. old and have two little boys. My husband says he hopes to one day have a girl so i figured 5 years should be enough time to decide. I got the Mirena last year and the only side effect i had was hair loss,BUT i'm not quite sure if it was the mirena or from just having another baby. But other than that I ABSOLUTELY LOVE IT! I have been reading all these reviews and they were almost all negative I was wondering if something was wrong with me. Since I got the Mirena last year I lost weight, no more cramps, lightened periods, and a better sex drive(probably cause I don't have to worry if im going to get pregnant, I feel safe). So would I recommended the Mirena , YES but it clearly seems that every woman's body is different so it might be great for one person and not so great for the other.

I don't know where to begin; I have a text box in front of me that says "add a new side effect of the Mirena" but all I see are the same side effects over and over. That, in itself, speakes volumes. As for myself, it's been depression, weight gain, exhaustion and yet unable to sleep, pain down to my knees - of course all of these symptoms can be explained by everything else in the world - who, these days doesn't have money problems, stress, employment fragility, etc.? But I know myself, and this is wrong.

I had mine put in March 2009 and after a month I told my doctor I wanted it out. She said I didn't give it enough time (apparently six months is the magic number).

It's now been three months and getting out of bed is an act of heroism for me. Sex is out of the question (well, we have given it a go a couple of times and he can indeed feel the strings, contrary to what I was told - perhaps it's because he's - er - oh, never mind.)

I bleed erratically and it stinks; if I hadn't lost my sex drive already I'd be put off just by that.

I got the thing not for birth control but for pain and bleeding (not that it makes a difference)- it has made the pain worse, so I don't understand why I'm so nervous about asking my doctor (tomorrow - Monday) to have it removed?

Prescribed Avelox after previous antibiotic could not clear up sinusitis. Avelox cleared it up within three days, but I feel worse now. Extreme agitation/anxiety, tremors, twitches, no appetite, boughts of depression, dizzy, lack of coordination, accelerated heart rate, leg shake, cold extremities, very strange, vivid dreams. Doctor told me to stop taking and side effects should clear up in a few days ( I hope). This is nuts. I feel like I am going insane. I could not go to work for three days due to side effects.

I have had my Mirena for 2 years.I have not periods but i still do have cramping sometimes. It is bearable though, it is a good option for me. The first few weeks were painful, but it does get better, give it a few months before getting it out if you are considering that route. The only real problem i have had, is mine "creeped". It is moved up high in my uterus and the strings are no longer visible. I have to get a ultra sound every year to determine the location. This will cause me to be put under and have day surgery to have it removed. I will cross that bridge when i get there. HAs anyone had one removed that had creeped?

I am a 44 year-old woman. I have been taking Topamax for 13 years! I take 100mg at bedtime (would NEVER take it during the DAY--that's ASKING for sedation). I take it along with 400mg of Wellbutrin & 30mg of Lexapro!!! I've taken various doses over the years. It was initially prescribed as a mood-stabilizer for my bi-polar II, and so happened to control my migraines. Happy Days!

When I FIRST took Topamax I remember having the strange feeling of small miscroscopic "fish" (or something) swimming under my skin, across my cheekbones and over the bridge of my nose. I never got a rash or anything. I did not feel that this passing side effect was anything I "couldn't deal with" as the medication stablized my mood without the HORRID side effects of Lithium, Depakote, Valproic Acid, etc!!!

All this time I have done very well and have NEVER had any health problems from the Topamax. I am VERY confused by folks who claim it gave them "mood swings"--as its effect is to make your mood stable!!! I don't understand how that could happen. Also this is a LOT of people having MAJOR effects from VERY low doses of the drug (50- 75mg mostly). Perhaps folks are medication sensitive OR something else is going on as well???

The nuvaring should not be legal. It made me insane and violent and gave me racing thoughts. I could never sleep. I was mean to people. It made me itch like hail!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

P.S.- Here is a comment from my boyfriend who got very upset because of my side effects on the NR:

"She went crazy one night and threw something across the room for no reason, because she said something to me that made me furious. She was completely irrational and i though she was being possessed by Satan. Than, we found out it was THE NUVARING ALL ALONG!"

I can't believe this!! I was searching the internet to see if there were any side effects from the mirena as one gets closer to the end of the Mirena life and I came across this site. I'm so blown away. I am getting my Mirena taken out in a week because it's been 5 years that I've had it in and I NEVER realized all the problems I've been having in my life was because of the IUD!! This whole time I thought it was just me and I was going crazy. So looking back on the last five years it's all making sense to me! Not only was the pain so unbearable getting it in, but the pain in my abdomen was so bad for 2 weeks straight, and no let up with the pain, that I almost passed out from it. My horrible boyfriend at the time told me suck it up. I said a prayer one night praying for the pain to go away and that if wasn't gone by the morning I was going to go get it taken out! I woke the next day and the pain was gone. But this wasn't the end. I developed depression ( I thought it might have been because of the crazy relationship I was in) which I'm STILL prescribed for and I also severe anxiety attacks,which I NEVER had before in my life! dizziness, lower backaches, crying fits, extreme fatigue and copious amount of hair loss, right around my hairline. I used to have lustrious hair which I had to have two hairties in to hold it up, now I can use a tiny little jaw clip to hold it all up!!. Never in my wildest dreams did I think it was because of the Mirena. I thought how great it was that I got it put in and didn't have to worry about it for another 5 years, since I have a terrible time taking regular contraceptive pills ait the same time every day. My memory has definitely been affected and another symptom I never thought would be possible is the weight gain. A year ago I was diagnosed to be Pre-Diabetic and have had to change my diet and exercise. You think I would have lost the weight, NO, quite the opposite I have actually gained more weight. I have little to NO sex drive and I USED to have a very high sex drive. Now this is all making sense to me. I really wish I had found this site sooner! Like 5 years ago!!! So thank god I am getting this thing taken out of me next week. I am opting to get a diaphragm fitted and getting all these harmonies out of my system, maybe I'll go back to being my old self! (tears in eyes as I am typing this!!! ) All these years....who would've known. I am still in shock!!!!!

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

I got a couple of kenalog shots in 2004 and 2005 following a surgery that left scar tissue on the bridge of my nose. I never had any bad side effects. I wanted to follow up and get more but the cosmetic surgeon that previously gave me those shots what not accepting my insurance any longer so I went to another plastic/cosmetic surgeon. He told me that I would need a revision and a Kenalog shot would not be beneficial. I pointed out another area on my face that I was concerned with and he agreed to inject the kenalog into a scar on my eyebrow which caused an indentation on my forehead! He won't admit this is a side effect from the kenalog shot. He even tried to convince me it was a frown line, but I know better. I have it all the time even when I'm not making expressions and it's only on the side of the injection.

Hello All, My Levaquin nightmare began on June 18th, 2008. The side effects I had were so unbelievable, most of you, if not all of you will believe this. I had severe night sweats which would transfer over to a extreme cold chills, which would allow me to sweat like crazy. Bathed in Sweat. I thought there were small needles all around me and poking me everywhere. My feet, toes, knees and buttocks tingled like there was no tomorrow (and still are to this day). When and how can I make these side effects go away. I'm sick of them. I no longer have the night sweats or the bitter chills, I'm now totally aware of want is going on around me, while taking the med and several days after I couldn't even tell you my name. The bridge of my nose, and running across to my ears tingled like crazy and my ears rang all the time, and they still ring once in a while still. I need to know when this feeling of tingling in my hands, feet, knees, legs and humming in my ears will go a way. Help! I think this drug needs to taken off the market. I took a total of 17 pills. My first scripted was for 15 days and by not knowing any better less then a week later and another doctors appointment, and one more script, which I filled. I took two pills from that bottle. My husband called the doctor and she told him this wasn't normal. She told him that I was to stop the med asap, which I did and I'm still having these awful tingling. If anyone, anyone has any suggestion of how to get those med out of my system I would certainly appreciate it. God Bless each and every one of you. May you all find relief.

I was taking 500mg three times a day. After 1 week I developed severe joint pain and swelling in my fingers. I got an itchy rash on the bridge of my nose and over my eyes and inside my nose. The joint pain continued to my knees and toes. I have been off of the medication 3 weeks and I am just starting to feel a little normal. a different doctor put me on 800 mg of Ibupropen 3 times a day and after reading up on the side effects of Cephalexin I began taking Benadryl which has helped a lot.

I am in my second week of this pill and I suddenly developed a rash all over my face, mostly on my cheeks and on my eye lids near the bridge of my nose. Has anyone else experienced these side effects??

Please let me know if a class-action lawsuit is ever filed against this Pharm Co because I will file a suit to get this dangerous drug off the market. Yasmin/Yaz almost took my life in January 08. My OB/GYN put me on Yaz in Oct 07 for bad periods and cysts on my overies. Within a month my entire personality changed and I started losing my hair. I experienced a complete loss of sex drive, became depressed and was either constanting crying or raging at someone. However, my adult acne did clear up. On 1/27/08 I experienced extreme pain in my calf that moved up to my thigh within 48 hrs. I went to the ER and was told that no only did I a condition called DVT (Deep Vein Thrombisis-blood clot) in my leg but that the clot had broken off and moved into both of my lungs and I had bi-lateral pulmonary embolism. I can't even describe how incredibly painful this was. I was admitted into the hospital for 1 week and was put on powerful blood thinners, which I will be on for about a year. It's now been nearly 6 months since I was diagnosed and the DVT and it is still in my uppper thigh. But am grateful to be alive. If you would like to contact me I would be glad to answer any questions regarding this situation and my email addy is ****** PLEASE DO NOT TAKE YAZ OR YASMIN OR LET ANYONE IN YOUR FAMILY TAKE THIS MED, IT COULD KILL YOU.

Awful, terrible, unbearable painful anxiety, panic and depression that just would not let up after a 7 day dose. Each day it got worse and I didn't realize it was the Avelox. It took weeks and weeks to get out of my system, with the help of a doctor. This was truly the scariest ride of my life. I wanted to jump off the bridge to end the suffering but I knew I didn't really want to die, I just wanted to feel better.
I've never been depressed in my entire life. It was an unfamiliar feeling to me. The thought of suicide never entered my mind until this antibiotic.
This experience was unreal and I was robbed of months of my life because of it. So were my boys and husband. I thank god for the peace I have now and that it's over.
Don't take avelox. Even though it helps some, you never know if you'll be the one that will have a rare side effect. Feel free to ask me any questions.

I was on Paxil for 12 years.
The early years I struggled to stay awake then gradually over 4 ti 5yrs I developed a boundless energy, with a constant elated and irritable mood, my thoughts and behaviors leaned towards the aggressive while highly confident. Never used a winter coat with temps well below freezing, I was always warm. Never needed more than 2hrs sleep each night.
Developed muscle aches, rash on both cheeks and along bridge of nose.
I read up on Paxil and discovered that these symptoms were Paxil related. I took myself off of it. I was on 20mgs then one month of 10mgs after that I quit cold turkey. While withdrawing I felt like my head was in a wind tunnel, a constant whooshing sound going round with dizziness, brain jolts, agitation, anger and crying, After 1 month of being off I began to feel better. If you want to quit you just have to tough it out. Once you get passed the withdrawals it is well worth it. I understand the link between school shootings, criminal behavior and serotonin reuptake inhibitors. It is wonderful after quitting to be in control of your thoughts and actions once again. I suggest you never start taking this medicine as it will be a nightmare withdrawing from not to mention the psychotic behavior it is known to cause in some cases.

I'm starting to see small itchy patches of skin in random places on my arms, and even above my eye. I have only taken lamictal since Feb. and on a low dose i experienced no problems it is the first medication that has ever worked for me, I'm Bi-Polar II. Once they stepped me up to 200 mg i got really sick and started to develope the rash...Does that mean i have to stop taking it? I'm really confused.

redness under my eyes on the bridge of my nose as well as on my arms