Excuse symptoms and conditions

I had been on Depo for basically 14 years, I came off of it, got pregnant 3 months later and after the birth went back on it. I had gained a lot of weight with it and had all the side effects plus so when I saw mirena I thought finally something better for me. I had it inserted in aug 2008. Other than painful insertion, like labor delivery contractions the rest of that day and some the next everything was fine. I didn't get my periods back, the only thing I liked about depo, and my weight was coming off and I was actually wanting and enjoying sex again. . A year later, and 15 lbs less, thought I was still doing good. Well I thought maybe my teenage daughter had jinxed me because I was bragging about still not having a period and I started, well a week later I am still having some sort of a period. It's very light and spotty, just when you think it's gone away, well there it is again. I have been noticing vision issues, I figured it was from where I had lasic done several years ago was starting to go but after reading everyone else's posts I think that's not it now. Everything I was experiencing, the back pain, blurry eyes, feeling sad, lower abdominal pain, I made an excuse for until now. I have recently started to loose my sex drive again. I hadn't had any, or so I thought, problems until several weeks ago. My problem is I can't take the pill, I don't want the depo back because of the side effects, the patch won't work for me so I am not sure what is left for me to take, I saved up for this and put so much money into it and now after reading everyone else's post realize that this BC is not for me either.

I have had Mirena for 18 months now. I love it. I have had no side effects that you all are describing. I have 4 friends that switched and all love it and only one had to have a follow up to have the strings shortened.

As far as the weight gain, ladies, let’s be honest. We are not 18 anymore and as we get older it is only going to become more difficult to keep weight off. Blaming it on a B/C....lets think about that last chocolate bar we ate because we were busy carting the kids off to a sports practice HMMM....
With any drug comes side effects, headaches, nausea, and some other terribly worse, but lets again be honest, all of these were pointed out in the literature available.

I just thought I would take the time to write my support as this does work and work well for some women, just not all, same as any other form of B/C.

Im so thankful i found this site, i was put on lisinopril about 2 months ago, i woke up one morning and felt dizzy took my bp and it was really high, i had never had problems before so i was surprised, went to the er where they check my blood and did an ekg, everything was fine, i have been so tired lately, my sex drive is completely gone, im having tingling in my hands every night, and my heartbeat is always elevated, my doctor is giving me an excuse of being over weight, well im only about 20-30 lbs over weight and never had this problem when i was 30 lbs heavier.. i have no energy to go to the gym, i was working out 3-5 times a week before, now i do good to get a full days work in, im always feeling shortness of breathe, im so sick of this, after reading this forum i have decided to stop taking it and hoping i get my energy back so i can get back to my life thanks to every one and their post.

EFFFF Levoxyl!!! My life has been really, really difficult since being on this medication. Reading all of your posts truly makes me feel like I am not alone in my struggle, anger, and frustration! If we could only sit in a room and talk about this face to face, how much better we might all feel. I think there needs to be thyroid support groups. Does anyone know of any?

I went back on Levoxyl about 2 months ago, because I was feeling tired again. I took myself off of it a year ago because I felt like I didn't need it anymore. I wasn't feeling great being on it and I had given myself a year on it already. Which by the way was a year from hell. I experienced depression for the first time in my life, gained about 20 lbs. from binge eating (never had an eating disorder or weight problem in my life), was fatigued constantly, then blamed myself for being so lazy all the time, lost friends because I canceled soooo much on hanging out, "I'm really sorry but I'm just not feeling good." Yeah that excuse gets really old to people with a normal functioning endocrine gland. Mind you I was diagnosed with this at 23. Sure I am mad that I have this problem, but when I am trying to get myself well and take the steps necessary per my doctor, it's really frustrating to just not feel like yourself. During the year off of it I took a natural thyroid support. Feeling fine, I slacked on taking the support thinking I had kick started my thyroid.
Two months of being back on it and I'm done! In a moment of emotional anger I threw my Levoxyl pills in the toilet. You know what they did...expanded to the size of a bazooka joe bubble gum piece. Uh that's big considering it's such a small pill.
I went to my doctor today because I've been experiencing bloating, pain and constipation for 3 weeks now. He told me to drink coffee and take benefiber, because perhaps I'm not getting enough ruffage in my diet. Just to see if I'm crazy about the expanding pill, I dropped an advil and tylenol in there. They simply fizzled down. I think these meds are making me bloated etc. and it's not worth it to me to feel this way. My body is telling me something is wrong and I need to listen!!
I eat right, take vitamins, drink PLENTY of water etc. and I still feel crummy.
I have been doing research online and have found a product called IODORAL. It is Iodine and Potassium Iodide. I have read many posts from people stating that this product has given them energy, helped with fatigue, their memory, overall well being. What was shocking for me learn is that Iodine helps fibristic breast tissue along with other parts of the body. Did you all know that 30 years ago breast cancer affected 1 in 20 women, and now it's 1 in 8 ???! Iodine used to be part of our diets. It has since been depleted from our soils and other foods. Bread used to be made with Iodine. Now Bromine is used in the baking process. Did you know that Bromine blocks the thyroid from producing necessary hormones for function. I bought myself some IODORAL and I'm going to see if it works. I am not a doctor but I am a person who is very in tune with their body. The bible says that there IS A CURE for everything on earth. I pray that all of you who have posted on here and are in discomfort do not give up your hope and find a different doctor or start doing your own research and be your own advocate for your health. There has to be something better out there! Something that isn't hurting our bodies! I am not giving up hope yet and neither should you!

My son was put onto 4mg Singulair when he was three years old. He is now six years old. For the past three years he has been a very quiet child, to the point that people commented on how shy and withdrawn he was. He never wanted to go anywhere or do anything. His favorite activity was lying on the couch watching tv. He was always thirsty, frequently went to the toilet,often complained of a sore stomach & had several bowel movements every day, did not sleep well at night, was often grumpy, could not concentrate for very long, was frequently ill with cold-like symptoms and did not really like you to touch/hug him. At the beginning of the year he was diagnosed by an occupational therapist as having low muscle tone. In March of this year, his pediatrician increased his singulair to 5mg. He began having terrible pains in his legs, to the point that he would cry and be unable to walk to the toilet at night. I took him to my GP who did every blood test under the sun and x rays of his pelvis and legs. He could find nothing wrong. The only thing that had changed was the increase in Singulair. I had a look on the internet and found this website. I immediately decreased his dose to 1/2 a tablet for a week and then 1/4 tablet for a week before taking him completely off it. Within a few days our whole family and his teacher and therapist noticed a huge change in his personality! He talks all the time now, he laughs a lot, he loves playing outside and has lots of energy. He teacher says he is much more receptive at school. His occupational therapist says his muscle tone has improved. He has not had one single leg pain since coming off the medication. He is sleeping well at night, his stomach is never sore and he has not been sick at all. Not even one little sniffle!! Best of all he is a normal, affectionate little boy. I feel very angry with the manufacturers of Singulair and with his pediatrician, it feels as though my son has lost three years of being a child. He felt terrible all the time and I had no idea! I have told everyone I know who has a child on singulair to look at the side effects.

I am SO glad i found this website. I am 18 and have been on the nuvaring since i was 16. I have been off of it for almost 3 weeks and I feel amazing. I got the nuvaring because it was easy and I was bad at remembering pills. Since I have been on the nuvaring i feel like a totally different person than I used to be and im not exaggerating.I have absolutely NO sex drive, i have been severely depressed and low self esteem because of how much weight I have gained because of it. A total of 45 pounds! its DISGUSTING. I eat very healthy and exercise so there is no excuse for the weight gain and I seem the starve myself at times and not a pound lost. I am now off of it and my cravings have gone away, I am sooo much happier, and guess what! I want to have sex again! I would not recommend the nuvaring to anyone!!!

I was prescribed budeprion150xr on April 6 after an ER visit having MDD and took over 6mg of klonopin..anyway during the day and a half stay I asked the nurses desk if I could get my bupropion SR 200mg and was working fine and they said they would call the hospital pharmacy and never got at 7am,12pm,nothing then I talked to the attending doctor at 5pm and told that I couldn't take it. I had severe headaches and ask also for Advil or Tylenol..nothing. Next day same excuse...horrible hospital. the prescribed me the newer budeprion. took it next day and felt sleepy and more depressed I slept three hours in the afternoon,feel irritable,robotic and an urge to leave and never come back to where I live. 7 days of hell..I am going back to bupropion 200mg sr...what a nightmare!!

i had the mirena inserted in sept of 2007 after m son was born. this was a good option for me because i can't remember to take pills regularly, and my OB said that she's seen people gain a ridiculous amount of weight with the shot...but i needed something that was going to be easy for me (and as a plus sized woman already, weight gain isn't an option). THIS was easy,. i had no problems...insertion was easy, bleeding stopped after about 5-6 weeks, and i haven't had a period since a couple months after that!

i was talking to my sitter (close friend of the family) and telling her how my hair has been falling out lately. i had chalked it up to stress at work, but she said her sister in law had the same problem, and that it was a side effect of the mirena. i started to think back, and i've always pulled a few hairs out after a shower, and it's gotten worse in the past year, but the last few months have been insane! i got out of the shower the other day and my hair had parted funny while i was drying it, so i was running my fingers through, and found about a quarter sized bald spot! after further inspection of my head, i found two smaller spots...very thin, but not completely smooth like this big one! i was horrified! and of course it's right on top of my head, just off the center...very difficult to hide unless i wear a ponytail...which then cracks the rest of my hair off! i can't win!

so then searching for other side effects i was unaware of, i find this site and a whole bunch of other stuff i've been experiencing, not relating it to mirena. i have no sex drive, my arms tingle at night (which had me thinking i was becoming diabetic), lack of patience and mood swings (which i blamed on my husband being an idiot), headaches (blamed these on the high blood pressure. why was this prescribed if i have high blood pressure?), leg pains (blamed this on the new shoes)...everything had its own excuse. but putting it all together...it's likely because of mirena!

i have my annual appt tomorrow, where i will be discussing this AT LENGTH with my OB/GYN.

OMG!! This is insane, I thought I was going crazy, I started YAZ about 2 weeks ago, I usually try to maintain healthy and workout a lot, but in 2 weeks i gained like 10 lbs out of nowhere!!! I am freaking out! I completely lost sex drive and as well as other said completely dry, nothing can make me wet, I also notice that I started getting a really heavy discharge everyday, Oh and depression (mood swings, snap at everything I feel like I don't want to live anymore, I don't care for my job as I used to or school...I feel helpless) I stopped YAZ 2 days ago and so far i haven't notice any change...I am still very moody and SSSOOOO tired, I can sleep all day and all night with no problem and when I do try to get up is like a magnet that's keeping me in bed, its awful!!! When does it get better???? Anybody knows??? I am falling apart!!! HELP PLEASE!!!

My son (14 years old) was given levaquin for a sinus and ear infection
2 weeks ago. Around the same time he began practices for his high school baseball team. He complained about his legs being stiff and aching. We assumed it was the intense practices causing his muscles to ache. After a week on the drug, he could barely walk and his knees were swollen. We were very concerned and looked up the side effects of levaquin on the internet. We were shocked and angry when we found out that levaquin should not be given to children under the age of 18 because on the possibility of joint and tendon problems. Today we went to the orthopedist and he drained a lot of fluid off of both knees (it looked like about a 1/2 cup from each).The doctor thinks it has to be a side effect of the drug, because the symptoms began at the same time. He doesn't
think after examining the knee and having him perform certain tasks that he has damaged any tendons. He has all the symptoms of rheumatiod arthritis. He is very athletic and plays competitive sports and we are praying that his knees are not permanently damaged by this drug. Parents please research all drugs and there side effects before giving them to your children! Doctor's DO make mistakes!! The pharmacist failed us too.

One person here said:
>My MD attributes the issues to aging. I going for a second opinion and third if necessary. I am told by my MD that there are no studies showing these side affects for this medications.<
"Aging" is the oldest excuse in the book for not investigating a medical problem. That LAZINESS. Doctors can get lazy, like any other worker.
The reason there are "no studies showing these side effects" is that studies are rarely done once a drug is FDA approved. They wouldn't do the studies at all if the FDA didn't require it for approval. When they do the pre-approval studies, they are careful to select people who have few health problems; they are not studying a good cross-section of the general population. It's AFTER a drug is on the market that the REAL side effect profile shows up. Doctors don't like to blame drugs for symptoms because they are part of the system that pushes drugs on the public. They don't want to get caught up in a malpractice suit, but pushing drugs is their bread and butter. Sad, but true. Slowly, more of them are turning toward more natural approaches to disease management. However, YOU remain your own best advocate.
I am going back to taking natural supplements like Hawthorne leaves and flowers (stronger than berry.) I resisted the drugs for years, and after reading all this stuff, I remember why. My mother struggled for years with the side effects. I'd rather die slowly of hypertension!

i been on warfarin since august 08 - its now end of feb 09, i have not noticed any serious side effects apart from blood in nose when wake up and snotter for the first time each day (excuse that term) .
i have been sitting under newly installed lighjt at work and find it to be very hot on my head... everyone else says its not, but i cant stay there after ten minutes... its mildly uncomfortable.. and it got to thinking that maybe warfarin can effect the sun and the taking of the tablets, im on 6mg a day and i have heart problems, heart failure and cardiomyopathy, i would like to here from any one that has problems with sun...... and after how long hair loss and teeth problems came after taking it - im only 24 but worry about it thank you for your time i also get fatigue

I just wish I could wear a sign that says: I'm sorry about the last 3 years. I have an excuse why I was a complaining bitch.

UPDATE:
I had mine removed 5 days ago. After 12 hours, I had a burst of energy... was still really achy, but mentally ecstatic.
The next day was not so good... the high was over, (and I was coming down with a cold), so very achy joints. I ate a lot of chocolate!
3rd day was so-so. I was in control of my emotions, but really achy. I found an old Rx for Toradol that worked well. Ate more chocolate.
Yesterday I felt fantastic, and today even better. I have had no cravings. My aches are 90% gone, without drugs, and I have not had any depression, anger, or feelings of despair. In fact, I found myself singing some goofy song from Dora The Explorer today, and my son looked at me really strangely and started giggling. I think I'm back!

THIS IS IN RESPONSE TO anastasia01 RUDE STATEMENT

Excuse me! Obviously, there are people who don't have any problem with Mirena or it wouldn't be on the market, so maybe you are one of those lucky people. Everyones body is different and responds to hormones differently, so for you to sit there and make a judgment like that when you don't know what kind of hell I have been through in the past TWELVE years of my life with hormone treatments or what other people on this page have been through, is absolutely ignorant! I am so happy for you that you have had no side effects and thats wonderful, but thats all you had to say. Attacking everyone else is so uncalled for! Don't judge people you don't know! Especially, people reaching out for help!

Here is my experience, I am confused only because I know part of what happened to me is my own fault.

To make a long story short I overdosed (intentionally) on a different drug called Lamictal. This is a seizure med. When that event happened I was on a course of Levaquin. I was on day four. I was to take it for 24 days for a sinus infection that showed up on a CT scan.

I know that this sounds horrible, but my overdose was small. No overdose is small though, but what happened to me just didn't seem right in comparison to the amount of pills I took. My mind is telling me I have no right to question anything considering what I did.

After taking the pills, I passed out and ended up being flown to a different hospital as my condition was worsening. They told me that before I left the hospital, my urine had already started to turn brown.. I don't know what that means.

When I woke up in ICU the doctor was yelling at me asking me what other drugs I took. He said that an overdose of Lamictal would never have causes what was happening. He asked if I was on meth or had taken Benadryl. I was sweating a lot, my heart rate was 150, my liver and kidney functions were bad, and the worst of it all, I had a CK level of 70,000. I had developed.. excuse my spelling... rhabdomylisis. My whole body hurt. Every single joint in my body was hurting, I could not stand and I could not walk. They told me that I was going to probably have to go on dialysis. I ended up being in the hospital for 8 days. My numbers returned to normal after 7 days of leaving the hospital.

The doctor there still thinks I was lying about what I took because what happened "Makes no sense." When they found me in my apartment they said I had "Serotonin syndrome." Which is caused by antidepressants.They said that the muscles in my body had gone completely ridgid and I was having a seizure that they could not stop. What they told me is they couldn't move one muscle in my body. My doctor said that they assumed that I o'd on my antidepressants too. Which I didn't.

Anyway, it has been a little over a month since the event, and that sinus infection is again being treated with Levaquin. I will take my 2nd dose today. Since that day I have been off all of my meds, but I am starting some of them back up. My Lamictal, my synthroid and now this Levaquin. I am scared to death. I have been searching the internet and all of a sudden I started finding that levaquin caused rhabdomylisis in several patients... although "rare."

Do you all have suggestions for me? The part that makes this the worst is YES I did overdose on pills. I assume this is why no one has really looked into why I had such problems. Should I stop taking this pill right away? I suppose most of you would say yes. I'm just not sure.

Here is my experience, I am confused only because I know part of what happened to me is my own fault.

To make a long story short I overdosed (intentionally) on a different drug called Lamictal. This is a seizure med. When that event happened I was on a course of Levaquin. I was on day four. I was to take it for 24 days for a sinus infection that showed up on a CT scan.

I know that this sounds horrible, but my overdose was small. No overdose is small though, but what happened to me just didn't seem right in comparison to the amount of pills I took. My mind is telling me I have no right to question anything considering what I did.

After taking the pills, I passed out and ended up being flown to a different hospital as my condition was worsening. They told me that before I left the hospital, my urine had already started to turn brown.. I don't know what that means.

When I woke up in ICU the doctor was yelling at me asking me what other drugs I took. He said that an overdose of Lamictal would never have causes what was happening. He asked if I was on meth or had taken Benadryl. I was sweating a lot, my heart rate was 150, my liver and kidney functions were bad, and the worst of it all, I had a CK level of 70,000. I had developed.. excuse my spelling... rhabdomylisis. My whole body hurt. Every single joint in my body was hurting, I could not stand and I could not walk. They told me that I was going to probably have to go on dialysis. I ended up being in the hospital for 8 days. My numbers returned to normal after 7 days of leaving the hospital.

The doctor there still thinks I was lying about what I took because what happened "Makes no sense." When they found me in my apartment they said I had "Serotonin syndrome." Which is caused by antidepressants.They said that the muscles in my body had gone completely ridgid and I was having a seizure that they could not stop. What they told me is they couldn't move one muscle in my body. My doctor said that they assumed that I o'd on my antidepressants too. Which I didn't.

Anyway, it has been a little over a month since the event, and that sinus infection is again being treated with Levaquin. I will take my 2nd dose today. Since that day I have been off all of my meds, but I am starting some of them back up. My Lamictal, my synthroid and now this Levaquin. I am scared to death. I have been searching the internet and all of a sudden I started finding that levaquin caused rhabdomylisis in several patients... although "rare."

Do you all have suggestions for me? The part that makes this the worst is YES I did overdose on pills. I assume this is why no one has really looked into why I had such problems. Should I stop taking this pill right away? I suppose most of you would say yes. I'm just not sure.

My son is 12 and has been taking Singulair for the last ten months...he has been getting moody and upset for no good reason over the last 3 months and I put it down to "hormones" starting to kick in. He has now gone to feeling very sad and has even told me last night that he has thought about killing himself several times and feels he can't go on, or cope and feels lost and lonely or unwanted and in the way. He is confused and does not understand what is happening to him. I have just realized it may be the Singulair and will be taking him off it immediately. I'm hoping it is this as if it isn't I feel totally helpless as to how to help my child. Please say a prayer for him. He used to be happy go lucky.

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

I've been on nuvaring for four months now. I've been raving about it to my friends and only recently started to realize that maybe it isn't as great as I'd thought. Here's the thing... I have gained weight, lost my sex drive (which at 20 years old is terrifying), felt my self-esteem fall through the floor, and feel stress/sadness weigh on me even on days that I am truly enjoying myself. (Oh and excuse the ick-factor but I've now also have discharge everyday which is seriously annoying and frustrating!) I've been attributing all of this to my lifestyle of being stressed out in college, not knowing who I am, worrying about my relationship... I've felt so much self-loathing and disappointment in myself, feeling like I am failing myself and my boyfriend. The thing is that I'm not one to blame things like this on medications, and I don't think that there's any way of truly knowing if the changes I've felt have been due to the ring or just my life as a whole. I've tried every other birth control and hated it so now I'm conflicted if I should stop taking it or not. I'm way too paranoid to just trust condoms... so I don't know. Take it for what you will - in many ways it has been a great form of birth control (no babies, right?) but if these changes I've felt ARE due to the ring, then I would NOT recommend it.

I have been on the NuvaRing for 7 months and Thank YOU all for your helpful comments. The last 7 months I have been this crazy, emotional, roller coaster, just like the rest of you. I have made excuse after excuse for all my emotions and let it happen because I thought it was just me. I have recently started feeling the headaches about 2 months ago, I didn't even imagine it was because of the BC until I read this. I have never had headaches like this before, it was never a problem I had. This is the first BC I have ever taken and I mean it was crazy .. I started telling my boyfriend that i thought something was wrong with me and that I thought it was something serious but I even went to the doctor and he took all my blood work, we even did a pre diabetes test and it all came up normal and healthy, so I just thought it was me and I thought I was crazy. Another thing I had like the rest of you was NO SEX DRIVE, I mean once I got started, I liked it, but it was hard for him to get me started. Anyway, this website explains a lot, it just sucks that it took me 7 months to realize that all of this could possibly be my BC. I took it out 2 hours ago and I will post again to let you know what happens next. Note to all the women taking this Ring: If you have all these side effects then stop or at least try one month off of it because I have never had health issues and these side effects did not start until I started the NuvaRing, don't wait until it is too late because while I was looking for this website, I saw other websites about lawsuits against NuvaRing for blood clots, stokes, and heart attacks, and although that didn't happen to me (so far) I don't want it to happen to you.

Hello All;

I have had the birth control from hell since 2005 and have had all of the side effects you girls have listed. I am having mine out this Wed. SURGICALLY! I have had two transvag. echos and the bloody (excuse the term) thing is in place, however three Dr.'s could not find the strings and after much rooting around my new wonderful OG/GYN has scheduled me for surgery to get out the"retained IUD". On the positive side, we did find my lost car keys! Ha! It may have been mentioned in one of the postings, but has any of you had this procedure? AND just recently I got ahold of the Physicians Prescribing Information so now I feel dumb. Has anyone noticed 1) Under Drug-Drug Interactions...the effect has not been tested 2)Carcinogenisis...Long term studies....has not been tested...O.K. I get the feeling as someone mentioned...we are the long term study!....If anyone has had to waddle to the hospital (sorry, I have a few fleeting moments of humor) to have this procedure (gotta love the medical term, right up there with discomfort) can ya let me know what happened?

I have been on Effexor 75mg and at first experienced extreme drowsiness and extremely dilated pupils. However, after the third week these side effects subsided, and I switched from AM dosing to PM dosing which helps with the drowsiness. The one thing I did notice though is that, though my anxiety and depression are gone, I have seemed to develop a new habit, or not new, but whenever I go shopping, I end up spending a lot of money and I don't really worry about it or care. The first month I burned through my credit and still, although I know it's a problem, don't feel any anxiety over it. Before the anxiety would stop me from doing ridiculous spur of the moment spending or other silly decisions, but since I have been on effexor I seem to not care anymore. I do love this medication however, and have learned over the past few months that I need to monitor my decision making more closely, and not based solely on my emotions, since I am always happy and carefree. Has anyone else experienced this?

I had the Mirena put in March of 2005 and I thought I loved it. UNTIL...... I started doing some research. I have had cysts on my ovaries since January of 2006 and questionable lumps in my breasts, very fatigue, very little sex drive,weight gain (typically weighing 108 I now weigh 122) and head aches every day. I always had an excuse until one day a light bulb went off it has to be the MIRENA. So I researched the side effects of MIRENA and behold I found everything I was experiencing listed about - buyer beware type thing. I had the MIRENA removed today. The cysts on my ovaries are about 2cm big and the lump is about 6cm big - I pray that having this thing out of me will resolve all of the problems I have had. I will keep you posted.

I have been on Norvasc for some time,but was switched to the generic form a little more than a year ago. I have been very unhappy with the quality of the pill from Mylan Labs. It dissolves in my mouth, tastes horrible and sticks in my throat. Last month, I had it go down my trachea and was coughing it up for 2 days, which included alot of burning. I asked my doctor to prescribe the name brand but she refuses, stating state drug laws as her excuse. I know it really has to do with my insurance company's formulary and she just doesn't want to go to the trouble of getting it approved by them. I tried calling all the local pharmacies to see if another company's version was available ,but they all only carry Mylan's version. I take a lot of prescription drugs for several chronic health disorders, and several supplements and vitamins and can swallow a handfull of pills at one gulp, so I know this problem is not my pill-taking technique. I also started to experience swelling in my feet, ankles and hands about the time of the switch to generic, which I never correlated to the generic Norvasc until now. I told my doctor I will not take the generic from Mylan and am awaiting a call back from her as I sit writing this. I am having surgery in about a week and can not afford to be playing around with my meds, but this is important to me. No one should have to accept an inferior product. By the way, I'm writing to Mylan, too.

HA. My doctors office must be trying to kill me. I was recently switched over to lo24 from the nuvaring. Ive been on it for about 5 days now, and already am having a break out, with moodiness. I found this sight when I decided to do some research on my "new bc", and am glad i did. I called my doctors office today to find out what i was on before the nuvaring, and they said lo and behold, Loestrin 24. I can now SAFELY connect my mood 2 years ago to this stupid pill. I became hysterical, suicidal, had horrible break outs, couldn't look in the mirror. Now by all means I am not trying to use a pill as an excuse for going absolutely CRAZY, but before I was on the pill I was actually happy. I almost ended up in the hospital from the depression this pill caused me. I wouldn't recommend this pill, and after linking my crazed episodes to last time I took this pill, I am going to throw this pack out right now! beware!