Earth symptoms and conditions

I seem to be the only person on earth who developed fat atrophy in my left eyelid, after receiving two shots of Kenalog for chalazions in said eyelid. I'm just heartbroken at the way I look now. The doctor told me there would be no side-effects except for a possible whitening of the skin, which I was not concerned about, since I am light-skinned. What happened instead is that my left eyelid is now asymmetrical to my right one and worse, it also has a droop. I have consulted an occuplastics surgeon who has just informed me that it's a permanent condition and the only way to fix it is reconstructive surgery, which will be difficult because of the size and delicacy of the location. In other words, it will never be the same as it once was. I really liked my eyes and if I had known that this was a possibility, I would have just left it all alone. It's disgusting that Kenalog is not used as a last measure. It's a very, very damaging drug that has serious side-effects. I have written the FDA.

I'm sorry if someone has covered this already... my grandmother is actually the one on Prednisone because she was diagnosed with peripheral neuropathy about a year and a half ago and I believe they recommended it to help her strengthen her muscles so she could walk. It has really taken a terrible toll as she is now unable to walk, and even using a walker can be stressful and difficult. Once she was put on Prednisone they continued to increase her dosage and because of it she now has terrible tremors. It kills me to watch her go through this and wish that I could fight the illness for her. I just want her to be able to eat without feeling so stressed out because her hands aren't steady. The doctor did say that the medication is causing her tremors, and we were relieved to find out that it wasn't Parkinson's, and now they are beginning to wean her off of the medication but she is still taking it at the moment. If anyone has finally tapered off from the medication, who originally had tremors, did you find that your tremors did go away once you were off the medication? How long before the shaking stopped and you felt better? I just want to give her hope that after she is off the medication there will be some relief. I feel awful knowing there is nothing I can really do but support and be there for her, and do some research. If anyone could help me with my questions it would be greatly appreciated. I'm sad to hear other people's terrible issues with this medication and as far as I know I have only heard negative responses to this drug, so it's unfortunate that in this day and age they haven't found something safer that has the same effect that doctors are looking for in a medication. I wish everyone a safe and happy recovery.

I just went in for my second shot of Lupron (out of a series of 6) for treatment of stage IV endometriosis. The most noticeable side effect I experienced was during my first menstrual cycle after my first dose of Lupron. I had never experienced menstrual pain or cramping (even though I had advanced endometriosis) until after Lupron. I have a fairly high pain tolerance and yet the cramping for the first 2 days of my period were almost debilitating. I had extremely heavy bleeding and have had spotting daily ever since (app.18 days). I have gained about 3 pounds because I have no energy at all. I'm usually active and work out 4-5 times a week but by the time I get off work, I'm too fatigued to do so (hence the weight gain I guess). I have hot flashes and night sweats all the time. The most recent side effect is high blood pressure. I have never had high blood pressure in my life (I'm a healthy 25-year-old woman) and when I went in for my 2nd Lupron shot today, they told me I all of a sudden do. I don't seem to have mood swings but do feel depressed and sometimes more anxious than normal. I have experienced a decreased interest in sex as well.

My husband was prescribed 500 MG of Levaquin for 10 days due to respiratory infection. When I got the medicine home, I read all of the warnings and possible side affects. He is 61 and has had tendon damage in his shoulder and his lower leg from taking Cipro two years ago. He had severe joint pain from Bactrim and hallucinations from Flagyl. From these previous antibiotics he still suffers pains and limitations of movement. What is worse is that they prescribed Prednisone with the Levaquin. It clearly states in the warnings that Levaquin taken with Prednisone increases the likelihood of tendon damage. The warnings state that people over 60 have increased risk of tendon damage. Why on earth did his doctor prescribe this? My husband is 61 and was too sick to research all of this on his own. It has obviously become more profitable to make people sicker.
I found this forum and called his doctor. I refused to give him this terrible Levaquin and asked for a prescription for something milder. The Doxycylene seems to be working just fine to clear his infection.
A word of warning to all to not drink the Kool Aid that they give you without asking questions. Any health care system that sustains itself by keeping people ill is a bad one. Think about it. If people are healthy, then where is the profit?
This Levaquin sounds like some kind of bad snake oil to me and I am thankful to have read the warnings and then found this helpful forum. I am so sorry for the pain that most of you have suffered and are suffering. We are living with damage from antibiotics and we understand your anger. Take good care of yourselves.

It has been almost a year since my father took his own life after being prescribed Avelox. He was given the drug by IV in the hospital and then by mouth at home. My family is still in somewhat of a state of shock. We dearly loved this man and miss him every day. The past year has been a real strain on my mom and I know it will ultimately affect her life span and the time that she will have here on earth with us. As I keep reading your stories I encourage everyone to report the side affects to the Food and Drug Administration. No family should have to endure the pain of this last year.

God bless each of you.

mika 0408

I have been on YAZ for 6 months and have had so many freaking side effects. How on earth these people think its okay to sell these drugs to people is freaking ridiculous. I have gone to various doctors since about a month after i started yaz, and every visit corresponded with a known symptom of yaz. i am so happy my boyfriend found this site. he's been so worried about the fact that i barely even wanna be kissed anymore and after learning about the reduced sex drives of like a thousand other people from yaz, it makes sense. i am soo pissed off that anyone would do this. i just quit taking the pill and hopefully everything will go back to normal.

My 13 year old daughter had her third shot on 02/16/09. Her first two shots did not seem to be a problem. She said her arm hurt really badly after the shot, and the next day she complained of leg pains she hadn't had before. Within a few days, she had a high fever with body aches like the flu, except it wasn't the flu. She felt better, but a week later she still had a low grade fever. She was tested and had strep throat, and was treated with anti-biotics. A week later she started having stomach cramps and diarrhea. It's now March 18th and she still has diarrhea. I think it's criminal this vaccination is being given to our young women. How on earth could anyone think "possibly" preventing HPV and/or cervical cancer is worth the risk of what my daughter and so many others are having to go through?

I can't believe I found this. I am a 34 year old female who went on Yaz about 1 year ago.I have had zero sex drive, nothing. The hottest man in the world could wink at me in traffic and I would role up my window. Nothing and there isn't enough ky on earth to fix this problem.Needless to say my husband is feeling rejected and annoyed. Everyone has told me it because of the baby, who is now three. Through the rest of the pack out. Now I want t o know how long it takes to clear my system. Anyone else with the chest pains?

Hi . I am a 69yr old male. My doctor has recently increased my Lipitor from 20 to 40mg. My cholesterol reading was 3.6 which he considered to high after a quad bypass. I am suffering painful cramps down the front of both lower legs as well as cramps down the back of my lower right leg. I plan to revert to 20mg to see if the cramps stop. I am not sure if I should stop completely.

2 days ago I just happened to come across this website. I was in tears reading all of your stories. It sounded like it was me writing! You have given me the answer to all my misery over the past 3 years! My marriage nearly failed from all of this. I was married in July 2005, had a son in March 2006 and immediately had the Mirena IUD inserted. I thought it was the best thing on earth! No side effects... that I was aware of!! It all came on so gradually that I blamed my symptoms on post-partum hormones and a change in life-style. I remember I became a total bitch towards my husband very shortly after I got the Mirena. I gave up exercizing, ate like crazy (partially probably due to breastfeeding), and I had absolutely no sex drive, which was a 180 for me, because previously I wanted sex everyday! I blamed this on hormones too, or maybe my weight gain... just not feeling sexy anymore. When my son was 12 months old, I had the Mirena removed, only to try to get pregnant. We had a daughter in December of 2007, and I immediately had the Mirena re-inserted. As time went on, I was the bitch I was after my son was born.. again, I blamed it on my hormones. My back was killing me all of the time.. I blamed that on having to carry my daughter around. Then the insomnia hit me.. wow! I would lie awake in bed till 6:30 in the morning, and this was after my daughter finally started sleeping through the night. Maybe I had insomnia the months prior but never noticed because I was up all night long with my daughter anyways. I was miserable, depressed, moody, and incredibly mean towards my husband (thank God not towards my kids). He's a saint to still be here. Last summer I started getting pain in my joints. Some days I couldn't lift my kids because my wrist was so sore... or I was limping because of my hip or my knees. I was also incredibly depressed at this point. I was getting virtually no sleep, was pissed off at my husband all the time, and looking after 2 kids was draining me. My husband, being non-confrontational, was lying to me all the time try not to rock the boat. I found out he was lying to me, and I thought he was having an affair. I was crying all day everyday... finally after everyone told me I was depressed, my doctor put me on anti-depressants, and a bedtime pill called Elavil to help me sleep and to help with my joint pain. We went to marriage counselling (still are). After 2-3 sessions with an amazing counsellor, we realized I was not suffering from depression. Thank God, because the anti-depressants were making me even more miserable and I was binge eating like crazy! My husband and I, with the help on counselling, have since dealt with all of our problems. So why am I still so unhappy? Why is my join pain coming back? The Elavil is not working for my pain anymore. My body feels like I have the flu. Achy, but more intense and joint-specific. I have no energy or motivation to do daily tasks like laundry, clean the kitchen, or even take a shower and get dressed. When my kids wake from their nap, I feel like crying because I don't feel like a good mother is caring for them. 3 days ago I was with my husband and kids and had to leave because I began to cry. My husband came to ask me what was wrong, and I just said that I was in so much pain, I couldn't stand it. The truth, which I did not tell him was: I literally could not take another day like this. If I don't get better, I don't want to live anymore. I was not contemplating suicide, but I'll tell you this.. if I hadn't found this website when I did, who knows what I would have done!
Looks like I know how to make a long story even longer! LOL.
My husband and I went out for a romantic dinner on Friday to celebrate Valentines. I told him what I had discovered.. actually, I just handed him this website on my iPhone. AS he read your stories, we both were in tears! The last 3 years should've been the happiest of our lives, and we were robbed by this devil-IUD!!
Last night I couldn't take it anymore. I was crying and my husband said, "why don't you just go to a walk-in clinic and have it removed?" So I did! It was painless and I have no bleeding or cramping as of yet! I don't know if it's psychological, but I feel terrific today. My joints are achy still, but my mental state is on cloud nine! I have energy today and have been playing with my wonderful adorable kids all day. Let's hope it lasts. I will keep you all posted!
I hope my story helps someone as much as you have all helped me. You have saved my marriage, and probably my life. Thank you all!!

I'm surprised at all the comments about Mirena...about how painful the insertion was and how horrible the side effects are. I can honestly say that I've had NONE of those issues.

I'm 28, and I've had Mirena for 2 years now. I have NO children, but the procedure was NOT painful. It was slightly uncomfortable for a few moments while she inserted it, but I did not receive any anesthetic. I had slight cramping for a few days, which is normal. Over the course of several months after having the Mirena put in, my periods began to subside and after about 4 or 5 months, I had no period at all.

I have noticed absolutely no difference in my sex drive, weight, mood, hair growth, etc. I recommend Mirena to anyone who is interested in it.

Of course, every woman is different! And, our bodies all react differently. So, if you're interested in Mirena, please don't make a judgment call based solely on this message board or any other message board, for that matter. Some of us have had horrible experiences. Some of us have had great experiences. But, your decision should come from the ONLY two people who know YOUR body best: you and your doctor. Good luck!

I posted a while back about the symptoms I was experiencing from Yasmin. Well, I've been off of the drug for just about a month now. My libido has DRASTICALLY improved, my moods are better, and I am getting along with my boyfriend like I haven't in a long time.

The only problem I'm now having is that my weight is continually creeping up. I have been very busy with various things for the past few months (searching for and finding a new job & new apartment in a different state, going on a week-long food-filled vacation, packing, moving, unpacking etc etc). I thought that I was up a few lbs (3) as a result of being very busy and not having as much time to commit to exercise and eating healthy. Don't get me wrong, I have still been exercising and eating healthy, I just haven't been able to commit quite as much time as normal to these things.

In the past two weeks I have gotten back into my old routine and have been doing 60 minutes of cardio approximately 5 days/week and really not eating very much. Most days I have eaten a big bowl of oatmeal for breakfast and not been hungry until dinner. Since I've gotten back into this routine I have done nothing but gain MORE weight. Additionally, I have absolutely no appetite. My stomach looks poochy and my pants are getting tighter.

I have been able to keep my weight in the same range (127-129) since I started running, 4 years ago. It would VERY occasionally creep up to MAYBE 131, but I haven't seen a higher number than that until now. I feel that I literally LOOK at food and gain a pound.

Has anyone else experienced this? Could it be that my hormones are just adjusting? Honestly, I'd almost rather deal with the side effects of Yasmin than deal with gaining weight as a result of not being on it.

I was diagnosed with bronchitis a couple of days a go and was given a 5 day course of Levaquin 750mg. The doctor also gave me a prescription for the Z pack in case Levaquin did not work. Before I went to the doctor I had a fever of 102 for 5 days so I was ready to take anything. That evening Nov. 11th 2008 I took my first pill... and my last one. The onset of side effects started within 3 hours. It began with an extreme blinding headache and a very stiff neck. I finally fell asleep and had the most intensely bizarre dreams which I woke up from several times to find my self drenched in sweat. The night sweats were extremely intense and followed me through to the next day. I could not stop sweating... My head was pounding in pain, it felt as if my brain was swelling though my fever had subsided. I proceeded to turn the tv on to try to distract myself, but as I was doing so my mind was racing and I found it very difficult to organize my thoughts. My vision was very isolated meaning that I felt like I had lost my peripheral vision all together. I was unable to read silently without hearing the words in a loud voice in my head...very very strange. I had zero appetite and experienced serious diarrhea the next day. This drug felt overwhelmingly powerful kind of like dropping a nuclear weapon on a small village. I felt like my body was on fire for a moment as if i was given chemo therapy. While trying not to panic I realized that a lot of my joints were cracking. It was then I decided to go online and do some reading about this drug...WOW... I mean WOW... How do scientists manage to create a drug that can actually snap tendons... We can't cure anything but we sure can napalm the hell out of anything. That being said I decided to call my doctor and said WTF were you thinking giving me this!?! Needless to say it took about 60 hours for the one pill to wear off. I am terrified to think what would happen to me if I had finished the 5 day course. I know the one pill caused some damage, hopefully nothing permanent. I am now on the Z pac and it is very mild in comparison. Please listen to your body as I did and immediately discontinue use if you experience any side effects. I firmly believe that this drug is something you take only if you are dying and there are just no alternatives ie Anthrax.

Add me to the list! I have been on 300 mg Wellbutrin for the past few years. My hair is falling out and you can see my scalp. Just like many of you, I went the thyroid tests route, to no avail. I'm so thankful that in my desperation I did a search on hair loss and this drug. I will see my doctor and get off this stuff as soon as I can. It does help with depression, but who on earth can deal with watching your hair fall out on the sink and on the floor and down your back....I'll take the withdrawal headaches, as long as I have some hair on the outside of my head. Thanks to you all for writing about it. We are not crazy!

I got Mirena put in Feb of 07 almost a year after my second baby. I thought it was the greatest thing one earth for almost the next year and a half. I always had light periods so I stopped having periods completely since it was put in. I had no side effects whatsoever until Aug 08. I started having mild headaches that turned severe and did not go away for over 20 days.

That was my first sign. I started having pelvic pain (which has since gotten much worse) resembling ovarian cyst pain. I started bloating like crazy and my clothes were very tight and uncomfortable. I started experiencing pregnancy symptoms which worried me so I took a pregnancy test and it came out positive. I took another one later and it came out negative. I went to my regular Dr (because she had to order the tests for insurance purposes) and their tests came out negative. I've been pregnant 9 times (7 miscarriages) so I don't need a pregnancy test to tell me I'm pregnant. I know I was but my lack of periods wouldn't allow the uterus to hold a pregnancy.

I looked up my symptoms online and found hundreds of women with the same experiences. My Dr looked for the Mirena and couldn't find the strings or the device so she ordered an emergency ultrasound (lucky for me I have great Drs). They found the Mirena pushed further back in my uterus and that I had a large cyst (which I already knew I had from all my pain). My headaches got worse, my uterus pain got worse, I had back pain like crazy, I became so tired I could hardly move, and I was constantly nauseous. With a husband, 2 kids, and a job there was no time for all of that. I talked to people at work recently and they said when I was experiencing the best of my symptoms they were talking to me and I was looking at them like I was telling them to F*** off with my facial expression. I had to explain to them that it was the extreme headaches and the pain I was in and not them. I didn't realize it got so bad that my facial expressions showed it!

I went to my Ob/Gyn for an appt I had scheduled weeks before my pain started and told the PA about my symptoms so she looked for the strings and found them so the Mirena was back in place. She asked if I wanted it left there and I told her HELL NO. She pulled it out immediately and called it a demon, which makes me believe she knows about the horrible side effects. She didn't try to talk me out of it at all, not that I would have let her. Both of my Drs were very understanding to my need to have it removed and were willing to do it.

After I had it removed I continued having those symtpoms but they are beginning to fade off. I did have one day where I woke up and I was a raging B**** from the minute I opened my eyes and I don't know why. I apoligized profusely to my family and I knew it was my hormones but I could do nothing about it. Later that day I had my first ever anxiety attack and I freaked out. It was TERRIBLE. I've had continuous spotting since then. All these are our bodies' way of telling us to stop polluting our poor bodies. It's called "the crash"

Well ladies good luck with your little demons and remember the side effects continue until your body can regulate itself again. Don't give up cause it will get better.

I am a grandma to a 41/2 year old boy named Trevor. He has been on Singulair since he was 18mos. old. I am here to tell I am furious and heartsick to think that he has been subjected to a medication that can do the things it has done to him. I have NO DOUBT that Singulair is the problem. Our daughter and son-in-law have been at their wits end with
him and was one phone call away from taking him to a therapist (they needed one too!) The phone call to me on Monday, July 28th, was out of
sheer desperation. My daughter wanted me to look up the side effects for Zirtec. After looking that up and not finding anything I happened to remember that Trevor was also on Singulair. The actual side effects listed
didn't ring any warning bells with me. Somehow I happened onto this website and OH MY GOSH I flipped out and cried through every letter written by parents with the same side effects Trevor has. The compulsion, anxiety, anger and (heaven forbid) the threats of wanting himself, or someone he loves very much to die.This is absolutely unheard of for someone his age. I'm ever so thankful I found this website. Trevor was taken off Singulair that very day and within 3 days we had the sweetest,
most normal 4yr. old, on this earth. When I think what could have happened
had he stayed on it any longer...I can't!!!

I have been on and off Singulair for roughly a year and half, and after reading some of these posts I have a much better understanding of where some of my feelings are coming from. When I first began taking Singulair, it really helped me breathe a lot better and I was convinced it was the best drug on earth. Slowly, over time, I began to notice that I was becoming slightly more irritable but didn't really think much of it. I got off the drug for several months because I don't enjoy being on medication. I wanted to see if a nutritional approach would help me ward off my allergies. After a few months of being off Singulair, I began to have difficulty breathing during allergy season and went back on the drug. It really helped my breathing in a big way; however, my irritability began to return. I thought I was just becoming overly stressed, but when I heard about the moodiness that can be caused by Singulair, I decided to once again get off the drug. I was off of it for several month, and have recently begun using the drug again. I haven't even made it through my first 30 days and I'm becoming a monster!! I'm yelling at my wife like crazy. I seriously felt for the first time in my life that committing suicide would be a good thing and I keep telling myself in my head how bad I suck! My temper is off the charts! I feel like I literally have no way of holding my rage back. It's like I'm an audience member to my own MMA fight. I'm absolutely getting off of this product tonight! I will keep you posted on how I feel after a couple of days not taking this drug.

I got all those problems but the higher the dosage the more attacks i had.Another neurologist think that i just have pseudoseizures-paranoia attacks.Anyways the doctor screwed me up,he gave me 5 years ago something different and my seizures started daily than switched me to lamictal.I must say that sometimes i have or HAD electricity in my left hand all the time and once a women touched me and got stunned lol.anyways lamictal is bad,i didn't have any side effects like loosing hair but i did have A LOT of head hecks.I must share something with you,when i read epilepsy.com it seems that my seizures called myclonics in the end they are not but they similar in effects.Myclonics its seizures that happens only in the morning.Heres the catch for me,i figured out that if i won't close my eyes the first hour after i got up and went to the sun outside than i didn't have seizures.Its not a real solution so i decided to raise the lamictal from 175 which was ok for me to 200-250 like the good doctor said,just made me worse.Now i started dropping it by 25 mill each week and i must say i feel better only a little tired after 5 years that my body got used to it.Anyway if any of you have myclonics than don't close your eyes.BTW i have AURA-feeling before the seizure but luckily for me after a second if i open my eyes nothing will happen although i don't always take notice of it.In midway it would happen if i seat in front of computer and will lose attention if someone will call me or whatever but its a mill-sec seizure,barely noticible if at all and i never get "disconnected" from reality!!!
the ONLY thing which is bad for me is that except that im sick now my blood pressure is huge-140/82 and pulse 106 which is being like that for couple of days but i will get trough that.Since i lowered my dosage my midway seizures stopped,now im on 100.

P.S=Check yourself with the neurologist with a different one preheps.IF you can describe the whole seizure it means you don't dispatch from earth which mean it might be psydo seizures which are psychotic and not epileptic,the most important thing is that if someone takes lamictal or any anti apileptic drug even tho he doesn't have real seizures the medicine can do this.I got screwed and now i try to get over it,the doctor trowed me on woods with tablets after having a first seizure WHICH IS WRONG because you sepused to get tablets only after 3 attacks and after describing seizures and doing eeg tests to make sure that you DO have the problem.

Anyways remember what i said about the closing eyes in the morning part,if you close your eyes and feel weird keep them open at least those that have them after they wake up,that was a solution for me and it can help you to...MY doctor said everyone like me but i think he is laying,the other neurologist said my doctor was wrong probably about the seizures,i think i have both but i do know that believing and saying that you don't have anything WILL help you and lower your seizures,after speaking with the doctor i actually started to believe i don't have anything and walla i have almost NADA,today i had zero!!!! :D

OF course don't lower dosage without first consulting with someone expert,but since i know i can control basically every seizure i have and i know what to do to avoid it i let my self start dropping dozes!!!

GOOD LUCK my friends believe in yourself and if you want some personal info leave your msn i will add you and try to answer you the best i could,i was researching my self trying to figure out the core of the problem for 5 years but after 6 months knocking my head in the pipe when i washed my face i learned what i should avoid to minimize the chance!!!Try that

I'm 31 and started taking Effexor a week ago 75mg to begin with. Today I'm doubling the dose. I am mourning for the loss of my husband whom I have been together with for three years and married for 4 months! In a week I had a serious nervous breakdown due to an obsession in my mind; related to getting his personal belongings from his family. But today when I think about my feelings, it seems as if they're all lost. Or they are buried even deeper inside of me. I can't cry and this is uncomfortable. One day I'm seriously aggressive, another day I'm the easiest person on earth, then another day I'm fighting with my emotions like missing him bad. I had suicidal thoughts as well. When I look back, it seems overwhelming what I felt due to this medicine on top of my deep sorrow.
I don't really know how this dose doubling will affect me, but I'm anxious!!!!!

This is my story. My daughter 14, the most precious child ever born. She has a wonderful disposition always happy, loving, and determined to succeed in whatever she does. She just brightens everyone’s world.
She suffers from severe seasonal allergies and mild asthma. She takes approximately seven allergy/asthma medicines a day during peak season. Over the past two years she has been taking Singular as one of her medicines. Being 14, sick of taking medicine she would not take the Singular on a regular basis. Approximately four months ago “MOM” says, if you take nothing else take your Singular it will work both for the seasonal allergies and your asthma. She has been taking this regularly four the past four months.
She became paranoid, she became a compulsive eater and bites the skin on her fingers. She would eat and chew on her fingers at the same time, until she choked. She had so much anger, she could not even go to the mall without temper tantrums.(As a child she never had any tantrums ) Always afraid. Severe depression set in. She would cry at a moments notice. She would say, I have a very sad life, sad very sad, nothing makes me like this, I’m just sad. She felt she should go live with the homeless people. I asked her why, she didn’t know, she felt maybe that’s where she belonged. Nightmares and sleepless nights.
She needs help quickly. Before calling the Doctor, I went on the internet and entered Singular and depression and I found 1900 entries, all people telling me what I was experiencing. Could this possibly be the answer for us? I called her Dr and told him what I thought, he said he has never had anyone that this has happened to. He hoped it was the answer, but really didn’t think is. He said if it wasn’t the answer she would need therapy, mood stabilizer and Prozac.

Its day four off Singular, she smiling, no tears today, no temper tantrums, looking forward to school next week, wants to play volleyball next year, singing in the car,
I hear that happy voice again.(Hi, Mommy!!!!!!) Every once in a while a glaze comes over her face. She isn’t a 100% back, but I know it is coming.

To all the people that don’t have the happy ending, I will pray for you and hold you in my heart forever.

June 2, 2008

I've been on Xalatan for 10 months. At first I had only red eyes, but after two months my vision got blurred. So I got new glasses. One month later I needed new glasses again. The cornea began to swell and finally I had a macular edema. After having stopped using the drug, my vision still remained bad.
Why on earth do doctors still prescribe Xalatan???

I work in a health care system and we have used levaquin for this last cough, cold and flu season. It has worked wonders for the various upper respiratory infections.

No one has developed rashes, boils, or bone/muscle pain. After reading the first response, her abnormal reaction sounds more like a bad case of shingles.

Then, I read the last post where the person drank two glasses of whine to help with the blah blah blah. Mixing alcohol with any type of medication will not help with Your sypmtoms were a "full fledged panic attack" as you stated from the beginning.

Nothing but idiots posting here!

My son is 21 month old and he's been taking singulair for two months now, and I can notice that after he started taking it he is having nightmares. Every night he starts crying while sleeping without any reason. So I am wondering could it be possible that these happens because of singulair just in 2 months or there is something else. Doctor told us to continue giving singulair for 6 months, Shall I stop giving it or not?

I'm just posting an update on my daughter tomorrow will be 1 week since she's been off of it and she's doing great! laughing,singing,playing with her sisters and happy again. It makes me really mad when people come in and say this is not true. How about you rewind my life back five years ago and live my life. With a child that acted like she was a demon filled with hatred and wanted everything in my world gone. Have the people forgotten how just a year ago our pet food was poisoned,our own food, our childrens toys, our drinking water, and now our medicines? We don't live in the kind of world we use to..where doctors use to listen to you and stayed in the examining room longer than just 5 or 10 minutes. How on earth can you really get a true diagnoses these days. All I know is that my daughter for the first time in 5 years is happy again and not destroying everything in sight. Never again will I put her on Singulair again so a big company and their share holders can make a huge profit for themselves.

I kind of think CNN and the FDA are intellegent enough to figure out that they should NOT get information off this website. What makes everyone think all these posts are real? First you have to weed out the pranksters who post here for fun, then you have to weed out the competitors to Merck who post here to bust chops, and then you have to weed out the ones who really have a psychiatric condition and get their jollies by posting made up stories.....shall I go on? This is the INTERNET people!!! Anyone with one, two or ten verifyable emails can sign up (I have 11 email addresses myself). I have been intrigued to see the same people posting under multiple user names. Then you go to the other boards and see them there. If you really study these messages you can figure them out. So my point is, NOT ALL THESES STORIES ARE REAL. I think I would be generous in saying 25% of these posts are legit. I would hope that no government agency or news agency is going to risk their reputation on a public forum message board.