Disaster symptoms and conditions

My experience with Topamax was unreal. My doc gave i to me for anxiety/depression/weight loss. The weight loss began working right away but so did the disaster. By the time I had been on Topamax four months I was fired from my job, having an affair with my husband's best friend, spending $1000 on a credit card no one knew I had and spent 10 days in a psychiatric ward. There they determined that the Topamax had made me manic. A feeling of unreality had set in along with an intense feeling of well being, and aggressiveness. I am putting my life back together now after getting divorced, finding work in a new field, and trying to repair the damage done to my relationship with my kids.
My best friend called me tonight to tell me that her daughter who is also taking Topamax has become almost anorexic, is also getting a divorce, is now on medication for heart palpitations and will not speak to most of her family. It IS dangerous!!

I am a 38 year old female on Lisinopril for approx. 2 months on and off. I am in excellent physical shape and ideal weight with a family history of hbp. I immediately noticed negative side effects from this drug. Extreme fatigue and confusion the first day I took this pill. The first month it was in combination with water pill and that was a disaster. I could not stop craving salt. I stopped taking this on my own and went back to the Dr. She then prescribed the Lisinopril w/o the water pill and the salt cravings were not as severe but I was constantly hungry! Yesterday I decided to not take the pill and see how I felt and of course I was NOT tired or having any unusual hunger issues. There was an immediate difference! I also have the dry cough which until now I thought was something I had p/u from one of my children and could not shake. This drug is ridiculous. I have taken meds for bp on and off through 2 pregnancies over a 10 yr. period and the pills are worse than being pregnant as far as exhaustion and cravings!!!! This is very scary and I know hbp is deadly, but there are other meds which do not come with all the negative side effects. I will keep experimenting until I find one that works for me. This pill is headed for the trash!!

Hi everyone. I am a medical professional and former user of the nuvaring. It is true, birth control as well as most medicines does affect everyone differently. However, I was an absolute emotional disaster (frequently contemplating self-harm) while I was on this medication. I initially attributed the mood swings to my then current stressful situation. When I finally graduated from NP school and my stressors were alleviated, my depression persisted. Within a week of stopping the NuvaRing, I was back to my old self and have not had any of those symptoms since. It is a rather large dose of hormones so if you're feeling these symptoms as well, perhaps you should contact your provider about a more appropriate method of bc.

I read with interest several of the posts here. I have been on Lipitor for about 5 years. I have been experiencing leg pain, back pain, neck, and hand pain for likely 4 of the last 5 years. I have arthritis, I thought. Two weeks ago I ran out of Lipitor. I read several other forums where Vitamin C and Omega 3 were suggested as a possibles to replacing the Lipitor along with generous amounts of water. I said, What the hell, I will give that a try. Within days of stopping the Lipitor, most all the pain has subsided to the extent that I have not had to take any other Pain management medications at all. I was prescribed Perocet for the pain I have been experiencing. Two weeks ago, I had a tough time opening a bottle of soda, or even a relish or pickle jar. Today I can! Coincidence, I think not!!

I was given Levaquin for a prostate infection. They prescribed me 750 mg for 30 days. I have been off of the drug for 3 weeks and I still have pain in my tendons. Shoulder tendons, knees, elbow and hands. How long can this last? I feel like I am dying.

When my daughter was 15 her dr suggested she get the vaccine. Trusting the doctors advice, i ok'd it. The first two injections were fine. Immediately after receiving her 3rd, her arm, neck, and shoulder got really sore and then about two weeks later she developed severe pain in her upper abdomen causing her to pass out. That was on November 22, 2007 and she hasn't been the same since. She has suffered severe pain, nausea, dizziness, fatigue, IBS, anxiety attacks and depression brought on by the sickness. Our life for the past year has consisted of going to doctor after doctor trying to figure out what is wrong with her. She has been diagnosed with mono, UTI's, had her gal bladder removed, etc. Funny, they diagnose her with all these things but no treatments have worked. She went from being a very beautiful, active 15 year old girl with lots of friends and activities to barely being able to get out of bed in the morning. My question is, does anybody know how to help or what to do ?

My 3 year old is on 5mg of singular daily for her constant allergy issues and has had NO trouble at all with it. Her personality has not changed.. she's happy, outgoing, friendly and MUCH better than she was before she started the medication. Prior to starting she was constantly dripping from her nose, she had both ears filled with fluid, had bags under her eyes and was tired and grumpy all the time, due to allergies we could not get under control with other over the counter or prescription meds. Since being on Singulair she's been 100% better than she was. I'm sad to hear that others are having so much trouble with it, but I can say that I am happy my little girl is feeling better.

To send a report to the FDA about Lipitor and the side effects, go to ****** Hopefully, if enough people will complain about this dangerous drug, the FDA will ban it and it will be off the market.

Today is 4years exactly that Matt had his one and only asthma episode,that sent us done the road of singulair disaster,7 months of the drug now thanks to Kate who went public with her story.Each new day brings more hope for a full recovery,although the road is long and strewn with guilt and anger.First i was angry with my doctor,then Merck now the FDA,but the guilt always stayed with me.Ive spent hours on wouldas couldas and shouldas but none the less it is what it is.I have had an education in things i really didn't want to know,the medical system,the justice system,and our government.I have written hundreds of letters reported 3 times to the FDA,never a response other than your email was received,called and reported to Merck twice,they were always ready and willing to take my info,so today i wrote to the FBI asking if they could investigate corruption at the FDA,proberly they will laugh and trow it out,or maybe even put me on a list of some kind,but i will leave no stone unturned until some one explains to me how this happened in America

I am a healthy female with little to no history of adverse reactions to medications. I was prescribed a 10 day dose of Levequin (500 mg) for a minor but stubborn skin abscess. After the third day, I woke up with significant joint soreness in my fingers. Progressively the soreness spread daily to my wrists, elbows, ankles, knees, hips, etc. I did not suspect the antibiotic at first, but I know my body, and I know something was WRONG.
After my 8th dose I decided to look online...it is at least good to know that what I'm experiencing is definitely from Levequin. Thank you all for sharing your stories.

I especially found MERCEDESLANE posting on April 15th interesting. I guess this person works in the health care system. Considering this uncompassionate individual, who apparently wants everythone to know he has a Mercedes, can't spell (whine), and does not have basic grammar skills. Wow...my faith in the our health care system is stronger than ever. But what do I know, I'm just an "IDIOT" with shingles that needs to have a couple of glasses of whine while I pop my remaining Levequin.

I just came back from my GP and I am off work now until the end of the week and it's all because of Yasmin. I decided to go on the Pill as I started a new relationship and was told by my friends that this was the best pill available on the market. My doctor put me on it as well but from day one it's been a disaster. I am very thirsty, it makes me go to a bathroom every 20 minutes, I became very moody, irritated and almost depressed. And this is only after 6 days of taking it!. My breasts are very sore, I feel completely out of place, hot flashes and mood swings.I feel like a zombie. I cried in a bathroom at work today. I cried in my manager's office today as she wasn't sure what was going on with me. Thank God, she was very supportive and understanding. It was her who encouraged me to stop it straight way. The doctor I went to see today said to me the same thing - to get off it straightway. Hopefully I will become a normal person soon. I will be trying another type of contraception but will never go back on the pill again. In six days it turned me from a happy person into a person that I can hardly recognize as myself. And from reading all the comments which have been posted here, it makes me think that it's not worth it. I will be trying another method of contraception but will not be messing up with my body again. The price to pay is too high.

A plastic surgeon injected Kenalog in two places underneath my chin to dissolve small spots of scar tissue. The result is a disaster. I have a dent on one side and a large burned looking, atrophied area on the other. He did not advise me that there was any possibility of this drug eating my healthy tissue -- said it would probably not do anything. I did this on the spur of the moment and am angry with myself for not researching the drug first.

Has anyone who has had these "dents" had their atrophied area fill back in?

well this is my first time hearing about these conditions. i was just aware of it by my mother when i told her ive had these lympth nodes by my pelvic area for about a month which is a month later after my last injection of the gardasil shot. throughout my entire injections ive nevered experience any sie affects not untill my last injection but my side affect are the lympth nodes. the story my mother had told me was about a girl around my age(16) who had gotten paralyze from the injection once she discover her lympth nodes but difference with her and i,she had soo much pain frm themas in pain to walk maybe swelling had occurred. As i read through all the articles of women and teens had experience such horrible side affects from this injection i have came to realize after my second shot ive myself experience hair loss an as of right now my hair is so thined out that when i pick up my hair there bald patches in th front but question is could this be a gardisil disaster? see i didn't worry much about it due to family memeber will constantly tell me no more hairspray or anything and let my hair down because too much of all of it could be the cause of my hair falling out. but till this day i am still losing an enormous amount of hair even after my injections of the shot. should i be worried or should i wait it out as i was??
-ally

Just had Mirena put in two days ago (Friday). This is Sunday and tried to workout and couldn't finish. I usually do pilates on a reformer everyday. I feel tired and crampy. I never looked up Mirena on the internet before I had it inserted and feel scared to death. I don't want to bloat or constantly spot. I have a great sex life with my husband and constantly having to worry about bleeding will make my sex life a disaster. I will keep everyone up to date on what I am going through. I sure hope I don't have any problems with this. I was pregnant with triplets 6 weeks ago and lost them and decided I better get on some great birth control. My doctor thought this would be great for me to go on. Lets all hope the cramping and light bleeding stops.

I was on Yasmin since 2001. I LOVED it, it was great for me. At the end of 2006, I read about Yaz and asked my doc to switch me and so he did. I developed hives and cystic acne all over my face and back. It was terrible, and I thought it would get better but it got worse. So after 3 months of Yaz i went back to Yasmin. I currently have no health insurance and have been paying out of pocket for it. EXPENSIVE! but worth it. I never had any negative side effects while on Yasmin. It actually was beneficial for me, cleared up my skin, no more ovarian cysts, lighter periods and little cramping. For me Yasmin works great. Until I had to stop taking it 2 weeks ago, everything was rosy. I moved from NYC to Upstate NY, 300 miles away, and transferred my prescription for Yasmin. When it ran out last month, I called my doctor in the city to request a refill and he declined without me going to visit him for an exam since it has been over a year, which is ethical but BAD for me, because it's not convenient or cost effective for me to get to my doc 300 miles from here. So I went to Planned Parenthood and they refused to prescribe Yasmin for me because I checked the box in the health history that asked if I have ever had a history of headaches. I have gotten tension headaches for years but none in the last few years and they told me that because I checked the box they can;t prescribe anything with estrogen in it to me. I was so mad, I walked out without my exam. I called my doc in NYC and am taking the train down for an appointment this week. Unfortunately, I have to spend a month off Yasmin. I have been on one pill or another since 1993, so I know what works for me by now, and Yasmin has been a GODSEND. I am currently a disaster. I have developed severe cramping and bloating in my abdomen, which is normally flat as a pancake thanks to working out a ton, I am ravenous and want to eat EVERYTHING, I am moody and have developed a few large painful acne cysts on my face, and so far it's only been 2 weeks off, 3 if you count the placebo pill week. I want to kill someone. I am totally miserable. My mood was level all the time on Yasmin and I never had acne and my ovarian cysts had ceased. Did I mention that I am miserable? I am experiencing extreme fatigue as well. I am actually considering going to the county clinic tomorrow just because I can't take it anymore. I'd sooner take the morning after pill (which Planned Parenthood gave to me to take before they gave me a script for some stupid progestin-only pill) to trigger my period, which I think I am going to do, and order a month of Yasmin through an online Mexican pharmacy, just to get this nightmare to cease. I'm going to go do just that right now. I can;t take it anymore.

I received my first shot of Gardasil in January 2007. It could have started sooner, but about a month later my hairdresser noticed a bald spot in the back of my head. I rushed back to my ObGyn and asked her if the Gardasil could be the cause as nothing else had recently changed. She said that she had not heard of this, but she referred me to a dermatologist. I asked him if my hair loss had anything to do with the Gardasil. He replied that I had Alopecia areata and one thing had nothing to do with the other. He advised that I continue with the Gardasil and that he would start treating me for the alopecia. I wish that I would not have listened. I don't know what would have happened if I had stopped then, but I didn't I proceeded with the treatment to the end now over half of my head is bald!!!
I don't know what to do. I keep going back to the dermatologist for treatments for the alopecia, but it just keeps getting worse.
If anyone has had a similar experience and would like to share or has found some other treatments that work, please post a reply.

Melissa

I am posting this as a new post. I am not against Singulair. I am against withholding negative side effects from the patients. I am against promoting that Singulair is safe and effective for everybody on the planet.

My entire family is health care. My father was a surgeon. I worked for a pharmaceutical company. Pharmaceutical companies are supposed to ethically invent drugs and inform everybody about the safe and effective way to use those drugs. Pharmacists are supposed to police the prescriptions and dispense the correct dosage. Then pharmacists are supposed to be aware of side effects and drugs interactions. When necessary, pharmacist are supposed to intervene to prevent a mis- communication from turning into a disaster. Doctors are supposed to review the recommendations of pharmaceutical companies (who are policed by the FDA) in order to determine if their diagnosis matches the profile of drugs known to be therapies for certain symptoms. I, personally, am madder than hell at Merck. Singulair could really be a good therapy when it is needed. It could correct some bad stuff that happens short term. Why does Merck's need to make every drug a major block buster money maker ruin the market for Singulair?

Wow what it is with all these doctors not knowing these side effects, don't they know that there butts are hanging in the wind,the law protects the drug companies ,but doctors you are not immune

We have been through hell for the past three years with my son, who is now 18. He went from a very happy, confident kid who had lots of friends, loved playing several sports, played the piano, enjoyed going to school where he got straight A's, to a complete disaster. I cried when I read many of these postings. All these stories sound so similar to ours. He had trouble sleeping where he couldn't get to sleep at night and then his sleep would be very restless (one time he punched a hole in the wall in his sleep, several times he fell out of bed) and he would be all twisted up in his blankets in the morning. Getting him up in the morning became a complete nightmare, I dreaded getting up in the morning because our mornings had become so stressful. He just could not seem to wake up no matter what method we tried and sometimes it could get quite ugly. We took him in for several sleep studies which didn't yield any results. He started feeling sick all of the time with frequent stomach aches and ended up missing alot of school. We had a CT scan done on his abdomin which didn't show anything abnormal. Because he missed alot of school he fell behind and his grades dropped, he stopped hanging out with all of his old buddies and he started getting into trouble. There were days when he would be rolled up in a ball in his bed crying, telling me that he couldn't stand the thought of going to school. This was not the son we knew and we, like most people with teenagers, figured it was just a phase and would go away. Unfortunately, he ended up getting thrown out of school and has moved out of state. He will not be graduating with his class this spring which is a tragedy. Although he has been away from us now for 10 months, we keep in touch regularly and he is doing great (he stopped taking Singulair well over a year ago). He has had a steady job that he loves for the past 10 months and is apparently able to get himself up in the mornings and to work on time. He has been living on his own, paying rent and all of the other associated expenses that go with this, he has not asked us for any assistance and appears to be coping very well. He has made a lot of new friends and seems to be thriving. We are very proud of him! He would like to get his GED and go to college. His transformation has been dramatic. The frustrating part is that it didn't have to be this way. We feel like we have pretty much lost the last three years of our son's life, and we're not sure when he will be coming home. We all miss him terribly, especially his brother and sister, there is a big hole in our family. And the stress of the last three years has taken a toll on our family. I have passed some of these postings on to our Dr. I hope all of the information on these postings will help to spare other families the sadness and heartache that we have gone through. If there is going to be a class-action suit I would appreciate receiving any information regarding that.

DISASTER! WITHIN 45 DAYS AFTER 4 MONTH SHOT I HAD LOST ALL UPPER BODY STRENGTH, QUIT GOLF . PRE-LUPRON I WALKSED 2-4 MILES EVERY DAY, AFTER THE 2ND SHOT , I COULDN'T WALK 100 YARDS, WAS IN 24 HR., AGONY FROM LEG PAIN, DEVELOPED NEUROPATHY. SIMPLY, IT TURNED A VIGOROUS 83 YR OLD INTO A FEEBLE OLD MAN IN 5 MONTHS.

About eight to ten years ago i had a violent reaction to lactaid. I had taken it numerous time before with no problems and then I woke up one morning - had a bowl of cereal and a lactaid pill - within the hour I was experiencing severe stomach pain along with vomiting and diarrhea. I thought it might have been due to the fact that i had had very little to eat the day before and only a bowl of cereal that morning with the extra strength pill.

the following weekend i was brave enough to try it again with some ice cream at night (this time i had a full stomach from dinner). BIG mistake - this time it was worse - the stomach pain was out of this world (i have a high pain threshold but this had me in the fetal position) and i couldnt leave the toilet and trash can for a few hours. My girlfriend was scared and called one of those nurse hot lines. they told her to coat my stomach with some kaopectate - which seemed to help. I checked the bottle of lactaid - and the expiration date had passed - so i threw it away and swore off of lactaid pills. fortunately they came out with the lactaid milk!

Fast forward to now - never touched the stuff again. well the other day I was out of lactaid milk and my wife (yes the same girlfriend) had picked up some samples of lactaid pills at a trade show - so I guess with the passage of time - I forgot how painful and miserable the other experiences had been - so i took the pill. Nothing happened!

Last night i decide to take another one because i had a craving for ice cream (had been awhile!). I figured it was ok since i had no reaction a week ago. Well sure enough - within the hour I was on the floor in severe stomach pain - followed by vomiting and diarrhea. This time we had kaopectate in the house - so i started taking it - well i just threw it right back up.

This episode lasted about an hour and a half this time. There was a metallic taste in my mouth about the third time i vomited, and the fifth and final time, there was puddle of yellow liquid that came out at the end.

I was put on Tricor and it was a disaster. Goal was to lower LDL and I had already had negative results with Zocor (neuropathy). After a a couple of weeks I developed low back pain (near the kidneys), followed by excessive urination and related pain. Also right hip pain. I went off the drug and still had ongoing pain in my right hip and groin. Low back pain, knee pain and neuropathy in my feet. I'm a type 2 diabetic in good control and had bypass surgery so they wanted my LDL cholesterol lower than the 73 I achieved with diet alone.

I also experienced foot drop in right ankle with no strength in heel/ankle and neuropathy in both sides of my ankle. Three weeks after going off the drug I am just now recovering but continue to have hip pain, low back pain, 50% less strength in ankle. Also groin and testicle pain. I subsequently read that being on a blood thinner like Warfarin may be contraindicated which my Cardiologist did not mention.

I'm a 26 year old female and I've been on Topamax since March 2007. It has completely gotten rid of the debilitating headaches I experienced 3-6 times a week. It also got rid of my anxiety. I got my life back, my antidepressant kicked in at the same time. I experienced all the usual side-effects, tingling hands and feet, forgetting words, memory problems, loss of appetite, but was COMPLETELY pain-free. I still am. However, I never remember anything now, forget whether or not I did something, paid my bills, etc, lose things constantly, and I have lost about 20 lbs. Not good. I look anorexic. I have bones sticking out. Eating is hard. I forget to eat and drink all day and food is just unappealing. I feel fuzzy and stupid and slow. Not sharp like I used to be. It has killed my confidence and self-esteem. But I was wondering if any women out there got yeast infections while they were on Topamax. I've had one monthly since I started it, and my doc said it's a rare side effect. Oh yeah, I've had mild hair loss and mild to moderate acne now. This drug, it is such a 50-50. Living with chronic pain, those headaches were awful. But doubting yourself is awful too. Anyone have similar experiences?

As others have pointed out, BCs affect everyone differently. Before my children, I took Ortho Tri-Cyclen without incident. Loved it. Then after my children, I had a tubal ligation and was not on BC for over 7 years. But due to the onset of adult acne and extremely oily skin, I asked my GYN to put me on Yasmin to clear up my face and chest. What a disaster that was!! The first two months were OK, but the next five months were agonizing. My symptoms included significant weight gain (15 pounds), larger but painful breasts, sleeplessness, anxiety, anger/irritability (more than my normal septic self), heavy spotting between periods, slight vaginal dryness and an unpleasant body odor. I quit the pill this past September out of sheer frustration. The interesting part was that I did not tell my husband that I quit taking them and he asked me about a month later if I was still taking them. I answered no and he said that he could tell because now I smelled and tasted "normal". So ladies, be aware that aside from the anger issues, your partner may be suffering in other ways. I'd rather have blemished skin than deal with the side effects. And now that I have been over 3 months free of BCs (I am not taking any chances with trying others), I lost almost ten pounds and all of the weird smell. My period is longer than I'd like but has gone back to normal and although my skin is still very oily, I have found a facial product to combat the acne. Email me if you liked because there is more to this story than I have time to write.

I have been taking this for 3 days and I am a little worried. My legs feel kind of tingly and sore (started about an hour after i took the 1st pill). I am not swollen or anything...this is pretty much my only side effect, but I can't get a hold of my obgyn to ask her about it, since I have to wait 2 months to get an appointment with her...I dunno. The leg cramps can't be a blood clot this soon? This site is really worrying me now.

It is not a shooting pain like they say in the pamphlet Warning Signs, just kind of a dull pain. I had a lot of leg cramps as a child and this feels just like it, but more mild.