Heartache symptoms and conditions

My 14 year old daughter received her fist Gardasil shot in Sept/Oct 08. Soon after she started losing her hair and thinning. Now it is coming out in handfuls. She is so upset and I believe that she is becoming depressed due to the emotional heartache. She has not received any more shots. Anyone who reads this don't give this to your daughter.!

hi all. i had the mirena put in January this year. i also noticed a lot of the side effects that a lot have mentioned, my biggest issue was the hair loss. i went back to the GP who said it had nothing to do with the coil and put it down to stress. it was strange that it happened just a few days after having it inserted! so i had it removed in march. however i have noticed that my hair is still lifeless and falling out. im 26 and shouldn't be losing my hair. please can anybody help in telling me if they had the same experience and how long did it take to stop. im very worried about it. all of you ladies out there think twice before you have this device inserted its more hassle and heartache than whats it worth. if any body can help me please please do.

I was prescribed singular on Friday for my asthma and allergies - I took the first dose on Saturday night - slept like a baby and felt really great Sunday (the best I'd felt for a long time!) but that changed Sunday night - after taking my tablet I went to bed - it took me until 4 am to finally fall asleep because of the noise in my ears and this overwhelming feeling of unrest in my mind and body. Around 4.30 am I apparently woke my daughter by leaving my bedroom sleepwalking - I even managed to change the top I was wearing before loudly opening and shutting my bedroom door then walked half-way down stairs turned then went back to bed - I'm 44 and never, in the whole of my life, walked in my sleep! All day Monday I just didn't feel myself like the world was an overwhelming place to be! I didn't take the next dose but feel absolutely drained and on edge - I'm told it'll take a few days to completely leave my system - wish I'd never even tried it!!!!!

The medical professional is particularly unhelpful in this matter. Talking with medical personnel about fluoroquinolone poisoning is a go-nowhere exercise. In an era when Monsanto genetically-modifies our seed stock you might think medical caregivers would advise us in advance that their prescription antibiotics mess around with their patients' DNA. (IT's that deregulation thing, yes?)

I experienced painful calves and a strange dream, possibly a nightmare, immediately, e.g., on the very same night, after having injested one Levaquin dosage for a prostate condition and maybe a year after separately having taken cipro for a week to combat traveler's diarrhea. The post-Levaquin early evening dream was strange insofar as I rarely drempt, and I never recall having been roused to wakefulness by a dream shortly after having gone to bed. Early on I did NOT associate Levaquin with the really terrible symptoms that I experienced within 60 days of having injested Levaquin.

My wheels fell off when I entered a period of insomnia. I thought my sleeplessness was stress-related because my health history includes a major depressive episode 11 years ago. I presented myself for help to a psychiatrist who prescribed a small dose of an atypical antipsychotic as a sleeping aid. My drug-induced sleep felt like a coma that lasted each night for a couple of hours. There were heart palpitations, agitation, panic attacks, racing heart, racing thoughts, insomnia, depression, paranoia, poor cognition, body shuddering, muscle twitching, night sweats, and pain in both Achilles heals. The symptoms filled a note book page. I felt like Jean D'Arc who was being burned chemically at the stake from the inside out. I would rise in the morning and then minutes later fall back into bed. I could stare off into space and completely lose track of time. I could not even find the right words in mid-sentence. I could not fill-in the registration papers when I presented myself for a second opinion at Mayo Clinic. I became a full babbling idiot. My wife said that I had retreated or devolved into some kind of primate or ape who communicated solely his emotional states by means of eye contact only.

I asked my doctors if the sum of levaquin and cipro had pushed me over my peak quinolone tolerance level. Or was it the medicine that the psychiatrist had prescribed to make me sleep? . I was no stranger to depression and I knew my symptoms were not merely emotional or psychological in nature. Why did I always feel as if I had been poisoned? The psychiatrist decided my paranoia warranted higher med levels. I declined the advice and stopped taking the meds altogether. My anxiety today is lower, my sleep is improved but fitfull. My neck aches. My head feels as if it were in a vise. It's not a headache and it's not painful, but there is a tingling, crawling, scorching sensation at my forehead and behind my eyes as if someone had beat me with a pillow and then filled my head with novocaine.

I'm not sure there's a moral to the story. It might sound a tad over-the-top, but I think we're faced by a pharmaceutical plague. There's really no excuse for the absence of informed consent. There is nowhere above ground, e.g., nowhere on main street, and no-one with whom you can speak in order to take the full measure of fluoroquinolone poisoning. If you are at this URL merely to find out about the FDA's recent black box warning re: Levaquin's link to ruptured tendons, you are in for peep into hell. Read the other thousands of postings on this site, and decide for yourself who bears the ring of truth.

Ok i have read some of the post and now i am a bit scared about what i have done to myself. I had this put in Sept 23 2008 so i have only had it for about a week. I have two children 18 months old and 2 months old i am 22 years old and cant afford to have any children let alone any more children. So i chose mirena since i got pregnant with my children on the pill and the patches pill with my last one and the patch with the first one.

I paid 878.38 to have it put in and so far i have noticed that i have some poking and sometimes stabbing pain in that area and i have really bad gas and i am afraid to push to have a bm scared that i might push it out since the cervix is still dialiated. so far i don't want to have it removed but wanted to know.

Has anyone had it fall out?
and also what about weight gain, face compelxion,

Im not so worried about sex drive i didn't have one with my boyfriend before i had it put in. I lost my sex drive after i had my daughter who is 2 months old i actually lost it before i had her so thats not a major concern of mine that i think has a lot to do with bi polor anyways and the meds i take. And i haven't noticed any changes in depression maybe because i already take 3 different meds for manic bi polar syndrome.

I have notice some pimples popped up on my chest in the last few days but i thought that could be due to the heat and i was out side for a few days doing a yard sale.

Does anyone have any advice.

Hey everyone ,The advocacy website is up and running for you to sign on. Please click on reply and you will see a link .Please take the time to view this site and sign the petition,this is how you can help and we appreciate all the help we can get. Kate Miller

Our daughter is 17. She started taking Singulair June of 2000, 8 yrs ago. Upon hearing the side effects I insisted she stop taking the drug due to the fact that she also showed extreme signs of agitation, irritation & was always angry & frustrated by everything & everyone around her. Her standard comment was " I know I'm mean & rude". As a parent you know your child & we knew something wasn't right but never suspecting this drug. She as a young child never exhibited any of these signs. She was evaluated by 2 psychiatrist in these past 8 yrs., ADD was one of the diagnosis & our concerns that there may be some bipolar symptoms. After taking her off the Singulair there has been an obvious improvement that is evident to all the family members. The Singulair did an outstanding job of helping with her allergies which are severe & also contributed to multiple sinus surgeries. But the trade off? We are absolutely convinced & she is too that the Singulair had a debilitating effect on her personality. She once again talks, laughs & is such a joy & pleasure to be around. I will add that she never felt any suicidal tendencies, but just severe agitation, irritation, impatience & her reactions to situations & people around her were completely out of balance. I will always be convinced given our experiences that Singulair was completely responsible for 8 yrs. of heartache for us as her parents & 8 yrs. of misery for her.

Concerned Citizen; I just went to Singulair.com and the website is quite good. Any practitioner would know to look at the product PI which is right there and the pharmacokinetics section tells you how it works. Put your glasses on.

I have previously posted; my 17 year old son, A.J., committed suicide in October of 2007. I have filled out two FDA reports, written to Dateline and I will write to every that I can. I'm not getting an attorney. I don't want anything. If it would bring my son back, then yes, I'd put up a fight. I'm interested in providing medical statistics to Merck and the FDA. I'm interested in education and truth. I believe Singulair is a dangerous drug, no doubt about it. But I beg all of you, gather medical records and provide them to the proper entities. Be interested in education and statistics. Not money. It won't bring back the lost years when your child was miserable and bouncing off walls. If you've taken your child off of the drug, you have most likely solved the problem. Thank-you. Kate Kendle

My 20 month old son was perscribed Omnicef for a persistant ear infection. Two days after he started the medication, our sweet little boy turned into the Demon Child, that wouldn't eat, wouldn't drink, wouldn't sleep, would scream with terror, or pain every 20 minutes...

He had loose stools as well, but since he wouldn't eat or drink that only happened about once a day.

We took him to the hospital and they ran tests, but could find anything wrong, "It must be the pain of the ear infection..."

My wife and I were going crazy with him, and didn't know what else to do but love him and not try to kill each other from lack of sleep.

About a day after the medication was finished he started to eat again, and within 48 hours he was sleeping though the night. As a matter of fact he could not get enough to eat. He was going to gain back the 5 pounds he lost ASAP.

The real kick in the pants is that he still had an ear infection in both ears and ended getting tubes in his ears two weeks later.

We are taking the precaution to never let him take cephalosporin derivatives again.

I can't believe that the manufacturer of this drug does not list these behavioral reactions in the small print. It would have saved us a lot of heartache if we had known and could have discontinued the drug.

I have been taking toprol since Oct. for a heartache I had.
I also am a diabetic and have noticed that since taking
Toprol my sugar levels have dropped to normal. Does anyone
else have this side effect for Toprol?

I had the "moon face" For me, after my body adjusted to the pred., and it really never fully adjusts, but it gets used to it somewhat, I started to lose a few pounds here and there and my face looked a little better. It depends how many mg. a day u r on it. I was on it for 4 yrs. and have been off of it for 5 months. It's getter smaller since I've lost more weight. It makes u hungry and nervous and u eat because of both. It's hard to lose any weight, I know. It seemed my brain worked overtime while my body was so sluggish, but yet I couldn't sleep. It's all part of the pred. I could never seem to get interested in anything. Even now, I'm just starting to get interested in things I used to like, still slow going, but I notice a difference. Try excercising. it was extremely boring to me, but I tried. Couldn't concentrate unless I could use my bike in front of the tv. I promise, it does get better. I wish we didn't ever have to take pred., it causes such heartache in so many areas of our lives. It does wonders for so many reasons but the side effects r so horrible. Take care and God Bless u.

For those of you mothers that think that "drugging" your children is wrong, I wish to God that my parents would have when I was a child. They thought the same as you and I suffered because of it. They were both school teachers and didn't want to admit that their child had a problem. I have been diagnosed wt ADHD and now take medication. I only wish I could have stopped the heartache I experienced throughout my childhood. Spending those "10" extra minutes a day didn't work for me. I remember many nights when I sat down to do my homework and I just cried. My only memories of school were those of me throwing my books across the room, tired from looking at a wall for hours, clueless. I suffered and there was simply no reason. For this, I never forgave my parents. Later on, my mom told me that she had the choice to put me on medicine and she didn't think that I needed it. Now she admits she was wrong. Don't be selfish Mothers.............

To Kay who just recently posted, HANG IN THERE....I was on Yasmin for nearly 2 years and suffered from depression, rapid heart rate and severe anxiety for the last couple of months of taking it before realising it was due to Yasmin and getting off it. I have now been off it for 4 months and everything has been getting better each month...however, the main symptom that has lingered has been ANXIETY. Prior to Yasmin, I have never in my life had an issue with anxiety and each month (mainly around ovulation and period time) I get obsessive/irrational/negative thoughts and become more panicky and anxious. Each month has gotten better, but I am aware of it taking anywhere up to 7 months for some women for these effects to completely go. Be sure to cut out any caffiene as this only makes it worse. Also, I tried magnesium supplements as I heard it can lessen anxiety but it only made me worse so I stopped. It DOES get better but it takes a while. I think we almost need a website for those who have STOPPED taking Yasmin as much as those suffering whilst on it. GOODLUCK and take care.

WARNING to the guest who posted a reply to desperate boyfriend about the fact that you are now on Yasmin and feeling great...I too thought Yasmin was great for a year and a half until I was completely taken over with depression, dizzy spells, rapid heart rate and anxiety. Please watch how you're feeling as I would not recommend Yasmin to anyone, and would not wish my experience on my worst enemy. Do not be lulled into a false sense of security cause it seems to be ok at the moment. If I had been warned of the possible effects of this pill I could have saved myself and my family a whole lot of heartache.

Lots of hugs out there to those getting off this awful drug. It takes time, but you will get better and get back to your 'old self'!!!