November 28th
2007
9:42 AM
I didn't really have any side effects with Relpax. The most wonderful thing was that it made my headaches go away. Of course my Dr freaked out when she found out that I was taking them on average 3x a week and switched me to Topamax because the frequency of my headaches meant that I had chronic migraines. I HATE Topamax. It gave me a lot of side effects and I still have my headaches. I want my Relpax back!
-- By lbs12 | Reply | (1) replies | Private Message me
October 24th
2007
7:10 PM
I had the Mirena IUD inserted on October 10th. I had it switched from the copper IUD because I was spotting dark brown blood prior to my period, so my gyno recommended the switch. I spotted for the rest of the day, then stopped for two days, then began what I would call my period, since I was due for it later that week anyway. I am still bleeding, but I'd like to believe I'm nearing the end, since it seems to be lightening up. I expected my period to be fairly long after insertion.
The day after insertion, I experienced severe itching and swelling down there, and decided that I must have a yeast infection, but both symptoms are listed as side effects on the sheet I got from my pharmacy. I treated the infection, but still itch from time to time... I'm wondering if it's the hormones in the IUD.
On the weekend of October 19th, I lost my appetite, my sex drive, all sense of sexual pleasure and my ability to acheive orgasm. I ate three meals all weekend long, and only because I felt that I should eat, not because I was hungry. Sexually, I felt friction and not much else. Upon trying to climax 4 seperate times over the course of the weekend, I failed at all 4 attempts and all I got from my efforts was sore muscles, frustration and tears from being so upset by it. I have never experienced problems with sex or climaxing in the 14 years I've been with my husband. However, a couple of days before insertion, we had had sex and it was fabulous, as always. I climax every time we have sex, so it's been very upsetting.
I weighed myself today, just out of curiosity, and since the insertion, I've lost 7 lbs. I'm not dieting, not exercising, not even trying to lose any weight.
Upon calling my gyno and discussing my symptoms with her assistant, I was told that it couldn't be the Mirena, because the amount of hormones in it are so minute that they wouldn't affect anything outside of the uterus. I was told that something else in my life must be causing my sexual problems. !!! I don't think so! The IUD is the only thing that has changed in the past 2 weeks! And how do you explain a sudden loss of 7 lbs??? She didn't want to say it straight out, but she was trying to tell me it was all in my head.
I've had sex again since my failed attempts, and it's getting better, as is my appetite, so I'm hoping that my body is simply adjusting to the new IUD and getting used to the hormones. I have not been on any medication or hormones in the past two years, as I've been pregnant and then breastfeeding, so it might be quite a shock to my system.
If my inability to acheive climax continues, I am going ot have the IUD removed and have another copper IUD put in. My sex life isn't worth this.
-- By ddr_74 | Reply | (5) replies | Private Message me
October 24th
2007
6:44 PM
I've had side effects of hearing conversations and thoughts but, I can not tell from what because I was on so many things. Monday, my lamictal went up from 75mg to 100mg and over the past few days my mood has gotten worse, my headaches have increased in frequency, my appetite has increased and my hallucinations have returned.
-- By sarabader | Reply | Private Message me
August 21th
2007
8:11 AM
I've been on Topamax for about a year. I think the worst thing that happen to me is I totally forgot my childs given name. We have called him a nick name all his life but I'm his mom!!! I was so upset I thought I was going crazy! I still get headaches daily but I know topamax has been the best meds I have been on so far. I have heard that if you combine Relpax with topamax it helps so if anyone has any information, let me know.
-- By lemondrop | Reply | (2) replies | Private Message me
May 28th
2007
9:24 AM
I have been taking lisinopril for about 5 years for hypertension (160/110). I first started at 10mg, 20mg, and now at 40mg daily for the last couple of years. In retrospect, I have noticed momentary bouts of short intense vetigo. Recently, as in the last week, the frequency of these bouts of vetigo have increased to 4-6 times a day and intense fatigue and headache has crept into the equation also. I will talk to my doctor regarding this, but would be really interested in exploring the holistic approach to hypertension management and get off the lisinopril.
-- By recray | Reply | Private Message me
December 30th
2006
11:14 PM
I was on Topamax for 3 weeks, and only got up to 75mg/day before insisting to be taken off it. I felt drunk all the time, couldn't concentrate or find the right words, my hands and feet were numb and tingly all the time, I had awful heartburn/belching for almost 3 weeks straight, I couldn't sleep, and was very nauseous all the time. I may have stuck it out a bit longer, but I had 5 migraines in 12 days, which was an increase in frequency compared to before taking the Topamax, so I didn't feel this drug was working for me. Today was my first drug-free day, and my head is so clear, it is just great! My feet are still tingly though, so I'm hoping that will go away soon...
-- By jrocco66 | Reply | Private Message me
August 19th
2006
12:26 PM
kenalog helped the pain in my back. I do have some stomach upset, heartburn mostly that I didn't have before. I had a little anxiety and some heart palpitations but now at 3weeks lafter injection I feel fine. I believe when administered properly and at the right doseage and frequency this can alleviate pain in a lot of people. It did me!
-- By skalos19 | Reply | (1) replies | Private Message me
August 7th
2006
5:20 PM
Seem to have blurred visionat times since using Flomax, doesn't seem to helpflow that much, had seed therapy for prostate cancer 2 years ago, my problem is frequency of having to urinate, also noticed muscle pains in knees etc, lack of energy etc?
-- By pvbh | Reply | Private Message me
May 10th
2006
6:51 PM
My son is 18 month old, and was diagnosed as an asthmatic since he was 6 month, (because of the frequency of his asthma attacks). He start on Singulair on May 01, 2006 and he have been taken it for 10 days, Two days ago he start having a bad rash and he is asking for water non stop, 8 or 9 bottles of water a day, maybe more, we do not think this is a normal behavior, because babies usually never drink that much water and, he is more active than usual, he screams, cry, and runs non stop. Have someone had the same problem with the polydipsia (abnormally large intake of fluids by mouth). Thanks for this site, It have been very helpful!
-- By kyrin | Reply | Private Message me
February 23th
2005
2:13 PM
Levaquin is probably one of the most damaging drugs in the market. I was given Levaquin 500mg for 20 days by a Urologist for a possible urinary infection. (It later turned out that the frequent urination for which I was given this medication had nothing to do with urinary infection and all the symptoms remained the same after completing the 20 day course, but that is a different story).
Now about the side effects. I started having on and off chest pains about a month ago and now the frequency of those chest pains have grown to almost persistent chest pain. It is getting me very nervous. I also notice my left knees are sometimes totally limp and unable to move.
Those doctors who prescribe this medication without becoming aware of its side effects and not informing the patients about its side effects should be prosecuted to maximum extent by the law and it should be considered a felony to prescribe this medication without considering alternatives.
I would like to know if anyone has noticed any of the symptoms getting better with time. I am curious to know if we can expect any of the symptoms to get better with time or worse? Also, I would like to know if anyone has been able to treat any of the side effects.
We need to get a petition together and file with FDA about Levaquin and its disastrous side effects. How can FDA approve this medication without a thorough study of its side effects?
Looking forward for any responses.
Thanks.
-- By razam2 | Reply | Private Message me
February 13th
2005
5:08 PM
My doctor put me on 40mg Lipitor about 4.5 months ago. My cholesterol at that time was about 220. The Lipitor has reduced my cholesterol to about 105 but not without serious side effects that I began noticing about one month ago. I am a diabetic, BTW, but but sugars are well-controller. The first thing I began to notice is that my thighs felt cold all the time, sometimes even burning--but only when I sit down. If I put heat on them, it goes away. Putting cream on them goes away. Another thing I was getting these migraine headaches that affect my vision, causing blind spots. I've them before but never with the frequency of the way they are occuring now. The last two big things is absentmindness and extreme fatigue....whew. Well, I stopped taking Lipitor today and I feel better already. Diminished fatigiue, for sure.
-- By freemarketer | Reply | Private Message me
August 25th
2004
5:04 PM
transition to seroquel for my 11 yr old son was just completed, over the period of coming off one medication and being switched to this, there has been a marked increase in mood swings and agression culminating in a full blown rage this evening.
These symptons have increased in frequency and level with each increase of seroquel and leveling off of the other medication.
Tonight was his last dosage, as one hour later he was literally out of control, agressive, destructive, and physically abusive.
-- By mistofmourn | Reply | Private Message me
July 24th
2004
4:22 AM
Hi all, i live in NY and have been on synthroid. since i was 34 i am 50 now. Because of the huge normal range it is very easy to take too much synthroid. Doctors also do not know how to prescribe it...It is better to take a little bit less then move the dose up. Mohammed Ali( the prize fighter) thought that taking synthroid would make him a better fighter ,stronger etc... he took synthroid, though he didn't have thyroid issues, and became tired and sick.
So from my experience too synthroid much causes constipation, muscle cramps in the calves first , then everywhere, like your butt and then your pelvic floor which in turn can cause frequency. Your feet swell, you get much more tired and irritable then depressed. Your heart races then you have episodes of shortness of breath and horrible crushing anxiety. Also your hair falls out..
Also as you go into menopause with less estrogen you need less synthroid , (pregnant women need to take more)but NONE will tell you this so you just get sick all over and think that its just menopause!
I truly believe that there are millions of women out there with "fibromyalgia" who are just simply just taking too much synthroid... if 1.25 is the full replacement dose why would anyone be taking 1.65?
I am not a dr but i have come to see that they never suspect this medicine for the harm it can do.Part of this is that it is the most prescribed medicine in the country and the company who makes it is very powerful. And if you think that drug companies care if their meds make you sick than you should read about the Delcon shield and how the makers knew that the string wicked germs up into the uterus and they sold it and hid the results! I was not able to have children thanks to the good makers of this product.
so back to synthroid, I was taking .1 of synthroid with my numbers in the normal range and i had constipation frequency , muslce spasm in my calves,hair falling out , fatigue irritability , shortness of breath with anxiety... over a few weeks i moved my dose down( with email to dr) to a spilt dose of .025 in the am then 12 hours later .025 in the evening and ALL of the symptoms WENT AWAY! my advice to anyone who has the symptoms above is to tell their dr that they want to on a trail basis see if their symptoms are alleviated by less medication.If your dr says no ,FIND A NEW DR. , these are quilty of life issues and many drs are to busy to elp you titrate your dose , dont give up , you are only here once and you can get rid of the symptoms!!!
-- By sluglike | Reply | Private Message me
March 31th
2004
1:55 PM
began 10mg of Singulair for asthma following a bronchial infection about 4 weeks ago. I have been experiencing increased muscle cramps in my toes,feet,legs and hands. I went without it 2 nights and have already noticed a slight decrease in the frequency of the muscle cramps. the pamphlet accompanying the prescription said nothing about muscle cramps. apparently it IS a definite side effect.
-- By woodnymph1_2000 | Reply | Private Message me
June 4th
2003
6:55 PM
Ativan is a complete life saver. I was experiencing criple-ing panick attacks and sleeplessness. I take an ativan whenever one comes on and it levels me out. It has actually decreased the frequency of panick attacks.
-- By michelle82 | Reply | Private Message me
Levaquin (2) Singulair (2) Topamax (2) Relpax (1) Kenalog (1) Elmiron (1) Mirena (1) Celexa (1) Ativan (1) Lipitor (1) Flomax (1) Lisinopril (1) Seroquel (1) Evista (1) Synthroid (1) Lamictal (1) Accuzyme (1)
December 5th
2007
7:26 PM
I have been on Celexa for a little over a week for panic attacks/anxiety. The first 2 days I took it I felt like I was in a dream, light headed, tingly, pretty much just intensifying my problems in the first place so I stopped taking Celexa for a few days.. then I spoke with my doctor and she said to try taking it at night instead of the morning. So I began taking Celexa at bedtime. I didn't have much side effects except for a little trouble sleeping, but I actually was starting to feel "better", for about 4 days I was feeling really well and resuming normal activities. Then out of nowhere on that 4th day in the evening I got a really bad panic attack, and for the past 3 days since I've been feeling high anxiety and panic again. I don't understand, because I really felt like I was getting better. I told my doctor what has been happening and all she said was that its normal to have set backs and to continue the Celexa. I'm also taking Ativan to help control the anxiety until the Celexa "kicks in", but in the past few days nothing has been seeming to help. Has anyone experienced this? Is it because I've only been on Celexa for a week? I feel like I am going crazy being back in this lightheaded fog.
-- By brer1996 | Reply | (6) replies | Private Message me