3x symptoms and conditions

I have been dealing with Total neuropathy of my feet and legs for 18 years now and i was taking neurotin 300mg 3x's a day and that was not even putting a dent in my pain. 2 weeks ago I fell in the shower on Monday and fell down my stairs Tues. ( due to not being able to feel my feet) and I sprained my whole body and was in major pain. My Doctor prescribed 10mg flexeril and 50mg of tramadol. It has been a miracle for me!! the pain is gone from my nueropathy, I haven't slept this good in many years & I am hoping that after talking with my Doctor i can continue taking this ! What a difference this has made in my life. However the second and third day I was severely grumpy but I was aware of the fact so I was able to minimize it!

i had mirena for an yr and a half. I began breaking out( thought it was stress) but i couldn't control it and the acne was real bad around my mouth and chin area( thought i had something). I suffer from migraines and it did help with that. Moody, depressed. I am normally a happy over jolly person but within this last yr. ive changed to a moody chick. Always tired. dizziness and i just felt like a different person. Like so many women said . You think your losing it but all the time its the Mirena. I really didn think about it that way until my friends told me i ve been like a devil. And how i just lash out on ppl for no reason. But i went to the doc 3x about the acne and how my partner was able to feel the string and they were able to cut the string. but my face still looks crazy and lil on my chest and shoulders(ACNE).O breast tenderest and back pains. I am only 22yrs ol. My cousin said it caused her hair to fall out and lost of weight. I was losing and gaining. My weight was every where. And that caused white stretch marks.O just hand it removed feel better already but start bleeding. O my period did stop a lil and i did have a odor before i start spotting( never had odor problems and never was a cramper). I had some of the worst cramps ever and was a cramper. I quite sure theres more stuff but can't recall everything. My mom said they using us as test dummies.

I was diagnosed with pneumonia in Nov 2008. When I was released from the hospital, my doctor prescribed bactrim (2pills 3x daily).
After a short time I had noticed body aches and my legs and joints felt as if I had been hit with a bat.
The primary side effect was a rash like skin irritation all over my body.
What started as itchy red marks, began to dry up and my skin was flaky and hard (back, arms, chest, legs, stomach, neck, face and ears).
I was admitted back into the hospital.
The rash and itchiness cleared up. Yet, now my body is full discolored with dark blotches where the rash was (back, arms, chest, legs, stomach, neck and face).
I'm totally humiliated when I'm in public because the discoloration is clearly visible and it looks as if I have a disease.
In addition to that, I can't even wear most of my wardrobe anymore because I hate to expose my skin.
Looking at my before pics is a sad reminder that I've been scared for the rest of my life.
I've consulted an attorney who quickly told me that I had no legal recourse.

I was prescribed this drug in hopes of keeping thyroid nodules and goiter from growing larger. My TSH levels have always been in the normal range throughout my life, so the theory that "normal TSH' means a working, normal thyroid is absolutely untrue. I am a prime example of a person who's numbers have always remained normal and yet their thyroid does not work properly. I have decided to discontinue this drug after 3 months of use. The weight is packing on faster than I can diet and exercise it off. My face is puffy, my stomach bloated and looking pregnant, and now retaining water. Anyone who does not believe that Synthroid causes weight gain, I welcome you to try this drug. It does the exact thing it claims it is combating. I am not hypo with levels of 1.07 and yet something odd is occurring within my body with this synthroid. I'm praying that if I stop the drug I might return to some form of normalcy soon.

wow, guys, so...i have had mirena in since April 08, and experiences minimal side effects that i was told would happen. slowly but surely though other things kept coming around, including:
-10-15 day periods
-constant cramping, extremely painful at least 2-3x a day on either left or right side
-no sex drive
-high irritability at unpredictable times
-muscle cramps
-headaches about 2x a week
-nausea at least 3x a week
-fatigue about 2x a week

When i first got on i thought all these people complaining were whiney, whusses. but now i see that all these little annoying things add up, and aren't good.

so i am getting mine taking out tomorrow, and the only form of birth control i will use is the easy fertility awareness method. charting your cycles is natural and fairly easy, and can help you avoid pregnancy, or get prego. Taking Charge of Your fertility, by Toni Weschler is the book i use, It is totally the fertility bible! Man-made hormones are just going to screw you over eventually, why not try just educating yourself and knowing when not to have sex, or to be protected? It worked enough for me before i got prego, i got pregnant exactly when i wanted to. I just went on mirena cuz it was easy, paid for by insurance, and i didn't have to avoid sex with my hubby that one week a month, haha now i don't even want it. funny stuff, eh?

I will try to up date after i get it taken out to see if i get the same relief that many of you felt!

I began to experience upper body itching (arms, back, and upper chest after taking TobraDex drops for two days. (perscription was for left eye, 3x per day for 4 days) After 8 days the itching still does has not gone away.
The level of itching is similar to what you would experience with a low level sunburn with light skin flaking. It's rather interesting, I don't really feel an intense itch on my back, but when I start to scratch it really feels good to just scratch and scratch. And no, I do not have sunburn.

I am a 34 yr old mom of 2 and have had my Mirena for 4 and 1/2 years. I actaully have been having a great experience, but again, have the same weight gain issues with almost no loss, no matter what. MY BIG QUESTION: has anyone else experienced mysterious vaginal discharge and symptoms? Starting about a year ago, I began having mystery discharge and have been to 7 different doctors who have tested for everything under the sun, and FOUND NOTHING. they can see it, keep giving me yeast treatments. etc, but in 2 or 3 months, it is right back. There is a pungent fish odor, especially after sex with my hubby, which Dr's have been saying is normal... MAYBE NORMAL FOR THEM, not me!! I actually thought it was due to a lack of hormones now that my IUD is ending is life.. However, I did have a couple of crazy panic attacks, which I have never had, the dryness for sex and friction is intense, and my hair has been thinning, which I thought was just me... Can anyone let me know if you've had the vaginal symptoms... I know no one wants to talk about it, but I have to ask!!

Headaches??? Really i have been getting headaches recently
I hate the new HFA inhalers
I have been a chronic user of the old inhalers for years and i never complained, I actually really liked them. I have been on a ventilator 3x and I am only 24 years old. The most recent hospitalization was the worst. I have been found to have an under productive heart. They did exploratory lung surgery and also gave me a chest tube and took numerous lung samples. I honestly believe that this was due to the new inhalers. Whenever I take the new inhalers I feel slightly better (not much) approx. 1/3 of the the way the old ones made me feel. I feel slightly better after about 15 minutes, but as soon as I take it I actually have a harder time breathing and it just SUCKS!!!

I'm glad I thought to check to see if Wellbutrin might be causing my hair loss. I had some natural thinning at my temples before and started using Rogaine for women with great success. Then after my mastectomy and breaking up with a guy I went on Wellbutrin. I am currently taking the 150mg three times a day. I am losing so much hair it's scaring me. It comes off my head all day long. Like others have said I also have a handful in the hour, another handful in my comb and then it just continues to jump ship all day long. I have lost at least half of my hair.

My Mirena Removal....
So i posted here a few weeks ago after I found this site. I had EVERY side effect listed and was so freaked out that i immediately made an appointment for removal.
For those of you reading and wondering what the removal is like..
Well, NOTHING like the insertion. I was so so nervous and it was over before we actually started. The DR was surprised that i was back in his office to have this removed. He then proceeded to do an ultrasound to be sure it was placed properly before removal. And yes, all was OK on the position of it. I explained to him my reasons and he looked at me like he had never heard this before. I honestly can not imagine with all the women he sees that NONE of them have complained. But...as I was getting dressed afterwards, I took a good look in his office. There was Mirena literature ALL over the place. In fact, that was the ONLY thing he was advertising. Not to mention...they made me pay up front with the insertion back in Nivember...billed my insurance and I still have yet to receive my reimbursement. Oh yeah, and that...they charge more than the actual Mirena costs, then they bill your insurance for the price they know they will pay and the DR then makes about $150 profit. Nice.
Ok, back to my side effects post Mirena. The removal was not painful at all. I did spot for about a week- nothing too heavy but it was clotty and def there.
A couple of days after the removal it felt like I was coming out of my skin something terrible. I figured this was my body adjusting to the lack of hormones. I also had some headaches.
It has now been 2 weeks and the spotting has disappeared. I also can see the bloating of my stomach is starting to go away. It looked like I was about 4 mos preggo while I was on it. I also have an increased sex drive. And sleep-- well let me tell you, I have not slept this good in a very long time. I am actually sleeping more than 6 hours now and the night sweats have also discontinued.
I can't believe EVERY time I come to this site and look up Mirena ALL the people that have posted their experience as being negative. Yet, the DR looks at me like I am crazy! I have been seeing him for years and I have never complained about something like this. I really am so happy that I have it out and wish I would have done my research on this prior to insertion (which was one of the most painful things ever!)
So..for those of you out there that are either contemplating having it inserted...I say NO WAY. And for those of you out there that are nervous about the removal or not sure..I SAY YES, DO IT! For our bodies to be reacting this way, it is clear to me that it should not be inside of us. Listen to your bodies...they really do speak to you and let you know when something is not right. Forget about the DR saying it is safe or he has not heard of any of these side effects...YOU be the judge.
Good luck! And I promise it gets better once you get that lil' demon out!
Mona

My poor 6 yr. old daughter has been taking this awful medicine since December. She has been complaining of stomach pain, headaches and not being able to breath. I called my doctor a few weeks ago to see if it could be from the Singulair she was on.. they told me "probably not". During her dance class she had to sit down because her stomach hurt so bad. I was writing everything down that she was eating (we have an appt. w/an allergist in 2 weeks.) .. thinking maybe she has food allergies now. She is constantly trying to clear her throat and telling me she felt like something was still coming down her throat. Until I found this site, I had no idea why she was behaving this way. I started putting blankets down on my husband and my floor because of her "bad dreams". This little pumpkin has always been an awesome sleeper, but at least 3x's a week comes running down the hall crying about her nightmares. I walked into my docs today with a print out of Merck's own website listing the side effects of this horrible med. She looked at me and said "you get the credit for diagnosis on this Mom!".. Praise God He led me to this website! My poor daughter will playfully start to feel better now that we have taken her off this junk!

Thanks for all these posts! My 4 year old daughter has a history of allergies which have in the past led to sinus infections and bronchitis. We used Xopenex and Pulmicort with the nebulizer along with Vazobid and Delsym and cleared up the bronchitis during Christmas 2007, but her pediatrician suggested her taking Singulair as a preventive medication for her allergies. This medication has turned our household upside down. She has taken it every night for 3 weeks and the side effects are the same as others have posted.......aggressive behavior, severe defiance to simple tasks, nightmares, stomach cramps, wetting accident at school (first time ever), weight gain, bruising, and vomiting. When told "no" she replies with wanting to kick me and tells me she doesn't want me as a mom anymore. The devilish behavior is intolerable. She was never like this before she started taking Singulair, and I am so thankful that I found this website quickly enough to put 2 and 2 together, and I am taking her off of it TODAY!!!

Hi All,
Just wanted to share a positive Lupron experience. I began Lupron in Dec 2005 and ended in Jan 2007. I took monthly Lupron shots for a year straight. However, my Dr. prescribed an add back drug called Norethindrone which I took once daily the entire time I was on Lupron. The only side effect I had was about a 10 pound weight gain. When I asked my doctor if this was from the Lupron he said maybe 3 or 4 pounds of it. I was eating right and exercising during this time period but was still gaining weight. About a month after I came off Lupron I began losing weight and was able to fit into my old clothes a few months later. I am sure it was the Lupron that caused me to gain weight.
If you are taking Lupron without any add back drug, this seems when all of the other horrible side effects come into play. Just wondering if anyone had a really bad experience even while taking the add back drug.

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!

Omnicef is actually one antibiotic my 2 year old has little trouble with. The red stools are alarming but at least they are solid. Currently he's on Augmentin which has caused horrible rash and loose stools.
The other nice thing about Omnicef is the dosing schedule.Usually once or twice daily depending on the infection. The 3x daily with Augmentin is way too much stress for me to bear,and for him even more so. Seeing his poor little red butt makes me cry with him. Since the two drugs can be used for the same infections, I will be asking for the Omnicef first from now on. Omnicef seems to clear his infections very quickly. The Docs really should forewarn about the red stools though, they are quite scary,even though they are typically harmless.

I took 10mg lipitor for 9 months and started having horrible arm pain that would not go away. Then the pain became mixed with weakness and I could not even lift a grocery bag. I am 53 and of good weight and I thought, good health - other than the elevated cholesterol level. My whole family has the elevated levels and there was an uncle who died at 43 of a massive heart attack. So, gave it a try. I got to where I thought I had ALS for sure. The leg twitching started in my calf and moved down to my feet and kept up even now. I have been off lipitor for 8 months. My strength came back in about 3 weeks and has progressively been better. The twitches are still here but am now taking 3 doses of CQ10 3x/day with Bcomplex and folic acid. All is helping and I am hoping the twitches stop. I will not ever take this again.

I took 600mg of Neurontin 3x a day. I started to get gas during the 5 years I was on the pills. At 1st, I only took the pills 2x a day and it wasn't terrible. Later I had to start taking the pills 3x a day and after my 2nd meal of the day, I would get intestinal pain, bloating, and gas! It didn't seem to matter what I ate. My doctor gave me a zillion tests and could never find the cause of the problem. I had surgery for my neck 3 weeks ago and was weaned off of the Neurontin. For 3 weeks now, I haven't had nay of the gas!!! It was the Neurontin all the time. I am so glad to be off of the Neurontin.

Cure for side effects? CoQ 10 helped me it could help you to. I don't think the private mail on this site works. You can contact me: seekers999@hotmaildotcom if you're a real person you know what to do with the"dot"... "." But nobody needs me, do the research yourself! checkout coq-10 and how lipitor and other statin drugs deplete your body of it causing muscle atrophy. (see my previous post for link)
I don't recommend websites or charge (even though I'm on social security disability w/kids and financially challanged ;-) I;m just trying to help people get better by pointing them in the right direction.

I was crippled up on crutches! Worst pain in my life! Couldn't even get to the bathroom 15' away WITH THE CRUTCHES!! If felt like muscle was tearing with each step, within a week the pain was gone!! The mental fog was gone also and I quit taking the Prozac, but this might have been also due to the Acetyl-L Carnititne.(500mg 3X a day)

I just know that stopping the lipitor didn't stop the pain and confusion!

God Bless all as they try and work their way through these terrible side effects! Remember I had to increase the coq 10 to 900mg a day before I saw benefits on the 3rd day.... There is hope! I hope it works for you!

I was on Lipitor for over 4 years but had my dose increased about 7-8 months ago. During that time:

1. Loss of energy (sometimes severe)
2. Muscle cramps at night in thigh
3. Pains & numbness in feet
4. A kinda of fog in my mind at times, hard to think
5. swelling in both feet
6. Easily injured in feet and knees, and slow to heal. the smaller muscles in the legs and feet

I finally realized it was the Lipitor and stopped immediately but the symptoms DON'T! What I found out is that Lipitor depletes the body of
Coenzyme Q10 (Coq-10) an important part of our bodies heart and muscle health. I was crippled unable to walk for over 2 weeks! On crutches, it felt like I was tearing and ripping muscle with every step, in my feet. I was taking 300 mg of Coq-10 a day. I found a web site that stated to take 900 mg, after 3 days I could tell a small amount of differance. 3 days later I was off the crutches. I was also taking 500mg 3X a day of
Acetyl-L Carnitine but it is the Coq-10 for sure! With in a week, ALL SYMPTOMS WERE GONE!!
Unfortunately if you stop taking the coq-10 they come back, I found out the hard way. Apparently your muscles have become extremely weak and need to build back up. You need to take the Coq-10 until that is complete and I hope you can stop after that. You can get Coq-10 at supermarkets, heathfood stores etc... BUT it's much cheaper on-line. feel free to email me for more information or questions.

I can't believe what I'm reading, I too have been on Lipitor for four years now and in June of this year my right leg began bothering me, feeling crampy, foot felt like it was asleep, ached every minute, hurt to move my leg during sleep time. Continued to get worse everyday. Went to doctor, thought to be a strained muscle. But this was only in the calf of my leg, not my whole leg. All this time continuing to take my lipitor. Then this month, it became the worst, I got up one morning and couldn't put my foot on the floor, couldn't put any pressure on that foot at all, the pain was unbearable. Went to emergency and the doctor there advised me to get off of the lipitor. I've been off it for three days now and today I can actually put my foot on the floor, I do have to use a cane to walk but it feels ten times better. This has caused me to lose time at work plus ruined a week of vacation for me. This drug should be outlawed! Everyone beware of the side effects, it took me four years to see any but now I'm paying the price.

I am a male 46 years old and recently came upon this site. I have been on Lisonopril for about 6-8 mos and have had tremendous side effects. The skin crawling at night (heebie jeebies, and skin tingling) horrible saliva and constant spitting. heavy mucus in my nasal passages and throat that made me vomit. The dreams.............. my God .......... the dreams!!! I dreamed i killed my son for gods sake, have had weird and veeeeery vivid nightmareish dream activity. The shortness of breath and pain under my collar bone and up my neck,,,,,,,,,, also scared the hell out of me. I can only work a half of a day, and i am fortunate that i own my own business................ however anyone who knows you have to be there........... the ONLY fortunate part is no one can fire me. I am not sure if my business is suffering from my lack of being there, but i feel guilty as hell. Throwing it away!!!!!!!!!!!

WOW!! I can't tell you how glad I am to have found this site and learned about all the side effects from lisinopril. I've been on lisinopril since about January of this year...12.5 mg. Been back to see the doc 3X since i've been on it. I complained about chest pain and coughing. I've had EKG done on me 3X (including the one done recently when I checked my self in at the ER at 2:30am) also did the treadmill stress test. I've also been referred to and did see a pulmonary specialist where they checked my lung capacity/function due to the shortness of breath. I've been friggin joggin' 7 days a week for 3 months (used to do 3X/wk) to combat the fatigue, shortness of breath, tickly & scratchy throat causing me to cough to try to clear it, tingly arms and legs, chest pain (kinda like pressure or cramping, real discomfort)...and yes, i feel like my days are numbered. It's been such a life altering experience. I'm stopping lisinopril starting today. I hope the chest pain will get better. Will post again in a few days and let you all know how I feel. Thank you all again for taking the time to post your experiences. God bless!

while taking adderall xr 25 mg. twice a day i have experienced numbness or a tingling like feeling in my right thumb. anyone out there had this with adderall xr? i can't imagine what else it could be. i also have severe headaches and seem to live off tylenol!!!

I am 53 years old and have been on 10 mg of Lipitor for at least 5 years. For the past 3 years I have been experiencing tight muscles in my back and muscle spasms on my right side. I have had the following tests done - all of which came back negative: CT scan, Ultrasound, MRI, gall bladder scan, kidney scan, pelvic exam, even had a colonoscopy (that sucked), and went for physical therapy which the therapist said I had weakness on my right side. The doctor never even suggested to stop taking Lipitor but after reading these posts, I'm stopping myself.

I have been taking Lipitor for about 5 years now and have had numerous things happen to me. Just trying to find out if they relate to the Lipitor or not. Have developed extreme fatigue and depression over the years. Always seems like I am in a fog. Have tried numerous anti-depressants trying to conquer this. Nothing seems to work and the problems continue. I was thinking that I just have to live with it and then I thought about the Lipitor. Has anybody experienced any of these symptoms too? I am on 20mg.