Doctors office symptoms and conditions

I am 26 years old and have 3 and 1/2 month old son. i recently had mirena inserted and will be having it removed first thing tomorrow when i call the doctors office. i have ready numerous blogs and have a hair loss problem as well. I know that after u birth a child u loose hair as well as when its cold out as the air changes and may cause ur hair to be more dry and break etc. That is not the case here, my hair line on both sides is thinning as well as the front top part of my hair line.when i wash my hair it comes out way to easily and not the normal shedding when u wash and scrub ur hair. I have very long, thick thick hair so it took a few weeks to notice, but i know this is not normal.The first thing u can do is go to the fda website and find ur region complaint line number and call and report it. they take this serious, as they called me back a few minutes after i left my info with the young lady on the phone. if it is not reported to them they don't know to pull the product. it is even posted on the mirena web page to report any side affects u feel are not normal, or something along those lines. drug reps are surely not going to tell ur doctor this is more common then the 5% the info on the web page says. If u do not know medical terms or what u are looking for, ur likely not to see it and its not listed in "common" side affects like it needs to be. Please help by calling the fda in ur area so that this can be further looked into. i have only had the iud for 7 weeks and already notice this and caught it. I have read a ton of post on other pages and feel so bad that so many people did not catch it for awhile. Like most said, they thought age or an imbalance in their body was the causing factor. if i find more info i will post, hope this helps, and if u have any info for me please send it-

I'm am really ticked off! Today at the doctors office, the scale revealed that I've gained 17 pounds in a year. And it's all thanks to the Abilify! I was previously on Seroquel and I never gained an ounce. I'm just so mad right now. I mean, when I was on Seroquel, I was tired all the time, but at least I was happy and I was able to lose weight just fine. But with the Abilify, I can't stop gaining weight. I haven't been cheating at all and I exercise like mad at the gym. I use to weigh 165 pounds and was a size 8. Now I'm 182 pounds and wear a size 12. I hate being overweight. I'm huge and if I don't get off the Abilify, I'm just going to get more huge and I'll be back at 242 pounds if not more. I want to wear a bikini one day and have kids, but now I can't do that stuff! I'm physically too FAT!!!

When I took SMZ-TMP DS; The day after i could not move my legs without being in agony pain. I didn't think anything about it. The next day i had painful, red knots on my ankles and as the day went on they started to grow in size and more started to appear. I immediately stopped taking the drug and called my doctor. I could not sleep cause I was in so much pain. I would lay still on my back but when it was time to get up in the morning i had to literally lift my legs with my hands and get someone to carry me to the doctors office. He said that I had a very interesting case and that to never take this medication again. Right now I am still in a lot of pain and taking anit inflammatory medication to help with the knots and pain. I am still in bed not getting up and now I have 40 knots on my legs. He called the knots Erythema Nodosum. My tissue got infected with this medication.

Well I had Mirena inserted yesterday and immediately after I was in the worse pain ever. I suffer from dysmenorrhea and it felt one of my worst days I was in the doctors office for 2 hrs. I finally got a shot of Toradol for the pain which made my right numb.About an hr after i threw up and was still in pain. I slept collectively for about 15 hrs and had to take 2 aleve when I woke this morning. Hopefully I won't have any of the above mentioned symptoms. I am so scared to have this thing taken out.

Oh boy. So it started with this sentence in my obgyn's office "is there anything to help the EXTREME cramps i get every month?" to which he replied "oh yes there is the mirena" and it went on to ask him what it does. oh it sounded so wonderful! but....FAIL! my daughter is nine months old now so i guess i have had it for 8 months now. got it in right after my check up. I have lets see....i wrote these all down. Sex Drive..GONE. increased weight gain which is that i weigh more now then when i was pregnant and have changed everything and i keep GAINING more weight..cramps regularly there not bad but they are everyday. no energy i cant even do the dishes without getting tired. heartburn everyday, if my stomachs empty i have heartburn so it doesn't help me trying to lose weight! I have become more moody and when i say more i mean i have clinical bipolar disorder and it is HORRIBLE with my anger and depression and my always crying. I get pain in my joints and mostly my right leg goes numb (idk if thats mirena but it didn't happen till AFTER mirena happened). I have always had AMAZING skin...now i get acne all the time its unbelievable. i get dizzy and sometimes i cant even hold my daughter! and the migraines are the worst of all...no the worst is the no sex drive! All this and i was never told the cons in my doctors office! Isn't that against some code? Here is the topper on the cake. two weeks after i had mirena inserted my obgyn was asked to leave the practice and they refused to tell me why. Shady thats what that is.

I had mirena put in in Oct 08. My symptoms are: dizziness, sweating, nausea, (these symptoms can be mild and brief (seconds); or last a few minutes. I had severe dizziness in May and June of 2009. I also get acne on my shoulders, neck, face, and my T zone is very oily (especially my forehead). I am using good acne products to try to combat this problem, but I continue to have a problem. Some of my acne is like welts and I even have this going on on my scalp. I wrecked my car in December 2008. At that time I was very foggy headed. I blamed the foggy headedness on being stressed and overworked. I am 40 years old. My children are 10 and 13, therefore I know my symptoms are not post pregnancy. Today, I questioned if I wasn't going through early menopause. My doctor said this mirena would be wonderful and that after six months I would not have a period anymore. I have a period every two weeks. My periods are very light, but I still have them every two weeks, and they last for two weeks. I have been wondering if my body will adjust, and if I will eventually get to this heavenly place of now periods and bliss?

I've been on Yasmin for about a year and a half now... This is my first time really using birth control. I tried BC in my teens but hated the side effects so I got off them right away. Now that I am in a serious relationship and we're both in agreement we don't want to get pregnant until after we're married, I decided to start BC. I've had a few side effects but didn't really think much about them until I went for my annual pap last week. My doctor asked how the Yasmin was going. I told him that I've noticed I have little to no sex drive. He basically said that's not typical for Yasmin. I decided to get online and research side effects, that's when I came across this website. After reading several of the responses, something just clicked... I have many of the same symptoms!

I have never in my life experienced migraines until I started Yasmin. Fortunately I've only had a few since I started but nevertheless, not fun. I do however get frequent headaches. While I'm on the subject of my head, my memory seems to have slightly diminished. I often have a hard time remembering the simplest of words, causing me to misspeak often. I even have a difficult time remembering what I did a few days before! I've always had a very good memory! Has anyone else experienced difficulty with your memory??

About 4 mos after being on Yasmin I had a really weird uncomfortable pain just above my inside ankle. A few days later that pain had traveled up to the inside middle portion of my calf. At this point the spot where the pain resided was now discolored, looked almost like a bruise. Within a few hours the pain had moved up my leg just below my knee, still on the inside of my leg, again discolored. To make a long story short I went to my doctors office and he said I had a blood clot in my leg. He told me to keep my leg elevated and apply heat that it should be okay. I haven't had any bad cases like this again but I do occasionally get a similar pain in my leg but the pain seems to subide after a day or so. Ladies, if you experience similar pains and/or discoloring on the back of your leg(s) make sure you see your Dr. This can be deep vein thrombosis which are dangerous blood clots, they can cause pulmonary embolism's- blood clots in the lungs.

In addition I've had many other side effects including: little to no sex drive, severe dryness down below (kind of causes problems in the bedroom...), slight vision problems (I usually have near perfect vision, now I often feel like my vision is blurry), odd colored periods (brownish colored), sticky mucusy periods, a very sharp yet dull and uncomfortable pain in my right breast (at least once a month), frequent Urinary Tract Infections, mood swings (had a bad one this morning, threw a fit because my hair took forever to dry- so trivial, right?), severe melasma (hyperpigmentation) on my upper forehead and the top of both cheekbones, and last but certainly not least very low energy.

I actually have a follow-up appt this afternoon with my Dr. I am going to ask him about other options for birth control. Thank you to all of you for writing about your symptoms! Your comments have really helped! Good luck to all of you!

I am so glad I found this forum. I thought I was going nuts for the past few months I was on Mirena. I'm 31 years old and healthy. My daughter is 19 months old and I had Mirena put in back in Dec of 2008. Since I was BFing, I did not get a period until June. Since June, I've had cramping basically everyday, a few days a month I feel nauseous (which I've never had, even when I was pregnant), I'm hungry all the time, I'm exhausted all the time (even though my daughter sleeps through the night and I sleep 9-10 hours a night). My husband calls me lazy, but I swear it's the Mirena. I had more energy when my daughter woke me up all the time. I'm annoyed I'm not loosing any more weight since I force myself to go to the gym, but sometimes I feel like crap that it's hard to get a good workout. I also have zero sex drive. I called my doctors office about the cramping as a side effect 2 weeks ago, and the nurse said she never heard about it and would have the doctor call me. Of course, the doctor did not call me, so I just made an apt to get it out. The earliest apt I could get is in 11 days. I hope I last that long! I tried to pull it out myself but I can't feel the strings. I know remember my doctor saying she cut the strings. I was trying to just deal with the side effects since I love the effectiveness of the BC (I'm really fertile), but will take my chances with a pregnancy and use that as motivation for my husband to get snipped. To the rest of you out there, trust your instincts and if you notice something majorly wrong, don't let the doctors dismiss you.

****KENALOG CLASS ACTION LAWSUIT****
Need a list of people that want to join Kenalog class action lawsuit A.S.A.P Please email me with name,state and all side effects. Include if you were treated for the side effects from a Doctor and/or hospitalized.
******

I just had scar revision done with my own body fat to correct an injection site necrosis from kenalog. The cosmetic surgeon advised that it sometimes takes more than one graft. This procedure is expensive and a lot to go through, but the only other choice seems to be to wait two years to see if it goes away. I had the injection in October and it only seemed to be worsening. Does anyone know of an attorney wanting to take these cases? My next step is to picket the doctors office, since he has not agreed to pay for my surgical reconstruction. I'm in the panhandle of Florida if anyone would like to join in the fun.

My husband stumbled across this website and first I would like to thank everyone who have posted their experiences on the NuvaRing. Because of you guys I now know I'm not losing my mind.

I started the NuvaRing March of 2008 and I started getting dizzy spells May 2009. I actually got my first dizzy spell when I was driving. Everything started to spin very fast!! My husband had to grab the wheel and tell me how to slow down and how fast to do it. That was the scariest thing ever!! My head felt a numbing sensation in my head. I had a pain above my left eye and it would shoot up my head and down my neck. The dizzy spells would come whenever, once every 8 days to twice in one day. I have had an MRI and an MRA done and nothing. The docs have had me on so many migraine meds to try to get a handle on this and nothing has helped. My longest migraine lasted for 14 days, that was in May. This month (July) I got a migraine on the 13th, took the ring out on the 21st, and had a dizzy spell this morning but this afternoon and especially this evening I feel amazing.

Since getting on the NuvaRing, like so many of you, my sex drive does not exist. It has caused so many fights between my husband and I. Its hard to tell him that he is still attractive but I can't explain why I'm not excited. So thank you for writing your experiences. He got to read that I'm not the only one and I wasn't making it up.

These last three months have been hell for my family and I. I have been like Dr. Jekyll and Mr. Hyde. So much tension has caused everyone to walk on pins and needles when they are around me.

So lets sum it up here, after being on the NuvaRing for 14 months I started getting dizzy spells, migraines, nausea, neck pain, twice I've puked because of the room spinning so damn fast, and very very VERY low sex drive.

I'M NOT CRAZY!!!! :)

Got Mirena put in 2 months ago. Side effects: hair loss, slight weight gain, bloated stomach (can't even suck it in anymore), 2+ week periods, spotting, tired all the time, foggy headed (Like I need a cup of coffee)...

I'm 39 years old and have 2 kids (youngest is age 2). I don't like BCP's and was sick of condoms so I thought I'd try Mirena. Especially since my periods were starting to get heavier (guess it's my age). The insertion was extremely painful. I yelled out in the doctors office. I turned pale and got sweaty and lightheaded. That I didn't expect. I was okay the next day. I soon noticed that A LOT of hair would shed out when I washed my hair, brushed , etc. Not a normal amount at all. It's been 2 months now and my pony tail doesn't even feel the same. I've lost a lot. It's everywhere. Have to put it up when I cook. Thinking of calling my doctor this week to get it removed. I haven't had sex anyway since it was inserted b/c of the LONG periods anyway. It's just gross and stinky. Plus I'm so bloated. My pants fit differently. I've only gained about 3 lbs. I really wanted Mirena to work too. I think about the side effects too often and it's affecting the quality of my life. I'm in tune w/my body and this is the only change in my life so I know it's a real side effect. When I mentioned this to my doctor she said she had only really heard of women complaining about the bleeding pattern and moodiness. She had never heard of the hair loss but now that I read this site, I see it's quite common. It's listed as a side effect too on the medical websites. Good luck ladies. I'm making the call this week.

I had the mirena inserted Dec. 4. 2008. I't worked really well the first couple months i thought i really liked it. until a couple of weeks ago i started getting really dizzy i thought i would pass out. I also got really tingly in my feet and my arms the most. and i have gained a lil weight that i just can't seem 2 lose no matter what i do. i thought something was really wrong with me until i googled dizziness with mirena. just 2 see if that would have anything 2 do with my symptoms. and yes apparently it does. i called every doctors office in town and nobody believed me that it was the mirena doing this 2 me so they wouldn't remove it. so i'm having my sister in law remove it 4 me today since she's a nurse. i can't wait. HOW LONG DOES IT TAKE 2 FEEL NORMAL AGAIN??????

I'm 15 years old and i've been taking prednisone for a few months, and from what i've read i'm on a really high dose. i was diagnosed with rheumatoid arthritis and another autoimmune disorder concerning my muscles at the same time. my doctor told me prednisone was my only choice; it was either that or i would lose the ability to walk. he told me there'd be side effects, but i had no idea it'd turn out like this or i would have fought harder for another course of action. i started out on 30mg twice a day, and since then was weaned down to 20mg twice a day and now i'm down to 30mg once a day. i've been looking up a bunch of information trying to figure out if there's a way to lessen the side effects or any hope at all that they will get better. apparently there isn't much. after reading a bunch of these stories i gotta say i'm not feeling great about this. i totally understand everything everyone is going through. i'm sure you can imagine what it's like being smack in the middle of high school with a huge puffy face, acne so bad on my face, chest, back, neck, and shoulders that wearing a bra could put me in tears, and mood swings so bad i've lost friends over it. everyone knows how brutal high school can be, where appearance and attitude are everything. and i try to tell my doctor about it and he literally looks at me like i'm a whiny teenager and says "you're just going to have to deal with it." and people like my mom and my closest friends don't get it either. nobody understands how beyond frustrating it is. i'll get into the worst moods and not have a reason for it, but i'll stay angry for hours or burst into tears over someone looking at me the wrong way. it'll get to the point where i have to isolate myself from other people because the abrubt mood changes get so bad. as bad as i hate to admit it, the pain from the arthritis is gone now and supposedly my muscles are doing better too. developing arthritis caused me to have to quit cheerleading, something i've loved doing for 6 years, because the pain got to the point where i couldn't get my arms above my head or bend my knees. however, i'd almost rather deal with the horrible joint pain than deal with the side effects of prednisone. if your doctor gives you and alternative method, take it. i've always been confident in the way i look and really outgoing and happy and now i sometimes catch myself thinking about suicide. that's shocking to me because i've got so much going for me, but this medicine makes me miserable. and when i complain about it, anyone i'm talking to just looks at me like i'm being a cry baby. my mom does too, she'll say things like "you just have to do this. i know it's not what you want but to be honest i'm sick of hearing you bitch about it."
i feel a little better knowing other people feel the same way - like nobody gets whats going on with them. the prednisone does give me days of really great euphoria and days when i feel like i could run a marathon, but waking up in the morning to the acne and huge face puts me to tears every day. i have to pee all the time, usually getting up at 2 or 3 am. i don't sleep well anymore and i do sweat all the time. which also sucks being a teenage girl. i'm always hungry, and when i eat i never feel full so i don't know when to stop. my neck and face have put on so much weight that when people see me in the halls or out and about they ask me what happened. mind you these are people i don't talk to, just ones i know from classes or whatever. and it's pretty bad when teenage boys i've never really talked to ask what happened to your face. kind of a blow to the ego, or whatever is left of it at this point.
i'd like to know if, as my dosage gets lowered, the side effects will diminish and when i'm off the prednisone completely if they will disappear altogether. any help there?
or if there is any way to help the acne or puffy face

my doctor just put me on something called methotrexate or something like that to help wean me off the prednisone, and does anyone know what those side effects will do? or if they'll affect the prednisone side effects?
i'm constantly obsessing over gaining weight and what my skin looks like and what i eat and how heavy my face feels and the occasional pressure in my eyes to the point where i just want to be put out of my misery.
and after reading other people's stories i really don't understand why this drug is still given out as freely as it is. but maybe all doctors are like mine, they just don't get it.
best of luck to anyone who's on prednisone, my heart goes out to you; i'm right there with you
sorry this became like a book it wasn't meant to be this long

June 11, 2009
Just for all of you out there...I had the MIRENA put in May of 2008.I was anemic and had it inserted to help with menstrual bleeding. I am through having babies, so i didn't need it for birth control. My husband has had a vasectomy. I am having it surgically removed tomorrow because of an unsuccessful attempt at my doctors office on Wednesday. It is going to cost me $5000.00 to have it removed!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! $5000.00!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! I have had terrible side effects that my doctors profusely denies could have anything to do with the MIRENA. Funny how I didn't have them before the MIRENA! Think twice before you have this put in! I can't imagine if i had waited 5 years to have it removed!!!!
K.

Hi I'm 36, with high blood pressure. I have been on 25mg/day hydrochlorothiazide since July 08. I went in for normal 3month check up and Dr tells me that my bottom number is to high, so she gives me yet another pill to take(yep you guessed it) Lisinopril. I filled the RX in the morning, by lunch time, I felt sick to my stomach, dizzy, everything hurt. I thought I had gotten the flu. This was just 2 days before my daughter and my mothers birthday.(both the same day) We had big plans after all you only turn 18 once. I put a smile on and went to the party, but it was living hell. My Fiance' noticed that I didn't start feeling bad until after I had taken that new pill. I only took 1 a day for 3 days and it took me over a month to feel half way normal again.

I had a kidney removed at the age of 19. I recently had a UTI and was prescribed sulfameth/trimeth ds for it. With in an hour after taking the first pill my hands turned bright red and were uncontrollably itching and then the rest of my body started to itch, with in about 2 hours it felt like i had been beaten up my entire abdomen hurt (movement like coughing and breathing hurt the most) By the end of the day when it was time for my second dose i was beginning to get really concerned, but i took the second pill thinking i needed to protect the only kidney i have left. The next day i wasn't able to go to work i was in so much pain in the abdominal area. I also feel light headed and short of breath. I DID NOT receive a drug facts paper with the side effects like u would with any other drug ive ever gotten and im starting to wonder why. So I called the doctors office that prescribed it to me to see if it was an allergic reaction or side effect and it took them 2 days to call me in a new prescription! Heres hoping it didn't harm the kidney i have.

I had my Mirena put in on April 7th 2009, so about 3.5 weeks ago. Immediately I regretted my decision, the intense pain and cramping at insertion was not what I was expecting or bargained for. I had to sit in the doctors office for 45 minutes till I could gain my composure back and I have a high tolerance of pain. That night I could not sleep, I got 3 hrs sleep for the first two nights, only 6 on night 3 and it hasn't gotten any better since. Hot flashes, headaches, back pain, moodiness with my children and the constant bleeding since insertion combined with the insomnia is enough to make me have this thing removed. I called my doctor after another night of 3 hrs sleep last night and I am getting it removed at 1:30 today! I can not wait, especially after reading all of the stories on here I know this is the right decision for me. My greatest concern is now what? Will my insurance pay for me to have tubal ligation now after having paid for this only 3 weeks ago? That is the chance I will have to take. A mother of 3 little ones needs her sleep for her sanity!

Okay, I had Mirena put in by my doctor a little over a month ago. I had my first period as scheduled, but I bled for 2 weeks. I have been spotting ever since. This is getting on my nerves. My question to everyone else is this: has anyone noticed a metal or copper smell with their discharge? I seem to be having more discharge than usual, and it has a coppery smell. It doesn't matter how many times I take a shower, it's still there. I am currently waiting on a call back from my doctors office. This is frustrating me more than anything. It is making me smell like I'm dirty. UGHHH. I'm leaning more and more towards getting myself permanently fixed because nothing else is working for me. Someone please help me. I can't help but think that I'm not the only one having this issue.

Thanks

Well I wrote yesterday and told my story about the Mirena I called my doctors office this morning and made an apt to have it taken out they asked me what kind of insurance I have and I told them medicaid they told me since I had that she would have to ask the doctor that put it in because if you have medicaid they like for you to keep it in for a few years to get your money worth. I asked even with me with me having all these symptoms she said yea when I told her I have been bleeding for a week and a half now she said your probably just having a miscarriage (like it was nothing) I was so pissed off. So she called me back after she talked to my doctor and told me she wanted to see me for a physical in the morn I asked if she can take it out tomorrow and she said it depends so we will see.. im going to tell her if she don't want to take it out I will (don't really want to do that) I'll post again tomorrow after my apt.

I had the most horrible experience with this medication. Part of it was due to my doctors poor care. On Monday I started at a new doctors office which is rather large. I gave him him my history with migraines and told him I was finally ready to start some sort of treatment. My previous doctor in the town had often recommended that I take something but I didn't want to take a daily medication. I am a fairly healthy 21 year old who gets between 5 to 10 migraines a month and many more headaches a month. I told him that my doctor and I had always concluded that my migraines were stress related. I told him that I have been experiencing a high degree of anxiety (I am a junior in college and it's the last week of class before exams.) He recommended Topamax and told me that it was an anti-seizure medication that was often used to treat migraines. He warned me that if I had any trouble with speech to let him know immediately but other than that he hasn't seen any other problems. He prescribed me 50mg twice a day,which he did not titrate as he should have. I took the first dose before bed Monday night and woke up so dizzy Tuesday morning I missed my first class. The dizziness passed and I just thought it was an adjustment period so I took my morning dose. I began to feel some tingling in my hands and feet and my reflexes were slowed (I felt like a drunk driver) I am a manager at a retail store and I forgot to do some of my most basic tasks. I took my evening dose and was described by fiancee as zombie. On Wednesday I woke up very emotional and cried a lot but didn't really think much of it. I took that mornings dose. By midday my anxiety and depression was so high I became suicidal. I had a panic attack while driving, i stopped off at my place of work because i couldn't drive anymore and my manager informed me that I was having a panic attack. I had never had one before. I have not been taking this medication for 48 hours but it has not left my system yet. I sought out counseling and am no longer depressed but I still have a great deal of anxiety and have been on the verge of two panic attacks today. I can write today, which I could not do yesterday. I do not recommend this medication to anything. Especially after what it did to me in just 3 days.

I am a 24 year old female. I got diagnosed with walking pneumonia after having a chest X ray at my doctors office. The doctor prescribed z-pak. I went home and took the first 2 pills and about 2-3 hours after taking it I suddenly experienced uncontrolled rapid heart rate. My heart was pounding so hard i almost fainted. I work in the medical field, and knew immediately that I was in trouble. My husband drove me to the ER, where I was admitted with a heart rate of 186 beats per minute, I honestly felt like i was going to faint, or die. Once they ran several tests and ruled out anything major IE blood clot, they determined I was having an extreme allergic reaction to the z-pak. They gave me IV benadryl and steroids, which immediately started to bring my heart rate down. I do not take any medications ever, other than supplements, this is the first time in 9 years that I have had to take an antibiotic, and this was the only prescription I was taking that day.

Ok, so here is a new one for you. I have had migraines for a very long time, since I was a teenager, and never really sought physician treatment because in our family a headache was "nothing to cry about". So, now that I am married with 4 kids and an advancing career, having migraines on a weekly basis isn't something I can live with anymore. So I went to my doctor. He said what about preventing them with Topamax. I know what Topamax is, I'm a nurse, I know what the potentials are, but I had not really heard of the side effects when using it in a perfectly healthy person. ANd I must say it has to be my own fault for saying "sure" and not investigating first. WARNING= Topamax is a drug for seizures, effecting the central nervous system, and will have effects on a healthy person's central nervous system. Now, not doing my research I will also not have known that you are supposed to be titrated very slowly up with increasing doses, starting at a suggested dose of 15-25 mg per day for the first week the 50 then to 100, etc. I was begun at 50 mg/day for a week then 100 mg a day thereon out. Please, if you experience the symptoms the pharmacy warns you about, but they are exaggerated, go back to your doctor!! Here are my symptoms by day
Days1-3- Normal effect- tingling hands/feet, taste loss of some drinks, foggy unable to think clearly
Day4-5- horrible head pain, back of my head, not like my migraine pain, stabbing and pins/needles in hands/feet, still can't taste, nausea, dizziness, confused (like I couldn't find my way to my doctor's office confused)
Day 6- And I am entirely embarrassed to say this one because I am a nurse, and I know what it implicates... Pseuedoseizure. I was in the doctors office, in the waiting room and I could not control my muscles. I knew it wasn't a seizure because I could hear some of what was going on around me, but something was not right. I couldn't move anything and I didn't remember everything. And all the above symptoms, along with. But, naturally normal CT...
Day 7- It happens again... And this time I have some right sided weakness and all the above, that's it, it has to be the Topamax, we are done. It's only been a week, so cold turkey.

That is my experience with Topamax, and unless I am actually seizing, it is a journey I will never take again, I have 4 little ones that depend on me too much. PLEASE research before you try whatever is handed to you!!

Abilify was recently added to my medication of Depakote 250 x3 (i have been on this for 10 yrs), Zoloft 40 mgs (8 years), and Buspar 40 mgs (8 years). I started taking Abilify last Tuesday the 17th of March. The first night I took it I had trouble sleeping..(but i also had some caffeine that night)...for the next few nights I still had trouble sleeping...I also noticed an increase in my pulse, rapid heartbeat...and my blood pressure! This past Saturday, my blood pressure was 141/91 which was my left arm, then my right arm was 138/90. My resting pulse was 90+ with my heart pounding. I went into work today (i work in a doctors office) and had a nurse take my BP and it was 153/95...now my BP is normally 120/60...the lowest its ever been is 90/70. So to have my BP this high is very strange. I called my doctor and she advised me to stop it ASAP and to call her if i have any more problems. I already have a scheduled appointment on 04/01/09.

March 3, 2009
I returned to the doctor today to get a different antibiotic because Avelox made me worse off than the sinus infection I had. I stopped taking it about two weeks ago and still have side effects from the drug. My doctor had given it to me about two other times. The last time I recall was in November. I didn't finish taking my prescription then either.
I thought maybe I was having flu symptoms also, but it was the drug making me more ill. RASH, HIVES, RED HANDS, SWOLLEN TONGUE THRUSH, BUMPS ON MY TONGUE, TINGLING IN MY BACK, VOMITING,HEADACHES, PAIN IN MY STOMACH NOT LONG AFTER TAKING A DOSAGE. FREEZING HANDS, THROAT FEELS LIKE IT'S CLOSING UP AND DIFFICULTY SWALLOWING, COULDN'T GET OUT OF BED, MUSCLE FATIGUE, ACHES WEAKNESS, JOINTS HURT, TINGLING IN HANDS, ANXIETY,CRYING SPELLS, NIGHTMARES, SKIN SENSITIVITY, INSOMNIA, THEN EXTREME FATIGUE, DIZZINESS AND LIGHT HEADED UPON STANDING AND/OR GETTING UP FROM A SITTING OR SQUATING POSITION. EVERYTHING HURTS ALL THE TIME IN EVERY MUSCLE...... I BASICALLY FEEL LIKE I AM DYING.
My fiance thought I was totally losing my mind. I was moody, aggressive, irritable, depressed etc... I felt like like a different person.. My fiance of course got sick also and his doctor prescribed it to him. His side effects included muscle aches and pains and extreme fatigue and mood swings. I looked up some side effects when I was started taking it a few weeks ago, but didn't pursue the research until the side effects got worse. I took it for 7 days this time. My fiance took it for three days. I called him at work after seeing this website and told him to stop taking the medication immediately. I am still sick with a sinus infection, and a whole slew of other crap going on. I called the doctors office and went in right away to get a different medication. To no avail, when I went to my doctors office there was a rep from Avelox there. I said don't give that Avelox to anyone sarcastically. I then saw his tag on his shirt and his bag full of Avelox samples. He asked what type of symptoms I had and I told him.. He said he would report it to the company.... What do you think they will do about it? MOST LIKELY NOTHING. I am an educated person with the capability and time to research anything I need to and I will do my best to dig up the most dirt I possibly can about this horrible medication. They need to stop pushing these meds on doctors to give us and make us more ill than we were to begin with. I JUST HOPE MY AILMENTS AREN'T PERMANENT. People try to make light of the situation because they don't want to be sued. I think the FDA needs to be revamped and the Government should stop letting these pharmaceutical companies poison us. I AM NOT EXAGGERATING EITHER! DO NOT TAKE IT.
I have been going to my doctor for about fifteen years and she never gave me any medication that had made me this ill. I get samples a lot because I have no insurance. Sometimes she gives me scripts. Today I got Zithromax which always worked well for me in the past. Very little side effects. I realize that everyone reacts differently to certain meds, but come on now! It isn't just a coincidence that all of us commenting and complaining here are imagining these horrible side effects! Today I got Zithromax which always worked well for me in the past. (Very little side effects).Then why did I ever have to take Avelox if there are other antibiotics that will make me better not worse. They push these meds on doctors to give to us that's why! I always trusted and admired my doctor. She always treats me well and does right by me. What is going on with these medical companies?! SOMETHING HAS TO BE DONE ABOUT THIS!