Memory problems symptoms and conditions

I'm 24 and just recently finished my lupron treatment for endo. I'm still having some of the side effects and have yet to start my period again. I honestly would've rather had surgery again for endo than go through months of the side effects. The memory problems, overall fogginess, night sweats, insomnia, mood swings, hot flashes, and just the stress and complete crappy quality of life I've had most of this year has completely affected all aspects of my life. It's not easy at work, at home with my husband- surgery took a day or so to recovery from and this has been a nightmare for months and months. I'd really think about it and research the benefits for you vs the side effects before doing it. If there are any other options- I'd absolutely consider them.

I have had several things but am not sure if they are due to the mirena but I have always been good tell I got mirena
here are the symptoms I have

severe bleeding 8 months straight
head aches
increased appetite
weight gain
dizziness
faint
depressed
really moody
mean
angry
tired extremely
cant sleep well
memory loss
memory problems
blurred vision
and recently extremely painful sex
it hurt so bad It was all I could do not to cry
it felt as though I was in labor
I did not have the heart to tell my husband i was in pain cause we rarely have sex due to the constant bleeding
it is the best birth control I have ever heard of cause you cant have sex if your bleeding all the time. I want to remove it but getting a hold of my doctor is like a joke and I don't know what to do cause I need my memory I have a family that needs me as i used to be not the mean upset all the time me.

I never really thought I was having a problem with Lisinopril which I have been taking regularly for 6 months. I am a 54 yr old female and going through menopause. I thought the memory problems and tiredness was due to this, never associated it with the drug. I really do not have a cough, just a kinda post nasal drip that causes me to clear my throat often and I am stuffy a lot. Now after reading these post, I wonder! I will stop for a while and see what happens. I do not think I have a blood pressure problem yet but the doc said since my mom did and mine fluctuates (most times in his office) and menopause, I should take it. Will keep posting

I have some memory problems, forgetfulness, and "foggie" feeling. My co-workers have noticed the change in me - these symptoms were gradual; also trouble with insomnia (always had some trouble sleeping, but it seemed to increase with the lovastatin; some shoulder pain, and more headaches too.

I have been through hell with this drug, well i'm sure it was this drug, I have had minor anxiety in the past, but the anxiety i had the day after taking this was off the scale, I couldn't sleep, eat, or function in my life at all. I started to become very depressed and go into despair. I even had suicidal thoughts which freaked me out and is not like me at all. I was even taken to A and E at hospital it was that bad. I finished on Sunday and seen a bit of improvement, I was not as anxious and irritable. Today it has came back a little, I seem to have some mental confusion and memory problems also. It has been a long dark road, and I entered some scary dark places that felt horrible. Im usually so upbeat and busy. It was so not like me. I took this medication for 11 days at 100mg twice a day. Like I said i finished on Sunday, I still feel very unreal (dreamworld) depressed at times, no appetite yet and struggling to relax.

How long will this take to pass? please help I feel im going crazy

itching of scalp, face.

I have been on this horrific drug for just over two years and have wanted to be off of it since the six month mark...i am not on it for depression but for focus...FOCUS, i cannot begin to describe the memory problems that i have...i can be standing in front of a person i have known for years and i will not be able to come up with their name or how i know them...luckily it does not seem to cause problems with my actual work but it is rather embarrassing when your boss walks up and you have to think hard to figure out who they are...side effects...i have gone from being a so called gorgeous man to a frumpy 30 lbs heavier man, and i still run five to ten miles a day and i eat less than i ever have...try to explain that...it is almost like i am swollen...i have horrible dreams, i sweat, i panic, i shake and i have a constant feeling of having a heart attack...try and live thinking you are having a heart attack when you are not but then again do you really know...in other words what if i have been desensitized to thinking i am actually having a heart attack when i actually am, may i rest in peace if that is the case...

when i have actually tried to come off the pills i have been violent (i never have been before in life), irrational, can't sleep, double vision, electrical shocks just by moving my eyes, can't move and bruise to the point that i look like a junkie who has injected himself everywhere...

my doctor never warned me of any of this, nor can i find it on the wyeth website (with the exception of the memory issues, which was not there when i started taking the drug...

i am so very sad over all of this...don't become like me

I took lupron for about a year or so back in 1999. I don't remember a lot, just the hot flashes, etc, that I was warned about. I began to have memory problems a little. As the years passed by, it became worse. It is 10 years later and I have no short term memory. I have searched and searched to figure out what is wrong with me. My memory is gone. Its a sad thing, that this shot is still being given.

I am 22 years old and I have never had any children. I do not understand what made the doctor think that this horrible device would fit in my uterus. When I had the Simply Mirena inserted in March 2008, I almost passed out, (since he inserted it wrong once, he had to pull it out right after and do it again). I think of myself as a pretty strong person, but I literally cried out, and I almost fainted while paying my co-pay at the receptionist's desk. My husband had to come pick me up from the doctor's office because I couldn't even walk to my car, but I wish that was the worst of it.

Within one month, I started feeling VERY depressed so my doctor put me on Effexor XR (which started a whole bunch of other problems), but now that I have been off of the Efffexor for a while and I am noticing problems that I had been blaming on the Effexor.

Here are some of my symptoms...

- Weight Gain
- Feeling tired, weak, and depressed.
(To the point that I will sleep for 18 hours if givin the opportunity.)
- Chronicly Dry skin
- Constipation and Diarrhea
(I haven't had a normal BM since I had it inserted.)
- Memory problems
- Cannot concentrate
- ABSOLUTELY NO SEX DRIVE!
(And when I do have it, It hurts for days afterwards.)
- Lower back pain
- Stabbing pains in the uterus
- No menstrual cycle
(I would spot for the first few months, but now it is completely gone.)
- Massive mood swings
- Nausea

Well of course my doctor thought for sure that this was my thyroid, so (without medical insurance), I went and got all my blood work done thinking that I would finally have an answer to my health issues... NOPE!
I received the results today and found out that my thyroid was perfectly fine, no anemia, good blood counts... Nothing.
Now not to say that I am not happy that my thyroid is okay, but I just wanted an explanation for all of this. SO my doctor sends me to see my NEW Ob-Gyn, to have this "Thing" aka Simply Mirena, taken out of my body. After reading all of the problems that the other women have been having, I am CERTAIN that this is the cause of all of these problems.

I would like to thank all of you for opening my eyes to something that was so obvious. I have an appointment to have mine removed next Friday (I'm not as brave as some of you ladies to take it out myself). I will keep you all posted on my progress.

I have been taking Wellbutrin 150 generic bupropion 2x daily for one month. I have been experiencing very noticeable and disconcerting hair loss (a la 'male pattern baldness'). RAPID. I took the shears to my head because I was going crazy at the amount of hair I was losing (that seems to have slowed the process!)

Also, extreme memory loss. I forget the names of friends and family; sometimes myself. I will call people the wrong name by accident. More than a few times, I've stopped mid-sentence in conversation, forgetting what I was talking about. Almost like I've been put on 'pause' for 15 seconds. The crappy thing is that I'm sure that the person can see that I'm struggling.

I am very scared to drive: 35 mph seems like I'm playing a drugged up video death game. There have been episodes where I feel like I've been sleep-driving. Sort of like an out of body experience. Which freaks me out because I manage to make myself aware of the danger in the situation but the body/brain connection seems impaired.

I am/was an avid reader (3-4 books per month) but I have completely lost interest and the couple times that I have tried, I couldn't read half a page before quitting. I read the same sentence over and over without making any connection. The same with my writing. It has become a chore.

Also, extreme impatience at the smallest things which before I would have not been bothered by. Sometimes even seething anger, which is very out of character. Since I've been on Wellbutrin, I can no longer tolerate the "cuteness of children" antics and such. There are no 'minor' annoyances anymore.

I told the doctor of the symptoms I was having, not attributing them to the Wellbutrin (which I now call 'Zombie') and I was completely dismissed. The hair loss and memory problems he attributed to stress, and he wanted to up the dosage to 300mg and prescribe Xanax (which I call 'Mind Eraser' from previous juvenile dalliances).

I don't like ANY medications...Which reminds me...I forgot why I'm even taking it...the doctor suggested I should take it after telling him I felt like crap after a bout of Lyme Disease. I laugh at the completely unnecessary BS I've put myself through for a month!!!

I feel like I have little choice other than to wean myself off. I will most certainly NOT keep my 3.5 GPA this next semester if I continue taking this drug. I am glad I found this site, because the doctor looked at me like I was crazy when describing the symptoms. Now I know what to blame/quit.

***ON A VERY IMPORTANT NOTE, I WAS ABLE TO QUIT A PACK A DAY CIGARETTE HABIT AFTER TWO WEEKS!!! After 10+ YEARS of trying patches, gums, lozenges, and even chewing tobacco (ick) I've been able to go two weeks without smoking. Wellbutrin has made me FORGET about the habit.

I am taking the generic Bupropion at 300mg per day. I went up in dosage to 300 last month, I'm about 1 week in to my 2nd refill on the 300mg. I am having TERRIBLE side affects right now. At this moment I'm at work trying to concentrate on even saying the right words on the phone - I have no sick time left so I can't go home - my hearing is jacked up. Things fade out and then come back so loud. I feel as if I'm drifting off to sleep and things get quiet and then WHAM someone will say something to me and it's so loud like someone woke me up from a nap. My vision is a little blurry, and I can't remember things. Fortunately I can get away with this for another day at my job, I started feeling like this yesterday, just today started thinking it was my med. I'm not on any other meds. I'm dizzy too. The worst part is I can't remember conversations. At the time of, I know what I'm saying though slower, but if I'm having a lengthy conversation I will probably forget what you said at the beginning. The confusion is what makes me the most upset. Things that I know, little things like someones phone extension, I can't remember and have to look up. The weird thing is all these symptoms come in waves. I'll have a moment of 'normalness' and then right back into the symptoms. I'm even having trouble typing right now. - I'm not hungry and after reading this site I now know why I'm itching all over.

I got on this website looking for a 'quick fix' like eating a big meal, but see I'm going to have to rough it out another day here in la la land. Wellbutrin was working for me in the beginning, 150 mg for 2 months, increased energy, good attitude etc, then wore off a little so we uped it to 300mg. I'm going to go dwn in dosage, try taking the 150mg tomorrow and see how I feel. I hope this wears off!! I am curious to know if you can cut the dosage of 300mg pill Buproprion to 150 by cutting it in half? I just got that refill so I was wondering. Today is going to be so rough! I went straight to bed yesterday after work and guess I will be doing the same tonight. Oh great, my coworker just asked if I was "ok" because I'm being so quiet. Yikes. I've read this email about 5 times to make sure I don't repeat myself since I can't remember!

I am 62, have been on one or another anti depressant for 20 years,was on prozac for about last 3 years It seemed not to be doing the job,therapist started me on wellbutrin, the generic Bupropion,sex life was better,BUT I would rather have hair on my head than having orgasm. been taking 200 mg about 2 weeks,hands full of hair after washing my hair.I have noticed SOME memory problems,thought it was my age,ALWAYS have had a good memory, going off slowly,100 mg a day for 7 days then nothing,I also take anxiety meds,going to see if that may be all I need .If not back to the prozac

Wow, thank you all for your postings. I just wished I had found this before I had Mirena put in. I had it placed in Feb 2009, it's been exactly 5 months. I have been extremely tired and agitated. I didn't really associate this with the Mirena until reading the other posts. My hair comes out by the handful (with root attached), I never have solid stools, I have gained about 10 pounds even though I have been trying to lose weight through a diet and exercise program. All the weight is in my stomach and people keep asking me if I'm pregnant. I started to wonder if I could be seeing as I was crying all the time, extremely moody, and that I look at least 4 or 5 months pregnant. All pregnancy tests have come back negative. I got this put in the day before my fiance and I got engaged ( not knowing at the time) and last week we were about to call of the wedding because of my emotional state and constant conflicts. I have to wonder how much of this is caused by the Mirena. I have already made an appointment to talk to my doctor after reading what all these other women have been through. It's just so tough because with any type of birth control their are side effects so I don't want to make it out to be like this is the worst thing ever, it may be exactly what someone is looking for, but just be informed that there are some side effects because I like a lot of other women on this post was lead to believe that there were no side effects or very little side effects.

I have been on Lipitor for almost 5 years. I started with a low dose of 10mg for 3 years but my cholesterol did not come down significantly enough so the dose was increased to 20mgs two years ago. I have noticed my hair thinning almost immediately after being put on Lipitor but when the dose was increased the hair started falling out where now it is noticeable, at the front along the hairline, on top and at temples. It has become another problem, at this point, like having high cholesterol. It seems to be happening now at an accelerated rate and my scalp is visible from my hairline 3 inches back. Styling is now impossible without coming the hair all the way forward from the crown, what's left of it. I had no idea hair loss was a symptom of Lipitor until I thought about when it started and the fact I take no other medications. There is no history of this type of hair loss in my family. The Lipitor brought my cholesterol level down to preferred levels but if I stay on it much longer I will be bald on the top and sides of my head. I'm worried it won't grow back.

I was placed on Topamax, off label, for suspected bipolar illness (now disproven). My cognition, word finding abilities, memory has been so adversely affected that I am now on disability. I had 5 kidney stones due to the development of Renal Tubular Acidosis, nearing renal failure (a side effect doctors don't warn patients about). This in turn led to osteomalacia, softening of the bones, only discovered after I broke all three major bones in my leg and snapped off my foot stepping off the lowest seat of a bleecher. I've suffered tingling in arms, hands, legs & feet (nerve damage), lesions in the brain, muscle spasms, heat & cold intolerance, insomnia etc... Although I lost weight, I gained it back (then some) as soon as I reduced the dosage of 800 mgs. Upon stopping the drug to save my kidneys, thus my life, my kidney function returned to almost normal within a few months, although there is residual damage. All other side affects remain two years later. Losing weight is not worth dying! Beware of this drug being used off label! I would never trust this drug!

I have pretty serious memory problems, and I notice the problems at work. Maybe the stress of work makes it worse at work than at home. But my boss and i talked the other day, and I said I felt scattered - she said I come across as very scattered, forgetting stuff, not following through, etc. I said I would write things down more to help me remember, and she said maybe I might try a different drug (she knows about my bipolar - I told her, and I use a service dog to help with anxiety and tardive dyskinesia from another psych drug). When your boss tells you to maybe try a different drug, it's a bit scary - am I going to lose my job?! But when I forget to take the Lamictal even one day (I take 200 mg. in the morning) I can feel the difference within 24 hours - agitated, depressed, irritable, impatient, etc.). So I have to be careful to take it every day. Along with my other meds...
I don't want to go off the drug, but the memory and cognitive crap is really hard. It's nice to hear I'm not alone.

I am 72 years old and in 1995 I had an artery blockage and had angioplasty.Upon my release from the hospital I was put on several prescriptions, beta blockers, cholesterol, Aspirin, Vitamins, etc. which I had been taking regularly for 13 years without any problems. In 2008 after having chest pain and going to the hospital my heart doctor advised me I had Atrial Defibrillation and put me on Warfarin and also told me to stop taking all the vitamins I was using along with my daily aspirin dose and one of my prescriptions. Since then I have had constant shoulder and muscle pain in my arm and leg. I have had several treatments by a chiropractor and several physical therapy treatments and the pain has not subsided. My memory has gotten worse also however I thought that was due to my age until I read some of the above side effects of Warfarin. I definitely have a lack of energy and also changed my diet due to the Warfarin. I have informed my heart doctor about the problems and he advised it is not due to the Warfarin. I don't agree with him after reading all the posts, but I am not a doctor. I will continue my prescribed dosage and Pt/Inr tests as schedule for a while, but if my pain etc doesn't get better I will probably do like the lady's posting and stop the warfarin on my own.

I have been taking Yaz for six months now, and I'm stopping after I finish this pack. I've been on it this long because I thought at first the side effects caused by it were just the beginnings of aging for me (I'm 25), but the acceleration of my problems has been so noticeable that I can't be in denial any more! Basically, here's what I have:

-thinner hair that comes out more easily and doesn't grow back as fast (it would be nice if this were restricted to "unwanted" hair, but this actually includes my eyelashes, eyebrows and head hair, which have all gotten noticeably lighter and thinner)

-CELLULITE, which I never had before...not only on my thighs but on my bum and CALVES, I didn't even realize it was possible to get cellulite there!

-spider veins on my upper thighs, again, never had this before

-very decreased sex drive

-thinner skin with less elasticity

-memory problems

-much increased vaginal discharge

Now, it's not all losses...my boobs are bigger when I actively take the pills, and my skin has become less acne prone...but is all that other stuff really worth it??? I think not.

I took Ambien for 2 years. I had all of the common side effects: hallucinations, memory problems, loopiness, nightmares, etc. However, I eventually started smelling smoke all of the time. Since Ambien was the only drug I was on, I stopped taking it. After a couple of weeks, the smoke smell faded. Life went on as usual, and I became pregnant and gave birth to a beautiful boy. That night I couldn't fall asleep even though I was exhausted. I tossed and turned all night, and the nurse started showing concern for me. She asked if I wanted to try a sleeping pill, and contacted my doctor. They ended up giving me an Ambien that night, and that night, the smoke smell returned for a few days. Fast forward several months after giving up Ambien completely. I developed a nasty head cold that gave my sinuses a pounding. That was when the smell returned. I began to piece things together, and went to the doctor. I asked him if he thought the Ambien damaged my sense of smell and if sinus conditions like congestion, allergies, and sickness exacerbated the problem. He did first check me for a brain tumor, but agreed with my assessment. He has seen thing like this happen to people, although not specifically with Ambien since it was a newer drug. He thinks a combination of the drug and sinus problems permanently damaged my olfactory nerves. He told me to try Flonase, and within a week of smelling smoke, it goes away. seven years later, the smoke smell still comes and goes, but actually cues me to what is going on in my sinuses at the time. I know when my sinuses are congested or irritated, and I take Flonase for relief within a few days to a week. Not saying everyone will have this problem, but it is something to be aware of...

I started on the 27th of April and by the 29th I had burning in my back and severe pain. I then got chest pain and tingly in my arm. Over the next few days, I got anexity, the depression, confusion, poor judgment, depth perception problems, muscle spasms and almost wrecked my car.

I had memory problems, irritable, uneasiness feeling, etc.

I then had problem with my hip and I am only 35!!! I can't pick up my baby without feeling faint.

Today my eyes started yellowing.

I reported all this to the FDA MEDWATCH and to BAYER the makers of it. Maybe if everyone did this, they would see there is more of a need to help others. PLEASE do the same. A quick internet search would help you find what your looking for.

I received yet another email from someone who has had a recent MRI due to memory difficulties and the MRI indicated brain shrinkage. This drug is breaking the blood brain barrier, causes depression, and is shrinking the brain. I know of 3 people who began Lisinopril and over a period of less than 2 years, have had MRI and their brains indicate shrinkage. We are wondering why Alzheimers is becoming an epidemic. More people are being prescribed Blood Pressure medicines at earlier ages, particularly Ace Inhibitors because they are cheap and these drugs are pentrating the blood brain barrier and causing a drug induced brain damage that mimicks Alzheimer symptoms. It begins to appear as depression, so, they treat the depression with anti-depressants. They improve for a period of time and then the symptoms of memory loss, difficulty retaining, concentration issues, mental sluggishness begin to present again. The Doctors are in denial, not us who are posting these symptoms. The obvious is oblivious. You cannot take a healthy individual who never took anything more than an aspirin and within 17 month of taking this medication have depression, memory issues and brain shrinkage. I hope if there are any Doctors that read this site, they pay attention to their patients and watch those people on Ace Inhibitors who then follow a pattern of memory problems and depression. It's much more than depression. I bet if all those people who experience memory difficulties got and MRI, there brains would show shrinkage.

50 y.o. female suffering from severe depression (or so I thought) since mid-teens. Finally sought professional help 8 mos. ago - diagnosed w/ bipolar disorder/depression/anxiety. Lamictal (now up to 300mg/day) has literally been a life-saver for me. I feel calm, rarely depressed, a bit more patient w/ myself and others, and the suicidal thoughts I've had for 30+ years are gone. I feel happy. The side effects, however, are disturbing. W/ the higher dose, I feel emotionally well but the memory problems are scaring me. When I write, I know which words I should use, but now I frequently omit or misspell words - not a problem before. I've always been a fast, accurate typist but I feel clumsy when typing and frequently hit the wrong keys. I misplace things and since I'm a bit OCD about losing paperwork, etc., it's happening. My job requires me to handle important financial docs. for people and I'm worried that I'll miss or lose something. Some days I can be very articulate w/ great use of vocabulary and other days I feel lucky to put a string of words together that will make sense. I'll lose a thought in mid-sentence. My doctor recommended that I take 1 mg of folic acid per day; it seems to help the memory issues and I may increase that amount. I grind my teeth at night so badly that I'm wearing a night guard to avoid ruining my molars. I find myself frequently rubbing parts of my hands together - especially when my hands aren't otherwise occupied. My dreams are vivid and I recall most of them, which is a pleasant side effect because I went many years without remembering my dreams (maybe due to alcohol abuse?). Another unpleasant side effect is clumsiness. I'll reach for something and miss it or jam my hand into a solid object, I drop things, I hurt myself more often - stubbing toes, smashing fingers, and cutting my hands more often in the kitchen. My doctor has put me on two different anxiety meds but the side effects were not acceptable so I stopped them. I'm considering lowering the Lamictal dosage to see if the memory issues improve; I can deal o.k. w/ the other side effects. I can't imagine not taking this drug, so I'll most likely endure the side effects for as long as possible.

I am in month 4 of a 4 month Lupron shot that my doctor gave to prepare for surgery. I was told I might get hot flashes, loss of libido, increased urinary symptoms for a few weeks. No one said anything and there was absolutely nothing in all the drug leaflets they gave me that would have prepared me for the the horror story that my life was about to become. As if having cancer was not bad enough.Since day 2 I have suffered so many bad side effects that I have lost count. The worst is insomnia and nothing has helped including high doses of Ambien. They suggested Lunesta but my health insurance company balked and even if they had said yes, my co-payment would be unaffordable. This stuff is more expensive than gold. I am exhausted all the time. I have terrible memory problems that are so bad that I can be talking to some I know really well and not remember their name. I am unable to concentrate on anything, my mood swings are unbelievable, I feel mentally disoriented and dissociated all the time, high blood pressure, racing pulse, high blood sugar, hot flashes, raging night sweats, dizziness, bad balance. The side effects that I can handle include nausea, headaches, diarrhea, joint and muscle pain. I am supposed to be on Lupron for 2 years. The only difference I see with my Lupron experience and others here is that my gender is MALE and I have early stage prostate cancer. Being male, my other serious Lupron side effect is complete impotence which is going to go on for a long while due to the radiation. I had radioactive seed implants into my prostate gland done a week ago and I have to follow this with 5 weeks of beam radiation. Lupron seems to be an equal opportunity drug. Lupron has messed me up so badly that for the past 5 weeks I have been off work on disability status with no chance of going back for at least a month and my Dr thinks that may be optimistic. No one seems to know how long it will take to get back to some kind of normal. I just could not function at work and ended up in my doctors office having a complete emotional meltdown. I would caution anyone, male or female, to consider Lupron very carefully before having it.

This site has helped me feel like I'm not alone. Thank you to all of the previous people who have written in about Coumadin. I am not the normal DVT/pulmonary embolism survivor. I just turned 37, am a runner, organic/healthy eating Mom of three kids. I had a PE, two weeks to the day of my plastic surgery (breast augmentation and liposcuplture). I am currently on 7.5 mg of Coumadin daily and my INR levels have been pretty consistent. I just stepped on the scale tonight after feeling "fat" and was shocked to see I've gained 12 pounds in almost 6 weeks since starting Coumadin. Yikes! I am hungry all of the time. I've also had memory problems and my hair is more coarse. I hope I don't have to be on this for too long. They say 6 months for me. Good luck to every one.

Have been taking topamax for 4 months and now have hand and feet tingling. major spelling and memory loss issues. My question is Does any one else have HIP PAIN??? I can't think of any reason why I have it now... except for the addition of the topamax.Thanks, TL