Sensations symptoms and conditions

I was prescribed levaquin also. I was given a 5 day supply. While taking this drug, I experienced severe diarrhea, major gas, and also had numbing sensations a few times in my hands....very strange drug...all the side effects did seem to go away a few days after I finished taking the medication.

OH MY GOSH! I thought I was crazy until I found this site. Ok, I had my Mirena inserted January of 2007, and IMMEDIATELY experienced joint pain, pain in my hands and feet, and it's 22 months later.. the pain NEVER went away. I thought because I was a very hardcore athlete when I was younger, that this was par for the course, that I will be getting arthritis. I'm 34 years old. Crazy to say arthritis at 34? I think so. Well, I have been researching my symptoms for months and months online and gone to a few different doctors over this. My symptoms include chronic fatigue, headaches (on a good week 4 days out of the week), joint pain in my hands and feet, sensations in my hands and feet that feel like they are swollen (but they aren't), upper and lower back pain, heart palpitations, leg cramps, hair loss, ABSOLUTELY NO SEX DRIVE AT ALL, muscle fatigue, and I've gained 40 lbs since I had it put in... OUCH. NONE of this (except for headaches and some depression) was experienced before the Mirena. Funny, I never linked it to the Mirena. I've had my thyroid checked, been diagnosed with carpal tunnel (lol what about my feet? Good doc!) had blood sugar checked (nope, not diabetes!), well, now I'm on to getting checked for fibromyalgia. Kinda wondering though, if there is a link to fibromyalgia and Mirena, like it could induce it? Sounds like so many of you have the same symptoms, and many have thought the same things... fibro, diabetes, lupus, ms, hell, I even though lyme disease at one point. This is ridiculous... I'm having it out this week.

Lisinopril causes burning and tingling sensations in your feet (peripheral neuropathy). The neurologist insists that the Lisinopril simply "unmasked" a hidden glucose problem. My primary physician does not understand what that means. I have stopped taking the drug. It has been over a year and the side effects remain. I tried 10 sessions of acupuncture which seemed to alleviate some of the pain & discomfort in my heels and middle of the feet. I have started a treatment of folic acid, B1 & B12. I also recommend diet & exercise. I was prescribed gapapentin by the neurologist; it alleviates the side effects but does "cure" it.

Hi, my name’s M. and I posted my story on here about a month ago. Unfortunately, I’ve made no progress. I was hospitalized again mid-October for numbness and tingling sensations in my legs, which is a symptom of guillian-barre syndrome and supposedly needs to be treated very carefully. I had an mri of my brain again, this time including my spine to check for possible tumors. I was sent home the next day, negative for guillian-barre, but having received no answers. I was crawling up the stairs by this time, and was too weak to walk without holding on to furniture to support myself. My legs felt like cement blocks, and the neurologist specifically said, “I don’t know why you can’t walk.”
Since then, I’ve developed acute mononucleosis, which increases my fatigue and muscle pain, and causes me to sleep about 15 hours a day. Recent blood work also showed I was positive for an autoimmune disorder called Myositis, which is a painful disorder that causes the body’s immune system to attack its muscles and connective tissue. I was referred to a rheumatologist, who was the least sympathetic person I’ve met in my life, and told me my physical exam was perfect, so she felt the Myositis must have been a false positive. She re-ran the blood work, and the Myositis was negative. This is of course a relief, but how we’ll ever know which test is correct, I don’t know. The rheumatologist did notice the weakness in my legs and my difficulty walking, and suggested physical therapy to help gain my strength back. She also prescribed an anti-inflammatory medication that took away almost all of my pain. Thank God, something finally worked for me. We then saw the physical therapist who said, “We can probably make you stronger, but I’ve never seen anything like this before.”
I’m seeing an osteopathic specialist who is convinced my illness is directly related to Gardasil. Through ancient medicine methods, she introduced a vile of Gardasil to my system and noticed an immediate weakness. I’m not sure if I totally believe in her practice, but the fact that she noticed a rejection to Gardasil the minute she introduced it is enough to convince me. She believes that my immune system was basically poisoned by the vaccine, which is causing it to fight off things I need. She also said it probably doesn’t recognize the mono as an infection, and decides not to fight it. For a normal, healthy person, mono can last up to 3 months. For someone like me, no one knows how long it could last. It was my immune system’s weakness that allowed me to develop mono, and it was the Gardasil that weakened it in the first place. So thank you Merck, for yet another thing I have to deal with.
And that brings us to today. I’ve missed about 30 days of my freshman year, so I’m assuming summer school will be necessary. My high school won’t provide a tutor, so I can only take my core curriculum classes, and am having difficulty keeping up with just those few. I’ve gained some strength in my legs, and it’s a little easier to walk with the anti-inflammatory, but I still can’t walk very far without resting. I’m also taking an anti-depressant to help me focus-hopefully it’ll lift my spirits. Since I received the vaccine, my periods have been painful and irregular. The constant nausea, headaches, and occasional stomach pain/joint pain continues, along with extreme fatigue.
The doctors make me feel like a crazy person who faked this to get out of school. How could I possibly fake nausea for thirteen weeks straight, and pain that kept me up crying almost every night? How could I fake my difficulty walking while it’s causing me to miss both of my volleyball seasons? Before this, I had hardly missed a day of school in my life, and refused to stay home whenever I got the flu because I hate falling behind. I’ve played volleyball tournaments with sprained ankles and chipped elbows, I can handle pain, and I’m not a baby. If the doctors would take five minutes out of their time to try to get to know me, maybe they would see that. And the few who actually take the time to be pleasant don’t listen. They tell you they know, that they understand, but they don’t. They won’t drag themselves out of bed in the morning feeling nauseous and half asleep; they’ll be able to walk into their office without feeling like they want to collapse, and they’ll go home to the people who care about them and will actually be awake long enough to enjoy their company. No one will tell them they’re insane, and the worst part is that most of them won’t take the time to realize how blessed they are just to have the ability to do those things. How can the doctors not have sympathy when they’re the ones who put this poison inside of me?!
I know I’m very lucky compared to girls who have experienced more serious side effects, and am thankful that we were able to make a connection between my illness and Gardasil after the first shot. But I’m living proof of what just one stupid shot can do to you-how can you put yourselves or your daughters at risk of what I’ve gone through? The benefits are not just worth the risk..
My 15th birthday is coming up in just a few weeks, and all I want is to be normal again.

I am 39 years old. I have been taking Lisinopril for nine months now, for my High BP. For the first 7 months I had not really had any annoying side-effects other than a mild dry cough. But for about the last 2 months I am having a really odd sensation in my heart. It seems like a flutter and it goes across my upper chest area and into my throat. At times they are mild and other times, during a lot of moving around, I have more aggressive sensations. One night while in bed. My wife got her stethoscope out, (she has a medical background) and listened to my heart. She told me not to tell her when I get the sensation, but to let her try and determine when I have the feeling. this nailed it as soon as I had one. She said that it seems that my heart if pumping too quickly. Meaning that I may have a Premature Ventricular Contraction. This has really scared me. I am scheduled to see my Doctor tomorrow. In my last visit which was about 3 weeks ago, I had brought this up to him. He didn't really try to hear my heart on his own. He just listened to what me and wife were explaining about the sensation. I had hurt my leg about the same time this started happening, and I was taking large amounts of Ibuprofen. So he partly chalked up to Ibuprofen and maybe a drug interaction and stated that I lay off the Ibu and see if they go away in 2 weeks. And if not, he wants to do a Holter Monitor on me to see what may be happening. Well they haven't stopped! I am thinking maybe I should ask for a different BP med. I still want to do the Holter to make sure, but I think it may be time for a change. I have only heard of this fluttering feeling happening to one other person. Has anyone else out there had this same scary sensation? if so please let me know what you have done or have found out. Thank you!

I have been taking Lisinopril for about 2 months now, I haven't experienced any of the side-effects until recently I started waking up with numbness on my left upper leg. Overall I get weird sensations, mild numbness & tingling on my arms, fingers and feet. Thanks to this site, I realized my overall changing sleep patterns and numbness can be attributed to this medication. I will call my doctor to see if I can stop taking it. On a side note, my BP is definitely lower. I am 29/male.

I am on Wellbutrin SR 150. They started me at 1 pill once a day. After three days to 1 pill 2x a day. Last night was a "clutching my rosary" moment. I fell asleep and woke up a couple of hours later to go to the bathroom. I had INTENSE ringing in my ears - like a freight train. I was very dizzy. By the time I got down stairs and went to the bathroom I was so dizzy and disoriented I knew I couldn't stand up much longer. I ended up crawling around on the floor praying with my head down on the floor. I had HOT, I mean like FIRE sensations shooting up from my abdomen to my head. These subsided more and more over the night as long as I kept my feet elevated and lay flat on my back.

Has anyone had ANYTHING like this? This is just AWFUL. It hasn't been a week yet, but I'd rather be seasonally sluggish than EVER go through this again! I am waiting for my doctor to call me back today. I did NOT take a pill this morning!

I have been on Aviane since January. I started taking it for extremely painful cramps that induced vomiting and dizziness. I wasn't taking it for birth control, acne control, or anything else. It worked wonders for my cramps. I had a regular period, no spotting, and no excruciating pain. That being said, the rest of my life was awful. I break out like crazy, put on a little bit of wait (nothing to really complain over), and worst of all, I have been in a hazy slump since I started taking it. I wouldn't say its been depression, but it is definitely a fatigue that I can't shake. I don't care about my friends or boyfriend or family until something or someone makes me aware of my blatant rudeness and apathy and then I burst into tears and cry for a whole day. Its awful, and I plan to not start the new pack on Sunday. I'm cutting birth control entirely and hoping it will change things. Has anyone else done this? I'm kind of scared of the side effects of stopping...

For the first time in 10 years I chose to go to a medical doctor instead of my usual Homeopath to receive treatment for a UTI. 2-3 weeks after taking Cipro My knee would suddenly give out while I was walking (no pain, yet). A week or so later the tendon behind my knee starting hurting. Another week the front of my knee hurt. Another week and it’s as if my muscles & tendons in my calfs completely froze. I could not walk. Excruciating pain at even resting feet on floor...could not bear any weight or pressure. Also swelling, strange crawling sensations, pinching pains, dull ache in leg bones, stabbing pains, tearing sensations in calfs...it seems to be a little different every day. Also some insomnia and anxiety, shortness of breath, and a strange sensation that my throat or tongue was swollen so I had to sleep in a raised position because it felt like I was suffocating when I laid down. Now 8 months later...only very slight improvement. I can grocery shop for about 20 minutes before I’m so exhausted and in so much pain that I’m sweating. Cannot lift or carry anything that’s even slightly heavy because it puts too much strain on my legs. When I can walk, I walk funny - kinda like Frankenstein’s monster (straight-legged) and also limp. I never thought at the age of 44 that just grocery shopping would be enough to wipe me out for 2 or more days. And yes...depression too. Who would’nt be? If you have any advice please share it with me.

I am a 56 year old that had an aortic valve replacement 51/2 years ago, I have been on toprol only 12 mg a day for around 4 years I have had minor side effects, cold feet, cold hands, optical migraine headaches (once in a while). I was on the real toprol for years and then the folks at walgreens offered a generic and I excepted, things were fine and I was rolling along until they chaned generic brands from SANDOZ to ETHEX, I seemed fine on the SANDOZ it even looked the same as the real thing, but when walgreens gave me ETHEX (which is a round pill about twice as large as the other) I began to feel sensations in the middle of my chest and sometimes while taking my pulse it felt like my Heart stopped or skipped a beat, this scared the shit out of me! I took about 22 days worth of EHTEX and the symptoms kept getting worse, I finally called the Cardio folks and they suggested that I wear a Holter monitor for 24 hours, which I did and felt that I had a few Heart stopping moments along with a odd heart burn sensation in the middle of my chest. Two nights ago I found some of the SANDOZ that I had saved for vacations and began taking 12 mg of that instead of the ETHEX today for the first time in nearly 3 weeks I had NO Heartburn problems and NO Heart stopping experience, mind you this was only day one! Looking forward to day 2 and now that I have read all of the side effects from all the good folks on this site, that are not listed when you purchase the drugs, my opinion is that all GENERIC drugs that are suppose to be IDENTICAL to the real thing is a huge lie! What the hell is the FDA doing? Are they trying to let the GENERIC FOOLS poison all of the good folks that actually need these drugs without doing or maybe reading the test results? Or maybe the drug company's have so much clout that they can grease a few palms and get there GENERIC shit to market. To think that these drugs are suppose to be IDENTICAL and then to receive a pill that looks NOTHING like the real thing and when you bust it in half it's a different frickin color (ETHEX)!!!! What was I thinking taking this GENERIC piece of garbage! The GENERIC buttheads along with the real manufacturers should be required by LAW to list ALL ingredients on the label so all of the good folks can read and compare to see what there swallowing and putting into there bodes! I hope to get off of thos drug soon but if I don't rest asure that I will seek out the real thing. I was so freaked out by the side effects that the Cardio Doctor scheduled an ECHO for this Friday, I think the valve is fine but we will find out! Good luck all!

I take Simply Sleep once in a while just to help me fall asleep. I'm a 120-pound woman and one pill is usually enough. Last night, my mind was racing and I decided to take both pills. BIG MISTAKE! I had very weird sensations in my legs that still continue (it's now 11 AM, 12 hours after the dose). I guess it could be a form of Restless Legs Syndrome, but I've never had that before. These sensations (tingling, numbness, a desperate need to move) were enough to wake me up in the middle of the night and keep me awake, even though the rest of my body was tired. I'm dragging today -- a combination of no sleep and the residual effects of the sellping pills. My legs are still not right. They feel weak from the hip down when I'm sitting.

Has anyone else developed extreme sun sensitivity? I have many of the other side effects listed here, but 6 months ago my dose was increased and I became so sensitive to the sun that I can't go outside for even a minute. I get a deep tissue burning (not a sunburn on the surface) and tingley or chills sensations. I have been to the Dr. and stopped taking it one month ago, but so far no improvement. Please, i would like to know if anyone else has experienced this.

I began taking Wellbutrin 2 weeks ago and started on a 150mg dosage. I was on 150mg for one week. The second week, I went up to 300mg per the psychiatrist's instructions. I was feeling really angry some of the time and decided to stop the medication. Prior to the last 2 weeks I was taking 40mg of Paxil, which I stopped after the first week of being on Wellbutrin.
The anger was uncomfortable, I stopped taking the Wellbutrin and within 36-48 hours of being off this drug, my feet began to itch mildly at first. Within about 30 minutes of this "mild" itching, the sensations got worse. My feet felt like they were on fire. The only relief was putting them in hot water in the tub. I was screaming with frustration and pain. I attributed this to the cold turkey stopping of wellbutrin. But since I had been on it only 2 weeks, I didn't think anything would happen. Big mistake. After 2 hours of having feet in tub, on the phone with a 24-hour nurse advice line and pharmacist, I went ahead and took 300 mg. The itching stopped within 2 hours. This was a freaking nightmare ! So I am weaning myself off. The doctor who prescribed this, who I spoke with the following day, said...well..stop taking it. Doesn't make sense because when I stopped that's when the extreme itching happened. It's crazy. I'm weaning myself off and taking Benadryl. I also got some hydrocortisone cream. There are scabs on the top of my foot from scratching. No more. I've been on anti-depressants for over 10 years now and I want to stop ALL OF THEM. Within 2 weeks, I should be "clean". Just know that this itching...was so intense I was crying and screaming because there was no relief.

I've been on Lamictal for about 5 months now. I recently have had some horrible side effects. I've had the acne, brain fogginess and weight gain all along. About a month ago I was hospitalized for having a blood phosphorus level of 0.6 which is dangerously low. The symptoms around that day were nausea, feeling like I couldn't breathe, hyperventilation, heart rate of 120-130, tingling sensations from my nose to my toes, diarrhea and almost blacking out. Of course, the ER doc thought I was having a panic attack and told me to breathe into a bag and try to breathe slowly. NOT from a panic attack. Granted, I was panicking because I was scared. Has anyone experienced this low phosphorus problem?? I will be coming off of Lamictal in the next week. Hasn't made my depression, panic attacks or sex drive any better. thanks.

I am a 38 Yrs old and I took myself off Yaz 2 nights ago after being on it for 2 weeks. I still need to call the gyno and inform her. My personality completely changed, my moods terrible, snappy and extremely short fused, i think i'm officially banned from the dunkin donuts at the end of the street after yelling at them for screwing up my order-normally i'd let it go and just get it fixed, no patience whatsoever. I'd never been on birth control before, and I'll never go on it again after this experience. I didn't even want to be with myself. I can't believe my boyfriend didn't dump me after Sunday. The side effect i find odd and worrisome the most is, and I still have, pressure in my head and throat and tongue, it's dissipating as of today but started last Thursday (about a 1.5 weeks on the yaz). Has anyone else experience the head pressure?

I am taking Septra for a sinus infection. I am consistently, ridiculously nauseous all day and all night since within two hours of my very first dose. Taking this medicine with lots of or little bits of food, milk, bread, soup, peppermint tea, ginger, etc. doesn't make a difference.
Food smells make me wretch. I can't even wash the dishes because of the leftovers. Even simple mention of some foods makes me gag.
I also am sick when the road curves too much ahead of me, I see spinning things, and moving my eyes too quickly.
I have never been this nauseous in my life. I find it disturbing.
Vomiting does not relieve the sensations. My vomit tastes very bitter.
I suspect the accompanying headache is from dehydration caused by the low food intake and diarrhea.

Im 17 years old and my doctor asked me to try this new birth control......it's terrible i'm on my second pack and only have one week left until my brown pills!!.....my breast got swollen first and then they became tender....but by night fall the tenderness goes away and returns 2-3 hours after i take the pill the next day. im ALWAYS bloated even when i awake in the morning.....i suffer from headaches from time to time and even feel tingly sensations in my right arm....i bled for about a day on my first set of brown pills and had some spotting here and there.....and not to mention i gained 5 pounds!!!....im way to young for this so i'll take my 3rd pack of pills and see how it treats me but if it doesn't get any better i'm starting some new pills!!!!!!!

I have been on Warfarin for two years now and on it for life, i had a blood clot in my left leg. While i was reading everyone's side effects, it was like i was writing it myself...I experience the same symptoms........Foggy mind, short term memory loss (i even have a notebook now wherever i go now), fatigue, thirsty all the time, headaches, strange sore sensations in my legs/body especially when its cold.....all of which i am told Warfarin has no such side effects and that im imagining it.........i have been told this over and over and over. Im soooo glad im not crazy lol and that there are also people out there that are experiencing the exact same stuff that i am.

I am glad sites like this one exist because it makes it easier to become educated on all the different side effects women have. Of course, its a completely different experience for each and every one of us, based on our biological clock, hormone levels, etc...I've been taking Loestrin for about 9 days now. The first three days I was extremely irritable and moody. Everyone noticed it and pointed it out because its so unlike my character to be that way for no reason. I was snapping at people and I felt very sensitive. I've felt light-headed and weak but many of my back pain medications make me feel this way so I am unsure as to whether I should attribute the sensations to Loestrin. After the fourth day, I've felt normal. The only thing that concerns me now is that I started bleeding this morning. My doctor said I have what's called breakthrough bleeding and I hope it doesn't last longer than a day or two. I've never taken any oral contraceptives in my life and hope this regulates my excessively long periods (think 5-7 days).

Hello ladies. I have had the Mirena removed now for about 2 months and i feel a lot better. I am not sure if i posted here or another forum but i have experienced terrible side effects from this thing being in my body. my side effects included

painful joints( i felt like a 80 something year old)
lower back pain
Chest pain ( which i still experience on and off now)
numbness on my fingers and toes ( which i still have to some degree)
sharp abdominal pains
extreme anxiety
tired all the time
spasms in my hands and legs especially my left side
headaches and the list can go on and on.

My doctor did not believe the mirena was causing all of this even though i had been a very healthy person with no medical complaints at all before the mirena was inserted.

Did i read somewhere about a class action lawsuit? Because i will definitely look into it for all the suffering this thing has put me through.
Thanks everyone for posting. Information is power!

It`s very disturbing to read all these stories.

I really feel for you.

My experience comes from seeing what happened to people close to me. They all took statins.

I started to look for information on statins, and other medications, in 2004 and it continues to this day although two of my relatives are dead.

I have nothing to do with the health or pharmaceutical industry.
I saw the suffering and it made me very angry.

I am an ordinary lady in her sixties who live in Sweden.

The situation is almost the same here as in the U.S.

There is very little discussion about risks/benefits with this kind of medicatications - or others.

I think it`s a good idea to turn to the Internet and books to get other views about the cholesterol issue.

Is it really true that it`s the cholesterol that is causing heart disease? Are you sure?

Please visit:

www.thincs.org,

www.ravnskov.nu,

www.spacedoc.net, www.statinalert.org

Also search for "Stopped our statins" on Google.

You will find a lot of information. Under "print articles" you will find a very informative article from The Weston Price Foundation.

Also search on the names of the different authors below.

Here are som books:

The Cholesterol Myths (Uffe Ravnskov)

The Great Cholesterol Con (Antony Colpo)

Book with the same title (Malcolm Kendrick)

Overdosed America (John Abramson)

The Truth about the Drug Companies (Marcia Agnell)

There are many more.
For forther information about these books turn to the Internet.

It´s good to have some other information than the one given by doctors because most of them have been "educated" by the pharmaceutical companies themselves - and why should they talk about risks, side effects etc. They are interested in profits.

Finally - here are some side effects that I have seen:

pains in legs, hands, elbows, shoulders, knees, hips, cracking noise in ribs, muscle weakness, loss of hair, head ache, burning, tingling sensations in hands and feet, numbness, difficulties to swallow, loss of taste, ringing noise in ears, cramps, insomnia, irritation, depression, difficulty with short-term memory and then advancing into more serious problems.

These side effects - i 3 different people - all over 65 - did not come at once.

All of them had taken statins for years (Zocor)

It doesn´t matter which product -all statins have similar side effects.

My relatives also had some other medications which makes it even easier for doctors (and patients) to say that it`s just old age.

I am happy for those who get problems right away because then there maybe a chance for the patient and the doctor to see that there is a connection.

You really have to look out for yourself and the people around you!

Good Luck.

I wrote the message below on March 9th, 2008, but I think it might be useful if I repeat it.
_________________________

It`s very disturbing to read all these stories. I really feel for you.

My experience comes from seeing what happened to people close to me.

They all took statins.

I started to look for information on statins, and other medications in 2004 and it continues to this day although two of my relatives are dead.

I have nothing to do with the health or pharmaceutical industry.

I saw the suffering and it made me very angry.

I am an ordinary lady in her sixties who live in Sweden.

The situation is almost the same here as in the U.S.

There is very little discussion about risks/benefits with this kind of medicatications - or others.

I think it`s a good idea to turn to the Internet and books to get other views about the cholesterol issue.

Is it really true that it`s the cholesterol that is causing heart disease?

Are you sure?

Please visit:

www.thincs.org,

www.ravnskov.nu,

www.spacedoc.net, www.statinalert.org

Also search articles etc on "Stopped our statins" and on the names of the different authors below.

Also read:

The Cholesterol Myths (Uffe Ravnskov)

The Great Cholesterol Con (Antony Colpo)

Book with the same title (Malcolm Kendrick)

Overdosed America (John Abramson)

The Truth about the Drug Companies (Marcia Agnell)

Malignant Medical Myths (Joel M. Kauffman)

There are many more.

Please look on the Inernet for more information about each book.

It´s good to have some other information than the one given by doctors because most of them have been "educated" by the pharmaceutical companies themselves - and why should they talk about risks, side effects etc. They are interested in profits.

Finally - here are some side effects that I have seen:

pains in legs, hands, elbows, shoulders, knees, hips, cracking noise in ribs, muscle weakness, loss of hair, head ache, burning, tingling sensations in hands and feet, numbness, difficulties to swallow, loss of taste, ringing noise in ears, cramps, insomnia, irritation, depression, difficulty with short-term memory and then advancing into more serious problems.

These side effects - for 3 different people - all over 65 - did not come at once.

All of them had taken statins for years (Zocor)

It doesn´t matter which product -all statins have similar side effects.

Search for "Stopped our statins" on Google. It´s a very informative site and under "print articles" there are som articles that you can take along to your doctor for discussion.

I particularly like the one from Weston Price Foundation
and explains the different statin studies and side effects. .

My relatives also had some other medications which makes it even easier for doctors (and patients) to say that it`s just old age.

I am happy for those who get problems right away because then there maybe a chance for the patient and the doctor to see that there is a connection.

You really have to look out for yourself and the people around you!

Good Luck.

Hi,
I just found this site and was wondering how long it takes this horrible drug to leave your system. I have been taking it for a year and have suffered the WORST depression and anxiety attacks from it. I have been lucky enough to have never suffered from any of these symptoms in my entire life and my heart goes ou to those who live with it every day
So far I have lost my job, any chance of sleep, and I can barely get out of the house in the morning. Its having a direct affect on my marriage, I have lost all intest in my hobbies, unable to concentrate, I'm just a wreck. I just saw my Dr. last week and she made my dose smaller (25 MG) for the past week and I feel worse. Is there any ending to this?

I've developed a twitch in my right eye in the five days I've been taking Yaz. No other new elements have been introduced to my routine in that time. I'm going to stop taking it today, the sensations are too distracting.

I am so glad that I found this site. I was put on Toprol in January and Just recentky i have panic attacks, chest tightness,tingling and numbing sensations in hands and feet, and i am deperessed. I also have some difficulty breathing. My Dr. told me that I am depressed and these side effects are from depression and not the medication so she gave me Zoloft, which I am not taking. I am not crazy i know that my symptoms are from the meds. i am going to wean myself off and pray i can be "normal" again. This is the worst time of my life and I pray that I can do this.