Single mother symptoms and conditions

I am a single mother of 2 children, I wanted to quit smoking so my doctor said to try Bupropion ER150MG for a 1 week and 3days The first week it was 1 pill a day then 2pills from there on out. The affects hit me the second day it has helped with cutting down on smoking and it makes them taste very plain and nasty. I have these systems/side affects already>feel slow, dry mouth, horrible taste in mouth, food and sodas taste nasty food has nasty taste as well and headaches first week. Very emotional ever since I started taking 2pills, just a thought and I would tear up. Like today this morning I was emotional and around 1o'clock I was Bitchy and irritable. I feel drudged honestly. Totally not me I only get emotional when on my period and Bitchy hardly ever! Sleep well lets say I wake up a couple times every night since I have been on it period. I am a deep sleepier too. I have no clue on what to do if I should give it more time or tell the doctor I'm done? I just want to quit smoking with something thats not going to affect me like this. I have no anger problems or anything like that just smoking. I am actually under weight for my age I don't know if thats why it has affected me so quickly 5'5 and weight 107-109 26yrs old I have not been eating as much as I usually do and have a high metabolism and I seem that I have gained a pd or 2. Don't understand I just think it's mess me all up. I waited an hr or two later to take my next pill tonight and I felt so good like myself, I will also say it seems to leave my system within 9 to 10 hrs it suppose to stay in your system for 12hrs but not me. If anyone can help me on advice feel free to email me please ******Thanks Mel

About 4 months ago I took 7 days worth of Levaquin after my sinus surgery. It was a preventative measure, I never had an infection. A few days into the prescription I started having tendon pain in my knees & ankles. I couldn't sleep, I was having nightmares, I was emotional, anxious and drained. My doctor told me to stop taking the Levaquin immediately. 4 months later and I am still suffering from entire body tendonapathy, neuropathic pain, joint pain, skin sensitivity, severe migraines, temperature sensitivity, twitching (muscles convulsing), basically my entire body hurts. Some days are a little better than others but not by much.

I have been to rhuemetologists, neurologists, pm & r doctors, physical therapists, acupunture, orthopedic surgeons, & allergists (in Chico Ca, & @ UC Davis in Sacramento Ca). NONE OF THE DOCTORS KNEW WHAT TO DO. My general physician actually told me to "go home and wait it out" because there was "no hope of finding help" (I'm not kidding). I've had tons of blood tests with fairly normal results. Thankfully I have a wonderful neurologist who has taken some interest in my situation. All of the other doctors told me that my case was very rare & that they had heard of such side effects but had never seen any patients with them! After some research on the internet I seriously doubt that my condition is as "rare" as they claim.

I am only 28 years old, I can't walk, I can't work, and my life has been turned upside down. I was very healthy before, I don't have a family history of health problems, nothing like that...it was the Levaquin.

Here is what I am currently taking: Lyrica for neuropathic pain, twitching, not being able to sleep etc., and oral morphine for the severe pain, Milk Thistle to promote glutathione (important because it helps your liver detox), Magnesium Malate (also helps detox), a multivitamin, vitamin c, and fish oil pills. I also attend acupuncture 2x per week (honestly feel some relief from it). Also, I heard that glutathione infusions are helpful but I haven't tried them yet. At this point I will try anything.

IF YOU HAVE HEARD OF ANYTHING OR ANYONE WHO CAN HELP WITH THESE DEVASTATING SIDE EFFECTS PLEASE LET ME KNOW.

~J.

I thought that all the problems I've had the last 3 months that I've been on Yaz were unrelated....I thought between stress, IBS, my job as a teacher, and being a single mother, that all my problems are just stress. I've been on the pill for three months. I am taking the pill to help with adult acne and mood swings. I really think that it has helped both of those things. However, the last month I have noticed some symptoms and I think that maybe I can tie them all to yaz???? Here's the list:
Headaches
Weight gain
Muscle cramps
Extreme GI problems (worse than my normal IBS)
Blanking out (short time frames where I do weird things and I don't remember them). Is this a symptom? I haven't read about this one. I'm scared to death I have some mental disease or something! Anyone else have this problem? I am so scared that I've lost my mind and have gone crazy.
Night mares
Anxiety
Panic attacks (I think)
Abnormal heart beat

IF YOU FEEL/EXPERIENCE ANYTHING ABNORMAL FOR YOU OR DO NOT FEEL QUITE YOURSELF SEE YOUR G.P./NURSE AND SERIOUSLY CONSIDER GETTING THE MIRENA COIL REMOVED
This medication may be suitable for some people but if you experience any of the following, I urge you please, please please, 'demand' that you want the Mirena removed. My symptoms were noticeably worse around my time of ovulation. I've also found out that people previously treated for/suffering from depression should not be prescribed this medication. (I've been on Prozac in the past). I had it fitted in Aug 2007 to combat very heavy periods and severe PMT at the recommendation of my G.P.and had it removed Sept 2008. Symptoms I experienced :-

Dry/furry mouth
Headaches (over time these became migraines)
No concentration
Poor memory
Lethargy (constantly tired and drained)
Smelly discharge (still noticeable straight after washing)
Very heavy legs
Numbness in my legs
Joint pain and clicking (mainly in my shoulders and knees)
Developed facial hair (mainly under chin and jawline)
Hair loss
Weight gain around my stomach (without increasing my food intake)
Feeling constantly bloated.
Spotting randomly for duration of Mirena being fitted. (Brown spotting)

Panic Attacks ( awoken in the middle of the night with them) escalating to the following:-
Palpitations (for no apparent reason)
Clammy/sweating palms and feet
Aggitation ( during an episode if someone was talking to me I wanted to really yell at them 'Just shut the **** up! You're doing my head in!)
Feelings of madness (actually wanted to run away from my own mind)
Pins and needles/Tingling in my hands and feet
Electric shock like surges going through my body (my nerve endings were obviously suffering)
Muscle tremours/shaking (mainly arms and legs)
Eyes became extremely light sensitive
Heightened awareness of sound

Insomnia
Terrible nightmares
Depression
Feelings of detachment from the real world.
Visual disturbances
Episodes of blurred vision

These symptoms did not appear straight away but appeared gradually and with more veangance the longer I had the coil. The more concerning episodes I experienced happened after about 3 months and very erratically. I could not predict when or what time of day I was going to have an episode or pinpoint any reason for bringing on an attack. I had no control over the effects, was absolutely petrified when I experienced a panic attack and just had to ride it out.
All my G.P. did was prescribe me anti-depressants to which I reacted badly. Blood tests also failed to show anything abnormal.
I even tried herbal medicines as an alternative and experienced similar reactions to the prescription drugs. I've now become very pill-phobic and would rather ride out and get over symptoms myself. Paracetamol & Ibuprofen being the only medicine I trust to take now. I had a horrendous year and everyone suffered. Not only my family, but I was signed off of work for 3 months. It was a very worrying time for my husband and my children, who all had to keep an eye on me and witness the effects of my symptoms. On looking back now, I don't know how I managed to function at all and even do my job. Most of the time my energies were spent concentrating on trying to appear normal and held-together to the outside world.
Although I feel 100% better in myself, I noticeably experience more migraines and headaches than I ever did in the past, along with palpitations, usually during my week before. Two days before it I often really feeI like I'm losing the plot! I also really bloat up now a week before my period, feel sick and have a feeling of being ' very full', so am hungry but don't really want to eat. One of my big toe-nails has gone black over the past few months and not through injury. This has just been sent away for analysis. The one on the other foot is raised/ridged/thick/yellow, but normal growth has resumed half-way up now, which I feel co-incides with the state of my health on having Mirena removed. The nurse I saw recently explained that it is true that nails and hair show the history of our health so, for me, this would seem true.
I wish I'd been made fully aware of all possible side-effects of this medication and am now actually concerned that the effects I've suffered may have left some permanent damage.
In spite of all this, it's so good to be me.

First I want to say, after reading several posts, that it seems a lot of you are taking Topamax without food, which may be causing your "spaciness." My doctor suggested always taking it with food, even though it says with or without food, and I only experienced spaciness the few times I took it at bedtime without food. Once I started taking it with breakfast and dinner, that never happened again.

I am a 48 year old woman, prescribed Topamax in September of 08 for migraine associated vertigo without headaches, with facial numbness. The first thing I noticed was I immediately had headaches, which to me indicated it was dehydrating me as that is the only time I get a "normal" headache. So I knew I had to drink a lot of water. Soon after starting Topamax I developed a dry cough that lasted the entire time I was on the med. I did not relate it to the drug at the time, however. It never even occurred to me. After about two months on the drug I started having trouble breathing with extreme dryness in my airways. I was prescribed an albuterol inhaler which did not help. I was then prescribed a corticosteroid inhaler which also did not help. I thought the trouble breathing was from taking Nadolol which I was prescribed for occasional heart fluttering - the neurologist said this was a normal side effect of Topamax. I stopped taking the Nadolol but the trouble breathing continued. I also had more migraines with vertigo and facial numbness than before I started taking the drug. I hoped it would eventually stop and the drug would kick in to help the vertigo, so I stayed on the drug. I had very minor tingling in my feet, but it was tolerable. I became very stressed out, had trouble sleeping, depression, my face started breaking out in November (and still is), I lost interest in everything that I normally enjoy - reading, photography, following politics in the news (sort of an obsession of mine). In December I was so depressed that for the first time in my 11 year career I started canceling appointments and eventually took three weeks off from work to "re-group." In January the neurologist decided that we would increase the dose from 100 mg to 150 mg for one more month, and if it did not get rid of my migraines with vertigo, we would discontinue the drug. The first day on the increased dose I had a killer headache, and I drank 150 ounces of water before it went away. That night I did not have to go to the bathroom during the night, unheard of for me. That's a lot of water to drink and not have to pee. Within two days of increasing the dose, my cough became much worse, and within three days, the breathing became more difficult. Within five days, I was having trouble speaking because my airways felt so dry. I called the doctor the next morning and he said it was not the drug, but if I wanted to, stop taking it. So I went off it cold turkey, per his instructions. I had rebound migraines every day for a week or two and my heart was pounding, sometimes for three or four hours at a time. Eventually the cough and trouble breathing went away, however, I had to continue drinking lots of water or I would notice that I didn't have to urinate, sometimes not at all. Again, unheard of for me. I saw a cardiologist at the neurologist's urging and they said the heart pounding was just anxiety. I disagree, as did another doctor of mine. We both believe it was withdrawal. I have now found out (by getting copies of my medical records) that the neurologist is now attributing all of my side effects from the Topamax to "somatization." In other words, psychosomatic - not a side effect, but just a way of getting medical attention. I am seeing a few people on this board who have also experienced a dry cough and trouble breathing. Can I have the same side effects as other people and have them still be psychosomatic, even though I had no idea those side effects could occur? I don't think so.

I have a theory that Topamax interferes with hormones which causes a lot of the side effects like lack of concentration, memory loss, anxiety, depression, insomnia, acne, and hair loss - all symptoms of peri-menopause and menopause. Ask any woman in her 40's or 50's if she has these symptoms and most of them will say yes. My face has not been this broken out since high school! My hair is falling out at a rapid rate. I won't even bother mentioning these to the neurologist. He'll just say it's not the drug.

I'm very frustrated and not sure what to do at this point. The neurologist has me taking a supplement called Migrelief now, but I think it takes three months to kick in, so I have no relief at this point.

Has anyone else experienced the trouble breathing with dry cough? I don't believe for a moment that it was psychosomatic.

2nd week into Chantix experience. Smoking is WAY DOWN, from a pack a day. I am so nauseous that I cannot eat/think function etc. I had better be smoke free after experiencing this lovely side effect. Also, Type I diabetic, single mother of a 2 year old and a smoker since age 13 or 14 that's 25 years of smoking.

I have been on Yasmin for almost 2 weeks, and I have been nauseous, vomiting, huge sore breasts, headache...it is like being pregnant for real..again! I hate it and I am seriously wondering if there is anything out there that is not going to make me sick? I am 39 years old and I don't plan on having any more babies. I have one beautiful 3 yr. old right now, and as a single mother I need something that won't bog me down. Any suggestions?

I was so amazed to see so many people having the same side effects as I am. I thought I was just stressed out from working full time, being a full tine student in college and a single mother of a 3 year old. I have not had this much acne on my face since I was in high school and I am 28 years old. I have gained so much weight that most of my old clothes don't fit anymore and I don't have the money to buy new clothes. My mirena was inserted in May 2008. After reading these blogs, I think I will get it taken out, but I would hate to get back on the birth control pill and I had a bad experience with Nuvaring too. I read in a magazine that what Mirena does is make the uterus uninhabitable for the fertilized egg to grow, so this means we are pregnant every month and pass the fertilized egg out with our menstrual cycles.

My daughter had been on singulair from the time she was 8 yrs old until she was 14. This will sound as if I am a horrible mother but I just thought that she was a raging bitch. Without my knowledge, she stopped taking her Singulair for a few months and she became a different person. She was so sweet and loving. One night she came in my room having an asthma attack and I asked her if she was taking her meds, she admitted that she had stopped taking her singulair and I got on to her and immediately got her prescription refilled. Within a few days of taking the singulair she turned into a raging, screaming emotional wreck, a TOTALLY different person. I feel so bad that for 6 years of her life I put her on medicine that caused her to have screaming, uncontrollable tantrums, and severe mood swings that caused her to be miserable. It does seem to be the only thing that effectively controls her asthma symptoms but the emotional havoc that is causes her and the people around her is not worth the benefits. We have an appt. with her doctor to see what other options we have.

I'm trying to wean myself off Geodon and I had a minor, panic attack,. My doctor won't help me because she said I need to see a psychiatrist but I can't afford to see one. Does anyone know how long the side effect last when you get off Geodon. I am a single parent and have a job I need to function at so any advice will help. I have ,anxiety, all the time the doc had to prescribe some anti-anxiety medicine which I never had anxiety like that before. My symptoms on the medication is sleeplessness, restlessness, loss of appetite, can quit moving, racing thoughts, depression.

I have waited long enough to tell my story. I am a 29 yr old single mother of 3. I started YAZ in Feb of 2008. I took it for 11 days. ELEVEN DAYS. It was about 4 days in that the headaches started. I couldn't stand light, I wore hoodies and sunglasses. I was nauseated. Saw double, black spots. Motion sickness.I could barely make it to work. I was out of control. I did not have control over my mind. I was crazy. My friend almost took me to the hospital to have me committed. There is no history of this in me or my family. The headaches would last from the time I woke up til the time I would go to sleep. Painkillers was the only thing that would keep me asleep through the pain. My dr immediately stop the the pills. I saw an eye doctor and they found nothing. They ordered an MRI. They found T2 Foci scattered throughout my brain. VERY unusual in someone my age. What that is, is my protective covering of my brain cells had been damaged there were gaps in its covering. I soon developed a stutter and a slur in my speech. The pain then moved throughout my whole body. They said fibromyalga and daily migraines. I'm now on topamax daily which gives me breaks in my headaches. I still get them daily. I still have pain in my body daily and I'm on painkillers daily. I have found a new dr who is wonderful. Who has recently taken blood. Who thinks that maybe it could be lupus. So I started researching Lupus...my symptoms and rashes match up. There is also a DRUG INDUCED LUPUS. and ORAL CONTRACEPTIVES is a KNOWN drug that can cause this!!! BUT IS THAT ON THE LABEL???? NOOOOOOOO!!! I was perfectly healthy before yaz, in kick boxing and now I walk and have the memory of a 60 yr old and my brain is permanently damaged. I have another MRI coming up to find out if there is more damage and I will find out the results of the blood work to find out what is wrong with me...but I blame all of this on YAZ and I hold them responsible. I SAY CLASS ACTION LAW SUIT....just have to find a firm with big enough BALLS to do it!!!

I had the Mirena inserted in March of this year (2008)! I hate it! Shortly after having it inserted I developed huge painful cysts on my ovaries. The doctors insit that the Mirena didn't cause the cysts but b/c there isn't enough hormones in the Mirena, they cyts aren't going away on their own. I had the cyst aspirated which caused the remainder of the fluid to leak out causing an infection in the lining of my abdomen. They put me on a heavy dose of antibiotics and hormoned to get rid of the cyst. For about a week I felt better until the pain came back worse. The cyst had not only come back but gotten bigger. I have to take a double dose of birth control pills now to get rid of the cysts.
For the past week I have been having pain again and not wanting to tell anyone b/c I know they are just as tired of this as I am! I can't sleep at night which makes it nearly impossible to get through the day. My doctor had given me pain medication the first time I had the pain to sleep at night but they are gone and I'm afraid to ask for more at the risk of sounding like a drug addict! I can't take these pills during the day b/c they make me loopy and tired and I am a single mother of a 3 year old little girl plus I work full time! What kills me is the that I had the Mirena inserted b/c I can't handle the extra hormones or remember to take the pill everyday! I can't deal with it anymore. I have gained almost 12 pounds in the last 2 months and I am afraid to exercise b/c of the cysts. I am hungry like I was when I was pregnant and tired all of the time and don't enjoy the things that I used to do. I cry at everything..good or bad...and I just can't take it anymore.
I will post back more when I have this thing removed and hopefully will have some good news.
I do feel like I have to say that I hear about Mirena from a co-worker who absolutely loves it!! She has had no side effects and has had it in for 7 years now! So it's not for everyone...but if you feel side effects...listen to your body and have it removed!!

I have a seven year old Daughter that has been on singular for 6 years. The first 3 years she only took it occasionally but the last 3 years she as taken it every day. Also in the last 3 years she has had trouble sleeping all the way through the night she would wake up because of night mares and was afraid of sleeping alone and having mood swings that you would not believe she would go into rages that would leave me in tears because of not being able to help her and after about a year of that i took her to a Psychologist she was given a sleeping pill and was tested for learning disabilities. when they test a child they also ask the parent and the teacher a lot of questions about different situations the results of that test made it sound as if all of this behaviorally problems with my daughter was my fault be cause i did not have a good support family i think that was because i am a single mother but they also said there was nothing essentially wrong with my daughter. all of the things that i have read tonight sound just like the problems that i have had with my daughter and my daughter will not be taking Singular i know that they say that we should not be stopping the medication without talking to our doctor but if singular is the reason my daughter is acting this way then i can handle a runny nose better than a scratching bighting hitting whirlwind that she becomes in her rages

I had been taking Lipitor for well over six years to help lower my Cholesterol count with no know side affects. A problem developed about two and a half years ago with nerve damage that gave me excruciating pain in my shoulder and arm. After an MRI and three cortisone shots I was referred to a neurologist for help. He had no idea what was causing the problem.

About six months after many doctors could do nothing for me, and referring me to a physical therapist, my wife showed me a story in a magazine, which I can no longer find, that talked about problems with Lipitor that had not been properly documented. The article talked about exactly the side effects I was having. The article said there was a problem with nerve damage. It had been well documented that some people had muscle problems, but it was not know there could also be a problem with nerve pain.

I contacted my doctor and stopped taking Lipitor. Two months later, the pain just disappeared. The very day the pain ceased, I had a visit from a good friend of mine who is a Radiologist and who had studied Lipitor because of a problem he was having.

He explained that Lipitor was doing the job it was supposed to do, namely keeping the liver from producing all fats. The problem I was having was that I had injured a nerve and Lipitor was keeping the liver from producing a particular fat needed to help heal that nerve. It seems that the myelin sheath around the nerve needs that fat to help the nerve heal itself, and Lipitor was preventing the production of that particular fat.

Once I quit taking Lipitor it took about two months for the healing fat production to do it's thing. Recovery of the nerves in that arm has been very slow, but they do seem to be healing now.

I thought this was such an important finding that I notified all the doctors I had seen about this problem. To my great surprise I heard from no one. Not even a thank you. I guess that since they didn't find the solution, they just were not interested.

I hope this discussion helps someone else. Thanks for listening.

I have been on Wellbutrin for about a month. I am 31 and have never dealt with depression in the past. After a year and a half of one stressful event after another I started to feel life was just not turning out the way that I thought, but really thought that this was my life. After having some serious issues with my two kids, I am a single mother, I new that I needed to see a doctor. I couldn't get out of bed, felt detached from my family and pets. I had pushed the people who were most important to me away. After doing a lot of research on the internet I decided to discuss this med with my doc. At first it was pretty rough. Sleeping schedule was crazy, I was only sleeping a couple of hours a day but when I woke up I was not tired. I was extremely emotional. Crying for six hours straight one day. These are the only side effect that I had, but I felt much worse than I did dealing with my depression, which was pretty bad. HOWEVER, I continued to tell myself that these are side effects and I was willing to stay the coarse in order to get the benefit from treatment. During this time, I did have some good days or parts of good days which really gave me hope that eventually it would work. After about 3 weeks I felt better, the long bouts of crying had stopped and my sleep schedule returned to normal. Everyday after that I have felt more and more like myself. I didn't fully understand how depression had really affected all aspect of my life even in small ways. I think that I can't feel any better and then another day goes by and I realize that I can. The greatest thing is I can still feel things, can still get upset and have a good cry without it ruining my whole day. I think that is important as I am dealing with some very serious personal issues, thus the reason I need meds, but I know the importance of learning to cope with these issues as the are never going to go away. I feel like I have been saved and didn't even know that I needed this much saving.
I say all this because in my extensive research I have read a lot of these comments on many different sights and really didn't see myself or my experience. I have only read things that are scary and would make me think that depression is better than trying this drug. Everyone is different and the way they react to drugs is different, I completely understand that, but this drug has had an amazing affect on my life and the lives of my loved ones. If you have just started taking this and you think it is making you worse I beg you, stick with it, let the drug stabilize in your body and then decided if this drug is for you. I know that it is hard but there was a light at the end of my tunnel and there could be for you. Do not let a couple weeks of side effect put you off, or others negative experiences, if I had done that I would not be where I am. I know that I am getting better everyday. Remember this is a serious disease and it can not be fixed over night, if you had been prescribed an antibiotic for an illness you would expect for it to take some time to take affect. This drug is no different.

I was on the ring for about two months. It seemed great. My best friend had told me about it. We were loving it. Our boobs even went from a B cup to a C cup. I don't know about her but I know I took it the correct way. Then she came down with a "nasty flu" was what we had to tell her parents, but really, she was pregnant. She ended up terminating the pregnancy because the doctors said it was likely the child would have problems since she was 4 weeks pregnant and was still on the ring. I was a total different case though. I didn't even have any morning sickness until I was 6 weeks pregnant. I went to a specialist and they did an ultrasound and nothing seemed to be wrong so I became a single mother at 18. (I caught my boyfriend cheating 5 months into it). I have since then met at least a dozen other women that just so happened to be that one in a million percent with me.

I am getting mine removed FRIDAY!! And Friday can't come soon enough. I am kinda bummed tho for having to go back on the pill but I can't hack this ANY LONGER!!! One of my friends works for a GP and I went to him because of some of my side effects. The flu like symptoms minus having the flu (had it for at least 2 to 3 mos now) NO sex drive (causing trouble with my marriage. Hubby is taking it WAY to personal), swelling in my hands, feet, legs, and face. (my face will feel flush and BAM I'm swollen!!) VERY BAD MOOD SWINGS!!! Very Bad isn't the word for it!! There are no words to explain my moods!! ANYHOW..... I sent this to my friend to read and she pulled it up at work. Well the GP said that this isn't a reliable place to go for information on the side effects. "There are NO positive side effects to anything." Which is true BUT he seems to think going to Web MD or some sight like that is more reliable than here. And that this sight shouldn't scare me and he wouldn't urge me to have it removed after reading this. (OH YEAH I forgot to mention joint pain, I have HORRIBLE joint pain in my hands, wrists, elbows, knees, ankles, and feet. The worst of it is in my wrists and elbows) Back to what I was saying. To that (this sight not being reliable) I say go to Web MD and post there too! I pray that I can get back to me after this comes out!! I hope it don't take too long either! I MISS the old me and HATE the new me!! But FRIDAY HURRY UP AND GET HERE. And for anyone who has had it removed........ anything I should be repaired for??? Thanks for your time!

I've been on Topomax for about 3-4 months now. I've had memory loss, slurred speech, decreased concentration (I have to re-read something several times to understand it) tingling in the hands and feet, depression, increased anger, loss of appetite, weight loss. I'm now at the point where I have a rash on my leg, severe nausea, and abnormal bleeding. I going to follow up with my neuro and PCP to see what's going on so we'll see. My migraines have decreased from 3-4 a week to maybe 1 a week, so it has been worth it so far so I can function for work and for my kids as a single mother. I've suffered from migraines for about 10 years and can't take the pain no more!!! If anyone has experienced the nausea, rashes or bleeding please reply.

I am on my third cycle and I am not taking this pill ever again! I deal very well with stress. I am a single mother, i went through an abusive relationship with my sons father, I have a high stress leval career...through all that I never felt like there was not a light at the end of the tunnel. All of a sudden I am depressed, I can't function, I can't stop crying....now that I have read every one elses comments about heart palpitations, and cramping-I have felt the same thing! I just never associated it to Yasmin. I feel sharp pains in my head that last for a few seconds, I have had several breakdowns and lost my temper easily with my son....if anyone is considering taking this DON'T. The depression pain is almost unbarable and NO ONE shoudl have to deal with this!

Jennifer

I have been on this med for 2 years due to panic attacks and many of the side effect that i have read in the forum i have had but also i have had numbness of the lower arms, tingling in the lips, the nightmares, the shock in the face and side of the head,agrivation. I no longer have patience with my children and seem to be yelling all the time/ It did seem to help me at first and the panic atacks have all but gone completely but now i am getting depressed because l feel fat as l now weigh 70 kilograms and before zoloft only weighed 57 kilos. So l guess all in all there are good and bad things about this medication. i have also found myself drinking more alcohol than l normally would and have become disinterested in alot of things and found that now my negative thoughts are returning. And i have a sickening fear of death: single mother of 2, 36 years old zoloft 100mg 2 years.

I was recently diagnosed with a UTI and was prescribed Doxycycline for it. I had taken 5 of the 7 days of the script, with no relief. I went back to the Dr. and was given a 7 day sample of Levaquin. I took one last evening around 8pm, and needless to say...I got about 4 hours of sleep. Not continuous sleep either, that was in about 30 minute intervals. The nausea set in, my head started pounding, I was freezing and hot all at the same time. When I finally did get to sleep, I had horrible vivid dreams, woke up completely drenched, my heart racing, out of breath, and my head still throbs. I am also having trouble swallowing. I am so wiped out I can barely type this message. I can barely climb the stairs without having to sit down and rest afterwards. I did not get any kind of side effect leaflet due to this being a sample, and thought I would look it up on the Internet. Well...I am glad that I read this before looking up the general side effects, as I will not be taking the remaining 6 pills. I am a single mother with 3 small children, work full time, and definitley do not have time in my schedule to feel like this!