Hope you feel better symptoms and conditions

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 had Mirena IUD since July 06. Since then I've had incredible mood swings and have been so emotional. I basically was forced to quit a dream job b/c I had trouble being "professional" - that is keeping my cool and not having temper tantrums and snapping at people. Now, with no co-workers, I am doing it to my in-laws. I yell at my kids like I've never yelled at them before. They are scared of me at times. I was forced to see a counselor on 2 occasions when I had incidents at work and was suggested to see a psych for medication for my depression. I am against doing that. I had been trying so hard to lose weight and just wrote it off as being 35+. Just this summer, I started having pain in my right upper thigh and groin area which would radiate all over my leg, knee, shin, hip, low back - just depending on what I was doing. They couldn't figure out the prob so I went through a series of epidural steroid shots which have not helped much. Also, in the past year or so, I seem to not be as mentally sharp. I have trouble recalling names and facts that I should know. I feel like I have early Alzheimer's or something. Also, have that issue with my eyes where I sorta need reading glasses. Eye Dr. said I was a little young at 36 to have that. Have trouble getting things done and staying focused. Feel like I have adult onset AD&D. Other things that are more occasional include: not healing as quickly from minor scrapes and such, some drop in sex drive with some discomfort during sex, some hair loss but I've had that in the past from time to time, dizziness at times, shortness of breath, a cyst which I've never had before. I called my ob/GYN today and I am getting this out of me ASAP. I will definitely miss not having a period but we naturally have a period and it must be for a reason. I would rather deal with that.

I am a 26yr-old, another victim of Yasmin.

My story's gonna be a bit long, but hope you can bare with it.
Please also forgive me for my incorrect grammer as English is not my mother tongue....but I hope I can get my message across to all of you.

Here it goes!

Ever since I had my first period at a late age of 18 (I was anorexic and severely underweight btw the age of 14-15 when I was supposed to start my mensus had I been healthy,,,,), my mensus had never been regular.

I only had about 3 full-fledged mensus per year, with occational spotting.
Apart from that, I was a happy, bubbly, cheerful lady.
Nevertheless, worried about the side effects of "not shedding", I made my first visit to the gyn.

The Dr. ultrascanned me.
Both my uterus and ovaries were normal in size.
She ran a blood test for my hormones and thryroid level.
They both came out fine.

So then she recommended me to take Yasmin, which will help to regularise my cycle and "shed" all the accumulated lining.

I was quite happy during my first box as I lost my water weight, and my skin cleared.

But then the nighmare began......

Half-way thru my second box, I suddenly became sooooo depressed.
Sure, I did have some ups and downs prior to taking Yasmin, but the ones I'm experiencing while on Yasmin is just beyond anyone's imagination.

Prior to taking Yasmin, I was confident with myself, which I believe made me an attractive person.

HOWEVER, ever since the onset of depression, I seem to have lost all the confidence in me.

All that "self-esteem" I used to possess is now GONE.

I feel so insecure about myself, and don't feel good about myself even when I'm in my favourite outfit.

Before Yasmin, I was so easily "turned-on" !: listening to my favourite tune turned me on, watching drama with my fav actors turned me on, thinking about what to have for dinner turned me on.... just about any thought was enought to mass-produce dopamine in my brain.

But these days, none of these make me happy.
Nothing makes me happy, but anything can make me go DOWN.

I've been off Yasmin for 5 days now.
I do feel slightly better than 5 days ago.
But I'm suffering from elevated heart beat around midnight, which is making me insomniac.

But my biggest concern is ;

WOULD I REGAIN THAT "GLOW" IN ME?
WOULD I REGAIN MY CONFIDENCE?

Also,

Is taking Evening Primrose Oil beneficial to regain my peaceful hormonal level?
Can I start taking EPO directly after stopping Yasmin?

By the way, I notice that I look older (as in aged) ever since taking Yasmin. Does BCP make you age faster? Or am I just imagining things out of depression?

PLEASE HELP....

Thank you for spending your time to read my story,,,,,,

I have been taking OMEPROZOLE for around 9 months for Barretts Asophegus reflux.
In general I was beginning to feel I was very ill with symptoms mainly: hot flushes, my face was burning for a few seconds, dizziness, stomach cramps top right mainly, feelings of diareah, and dry mouth.
Has anybody else experienced any of these symptoms... my GP is sending me for a scan on my Gall Bladder, but in my mind all these cramps are associated with Omeprozole... I cannot stop taking it or I get severe pain between my shoulder blades with reflux burning.
Maureen.

I wish I had seen this page BEFORE I finished 5 days of Levaquin 500. The meds were prescribed for a post-upper-respiratory infection hacking dry cough that had been going on for nearly 3 weeks. I finished the meds 4 days ago and still feel super crummy. Levaquin did nothing for the cough (acunpuncturist stopped it with with several well-placed needles in my outer ear) and - before I saw this page - thought of asking the doctor for another round since I was still sick and seem to be getting worse. I have intermittent headaches, a racing heart, blurred vision, am so tired I never want to get out of bed. I'm also having a recurrence of sciatica in one hip and thigh and - new symptom! - the foot on that side is so sore it's hard to put my weight on it. I was told to report any joint or tendon pains but, according to the doctor, "they are very rare." I'm sure he told me about the symptom to protect himself "just in case" but it was clear he really didn't believe there would be problems. I took the medicine for three days, then stopped for a day because I didn't feel well. Then I thought, "Suck it in - there's only 2 pills to go and then you won't infect anyone. You don't want to be Typhoid Mary for the next antibiotic-resistant killer strain of some bug or another, do you?" I am devastated to think these symptoms will persist as long as people on this site say they will. I keep thinking I can sleep this off, or that I'm really sick with something that requires a different antibiotic. ( And how stupid is THAT?) But, from what I've read here, that's not likely to be the case. I'm 67 years old and already have compromised immune system plus sleep apnea, high blood pressure, narcolepsy, and asthma. Is there anyone out there who has been able to resolve these symptoms in less than three months? I refuse to believe I have to feel this way for the foreseeable future. And boy, am I mad! At myself as well as at the doctor. I usually research everything before I take it, but this one just slipped under the wire.

I am a 56 year old female who was very active ranching, balng hay taking care of irrigation etc. 3 years ago I had pain in my left arm and my heart was racing went to the E.R. where they did a 12 lead ekg. Could not find anything wrong other than my blood pressure was up to 160/90 they gave me ToprolXl 100 mg and told me to see my primary care physcian. Which I did. He continued the medication.

Since that time I have complained to all of the symtoms I have seen on this site. With one exception. Two months ago I was watching TV and had double vision. It only lasted for a few seconds but noticed the next day my peripheral vision was gone. I made an appt with an opthomologist and he spent 3 hours with me and recommended an MRI which was conducted some 2 weeks later. I was referred to a neurologist who ran a lot of blood work. My first batch of blood work showed a raging inflamation. They started testing for MS, lymes, lupus etc. Last week i met with my neurologist for the follow up blood work report. Everything is normal he says but by the way you have myathenia gravis. You get double vision again you call me I will give you medicine. Like I am a two year old.

I have researched myasthenia and the one thing you dont want to do is be on a beta blocker or a calcium channel blocker, as both of these will aggravate the condition. I called him to ask that he change my blood pressure medication. He says I wont do that. My primary care physcian is no longer in practice with the original medical group and has left the area. I saw him only 2 weeks ago and nothing was mentioned. The point is folks Don't trust anyone. Oh and by the way the side effects you are seeing mimic myasthenia gravis. Now no one knows what causes it for sure. Stress is a factor. But if you have not been tested get yourself tested. I may not even have this disease but I am getting off this medication and I am going to find out for sure what in the heck is going on. By the way I have seen a cardiologist last month without a referral because I wanted answers and he says there is absolutely nothing wrong with my heart...so why was I put on this medication? Heaven help us all.

Symptoms I have:
NOTES on health since day after I started the Lisinipril.
9-03-07 – started taking Lisinopril
9-05-07 – Saw Dr. for Bladder infection (left urinalysis with doctor). Prescribed a sulfite antibiotic for bladder infection.
9-06-07 – First symptoms began; trouble urinating
9-06-07 – Called Dr. Kuebals office to let them know that I was having trouble urinating. I also asked if they got the lab test (urinalysis) back yet. The nurse let me know that I had strep in my urine (very rare she said) but they will be prescribing me macrobid and to stop the first antibiotic.
9-06-07 – Began taking macrobid
9-11-07 – Unable to urinate at all
More symptoms after a few more days of taking this drug: Heart pounding in my chest, Achy skin, panic/anxiety attacks (hard to catch breath, heavy chest), Cold feet, hot sweats and chills, urinary retention, bladder infections, ultra sensativety (body to the touch), muscle cramps, arms, legs, back and neck feel heavy. I can't even lift my arms to fold clothes they get so heavy.
9-12-07 – went to the ER to get catheterized
9-14-07 – At hospitals request (doctor at hospital) saw a urologist although he thought that this was most likely a cause of the bladder infection and that I might have some swelling around the urethra or he also suggested that it might be caused by a tear or “stretch” in the urethra from not being able to urinate due to the pain of urinating. I didn’t not think that one, because as soon as I was not able to urinate, I knew that I would need a catheter until we figured out what was wrong.
9-14-07 – Removed catheter at urologist office
9-15-07 – Early am – went to ER again to get catheterized as I was still unable to urinate
9-19-07 – Went to CT Scan requested by Urologist
9-20-07 – Nurse removed 2nd Catheter at Urology Office and said to come back by four if I still could not urinate on my own.
9-20-07 – Researched Lisinopril to find UT could be caused by Lisinopril (medications.com) and saw the side effects that some people were having with this drug. Also learned that this was a derivative of venom from a Brazilian snake (thus the symptoms of feeling achy, sick, tired, muscle weakness and urinary retention
9-20-07 – Went back to urologist to let them know that I still could not urinate and they showed me how to self catheretize. Also, as of the evening of 9-19-07 stopped Lisinopril.
Between the ER doctors, my PCP and my Urologist, they have heard me complain about all of these symptoms but they refused to connect them to the Lisinopril.

OKay, I don't know if this has anything to do with Mirena or not, but I have had my implant since August 2006. Typically I am a very happy, healthy person. I eat extremely heathy (almost all organic, tons of vegetables & fish & almost no processed foods). Anyhow, for the last 6-8 months have have become VERY moody. I am often grumpy, I cry everyday, I have pain in my joints (I believe it to feel like arthritic pain). My finger joints are always sore. I am a fit person & am uncapable of opening a jar anymore. And, I have this nagging pain in my lower back to the left of my spine. Like I said, I'm not sure if this is because of my mirena implant, but I take no other medication, I don't even take OTC pain meds. I'm only 27 and consider myself to be very healthy. I'm not sure what else it could be. I suppose I will have it removed & see if I can become a normal human being again. I appreciate anyone else who can share their experience...I just want to know if I'm crazy or not???

I started taking yasmin at the beginning of the month suggested by my doctor for very irregular periods. I am 16 and have been irregular for 5 years and wanted a change. I also have very bad cramps or nausea when I am PMSing. I've never had any experience with a gyno and I didn't know what each kind was so I took her word for it. The first week or so I was nauseous before bed when I took it every day. Then 3 weeks later right before I was to start the "white pill" section I almos passed out in school. I was blacking out and shaking with a rapid heart beat and very dizzy. I went to the ER and the doctor said I just had "vertigo" and all tests were normal. After reading this and thinking I now have the stomach flu I have realized that Yazmin is the reason for all of this. I am glad that I'm not going crazy here. The past few days I've stopped talking it but I still have extreme anxiety (possibly caused by upcoming stress in school- i'm extremely busy and all over the place), dizzyness, shaking, nausea, diarrhea, vometing, random shakeyness and headaches. I hope this helps other women that have the same symptoms and are wondering what is going on- I know I was like that until I found this website.

I started on Advair 250/50 6/28/07 for continued wheezing, bronchitis problems even though I quit smoking 12/25/06. In mid July I began to have Lt knee pain, the dx from the Dr was "arthritis--you are getting older you know" I was 46 yrs old. I got a cortisone shot 7/24 since the pain was so terrible, the shot gave we 1 week pain free, then 8/10 I had #2 shot, same knee, again this shot only lasted 1 week, then pain returned with a vengenance. End of August I had an MRI done on Lt knee due to continued knee pain---this showed a menescal tear. So we are in the 1st week of Sept and the pain continues to worsen, now I have pain in Rt knee also. Grasping at various straws I re-read the Side Effects and Adverse Reactions to Advair. Imagine my surprise/shock to read under Musculoskeletal: arthralgia (Severe arthritic joint pain), bone and cartilaage disorders, muscle pain, muscle stiffness. Also wt gain.
Needless to say I quit the Advair..Even tho I had been on Advair for less than 1 month before my knee problems started . Next week I go in for surgical repair on torn menesci Lt knee, and so far so good with my breathing, but tomarrow I tell my Dr that "I quit the Advair, and the reason why I quit."

I was prescribed Doxy for my Rosacea and the first time I took it with plenty of water and vomited but I found out that it is better to have a full stomach of food instead. Now I have no problems with Doxy. I've been on it for almost 2 months now. I sure hope I don't have the symptoms that I have read in this site. Maybe I'm one of the lucky ones! Who knows? Good luck to all of you and hope you feel better.

Last night I bought 2 new shirts, was completely disgusted with my stomach and mid section. I had went to the doctor about 2 weeks ago for a cold, and when I was weighed, I had gained about 10 lbs in a month. I am completely disgusted with my stomach. I had a pooch down there since having my baby, but she is 19 mos now and since I had it inserted in April, I feel like a growing marshmellow. Sometimes I cant stand to even have my husband see me change clothes. Im about 195 lbs now...almost my PREGNANCY weight and I hate to get it taken out now since I just had it put in - in April. Also I have NO SEX DRIVE. My husband complains about it constantly and Im so tired all the time, I'm always saying how I could fall asleep. I keep attributing it to having a 19 mo old and working full time, but she sleeps through the nights now and I'm always tired. I've also had several dizzy spells that I can not explain. I'm going to keep reading these comments and it seems like I may have found what my problem is! Thanks for the help. I should have done my research before I went through the pain of having it put in. That would have been smart right?

I just want to say a huge THANK YOU to all the people that have posted their experiences here. I am so sorry to hear of your miseries, but you have prevented me from going down the same road.

I was prescribed Levaquin and my wife suggested before I take any antibiotics check on the side effects. Yikes! I have not touched one pill nor do I ever intend to. I will take my chances on the infection any day!

I had a stye/ staff infection in my right eye. It was swollen and severely hurting me. Well, my doctor put me on sulfameth and a eyedrop antibiotic. I don't mind taking the eye drops, but these pills are making me feel horrible. I am on 1 pill twice daily for 10 days. I asked the doctor and the pharmacist if this stuff causes constipation and they both said no. Well, I haven't been able to use the bathroom well since I started it. My muscles twitch, my eyes are sensitive to the sunlight, I can't go to sleep easily, I've been itching up a storm, and I have headaches. I want to just stop the medication but if I do then I will never get rid of this infection in my eye. I figured I'd stop the meds in the middle of the week. I hate feeling bloated and constipated. Has anyone else had the constipation effect?

Hello everyone. Thank you for sharing your stories. I no longer feel so confused as to what I am experiencing while on Prednisone. I was prescribed this medication for my back (I have a ruptured disc). I am 24 years old. I took a short five day treatment of prednisone about three weeks ago. I was very foggy and forgetful. I was tired and bloated. The worst side effect I have noticed is ACNE! Oh my gosh, I haven't ever experienced a breakout like this before. This breakout is a continuous side effect long after I stopped taking the drug. I went to the doctor again yesterday for a check up on the status of my back injury. He has prescribed a THIRTY day treatment and even more aggressive approach with prednisone!!!! I am so scared to start this treatment because of what I have already experienced. HELP! Does anyone know if the acne will clear up? Will it scar? Does anyone have any tips on this?
Thanks.

I have just come across this site, while looking to find out why I have been experiencing heart palpitations for the past two months - out of the blue!!! and usually "exercise" induced. I had some tests and have been told they are Premature Atrial Contractions "PACs". I started taking Yasmin in April, after having tried others over the past year (tri-cyclen lo and alesse) which did not work for me as the progestin was not strong enough. I am in my 40s and never took the pill before. Yasmin was great, it significantly reduced my "physical" pms (severe inflamation, severe bloating, severe sore breasts) which I experience for 2-3 weeks a month. However, sometime in mid to late June, I started getting palpitations/tremors out of the blue. The first episode freaked me out and lasted for about two weeks. At first I thought it was allergy medication mixed with my thyroid med, which can happen - but I cut out the allergy meds and still got them. They seem to come about 6hrs to a day after I fexercise/figure skate and they last from 2 to 5 five days. It's very irritating and nerve wracking, and I feel very agitated. I am also out of breath more than usual when walking up stairs, a little light headed and have some tightness in the chest. My legs also are weak, which makes no sense given my exercise regimen. I then lowered my thyroid replacement from .125 synthroid to .100 - too much thyroid med can cause some palpitations. Anyone who has mistakenly taken a second thyroid pill having forgotten that they already took one will understand. Even with the lower dose I am still getting the palpilations. I am totally at a loss as to why all of a sudden this is happening to me (perhaps perimenopause??). I have had the odd flutter here and there in my live, but nothing like this. It just doesn't make any sense ag ll. Can one's health just change like this overnight?. I am otherwise healthy, slim, have "lower" blood pressure (apprx 100-90/70-60)I skate 3 to 5 times a week, I have a full time job and yes I do push myself, but this is getting ridiculous. The only thing I can attribute it to is the Yasmin, ... but my symptoms only started after a few months not instantly, whereas it would seem that most of the the women here noticed the side effects faster. I hate to stop the Yasmin because I will have to return to pms "hell", but I suppose I will give it a try to see if the palpitations subside. At this point, I have been offered a low dose "beta blocker" and have refused. I am stunned to think that all of a sudden I have heart issues, especially since my Dr has always kidded me my that I will never have heart problems with my blood pressure. I will stop the Yasmin tonight and post another message in a few weeks one it is out my system. Here's hoping it is the Yasmin.
KarenSkaterGirl

hi guys,

finding your posts so helpful.
i've been on yasmin for nearly 5 years and its only just dawned on me recently that my:
-anxiety/mood swings/erratic behaviour
-body hair growth
-weight gain
-increase in discharge etcetc
could actually be from the pill!!

i was always so bubbly and strong but i seem to cry now at silly things and i just don't feel myself. i initially went on the pill when i was 17 because my periods were so bad but i'm not sure what to do now... change pill or come off pills altogether?!

i'd love some feedback if any of you have been in a similar position, thanks so much

xxx

I received a kenalog injection for coccyx pain March 2007. I have noticed the following side effects: nausea,heightened anxiety, insomnia, night sweats, loss of appetite, fatigue and severe generalized itching. It is now August and I am still experiencing these problems.
I have a question. Has anyone out there noticed their blood sugar
increasing? I am trying to see if this is separate or related to the injection.

Hi! I am a 36 year old female and have been on this HORRIBLE HORRIBLE drug (prednisone) for 2 1/2 years now..... Hopkins doctors still arent sure exactly what i have. My immune system is attacking my liver so to speak. My body is basically looking at my liver like it doesnt belong and is attacking it with large multiple lesions that is eating it away... the good thing is that it hasnt interupted the functioning of it yet but is leaving horrible scar tissue. I have been in and out of the hospital 13 times, have had just about every test imangable, 12 liver biopsies and they STILL have NO clue! They are leaning towards Church Straus desease and Wegners but the weird thing is i have half symptoms of both. The first year they had me on 80 mgs of prednisone a day which had seemed to put me in remission for about 4 months and then they came back even worse so i was put back on the prednisone, 80 mgs a day AGAIN along with 100 cc's of Methotrexate, another not so nice drug... i had EVERY SINGLE BAD SIDE EFFECT OF BOTH DRUGS!! This second time around was ALOT WORSE for some reason!!! My body DID NOT LIKE IT!! Nausea, hair loss, moon face, gained 40 pounds (and i was in great shape, worked out, i am 5'4 and was 110 pds!), EVERYTHING was swollen, legs, ankles, arms, neck, face, had the camel hump, fingers and especially my belly!!! UGH!!! Have bone, muscle, and SEVERE joint pain! Kaliedescope vision, dry eyes and then had mucus discharge (kindof like pinkeye), headaches, intestinal problems.... VERY CONSTIPATED and then the opposite!!! I literally felt as if i had turned into a man in my behind!!! Sorry to be so gross but thats how bad it was!!! Jaw problems, teeth and gums as well, skin sensitivity and have little bumps all over my skin (kindof like tiny little moles), itchy, broke out with acne and pretty much NEVER had more than 1 pimple a month, had facial hair (VERY DISGUSTING!!!! HAD IT WAXED EVERY WEEK!!!!) and then on top of all of that the swelling of my liver not to mention the PAIN! I was recently in the hospital again with 12 new lesions, pneumonia, and 104 fever. My doctors said the Methotrexate was the cause and i was having a bad reaction to it so they now have me on 100mgs per day of Azathiroprine. I am now finally down to a maintenance dose of 5 mgs of prednisone cause my body was starting to reject that as well. I thank god that i am now down to that dose!!!! It as only been 2 wks and the withdrawl symptoms are horrible worse then they were but i know what is to come =) loosing all this fluid and all of the HORRIBLE side effects i listed above. I will have to be on the maintenance dose of 5mgs the rest of my life and can live with that cause when my body gets back to somewhat normal i wont even notice that im on this CRAP!! I will be on the high dose of Azathiroprine for a few years and then on a maintenance dose of that as well for the rest of my life to keep whatever this is that i have under control.... the scary thing is is that they arent even sure that all of these meds will even work...... im a guinea pig..... The only thing that i am on out of all 25 pills/meds that i take everyday that works is my pain meds. Oh and i also forgot to mention that i had to be put on some "HEAD CASE" medication (thats what i call it =) ) for depression. Its a low dose but it does seem to help... I am terrified of what the future holds but continue to be strong and have an amazing support team... my fiance and family =) I dont even want to think about how i would be without them. I go back on the 25th of this month for my MRI so please who ever reads this keep me in your prayers as for all of you are in mine. I feel for each and everyone of you that has to endure this horrible drug everyday and i hope that everything works out you. =)

Sue =)

This was the most appauling medication I have ever taken. It made me incredibly irritable. I almost split up with my boyfriend because I was so unbearable to be around, and also got painful, recurring urinary tract infections. If you're female steer well clear of this one!

Currently on Biaxin XL on a 10-day medication for a Pneumonia infection. Experiencing: increased heart rate, sweating all day long with no fever “Chills” and a bad taste in my mouth.
A possible side effect that concerns me is I have been sweating “night and day sweats” all day long with no fever, since I started BIAXIN XL, I asked my Dr. and I was told sweating helps the body to get rid of bacteria but today is my 8 day of sweating, Strange !!!!
I have never had a problem with side effects in the past on any medication!!!
Anyone else experiencing sweating? Your comments will be appreciated!!!! Thanks,

hi alicethecamel. it might be worth getting another test done now you are off yasmin. when you are told your levels are normal ask for the actual numbers of your tsh. there is a wide margin to what the dr's and labs call normall. to feel at your best you need to be in between 1 - 2. a lot of people feel symptomatic at levels above or below this level. most labs normal is 0.3 - 3.0 but some are 0.5 - 5.0.
hope you feel better soon.

sarah

hi alicethecamel,
just a thought but have you had a tyroid test? you could be hypothyroid and the pill can cause you to becaome more hypothyroid,i had trouble with low moods, heavy period,clotting etc due to an underactive thyroid,it eased when i went on to levothyroxine but started up a again when i went on yasmin but a dose change sorted it out again. unfortunately my experience with yasmin was pure hell/anxiety/depression, emotionally unstable (and sometimes felt mentally unstable too!) regardless of whether you choose to stay on yasmin i would definately get a thyroid (tsh and ft4) test done.
best wishes to you,i hope you feel better soon.

sarah

hi jess,
the symptoms you have could well be down to yasmin,you may be hyper sensative to the effects of the artificial hormones,i think it depends what state your hormones are in before you start taking this stuff. i felt great on it for about six months,pain free periods,slight weight loss,reduction of cycle related acne etc. but then things started to change and i became ill both physically and mentally with no explanation,i felt that way for 1 year until i found this site and stopped taking yasmin,since then all my symptoms have pretty much vanished although they resurface briefly during ovulation-menstruation but that is because my hormones are still out of whack. my advice would be if you are feeling a bit off talk to your doctor and see if there is an alternative to yasmin,if you are starting to feel closteraphobic (sorry can't spell !) and never have before then i would think that yasmin may effect you badly mentally,something to do with oral contraceptives depleting seratonin levels,most of us on this site have had panic attacks/anxiety attacks along with agoraphobia or paranoid delusions,we are not mental it is this pill! some people do really well on it and feel sick for a couple of weeks then improve but i suspect if you are feeling bad after a few days then it may not be the right pill for you. sorry for the long post but it really upsets me when more and more women are being prescribed this rubbish that has nearly destroyed so many women here,all the symptoms we experience are to similar to be coincidental,the one common factor is that we have all taken yasmin.
best of luck to you whatever you decide to do,i hope you feel better soon.

I started on Levaquin for a sinus infection on Friday and by Sunday evening have the most unbearable pain in my feet, ankles, knees and hips. I could bearly move and took 3 ibuprophen and that took the pain away. I'll see if the pain comes back after the Ib wears off. I'm thinking it's the Levaquin.