Ssri symptoms and conditions

I've been on Zoloft 11 years alternating between 50 - 75 mg. This SSRI positively changed my life. From being depressed/anxious/obsessive compulsive I've managed to lead a full happy and productive life.

HOWEVER, the last three nights I've experienced terrible anxiety producing nightmares. Waking up shaking and with my heart pounding, I'm wondering if changing from Zoloft (brand name) to a genertic would cause this problem.

I switched three months ago without any problems. Has anyone experienced the same symptoms, and if so, had you switched to a generic? It seems these nightmares would have occurred sooner if that was the problem.

I am 18 years old. I started yaz three months ago. During my first month taking yaz, i had a really bad fever and started getting these electric shock sensations in my head. My heart was racing and I couldn't stop twitching. I was panicking and will skip the long er story but the doctor told me it was anxiety and an allergic reaction to my cough medicine and sent me home with vicodin and atavan. I got better and didn't have that sensation for the next week. However, I was growing increasingly anxious and panicky for no reason at all and would have long crying jags where I couldn't calm myself down. I am usually a very happy person, and I just feel so depressed. The shocks started coming again, along with the twitching and feelings of vertigo. I started thinking that maybe it could be the yaz causing it and went off it mid pack. I went to my doctor for the shocks and she had no clue. I had a mri of my brain and it came back normal. I have been off yaz for two weeks now, and have since seen a neurologist. She put me on an 80mg prednisone pack which she said would stop the shocks but only have me the worst migraine of my life and shaking so bad that I couldn't function or leave my bed for for four days. I went to a new neuro and am on an new migraine medication which seems to be working better as I am up and my headache is better. He seems to think the shocks are a result of yaz. Have any of you had this symptom, and the twitching? I feel like someone has turned an electricity switch in my body and I cant stop moving. I have no clue whats wrong with me and its really scary. The only way I can sleep at night is with ambien, and I cant stop twitching even during the day. If yaz can cause this why can they even sell this awful pill?

Now I am personally freaking out. I went to see my gyn this morning because I have had terrible anxiety and depression (I suffer from anxiety and depression anyway). I was hoping that it was due to a hormonal imbalance. Well..we didn't do any tests. She put me on the nuvaring to balance out any hormones...to give me a constant flow of hormones.
I am freaking out. I don't feel bad right now. I want this to help not hinder me.
Does anyone have anything good to say about it? I can't take any more anxiety or depression.

I took Lexapro for several years without many side effects. Yawing and sleep problems. Then I had an aortic anysrem and kept taking the Lexapro. Then for money savings I switched to Celexa. I started losing weight, great. Then I start talking like a drunken sailor. I couldn't find any symptoms of speech problems so I figure it was a stoke. MRI says no stoke. I am getting off Celexa and SSRI's all together. I think the panic attacks i was having was my body telling me something was wrong and the doctor and I didn't listen. I just about cost me my life. NO TO CELEXA.

My psychiatrist has me on two 20mg Adderall everyday. He just added Remeron to my cycle and it ruined everything! It's hard to find something for anxiety/depression that works with the Adderall well. I've tried everything but this one scares me. SSRIs and SNRIs usually make my head tingle, more anxious than usual, and unpredictable mood-wise. After starting Remeron for about a week, I had a massive strange hours long panic attack. I tried to slit my ankle, screamed and yelled things at everyone I came into contact with, walked off down the street three separate times (three diff. people had to come find me every time). My skin felt "creepy-crawly" and I was SO angry and couldn't get away from the anger. I'm still waiting on the Dr. to call me but I told his secretary I just am NOT taking it. I'll take the nerves, shakiness, and sweatiness ANY DAY over feeling crazy like that. Angry and wanting to die.. not for me.

I started taking Zoloft in Aug 2007 because I could not get sleep at night...tossing and turning - thinking about all the stuff I had to do the next day. Within a few weeks - that was so much better - my moods were better - and my performance at my profession was better because I could actually relax at night. I had lost all the anxiety that I have had all my life - and couldn't believe that there was something out there that could help me so much. I, at the time, would never in a million years think about stopping this medication. HOWEVER, fast forward to Nov 2008 - the zoloft is still working great - but my sex life with my husband is so bad that it is more like work for both of us...and reaching orgasm was almost nearly impossible. I just didn't desire sex...which is highly unusual for me. These affects of the med increased over time - and I was willing to deal with them - but the thing that changed my mind about it all was my weight gain. I chose to take Zoloft because it had the least chance of weight gain...or so I thought. I had gained 30 pounds since I started taking it. I wasn't working out as much - and so I thought that was it...but when the scale hit 200 - and then 210...on a frame that should be no more than 140 (I was a bit overweight when I started it) I freaked out. I had been working out and eating really well for three months, no alcohol - no extra hidden calories - to the 210 mark - and I had gained weight during that time. I was talking to my doctor one day and out of the blue complained that I had gained so much weight and it was really starting to bother me. He said, "oh yeah, that can happen on ssri's - in some people they can pretty much almost shut down your metabolism". I was in shock...he knew my struggle with weight to begin with - and here - now a year and some later told me this. Needless to say - I felt betrayed, but was then determined to get off zoloft. And so I have been with his help..and it has been one of the hardest things I have ever done...and I am still working on it. It has been two months and I am slowly weening off. I was on 100mg per day - and dropped to 50mg, and now I am taking 25...I get dizzy, the mood swings are awful...AWFUL - but I am doing it...and I will not ever take zoloft again. I never realized how addictive this med was - and just how much it affected me until getting off of it. However, the one thing that I have found to help with the withdrawal symptoms - even the dizziness is working out. It has been my saviour.
Just thought I would pass this along. The honeymoon period is great with Zoloft - it is when you see your body out of control that puts it all into perspective. Every person's body is different, but if you notice that you are gaining weight for no reason - and can't seem to lose it - tell your doctor. There are other drugs out there to help with symptoms that zoloft relieves that do not cause all these side effects...the ssri's just tend to work more efficiently. For all those with decreased sex drive - wellbutrin does not affect this or weight...but isn't as good about sleep.

Having breathing problems since taking yaz?-- I have been reading all the postings on ladies having breathing problems. It has been maybe 7 years ago now, but I feel a necessity to share my story. I had been on Yaz for 2 months. I became short of breath to the point I could not walk across the room without having to sit down. My primary dr did an EKG and immediately had me rushed to the ER for test. I was sent to different specialist and over $10K in test were done within a week. By this time I WAS ON OXYGEN! They ran blood work, test on my heart, lungs and checked my legs for blood clots. I ask my GYN if it could be the Yaz. (the only med I was taking) and he said no- never heard of such. I took it upon myself to stop taking it and guess what!---I immediately was better. I turned my oxygen tanks in, doctor's never diagnosed me and I never heard from them again. I am 34 and have always been healthy with the exception of this incident which praise God was resolved "in time".
However, I would like to share that I now have a Mirena. The first 5 years was great, I had it replaced in May 08 and I believe this second one is not agreeing with me. I bled for 5 months, have a very heavy feeling in the bottom on my stomach, lower back pain, & fatigue. My appt is Jan 29th to have it removed. ******

Hi,

To the first poster: bbk I had the same problem. I've been on Adderall-the regular kind, not XR-since my ADD diagnosis in June.

Whenever I start an SSRI: Prozac, Zoloft, Effexor, Lexapro, my Adderall stops working. I get exhausted, brain fog, and I also get an insane appetite.

I've done some research and the explanations I've found are that SSRIs tend to increase your insulin and lower dopamine. Adderall is supposed to increase dopamine. Basically, the SSRI interferes with the Adderall.

In one appointment with my doctor (while I was on Prozac) he actually admitted that most SSRIs raise insulin, Prozac being worse than others. Guess that explains why my blood sugar was always in the 60s and I felt horrible no matter what I ate or did.

If you're already overweight and insulin resistant it will screw you up more than other people.

I'm currently trying to find an anti-depressant that works well with Adderall.

Taking nicomide while taking Celexa and a b-complex for hair and nails. I read somewhere that nicotinamide may have anxiolytic effect. Not sure if this combination of vit B3 along with the other B vitamins and an SSRI is causing the SSRI to be less or more effective, but have experienced I think a tranquilizing effect, more noticeable at night. But at the same time I feel some depression and anxiety so I wonder if the Celexa concentration is being decreased secondary to the vitamins. I will stop taking all B vitamins for a few days and see how I feel. My work environment lately has been more stressful, too, so it's hard to say what exactly is going on. But will stop all B vits and see how I feel.

I was on SSRI's for a while (lexapro, zoloft) when I finally couldn't take the tiredness, weight consistency, and NO sex drive. So I tried Wellbutrin SR 150 2x a day. Started off at 150 for a few days and felt like I was given a new life! I had never felt so good. Then it was time to increase my does to the 300mg. I started getting headaches, dizziness, my ears are ringing so bad I can't hear very well anymore. So I went back down to 150mg per day. I don't feel as tired, but it's still there. The ringing won't go away and I am still dizzy. The funny thing is, is that I can almost guarantee it's the same time everyday. I get the dizziness and headaches around 3pm, they go away(most of the time I have to lay down) and by about 5pm they're gone, but by about 10pm they're back. And it happens every day like clockwork. I like the way I feel (minus the headaches and dizziness, and ringing) my brain doesn't feel "numb" like I did on the Zoloft or Lexapro, and I have lost a few pounds which doesn't hurt, but I don't think I should feel like this everyday. I want a medication that I can feel good on without headaches and dizziness. And PLEASE no ringing in the ears. It's good to know that other people are experiencing these side effects, I really thought I was the only one.

I have been taking Lamictal since October of 2007. I experienced some of the symptoms (muscle pain in the head and neck) before I started the medication. I have experienced panic attacks since July of 2005. I have had mild heart palpations since I was in my mid 20's (I'm 36 now). I have had what I would consider a below normal energy level since my mid 20's also. Ok so like everyone else I am thinking I'm a hypochondriac! However, I was diagnosed August 28th 2007 with having Lyme’s Disease and also Hyper-Thyroid (same time, same lab-work). Two weeks later I was diagnosed with Bi-Polar Disorder (this is one thing I knew I was battling but didn't know how to handle it). My physiatrist started me on Lamictal and I did the standard ramp up to 200mg. I also was started on a 90 day treatment of Dyoxicycline for the Lyme’s and Methimazole for the Hyper-Thyroid. I was very very weak and was only able to stay awake for short periods of time (4 to 5 hours max). Just an fyi, I am not overweight, lazy or unmotivated. I have the physical appearance of perfect health. This, I think works against me as the Dr's seem to think I'm just whining. Mater of fact; my Primary Care Physician never tested me for Lyme’s. I went to an Urgent Care Center which tested me for Lyme’s disease and I came back positive (they also tested my Thyroid levels and found the problem with my THS levels) I told my Dr the results and he insisted I have same test done again. Guess what, new tests, same results.
My symptoms today are very similar to what I have seen posted many times. Muscle pain (entire body, some areas worse than others), heart arrhythmia, racing heartbeat, intense palpitations, nausea, foggy “un-plugged” mind, fatigue, weak muscles, muscle cramping (especially after repetitive motion, such as strumming a guitar), panic attacks (much more severe) and the latest addition to the group, Insomnia. Muscles pain in my head, fore-head, jaw, temple, neck (front and back), shoulders, is terrible to say the least. The pressure in my fore-head (right under my brow) makes me feel like I need to close my eyes or rest (resting does not relieve anything). The front of my neck is so tight at times it feels like my jaw is being pried down. I could go on and on.
On my quest to find out what else is going on with my body I have had 2 Echocardiogram’s on my heart and abdomen, 2Nuclear Stress Tests, blood work out the wa-zoo, MRI of my brain, 2 CT’s of my Head and Neck, Chest X-rays, Endoscopy, Colonoscopy, and all revealing nothing.
Most doctor’s I have encountered seem to want to treat the symptoms, not the problem/disease. I believe I know why; we (the ones who are there for solutions) tell them what the symptoms are (how we feel). We of course are thinking “this will help with a diagnosis of the problem/disease”, when in fact (I feel); the doctor’s thought process stops there. They don't know what’s wrong with you but they do know what your symptoms are so....bingo, let's treat the symptoms. Don’t misunderstand what I am saying. I’m not saying, “Most doctor’s don’t know what they are doing” or “don’t take your meds”. I am saying you and I are one of the 20 to 30 patients most doctor’s see daily (100+ weekly). They may be caring and good people but they are just as human and fallible as you and I. My advice is this; (and I am taking my own advice) don’t always “pop” into your body what the doctor suggests/prescribes, without doing your own research. Heck most of us won’t buy a car or more importantly, send our kids off to a college with out doing your own research (we just don’t trust those shinny brochures). Your body and your health are worth you doing your own research. Just keep in mind, Pharmaceutical Reps are always at your Dr.’s office (sit in the waiting room for 10 minutes and I’m sure you will see one). Reps are paid to do one thing; encourage (push) the Dr.’s to promote use of the Pharmaceutical Companies drugs.
My wife and I have been doing our own research on Lamictal (after a year of taking this stuff) and the side effects associated with this drug. We have searched through many (many,many) web sites for information and we have talked with pharmacists and Dr’s for opinions. Although I’m am not thoroughly convinced that Lamictal is the cause of all of my symptoms, my wife and I have decided to lower my Lamictal slowly from 200mg to 100mg. I am now taking 150mg daily (three days now) and plan on staying at this level for a total of two weeks before lowering to 100mg. I do fear dropping the dosage to quickly (potential side effects) or lapsing into a mania. To help avoid a manic episode my wife and my immediate family are all “up-to-date” with my course of action. They are on “Red Alert” and have promised to keep a close eye on my behavior patterns and moods. (I don't want to put them through another hyper-mania episode, its much too devastating). I do want so badly to feel healthy and alive again and at this point I am rather frustrated with the Dr.'s ability to help me achieve this goal. Remember it is called “Practicing” Medicine. So now I’m going to practice a little, very carefully and cautiously.
As a foot note; I have recently (past two weeks) been re-tested for Lyme's with a negative response. I am keeping in mind Lyme's test are very inaccurate (still hoping this one is accurate). My thyroid is under control and normal, so.... let's see if dropping below 150mg of Lamictal will eliminate some of these other symptoms. I will keep you posted.
Erik

I have been on Paxil off and on now for about 5 years.... the current length of treatment for the past 1 1/2 years. I need to be on it ( or something for that matter ) for my panic disorder. I am a 36 year old nurse/ manager and some days was almost debilitated by panic attacks. Depression was part of it, but not nearly as much as panic. I must say, that I have been experiencing memory loss now for about a year.... I thought maybe it was due to overwork/ stress...which I do understand it COULD be. However, I find it interesting that I am seeing so many more people with memory loss than I imagined. Is it due to stress in this type of people's lives, or is it in fact, the drug Paxil?
Keep in mind this is an SSRI ( Serotonin Reuptake Inhibitor ) ~~ even though there is no solid evidence (YET!) this is a side effect of the drug, I would bet my license on the fact that that it is!
I have tried time and time again to wean myself off of Paxil.. ( with and without my Dr's advice )--- I did succeed for a few years to be without the medicine, however being on a slew of other meds in the interim did not help as much for the panic as does the Paxil. Paxil, honestly, scares the hell out of me!
Besides the "numb emotions", memory loss, sexual appetite decrease, yawning, lack of sleep, etc... the side effects of coming off of it are worse! As I read earlier, it IS addictive, indeed! The brain gets used to the drug being there ( as with any addiction ), and the "surges" of dizziness, sweats, and out-of-body-like experiences I experience coming off of the drug are excruciatingly harder to bare than the depression itself. Those above symptoms of withdrawal are just that....withdrawal!
Once your body is "allowed" to reuptake serotonin (as it is supposed to), this is when those symptoms raise their head...sometimes for weeks or months until they subside.
I would welcome anyone with help on this matter---is there another Drug out there that can help with anxiety/depression symptoms, and not cause the plethora of side effects we have all discussed here?
Diane

One 37.5 mg Effexor XR and I thought I was a dead woman. I was BURNING HOT for 12 hours. I had a massive headache and I felt like I swallowed a brick my stomach hurt so bad. I was vomiting and trembling bad. Doc said he would consider that an allergic reaction and prescribed Celexa, which took 3 days to make me hypermania and I almost called 911 when my G.I. tract started burning. So this week he gives me Cymbalta, what is he NUTS? He let me try a small amount of xanax which doesn't give me side effects, it just releases that feeling of impending doom that I have 24/7. He says I can't have any more though, it might get me addicted. I can't imagine it being worse than what I have found online about SSRI's.

HI I AM 37 YEARS OLD AND 1 WEEK AGO I WENT TO THE DR FOR HEADACHES EVERY DAY, AND MY DR TOLD ME IT HAD TO BE DUE TO STRESS, BECAUSE MY BLOOD TEST AND PAP SMERE CAME BACK NORMAL AND I WAS PERFECTLY HEALTHY. SHE PRESCRIBED CELEXA AND SAID THIS SHOULD HELP. ALL OF A SUDDEN I HAVE NO SEX DRIVE, HEADACHES, NAUSEA, DIZZY, LOSS OF APPETITE, SHORT OF BREATH, MOUTH IS DRY, VERY EMOTIONAL, MY WHOLE BODY ACHES. IM GOING TO THE DR. AND HAVING HER TAKE ME OFF I WOULD RATHER JUST HAVE THE HEADACHES. DOES ANY ONE ELS HAVE THESE SYMPTOMS?????

I am 30 years old and have been put on Depo Lupron after a laproscopy to help with endometriosis. I am 2 months into a 6 month course (one shot every 3 months) of Depo Lupron and my life has drastically changed. I started feeling life altering hot flashes and night sweats two days after the first shot and nearly drown myself in sweat 24 hours a day. I experienced a little postpardum depression after giving birth 6 years ago but have found myself sunk into a sinking hole of depression and anger like I've never felt before. I bawl at McDonald's commercials and become enraged if the dishwasher isn't loaded properly! I am ecstatic one minute and severely depressed the next. I have even had thought of suicide since being on this shot. I am normally a very outgoing, athletic, cheerful, happy person - but since taking this shot, I have become a stanger in my own head. I tell my family all the time that I need to "go stick my head in the freezer" to cool off because of the horrific hot flashes. I have to carry a handheld fan with me 24 hours a day and sleep with ice packs to keep cool. Since the shot started 2 months ago, I have lost all sexual drive, am thoroughly exhausted by 9am and find myself crying at my desk at work by late afternoon because I am so tired. My family thinks I am going crazy and I've never fought more with my husband. My daughter has gone to grandma's for awhile because I'm just so tired and irritable that I feel like an awful mother. Migraines have also come full circle since the onset of the shot as well as blurred vision and shaky hands. I'm a little achy throughout the as well. I know that everyone responds to medication differently, but I'm finding a lot of people with the same side effects as myself and have to wonder why the doctors don't warn patients about these types of problems before prescribing medications such as Depo Lupron. I don't think I'll be going back for the second shot. Could it get any worse?

I have been on Lamictal for about five months for bipolar II. I has been increased slowly over these months and I am now up to 300 mg a day. I have a tendency to sometimes forget things but remembering numbers has never been a problem for me. In fact I can look at someone's tag number driving down the road and remember it for days. Phone numbers of people I have known for 20 years would stick and I wouldn't even have to call them on a regular basis to know the number. However, recently while trying to use my bank debit card at the store I was asked to enter my PIN number and totally could not remember. I tried it several times but it never came to me. I felt like a fool!. At this time, that was three days ago and I still cannot remember it!

This is very, very distressing to me. I feel like something has been wiped clean and that I will never get it back.

My Lamictal dose has been increased in the last couple of weeks and I thought maybe Lamictal or one of my other meds could be making this happen so I started researching and found this site where other people were complaining of memory loss while on Lamictal.

Headaches are another common side effect for me while on this med. It has really helped me emotionally and I need to know if the memory loss is just going to be a temporary thing and it will get back to normal or if I will be forgetting more and more over time. PLEASE HELP!!!

Left-sided chest pain from about one week onwards of taking 20mg of this drug; been on it for less than a month. Had lots of heart and lung tests in A & E to no affect, ie, they cannot find anything. It is intermittent, about 3-4 times daily, from one quick stabbing pain to about 10 mins; it gradually dies down. Taking deep breaths is not advisable due to the pain, but I just take more shallow breaths. These episodes do not bring with them any other side-effects, although of course I usually stop what I am doing. Nothing particular brings them on, I can be just lying in bed with eyes closed and have just woken up. I have been on this drug last year without chest pain. Not taking it for depression; taking it for although health worries, with my left thigh feeling 'strange', therefore, I think I have every muscle wasting disease under the sun. No therapeutic affect as yet. Is the chest pain due to the drug or something else? I could only find chest pain as a side-effect on the *****website; not in the British doctors formulary (BNF) at all. What's going on? I am close to asking to change to Cipralex, similar to Paroxetine.

I am soooo glad I found this website!! Please read further!!!! I had a horrible experience on the NuvaRing. Can't even begging to explain, but I want to express my knowledge to anyone that is on this site. I think doctors should ask every patient that requests the NR if they have had or have symptoms or have been diagnosed with depression, or at that, any mental illness. With women most mood disorders are somewhat hormonally linked along with some kind of chemical imbalance. The ring has a very strong hormone in it that can cause all sorts of problems for women in this category. However, it is probably great for some people. I was only on it for 2.5 weeks and I was screaming at my fiance for no reason then I would lay in bed and just feel hopeless and cry for hours. I know I have suffered from depression for a great deal of my whole life, but I had it under control until I put that little devil inside my vagina. We, my finance and I, thought it would be great to not have to keep forgetting pills and having a pregnancy scare once a month. We didn't link the two together until I told my therapist that I started the ring and he told me to immediately take it out!!! He said DEPO and NuvaRing are a big "no-no" with mentally frustrated patients. So, to all you ladies out there, the ring is good if you have never been to a psychiatrist!!! If you are on any type of SSRI or Benzo's then you obviously have a mental thing going on....stay away from these type of BC's because they are just simply toooooo strong. I hope this helps doctors and patients.

This medication was a life-saver for me when I first started taking it 7 years ago. Unfortunately, every so often it would stop being effective. My Dr. would up the dosage until I was on the highest and could go no future. So I set out to titrate off, which I did very slowly, but it was hell. The worst was when I was finally done. I felt like a junkie. I was shaking, having crazy brain zaps that made me feel like I was being shocked every time I'd close my eyes. I was sweating like a pig. My sleep was was filled with terrifying nightmares that left me screaming out in my sleep. I am 5 weeks off and still experiencing nightmares, and a few mind-zap things-but nothing like they were when I first started to come off. Yoga and meditation seemed to be the only things that helped. Each day I wanted to take it again just to feel normal. No one can believe that a common SSRI can have such horrible withdrawal effects, so I am on a quest to educated everyone I know.

My name is Candyce Donovan and I am a healthy 38 year old ---healthy except for an occasional cold or sinus infection. A few years ago I was put on the drug Singulair to help cure an allergy type infection. I was only on it for a few weeks and discontinued it myself because it was making me worse. Earlier last year, I went to a different doctor for the same type of thing and was put on the drug again. At time while on the drug I had a few "episodes" where my body was shaking while I was sleeping and I thought I was just having a bad dream. Then in August of 2007, I experienced 2 grand mal seizures while sleeping each one lasting about an hour from the time I had the seizure til the time I came out of it... and was in the hopsital for 2 days. I had numerous tests done and things like a brain tumor etc were ruled out, and it was the conclusion of the ER doctors that my seizures were brought on by a very bad case of sinusitis as that was the only thing that showed up on my tests. At that time my sister brought in the medication that I was on at the time...the Singulair...and the doctors said that that would not cause seizures. The Neurologist that I went to disagreed with them and said that we would never find a cause. I continued on the drug until early December , having another seizure in November. I have now since November, moved in with my sister for the 6 months or more that I have been with out my license as in NY state one cannot drive for 6 months after having a seizure....you have to be totally seizure free for those 6 months, and it was the advice of the doctors to not stay alone. I went to see another Neurologist who again said that there would never be a known cause for the seizures, and in fact he diagnosed me with having epilespy/seizrue disorder....up until August I had never had a seizure. An uncle of mine had seizures when he was a baby that lasted until his teens but the Neurologist stated that he didnt think that was passed on to me. With the recent findings with the Singulair drug that are on the website now...I am finding that I have had many of the side effects and I believe this was the cause of my seizures as my seizures co-incided with the frame time I was on the drug.

I'm a 35 yr male and have been dealing with depression/anxiety for years due to current & past issues in my life. This post IS dealing with singulair side effects but want to give some history as to why I think it's singular and not something else. For the past 2 or so years I've been using xanax which has worked fairly well in controlling my anxiety, but my doctor preferred I stop taking it because of it's potential for abuse. I've been on SSRI's before and I hated them, so I did some research and decided to try wellbutrin which works differently from the SSRI's. I was still using xanax while ramping up on wellbutrin the end of February. To my relief, the wellbutrin started working wonderfully - felt like I could cope with life, increased energy, better mood, with no negative side effects (actually some positive ones) - the only problem I was having is I traveled during this time frame and developed a bad case of sinus rhinitis due to the climate changes. I've had chronic sinus problems my whole life so it's no surprise. I tried most otc meds and nothing was helping. In the meantime I was feeling so much better (other than the rhinitis) that I decided to start tapering myself off the xanax. When I got to the point where I'd stop taking the minimal dosage I would start getting physical withdrawal symptoms (headaches, dizziness, etc) which is fairly common after taking for a prolonged period of time. The side effects were strictly physical - no excessive anxiety or psychological craving My sinuses were still really bothering me so I had two reasons to visit the doctor - try to get something to relieve my sinuses and to get a short supply of a benzo with a longer half-life to ease the withdrawal from xanax. The doctor gave me a prescription for a month of diazepam and 9 weeks of singulair samples. That was 3 weeks ago. I immediately begin using the singulair, but still had some xanax left so I decided to continue on a minimal dosage and use it up before I went to fill my rx, which I just started several days ago. Coinciding with when I started taking the singulair, all the positive benefits I was feeling from the wellbutrin just suddenly stopped. My depression and anxiety came back worse than they were before - another persons post describes the change in me: feel very anxious, fearful, reclusive, depressed, that everything is going to go wrong, or is always wrong. I'll have extreme anxiety about small everyday things. I’m unable to concentrate. I've also become more irritable, argumentative, and aggressive. I have difficulty falling and staying asleep. I also experienced a very noticeable decrease in sexual energy after a very noticeable increase which is a side effect of wellbutrin. I can even understand the rationale for suicide just to be free of this emotional nightmare - not that I would do it - but can understand it. I couldn't figure out why I went from finally feeling good about life to suddenly feeling worse than ever before. I guess I didn't realize it right away because my sinuses were much better, but I know these symptoms began occurring very shortly after I started to take the singulair. I was trying to figure out what was going wrong with me and yesterday I did a web search on 'singulair side effects' (since it’s the only variable I could think of that changed within that time period) and came across this site and several similar ones. It blew my mind how many people were talking about the exact things I was feeling. Yesterday was my last dose. Does anybody know how long it takes for this crap to work its way out of your system after 3 weeks of use???

has anyone suffered from postpartum depression put on the pill to see if symptoms go away and was feeling worse? I swear this pill did me in. I am still dealing with ppd but it has been a month now that I stopped loestrin 24 and I feel so much better. I still have rough days though not to bad. I swear I am ready to file a lawsuite on this company and my doctor who kept pushing it down my throat instead of getting to the bottom of it they madi it worse with this pill. Good luck to everyone. I hope you do not have to suffer as long as I did

I'm so happy I found this site. I've been thinking I'm crazy or just getting old for the last 3 years while on Yasmin. I started taking it at age 29 and almost immediately after started having mood swings, extreme irritability and depression. I had previously been on Ortho Tri Cyclen and the Ortho Cyclen before Yasmin and was on them for MANY years and never had one side effect. I only switched in the first place because I like to have very very few periods and I run all my active pills together to forgo periods very often and I was having breakthrough on the Cyclen. Hence, the Yasmin trial.

I'm actually a doctor (which is why I CANNOT have frequent periods with all the accompanying issues), but I didn't even realize the possible connection between IBS and Yasmin. This needs to be studied and taken seriously. I never once had IBS symptoms until a few months after starting Yasmin. Now, 3 years later I have almost constatnt trouble, to the point everytime I eat I run for the bathroom, yet my weight has never been higher. I asked a GYN friend at work if they could be related and she said definitely no, but reading all of these "real life" examples, coupled with my own experience has made me think otherwise. Often, the symptoms will occur shortly after taking the pill, even when I haven't yet eaten breakfast. It's crazy!!

I'm going to switch either back to Ortho Cyclen or to something new ASAP and will report back. I'm both excited at the thought that my "IBS" might really be Yasmin related but also scared that it might not go away and therefore might really be IBS. I'll report back... It honestly never entered my mind that all of it could be the Yasmin. I had just moved, started a new job in a town I hate and I thought it was all stress related.

I've also had an interesting side effect no one has mentioned yet- my hair texture has dramatically changed. It isn't falling out, but has gone from VERY curly with a nice soft spiral curl pattern to very dry, straight and hard to manage. Nothing else has changed and now I'm wondering if it's not the DRSP. If pergnant women can have hair changes, why not women on the pill?? It's all hormones.

As always with a drug, there are always possible side effects. No one drug is perfect, and humans are so complex in their make up and they way they process drugs. Therefore, please don't judge your family docs or GYNs too harshly as not even the best doctor in the world can predict every side effect.

Where do I begin??? I have been taking Yaz for six months. Migraines! The worst migraines ever, I cannot function for one full day and sometimes more, the pain was so intolerable.

Hives! For the past two months, I keep thinking that I had a food allergy; even my doctor diagnosed it as that. After going to the allergist, I was told that I have developed an allergy to the Yasmin pill. No part of my body has been discriminated with this medication. Hives from the top of my head, in my eyes, right down to the bottom of my feet! This has been the worst experience of my life with this pill.

Fatigue to the extreme! I fall asleep sitting up and never feel rested. Yaz has caused me to go up two cup sizes so far, I went from being a 38C to a 40DD and I can't fit into anything. My boobs are sore a lot.

Weight gain, at least 20 pounds heavier. Nausea; Indigestion; Diarrhea & Constipation; Decreased Sex Drive; and Mood swings; Uncontrollable Rages; Severe body aches; Hot Flashes/Chills; Crying Spells; Blurred Vision; Lack of Concentration; Trouble sleeping; Dizziness; Shaking; Restlessness mainly after 9pm when I should be winding down to go to bed; Terrible night sweats; Never ending cravings for junk food; Inability to cope with stressful situations; Feeling of being inadequate; Can’t concentrate; Gassy; Hate family & partners; Irrational.

Kim,

please remember, that being off a bcp (not only Yasmin or Yaz) for only 6 weeks really isn't very long!! Most doctor's say, that it lasts at least up to 3 months for the chemicals of the pill to leave your body completely, because it's not only in your blood but also in your tissue, and getting out of there takes much longer than getting out of your blood!! (That's another reason why drinking loads of water is so important!!!)

So even if your hormone levels maybe at the same stage than one year ago, there maybe still the side effects of Yaz, that you're experiencing, on top of the hormonal problems you've mentioned!!

Please Kim, try to stay strong and give it more time, 6 weeks off that pill really really isn't enough to say, you have to feel well again at once!! This is no cold or a flu we are or were going through!! Hormonal problems can't be solved within a few days or weeks, it definitely takes months (should be clear alone by the fact, that our cycles last about one month!).

And if you feel that an antidepressant might help you, please give it a chance. I still don't know if you had already tried the Valerian, I've mentioned a few posts before (well, although, as bitter RN told, you should not take it together with other antidepressants as ssri or such!!). I found this a very good little helper during my hardest days. It always helped me to calm down and at night it helped me to sleep. Please think about it.

Best wishes to you and I'll send you all the strenght I have left over to stand this Kim!!

Silke