Possibilities symptoms and conditions

I've had my Mirena since April of 2009. Since, I've gotten severe cramps, irregular bleeding, loss of sex drive and motivation, lack of energy, severe mood swings, and MAJOR hair loss. My hair loss probably started around August. When I went to 2 doctors neither one of them thought it was from that. They are still testing me for possibilities. I'm thinking that maybe it's time to have it removed.

All I can say is OHMYGOD! I had no idea about all these side effects. I had my son April 4th, 09 and had the Mirena placed October 21st. Since then, I have been constantly spotting, I have headaches, and no motivation to exercise. I have been moody and felt overall like blah. I have noticed some joint stiffness and discomfort in my hands as well as muscle tenderness in my legs. I have not experienced any weight gain or loss at this moment, nor have I noticed a change in hair loss...but will definitely be aware of the possibilities. Well I have a appt. for my follow up, I am going to inform my doctor of my side effects as well as yours, and see if this really is the best option for me. The last thing I want is for this to inconvenience my life when I got it just for the opposite...Good luck ladies!

severe abdominal pain, colitis, inflamed colon, arthritis, staphylococcal, scarlet fever (which is the advanced stages of strep throat)hair loss, severe headaches.
2 E.R visits, 1 hospital stay of 4 days. When I informed doctor of the possibilities of gardasil vaccination -within MINUTES released daughter to go home and make an appointment with a gastrologist

Sorry to keeping annoying y'all with more posts from me, but I have another question. I noticed that my symptoms were worse with Yasmin's generic, Othello, than they were with Yasmin. I am not knowledgeable about generic drugs vs. brand-name drugs, but I wonder if there is something different about Othello that my body doesn't agree with. Just a thought... Any comments???? :)

This website is a joke! After I had my Mirena inserted 4 months ago I started reading on the internet about possible side effects. I was furious with myself that I hadn't Read up on this before the appointment. There were so many horrible reviews involving hair loss, weight gain, acne, and mood swings! I was so scared and actually thought about removing the Mirena that week. I then found multiple reviews on websites not owned and operated by other drug companies that are trying to scare people in order to prevent the sale and use of the Mirena and the side effects listed here were a 180 degree difference. I have not experienced any weight gain, in fact, I recently was able to shed 5 pounds from picking up running again (so it is possible to LOSE weight on the Mirena as well). I have had zero hair loss, have not had a pimple anywhere or any random hair growth. My live in boyfriend and I have discussed if we've noticed any mood swings or changes and my mood which is usually optimistic and positive has been the same since I had the Mirena inserted. My periods are much lighter and although they can last an extra day or two more than what I was used to, they are light and I have not had any cramping. I'm writing this review not because I absolutely love the Mirena, I think it's a fine form of BC but who LOVES their BC, isn't it all kind of a pain. The Mirena is by far the most convenient form of birth control and I don't worry at all about missing a day and the chance of getting pregnant. I'm writing this review because I encourage everyone to talk more with their doctors about the side effects and look around on the internet for REAL websites.

I have been on the NuvaRing for over a year. I chose it because the medication I was taking for a neck problem was not safe for pregnancy, but I wanted to have the ability to get pregnant quickly once I was off the medication. I had no side effects or issues at all while using NuvaRing. Of course there was spotting and irregularity when I first went on it, but that is standard when there are hormone changes. Periods got lighter and shorter over time, and that is one of the stated side effects. My neck problem is resolved and now I am going off of that medication. So I did not re-insert a NuvaRing this month. Wow, what a change! I am having horrible hot flashes and night sweats. So two possibilities as I see it: 1) these perimenopause symptoms are with me for the next few years and the NuvaRing was holding them at bay, or 2) my body was expecting NR and its associated hormones but since it didn't get them, the resulting hormone changes are causing short-term hot flashes and night sweats. I sure hope it is the latter. But either way, I can't see where NR is at fault. I would recommend it.

I took Yaz for a couple months and was fine during that; however, about a month ago my doctor switched me to Yasmin(I have been on BC for years however, the ortho brand). I've been in the most pain in the past month than I ever have and I'm usually pretty good with pain and just try to take advil or something... but the symptoms have only gotten worse. I finally decided to google my symptoms and I found a lot of people on Yasmin had very similar symptoms. I have the worst anxiety like there's a lump in my throat and sometimes I'm literally grasping for air and I always try to drink a lot of water or cough or eat or burp to make it go away but it doesn't until I wake up the next day (sometimes). Also, I have never ever experience migraines in my life, but the past month I have the worst headaches imaginable. It happens at least 4 times a week; at first I thought they were caffeine headaches because it would sometimes help, but the past 3 days my headache has pretty much been constant (usually located near my temples/eyes). I take probably 8 Ibuprofin a day and drink an excessive amount of caffeine hoping it will make it go away, but it doesn't. Along with these problems I've been feeling lightheaded more often and usually have to sit down immediately or else I feel like I'm going to faint. The biggest/scariest symptom is my heartbeat and chest pain. Heart disease is extremely dominant on my moms side and almost all of her siblings have already had at least one heart attack. Lately my chest will hurt extremely bad, then I feel like my heart rate is just freaking out; I can feel my heartbeat from anywhere on my body and it's very intense. And then because of all of this going on, I always start to freak out and realize i'm getting extremely anxious so I try to make myself take deep breaths but nothings works. The past 4 nights I've been up til like 4 a.m. because my heart rate is so high and my chest hurts so bad in every position I try to lay in that I'm constantly moving. I never thought about going to the doctor because I thought it would get better but now I'm starting to think I should... I'm just wondering if anyone else has/had any of these problems from this medicine and if you've done anything to get rid of them.

(a couple other minor symptoms I've noticed recently are: joint pain and rapid memory loss (I'll be in the middle of a sentence and completely forget what I was talking about and blank out))

My doctor thinks I might have PCOS, which is why I went in the first place after reading up on the subject. I've always had random periods, and if I miss a couple months, they can last up to a month with heavy bleeding. I thought it might be wise to go get some help in regulating. At 27, I'm tired of 15 years like this. She gave me Loestrin24Fe because when I took birth control in high school for about two weeks, I turned into a raging monster that would have attacked anyone.

I'm on my second week of the pack, and bleeding heavy. I have an opposite schedule than most people (I'm naturally a late night to early morning person and no amount of work changes it) so I take it when I get up in the afternoon (around 5pm). I've been bleeding the same way I bleed when I haven't had a period in four months. This? Is unacceptable. If I wanted unreliability, I'd have just avoided getting an OBGYN in the first place.

Reading the side effects and replies here, I'm also wondering if the weird episode I had last week is related. I woke up dizzy when I went to the bathroom. I remember getting dizzy twice in there at random times, nearly falling against my tub, and then falling in my bedroom, passed out for a couple hours. I also had a severe migraine, like no lights could be on, not even the computer as back lighting so I don't stumble in the dark. I'm lucky that I wasn't concussed, but this is just not okay.

Later today, I'm going to call my doc since I need to call my endocrinologist anyway for sick meds. And I'm stopping the pills today. I got off my bed after takeout last night, to clean up, and noticed this insane amount of blood underneath that bled onto the mattress. No more of this.

I'm glad I found this page. My husband has incredibly severe asthma and one of his doctors has decided that he needs to stay on antibiotics constantly (don't agree, don't understand, they won't listen).

Anyway, my husband showed up at my job today and told me he didn't remember dropping me off at work and he had no idea where he'd been all morning, he just "came to" in a KMart parking lot with 1/4 tank of gas missing. We stopped by the bank, stopped at a gas station for a coke, he dropped me off at work.....he doesn't remember anything but getting in the car at the house. He's seemed a little quiet, but he wasn't "out of it" or anything, but he remembers hardly anything from the last three days. After a few moments of sheer panic and running through possibilities (like a mini-stroke), I remembered the doctor had changed his antibiotic to Avelox and that I'd had a similar experience a few years ago with an antibiotic. I did some research on line and the side effects listing for Avelox was INSANE! Why do they prescribe this stuff so quickly??? We, too, received samples, so no insert was included - no warnings. He feels awful and he's sleeping as I type, and hopefully things will improve once it's out of his system: I've got my fingers crossed!

I have been on the NuvaRing for about three years now. It is great, I loved it. For the past year I have been experiencing the most awful cold sweats. They last for about two weeks on and off all day. Then subside for two weeks or so. I can not seem to find an answer as to why. My gyn told me that if it doesn't coincide with my period than it has nothing to do with it. She suggested a tooth infection...it wasn't. I am beginning to think it is the NuvaRing...although not sure because I have yet to find someone with a similar symptom. I just don't understand why now after I have been on it for soo long without a problem? That's the only thing making me wonder if it is a side effect of the NR or not. I took it out about two days ago....Has anyone experienced this reaction? This has really become unbearable.

I have had this thing in for 6 months and feel the side effects have gotten worse. I spoke to my doctor about the hair loss, fatigue, weight gain and general feeling that nothing makes me happy, she suggested I check my thyroid levels. My results came back as in the normal range, she said maybe I should check with my primary care to discuss other possibilities. She said the hormone in the Mirena is a really low dose and shouldn't be causing these side effects.
I still made an appointment to have this taken out because after doing a little more research I am completely freaked out by this thing. I have an appointment in 2 weeks and will let you know if I go through with it and if it does make a difference.

Yes, kenalog has many side effects with SOME people. I'm both a patient that takes kenalog and a third year medical student. I've been receiving kenalog injections twice a year during allergy season for the past 5 years. All I can say is THANK GOD. I can deal with a itchy/running nose, the sneezing, and the itchy eyes. What I cannot deal with are the asthma symptoms that act up whenever my allergies do. I get little enough sleep as is, what I do get doesn't need to be interrupted by waking up not being able to breath.
What must be realized here is that however many posts are on this and like sites, the people who suffer from the side effects are in the minority. For most patients this drug provides great relief with little to no side effects.
For those who said that their doctors did not tell them what they were being given, or warned about the side effects, yes, those physicians should have warned their patients about the possible side effects. HOWEVER, it is also YOUR responsibility as a patient to ASK what you are being given, and what the possible side effects are. Never let anyone just stick a needle in your butt without asking what the heck they're doing first. I'm not defending those physicians that don't tell the patient what they're doing; they are in the wrong. But they see tons of patients very day, most of it route. And many patients lack the knowledge to ask what they are being given, and what might happen from it. Even if the physician took the time to explain, a lot of people wouldn't understand or simply don't care. Don't be one of those patients. Ask your PCP: what is this drug? what does it do? what are the possible side effects? what percentage of patients experience these side effects?. Take some responsibility for yourselves.

When taking YAZ there is only one question to ask yourself, do you feel lucky? Well do you? I am the fiance of the daughter of y_oung_a_american_z_ombie who was laid to rest on Aug 4, 2008. (See posting) She was misdiagnosed with pleurisy by what we thought was a trusted doctor, and passed away from a pulmonary embolism. I want all who are planning to take this drug or currently taking this drug to know that YAZ is a silent killer. Be aware that although you may tell your doctor that you are on YAZ your doctor should look at ALL the possibilities when making a diagnosis. God bless and watch over those that have perished at the hand of this crap and also to the survivors who are telling the true story of this "Wonder drug"

My 9 year old son only took Singuliar for about 5 weeks. He had side effects almost immediately, he was so aggressive, angry all the time, headaches, stomach ache and feeling like he was going to throw up, bad nightmares, a horrible rash, biting his nails, not focusing in school and got into trouble all the time, no appetite but his little body seem puffy all over. He has been off this medication for 3 months and he is still not 100%. He cries at little things and still has the same rash and with meds it is not going away. He had to change schools as he still was having problems in school. He just seems like he is not the same little boy and something is just not right. I do not know what to do at this point. Doctors say it should be out of his system by now, but if it is than there is permanent damage to his brain as he is just not the sharp little guy he was. We have had to take him out of all sports. Anyone else having these same problems???

Hi ladies... I'm not surprised that you folks comprise most of the posting population considering the fact that this drug is prescribed to you. Well I'm quite interested in this drug and I do prescribe it to my patients however I am surprised at the magnitude of side effects listed here. I am based here in south-east Asia and I do prescribe Yasmin to my patients and I rarely here of these side effects. Perhaps this can be contributed to the fact that it (Yasmin) is available here under a different brand name however consists of the same chemical position. I am interested in the ones available in the U.S. Does anyone know how I may go about purchasing them. You can contact me personally on ****** thank you.

you can't seriously think you got PCOS from taking Yasmin. PCOS is a syndrome, and taking the pill is used as one of the treatments for it.
One of the possibilities is the it is genetic, and it can be caused by insulin resistance or problems in your adrenal gland. You can't possibly get PCOS from taking yasmin. And PCOS does in fact increase the risk for cervical cancer, cardiovascular disease, and Diabetes, but has nothing to do with taking the pill or not.

As a pediatrician I write for Singulair every day.
The medication is for allergies.
Allergies cause a cascade of event that I will describe:
adenoidal swelling, leads to snoring + sleep disturbances. Poor sleep makes the child tired the next day leading to less attentiveness, hyperactivity and eventually acting out.
Almost 4 out of five kids with allergies have those subsequent symptoms, and more.
Over the years the child poor behavior his parents, teachers and peers respond of criticism/ ridicule, and punishments, cause the child to feel inadequate, embarrassed, frustrated and eventually depressed and suicidal.

Yes, Singulair does cause behavioral change but they appear within the first couple of pills, the rest is due to allergies and lack of medical care, i.e. sleep, Singulair, and Zyrtec deficiency.
Allergy shots cause 4 times the incidence of suicidally than Singulair, and Ritalin 10 times more.
Check it, it's true.

Living with our 13 year old son for the last 7-8 months has been like H--L, and now to read about all of this, we've taken him off Singulair as of last night. We've been completely at a loss why the sudden shift in his behavior, and we assume too it was hormones. Now, he's just started seeing a chiropractor for his recently diagnosed scoliosis, so we thought maybe the scoliosis was affecting his moods, which it could be, but the Singulair sounds more like it. I myself have been seeing a chiro for 19 months for a very bad back and have seen the great results (I could barely walk and was waiting to meet with a surgeon - happy to report I've not had the operation after all), and I've just finished reading a great book I encourage you all to read called One Minute to Wellness (and I'm not religious at all but this book really opens up the alternative possibilities of chiropractic care). I had heard before how chiropractic care has helped many with asthma, so we're hoping that our son's chiropractic care for his scoliosis will also help his asthma. It is worth considering. Our kids health and our sanity are worth it.

My sister died of a heart attack after being on lisinopril for a month and a half.. She had no known heart problems..

She passed away in 5 am. The evening before she told me that she was going to stop taking lisinopril because of the side affects.

I miss her so much.

My 11 year old daughter finally told me been having suicidal thoughts since Sept. 07. Changed her class and started seeing a counselor. My 8 year old son says he can't control his body - often in a suffering tone. 8 year old son and 10 year old son having trouble concentrating in school and turning in home work - staying on task. Stopped Singulair - two weeks later counselor is ready to release daughter from thereapy. Much happier girl. 8 year old tells me he is on cloud nine - I think he trying to tell me he feels in control of himself and able to handle every day situations. 8 year old also had nightmares - gone now. I am angry that my children have taken this drug for the last 3 years every day. You always think medications are here to help -not hurt. I have learned my lesson. Dr's are quick not to blame medicine but try to rule out all other possibilities. Sometimes parents don't have time to do that. Just think, I could have lost my only daughter if this info hadn't come out.

I started taking Yasmin 2 years ago, and after about the first 2-3 months of taking Yasmin, I started experiencing horrendous pains after sex. Once my doctor figured out what was going on, I was diagnosed with Endometriosis. Not long after that, I was diagnosed with Polycystic Ovarian Syndrome. Now I am more than likely unable to have children, and am at risk for cervical cancer, cardiovascular disease, and Diabetes.
If anyone else has recently been diagnosed with Endometriosis, or PCOS after taking Yasmin....PLEASE reply or contact me!!!!!!!!!!!

I am glad to have read the post below me.

From the majority of posts on this forum, it makes it seem as though Yasmin is an evil poison that the medical community is using to destroy women. I was seriously frightened after reading all the comments. While I do believe all these women about the negative effects of Yasmin, there must be some out there who are pleased with this pill. Everyone's body is different. I have been on it for only 5 days now, so I can't really say anything yet.

I will report back after 3 months or so, unless I have gone bald, blind, insane and bed ridden with head-to-toe pain at that time. I guess that could happen but I really hope it will simply calm my awful menstruation and help my husband and I delay pregnancy while we work on being able to afford to at least take care of ourselves.

When a class action lawsuit is filed, let me know....this drug should be taken of off the market immediately. We started all of this with an OB/GYN that prescribed this “miracle pill” and now have had to go not only to our primary doctor, but also a psychiatrist, gastrenologist, college campus counselors, psychologists, psychiatrist, and the campus medical doctors; All the while, accumulating enormous doctor bills. All the doctors say, "No, Yasmin won't cause those problems" (except the college campus doctors..wonder why? Hmm.. could it be that they are not in private practice?)....well, I beg to differ. Everyone needs to give this website to their doctor so the doctors can hear from the patients that have taken this drug, and not listen to the pharmaceutical companies that are pushing this drug to be the "miracle pill". Maybe if enough people complain and go to the media, we can get rid of this drug!
My daughter who is 18 was put on Yasmin because of irregular periods, hormonal imbalance, etc. We were told it was the new “miracle pill”. It will make you loose weight, regulate your periods, clear up acne, you name it, it will fix it. Yeah, right.
She started taking this pill in March 2007. She was off at college but called to tell me she was experiencing horrible headaches, behind the eyes. She complained about her stomach hurting, but we just figured it was the stress of freshman year at college. Then she said she got where she couldn’t eat when she went to a restaurant. When she came home in May for the summer, I noticed a total personality change. For example, she was always a neat freak, and now she wouldn’t clean her room. The first day when she drove home, she started crying she was so mad about the traffic. Yes, she has always had a little road rage, but this was ridiculous.
By June, not only could she not be in crowds, like at a restaurant, but now she is having full blown panic attacks and IBS. We called the OBGYN and they said, “Yasmin won’t cause this, go see your primary doctor”. I knew that the only thing that had changed with her was taking the YASMINE. I knew it had something to do with all of this so I “Googled Yasmin” and this website (http://www.medications.com/se/yasmin) was the first one I looked at. All of her symptoms matched everyone else’s! I am so glad we found this website, it explained everything and I had her to stop Yasmin immediately.
So we went to the primary doctor, explained about the Yasmin and how we thought it was the culprit of everything. Of course this doctor also says, “Yasmin won’t cause that”. We told him to look it up on the internet and see how there are over 3000 complaints on this drug, more than any of the other drugs on the market.
Besides the emotional problems she starting having, her pulse and blood pressure was sky high, so he puts her on medicine for that, and puts her on an anxiety medicine and sends her to a psychiatrist. She is very thirsty all the time, and develops IBS. She can’t eat without having pains in her stomach. So, now we’ve have gone from having just irregular periods, to all of the above, plus a psychiatrist.
The psychiatrist doubles her medicine (and puts her Pamine for the IBS) because the panic attacks are gone, but she still is having a lot of nervousness, anxiety, can’t sleep at night, crazy thoughts, worrying all the time, etc. A month later he changes her medicine again, to Effexor. The first 2 weeks, she does okay, but the packet doubles the strength after 2 weeks. It takes 4 weeks for it to take full effect. Right after she doubles this medicine, it is like her senses are on hyper-mode. She can taste everything that is in her food (chili powder, seasonings, etc…), taste the metal in water, and she can hear someone’s phone vibrating, in another room.
Then she goes back to college at the end of August 2007, and it’s horrible. The Effexor is having bad, bad side effects. We called the psychiatrist that she was using at home and he doubled the dose. That was the worse thing they could’ve done. The side effects were worse than ever. I had her to immediately go to a psychiatrist on campus. She told him the whole story and he believed her! Needless to say we switched doctors. He then lowered her dose back down to ½ a dose and hopefully can slowly get her off of all this medicine.
The newest thing she has developed is being hypoglycemic. The campus psychiatrist sent her to a campus medical doctor and he told her that they would get to the bottom of this. He tested her for everything under the sun. Low blood sugar is the only thing they found. But, she hasn’t taken the Yasmin since May. No telling what the results would have came back like if it was done at the time she was taking Yasmin.
Thank goodness she has counselors and doctors there at the campus that believes that Yasmin can cause all of these problems, and are working with her. From what I have read from the people that have used this medicine, although most doctors do not agree, Yasmin takes like 6 months to get out of your system. I think I am going to believe the testimonials of the people who take this medicine, over a doctor who prescribes it.
If everyone goes to the media, their doctors, the FDA, congressmen, and make them aware of these horrible effects, surely we can get this drug off of the market! Does anyone know a class action lawyer that would pursue this? For my child to have to go through all of this is ridiculous, not to mention costly. What do we know of the long term effects this drug will have if it is doing all of this when you first start taking it?
If you have the same concerns as me about this drug, and would be interested in looking into a class action lawsuit, please email: ****** I would be interested to see how many would want to pursue this.

I was on Singulair for a few years. I started seasonally and eventually stayed on it all year. It kept my mild asthma and seasonal allergies completely in control to the point where I no longer felt like I had those problems. Even after cold viruses, my peak flows never dropped as far and it didn't take as many weeks to recover peak flow. As a singer, that was very important to me.
Then I spent a year barely able to walk from the severe leg cramps and pain and swelling. My GP was stumped and I had several diagnostic and blood tests that ruled out all the possibilities she could think of. Then I called up Glaxo and asked if it could be the Singulair? Yes, in rare cases it causes edema and/or muscle cramps. My doc took me off and the problems faded away and I'm back to walking. But now my asthma is not doing as well back on the older drugs. Sigh.

I'm sorry so many are having negative effects from Yasmin. I guess there's always the possibilities of side effects from any drug taken. I'm here to say that I've had positive effects from it and have never had any complications. I've been on it for over 2 years now. I hope all of you out there who's had negative experiences will find new meds and new hope.