Six months symptoms and conditions

I'm in the middle of my third month on Loestrin 24 Fe. I used to be on Estrostep years ago, before I had children, and now am on this because of the low dose and my age (37). The first month, there was some staining near the end, then a lighter period (mine used to be 7-10 days, around 5 oz of fluid). On Loestrin, it's about 4 days, only a couple of oz. However, month 2, in the first week of pills, I took one pill about 8 hours late, then a few days later, took a pill about 6 hours late. The day of the second late pill, by two hours after I normally took the pill, I was cramping pretty badly and started bleeding like a full period. The bleeding lessened over the month, but never went away. Light period following. Now, on month 3, about 2 weeks in without having been late on any pills, I have had spotting the last few days and light cramping. Plus, the one time my husband and I had sex about a week after my period, there was some brownish blood afterwards, which he hates. So basically, he now refuses to touch me.

I have also noticed being more emotional, like I felt the two weeks after giving birth, crying more easily. I think that might be lessening now, though.

I am going to call my doctor to see if he recommends trying it one more month. I do remember that it takes around three months for a person's body to get used to oral contraceptives, although the first pill I was ever on (Ortho Novum 7-7-7) made me bleed lightly the entire six months I was on it, and when I switched to Nordette 28 that problem was solved. I just know that I can't have this spotting continue since my husband is so sensitive to any hint of blood, and I don't relish the idea of never having sex again. NOT the way birth control pills are supposed to work!! ;-)

I was only on 25 mg of Topamax for two months and had to stop due to the terrible side effects of mouth numbness, taste aversion and severe dry mouth. Unfortunately, the side effects have gotten worse and persisted now for six months after going off this medication. My personal thoughts: Topamax is the worst drug on the market, has negatively impacted my life, and my neurologist could care less. These symptoms are with me 24/7 and only mildly helped by expensive mouthwash and lozenges specially formulated for dry mouth. Actually, eating certain foods makes these symptoms worse and I am afraid this is permanent, but can find no scientifically plausible evidence to explain such lingering effects. If anybody else has experienced such long-term symptoms after going off this medication, please share.

Hello Ladies....I am 56 and diaged Hashimotos disease 3 years ago.At the moment on 112mcg of synthroid....dosage started off low and have gradually worked up....So angry with drs...was seeing endo, but moved and using family practice...so frustrated with weight gain approx 25lbs since diag. Also does the word sweat ....mmmm perspire for all us ladies, mean anything? I can't even wash dishes without breaking out in to a sweat...mmm beads of perspiration....Dry skin, I own stock in Aveeno....Also....does anyone get "boil type" skin eruptions in the nether region...butt, inner thighs etc? Does anyone or has anyone done any serious research on Iodine? I try to eat as well as I can, was doing Weight Watchers and gained weight do ya hear me? I am questioning my idodine intake or lack of....Presently take mulit vit with 150mcg. Considering uping it and dc ing my synthroid...cuz docs have been useless....eat less, (how much more less?) exercise more...I swim so much I look like a freaking prune....Any comments?

I have had my mirena for about six months. I have bled all but two weeks of the six months. Because I am always bleeding, even when Im not "bleeding" I am having this brownish discharge. And just when I think its going to stop, I get this clear discharge that smells like sewage. I have never smelt anything so horrible in my life. I have had this three different times in the six months. I don't know what I am going to do. I got the Mirena when I started college because we can't afford a accident pregnancy right now. It was free with my insurance. Now, I have no insurance and I can't afford the 250.00 to remove it.

Reading some of the other side effects (after posting my most recent side effects) has made me think back a long time to when I was about 10 or so, and my asthma had been acting up- I was given a sort-of high dose of prednisone. For about two-six months after taking it, I had really severe knee pain, sometimes where I couldn't even walk around the grocery store. Eventually, it went away, and I distinctly remember my mom asking my doctor a few years later if it could be the cause (too high a dose and no weaning off), and the doctor said it was possible. Sometimes, I will have general knee pain for no specific reason, but luckily it doesn't happen very often.

I can't attribute this directly to my cortisone shot - however, I've noticed that the past few months I have been losing my hair. I can pull it out virtually by the handfuls anymore! I am only 24 - this doesn't seem normal and the only change I could point to is the shot. HAS ANYONE ELSE HAD HAIR LOSS THEY CAN TIE TO A CORTISONE SHOT?

I also noticed a change in my period. Nothing as extreme as I'm reading here - but I'm so glad to have read this - puts my mind more at ease to know have a cause for that.

I have tried other remedies - but the cortisone shot has been the only thing to actually work. Any other ideas?

IS THIS SITE AN ANSWER TO OUR PRAYERS?

A little while ago less than two hours, after a very emotional, difficult battle with my daughter, we had yet another heart to heart to try to do better. At the end of our talk WE PRAYED for guidance to know how to help the situation. So I'm here looking for a link to her behavior fron the ADHD medication and I see someone had posted about Singulair side effects. I was floored! I have never thought that Singulair was not a safe drug. No doctor has ever mentioned any negative side effects to me regarding it. The more I'm reading about it the more in shock I am. Have I and her doctors been doing this to my daughter? My 12 1/2 yo daughter has been on Singulair for probably 10 years. She was a 28 week preemie and had severe lung issues so it was a needed medication. Her behavior has worsened the older she has gotten. Because of mostly anger issues and problems in school about a year ago she was started on ADHD medications. We are currently trying to find "the right one" . I feel so awful. Could all her misery have been caused by this little pill that was suppose to help her? Why has her pulmonoligist continued to give it to her although she has not had any serious asthma problems in years? I think I will stop all medications and see what happens. My daughter has also been on amytriptylin for about six months also for severe migraines. What do you think? Should I stop all of them cold turkey or gradually decrease one at a time? I would GREATLY appreciate any advise.
Thank you

My daughter was on Advair, Singulair, and Zyrtec to control her severe asthma and allergies. We were so thankful that these medications kept her from having to be hospitalized 2-3 times a year for uncontrollable asthma attacks. About six months after she began taking these medications she began to have headaches, she had difficulty sleeping, she was irritable, she had stomach pains, leg cramps,and eventually depression and social withdrawal. She went from an outgoing and happy teenager to a bitter and angry person. In 2003 she committed suicide. Six months after her death reports started to surface about the link between singulair and depression and suicide. Perhaps for my daughter it was a combination of the three drugs. Whatever you do be cautious and do your research before taking any allergy or asthma medication. Go to the Singulair website and you will be astounded by what you read. Please try to get the word out about these medications.

My daughter was taking a deadly cocktail of Zyrtec, Advair, and Singulair. She was on these medications for three years. At the time we thought that it was fantastic that her severe asthma and allergies were finally under control. After about six months of being on the medications we saw her slowly decline into a state of depression and withdrawal, she had constant headaches, she couldn't sleep, she was no longer interested in any of her friends or activities. She went from a loving and sweet girl to an angry and bitter person. In 2003 she committed suicide. Six months after her death reports started to come out about the links to Singulair and depression and suicide. Perhaps it was the combination of the three drugs in her case. If we would have had any idea what the effects of these drugs were we would have taken her off of them immediately! Please spread the word about the dangers of Singulair, Zyrtec, and Advair. Go on to the other sites and read what people have been posting and you will be shocked. The Singulair survivors are banning together to try and get this medication pulled. Do what you can to spread the word!

TWO PIECES OF ADVICE:
DO NOT DRINK alcohol within 6 hrs and EAT right before taking Toprol. This should help with all mentioned side effects!
I have noticed that if I drink ANY alcohol within six hours of taking Toprol (before or after), my HR skyrockets to 190+BPM. I thought this might help others. Also, I MUST eat at least 2 slices of bread each time I take it. Otherwise, I will feel very dizzy, faint and have bad dreams.
If I eat, I have no side effects.
Also, there have been a couple times where I missed a dose or took it late and each time, I feel my heart starting to race and the PVC's coming back.

I have been on 25 mg of Toprol for 6months due to PVC's and rapid/ racing HR (160+)/ palps and BP spikes. My 24hr Holter (six months ago) showed 370 PVC's in one day, so I was put on Toprol. All other heart tests were normal. Anyway, it has worked wonders for me. I had another Holter done last week and there were NO PVC's and steady HR and BP. Since being on Toprol HR is 65, BP is 105/60 or so.

For all of the poor girls who are searching "mirena experiences" because you are looking for a sure thing contraceptive-
This site is only for people who have had BAD experiences. Read them all if you want, but take into consideration they are the 3%, or whatever number, that had problems. None of these women deserved it, asked for it, needed it, or wanted it, but unfortunately their bodies responded to it in such an ugly manor.

Here's my experience so far....Had it inserted 8/06/08. Insertion was fine. Felt that speculum more than I could feel the actual insertion of the mirena.
Slight cramping afterwards...not immediately-went home and for like 20 minutes had cramps lighter than my period cramps.
For the first week bled lightly, second week had an actual period, week three and week four just spotting. The doctor told me this can go on for up to six months...kinda worth it if you think about it.
No acne problems so far, my hair is fine (and trust me, if my hair was thinning, falling out, or anything like that I would take the mirena out!), muscles and joints feel like they did before pregnancy, still breastfeeding (I know that they say that the mirena will make you produce less breast milk-tell that to my breastfed 13 pound 24 inch long 2 month old. he would disagree)
My breasts are a little tender and at first I was slightly bloated (less than if I were on my period) but that has subsided. Abstained from sex for a month after insertion per my doctor's orders, so I will come back and post if there were any problems with that...NEXT WEEK! yay!
Know that I understand the side effects could show up later.

Now again, EVERYBODY will experience something different. We are interfering with nature. Birth control is one of the most unnatural things we could do to our body.

Again, since this site commonly comes up when searching the mirena, I want for women to know that it might work for them better than it did for others.

I am almost 41, and have had migraine headaches most of my life which I could manage with 800mg of Naproxen Sodium, or a Norgesic Forte, and when Imitrex came out, I could just administer that. Six months ago, my headaches got so frequent that I had to start taking my Relpax (similar to Imitrex) and/or Fioricet more than 2X per week. According to my neurologist, this is a no no, as both of those meds can couse rebound headaches. He started me on Topamax, 50mg per day. It did nothing. He bumped it to a 100, nothing. Now I'm a 200 mgs, I am still have a migraine in left temple as I write this. I have the tingling, the daytime sleepiness, but my mind is fine, and my appetite is just swell (regretfully). What the hell am I going to do now? Ask him to bump me up to 400 mg? Now I have these headaches every "F"ing day, and I can't take anything. I just have to suffer.

Topamax is NOT working!!!!!

I was prescribed /TWP DS 800-160 for a urinary infection. I have taken this medication before with no ill effects, but this time my hands itch all the time and I have a red, itchy rash on my back and stomach. I finished the prescription today, ao hope it goes away and so far the UTI I had is better. At least I don't have as much pain, but it required two prescriptions before is worked. I have taken this before with no noticeable effects. Is this serious?

My son was born March 2007, when he was 8wks old, to much of my surprise I found out that I was pregnant again. Mirena sounded perfect!!!! I had it placed 7 weeks after my 2nd son was born in Jan 2008. I had what I still assume is normal with any type of birth control method, irregular bleeding,cramping,some slight mood swings. That all seems normal to me when you mess with you body like that. Aug 1, 2008 I woke up at4am with awful abdominal pain sooo bad that I turned to my husband and said that I think I have to go to the hospital. I decided that if I could fall back asleep then its probably nothing major. I fell back asleep (or passed out, I don't know) The next morning I was hurting so bad I couldn't lift anything, couldn't stand up straight, felt weak and felt as though I had rocks in my stomach but had an empty feeling at the same time. The pain was all over my abdomen, stabbing, shooting,pinching. I also had pain aroung my belly button and a noticeable discomfort about my pevic bone. Finally I called my husband to come home, went to the hospital, they took blood, cultures, did an exam and did a ctscan. All normal! WHAT!! Aug 11th still having pain and now having MAJOR HOT FLASHES. I find myself getting so hot and irritated that I cant be around the babies because I am afraid I will yell at them. If I get in a little disagreement with my husband it will most likely end with me saying I want a divorce (I noticed another lady with that same problem) Today I had a ultra sound done and it came back what my (new) doctor says is normal. The problem with that is that one of my ovaries is split and is NOW shaped like a horse-shoe. I was pregnant for almost 2yrs straight and had lots of ultrasounds NOT ONE TIME did anyone say anything about a odd ovary. I'm just going to make a educated guess that it wasn't deformed till after the Mirena. Now I am wanting to remove it but feel like I should get every test known to man first to rule out any other possibility. I really don't want to remove it. I am afraid of getting it removed and even more of getting pregnant when I already have two 10 months apart and still in diapers.
My biggest question is wanting to know if hot flashes are related or if I might be having something else going on. Am I the only one with he hot flashes? I have them all day long!!!!!!!!
Also I noticed after reading other post that some other things may be related like, piercing headaches, itchy flaky oily scalp, weight gain, ear drainage, lower back pain, oily skin, increased smoking, in-grown hairs in inner thigh area, joint pain, fatigue, decrease sex drive.

Since my Mirena I have experienced extreme dry eyes. It is so bad that sometimes at night it feels like my eye lid is going to stick to my eye ball. I thought it was because I had lasik surgery, but that was six years before having the Mirena placed. I have been seeing an eye specialist and other doctors and no one can figure out the problem. My first guess was the Mirena because this problem didn't start until after the Mirena was placed. Now after reading other stories I'm really convinced.

I just started on Nuvaring a few days ago. I started on it, not for birth control but because I am going through terrible peri menopausal periods. My doctor is hoping to control the heavy periods and I will go for up to six months without one and then bleed so heavy I will almost hemorrhage. She is hoping to control this using the nuvaring. I put the ring in, and I've had a discharge. Its not thick or discolored, it is like clear water, like sweat almost, but it is smelly, I feel like I smell. I'm thinking it is the hormones smelling. Is this common? is the discharge common? Its quite irritating!!!! The darned ring doesn't want to stay up where it belongs either and I feel like its going to fall out although it hasn't as of yet so I guess it won't, even though I keep checking to see every time I go to the bathroom. LOL I don't have a big cervix, and it just doesn't "fit" I guess you could say!!!! It just floats about in there! Its not very comfortable! I can't feel it when I'm sitting but I still k now its there! I don't know if I like this!!!!

Just letting you all know, ( i posted two or three days ago) i had my mirena removed yesterday after nearly a year with it in, and I SWEAR i felt better INSTANTLY. the cramps ive had for three months straight non stop are gone!! as soon as she took it out the cramps stopped, i felt like i could breath again. And removal was not painful what so ever, i didn't even feel it. she had to tell me it was out. Hopefully i'll lose the extra weight i gained and the acne will go away along with every other side effect ive had. i never associated all of my troubles with the Mirena...but now i know! I think women need to be better informed about this device... i honestly thought about walking into the doctors office yesterday with every complaint on this site printed out and telling my gyno she should hand THESE out with their brochures telling women how wonderful it is. I didn't though, but i did try to tell her about everything i had experienced and i pretty much felt like she didn't even want to hear it. I will keep posting on this site through the next couple months to let everyone know how i'm doing. I honestly feel like if you've had mirena in for six months and it isn't working you should get it removed immediately and don't let your doctor try and convince you otherwise like mine did. WOMEN listen to your bodies!!! you know when something isn't right... forget what the doctors say and do what makes you feel comfortable happy and healthy.

I had 3 injections of lupron Jan Feb and March and I stopped. I still feel lousy, my bones ache. Ever since the first shot I have not felt good thinking that this would help me, it did not. I wish people would stop talking about the price of this medication and start talking about the side affects. I sit and cry from my aches, I won't even go back to any Doctor. Thank-God that it is only so severe 3 weeks out of the month. has anyone experienced such side affects. and by the way my period never did stop and I am still in much pain from that.

oh, my gosh! i have been on seroquel for six months. it has been horrible! sweating,dehydration, weight gain. the WORST has been costchondritis(severe chest pain), extreme hoarseness, and now muscle aches and tightness in my legs, arms and chest. my psych says he has heard of these side effects but has never seen them. am i poisoning myself?

OMG! I thought I was losing it. Have had the Mirena since April and have gained weight (an entire dress size) for NO REASON, been foggy, moody, no sex drive, joint pains, cramps, etc.I thought I was alone, Did I mention EXHAUSTED all the time and acne on my face and back-sever enough to get antibiotics from the dermatologist?
I also suffer with PCOS--does anyoen else on the Mirena suffer with PCOS? Would be interested to see how it has affected you. Tried BC pills and after awhile they stopped working then switched to the YAZ--DO NOT GO THERE--the worst Pill ever--so not many options for those of us with PCOS. Just can't wait to go to the DR and get this thing out.

I had 95% occlusion of the major artery in my heart July 2007 with no symptoms except slight shoulder pain on 3 occasions. They did a cath and inserted 2 stents. Started with Lipitor 10 mg. and my LDL dropped from 75 to 112. The MD wanted to double the dose, but I refused because of intermittent nocturnal nausea. MD switched me to another statin and I had immediate muscle involvement and severe nausea at night. She wanted me to try another statin drug and I refused. After a 2 month period of no statins, she put me back on Lipitor 10 mg. daily. I decided to cut the pill in half and take it twice a week, then move to every other day and gradually go to 10 mg. daily. Immediately, the nocturnal nausea started again. Last night I awoke at 2 a.m. with nausea, sweating, sore muscles around my rib cage. Still no sleep at 4:30 a.m., so I got up and tried to eat something. This has been the pattern every night since I went on Lipitor.

I don't know if I can take this any more.

CK

I have been on Vytorin for about six months. I just recently started experiencing numbness/tingling from the waist down to my feet. I have also experienced it in my forearms and fingertips. Two days ago, I woke up and my face was tingly. My muscles are very week, and I have no energy. I stopped taking it two days ago, but haven't seen any improvement, yet. Hopefully, I'll see some soon. I am drinking lots of water to try to get it out of my system. I am done with statins.

I was first diagnosed with depression when i was 18 years old. For 9 years i was on all different types of medication but for a majority of the time i was on Effexor xr. I remember when i missed a dose, just feeling so bad i would just want to go to bed but when i took the next dose it wouldn't take long to get back to normal. My memory has been shocking. So bad that i have trouble remembering what happened when my children were babies. I don't know if this is because of the meds or the depression. My father committed suicide during the time i was on effexor and i just could not grieve. I felt that when i cried i was just forcing it. I just didn't feel many emotions at all. My life took a turn after that and i had so much going on that i either didn't have any trouble coming off it or i just don't remember what it was like.
At the start of this year my life was very full and happy and i was so busy until one day i just felt as though i was going to die. For a week i sat in the emergency department at the hospital certain i was going to die and leave my three children without a mother. I was finally diagnosed with a panic disorder. I didn't care what they did i just wanted them to make it stop.(the way i was feeling) I was put lexapro but had a bad reaction to that so they put me back on effexor xr. I can only say thank god! I have been on it now for almost six months and i have decided to come off it again as i feel my life is back in control. The main side effects i have had this time on this medication have been, a definite decrease in sexual function, deep sleep, vivid dreams and my pupils are dilating differently. I have over the last week decreased my dose from 75mls a day to 37.5. I really don't remember going through all these side effects last time. I was on a much higher dose before too. I have had the worst migraines, i am so tired, my eyes sting, i have what i guess others have described as shocks. When i move my head or blink my eyes it feels like i get a shock in my head. I feel like i am looking through a tunnel sometimes too. Although i had this same feeling when i was first put back on the meds. Yes it is tough coming off it this time but i still don't regret taking it in the first place. Without it i may still be feeling the worst feelings i have ever felt in my life and i wouldn't wish it on anyone. The effects i am getting now are not even a glimpse of what i went through before i started.

I haven't had ANY bad side effects with NuvaRing. I started using it as a method of controlling my period. I was having a period every two weeks... but of course, NuvaRing fixed that. I've continued it for the past six months and the only actual effect was a bad mood a couple days before my period. I highly recommend using it. It's useful and so simple.

I was put on Effexor XR 75mg two years ago. After about a year on it, i decided i needed a stronger dose, so I was increased to 150mg. I felt happier than I ever have, but about six months in I started experiencing side effects. I have very vivid dreams. When they are good dreams, they are wonderful, but more often they are horrible nightmares, the most vivid nightmares you will ever experience in your life. This is the only real side effect, but it is bad enough i am thinking about discontinuing the medication. I know that the higher the dose of a medicine, the more side effects there are. There were no side effects at 75mg, but i felt more depressed than at 150mg. I also sometimes have other milder symptoms, but I also have hypoglycemia, so I don't know if the effects are from the medication or just a sugar drop.