Ulcers symptoms and conditions

Am on day three of Omeprazole for pangastritis, ulcers, acid reflux disease and duodenitis. I have cried every day. This is not like me. Mother died of stomach cancer so am afraid to stop taking medication following endoscopic diagnosis last Thursday. After reading this I believe I will have a discussion with my gastrointestinal specialist about just cleaning up my diet to the 'n'th degree.

Hi, I am a mother of 2, and not quite 23 years old and got the Mirena inserted at my 6 week check up after having my second. I read all the literature that the Dr. gave me and I was sure that Mirena was the right thing for me (no where in the brochures did I read anything about the symptoms Ive read about here or anywhere else on the internet). I started having incredibly horrible mood swings, bloating, fatigue, nausea (sooo bad, every day) back pain, neck pain, no sex drive (!!!), depressed, lazy, headaches (to the point where I thought my head was going to explode), constantly hungry, acne, smelled maple syrup constantly, complaining all the time about everything, weight gain (only 7 lbs but I just had a baby, I need to lose weight, and I'm nursing),chest pain, and some other symptoms but the most important one is the stomach pain i was having. The pain in my stomach felt like a knife, and I kept having pain in my right side. So after a few days of this pain I went to the dr. he ordered an ultrasound of my abdomen and I am scheduled to get that done Wednesday. My doctor thinks that I may have gallbladder disease or something else seriously wrong with me that we suspect is induced by the Mirena. Keep in mind that I've had this thing in me for about 4 months!!! So after my doctors appointment I typed into google "side effects from Mirena" and Omg, I wish that I had done that before I got the thing inserted, those brochures about the Mirena make it seem like a Godsend and I am all for a lawsuit due to the problems I am having and the depression Ive felt. My 3 year old has suffered from my mood swings, every time id feel it coming I had to make her go to her room :( that poor girl deserves to have a mother that is not so depressed and ill that she can actually play, and both of them deserve that really, and im doing the best I can.... anyways I removed it myself yesterday, i had a hard time finding it but I took it out and I feel as if a huge burden has been lifted, EXCEPT I have been cramping very bad, spotting and incredibly sick, i also read about this thing called "the mirena crash" no matter how long you've had it in, if the hormones were in your system then you are effected and can feel very ill from it (and it can happen to women who had no problems while on it at all, even after 5 yrs). Im hoping that I have nothing wrong at my doctors appt on Wednesday when I get the ultrasound, and it may just be a cyst, turns out that is a side effect of mirena as well, that and bleeding the first several months (oh yeah, I did for about 2 months maybe 10 weeks altogether) Im also hoping that my daughter whom I am nursing is not sick as well :/

oh and for anybody out there thinking that the only women gaining weight are fat to begin with, well I am usually 105 lbs, after my baby I weighed 145, lost some weight, went down to 130ish gained it all back then some, losing weight is easy for me because I diet and exercise like I should, now I am doing all that and nursing a child.... and hello weight, when it really should be goodbye... well goodbye mirena I WONT miss you!!!!

was give coumadin in November, and by April my stomach hurt so bad I couldn't stand the pain. i hac a colonoscopy, and sigmoidoscopy. This doc couldn't find anything wrong. Made another appointment, ad just had the colonscopy, and sigmoid again. I have ulcers in my stomach, and the upper part of my intestines.

I know it has to be the coumadin.

I am so relieved to have found this site... i have been miserable for almost 2 weeks, i broke out with hives last week and never found the cause but with that and some breathing problems they put me on prednisone. I have been miserable since, i couldn't eat drink sleep or do anything else at all pretty much and i have had diarrhea, and a ton of other symptoms... i feel bloated acid reflex muscle aches headaches dizziness chest pain & pressure very weak feeling mood swings and depression the jitters and heart racing and from what i read and researched this is all from the steroid prednisone.... thankfully the doctor ended my dosage sooner than it was prescribed and last night i took my last pill... i now am just wondering when or how long will it be till i feel myself again and can have a good nights rest?? I will never use this medicine again!! I am just soo relieved to have found some answers on here.

I was prescribed biaxin for bronchitis a little over a week ago. I took the first two pills and the next day I had a sore tongue with red patches and ulcers all over it and I felt like I had bladder infection. I didn't stop taking them. I took 2 more of the pills and woke up the next night with severe depression and anxiety. I stopped taking the pills altogether and I haven't slept good, it has been a week. I have anxiety every day, panic attacks and nightmares in the night. I am extremely moody, irritable, I have crying spells for no reason. This is really scary, I will never, ever, ever take this medication again. The doctor gave me lorazepam to help with the anxiety and told me it would take 2 weeks to leave my system, one can only hope and pray......

I'm 41, male, and have been taking Omeprazole for about a month now due to an H. Pylori infection that was also treated simultaneously with PrevPack and Sucralfate. A subsequent endoscopy found no ulcers, polyps or stomach problems; my entire GI tract down to my stomach is clear.

I was taking a single 20mg pill per day and had it upped by my doctor to twice a day, though it seems that twice a day is now worse for me. Foods that were fine with me on a single pill seem to give me problems with two pills.

Now that I am on Omeprazole alone (taking no other meds) I have had strange sensations, both mentally and physically. My legs and arms get tingly, I have sharp pains across my chest (as if I am doing a heavy bench press and my muscles are being pulled), my heart rate will speed up, especially if I am laying down, and occasionally I suffer bouts of all-over body aches which feel almost like growing pains.

Mentally I am feeling depressed, anxious and on one bad night I felt oblivious to the world, as if I could walk off a cliff and it would be no big deal; scared the crap out of me. Often I have trouble getting motivated to do anything and find that my only way to get around it is to try and absorb myself in a book. Any other chore or project I try, I start but just can't seem to finish; my mind wanders.

I thought this might be connected to angst about dealing with the pain and circumstance of the infection, but previous to my H. Pylori I had another physical trauma that caused me trouble and I had no mental side effects; I was dealing with it and understanding it as a result of getting older and my body doing what every body does as it ages.

Is it Omeprazole? I suppose I can't really say for sure but reading this and other forums I am under the impression that it is probably having side effects that are serious enough to cause concern. I could probably deal with most of the physical side effects but the mental ones are scary. I will stop using Omeprazole starting tomorrow and see how it goes, confining myself to foods which hopefully won't cause too much reaction and go from there.

I began taking Mobic about a month ago. I have some acne and rosacea, but I began to develop blister-like acne papules all over my face. I am an esthetician working for a plastic surgeon. I take great care of my skin and thought it would subside eventually. Then I began getting ulcers/blisters in my mouth and my stomach was quite upset. I then recalled a similar reaction to Feldene and few years ago and decided to stop the Mobic. The breakout subsided in about a week and my skin is back to normal.

I found this sight after exhausting all other searches on the internet. I had the Mirena put in after the birth of my son at my 6 week checkup. My son was born 6/24/2008 and I had the Mirena put in the last week of August. I didn't have any problems with the insertion and I did have bleeding for a while afterwards but nothing else. However, in January I began getting migraine headaches and had extreme nausea everyday. I thought I was pregnant but took a pregnancy test and the results came back negative. I went to a Dr. and had SEVERAL tests performed and found out that I had a Urinary Tract Infection as well which I've NEVER had before. They thought I had ulcers but after taking the antibiotics and the ulcer medication the nausea is back again. I feel very run down and moody as well. I never thought it could be the Mirena and assumed it must be something else but after running upon this website I'm considering having it removed because all other tests came back negative...what else could it be? I'm only 30 years old and the Dr. said I was very healthy and he could see nothing wrong with me. I will report back when I've had it removed and let everyone know if the side effects have gone away.

Wish I had found this info last night.
Ive been on the medication for 8 days. All was well until yesterday afternoon when my face got beet red. I didn't think much of it since my face does flush at times.
Last night, it seemed to be traveling down my neck and shoulders.
When I woke this morning, red face was still there but now I had broken out is rashes all over my body. As of right now they are still there and starting to itch.
I was on this medication for ear infection and also for UTI.
Never would have thought with 1 pill left Id break out in a reaction like this.
Hope it goes away soon.
Benadryl isn't helping me much

I'll be sure to add this to my list of medications not to take.

I have oesophageal ulcers and duodenitis, diagnosed by Gastroscopy exam. I have been prescribed 40mg daily for 8 weeks then follow-up Gastroscopy to check efficacy of drug regime. Seems reasonable to me to wait to see outcome. My reason for adding to this blog: Only been on these pills for a few days and am having headaches (though not severe); and have now become aware of duodenal pain;.

I also have experience gas, bloating and unbearable stomach cramps that almost prompted me to go to the hospital. In addition, one morning I woke up and my tongue was all black. Is this from the sulfur or is something else wrong with me? Yikes. I was using the GNC supplement before and it worked great, but I got a coupon for move free. I think I'll switch back and pay the extra money.

I originally posted about my 9 year old son on January 5th. Refer back to this for the symptoms. He had his upper and lower endoscopies on the 12th, and the lower showed numerous ulcers in the large intestine and at the beginning of the small intestine. The doctor insists that it has to be Crohn's disease based on just this and the blood work, which showed eosinophilia and elevated sedimentation. He is insistent that this has nothing to do with the Singulair and the dosage change. It's just a coincidence .... He' in the hospital for a week now. Watch for those stomach complaints! His started with poor appetite, complaining that he was full when he had hardly eaten, and vague complaints about eating giving him a stomach ache. It progressed to occasional diarrhea. It got worse quickly after that, just a few weeks.

I've been taking Omeprazole on and off for 6 months. I've been feeling increasingly depressed, anxious and apathetic - unable to get out of bed in the morning and having difficulty concentrating. Had initially thought that I was feeling like this because of the adic reflux and ulcers... having read these posts I now think that it could be because of the pills themselves. I'm going to come off them immediately and stick to herbal supplements and controlling my diet.

My 7 year old son has been on Singulair since this spring for a dry hacking cough and allergies. The Singulair worked great clearing up his symptoms. We have not seen any behavioral changes. Our doctor said he only needs to take it during fall and spring when his allergy induced asthma is the worst. Both times that I have taken him off of it for a seasonal reprieve he has developed a VERY PAINFUL STOMACH ACHE. He doesn't vomit, but he rolls around complaining that his tummy hurts. I have seen other posts concerning stomach aches when on the medication, but I am wondering if anyone else has had this experience when they went off of it. Even if he forgot his medication a couple of days, the stomach ache will present.

I have been on the NuvaRing for about 3 months. Just after I started it...maybe two weeks later I got the worst case of heartburn ever. I had never had heart burn before. I had just eaten a big meal so I thought it was that. Then a few weeks later I had another severe case of heartburn that lasted all day. I threw up and by night time my back was in so much pain I almost went to the ER. Finally fell asleep and woke up the next day and it was as if nothing had happened.
Went to the doctor and they tested for ulcers and found nothing. Had a few more minor bouts of heartburn in the next 2 weeks. Then this morning...same thing. Strong heartburn which has gotten worse through out the day and not my back is in serious pain. Just hoping to get to sleep. Called my doctor and told her about this possibility and she had never heard of this. She told me to remove the ring to see if there is a correlation. Removed it a few hours ago. If the heartburn goes away and doesn't come back I will have an answer.
I eat quite healthy and am not overweight. I exercise regularly and don't take any other medication. Has anyone else experienced this with the nuvaring?

Well, I got a call from my daughter's doctor's nurse and they found ulcers all over her small intestine. Now, the nurse procedes to tell me that they are so bad that they pill cam that she had to swallow to find them had a hard time even getting through the small intestine because it was so inflamed! I don't know if anyone else has had this problem or if they have found any articles about someone else going through this after the shot, but please let me know if you have, thank you!

I went to this web site because I want to help my wife. She's been on Jolessa for 8 weeks now. As of this week, her heart has been "fluttering" for lack of a better word. She went to the ER room and they said basically that nothing's wrong with her but she is experiencing premature ventricular contractions (PVC's) which are not dangerous (according to the doctors). She asked the doc's if she should stop taking Jolessa and of course they said,"no."

We're wondering if anyone else is experiencing this feeling with this junk? My wife is 38 years old, healthy, never had heart problems or disorders. As of the past few weeks though,she's been feeling down in the dumps, sluggish and has a slight mode change.

If anyone is experiencing a change in heart rhythm, since taking Jolessa, please post it here. Thank you.

Has anyone developed tartive dyskenisia. It is involuntary body movements. Mine are in the mouth, like I am sucking on my teeth . It is very disturbing and listed as one of the side effects. It can occur in other parts of the body, like tapping.

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

Hi, njcukett posted 2 days ago asking if anyone is still having abdominal pain after being off singuliar awhile.My 7 yr.old (on singuliar at least 3 yrs.) is still having pain.She also had bladder issues for the past 2 yrs.(Frequent dripping and urgency to void).This went unexplained by doctors.Over the past 6 weeks since she stopped taking singuliar,I have noticed a complete change in her stools.While on singuliar they had become grayish in color.She would have 2-3 of these movements a day.The color of her stools are now normal,but the lower abdominal pain is still present.So I am wondering if the pain is coming from the bladder, not the stomach.I am going in(without my daughter) to discuss this with her pediatrician next week.Singuliar also made her very anxious,do not want to add to that,by discussing this in front of her.For the people having abdominal pain,did the stools change while on singuliar compared to when off?Just curious.

I spent the weekend reading about the development of Singulair. The early studies recognized that the first phase of the acute asthma response bronco-constriction was probably not caused by leukotrienes. They identified histamines and prostaglandins as the probable sources. I don't think that changed because the Singulair literature states that it should not be considered as a treatment for that. Leukotrienes were a source of inflammation caused by eosinophils and mast cells present in greater numbers (than normal) in airway tissue. So, it was beneficial to find a way to decrease that.

The cysLT1 receptor was identified as source of the signals that tell the cells to produce leukotriene. The receptor, a gene, consist of 337 (they think) amino acids. They modified a compound that would bind to that receptor thus blocking the cells ability to produce leukotrienes. This compound is very specific. It was formulated to bind to the "model" receptor. This compound will not even bind to cysLT receptor sub-types. (That is the good thing.) There is an enormous amount of research that discusses the genetic variability of the chemical reactions that occur in the leukotriene (calling it this for simplicity) pathway. We are also seeing that a number of researchers would like to use gene profiles to predict whether patients will respond favorably to different asthma/allergy drugs. ALL PATIENTS HAVE A RIGHT TO KNOW IF IT IS INHERENT THAT SOME PEOPLE WILL NOT RESPOND TO SINGULAIR OR RESPOND ADVERSELY.

There are many studies from the 1998 era that conclude that montelukast is not effective for everyone. Those researchers stated that it can be predicted that those people who are going to respond favorably will do that within the first 14 days or so. That conclusion would be consistent with a genetic component for efficacy and safety of Singulair. Those doctors concluded that those who did not respond within that time frame should not take Singulair for fear of harming them. That makes good sense.

The Italian researchers wanted to know if there was more going on than blocking leukotrienes in the action of montelukast. They set up a "test tube" study regarding montelukast, the cysLT1 receptor, and some t-cells that they selected. Why? Researchers always have something on their minds. They observed the death of these particular t-cells.

Montelukast is a quinoline. We basically know of quinilines and quinolones as compounds that were invented as broad spectrum antibiotics. They work because they interference with bacterial DNA so they cannot replicate themselves. Montelukast is a quinoline modified to bind with the cysLT1 receptor (a gene) and prevent that gene from activating. That's consistent with what a quinoline/quinolone does.

So what does montelukast do in blood plasma if it does not bind to the receptor because of genetic mis-match? (If montelukast does bind, then a chemical reaction has occurred and the liver will break down the by-products. Montelukast metabolized in 10-12 hours.) What happens if it doesn't bind? How long before it breaks down? Does it produce toxic by-products?

I want to know what happens to lymphocytes such as t-cells just because montelukast is a quinoline. Maybe nothing but what's up with the Italians researchers? I want to know if montelukast has the capability to interfere with lymphocytes who can clone themselves. That could be a good thing under circumstances when these lymphocytes are causing inflammation. But it could be a bad thing in the case of normal individuals with no problems.

I want to know if the bad side effects are due to the fact that the body has to break down and metabolize a quinoline that did not bind to the receptor for which it was created. The side effects of Singulair are strangely similar to what is observed in the quinolones such as levaquin. I have not as yet been able to compare montelukast as a quinoline to levaquin as a quinolone. I am hoping to find something on these categories. There may be no reason to worry that they cause similar damage. But frankly, I think that there is. There is some terrible chit happening to some people. The scariest is the neurological damage.

All of these questions would be in the everybody pharma knows to ask category. I don't know where the answers are. I haven't found them as of yet. Maybe there are no answers. We have to remember that Singulair and Vioxx were released in the same year. They have continued to be drugs under the current executive management of Merck. If the Vioxx marketing promoters had their ghost writers, why not the Singulair marketing promoters. The genetic component appears to be widely accepted but we haven't heard one thing about even that.

I think that it is sad that maybe the marketing of Singulair as one stop shopping for asthma/allergies may have destroyed the original concept. I really think from reading the original work that they knew that they couldn't engineer a drug for one size fits all. Everybody gets harmed when information is withheld.

Shame on the allergist who yelled at the mother who wanted to discuss issues. Does he know exactly who is allergic to Singulair and who isn't? Get him a dunce hat. Just because Singulair is marketed for allergies does not mean that you cannot be allergic to it. See the power of Madison Avenue? The ad agencies focus group these drugs to death. The ad agencies cleverly craft the product information. A good piece of legislation would be to prohibit consumer drugs ads.

Update: My daughter has been off Singulair for 3 months and is doing so much better. She is not having anymore nightmares, heart racing, anxiety attacks. No more itching, headaches, stomach pains, depression. She is so much happier now. She is 7 years old and acting like a happy child now. I am so glad that I took her off it in December. She is not crying and upset like she used to be. We could tell that she improved within one week and is still improving. Hope everyone else improves like my daughter has.

Here is some perspective for you all. I take Singulair and do well on it and in ACTUAL studies it has one of the safest safety records. Understand that post marketing reporting does not mean there is a correlation between the event and the product. Throughout the life of a drug the companies must disclose any report of side effects reported to them REGARDLESS of causality. A popular antihistamine that is OVER THE COUNTER also has suicidal thinking/behavior listed in its post marketing section. However, just because patients who had reported having these thoughts while taking the product doesn't mean it was a result of the product! Maybe they had a depressive personality and were also on multiple other medicines to treat that. You must look at the "Adverse Reactions, Warnings and Precautions" sections of package inserts to see the side effects that were actually seen in studies. You can die from ulcers derived from over use of aspirin or ibuprofen. Decongestants can throw off your blood pressure and these events are documented in actual studies! Listen to your bodies when taking any med. If you feel differently report it to your doctor.

These are all drugs people, there are potential side effects. There are also side effects to those "natural" over the counter remedies that are not nearly as regulated by the FDA or studies by the drug companies.

To anyone out there who has experienced side effects to singulair timed to when you started it, talk to your doctor, stop taking it and see if it goes away. Same advice for any product prescription or over the counter medicine. Side effects can be a combination of many factors (what other meds are you taking?) But understand for many people this product is the safest and most effective treatment for them. The FDA and Merck are reviewing all information to see if there is any correlation to the reporting. But singulair been around for about 10 years and prescibed to billions of people and is known to be one of the safer medicines out there overall.

In between the legitimate posts on this site I get the sense there is a lot of ambulance chasing going on. People looking to cash in on this big drug companies. We want drugs, we want them cheap and with no side effects which is not a reality. Keep stepping up the regulation and make the companies hire more lawers to protect themselves and jump through even more hoops and see what happens to the price and access to new meds. Even better, see how regulation has impacted the development of new medicines around the world (here's a tip, it will dramatically decrease). Drug companies certainly aren't perfect but which industry is?

Please, when taking any medicine over the counter, prescription or herbal supplement listen to your bodies to see if the potential benefits of the product outway the risks or side effects. Report any changes to your doctor.

I have been crying for almost 24 hours now. I cannot believe what I am reading and hearing about Singulair. My son has been to hell and back again and again. I cannot say for sure the Singulair is the culprit. But after reading all of the other stories on this website, I am convinced it is a strong possibility.

My son is 11 years old. He has severe allergies and asthma. He takes many, many medications for this including Singulair. He as been on Singulair for about 8 years now (my best guess because he has been on it for sooooo long.)

My son was diagnosed with ADHD in pre-school. He has taken many medications for the ADHD, but none have ever done any good at all. We thought some of the medications even made things worse. Now, I'm not so sure.

After exhausting all the ADHD medications, our pediatrician sent my son to a psychiatrist and a counselor. The psychiatrist put him on 2 different antipsychotic medications. Again, neither one did any good and seemed to make matters worse. The psychiatrist sent my son to a psychologist to be tested for Asperger's. For those of you who don't know Asperger's is a high functioning form of autism. The psychologist ruled out Asperger's by diagnosed ADHD and Anxiety Disorder. He did not prescribe any medication.

For some unknown reason, I've only given my son the Singulair off and on for the last year. My son had the best year in school ever. However, his pediatrician was still not satisfied. He sent him to see another psychiatrist at Children's Hospital in Pittsburgh. We were told he is believed to have more than one disability. He is believed to have ADHD, Aspergers, Teurettes and a possible 4th medical problem that has not yet come to light.

We are scheduled to see a neurologist at Children's Hospital on the 15th of April to rule out any medical reasons for his tics. We see the psychiatrist again on the 18th of April.

I am so tormented by this recent news. Has all of these problems been caused from him taking the Singulair for so long? Although he has had his best year in school yet, he still has a lot of problems. Are the side effects of the Singulair permanent.

The other side of the coin is this: It is also very scary to watch my son not be able to breath. Asthma can also be life threatening. What is a parent supposed to do.

Also, I now don't know whether to keep these appointments that are coming up. I hate so much to put him through more. He has endured enough doctors and tests to last him a lifetime. However, what if it is not the Singulair and there is help out there for him that I am not aware of.

Please if anyone else has had a similar experiences e-mail me. I would love to hear from you.

God Bless everyone who has been through this kind of hell.

THIS IS MY 8TH DAY ON LAMICTAL 25MG AND I WOKE UP SO DIZZY THAT I ALMOST FELL OVER. I HAVE BEEN THIS WAY ALL DAY IT LIKE COMES AND GOES FAST. IM DIZZY NOW..
I HAVE NOTICED MUSCLE ACHES BUT I THOUGHT THAT IT WAS THE ATENONOL 25MG I TAKE FOR PALPITATIONS BECAUSE IT LOWERS YOUR POTASSIUM. IM THINKING THE LAMICTAL DOES THE SAME LOWERS YOUR POTASSIUM WHICH CAUSES THE MUSCLE PAIN AND ETC.. SO I BEGAN EATING BANANAS AND SEE HOW THAT GOES. MY DOC SAID THAT IF YOU TAKE A ANTIDEPRESSANT AND YOU ARE BI POLAR YOU CAN HAVE SERIOUS REACTIONS TO THE MEDS. SHE TOLD ME TO "NOT" TAKE A ANTIDEPRESSANT.
I WAS ON THIS MEDICINE BEFORE AND WAS UNSURE ABOUT A SIDE EFFECT OF ULCERS IN MY MOUTH AND STOPPED IT. I REALLY WANTED TO CONTINUE BECAUSE IT MADE ME FEEL GREAT(only got to 50mg then)
I HAVE ACTUALLY FELT PRETTY GOOD MORE GOOD DAYS THAN BAD EXCEPT YESTERDAY AND TODAY I HAVE BEEN REALLY TIRED ALONG WITH THE OTHER.
MY QUESTION IS WILL THESE SIDE EFFECTS GO AWAY???? AND I DON'T WANT TO REALLY EAT MUCH.
I REALLY LIKE THAT I AM NOT MOODY ANYMORE LIKE I WAS AND I GOT MY SEX DRIVE BACK AND I DON'T WANT TO GO OFF IF I DON'T HAVE TOO.. HOW LONG DO THE SIDE EFFECTS LAST??
AND IS IT WORTH STICKING IT OUT?