Constipated symptoms and conditions

I was on YAZ for about 4 months. And like all medications, i gave it time. In the beginning i experienced a lot of nausea, fatigue, headaches, and severe diarrhea. And instead of clearing my skin, it made my skin absolutely terrible. i stuck it out in hopes that my body would change, and begin to get use to the hormone but it didn't. I have been having GI issues August, have been through a Colonoscopy, and everything came back normal. Ever since stopping this pill, my body has felt so much better overall, but the GI issues are still there which concerns me greatly. Has anyone else ever experienced this? My bowel movements have changed completely, and all of the specialist i have seen, say that the pill wouldn't do this. I do not believe it. I believe that the pill has messed up my GI tract so much, that i can't have a normal bowel movement. I honestly do not recommended this pill to anyone. I am 18, and to be experiencing what i am especially going to school, is so not fun. Could YAZ have been the cause of all of this?

I have the mirena now for about 4 months, ive gone from and outgoing fun loving, keep fit person to a person who doesn't want to go out, i wont train cos ive abdominal cramps. Im getting panic attacks, heart palpitations.
My sex drive has hit the pits.... when i do manage do try sex it hurts like hell... my vagina feels all spongy on the inside.

My back hurts, im constipated, cos when i try and go i get cramps in my tummy.
My periods stopped which is what i love about the coil, but i pay for it another way with monthly bloating and cramps.
I never had period pain or cramps before the mirena.
I've turned in to a monster, my moods is a rollercoaster, i feel my husband is cheating or doesn't love me any more. But he does love me and isn't cheating, its the coil thats making me feel this way.

And for the body hair what can i say. I no sooner shave my legs and then they are back to looking like leg warmers. Facial hair is another, and then the pain in waxing.

This list is endless. there isn't just one thing i hate about the mirena but all of it. We had sex 2 nights ago and now i am bleeding so much that its like as if i just had a baby. I am drained yet i don't need iron tablets.
My husband is now going to have a vasectomy ASAP..

I have taken Avelox before with only minimal side effects nausea and diarrhea were the only ones I got but they were enough. I have been suffering from chronic sinus and ear infections for going on two years now. My doctor gave me samples again of avelox on Monday. Last night I had to be rushed to the hospital. After throwing up all day I got a severe headache. I felt dizzy and out of sorts all day but when I couldn't take the headache anymore I tried laying down. With this medicine you can't take any pain relievers so I thought if I just went to lay down maybe it would ease up some. Well it didn't, and before I knew it I was shaking uncontrollably with tremors and could no longer put sentences together. My head hurt so bad I just wanted to stab myself to make the pain go away. At the er they gave me an IV with something to help with the headache.Anyway after taking a Ct scan and not seeing anything on there the er doc gave me the ok to go home and gave me a script for pain meds. I was having hallucinations, anxieties, and could not speak correctly. I am still having trouble making sentences, I am stuttering, which I have never done before. And I can't get words to go together to make a sentence. The Er doctor wants me to follow up with a neurologist. My tremors still haven't stopped and now I sound like the guy from rain man when I am trying to make a sentence. This is pure torture and I feel like I am in someone else's body.

I've been on levothyroxine 150mcg for about 3 months before that it was 100mcg and so on. I have gain lots of weight and tired all the time. depression also, headaches. I hate this gaining weight, sleepy all the time and depression is from gaining weight. I thought this med is to up boost my thryiode but it doesn't seem to be working. my dr. said I'm on the highest dose there is. I don't know what to do any more. I was thinking about taking myself off this but not sure what will happen if i do. I hope there is someone out there that might be able to let me know if they are going through the same things what they are doing and how they feel now.

I am a 44 year old female with diabetes. I have high blood pressure and as a precaution was prescribed simvastian(zocor). I have only been on it for about 3 weeks...I have been feeling tired and very moody lately...but yesterday I woke up with my right leg swollen from the calf down my foot with severe burning pain and numbness. Now I have experienced Neuropathy in my left foot for years and somehow thought maybe this pain and numbness and swelling had to do with that...until this morning when I woke up to a severe pain in my right calf ( I immediately thought blood clot).. well I have a doctor's appt tomorrow to see what this is....right now Im sitting at work in so much pain and discomfort I want to cry...my feet are burning, my right leg and right shoulder are in burning pain...and my hands are numb and burning and in pain. I have to sit for hours at a time and cant just take a break when I need too...Ive only been taking this medication for 3 weeks and can not believe that all this pain and burning is from one little pill. Has anyone else had severe swelling from this medicine. Any other diabetics taking this medicine and having the same side effects? Im certain they are going to want me to stay on this medication and at this point after reading all these wonderful post, Im going to stop...Im even having difficulty in typing this post my hands hurt so bad. Im so angry that when I asked my Doctor about side effects he never mentioned these. he told me about being nauseated, constipated and so one...Ohh and I have also gained about 10 pounds in 3 weeks without changing my eating habits...anyone else have that? Thank you for letting me vent here. I was scared to death until I found this site. I was seriously considering leaving work and going to the ER room...Now Im just going to stop taking it and waiting this out till tomorrow....

I got my Mirena November 14, 2008, the day before my wedding. The pain was insane, I could barely stand up as I walked out of there and hardly made it through my wedding rehearsal that night. I cramped and bled for the first couple of weeks and then it suddenly stopped only to come back full force as a full period on my honeymoon of all times! My hair started falling out immediately, but until I read these boards I was blaming it on the dry winter air and all of the coloring I do to it. My migraines came back full force (I got the Mirena because my doc took me off of the pill because it was giving me migraines) mid December and I have gained about 10 pounds always feeling bloated. I've been feeling depressed lately and extremely tired! I thought it was because I recently lost my job and now that my life has calmed down I was starting to feel the effects of it, and now I know it was the Mirena! Thank Goodness it's now really me! Just in the last couple of days I've noticed vision problems, not really blurry, but kind of wavy vision...I was starting to blame it on the fact that it's time to have my eyes checked anyway (I wear glasses) but my eyes really don't change from year to year anymore, so wavy vision is a major problem! So, to summarize, 10 lbs gained in a month and a half, bloated, constipated, migraines, wavy vision, spotting, depression, tired constantly to the point of exhaustion (I can fall asleep on demand).

I'm making an appt with my doctor this week to have this thing taken out! I don't know what to do next. I can't have any more babies...I had one baby, she died in March 2003 due to multiple birth defects and the doctors don't know what caused them, I'm not going to do that to another child and I'm not going to go through that again. I can't find a doctor to tie my tubes though, so hopefully my husband can find someone to give him a vasectomy!

I have had great experiences with Levothyroxine. I am no longer tired, achey, grumpy, constipated. I feel great. I am only 27 years old and got my hypothyroidism from having my first child. I am excited that my levels are now normal after 3 months (TSH was 25.89). I was on .50 mcg now I am on .75. Feel great!
I am a medical technician and have found that a lot of people who start on a certain medication for hypothyriodism, such as Synthroid - do not fair well if they have to switch. My doctor always says NOT to switch...not EVER. She repeats over and over again to check my prescription every time I receive it. That means checking the pills against each other, because hypothyroidism medication is one of the highest missed - filled prescription. If I were anyone who has had to switch, I would demand to be put back on your original meds. Have your physician write up your symptoms with the new meds and make a recommendation to the insurance company that you NEED synthriod.

November, 2008 I started Januvia about 3 months ago while also taking metformin, glimeride. I previously took Actos but was gaining a lot of weight. Actos replaced the Avandia. The first few weeks on Avandia I seemed fine and the bs was okay. Gradually it increased along with severe painful spasms in my legs, trunk and daily in my neck. Eventually my hands began cramping. I also became severely constipated which is quite unusual for me. I then developed a series of upper respiratory infections. Since I was feeling awful I decided to research Januvia and its side effects. The manufacturer mentions the infections but not the others. As an experiment, I stopped taking the Januvia and within about 5 days, the painful leg/trunk spasms began to disappear. I'm contacting my doctor this week to find me a new drug....hopefully not insulin.

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

My daughter is a 14 year old mentally disabled child who will be 15 next week. She was prescribed Risperdal last month. Her doctor wanted her taking the lowest dosage ( 0.5 ). She's non-verbal. So to get you to understand her wants and needs she uses gestures. I noticed since she has been on the medication that she is always wanting to be held. Was very quiet. Sleeping a lot. She wasn't constipated like the others here have brought up, but she always had diarrhea. Was gaining a lot of weight as well. But it was what happened this morning that made me panic. When I was giving her a bath this morning I noticed that she had a white drip on her leg. I didn't think anything of it because it looked like the liquid bath soap. She gave me a hard time to take her out of the tub, so I put my arms around her from behind causing me to put pressure on both of her breasts. Milk shot out from both breasts. Of course as the mother who knows for a fact that her daughter is a virgin I began to panic. With the recent weight gain and the enlarging of her breasts, and now this, my mind began to think negatively. But from reading what I have so far here on this site I now see that it's happened to others and that it IS the medication.

I was diagnosed as having Bronchitis. I have cardio vascular disease; have had 4 heart attacks. A doctor prescribed Levaquin 500mg for seven days. I started getting pain in my left leg about the 4th day of taking the Levaquin. I started having difficulty breathing and found myself gasping for air especially at night. I just thought the infection was getting worse and I finished the 7 day of pills. After that time I got a rash on my body, shortness of breath continued, my eyes were swelling up, had little urine flow, got cramps in my feet, thighs, neck and arms and I gained 20 pounds of fluid even though I was not eating much and swelled up like a water balloon in my abdomen and down to my feet. I went back to the doctors office, had a different doctor which she said I was having heart problems. She ran blood tests to check the heart and liver, took another x-ray, gave me a drug to test my urine flow and when the results of the blood test came back I was told I had an enlarged heart, fluid in my heart cavity and referred to schedule an appointment in two weeks with a cardiologist.

Then the doctor asked me if the previous doctor knew I had heart disease and I said yes. This doctor informed me it looks like you had an allergic reaction to something. She then prescribed a blood pressure and diuretic for me to relive fluid and released me, I took the diuretic one day did not relieve any additional fluid became constipated and I immediately stopped taking the water pill.

I then went to a third doctor four days later since I got no help from the first or second doctor for the shortness of breath, fluid retention,swelling and shortness of breath.
This doctor asked me what medication I had taken I informed him Levaquin and he proceeded to tell me they were having trouble and bad effects in some people taking Levaquin. I felt relieved because I had read the warnings that came with the medication and I confirmed I had certain allergic effects from the drug. The doctor then took a blood and urine test told me to come back in four days until the blood test results come in. I am extremely angry at the medical profession and the treatment I have received for their failure to treat the side effects of the prescribed medication I was given, I even read Lefaquin has caused cardiac collapse in some patients so why on earth would a doctor prescribe this medicine to a person with cardio vascular disease? I am sitting here suffering the side effects and they are out of the office not having a concern to my suffering just lining their pockets Monday through Friday with cash, Our medical and drug systems are broken and no one is attempting to repair them to my knowledge.

I have been on Levoxyl for only 12 days after switching from generic Levothyroxine, which I was on for 3 years.. I have no history of any GI disturbances and the last 5 days I have been extremely constipated, had horrible stomach cramps, gas and bloating. I am on no other meds, so my Doc and I have concluded maybe Lexovyl is not the right med for me?. Am starting name brand Synthroid tomorrow. In addition to the GI disturbances I have been having headaches the past week as well.

Seroquel is awesome. I, at the age of 50 realized that most likely I was Bi-Polar. My swings we not drastic but were hard on me and people close to me. I am taking 300mg at bedtime. I sleep like a rock, wake up with a slight haze which disappears after my first cup of coffee. I feel on top of my problems and not underneath them.
I have a theory about the weight gain, something that may possible help. I noticed I was becoming constipated a bit. I think that when your food stays in too long, your body sucks out every bit of fat, etc. I bought some Metamucil, which works great to keep things moving quickly. I also have modified my diet to lean eating.
I am having one problem. I have a crick in my neck, on the left side. It is very painful, kind of like I have pulled something. We went out to a Christmas Party last night and I had a few drinks. The neck pain came on quickly. Anybody else have this?

Well, I have been off the NuvaRing now for about 2 months, but while I was on it, I experienced a range of side effects. After insertion, in about 3-4 days, I experienced heavy discharge & extremely high sex drive. But, by the next day, I also had a constant migraine and felt sleepy all the time. What I thought was strange was that I felt abdominal pain & realized that I was constipated. I thought nothing of it & assumed it was from my diet, but then my boyfriend was constipated also. Now, he's as regular as the sunrise & if he was constipated then there was something seriously wrong. After about 2 weeks of a constant migraine, I called it quits & removed the NuvaRing.

My doctor put me on Neurontin for nerve damage to my foot related to heel spur surgery. I started taking it on the 17th of this month with it having no effect on the pain (I was only taking one dose a day at 300 mg). He has since upped me to 300 mgs twice a day. I am now having problems with bladder control, infrequent headaches, sleeplessness, inability to climax and horrible bloating and gas. If I hadn't been on other pain meds for the past 8 months, I would stop taking it. Any suggestions?

I started taking Yasmin this past sunday, so far, so good...reading all these posts worry the crap out of me...i'm only really on this because i have really BAD pms, which people i know including my boyfriend thought it could be PMDD because how "crazy" i'd get, bad cramps and my period sometimes likes to show up almost whenever even when i track it....i'm a moody person already and so far i feel pretty good, pretty stable which is nice, i guess the only complaint is that i'm kinda constipated and i'm exhausted, but i'm unsure if this has anything to do with this pill or not. i travel constantly and eat bad food since i'm away at college so sometimes i have some issues....oh my sex drive is usually pretty fine, i haven't noticed anything there yet, i still think about doing things and want to...so, my question is what should i do? shall i continue to use it and see what happens, or should i stop it or get a different pill?? i go to therapy and i am also making sure that my boyfriend and immediate friends notice if i act a little stranger than usual....
and i was on a different pill back when i was 15 and i don't remember much of it besides i don't think i had any side effects so i've had a little experience with birth control before...

I took Lipitor for 4 or 5 years. I lost count. I am a type II diabetic and the Dr. threw tons of prescriptions at me. I was convinced all my problems were not the result of Lipitor because my sister's Dr. told her that if you had the muscle pain you would have it all over. Well I got sick of feeling like I was 85 years old. I am 57. I know I am not young anymore, but I couldn't sit for more than a few minutes without having trouble getting up. The right top of my leg hurt so bad some times that I could hardly walk . I also had really bad pain on the right side of my lower leg. I had pains in my neck and shoulders and attributed it to stress at work.Last, but not least I had terrible gas and bloating. The gas was downright embarrasing. Well I took it upon myself to stop taking it. Within several days I felt like a new woman! The minute I woke up one morning I could feel the difference before I even got out of bed. I felt like I had been given my life back.

When I called my Dr. to let her know she wasn't very happy and wanted me to come in. Well now she put me on Crestor and it's been two weeks and the old pains and gas are coming back. I am NOT going to take these terrible statins anymore. They say that the muscle and joint aches are rare, but that is only because most doctors won't listen to their patients. You know your own body better than anyone else.

I have heard that some of the "older" statins are not as powerful and they don't have as many side effects. Has anyone else heard this or had any experience using them?

All I know is that for now I am off statins.

My experience is also not a good one. At the end of June 2007 I was prescribed Cipro XL 500mg for 3 days for a bladder infection, at an immediate care clinic. Over the next two weeks I experienced abdominal inflammation to the point I looked 6 months pregnant. I returned to the same clinic where I was again prescribed Cipro XL but this time 1000mg for 14 days and waited for a urine analysis to come back. As this showed no infection I was told to continue the CIPRO and contact my gynocologist who could find nothing wrong. I was sent for abdominal and pelvic ultrasounds. Both came back clear but I was still in considerable pain and the inflammation had not gone down but was worse. In addition I was constipated constantly, a problem I had never had. From my gynocologist I was sent to my family doctor. Blood work was done as well as a barium enema. Nothing found, everything normal. As at this point, October 3rd I was having constant diarrhea with blood I was sent with a stool culture. Cipro XL has caused me to have a strain of C-difficile. As the diarrhea has stopped my family doctor feels I should not be given medication (not antibiotics) to clear the virus. With lots of fluids, probiotic yogurt, etc it will take time but it will go away. I will just have to put up with the cramping, bloating, head aches and general malaise I have felt since it was prescribed at the end of June. I only hope anyone prescribed CIPRO XL will think twice before taking it and perhaps request a different medication. There are others.

Took 2, 6day packs 4mg for 2 ruptured discs causing crippling back pain. Could not walk much at all or stand straight. Im 37 years old male, have always avoided any meds if possible.
Results:
Back pain went away after 10 days, along with good chiropractor visits, cold pack treatments throught the day and lots of lying flat on my back wearing a brace provided by chiropractor.
Side Effects:
-Sleepy during day, difficult to sleep at night.
-Slightly blurred vision.
-Constipated at times and loose at times, small amounts blood in stool three times.
-Frequent trips to urinate with uneven flow all the time.
-Have had slight occurances of heartburn.
-One week after 12 days treatment was over the pain returned more and more and I started to peel on my face without being in the sun, without redness and I have been well hydrated.
-Maybe depressed but may also be caused from needing to cancel scuba diving trip due to condition.

Starting to take 6 day pack again for returning pain. Wish me luck...thanks

Now I am off this medication ( for 3 months) I am no longer constipated!... cant believe this as this had been a problem for all the time I'd been on ACE inhibitors.
Also had the neck pain mentioned by the previous writer.... this is improving slowly too.I now take small dose of duiretic (Bendrofl,,) at night and feel I am alive again!!.

My dad has dilaudid in his pain pump that goes right to his lower spine. It has slowed down digestive system. Food is staying longer in his stomach and is not processing thru his system properly. As a result he is always nauseas. He is constipated also. At times he has experienced shortness of breath.

God bless you all for posting your experiences here.
Until now I was feeling like an alien or someone trying to find excuses.
I've had the device since 2004 and my life changed a lot since!
I had 1 month heavy bleeding, 1 month latter I got so constipated that I had to go to the doc. Now turns out that I developed IBS, the symptoms I began feeling since I put the Mirena.
My mood changed completely, I was full of joy, up for anything and I felt tired all the time, my libido decreased a lot as did my lubrication.
My face is now covered with acne and scars, the doctor denies that Mirena can be causing this but after lots of medication....nothing sorts it out!They will have to give up and do some more research about it.
I also lost my hair at the beginning and now it is growing everywhere - forehead, chin, cheeks, breasts!
I will visit my GP next week and ask to remove it. Even though I am very scared of the pain - as I had to have anaesthetic to put it on - I am now prepared to do it.
Only good things: I did not get pregnant and my horrendous periods have gone for 3 years now!

i've been on this med for a little over a month. lately i am very constipated with green stool, when i can go. sharp pains and gas. all this for mild acne. by the way, i take 100 mg once a day. nausea and sever heatburn if taken around 2 hours before bed:(

I have found since taking this drug that my bowel movements are very difficult. I am not actually constipated, but feel almost impacted. I have never experience this problem before, and attribute it directly to this drug. I am curious if I am alone in this problem.

Thanks

Is anyone having chronic shortness of breath with their Mirena? I have been tested for everything under the sun, and all tests have come back negative. I was even checked out for cancer! I am 22 years old, previously very healthy. I have no other symptoms, except the spotting and longer periods.

Frustrated,
Darla