Referral symptoms and conditions

I am so glad that I found this site. I had my Mirena put in February 2009 when my son was 10 months old. I wan't even looking for options for birth control. My doctor kept pushing it on me every appointment we had. I knew 2 people that had it and they loved it so I thought why not. The day I had it inserted I had major major cramps. But the doctor said I would experience cramping. Well the next day the cramps were so bad I was doubled over in pain. They felt just like contractions from active labor. After about a week they went away.
Then came the rest. Heart palpitations. Tossing and turning at night. Night sweats. My contraction cramps came more and more frequently. I started getting pimples and I never get pimples. Joint pain especially in my left shoulder. Mood swings like I've never had before. I don't even want to be around my son who is now 16 months old. Most days I feel like both him and my husband would be better off without me.
I went to my doctor in June and she told me they're was no way it could be from the Mirena. I then called the Mirena clinic. They told me the same thing and said not only would I have to go through my family doctor for a referral to have it removed, I would then have to wait 3 months for my appointment. Needless to say I felt backed into a corner.
I made another appointment with my doctor planning on telling her we were going to try and have another baby and hopefully we would get a better response.
Well in walked in a new doctor saying my old family doctor no longer works there! So I told the new doctor about my symptoms. She took out a pen and pad of paper and started writing everything down. She told me that it's rare for it to happen but few people have serious side effects. I felt like giving her this website.lol
Anyway, 4 days later I have an appointment on Oct 6th the have it removed!!! I am so happy. I will post an update.

I was prescribed this for Epididymitis (sp?) about 4 weeks ago (100mg 2x a day). After a week or so on the meds, I began to have a striking number of the symptoms that everyone else has listed previously: Chest/Ab cramping, feelings of swelling in random places, loss of appetite, dramatic mood swings, a high level of anxiety, crying for no reason, confusion and panic attacks...I called my GP today for a psych referral, and when he calls me back I'm going to ask to be taken off the Doxy. Thanks to everyone who posted, it helped me for sure!

i just got off of the phon with my ob's office having spo9ken to her nurse about YAZ. i have been on it for a month and for the last week i have been having pain in my calf and behind my knee. i am worried about a DVT or something serious. i wonder if a doctor would do some tests to tell me if i have blood clots or not because i am worried. the pill has greatly reduced my horrible pms symptoms but i don't want to dye of a pulmonary embolism! they may take me off of the pill, don't other pills also have a risk of causing blood clots?

I have been using Topamax now for 8 years off and on. I stopped the Topamax about 3 months ago, something I do once or twice a year to try and feel 'normal' again. Then last month I went to see my regular doctor because of numb, pale, swollen, achy fingers, swollen ankles and feet, and for a papercut on my knuckle that overnight turned into a radical staph infection. The NP ordered a full blood panel and the results came back positive for Lupus. I have had so much pain in my hips and knees, more frequent headaches (not migraines), insomnia and vision trouble. The past two weeks I have been super irritable and nauseous. I still need to have a 2nd opinion and/or referral to a rheumatologist, but is all of this related to taking the Topamax? I take 2 Imitrex injections if a migraine comes on and am hesitant to start the Topamax if it has indeed induced Lupus. Am I crazy or is this common??? THANKS for the feedback...SM.

so far, ive been on Yasmin for almost 3 wks. the first week i had no side effects but as time progressed i started getting abdominal craps with a watery vaginal discharge; it sorta feels like i'm having my period except ther's no blood. i'm constantly nauseous and i have no appetite. my legs can feel numb at times and i get these really sharp pains in my chest. my body practically feels tender all over. i'm really depressed lately and my moods change drastically. Is this normal?

I have used the NuvaRing for about 3.5 years, starting after my 6 week check up when my daughter was born in 2004. In the beginning I felt like it decreased my sex drive but also that maybe post baby body that caused that too. For three years I had no problems. I had noticed breast tenderness throughout but other than that no side effects. About 8 months ago it began with a missed period, then two periods in one month. My OBGYN recommended 'resetting' my body by taking out the ring until my next cycle and starting it up again. I followed his directions but the next cycle came along with a bladder infection followed by a yeast infection. Over the next 4 months I either had one or the other, continually visiting my doctor I didn't make any connection to the two. Stomach pain, chronic fatigue and kidney pain also added to the list. My doctor prescribed a series of medications followed by blood tests and a referral to a specialist. Over the summer my husband asked that I stop using the ring because my sex drive had hit rock bottom. After a few weeks of taking out the ring, the burning sensation during urination has gone away. Stomach cramps and back pain has ceased and no infection to date. I am in my early thirties and after a week off the ring I realized what they mean by 30's sex drive. My husband and I are both happy with the changes. I visit my OBGYN again in a few weeks to revisit non-hormone options for BC

I have now tapered to 10mg prednisone every other day and will end 75mg Cytoxan Aug 19th. Just went to the Dr. and she said protein is back in urine (bad) but also rising in blood. (good) I can continue to taper prednisone but will have to have another 24 hr urine speciman to determine wether I have to go on cyclosporine. Was originally diagnosed with Minimal Change Disease, but now she thinks it could be another kidney disease. Has anyone had successful tapering with the addition of cyclosporine? Does the urine protein ever get higher? What about side effects of cyclosporine.

In response to Wewe's post, I've been wondering the same thing. Since taking my daughter off Singular almost 2 months ago, I'm seeing a different almost typical kid. Four years ago about 2 months after starting Singular my daughter was diagnosed with anxiety. As her condition got worse she was diagnosed with depression. We started to see OCD and tics so they were added as a diagnosis It was determined that it was related to strep infections so she was diagnosed with PANDAS. She was started on Zoloft and klonidine. The Zoloft made her worse. Her fears of hurting herself got so intrusive she was hospitalized. Her cholesterol was high too. The Zoloft was discontinued and Prozac was started. She's had therapy all 4 years. She also neede physical therapy due to muscle and joint pain. Now she's doing better, off Singular. Does she really have PANDAS, OCD? I don't know. She's still on Prozac, we just did a slight decrease this week. Is this medication the trigger for underlying conditions. Learned behaviors can be unlearned, but are there lasting physical effects? If a gene has been turned on, can it be turned off? I wish we knew the answers to help all of our kids.

So nice to see that I'm not just imagining the adverse reactions. I've been taking Advair 250/50 for about 3 weeks now after being diagnosed with asthma/chronic bronchitis. I went back to my doctor the following week because I was still having chest pain, back pain, felt as if I still wasn't getting enough oxygen and mentioned that I was having a lot of difficulty with being jittery. He evaluated my breathing with a peak flow meter and since that seemed to be OK, he wanted to do an EKG - which he did and seemed to see something that warranted a referral to a cardiologist. So far the cardiologist has not seen anything out of the ordinary.
I'm thinking more and more that there is nothing wrong with my heart and that this is all being caused by the Advair. Has anyone else been referred to a cardiologist and found out nothing was wrong?

This is the 3rd time I have been on Wellbutrin. Once in 1999, then in 2004, and just started taking it again 3 months ago. The first two times I took it I had joint pain and a lot of muscle inflammation. This go around is different... Just recently, within the past few weeks, I started breaking out with hives, after taking it with no problems for three months! Started on my head and progressively got worse. I break out all over my body, head, legs, back, hands, etc. For some reason it seems to happen more frequently when I lay down in my bed to go to sleep (weird!) One other scary side affect is, I frequently stop breathing when I start to fall asleep, and wake up gasping for air. Has anyone else experienced this?
Since I had never experienced problems with hives the first few times I was on Wellbutrin, I didn't think it was the medication causing the hives. So, I cut my dose in half (50mg/day). The hives didn't go away, so I stopped taking it all together 3 days ago, but still continue to get hives. Does anyone know how long it takes to get it out of your system?

Severe hair breakage/loss. I've always had fairly thick hair - since starting Actonel 35 mg 1x/week, have noticed lots of hair breakage - The actonel is the only thing different in my life in the past 4 months, so I attribute the breakage to the drug - anyone else have severe breakage? This is in addition to severe left hip joint pain, jaw pain, and upset stomach. I'm not going to take any more Actonel.

My daughter has been on prednisone since October, 2006 -today is July 25, 2007. She is a 35 years old with asthma and allergies. Originally the pulmonologist thought she had ABPA (Allergic Bronchio Pulmonary Aspergelosis) and put her on 60 mg daily. This year has been a nightmare for her. That original diagnosis apparently was erronous, but she was kept on the high dose for breathing issues, with instructions to lower it as she could. As of today she is on 30 mg. daily. Side effects? So you know she is no "loser", she is a PhD in Biomechanical Engineering, has two patents to her credit, has spoken at numerous medical conferences (for vascular surgeons and cardiologists), and has had countless articles published in medical journals. Now she can't concentrate much less sit still, has not read a book in months (she used to read at least one book every week), she has two research publications that need to be finished but she can't focus on the work, is totally exhausted and needs to rest after only a couple of hours of mild activity, has a face she has described as looking like a mongoloid. Her beautiful, big, blue eyes are slits in her face. Clothes that fit yesterday wouldn't fit today - and those that fit today won't fit tomorrow. She craves food in the middle of the night and said she usually eats 2 bowls of cereal. She has terrible pain in her torso. Her esophagus has become so eroded she is on 6 different meds for that, and as a result cannot eat salads or raw fruits or anything that might irritate the lining of the esophagus. Her body is covered with huge dark bruises. The latest side effect made evident happened this past Saturday night. She fell striking her shins on a carpeted step. Her skin has become so thin that it actually burst open. She said it reminded her of when we'd blanch tomatoes in boiling water to peel them, and how the tomato skin would just burst open. That's how her leg was. That little fall cost a trip to the ER for stitches, tetanus shot, and antibiotics. Her husband is a career military, so since they married 1 1/2 years ago she's lived in 4 states, there's not much history among doctors. She lives now in Kansas and has started seeing specialists through the university there. We just wish she could go to Mayo Clinic for complete evaluation, but unfortunately military insurance doesn't seem to cover the best.

My daughter is 5 years old and has been on singulair for 1 week. i have already noticed a dramatic change in her behavior. she has become irritable, mean, nasty, and emotional. she has had me in tears on a daily basis. she has turned into a monster. we will be calling the doctor in the morning!

l have been on yasmin for 8 months and the pill was fine but l started to have a breast white breast discharge for the past 4 months. my gp says its normal and he refused to give me a referral

Bruce, don't take the shot anymore, go to a E.N.T. allergy Dr. & start the shots for allergies. I think these weekkly shots last for a period of at least 4-5 years every week. Check with your primary care physician for a referral. I'm gonna do just that!! No more Kenalog shots, there's to many side effects that hurt you in the long run!!!!!!!

I started to have balance-problems, problems with depth perception, falling, walking with a cane, experiencing muscle weakness, pain and spasms, walking with a walker. Finally had to stop working because I could not get around by myself. I'm a 61 year old female on Zocor for three years. I'm seeing my third (via referral chain) neurologist. No-one has ever made an association with my progressive debilitation and Zocor.
I am going to STOP taking Zocor. I feel deeply that it is the cause of my neurological problems. Very limited discussions on neurological side effects.

I am so glad I found this site. My son was put on Singulair a week ago for a mild case of asthma along with coughing after playing outdoors and constant throat clearing. The constant throat clearing had me worried and I had heard that it COULD be a symptom of asthma. A referral to an ENT doc found the asthma. Anyway, after several days on the stuff, I noticed that about 2 hours after he takes the med, he becomes feverish AND, his behavior was becoming increasingly aggressive. The other evening he got so angry about something he started banging his head on the table! This is NOT my little boy. His coughing had subsided but it didn't do anything for his throat clearing. So, I looked at the leaflet that came with the med and saw that fever and aggressive behavior can be a side effect. I stopped giving him the Singulair. Doing a google search this morning, I found this website and am glad to see that this is not my imagination and that others have also had problems with the constant throat clearing. Does anyone have anything to say about this?
I've left a call with his doc to see the next step.

I was prescirbed singulair a few months ago because i went to my annual check up with my doctor and he found that my allergies were "too high" specially after gone with surgery (tonsils, adenoids, deviated secptum etc) associated with sleep aphnea. i had my surgery about a year ago... well he prescibed me singulair and i took it for about one week and i didn't notice any change (good or bad) so i quit the medicine. today i went to the ENT that performed my surgery(another doctor) a year ago to do a follow up he read the referral that my primary doctor annotated in my record and told me .. that with singulair i will get rid of my sinus. i decided to do a re-search on the medicine and i am soo glad i fond this site. I am not even going to start my medicine. i rather deal wiht my sinus than with all the side effects associated with the medicine. good luck to you all.

I started yasmin (after my doctors referral) about 9 days ago....the horrible nausea started on about the 3rd day, and has continued...i don't know what to do..the worst is the past few days i've had a panic attack type feeling..my chest gets tight, can't breathe that well and then terrible nausea. I am now convinced its yasmin but i guess i'll wait it out till the end of the month. Previously i was on loestrin and did well, except two days out of the month i was moody/depressed and then it would clear up...if anyone has a suggestion of a pill that was good for them, please let me know.