Lips symptoms and conditions

I am 40 years old and was prescribed lisinopril/HCTZ 20-25 a little over two weeks ago. I went in for a little congestion and low grade fever. I am a teacher and have many kids out with the flu, swine flu, etc. and felt that I needed to get checked. I came out with 5 medications, one of which was lisinopril. I have never had bp problems in my life. I am almost certain that the nurse practicioner wrote me down for something else and the dr came in and changed. I am usually a very calm person but in the last two days have experienced what I thought was a panic attack and anxiety, horrible anxiety. I haven't been able to face my students which isn't like me at all. During the first week I took my students on a field trip and had a really great day with them- much less stress than a normal day. I got home and my bp was around 138/98. I thought that was kind of odd. It has been under control since I started taking it. On this same day, I got blistered on my face and wasn't outside much at all. I have Rosea and thought that it had been aggravated. I believe now that it was the lisinopril. I know that it has a diuretic in it, but it doesn't make me go frequently. Instead I get a sudden urge and have had two "accidents" recently. I have a sometimes dry, other times full of mucous, cough to the point of nearly gagging. My neck muscles were already stressed out and tight, but have gotten worse. I feel a tightness in my chest constently. My lips are so dry that they peel all the time. I have no appetite and when I do eat I get nauseous and almost feel like vomitting. I have been lightheaded and dizzy. I am not sleeping and feel extremely tired all the time. But these last two days have been awful. I love being around people and right now can't stand the thought of it. I am guessing that lisinopril has caused much of these problems. I am about to go see the doctor today and think they will want to put me on some sort of nerve pill. I hate that!!!! I have a plan to achieve everything that these meds are supposed to. Exercise, change my diet, go see the chiropractor, do more relaxing things for myself and take better care of me! After reading these blogs I believe that I am going to take myself off of lisinopril and see what happens. My hubby is also on it and just last week developed an oozing sore and his left cheek - could be the lisinopril. I will pray for all of you bloggers and those who are unaware. This is definitely a poison to our bodies. I think I even read that it contains snake venom. Is this true????? I will update in a few days. Good luck and God bless!

I started the antibiotic on sept 23rd at night. Everything was going good until Monday night. I started having problems sleeping. Tuesday I went to work tried to run but I almost fell. Went to the emergency room with burning pains in my chest and my legs and hands kept trying to make me do a back bend. The doctors told me there was nothing wrong with me and they gave me a shot for pain. It didn't help. I tried to walk my calves were really bruised. I could not go out in any form of heat. My lips would become white and I would have problems breathing. The doctor checked my sugar and said it was at 117 a little bit high for someone who wasn't eating. So he did lab on me. My medicine was for 2 weeks and 1 extra day. The doctors lab took about a week and by the time I had gotten the results I had already finished the antibiotic. He told me I had Steven Johnson syndrome and that I was his second case he has ever seen. My hands hurt to lift or touch anything. My feet swell and turn purple. My lips become white and I have some problems breathing. And that's because it's over a month already since I have taken it. I still haven't gotten my appetite back. During the 2 weeks of taking this medicine I lost 13 pounds. Doctor told me he was glad that I didn't get the blisters. I drenched my skin in Vaseline and then I would take a bath. I took about 5 baths a day and drank about 7 bottles of water. I should be better before Christmas.

I'm so glad to find this forum. I've been on Yasmin for 7 months since March 2009. My gyne recommended me to take it because of my acne problem, heavy period and cramps. Ever since I started taking it, I was happy about it. My face is cleared of acne and my period only lasts for 3 days and very light without pain. I was a happy camper until the 4th month into taking Yasmin. I started to have patches of rash on my right temple, then a week later on the left temple and upper lip too. At first I thought it was due to my new face toner. So I stopped using it. I didn't think it would be the pill as any allergic reaction usually would should up 1-2 months after taking it. The rash got worst after 2 weeks, it started around my waist, more like hives this time. I can't stop itching my skin even in my sleep. It was unbearable. The hives comes and goes. And it spreads bigger and bigger to behind my neck and back. I drives my NUTS and my skin is very dry. I saw my family doc, and he thought it was eczema/fungus. He gave me some steroid cream to apply. It helped but didn't make the hives go away. I kept looking for the cause of the hives, but have no clues. After I read many people who posted in this forum also suffered the same problem, I can conclude that Yasmin is the reason. I'm stopping the pill today!!!! Hopefully, the hives will go away soon.

My dad had taken Avelox 400 for 5 days prescribed by a doctor for Bronchitis. He is a cardiac patient as well. After 1 week he developed the following symptoms in the order: high fever, Swelling in the ankles and knees, mild jaundice, thick sputum, rashes all over the body, difficulty swallowing food, conjunctivitis affected like discharge from the eyes, poor mental co-ordination, skin tearing in the lips, diarrhea, difficulty passing stool, anxiety, confusion, low blood pressure, insomnia, slightly impaired vision. I only hope and pray he recovers soon. I really do not know why this drug is administered to people when there are other alternatives which are milder. This drug has not done any good to anyone.

I just started taking this drug three days ago, and I am already having such bad side effects that I don't want to take it anymore. I am only 29, but have a family history of high BP, and went to the doctor last week to find out my bp was 175/90. Since starting the drug, I've been getting dizziness, but last night took the cake. I woke up around 4:30 with horrible nausea. I ran to the bathroom where I fainted while sitting on the toilet lid, wanting nothing more than to vomit. I remember waking up and looking in the mirror, and my face was as white as a sheet, as were my lips. I looked dead, and it scared the hell out of me. As I came to, I suddenly had diarrhea hit me, and once that was over, I felt better. My husband thinks my body is trying to get rid of the drug. In addition to all this, I am having palpitations and feel that my heart is beating too fast. I know that part of this is nerves, because I'm scared of taking this medication, but the fainting and nausea ARE because of the drug. I called my doctor today, and she wants me to come in to get my BP taken again. I am so scared that she won't lower the dose or (better yet) switch me to something else, because my bp always goes up at the doctor's office when I get nervous, every time. Oh, and I also started metformin last week because the doctor tested my blood sugar and it came back 250. Could it be the combination? I don't know. I just know I have only been on this stuff for a few days and already hate it and feel that it's bad for my body! It's very scary.

I am on day 9 of Topamax. I have Depression and ADD the is controlled by 300 mg of Wellbutrin and 30 mg of Adderall daily. I always felt like this drug regimen was working but I was still having some days where I couldn't shake the blues. I saw my prescribing doc and he suggested Topamax. He started me on 25 mg and in a few days I will increase to 50 mg where it will stay if things go well. I am a 34 y/o woman, married and a preschool teacher.

So far, my side effects have been EXTREME thirst. It's so bad that my lips are actually a little chapped. As far as taste goes, things don't necessarily taste bad to me as much as I just don't have an appetite at all. I have lost 5 pounds in 9 days! However, all soda tastes flat to me. I have tried everything and it's all just flat. In the grand scheme of things, who NEEDS soda? My husband says that I have been a little sensitive lately but, I have always been an overly-sensitive person so, I don't know how much faith I put into that. But, as far as my cognitive abilities, balance issues, and energy? I feel more energetic than usual and I don't feel at a loss for words at all. I also feel even more patient with the children in my classroom. Oh, I have been nauseous off and on as well, which contributes to my loss of appetite.

Now, my dosage will increase in 5 days from 25 mg to 50 mg and I hope that I don't feel different after that increase. When and if I do, I will be right back here posting. I would like to thank those that have posted. It has given me so many good things to look for and has put my mind at ease a little. Good luck to all and best of health!

I had a severe upper respiratory infection and regular well known antibiotics wouldn't kick it. I went back to the physician who prescribed Avelox. Within less than 2 minutes of taking the first pill out of the bottle I started getting sensations of bee's stinging my tongue everywhere and my lips were tight, purple and swollen. Within just minutes I started having a hard time breathing and the whites of my eyes were really bloody. Next thing I knew I could literally feel and hear my heart beat in my ears and everything sounded like I was in a tunnel. Within 5 minutes of taking the pill an ambulance was called and by the time they arrived my blood pressure was 70/16 with over 240 pulse.

When I got to the ER they said I wasn't the only one with the same issue to this drug and 3 were within the week prior to my being there. When I said I had SVT Supra Ventricular Tachycardia the doctor said people with SA Node (Natural pace maker of the heart) issues which control the magnetic aspect of your heart biting it sends something in there to screw it up and make it a big mess. I wouldn't suggest this med to anyone as I did some other research on it through the web and their reports from the FDA and there were some pretty NASTY side and long term effects of it.

Needless to say; since this happened I've developed a panic disorder and my nervous system isn't working correctly. Again; be careful what you take.

My symptoms are much like others described. I was prescribed Bactrim for a recurring UTI. I have never taken it before and have never been aware of any drug allergy. I took the Bactrim two times a day for five days. On the fifth day I began to develop a fever, with very cold chills, then very hot. The lymph nodes in my neck and the back of my head swelled up that evening and were painful when pressed. The next day I stayed home from work and my temp was up to 100.1. By evening that second day, I had developed rashes on my elbows and feet. They were itchy and raised. The next morning, which is today, the rash has spread to my shoulders, arms and thighs. It is not raised, but is a mass of small red dots. My face is also very red, and I think that my lips feel swollen. It has been good to read here that these are likely the result of the Bactrim. Much better info here than I got by calling the pharmacist! The only reason I looked in to it being a reaction is that my mother in law has had allergies to sulpha drugs, and has mentioned rashes. I agree that it is also interesting to here that it has happened to others either after the prescription had finished, or right around that 5 or 6 day mark.

I am a 57 year old male took lisinopril for about 6 month. Had to go to er with Angioedema. Lips, jaws, and mouth swelling. The doctor in the er said that lisinopril did this to me and I should never take it again. It was supposed to lower my blood pressure.

I was on doxycycline for three weeks because the doctor believed I had Lyme disease due to the slight headache, mild fever, and aching joints that I was experiencing. I was fine for the first few days, but then I began to develop some unusual symptoms. The symptoms fluctuated day to day, but I was never free from one or more of these symptoms: severe headache, chills, night sweats, tingling in my arms, weakness in my legs, ear ache, numbness in my face (especially my eyes and lips), anxiety, depression, insomnia, pain in my eyes, and neck, and stiffness in my jaw. At the end of three weeks, I seemed to have more Lyme symptoms than before I began the medication. My Lyme test was negative, but with my continuing symptoms my doctor recommended that I take the medicine for ten more days, and retest for Lyme. The first day back on the medicine I was sicker than ever. I waited it out because the doctor insisted that it was the best thing to do. I finished the medicine, and the effects were less intense. My second Lyme test was negative. I am being tested for Fifth's disease (my son was ill with it just as I began to experience my swelling joints - a condition that can not be treated, uggh). I seem to get worse if I don't drink all day and night - a lot of water is needed, all the time. The effects also increase when I go to bed, recline on the couch, allow myself to become nervous about my condition, or over work myself through the day. I was at the pediatrician with my son yesterday, and mentioned my problem, wondering how long it could take to get the medicine out of my system. She told me it could be as long as a few months. It's been two weeks since I took my last pill.

oh my...thank god for reading this site...i so thought something is seriously wrong with me i had the mirena inserted in feb.. i have had the worst acne breakouts through my hair all my face, back, chest, legs etc, i have been having headaches and bad lower backache which i was seeing my chiropractor weekly, i get abdominal pain, discharge, thrush wont go, dry skin itchy, my eyes are sore and dry itchy, i have recently started forming blistery sores, tingly in my vagina, i am extremely moody i have just about ditched all my friends and giving up start arguments, i don't want anything to do with my son, i was suicidal depressed, paranoid, dry mouth lips, achy joints, insomnia, exhausted no energy for day to day lifestyle, cant stop eating lately and feeling as though im pregnant, feeling of burning heat in my legs, wake up in lather of sweat, swelling of limbs, i just had no idea what was happening, im so glad to know now whats causing this only after hundreds of dollars at dermatologist and chiro etc, i cant believe so many others are experiencing the same, just bit worried to get it out, and what contraception to use now,

Hi I have just been given metformin 500 starting of with a quarter of a pill twice daily working up to one pill twice a day (supposed to work up to 2 pills twice daily) thats as far as I've got but will not be going any further in fact have stopped taking them as I'm fed up with feeling as though I'm tired all day no energy can't remember names of close relatives and mood swings and feeling depressed my lips feel swollen and tingling.

After reading these posts I am more confused than before, because my experience is so far very different. I was diagnosed with DVT about two weeks ago and now take Coumadin daily; the Lovenox injections have been discontinued. The reason I'm so confused is I now feel the best I have in 5 (five) years.

Before being placed on the anti-coagulants I had memory and concentration issues that were progressively getting worse and greatly affecting my job, and had daily headaches. I had joint pain that made it difficult to get up after sitting for awhile; they felt constantly inflamed. I felt fatigued all the time and my muscles hurt like I had really pushed them; I just didn't have any strength, and had muscle cramps. I was constantly yawning and found my jaws hurt from clinching my teeth, subconsciously trying not to yawn. I was extremely sensitive to physical touch, even hugs hurt. I also felt extremely depressed and cried almost daily. My lips and left cheek tingled, as well as other parts of my body. Plus I would get the feeling of sudden pressure in my head (different from a headache) like it was going to pop off, and I my eyes didn't seem to track what I looking at and had difficulty in remembering or comprehending what I just read.

About 6 (six) days after starting treatment it completely changed and these symptoms are essentially gone. I have talked with my doctor and pharmacist and they are baffled. I am concerned this change, while welcomed, may indicate an underlying condition that is not yet diagnosed. Has anyone ever heard of such an impact from starting Coumadin treatment?

I am so relieved to see these posts. My husband started Wellbutrin 2 weeks ago. We are at the beach and yesterday he started experiencing itchiness followed by rash and welts that have spread and are huge now. He has them on his legs, under arms, around waist and on feet. This morning his right eye became extremely swollen and now his lips are HUGE.. At first we though an allergic reaction to seaweed until it started getting worse. I googled benadryl and wellbutrin to see if they could be taken together and found this sight. He has also been complaining the last week with chest pains and I see some people also experienced that. Thank you all for sharing for now I can see what is causing it and we are stopping Wellbutrin now.

I've been on Advair for a little over 35 days. I started to notice a swelling or feeling of sores or loose skin in my mouth or lips. Then I started getting a pain and burning in both the nipples of my breast. I am going to stop taking it to see if both symptoms go away. Come Monday I'll call my doctor.

I am on two 500 mg doses of cephalexin daily to help heal a bug bite..Still waiting for the biopsy to come back. Doctor suggested could be a brown spider bite. Definitely want to stop the skin deterioration and get the wound from where the bite was removed healed but the itching started on day 3 on my stomach and has now spread to entire torso, back, insides of arms and legs. I have tried aveeno baths, benadryl (knocks me out) and eucerin itch-relief. Today I coated my entire body with 1% hydrocortisone with little relief. HELP - I am scratching to the point of bleeding and now that I have read these other comments will NOT take another one of these pills. Any other OTC relief anyone has found?

I started taking Levaquin on Saturday for preventive measures for knee surgery. I had taken Keflex the week before and had an allergic reaction to it. Extreme itching on my hands, hips, shoulders and feet. I broke out in hives and my lips, eyes, hands and face swelled up. I quit taking Keflex and then a week later, they started me on Levaquin. So this morning, Tuesday, I had been on Levaquin for 3 days, I woke up feeling fine. I was up for about 10 minutes and the back of my head was itchy. I itched it and noticed that my fingers and hands were starting to swell. I took a sip of coffe and my lips were starting to swell. Within 10 min. I was swollen, itchy, in an extreme cold sweat, my throat was swelling and I could not breath very well. I grabbed my phone and called 911 and I could barely remember my address. I told the dispatcher that I was going to pass out and I did. When I came to I could hear the dispatcher trying to get my attention. When I got back on the phone after passing out, she said paramedics were on the way. They showed up about 2 min. later. My blood pressure was 101/53. I ended up going to the hospital and on the way there, they gave me a shot of epipedirine and benadryl. When I got to the hospital there were 8 people working on me. I got a shot of pepcid and a shot for the rash that was covering 90% of my body. I was still having a hard time understanding questions and was having a hard time staying focused to answer questions. I was in the ER for about 4 1/2 hours for anaphylaxis but they finally got it under control. Now I get to have epi pens to carry around with me since this was such a severe reaction. I was told to look into an allergy screening so I think I might see how much the insurance will pay on that and maybe get that done.

I was prescribed phenazopyridine Tab 200mg, same as above, for the pain and burning associated with a UTI. I had been taking AZO that was working just fine, as with any OTC med. the mg was low. Because of such a high mg on the phenazopyridine it works much better. The only problem I am having is the swelling of my lips, the blisters on the edge of my lips and a sore in my mouth. It works soooooo good, and the reaction isn't all that bad, I am still deciding whether or not to finish the medication, after all I only have 3 more!!!

Has anyone had side effects pop up after 3 years? Yes, you heard me. Three years. Hair falling out. Joint pain. "Foggy headedness." Chest discomfort. Gotta be that. Please share.

I too had bad rash experiences with Wellbutrin. I was on it maybe 3 weeks when all of a sudden, I started getting hives on my stomach and neck. Also my eyelids and lips blew up and i even went to the emergency room one day when the whole left side of my face felt swollen up like a balloon.
I was shocked when my doctor didn't think it was the Wellbutrin since that was the only thing that had changed recently.
Suffice to say, without her recommendation, I stopped taking Wellbutrin and have not had those symptoms again -- and it's a full year later!

I am 14 years old, and have had all three Gardasil shots. Now, this may not be much in comparison to what some of you are going through, and im very sorry for you. however, it seems that a very common side effect of Gardasil is a sore arm. I had my first two shots already, and i recently received my third. as the nurse was administering the shot, i heard the words "oops" escape her lips. Needless to say, this worried me. I was also getting another shot that day, so my sore arm on the day of did not worry me. However, in the days after the shot, slowly the bump from the *other* shot went down, as the one from the Gardasil remained. It is as sore as can possibly be, and has recently become quite itchy. I do not want these other side effects to occur, especially since i am going away to camp very soon. Should i be terribly worried?
please respond to this comment or email at ****** (no space... an htm just isn't allowed.)

I was on Lisinopril for 6 years, and feel as if I was robbed of those years of my life. I experienced depression, anxiety, racing heart, body heaviness, abnormal EKG's, chronic hives on hands and feet, extreme hives all over my body off and on, swelling of face, lips, eyes, hands and feet, extreme fatigue, and insomnia. I was sent to cardiologists, allergy specialists, psychiatrists, and then pain specialists when, after 2 years of Lisinopril, I developed extreme lower back pain. None of these doctors ever mentioned that any of these symptoms could be side effects of the Lisinopril. After 6 years, I one day ran out of the Lisinopril and did not have the money for a refill, and after only 3 days without the medication, all of the symptoms stopped, except for the low back pain. I felt like a totally new person, and was able to resume my life once again. Though I still suffer from extreme low back pain, I'd take that any day over all the other debilitating symptoms. I'm still not so sure that the Lisinopril did not induce the problems in my back, which continue even after 3 years off the Lisinopril. (As a side-note, my doctor put me back on the Lisinopril 3 months after I quit it, and within 3 days ALL the symptoms came back. Needless to say, I stopped it immediately.)

My experience was a seven day short-lived trip through hell on Topamax.

I began experiencing a constant headache for several months in February 2009 (no prior history of headaches). I am healthy 32 y/o male. After multiple MRI's and CT scans came back negative I had a very severe headache that sent me to the ER. The ER helped arrange for me to see a Neurologist, who after patient listening to my laundry list of symptoms concluded I was having migraines (even though I had no sensitivity to light, sound, or nausea). I had been doing a decent amount of research on headaches and didn’t agree that they were migraines but decided, he’s the neurologist, I should trust him. Let me also say at this point, I am not a person looking for a pill to cure my problems, but I was getting desperate as my headaches were ruining my life. I was prescribed Topamax.

I was suppose to start with three days at 25mg, then go to three days at 50mg, and finally up to 100mg per day. The first three days were uneventful when I hit 50mg and then 75mg…I was out of my mind. I read these messages and see people at 400mg with no problems…it makes me cringe to think of dosing that high. I stopped at 75mg…here were my side-effects. Tingling in my face, lips, hands, arms, and fingertips, chest pains (I do have GERD and it jacked up my GERD bad!!!), pain in the back of head, taste confusion (soda tasting flat), and pressure in my eyes and temples…But those are NOTHING compared to the complete feeling of anxiety that over took my body. I had a mild nervous breakdown at work, became paranoid to the point where I was afraid to do routine tasks. And the MUSCLE SPASMS…those are the worst part. I have muscle spasms all over my body, just random fluttering of muscles in my chest, arms, back, neck, head, and face! I became suicidal and had the worst night terrors ever, of things, that I wasn’t even afraid of.

I have been off Topamax cold turkey for four days now and the anxiety has significantly subsided. I have worked through a lot of the anxiety with my wife and I now believe that stress is the cause of my headaches, not migraines like I tried to tell the doctor…but the muscle spasms have not stopped (they have decreased) yet…but I can’t wait for the Topamax to leave my body.

I used to think these messages boards were part of the problem, but they are very helpful. Do your research before you put anything into your body…trust yourself and if you disagree with your doctor, get a second opinion. This has been a life changing event for me.

Health and Happiness to all

Does anyone have a problem with skin, like having dark sports on a face.
I have my mirena for about 5 moths now and just lately I've noticed about inch long brown spots above my lips. I live close to the beach(even though I don't go tanning)so sun is quite intense but i'm wondering if this might be a mirena side effect.Please let me know if you have the same problem.

I'm fed up. About 4 years ago I had a complete thyroidectomy and OMG my life has been a mess ever since, Yes, I needed the gland removed (it was a goiter pressing on my air way and esophagus), it needed to come out but OMG what a nightmare. Synthroid is a drug I can't figure out. I am convinced that this has ruined my life. I have developed chronic/non-stop head pain and pressure. My B.P. has gone up and now I'm on B.P. medicine. (still have severe head pain). It just never leaves me. E.R. visits/hospital stays and on and on. They treat me like I'm a complete lunatic because they can't seem to find anything organically wrong with me. Ummm-it hurts(my head). I am starting with a new Doctor who is a D.O. rather than an M.D. and I am praying that he finds what the **** is causing my pain. I feel like crap. The T.S.H. is in normal range but I have learned that the T.S.H. is not everything (even though my thyroid is gone). The isiots for lack od better description, are just too lazy to go the extra minute to find out what is wrong here. I just want to be able to function and this head pain will not let me do that. It is a nightmare and I have nothing but sympathy and empathy for anyone who suffers with pain on a daily basis.

The only constant is the Synthroid. Maybe I can't take this stuff. It has to be that my body just can't tolerate it and need something else or T3 added (I don't know). I just pray that this new doc can figure it out because I feel so helpless with this. My pain is always there squeezing and pressing. It is horrible. Maybe Synthroid is the culprit. Good luck to everyone.