Duh symptoms and conditions

About 2 hours after taking my 18th day of generic Wellbutrin XL 150mg. (Sun)the palms of my hands started itching like crazy! No bumps or anything, just intense itching. I immediately applied 1% Hydrocortisone cream to them and after about 10 minutes that pretty much made all the itching go away. I didn't want a replay of that, so I kept applying the HC about every 4 hours all day long, or after washing my hands. That evening everything was okay. Then the next morning, my hands started itching again...so again I applied the HC cream again, and headed off for work...they itched SO bad, and this time it took about half an hour for the HC cream to even begin to work. Then about 20 minutes into the hand itching, the soles of my feet started itching..too wierd! I was driving, so I couldn't apply it to my right foot b/c it was on the gas pedal, but I applied the HC cream to my left foot, ahhhh! Then as soon as I could, I applied it to my right foot. It took about 10 minutes, but it was soon itch free. When it came time to retake my med, I decided not to risk it. I called my prescribing doctor and she was off, and some other doc just said to take Benadryl. Duh, I was at work and #1 didn't have any and #2 it makes me so sleepy, I can't function. Then later on in the day, my wrists got welts on them, then my left elbow got a huge set of welts on it, and itched like crazy...then a few hours later, my left ankle got a huge welt on it and it looked like my ankle was swollen and both my feet and ankles had pin pricking sensations....a few hours after that, my right leg started itching behind my knee...I could feel a welt through my slacks...so again, I went into the ladies room and applied HC cream and it helped. By now I've used 1/2 the new tube of HC cream! When I finally got home, I pulled off my clothes and I had huge welts (hives) all over the back of my right leg. Plus, a big long skinny (horizontal) welt where my bra and wrapped around me. Since I was home, I could take Benadryl...so I took 4 tsp. and jumped into a warm (not hot) bath (they say to use cool water but I couldn't do it) with a cup of baking soda. Felt SOOOO good! By the time I got out they felt much better. I kept taking the Benadryl every 3-4 hours all evening but by the time I went to bed, I had welts on the back of my left leg also and on my buttocks and hips. My head kind of itched here and there in weird places, more like pin pricks but I have really thick hair, so I can't tell if I have any welts there or not. I stayed home from work today to continue on the Benadryl and making sure it doesn't get any worse. It hurts to sit here typing as my panty line is in the middle of a big 3" welt. The Wellbutrin XL seemed to be helping my depression and anger issues, but I assume the MD will put me on something else. I really liked it. It did suppress my appetite during the day but not much at night. Oh well! I'm glad I'm not the only one with these symptoms.

I had to stop taking AciPhex because of side effects such as sleeplessness and heartburn. Sleeplessness normally causes heartburn too. So that would only make matters worse. Every afternoon I would get heartburn. Duh.
I think FDA have put their IQ on mortgage to approve medications such as this.

I am 23 and just completed my series of Gardasil. The first shot hurt right away but the pain subsided a few hours later and I had no other reaction. I had the same occurrence with the second shot. I just had the third shot 3 days ago. The day after I had it done I experienced significant pain in my arm, collarbone and shoulder, chest pain,chills, headache, fatigue, stomach cramps, and swelling in my arm. I could barely lift my arm to do anything. I had the same symptoms the 2nd day and today I am experiencing a low grade fever, muscle pain all over, extreme fatigue after plenty of sleep, headache, chest pain and heart burn, swollen glands and throat pain. I am pretty sure this is an effect of this vaccine. If I would have known sooner I would have not finished the series. I would advise anyone out there looking into this vaccine to NOT go through with it. I have an appt with my doctor tomorrow to discuss this.

Well, I've had some hair loss on Diovan 80mg. been on it since about May 08 - had some leg cramps, even some joint pain, but that seems to have reconciled itself. Not too overly dizzy, some tiredness, but ok otherwise. However, got concerned about the hair loss....long/short, Dr. prescribed Toprol XL/Beta Blocker (he's been great recognizing my sensitivity to meds. I just am),...well, my God, just reading the Toprol printout first paragraph and let me tell you it ain't gonna happen, I am not taking that stuff....plus, it causes hair loss, DUH! In fairness, how can we expect the Drs. to know fully all the side affects, they are not pharmacists - best thing, educate yourself first with websites like this, and the FDA site before you ever fill a prescription again. Anyway, I'm going to stick with Diovan for a while longer and see how things go - will post again. Hang in there, because there's even worse out there!

My dermatologist recommended and gave me a sample of Neutrogena Healthy Defense SPF 45 after I had a treatment for a pre cancerous spot on my nose. I first purchased the SPF 30 as the SPF 45 was not available. I used the SPF 45 sample and the SPF 30 for two weeks with no problems. I then found the Neutrogena Healthy Denfense SPF 45 with helioplex and purchased it. Within two days of use I broke out in a horrible itchy, burning, red rash with watery looking bumps and dry skin all over my face and neck where the helioplex had been applied. I do not have sensitive skin and have never experienced this reaction to any other product. I reported this reaction to my dermatologist who recommended I discontinue use of the SPF 45 (duh!). I am on day three of the rash and it has not diminished although some of the bumps have scabbed over. I saw no warning on the packaging of side effects. I agree that the helioplex needs to be researched for these side effects and the consumer needs to informed.

I am sorry to hear of the trouble and pain that you all are having!

The common thread is the the DOCTOR didn't tell of the dangers and side effects. This is not at all unusual. I am employed as a Certified Pharmacy Technician for one of the largest HMO's in the country and have also worked for retail pharmacies. If I have learned anything at all it is this; ALL QUESTIONS REGARDING MEDICATIONS SHOULD BE DIRECTED TO A LICENSED PHARMACIST!! Day in an day out I see doctors, PA's and RN's who are all but clueless as to drug interactions, proper uses, side effects, even proper & safe dosing! Countless times the Pharmacist will catch and error and not only save the patient from a potentially fatal mistake but also save the doctor's license, yet they are not given the respect they deserve. These people go to college for 7 to 8 years and study every possible aspect of pharmacology. Our society puts such God-like faith in doctors and fails to realize, they have only studied pharmacology, if we are lucky, for a couple of classes for one semester. Graduates now, at least in my home state are earning the degree PharmD (Doctorate of Pharmacy).

Please, please, PLEASE, don't say "Oh, I have no questions, my doctor told me" or "If I have questions, I'll ask my doctor." ASK A PHARMACIST!!! Granted, even the best trained pharmacist can't predict ALL potential problems but their knowledge is far superior to the vast majority of doctors!

Another point to consider; doctors are greatly influence by "drug reps", salespeople from the pharmaceutical companies that tout a new "drug du jour" every week, bombarding the docs with free samples, promotional gimmicks while wining and dining them so they will push (prescribe) THEIR product over the competitors' or any older but just as effective medication that most likely costs less too!

Again I wish only the best to all of you and my heart goes out to you who are suffering.

Susan

I took levaquin, cipro and avalox in a 4 month period due to a severe sinus infection, back in Jan to april of 2006. I had tolerated it most of my life, but at that time, I had had 'neck surgery due to 2 pinched nerves, left shoulder operated on, major tears, due to extreme 'flat roof roofing repair' for 6 months trying to save our 'dream home from satan'. (we lost it, foreclosure)
I complained to my dr the next day, (and most every week) he ignored my halluciations, (actually "snickered" in my face), mood altered, ignored my complaints of feeling like a hot rake tearing my muscle and tendons apart. pain, told me to continue taking it:(, blame me for listening and NOT doing research soon enough, I learned later the dr is supposed to STOP the drugs immediately to rule out tendonitist to prevent pernanent irreverable damage AND it's not to be given to 'muscle challanged people'). after that 3rd round in a 4 month period, I told him I'd rather die than to take them again. mom always told me I was allergic to pennicilin, I wasnt, it helped clear my infection.

I now have hodgkins lyphoma, (affects men mostly, i'm female, 51 yrs of age), I shouldnt have 'this cancer'. My face started breaking out w/2 types of skin cancer, basal cell, and precancer A. keratosis eveywhere. I was 120 lbs, cut muscles, always had been physical. Now, flab, lost mucle strength everywhere. Every day now is filled w/severe pain and NO dr will listen, I've been called crazy so many times, I could puke. The dr's dont WANT TO KNOW because of the extensive lawsuits that will exist due to them NOT knowing side effects and stopping meds, it's their 'brotherhood', protect each other no matter what the patients 'cost' is, as in mine, complete mind and body destruction:(
To MOST people, this drug is okay. To many of us, it's a life destroying slow death. Cant work, cant get disability. Have reached for 'help to heaven' so many times, but never followed through:(. I still HOPE for some dr to listen and do necessary tests so I can sue the crap out of my previous g.p. He should have known . HOPE is a forbidden 4 letter word, yet I cuss like a sailor.
Peace my fellow quin sufferers, Sandie in S.C.

I am just about to burst in tears from reading all this information. Our daughter is 4 years old. She is been in Singulair (for her Allergies) since she was almost 10 months. It been quite a rollercoaster for us. We have been told she is ADHD (although can't be diagnose until 6), she has almost all the characteristics. hyperactive, mood swings vary between days, now leg pains, nightmares, etc. Two years ago our allergist took her off Singulair but our pediatrician didn't agree, so we went back.
It has been very painful because our daughter is such a bright girl; we don't want her to suffer, not to be accepted because she is acting like this. From reading all this information my husband and I decided to take her off Singualir. Hopefully we see some changes that can give us a sense of relief. Any words of wisdom?

Suicidal feelings... were the result of my taking Welbrutin. At first I thought it may be due to the depression that the med was for. After awhile, I stopped taking it as I was so lost. I stopped taking it. Then, I was crying nearly all of the time but I had no thoughts of suicide. So, I asked if I could change to another antidepresant.. I was given Paroxetine. My suicidal tendancies cleared up at once.

After a couple of years I had forgotten about the affects of Welbrutin and swiched back to it. Duh,,, Same thing happened. Sucidal tendancies. I immediately went back to the Paronetine. I am fine now.

Needless to say, I will not forget that again!

Karo

I am Bipolar, and I have been on many drugs. When I began taking Effexor, I was misdiagnosed and told that I was manic depressive. Anti-depressants can often make people with Bipolar worse. Effexor was the worst! My main issues were terrible, vivid nightmares and anger problems. The nightmares were bad, but after even one alchohlic beverage, I became enraged. I said and did things to my friends, that I would never do. I know you are not really suppose to drink on a lot of medication, but one drink? I became scared of myself and I am lucky to still have my friends.

I do know, that Effexor works for some people, because my dad is on it and he loves it. It just wasn't for me.

I have had and still have all these terrible side effects but no one seems to know why I swell so much.My hands and legs.i am 7 months pregnant and my gyno says I am dehidrated and need to drink more water then I notided(DUH) the main ingrediant in singulair is salt!!!!SINGULAIR OR (MONTELUKAST SODIUM 10 MGS).Hello!!!!No wonder I am so Bloated and Swelled!!!Any one else have this symptom????I have been on singulair for about 8 years now and will be looking for a natural alternative to treat my asthma after I have finished nursing my baby.Good Luck Ya'll!!!!!!

Dear Chrissy,

thanks so much...yes i take my pulse a hundred times a day...lol how can i not and last night the doc said u know it should not be this high, wont kill me but gotta get it donw,,,duh thats what im trying to do, and bingo today i received my period (happy new year).
I know its gotta get better read some post back in sept and some woman had lost the palpitations and high bp after 1 mth and i was just stressing
thanks for responding
Lisa

Wow! I am so fortunate to have run across this site! I am 51 and have very hbp so was put on Lisinopril in March '05. I had no idea that the terrible cough that I have experienced since then was related to this medication, until I read this.. The only reason that I found this was was due to me getting a list of my medications to take to the 'ENT specialist' due to my very long lasting cough and no sleep issues. I started to really notice this cough in June and I described it to my husband as a feeling of something sharp sticking me in the right side of my throat and then turning in to a spasm feeling that would make me cough like a smoker and still bring tears to my eyes*wiping my eyes as I type this* and still coughing. I have done this for so long now and I do have allergies but I have just gone through 3 ys of immunatherapy so I figured that was part of that issue. I have had a terrible 7 months and have seen 3 doctors of which none have said anything about this being a side effect! I am very angry for my 'lost' summer and no sleep! I have been put on a z-pak, kenlog shot, two different cough syrups with phenegren and nothing has helped. duh I also had two ugly bladder infections for no reason. and I had dirareah for 5 weeks. I work out and and really are pretty healthy otherwise but I have had a horrible year. When I read this site prior to going to the ENT dr. I shouted for joy to know that Lisinopril was the problem and I found it thanks to all of you. I took my info to my dr on tues and expressed my anger. All he said was 'let's try you on another one!" I have been on Diovan for 4 days and have had a horrible headache. Called the doc today.Now what? I am exausted!

has anyone had the withdrawl side effect from pred. of getting a fever every once in a while? What about muscle aches so bad u think u r getting the flu? By the way "jules777", don't send a message complaining of side effects from anything in your mind because we r not really here HHHHHAAAAAAAA DUH!

I am a 36 year woman who has suffered from depression and migrianes. In the past couple of years, my depression has been much imporoved by stopping the use of alcolhol (duh) and finding a spriritual way of living. I have been managing it with Wellbutrin 300 mg a day, and have felt pretty well. My migraines, however, have been ever present and have continued to be a problem 2-3 times a week. My docotor suggested Topmax as a solution, and frankly, all heard was it could help with my migraines and one of the biggest side effects was weight loss. Yippee! Fewer headached and weight loss? Practically a miracle!

I am usually very careful about researching any new drug I take before I even fill the prescription. I have to admit I did not do this with Topmax. I sincerely wish I had.

The first thing I noticed was the lethargy. It was all I could do to crawl out of bed, go to work, and then come home only to crawl back again. I also got very angry and depressed right away. After 7 days, I went to speak to my pharmacist in tears on my lunch hour from work to ask her if this could be from the medication. I had just spent the morning in a rage over nothing, unable to think clearly and I just felt really out of control and in a fog. She said most of the side effects should pass in 2 weeks, and to give it about ten more days to seeif things improved.

I took Topomax 100 mg for nearly a month, and decided after that I would rather have migraines than suffer from all of the side effects I was experiencing. My side effects included severe depresssion, anger, confusion, problems with memory and concentration even my speech.I was lethargic, had aching joints and muscles, and generally I was exausted all of the time no matter how much I had slept. I had no energy to do anything. I was confused, had problems muli-taskng at work, and became suicidally depressed. Something that has not been a problem in years.

I have ceased taking the medication all together after consulting my doctor, and am feeling a little better after just a few days. I hope to be back to myself soon. It has been a horrible experience, and I will never take another drug again without fully researching it's side effects.

I have been taking for over one month. 20mg one time daily, female 31yrs old. Adderall seems to be helping focus quite well. I am not as obsessed with having a perfectly clean house. I can slow down, read books and focus, actually LEARN something. Thats something I've never been able to do in 30 years, nice change! I experience a dry mouth and appetite decrease, slightly. Its a good thing, I can read instead of eat, or accomplish worthwhile tasks rather than let neverending task lists spin in my head while not producing much at all. Its been well worth the side affects. I've been against drugs for 31 years, finally realizing that to be able to break through and accomplish more in my life I would need some assistance. (I've read several books on ADD, tried to control as much as possible on my own with out meds, and to a small extendt I could. But awareness is all I could control, I could never really control the focusing. IT felt so difficult to try, as if I was playing tug a war with myself and at the other end, several people are pulling. Wht shopuld focusing be that hard for anyone???!!!! I was fine with myself when not medicated, however I could tell the ADD in me, was disturbing to those around me. I just wanted to be normal, and was tired of having teachers or private coaches tell me to focus. AS if their words/advise would suddenly be able to make a change in me. DUH!!!! This finally got me ticked off enough to try a different route. I think I'll stick with this med.
My doc swithed me to the generic brand, same ingred.....wierd side affects, paranoid, couldnt sleep, mentally I was a mess, like a scitco... got off of that after 5 days. Would have rather not taken med at all. But I understand, its all about trying to find the right dosage and you have to be willing to experiment. (just hopefully if you put children on this, they may not understand what wired side affects are happening, it took me awhile to notice in myself... you wonder if its just you, or if your imagining side affects,,,,hard to tell) They should take the generic brand off the shelves! I also noticed b/c it (generic)was in tablet form, the benefit of focus seemed to wear off way sooner than Adderall.
Now Im back on Adderall and doing better. ( not as well as before I took the generic, but possibly that my imagination) My doc said Addreall would last 12 hrs. It doesn't seem to last that long..... hard to know when its worn off.

Yeah ... great I'll take the Rx pain killers over depot medrol. People wonder why Paula Abdul acts so punchy... she's totally strung out on weekly depot medrol shots DUH! Well good for her if the people around her can stand it. Wait till the Ms Hyde side shows up. Side -effect ? anxiety; easy agitation & anger; hyper activity.

OMG! I'm NOT crazy! I'm 43 been on yasmin a little over a year for ovarian cysts.... I've had 3 migraines already this year. Daily headaches....even chest pain. I'm a nurse and been in denial I'm having any kind of cardiac problems. It didn't occur to me the yasmin could be causing chest pain. I've been living on Motrin, Aleve, Tylenol and Claritin for the headaches....they aren't working anymore....then it suddenly occured to me... BCP's! DUH!!!! My husband is a doc and when I suggested it to him he totally blew me off. I'd just started a new pack and discontinued them 2 days into the cycle. Already I can tell a difference in the vaginal dryness. I'm hoping my libido will increase too....since Yasmin I could give a rats *ss about sex! HA!
I find it fascinating how everyone's OB/GYN's think we're all nuts! That really annoys me!

thanks,
TKG

I meant to say that "ocular" and nasal steroids can become systemic if taken for long periods of time. Of course, oral steroids *are* systemic. Duh!

Wow, after reading the side effects at a web site and reading the stories at this forum I found out that I was experiencing the same side effects that I read here.

I was being treated for a bacteria infection in my lungs, so my doctor put me on the 500mg tablets for 10 days (he said this should kill off any bacteria left around in there), he also prescribed me the Advair Diskus for my bronchial tubes (took this twice a day (morning and night)).

Well, the side effects I noticed were the following:

bad taste in my mouth
loss of appetite
nauseua
loss of weight - 5lbs (which of course coincides with the loss of appetite, "don't eat much, lose weight" duh!)
sleeplessness
a couple of nights of sweating (didn't help that on those paticular nights it was humid)
anxiety and depression
loss of energy
Sunburned (mowed the yard one day with a tank top on, shouldn't have done that)

Today is my last day of the medicine, I feel the infection has subsided so we'll see. looking back, I think I should have taken this medication with food or something. I was told not to take this medication with any dairy products at least 2 hours before and 2 hours later from taking this medication. So I just went ahead and took the medication without food altogether.

I had been on advair since it came on the market. I have suffered from increased heart rate and increased blood pressure. I complained in Nov. to doctor who proceeded to decreae the dose. I continued to have the same symptoms and in addition was having bouts of tachycardia and possibly skipped beats that were very disturbing. I again went and this time was told that by decreasing the dose that it was only the steroid and that the salmeterol was the same in all. Duh, why did he decrease the dose when it had no affect on the salmeterol. Now he decided to stop it altogether. My heart rate is back in a normal range and my blood pressure has come down to a very good reading. I do not have the the increased heart rate. However what I am experiencing is an increase in pain due to arthritis in my joints. i am wondering if this is because I have stopped the advair and the steroid that is in it. Has anyone else had that reaction after long time use of advair and then stopping it.