Rash symptoms and conditions

I am a 70 year old woman, I have been on 20mg Lipitor for high cholesterol, 200 total and 25mg of Spironolactone for a not so high blood pressure, for 3 1/2 yrs. Oh, my God, the Spironolactone is a potassium sparing diueretic that is very dangerous and has many uses I didn't know about or the terrible side effects, it causes breast cancer. It's also used to treat women who have an over growth of hairiness, or on a higher dose to treat hair loss and I've gone bald on the top of my head! Plus all of the good foods we're supposed to eat for high cholesterol, fruit & veggies one isn't to eat on this drug, because of lot's of potassium, what a huge contradiction. And muscle pains, and rashes, (eczema, atopic dermititis) that I've suffered from both.
Anyway, Lipitor, had know idea about the side effects until I looked it up on the internet and read these posts on here.
I stopped taking Lipitor last week and Spironolactone 2 days ago.
I had cholesteral test last week too and saw my dr. Wednesday. He said it was okay that I stopped the Lipitor, but not the other one, why not the other one worse then Lipitor and why am I on this strong drug, geez.
The pain and burning started in my hip for no reason, then my ankles with eczema which started soon after Liptior, then my fingers, numbness, can't pick things up, tingling, burning. Then my feet, yes, just like all of you I have these same problems. This is not just coincidental, this is from the drug Lipitor. I get severe joint cramps in my legs, feet and fingers.
For now on before I take any drug I've prescribed I will thoroughly check for side effects and not take it if they're seriously impairing like Lipitor. I feel like a cripple and older then I should feel, I almost just felt like why live anymore if this is how it's going to be.
Since I've stopped Lipitor I feel a little better, I read that it causes permanent muscle and nerve damage though, oh I hope not, I can barely walk anymore or get up out of my chair. This is all drug induced toxicity of my system. Thanks so much everyone who posted for sharing and enlightening all of us who are suffering from this drug and others.
It should be banned along with Baycol, (a statin) which was banned a few months ago because of these same side effects. With the studies that it only helps maybe to prevent heart attack, well I'd rather be able to walk again and hopefully all this will go away, the rash, etc.

I haven't finished taking the medicine yet because I'm only on day 4, but I must say that it's clearing up the staph in my right armpit. My left armpit is still swollen and hurts like hell. My mother is an RN, and she's been trying to drain the pus and blood from the wound. It hurts so bad that I'm ready to just drive up to the local ER and have them lance it. How long does it usually take for Bactrim to clear up the infection? I'm taking 2 pills once a day for 10 days.

And another thing, I think why people are having nasty side effects to the medicine is because it's not mixing well with their body chemistry. My sister took Bactrim last year for MRSA, and she cleared up beautifully without any horrible side effects.

Thanks guys!

The product is terrible....massive rash and burning

My whole torso, stomach area and sides along with upper and lower arms broke out in an extreme rash which was painful, oozing, welts, open sores and some bleeding. This lasted from @ mid July 2009 to present, Nov. 2009. Using A&D ointment, oatmeal baths, many vitamins and plenty of water it is just now settling down to symptoms of pink(raw) skin and not so severe pain with still some itching and flakey skin.

I had that Kenalog and it's been a total nightmare...My doctor Dermatologist injected into my two index fingers on each hand. The itching has been insurmountable and absolutely horrible....I haven't been able to sleep, wash dishes, do anything with my hands....I am telling you I am about to go out of my mind. I went back to her..and now she put me on Prednisone and Singular...now I am reading the side effects of Singular. She never told me what type of shot she was giving me for the pains in my hands that i was getting. I have had cortisone shots for joint pain before...for I figured that what it was that she was giving me...later to find out it was this damn Kenalog. I would have never agreed to such a thing until I had looked up the side effects. This has been a night mare completely...

The itching is so bad, that I have broken the skin, I have a rash completely on both fingers. It so sad...and she's charged me a fortune for it too, and the second time I had to come back for help. What the hell is wrong with people..?

DON'T TAKE THIS DRUG...UNLESS YOU DO CAREFUL CONSIDERATION..!!!PLEASE

I was prescribed Bactrim for 10 days due to ear/throat/cough issues. After day 2 I had 102 fever, chills, sweats, extreme fatigue, and headache. After day 3/4 I started feeling severe doom and gloom. After day 5 I had insomnia and began having vision problems and felt like my eyes were "loose" in their sockets. I went back in, and saw a different practitioner, and reported my symptoms she thought it was my blood sugar and checked me for diabetes (which it wasn't). She ran more lab work, and chest xrays. Nothing came of it. On day 6 I began feeling a burning and itching sensation on my face, and throughout my head. Nothing helped. During all of this time I could not eat, and was extremely nauseated. I got online, and found all of my symptoms of Bactrim side effects. Needless to say, the bactrim is in the trash. In addition, last year my husband was prescribed bactrim for bronchitis, and ended up in the hospital. At the time they told us he had Scarlet Fever, but when we both went in this week, they stated it was an allergic reaction to Bactrim. He looked like he has a sunburn from head to toe, with a rash. He had 105 fever, and was severely dehydrated. I wish we would have been told that last year. They gave him a zpack this time, saying he was allergic to bactrim. I will never take this medication again, or have my family on it.

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.

After you read a representative sampling of this website's testimonials, you certainly ask yourself inter alia: Can this be true? Did thousands of people inject an antibiotic from the fluoroquinolone family, which crippled them for longer or for shorter? Most of us, I suspect, never really get beyond the initial litmus test: Did this medicine poison me or save me? (The answer depends, of course, upon the age, gender, medical condition, and most importantly, the DNA make-up of the individual patient. For hundreds of thousands of patients this antibiotic is a boon. For thousands of other misfortunes this antibiotic is a disaster.) But there is another important question here.

Who gains from self-revelation? To be sure individual sufferers gain certain emotional catharsis from posting their adverse drug reactions (ADRs) to levaquin. E-postings are one-way anonymous tracks that form ruts on a well-traveled trail of tears. Unless these postings are hoaxes written by mischievious gnomes, then they consitute prima facie evidence for a causal link between levaquin injection and sundry crippling ADRs.

Curiously, this e-forum cannot be used as a tool for organizing thousands of potential litigants who might coalesce under a class action lawsuit. Yes, we can analyze each other's anonymous revelations to see if they muster our respective sense of the "ring-of-truth" re: levaquin toxicity, and we may contact each other one-on-one, but no-one can harness this intoxicating communication's technology to reach simultaneously all respondents en masse as a bloc.

So, who wins? The emotionally unburdened e-poster who learns belatedly that s/he is not alone and that prescription medicine likely caused more pain than the underlying malady for which s/he is being treated? Or big pharma that continues to manufacture and market a medication that poses downside risk to many consumers who unwittingly incur more damage than therapeutic value?

Indeed, who wins in a forum where consumers anonymously reveal their symptoms and unconfirmed suspicions? The answer is big pharma wins. Pharmaceutical companies data-mine our postings to estimate the frequency and bredth of ADRs about which consumers complain. House statisticians estimate the ratio of active complainants : silent complainants, i.e., the ratio of complaints who show up on this website to the far heftier percentage of complainants who never post on this website because either they are technology-challenged or they are incurious. House actuarians proceed to estimate how much operating profits their employers must set aside to cover losses in out-of-court settlements or in awards made to plaintiffs in class action lawsuits.

I think this is how the game is played in a behavioral sink where billions are made in a deregulated marketplace that allows predators and prey to interact anonymously. Sorry to be such a downer, but I fathom only the desperate plight of tens of thousands of levaquin consumers for whom no monetary award ever will compensate them adequately for their suffering, and the hundreds of millions of dollars at stake in court awards if consumers ever brought to bear their aggregate numbers and draw a bead on their big pharma tormenters.

I think it a true horror and shame that pharmaceutical companies have not devised a test which determines in advance which patient safely may consume levaquin and which patient's DNA places him or her at risk. I suspect the genome technology is available, but would dig too deeply into big pharm's bottom line. The economics of "parachutes-for-everyone" is infeasible. We are all guinea pigs in a B-grade movie featuring Russian roulette, billion-dollar pay-offs, and an FDA that pretends not to know.

I was on 50 mg. then increased to 100 mg. After about 10-14 days on the 100's, I began itching all over ... broke out in a horrendous rash, especially on my back, arms, and legs. Went to my GP who quickly diagnosed a new BP med called Bystolic 5 mg. for a trial.
I've been on Bystolic now for only 2 days. Rash is driving me crazy! I realize now that when I was on the 50 mg. of Toprol XL, I was itchy ... but I never broke out in this huge rash until I had to increase it to 100 mg. I thought, because I was 52, it was *flushing* due to hormones. Boy, was I wrong! Dr. told me to take Zyrtec for the itching/rash.
Now, after changing to the Bystolic, I feel much better (B/P and heartrate). Seems like I was having an allergic reaction to the Toprol XL which is maybe why it didn't work as well. Even though the Bystolic is a much lower dose than my Toprol, my BP feels much lower, and so is my heartrate!
Toprol XL's big side effect is the itching and rashes which can be debilitating. Oh, I had horrendous nightmares on Toprol ... so bad, I didn't want to to go to sleep!

I was prescribed this as an inexpensive option to treat a long-term sinus infection in March 2008. I had no prior history of allergic reactions or prior health problems. After 3 days (6 doses) my whole body was in throbbing pain, I felt like my skin was on fire, and I was seeing spots, and had difficulty breathing. I initially had NO RASH or visible/external signs while taking the medication. I immediately stopped taking the medication and saw my doctor, but symptoms persisted for a week. My doctor prescribed prednisone, and had to up the dosage two weeks later when a rash formed over my torso and legs and persisted for 2 months.

Started taking the Zocor generic Simvistatin just 2 days ago. My legs hurt so bad that I can not sleep. My right knee is swollen to the point I have very limited range of motion and can barely walk up stairs. It is after midnight and I can't sleep. Also having some angina and my little toe on my right foot is somewhat numb. I will be contacting my physician about this tomorrow. My cholesterol was 105 and this doesn't seem to be worth it to me!

I was prescribed medrol by my GP due to an ongoing rash that needed to get under control. I believe I had the 40mg dose/wein pack. The first two days I felt as though I were on speed. Day 2 at the grocery store I stopped to take my blood pressure because I was sure my heart was racing out of my chest. Thankfully, it wasn't and happened to be palpitations that I was having. I had hot flashes where my face and chest would get red like a sunburn. There were the sweats and the leg weakness/soreness. I did have sporadic headaches but, nothing a Tylenol wouldn't alleviate thank goodness. I've read here that numerous people had very bad headaches. My last day on the meds I started to experience the fatigue. Today is my first full day off and I certainly felt flu like. Sporadic lightheadedness, weakness and fatigue that would all come and go throughout my workday along with sporadic energy. I'm glad that I found this site so at least I know that this is normal and will subside in a few days. Other side effects I experienced were worsening of my post nasal drip along with a funny taste in my mouth, mood swings, insomnia, hyperactivity and muscle aches.

I have been on this medication for 5 days now for acid reflux (or at least, that is what the dr. assumes I have. The doctor told me to take two 20mg pills in the morning before breakfast, and it seems to have helped some, since the Pepsid prescription did not seem to help me. I also am getting terrible pains on the side of my neck, and my throat hurts. Also have an ear ache that feels like an icepick being stuck in the canal. I also have a red spot now above eyelid like a rash, and all day i feel anxiety. I don't know if I should quit taking this. The stomach burning was terrible and is why I was put on this med. to begin with. So I am afraid if I quit taking this, the stomach burning will return. The dr. said 2 weeks of this, but I don't think i will last that long.

WOW! My Mom is 65 and having a lot of these same issues, rash, swelling of the hands and feet, itching, tired ALL the time, depression and she is really "foggy". Her feet are so swollen she cant walk! Her Dr acts like she is just seeking attention and just orders more blood work! After reading all of your comments I am sure its the Lisinopril! Her doctor told her she should NOT stop taking the meds because she could have a stroke! I am angry he is using this scare tactic. I live 2000 miles away but I ready to make a road trip to get this madness to end! She really needs to find a new Dr and stop using this dangerous drug!
Thank you all for posting these issues!

I stopped taking my Bactrim last night after a trip to the emergency room. From the first day of taking it for bronchitis, I started having headaches, pain behind my eyes and could not sleep well. On my sixth day of the medication, I started feeling dizzy and nauseated constantly. By day seven I was running fever of 101 and that evening, broke out into a rash from head to toes. My skin was itchy and tingling and it was getting difficult to breath. I immediately went to the ER. They have me taking Benadryl 3 times a day for 3 days until the rash clears up. I am not a fan of this medication….and I still have bronchitis!!

I had an infection on my foot (could have been Staph because it was very aggressive and painful with lots of swelling) and was prescribed 'Bactrim' or Sulfamethoxazole. Everything was fine for the first 8 days. My infected foot was healing.
On the 9th day, I developed a rash that I noticed first on my wrist and then my neck, inner thighs and my feet. I went to the doctor who said to not take my 10th and final day of Sulfamethoxazole and prescribed benadryl.
Later the same day (tonight), the rash has spread everywhere from face to toe. The itching hasn't been severe but it has been uncomfortable, sort of like mild pin pricks in random places on my body.
I'm going back to the doctor's office tomorrow since they told me to expect it to get a lot better by tomorrow. I'd be surprised if it gets better but it definitely has gotten worse.

I had back surgery in July and caught two infections from the hospital, Staph and pseudonymous. I had a picc-line put in and was put on Cipro oraly and Ancef. I got Steven Johnson syndrome from the Cipro and almost died. I looked like a burn victim and swelled from head to toe that was three weeks ago. They pulled me off the Ancef and Cipro. It took a week of me running 103 + temps and the dr. kept telling me its a virous until the rash showed up and my tongue swelled and private parts and throat started to swell shut before they decided to admit me. Then once all that was done and they figured it out they put me on impernem to kill both infections. They pulled my picc-last week and put me on Doxycycline. I have done my research and know that the two are related I asked my dr. what the chances were of a reaction again he told me less then 1%. Ha! I am seeing an infectious disease dr. by the way. Since I started the Doxycycline last Thursday I have developed hives I called the dr. and was told they are not worried about it because I am not running a 101 temp and I am not swelling, plus they don't even know if the Pseudonymous is cured. What do I do? If I go off the antibiotics I will die and if I stay on them I am probably going to die. My joints hurt all the time now and I am only 31. Do I look for a new dr.? Can someone please help me? This is the only website I have found so far where people have had the same reactions as me. These antibiotics are dangerous they need to be taken off the shelf. Thank you and good luck to everyone who is struggling with this.

I am 45 years old. I get the impression many of the ladies here are younger, as they speak of having younger children, so I will tell my side from a bit more "mature" (ie older!) perspective:

Had Mirena for a little over 9 months. My two MAIN side effects were a development of terrible cystic acne on my face, back, shoulders, hairline, behind my ears and straight down my spine, ending in a nice lovely rash just above my tailbone. These things were deep, solid knots under the skin, not average little pimples. Worse acne I've ever had, and at my age too!

Second, profuse sweating under my breasts and lower back, again just at my tailbone, right above my butt. After drying off from a shower, I'd run my hand back there and still feel soaked. This did not seem related to hot flashes. Just sweating, and I think that contributed to the acne, which was beginning to leave scars it was so deep.

I do feel like I gained weight, my pants were much tighter and I just felt bloated all the time.

Fortunately, no hair loss or emotional side effects. I've had anxiety for years and take Ativan (lorazepam) which keeps it pretty much under control. No loss of sex drive either. It seems there are a distinct set of side effects, and some get them in different combination than others, but we're ALL getting them one way or the other!

OBGYN said as the Mirena is only progesterone, I was missing the estrogen which were the 2 components of the pill I took for years with no trouble. He gave me a Rx for a low dose of estrogen. Now I am getting what I had in the pill in 2 separate forms, and having these awful side effects on top of it. It didn't help.

So I had Mirena removed 6 days ago. Luckily he found the strings, told me to cough, and pulled it out, no pain! I immediately went back on Alesse BC pill that same day, so no break in hormones, but I handled the BC pill fine all those years, so I"m just going back on it. Have been bleeding ever since removal, but I figure that is just my body "getting back at me" for not having periods for months. My first real one, due in about 3 weeks following the pill schedule will probably be the period from hell. Ok, I accept that. My uterus wants to get this poison toxic mess out of me, and I'm ok with that.

I'm crossing my fingers that I will miss the "crash" I've read so much about. As it seems to be mostly psychological, and I didn't have those side effects to begin with, maybe it won't be so bad, or at all. Of course that could just be wishful thinking on my part! So far, 6 days of having it out of me and I already feel 100% better! My face cleared up in a matter of days. The sweating stopped immediately. My pants are looser, although I still weigh the same. The bloated feeling is gone. I just feel thinner. Before, my profile in the mirror looked like I was 4 months pregnant! That too is going down quick. Good luck to all who have it removed. Things can only get better!

And don't let any doctor tell you you can't have it out! It's your body! You can demand whatever you want, especially if you feel like it is making you sick! Do not take no for an answer. You don't even owe them an explanation. Just a "Sorry, it's not for me..." at the most.

Good luck to all....

The dermatologist gave me Bactrim to treat acne, I took the first pill in the afternoon and at night time I was vomiting and had fever.The next couple of days the symptoms went away but then they came back with itching, rash and lost my taste buds.I stop the medication and I am hoping that this symptoms go away. I guess I am allergic to this medication.

I AM A 71 YEAR OLD MALE I HAVE BEEN ON LISINOPRIL FOR ALMOST A YEAR, THREE WEEKS AGO MY DOCTOR INCREASED MY DOSE FROM 10MG TO 20MG THREE DAYS AGO I STARTED TO GET LEG TINGLING AND CRAMPS, THEN I BROKE OUT ON MY UPPER LEG WITH SOME BRIGHT RED SPOTS ABOUT THE SIZE OF A HALF DOLLAR, THERE ARE SMALL BLACK SPOTS IN THEM AND THEY HURT LIKE RAW NERVE ENDS, IT IS VERY HARD TO WALK WITH THE PAIN OF MY PANT LEG RUBBING AND KILLING ME.
ALSO MY WIFE IS YOUNGER THAN ME , SEX DRIVE WENT OUT THE WINDOW, I THINK THAT IS PROBABLY BECAUSE OF MY AGE. BEEN THERE DONE THAT. I AM GOING TO TRY TO GET OFF OF THAT STUFF TOO.

What brought me to this site is the fact that I have a bitter taste in my mouth that gradually occurred since I have been on Simvastatin 40 mg for about three weeks. I have also noticed a strange burning/numbness in my heels only, which has also been gradual. I feel more sleepy most days and not what I would call fatigued, but just like I don't feel like doing anything. I eat more just to try to get the taste out of my mouth and don't feel like exercising. I also finally went back to my Pilates class and felt unbalanced when trying some simple stretches. I usually have excellent balance. I guess my question is: Are these things related, and are they going to just get worse?

I have a huge indention on my left hip, supposedly as the result of an injection I received 4 months ago. I got a steroid shot (not sure the name) for a rash and itching. No immediate side effects and then about 2 mos. later I notice a lump on my hip about the size of a marble that was brown discolored spot. Then I remembered about the shot and thought it was a result of that. Forgot about it until about 6 weeks later when I got out of the shower and noticed a huge indention about the size of a golf ball on my left hip. A week later, I started having pain at that site which would radiate across my entire lower back, down my leg and up my arm. Sometimes the pain was dull, sometimes like a bad burning sensation with tingling all over. I went to the dr. and he thinks the indention is from the injection but is sending me to an orthopedic dr. this week for more testing due to the pain I am having. Maybe related, or not, I found a lump in my left breast this week, had it checked and have to go to an imaging center next week for more testing. Could this be related?? Also I missed 2 periods after the injection and my last period wasn't normal. Please keep posting these comments from others. I'm going to call my dr. Monday to get the name of the injection.

I wanted to make sure I updated my post as I had a very bad experience with this birth control pill. I posted very serious suicidal thoughts, severe anxiety, no sleep, etc and after 5 days I called my doctor. He ran a few tests and noticed that I had developed a rash that I had paid no attention to. I was sent over to another doctor who confirmed that I was allergic to an inactive ingredient in the pill. My "side effects" were getting worse simply because the more I took the more I was reacting. I was immediately admitted to the hospital and given IV fluids to flush my body and shots to counter effect the allergic reaction. I have not taken bcp in over 15 years and there was no way to know about this in advance. I feel 100% better now, not taking any bcp at the moment and was thankful for the cramps that I woke up with this morning! : ) I guess from my story is make sure you are informed, I didn't call my doc, wanted to see if it would pass and was not aware of the "severe" side effects. I would have been told after day 1 to stop taking them had I been more informed. My experience is very unique and was in no way a direct result of the birth control pill name, but only of one of the inactive ingredients. Best of luck to everyone!

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.

My daughter had a kenalog shot for itching on May 2009. The doctor never mentioned any side effects to her. Now she has a huge indentation in her left buttock. She is only 18 yrs old and she is scare and afflicted because the dent is getting larger and disfiguring that part of her body. I read enough complains. There must be an action lawsuit against the company distributing, selling and benefiting from this drug. Some doctors also should be liable for neglecting to release the accurate potential damage (as it is known) cause by this drug. It is causing mental pain and anguish due to the disfigurement that it leaves and also constant concern about the growing destruction of the muscle cells.Enough damage have been done. Who will pay to correct the damage? ******