Last winter symptoms and conditions

Don't ever take this drug. I was hesitant when I saw the list of side effects. But my UTI was so bad and I didn't want to go back to the doctor for him to prescribe something else. Why he did not give me the same antibiotic that I had last winter with my previous UTI I have no idea. I had a 5 day dose. It went fine. Everything went downhill the evening of my last morning dose which was 10/24/09. Today is 10/26. The chills and aches immediately kicked in big time. I went right to bed with 2 Tylenol. It broke several hours later. Then the sweats began the next morning. Then the chills again last night. They are still here this morning. Because i am so cold I am sleeping in layers of flannel which is accentuating the horrid rash on my chest, neck, and back. The heat seems to be bringing it out. The doctor's office said I could take an OTC allergy pill but that will make me sleepy and I want to keep alert during this crisis. So I am going back to the doctor this afternoon for him to take a look at me. I may give him a piece of my mind for prescribing this crap to people. On my long list of side effects from my pharmacy is the phone number to report side effects to the FDA. It is 1-800-FDA-1088. We suffering patients need to unite against this demon drug so it is eventually pulled off the market. I was given Sulfameth/Trimetrhoprim 800/160 tabs for 5 days, twice daily, for an UTI. My pill bottle also says MFG AMNEAL - Generic for Septra DS tablets. No refills. Who want want to? Good luck to all the suffers of this doomed drug. I had to lose a day from work today and probably will do so tomorrow. And I have to somehow get myself back to the doctor today to hopefully get some relief. And living alone makes it even scarier. Something has to be done about this drug.

I too have been experiencing the same side effects listed by most of you. I have also been seeing a gastroenterologist for about 9 months now because of stomach issues. All symptoms point to gallbladder disease but the tests come back normal. I called my gyne today and they seem unconcerned with what I have told them and advised me to continue to take my pills until my annual visit in October. I'm done with this pack on Saturday and am thinking of going sans pills for the next month until my appt. Any advice on what pill I should switch to when I do see my dr.?

Persistent cough again this winter...last winter I coughed for 8 weeks straight.
antibiotics don't help either. --B.P.

My 19 yr. old son recently starting taking Levaquin for a tonsillitis (throat infection) and he has now had severe chest pains from the Levaquin. Has anyone else reacted this way from this medication and if so, what did you do to get the chest pains to stop. He has stopped taking the Levaquin, however the chest pains have not lessened. When he tries to eat something, the chest pains get worse. Please someone out there help me if you can! I hate to see my son in such pain.

Hi, my name’s M. and I posted my story on here about a month ago. Unfortunately, I’ve made no progress. I was hospitalized again mid-October for numbness and tingling sensations in my legs, which is a symptom of guillian-barre syndrome and supposedly needs to be treated very carefully. I had an mri of my brain again, this time including my spine to check for possible tumors. I was sent home the next day, negative for guillian-barre, but having received no answers. I was crawling up the stairs by this time, and was too weak to walk without holding on to furniture to support myself. My legs felt like cement blocks, and the neurologist specifically said, “I don’t know why you can’t walk.”
Since then, I’ve developed acute mononucleosis, which increases my fatigue and muscle pain, and causes me to sleep about 15 hours a day. Recent blood work also showed I was positive for an autoimmune disorder called Myositis, which is a painful disorder that causes the body’s immune system to attack its muscles and connective tissue. I was referred to a rheumatologist, who was the least sympathetic person I’ve met in my life, and told me my physical exam was perfect, so she felt the Myositis must have been a false positive. She re-ran the blood work, and the Myositis was negative. This is of course a relief, but how we’ll ever know which test is correct, I don’t know. The rheumatologist did notice the weakness in my legs and my difficulty walking, and suggested physical therapy to help gain my strength back. She also prescribed an anti-inflammatory medication that took away almost all of my pain. Thank God, something finally worked for me. We then saw the physical therapist who said, “We can probably make you stronger, but I’ve never seen anything like this before.”
I’m seeing an osteopathic specialist who is convinced my illness is directly related to Gardasil. Through ancient medicine methods, she introduced a vile of Gardasil to my system and noticed an immediate weakness. I’m not sure if I totally believe in her practice, but the fact that she noticed a rejection to Gardasil the minute she introduced it is enough to convince me. She believes that my immune system was basically poisoned by the vaccine, which is causing it to fight off things I need. She also said it probably doesn’t recognize the mono as an infection, and decides not to fight it. For a normal, healthy person, mono can last up to 3 months. For someone like me, no one knows how long it could last. It was my immune system’s weakness that allowed me to develop mono, and it was the Gardasil that weakened it in the first place. So thank you Merck, for yet another thing I have to deal with.
And that brings us to today. I’ve missed about 30 days of my freshman year, so I’m assuming summer school will be necessary. My high school won’t provide a tutor, so I can only take my core curriculum classes, and am having difficulty keeping up with just those few. I’ve gained some strength in my legs, and it’s a little easier to walk with the anti-inflammatory, but I still can’t walk very far without resting. I’m also taking an anti-depressant to help me focus-hopefully it’ll lift my spirits. Since I received the vaccine, my periods have been painful and irregular. The constant nausea, headaches, and occasional stomach pain/joint pain continues, along with extreme fatigue.
The doctors make me feel like a crazy person who faked this to get out of school. How could I possibly fake nausea for thirteen weeks straight, and pain that kept me up crying almost every night? How could I fake my difficulty walking while it’s causing me to miss both of my volleyball seasons? Before this, I had hardly missed a day of school in my life, and refused to stay home whenever I got the flu because I hate falling behind. I’ve played volleyball tournaments with sprained ankles and chipped elbows, I can handle pain, and I’m not a baby. If the doctors would take five minutes out of their time to try to get to know me, maybe they would see that. And the few who actually take the time to be pleasant don’t listen. They tell you they know, that they understand, but they don’t. They won’t drag themselves out of bed in the morning feeling nauseous and half asleep; they’ll be able to walk into their office without feeling like they want to collapse, and they’ll go home to the people who care about them and will actually be awake long enough to enjoy their company. No one will tell them they’re insane, and the worst part is that most of them won’t take the time to realize how blessed they are just to have the ability to do those things. How can the doctors not have sympathy when they’re the ones who put this poison inside of me?!
I know I’m very lucky compared to girls who have experienced more serious side effects, and am thankful that we were able to make a connection between my illness and Gardasil after the first shot. But I’m living proof of what just one stupid shot can do to you-how can you put yourselves or your daughters at risk of what I’ve gone through? The benefits are not just worth the risk..
My 15th birthday is coming up in just a few weeks, and all I want is to be normal again.

Praise the Lord! It is about time. When I read this in the paper yesterday I could believe it. I have been waiting for this to happen for two years now when i decided to take my daughter off this junk. I have told every single person i know what this stuff did to my sweet little baby whom is now 9. She too experienced nightmares, mood swings, anxiety, night sweats, stomach aches, headaches, constipation, urinary problems, leg pains, aggression. She has always been a normal kid for her age. She had always been in dance classes since she was 3 and loved it. Never ever had she been into trouble at school or dance but when she got on this stuff her teacher was calling me at least once a week about her being rude and very forgetful about everything. Her dance teacher told me she looked like she was spaced out all the time. And not listening. I noticed she was having panic attacks in the stores when we would be shopping. She cried and told me"MOMMY I DO NOT KNOW WHY I AM ACTING SO MEAN? I HATE MYSELF. I DO NOT WANT TO BE ME." i cried too and we started praying about it. I posted on this site 2 yrs. ago when i decided to take her off against her ped. advice. She actually got mad at me when she tried to put my younger daughter on it when she was 3. I told her no i was not going to give it to her nor was i giving it to my older daughter any more. She looked at me like i was crazy. And said my girls needed it. I told her i did not like what it did to my older daughter. We do not go to her any longer. It took a couple weeks and my daughter started acting like her old self. I do think it messed her mind up though. Singular is evil and should be off the market. It makes me sick to think back on what it did to my daughter. It was a complete nightmare!

I was prescribed Singulair last winter after a severe allergic reaction. I have taken it throughout the winter with no noticeable side effects. For the past several days, however, as the pollen count has risen, I have been experiencing strange symptoms. I feel a bizarre pressure in my head, and a ringing of sorts in my ears. Also, I can't sleep - I feel exhausted, and try to go to sleep, but I wind up feeling agitated and have to get up out of bed.

Hi. My eight year old daughter has been on singular for 6 months. She has had chronic stomach pains that she says feel like pressure. Her appetite is terrible. She always says she isn't hungry. I have to search for anything I think she will eat. She is very tall and very thin for her age. She grew an inch in the last year but gained no weight. First time her growth just stopped. No surprise as she doesn't want to eat. I took her to the doc several times and they think she has acid reflux and have given her 2 different acid eliminators ( which freak me out as well) Said she should see a gastroenterologist. We have appointment in March . I started reading this site and thought well maybe it's the singular. So I called her allergist and told them I was taking her off to see if that's why she has the stomach problems. They said I could since it wasn't a big trigger time(seasonal) and she wasn't sick with any cold or flu) She gets mild asthma when sick. Her allergist asthma doc thinks her stomach aches are related to the mucus dripping into her stomach. I have taken her off all meds to try to see if it could be the Singular. She also has been very tired and can't keep up in her dance classes. Her school teacher had to put her in the front of the class because she said she wasn't paying attention. She seems to lose it over anything that requires focus or attention.She also seems kind of depressed. She is worried that something is really wrong with her. This child used to eat normally and is gifted academically .Her tests results(taken while on the Singulair) went way down from last year. She was put in gifted pull out program from last year results but would have barley made it in this year based on her much lower scores. That does not make sense to me. Never has had attention or focus problems before. I will keep everyone posted. Does anyone know how long it might take to get this drug out of her system? Has anyone else had this kind of reaction to this drug? I also wonder whether she had reflux before but this made it worse? I had her blood tested for Celiac and general stuff and nothing showed up.I wanted to get the Singular out of her system before we see the G.I. doctor. anyway thanks, Elizabeth

My college age daughter was diagnosed with allergies and asthma last winter. She had a series of allergy test and results were grasses, dust mites, mold, cats, dogs feathers. Her main complaint was shorness of breath during exercise, boxing and lately tennis. She is a very healthy young lady that played tennis, ate healthy and stayed away from pop and junk food. This sudden breathing issue is baftling. She was put on Singular and the lowest dose of Advair. For 9 months she has been taking these meds and they don't seem to help. What's more baffling is that 6 months ago she developed an eye irritation, itching, swelling and redness of the eye lid. She has see 3 opthalmologists and 1 cornea specialist. They've all said it's "dry eye". Fine, but what is the cause.
I am one to read all the package inserts to all medications. As a professional, having sat on two Institutional Review Board for Animal and Medical Research at Henry Ford Hospital, I am well aware of all the possible side effects that can arrise with medications.
Recently I read up on Singular, I am confinced that there is a definite correlation of the eye problem with the Singular. I have told all the doctors and non seemed to want to speak with the allergist or work with him, or even consider that this is a possibility.
I intend to have her stop this medication and hope and pray that this will problem will cease. If any one has had a similar occurance with Singular, please respond.

I have used Advair since November, 2003, first 250/50, then 500/50 after a bout with broncitis and phneumonia, and now 150/50 since last winter. My only side affect that I think is a side affect is I have had an increase in blood pressure that caused me to have to take mods, and my eyes have been giving me a fit this past year, draining, mucus, blurred vision at times. except for those I am thankful for the drug. After having severe asthma all of my life, since I was 1 year old and I am now 56, I am a new person all together. Not one asthma attack since the second day after I started using the inhaler. Now I get an albuteral inhaler and it expires before I ever use it.

My daughter was born with a breathing condition(never pinpointed) that kept her in intensive care for almost 2 weeks. As she grew she seemed ok. Then pneumonia appeared at 1 1/2yrs. and she has been hospitalized 5 times since with various forms of pneumonia(walking, single, double) since. We moved from the city to the 'burbs and all seemed well. She would take the occasional Xopenex(Abuterol made her nuts). To make a long story short, after 2 years in the new house new symptoms appeared. All of a sudden there was coughing at night that would not stop. We went to a new Dr. and he prescribed Singulair. This was October of '06. Soon thereafter, the behavior began to get worse. Tantrums and extreme moodiness began to become more frequent and her school work began to suffer. We've just been informed that the school is recommending holding her back. When I talked to the teacher, she indicated that my daughter has gotten "worse" since Christmas. Teacher also does not believe that there are any learning disabilities. I know that it is the Singulair. She has the constant stomach ache and no appetite to speak of. All of the professionals are assurring me that Singulair is safe. She is not on this nasty drug any longer... Waiting for changes...

I have been on ADVAIR for approx. 1/2 a year. At 1st it seemed to help & still is with the asthma. But now I seem to have a real low resistance to viral infections or at least sinus related stuffiness. I have had a nasal problem with stuffiness/post nasal drip/ears popping & ringing and loss of taste for almost 2 months now. I went to my allergist's P.A. 10 days ago & got a script for amoxicillin 875 mg & I still am having issues. They thought I may have a sinus infection. Is anyone else experiencing nasal congestion & rhinitis while on ADVAIR?

Side effect, NONE. i have had this shot for excema for the past 20 years. My dermatologist died last winter, and I cannot find someone to give me this shot. I have had NO adverse reactions to this shot and no doctor will give it to me. I have excema all over my body and the new doctor gave me a cream that i have to apply to the 'effected area' 4 times a day. I just dont see how i could strip down 4 times a day to apply it to my whole body when all I need is this shot ONCE a year.

I am sorry for those who had a side effect.

I bruise easily and have ugly marks on armsor legs where I get injured very slightly. I have none of the problems that I have read above. I understand prednisone is for inflamation and I have COPD - bronchitis last winter. Am also taking Actonel for bone strength.

I was given Biaxin along with Fluzone 3 years ago for what seemed like just a nasty case of the flu. After a few days I felt 200% worse and wasn't sure if it was the Biaxin or the Fluzone, so just stopped them both and began recovering completly within 24 hrs. However, it was while I was taking the meds that I had my fist panic attack, and I continued to have them intermittently for over a year. I found out later that Biaxin is an erythromycin, which I've never tolerated well. If I had known that to begin with I would not have taken it. My husband tried Biaxin this last winter for a sinus infection. After his first dose, he vomited violently and felt like he was getting the flu. He skipped the 2nd dose and began feeling better. The next day, he took another dose and the same thing happened. He threw up within an hour and felt lousy for the rest of the day. Forget this stuff!