Severity symptoms and conditions

PREDNISONE.... a word that is unknown to the naive and despised by the the knowledgeable. Before i begin i want to tell you that prednisone for lack of better word F***ed me up. So heres my story with the pill. About a year ago i was officially diagnosed with Minimal Change Disease, now remember i am eighteen at the time, and was prescribed prednisone to cure the disease. Now being unaware of the severity of the drug and disease i casually continued life while taking 80mg per day of prednisone. Well this was good and all because it did in fact put me in remission, but the side effects were starting go surface. My face ballooned up "moon face", started experiencing random series of depression, became insomniatic, and unfortunately gained several pounds. Well this was not the end of side effects as for me. I continued with the medication and after 6 weeks of 80 mg i began my 5 week course of 60mg. Then after that i started 4 weeks on 40 mg and began tapering 5 mg every 2-3 weeks afterwards. Toward the middle of 60 mg the drug started taking its toll on my body as my skin lost its elasticity so i started getting gruesome strecht marks all over my body. I also became constipated for whatever reason most probably prednisone was at fault. I became very frightened actually terrified so i started to research about the drug in hopes of finding ways to avoid some side effects. In doing my research i found out very disturbing information regarding prednisone. Along with all the side effects that i mentioned above, prednisone also causes cateracts, glacoma, diabetes via insulin resistance, and osteoporosis. Now these i consider as the more severe permanent side effects as the list unfortunately is much longer. Finding out about the side effects i became extremely paranoid and started a very strict diet to hopefully avoid some permenat side effects. I admit reading about the information on prednisone created my paranoia and/or possible phycosis which ultimately led to my stress which led to my severe depression. Now this wasn't any old type of depression, i was sersiouly in need of some help. Everyone around me could tell something was wrong and really i dont blame then for in fact i felt as if my soul had died, the very essence of my being. Now magin if you can someone taking away your youth from you, sucking the very life out of you... thats exactly how i felt. To add along with the depression my grades became a wreck in college as i dropped several classes, lost a friend, developed problems with my parents as they tired to help me, and disrespected family relatives with my uncontrollable mood swings. A few weeks in of dieting and exercising i lost a lot of weight (15-20 pounds). As far as side effects non had changed i still had to deal with all that was mentioned above especially with the fragile skin that was a real burden as i had even a few stretch marks on my face from sleeping on my side. At this point of my long and what seemed to be a never ending journey i become exteremly weak. My body had no energy to run on as i refused to eat and when i did eat it was either foods that are considered free foods or protein nothing else. Everything at this time had been taken away from me including smoking marijuana (marijuana drops blood sugar as this would cause me to start feeling faint and lightheaded), alcohol (same as marijuana drops blood sugar), and the fact that i was not comfortable in my own skin (literally). I was driving myself insane. Everyday i was behind the computer searching for more and more. I was obsessed and became my worst nightmare. Oh by the way half in the medication therapy i showed 1+ grams of protein in my urine which my doctor possibly thought it could have been a relapse. This news i did not take lightly i had lost it and was prepared of comiting suicide. I cant lie, i really did not want to live anymore i just wanted to end this and suicide seemed like a very real and convienent possibility. If it had not been for my parents talking to me giving me a 3 hour speech and lecture i do not know what i would have done. Suicide at that point became out of the question because i could not do this to my family. So i went and purchased urine dip sticks to monitor the protein. The doctor had given me a 2 week window or chance to get back into remission or else he was going to prescribe me cytotoxic agents aka chemo therapy drugs. This was horrible news to me. So as i monitored my protein i found out of a very interesting trend. I noticed that my protein levels in the afternoon were in fact positive for protein and were usually up and down as far as how much but in the mornings i noticed i was always negative. Now this give me a huge bit of hope because when in researching about MCD months earlier i found out that there is a coniditon called orthostatic proteinuria which affects mostly young adolecent males and is a condition described as for some unknown reason there is protein loss in the afternoon when the person is upright and active then when they are supine or laying down the kidneys do not allow any portein loss. This condition is in fact harmless. I was very happy from then news and i told my doctor, he was somewhat doubting, but i don't blame him he is looking out for my best interest, but sure enough after the 2 weeks had past i went in again for my appointment after testing and i was negative for protein as i had expected. We began tapering after that point and i continusouly monitored my own tests at home and eventually i got off the steroid, actually today is that day after a 9 month period of heartache and distress. You know people say that they went to hell and back in a hard moment in life, well i went to hell stayed there for 9 months then came back. I feel so everyone who as ever needed to take steroids for long periods of time, i know its tough but believe it as it is indeed a potent drug and in most cases a miracle drug. It gave me a second chance at life and no matter how hard it was or how much pain it put me through i cannot complain for it did in fact cure me and thats why i can never hold any grudges. So thats my story i kno its not pretty but what can i say it is indeed mine whether i like it or not.

How about MUSCLE SPASMS?? My mom has had right leg and arm muscle spasms for the past 3 weeks, but has been on warfarin since end of March.

Centocor, the maker of Remicade, aggressively pushed physicians to set up infusion clinics, write for the drug and promised huge profits.Most of these infusion suites are run by nurses. The drug dose is calculated by a nurse and mixed into the iv bag by a nurse NOT A PHARMACIST. The drug, which can put patients at risk for serious infections and tuberculosis is not even mixed in a sterile IV hood !!! It is mixed out in the open air and exposed to contamination. In the meantime,Centocor downplayed the severity of the side effects. This drug actually caused LUPUS in a patient who subsequently won $19,000,000 in a lawsuit. The drug can greatly increase the risk of lymphomas and blood disorders with fatal outcomes. But the literature does not adequately educate patients and physicians on how to properly monitor the drug! The drug can cause memory problems, visual changes, and increased sed rate and increased c-reactiv protein.

I was on YAZ for only 7 days before I felt suddenly and completely crazy! On the Yasmin site there are several women complaining about YAZ side effects and asking if anyone is interested in starting a lawsuit. I feel there is enough severity and consistency in the complaints to start one. I don't believe a medication should be on the market that causes so many so much distress. If I could just save one women and her family from what we've gone through I would be willing to put quite a bit effort into it. Please respond to me or one of the women on the Yasmin site if you too think your suffering was enough that no one else should have to go through it. I read the side effects very carefully as I always do but I don't remember any that warned you may lose emotional stability. I had no history of such severe, or unmanageable anxiety, depression... . Please help us take this drug off the market, Imagine how many other women are suffering but either not looking on this site or stopping to share their stories.

I first started taking birth control pills about a year ago, and my doctor started me on Yaz, I continued to have an increase in headaches, nausea, and break-through bleeding, so she eventually switched me to Yasmin. To be honest for the first six months or so that I was on it, I was great, my headaches that I normally got decreased, and I didn't have any real side effects other then the expected break through bleeding the first months after starting it. Now I feel awful, my headaches come back with such increased severity I can't think and any medication I take for it doesn't work, during random times of the day I get waves of depression for no reason, I go through episodes of extreme emotion and the thought of even being close to my boyfriend at times sickens me. I didn't take any other drugs that could have interacted with the pill or increased the side effects as I know some people have implied. But I've never felt so horrible before in my life and I'm only twenty years old, I'm trying to get off the pill and find a different one, has anyone gotten off Yasmin and found a better alternative?

I've been taking Actonel for over a year. I slowly started getting foot and leg cramps, They have increased to total body cramping. From my neck to arms, sides, back, leg(calf), foot and toes. The severity is tremendous. My doctor just keeps giving me samples and prescriptions for this and that. Not addressing the cramping issue. Finally he decided since it's widespread, it must be fibromialgia. I can't believe it! I am going to stop the actonel, and see if it works.. Thanks for being here to vent.

i started taking yaz a couple months ago and developed a blood clot in my lung, a pulmonary embolism. i was hospitalized for a week in may of this year. i have visited many websites to see if other women have developed blood clots due to yaz and i have found a startling number of women that have developed blood clots, and a couple girls who even lost their lives. the side effects of birth control are explained to us before we start taking them, and it is expected that some women will experience the side effects, and this is normal. however, when a disproportionately large number of women start having serious health problems due to yaz, then something is not wrong with us, something is wrong with yaz. i have seen many women express an interest in starting a class action lawsuit and i am trying to do so. i have worked in a personal injury law office for the past 2 years and know an excellent lawyer looking to take on a case of this nature and magnitude. if you or your loved one has developed a blood clot, lost their life, or have developed another serious health problem due to yaz than please email me at ****** with your name and an email address i can reach you at. A class action lawsuit requires a large number of plaintiffs. I have already gotten a few emails but need many more before we can make this happen. please email me... help me and yourself.

What is the severity of the weakness that can be caused by this drug? What is the drug causes the weakness? What is the effect it has on the body that can do this?

I am truly sorry to hear about you Dad passing away because of this. God Bless!!!

I thank you all more than you could ever know. Reading these posts has made me feel so much better and I can now clearly put things together. I now know that I am NOT crazy and my husband was right - this thing is the cause of all my symptoms. The abdominal pain, the headaches, nausea (who wants to feel pregnant all the time???) the terrible skin (I have always been proud of my flawless complexion, even without make-up) the numbness in my fingers and toes, the moodiness and lack of desire to do ANYTHING, much less sex, the 4 month long period I have been having. I have gone from a super-social entertainer to almost a hermit who doesn't want company or to go anywhere, and just wants to sleep all day.
I am having it taken out today in an hour and a half. I pray I get back to normal soon. My marriage and work performance has been suffering terribly since I had this thing put in 4 months ago.
Has anyone else had a problem with the skin on their hands and feet peeling and cracking? This is a new symptom with started last week and is getting worse. Been taking antihistamines (2 types, once daily each) and no help. I knew it would be because I use the same products I have been using for many many years but gave it a shot anyway. My hands hurt so bad. Just curious to see if anyone else had this problem.
Can't wait to get this out.

My daughter has had a very difficult year, with many of the symptoms described in postings related to Yasmin. Please will everyone who has experienced the negative effects of this drug go to the website: www.FDA.gov and file a report. They do not ask for personal identification, but you can describe your symptoms, tests, hospitalizations, etc in great detail. You can also file a report with the drug manufacturer, but this will carry greater weight if your doctor files it on your behalf. Under certain circumstances, related to the severity of your adverse reaction, I believe the manufacturer is required to follow up with the FDA, and respond to your complaint.

I am a mother of four children (21, 19, 15 and 15) who have varying degrees of asthma and allergy. All of them have some degree of ADHD as well. The oldest took Singulair from grades 7 to 12. It was great for his allergy, but he had a depression which was attributed to his ADHD.

The second is still taking Singulair. She is highly asthmatic and it has been beneficial for her. The severity of her asthma went down to the controllable range, and her migraines (suffered since second grade) significantly decreased (documented side effect).

The last two, identical twins, began taking Singulair four years ago when they developed asthma as they entered puberty. They became oppositional, defiant, prone to rages, and curiously not hustling hard enough at their sports. Prior to this, they were solid, dependable students, with moments of inspiration - and aggressive athletes, leaders at their sports. We always thought the problems were related to puberty and the ADHD. More and more ADHD meds were applied. No more weekends off the meds - because our house would be destroyed.

As 2008 began, my own allergies flared. When the doc offered Singulair, I looked forward to feeling better. Within 48 hours, I could breathe at night, and the tightness in my chest went away. Even my allergic dermatitis improved.

Then a weird thing happened. I got lazy. I heard myself saying things like, "I don't care if I'm fat." I stopped doing my evening chores. I stopped pursuing my hobbies. I almost stopped making dinner. I was wondering why I didn't care, but I didn't care enough to pursue that, either.

Then it got worse. I couldn't handle the least criticism. I was in tears over almost anything. Within a few days, I was trying to find a way to leave my family. I just didn't care about anything any more.

The water-cooler crowd at work was chatting about the news reports about Singulair and suicide. I started to wonder: gee, doesn't depression preceed suicide? Maybe this hopeless feeling I had was related to the Singulair.

So I stopped taking it. 48 hours later, I started to laugh at jokes again. Five days later, I cleaned my kitchen. Now it's been three weeks and I'm back at my hobbies and loving life.

Two weeks ago, I realized that the never-ending laziness and argumentation we've been getting from our twins might be related to Singulair. I checked with the ADHD doc, and their general doc, and got the go-ahead to discontinue the medicine (although not both of them at once). I did this without telling anyone: not the twins, not my husband, no one.

Forty-eight hours after the first kid had stopped taking the Singulair, I came home to a grinning, hugging, 15 year old, who sat me down at the kitchen table to explain the strategy he'd designed to study for his upcoming exams. I was speechless and numb. I didn't tell anyone that he was no longer taking the Singulair (he takes a variety of vitamins and ADHD meds every day). The next day, my husband called me excitedly: the kid was cooperating with him! He didn't know what to make of it. I kept him in the dark for a few more days.

The other twin had been on a lower dose (5mg rather than 10 mg). I stopped his medication as well. The change in him has been more gradual.

Neither of them takes ADHD medicine now on non-school days. They are happy and cooperative. We ask ONCE for chores. There are still a few arguments and stormy moods - but I no longer wonder what's going to get broken next. And they seem to love working as hard as possible at their sports.

The good news is, we all feel better. The bad news is -- how did this happen? How can it be that such an obvious side effect was missed?

It's not like the effect of montelukast on the brain is unexplored. Try searching on "montelukast brain ischemia" - there are many studies that show that montelukast (Singulair) dramatically reduces brain swelling. What does it do for an uninjured brain? Does it dehydrate it? Deprive it of nutrition? If I had to characterize the behavior I saw in my twins, it's this: they acted the way hypoglycemic patients do, when they're late for their next snack. REALLY GRUMPY.

Or do some research on migraines and Singulair. There's an effect there, too. Many asthma patients on Singulair report that their migraines improve.

So the drug clearly affects the brain, and Merck's position that Singulair doesn't cause suicidal ideation is almost irrelevant. The fact is, montelukast has a significant, often-studied effect in the brain. That effect is not fully understood.

In our house, the effect of montelukast on the brain has been significant. We have dragged two kids to many psychiatric evaluations. We've spent hours and hours with teachers and principals and counselors, trying to understand why they just won't get their work done. We've used every performance-management trick in the books to get them to work - without much benefit. The kids have swallowed an awful lot of stimulant medication because it was the only thing that controlled their rages. Who knows what their teachers think of them - are they forever branded as the lazy kids? And we are lucky. From this forum, I've learned that it could have been a lot worse.

My story: I was prescribed Avelox for a small infection from shaving (foliculitus). I started taking this antibiotic the following day, it was a wednesday. Saturday night while bowling, I had what I consider to be a panic/anxiety attack, where I felt a disconnection happening between my mind and my body. I just wrote that instance off as just that, an anxiety attack. Well on monday I had a full blown attack and felt reality slipping away, and felt completely disconnected from my body and my surroundings. Everything became surreal. I went to see the prescribing physician, and she told me to stop taking Avelox, and that, this can happen to some people. Well I stopped taking it on that wednesday, and now its friday and I still feel completely disconnected from my body. I am scared and need to know if this will go away, I don't want to feel like this anymore. Does anyone know how long I will have to deal with this feeling?

I was on 200 mg/day of topamax for migraines. It did lessen the frequency and severity of the migraines. I lost 20 lbs and looked great. I felt horrible. I was suicidal and paranoid, cried frequently and thought that I was going to die. I was very tired, probably due to the topamax and the fact I was only eating about 500 cal per day on a good day, I was only rarely hungry and then would feel full after a few bites. I loved being thin, but was too tired to enjoy my life. I'm a nurse and couldn't remember anything, so I wrote everything down. My husband said that talking to me was like playing charades, because I couldn't remember the words for what I wanted to say. People would talk to me and my comprehension was very poor - it was like they were talking in another language that I didn't understand very well. I had always been sharp and quick witted, but on Topamax I was lost in a brain fog. I went off the drug under an MD's care. It took a while to feel like my old self, but life is now normal.

I was considering going back on it to lose the weight I put back on, but after reading all the other posts, I realize it's just not worth it. No, not everyone experiences all the awful side effects, but the side effects are not rare and some of them are horrifying. One of my friends who went on it couldn't even remember her children's names and she was on just 25 mg. I think this drug can make you feel like you are dying - just like a cancer patient at end stage. You don't want to eat, there is little enjoyment in life, your brain is foggy like you've been going through chemo and you feel incredibly sad as if you're going to die.

My advice would be to use the drug only if absolutely necessary. Try acupuncture, other migraine meds or seizure medications before this one. If you are taking it and notice that you are having extreme side effects, ask your doctor to be taken off it. If you can take it and the only side effects you get are a little pins and needles and an aversion to soda, go for it! But please note if you have strong emotional changes and try to eat healthy while on topamax.

I am a 25 year old, who was perfectly healthy prior to recently when I was diagnosed with Nephritic Syndrome and Minimal Change Disease and possibly FSGS (kidney diseases) I was put on 60 mg of Prednisone for 1 month then I was lowered to 40 mg for one month and I am then dropping to 30 mg. I am also taking Fosamax for my bones and a Vitamin D pill because my last lab test showed low vitamin D levels.

I am dizzy constantly and can not live a normal life, I can not drive or do any activities that I had previously done. My chest is so tight and constricted all of the time, my heart rate is so fast and pounds at my chest. I have no energy to do anything, I can barely open a door at times. I am beginning to grow unwanted hair on my face. My abdomen is always bloated. I have pain in my rib cage, and shoulders. I feel very sore throughout my entire body. I do not really sleep at night, so I look very tired all the time.

I have actually lost weight, I have no appetite at all. I am down 10-15lbs.

Now for the Pro- my Kidney Diseases are currently in remission and this has happened much faster than the Nephrologist had thought.

I am very anxious to getting my life back to normal and getting off the Prednisone.

Has any one else experienced increased heart rate, chest tightness, or rib pain?

I wish everyone the best in their roads to recovery!!

Was taking 300mg BID for seizure disorder (complex-partial with occasional progression to generalized) but had to stop because of severity of side effects: confusion, inability to remember words, depression, inability to concentrate, increased frequency of "aura" sensation/absence seizures, fatigue, frequent migraines, short-term memory loss (seems to have been related to medication rather than seizure disorder), dizziness, flushing, "drunk" feeling, insomnia (not sure if due to drug), loss of libido, occasional suicidal thought, etc. (There are others, but because of memory/concentration problems, can't remember them!)

I took it for severe epilepsy. I had two children on it fine, no problems. It put my epilepsy into complete remission, but for all the years I took it my life was destroyed by the emotional and mental side effects. Ended up homeless and in a domestic violence relationship, which I got out of when I stopped taking the poison pills. Coming off it felt like waking from a bad dream, but without epilepsy.

The effects which never went away were the dry mouth and no sweating, the enamal is stripped off my teeth. The mood swings and depression and exhaustion and memory loss and cognitive damage never went away. The loss of appetite and extreme weight loss(92lbs at 5'1" at first, 98lbs after tolerance) never stopped, nor did the constipation and resulting hemorrhoids.

Initial dose increases caused what I understand to be myoclonic spasms, which was a change in my seizure pattern, and other seizure pattern changes. The spasms came immediately after the final dose increase, were incapacitating in severity and lasted for about a half hour, and didn't fade for a week or two.

Did put epilepsy into complete remission.

I was prescribed this drug as an after operation precaution. I only took the tablets from Thursday- Monday after seeing the posts on this site!
I had been getting what i thought was heartburn on the day after my operation and assumed that the burning in my throat was from the tube placed in my throat during the anaesthetic. How wrong was I! By Monday night I was unable to eat or drink even my own saliva was buring me right down to my Oesophagus. I began to think that this was not normal as my breathing was getting weaker than normal-( i am asthmatic) constantly feeling dizzy, and to feel like someone was pouring acid into me ?? All sent warning signs. So i read the leaflet in the box to see the side effects. Surprise surprise i was getting the severe reactions to the drug. If only i had looked sooner! So i called my local gp first thing Tuesday, who advised i was being silly and that it was not the doxycycline!!! Even though i told him about the side effects. He then told me to continue to take them! Well I was not convinced and contacted the gp that operated on me and he told me to stop taking them immediately due to the severity of the side effects i was having. Its been 4 days now and the most i have managed to consume is 1/4 of a pot of yogurt. I also am a single parent with a 2 year old to look after so I am really struggling with the effects from this drug! I have seen that others are still affect by this for days after they have ceased the treatment. I just hope it calms down soon so that i can eat something. I am terribly drained and in so much pain, not to mention having to put up with the pain from the operation! I would advise that the first signs of discomfort on this drug stop taking it!

Anybody know if Prednisone and Levaquin are a bad combination together because that is what my doctor put me on and it almost killed me. No one seems to be able to find anything written that they should not be prescribed together. Doctors and pharmacies are all saying it is fine. I have so many side effects now that I don't think I will ever be back to normal. All I had wrong was a sinus infection.

I've been on Quasense for about 5months now. It's my first birth control, and I was happy with it until I was spotting a week before my wedding! After freaking out, it amazingly (miraculously) stopped a day before the wedding. So I decided to continue with it. It's been great until about 3 weeks ago. I have been spotting (sometimes more than just "spotting") for more than 2 weeks now! In addition to that, I'm convinced that Quasense has significantly contributed towards an increase in frequency and severity of my migraines!
Between the spotting and migraines... I had my doctor call in a prescription for Yaz TODAY.
Not surprisingly... the hubby isn't too thrilled with Quasense either!

hi, Finished a 6 day pack of Prednisone and am so very tired. I feel a bit sick and have hot/cold flashes. More than the normal for my age. I do not feel energetic. I don't know if it is the winter and gray sky doing it to me, but I don't think so. I feel so blah. Could this be from the Prednisone?
Thank you in advance for your help.

I am one of those women who spent years on Yasmin and more recently on its follow-up Yaz. I heard "low-dose" formulation and just assumed these would be the right pills for me, since I had moderate PCOS. Well it's taken me a long time to figure out that the introduction of these pills coincided with an increasing frequency and severity of mood swings and tension. Over the years the mood swings have included angry outbursts and irritability. I did like the predictable periods and absence of cramping. But that was definitely not worth the psychological and emotional suffering I've been through and put others through. I took my last Yaz pill today. I hope I get my normal life back, without the PCOS.

I got Mirena put in December 20, 2007. Getting it put in was the most painful experience of my life and I handle pain really well. I'm 21, no kids. I spotted all day and had the worst cramping and searing pain all day. I took pain relievers constantly all day and it did NOTHING!! I suffered through the night and had to go to the emergency room to have it removed. Apparently the doctor told me my body was rejecting it and it was forcing its way out. Well getting it out was a relief. That is until the next day I still had the swollen stomach and severe cramps still. I also started bleeding heavier than I ever had in my life. It's been three days since I got it removed and I'm still bloated, swollen, in pain, and miserable. This was the biggest mistake of my life!! I wish I had found this site before I got it because the pamphlet I got on it didn't even touch the severity of the symptoms. I would NOT recommend this to anyone. It will be the biggest mistake of you life!!!

I think a very, very important thing to keep in mind is how differently medications will work for different people. While it seems many of you have had horrible experiences with it, I surely don't think this is the case for everyone, including myself. I've been diagnosed with bipolar-II and have been on Lamictal for several months, currently at a dose of 150mg. I've found it had dramatically brought down my rapid cycling and decreased the severity of my depressive episodes. Though I still have mood swings, they are less frequent and less intense/disabling.
As far as side effects go, I've never been one to experience many side effects from any medication I've been on. With Lamictal I've begun having headaches and also difficulty with focus, concentration, and short term memory. I'm much more spacey than usual and often will get distracted while having a conversation with someone and forget what we were talking about. My psychiatrist believes these indicate ADD and has prescribed me Ritalin, which I refuse to take because I'm convinced that these problems are side effects of the Lamictal. I've experienced weight loss, but this also may be due to the 200mg Wellbutrin I am also taking.
Although I've experienced more side effects with Lamictal than any other drug, for me I'm willing to continue giving it a try because of its effect on my moods.

60 yr old/young female: I started generic toprol (metoprolol 50mg xr) yesterday (11/22/07). Took about 3:00 PM. The next morning around 6:00 AM, I had a hot flash that equated to one you would have if you had taken niacin. Body was burning and I was sweating. Looked in the mirror to see if I was flushed, because of the severity of the hot flash I thought my body would be totally red. It wasn't. I called my pharmacist to report this event. He researched and found no evidence of such. He did say that it did not rule out the possibility that it was caused by the Toprol. Asked me to keep him posted as his customers were the ones that helped him be able to report side effects to other. Well I found this site and low and behold I have read of the hot flashes and all of the other problems. I will not be taking this medication. I am not a pro medication person anyway and related that to my dr, but at some point you feel you have to have trust in someone. I don't trust medications. I know at some point in my life I will probably have to take something, but not Toprol. Sounds as though it will cause more problems than it will cure. Thanks so much for your input. It will prevent me from having to wean myself off this mess. Oh yeah, I was also feeling the depressed, anxiety mentioned. Not at a high level , but just knew I wasn't myself. That was after just one dose. I can't imagine how it would have progress. I feel very blessed.

i am taking allegra 120 for the last 6 days. at 1 pm. i feel drowsi and tired and fatigue feeling. feel like lie down always. is it due to allegra i dont know. can any body help me. please. regards.faseehuddin