Mg dose symptoms and conditions

Joint pain in fingers, joint pain in knuckles, wrist weakness after a week on 10 mg daily dose of Zetia. Amazing reduction in bad cholesterol and triglycerides when used with daily maximum 80 mg dose. Zetia was discontinued because of these painful side effects. 68 year old male.

My 11 year old son started singular in March of 2009 for exercise induced asthma. Within weeks he started having symptoms of heartburn - which he had never had before. I brought him back into the dr. mid June- they said wasn't related to singulair and actually increased his does from 5 mg to 10 mg. Since increasing his does, he started experiencing, daily headaches, stomach pain, leg cramps, night sweats w/ shaking & overall FEAR. Last night he was in tears - he kept saying there is something seriously wrong with me - I can't stand feeling this way he was afraid he was going to die and didn't want to go to sleep.

Last night I did my own research and found this board. THANK GOD!
He didn't take his singulair last night & he never will again.

I called his dr. this morning to tell them I think he is having negative side effects from singulair. They actually told he it was "HIGHLY UNLIKELY" his symptoms were related to singulair and NOT TO STOP USING IT. They instead said I should start giving him pepcid. I told them he had stopped it - for good and that we need a plan B for is exercise induced asthma. Looks like my plan B is finding a new Dr. that isn't in bed with Merck.

Has anyone had any experience with a NATURAL approch to controlling exercise induced asthma?

I am 74 years old and have been taking 50 mg dose of Amitriptyline for 12 years and I take it two hours before bedtime.

Recently it has been causing sleep apnea. I am now taking 25 mgs, two hours before bedtime at 8pm and need to know what time should I take the second dose in the am? I took it this morning around 9am and was sleepy most of the morning. I am guessing this has to do with how long between the dose the night before and the am dose was taking.

How long between these 25 mg doses should I take them.

Thanks Much. D.

Another one of many sleep aids prescribed to me it did not work at all 15 mg dose I asked my doctor if I should try two he said two was max dose and that if one did not work at all two probably would not and he told me to toss them.

This is the 3rd time I am taking levaquin in about 3 years. I had a MRSA type infection in my eye 2 years ago that I got in the hospital visiting my dying mother. She by the way died of a mysterious"infection" in her spine but frankly reading all of this I suppose it could have been caused by levaquin because they never found an infection but she complained of so much pain in her spinal collumn that they had to put her of morphine. No cause was ever determined but she was a dialysis patient and was given Levaquin on a regular basis for the infections that are common with having a stint in her arm. Her circulatory system collapsed and they could not do dialysis on her and she died after a week.
Getting back to my situation. I got the infection when rubbing the tears out of my eyes and woke up the morning of her funeral with a bad infection in the eye. Was going to eye doctor every week for 3 months thought I was going blind. Took 3 months of 750 mg dose. And multiple eye ointments. My eye sight took a hit and I now need to wear glasses for driving always. Used to have near perfect vision before this. This past year I took it again for Lyme's disease and after about a month after I developed and nerve or tendon pull in my neck that they could not explain how I got it. But I went to the emergency room and they gave me a neck support to wear.
Just was on Levaquin again for upper respiratory infection. Woke up in the middle of the night second day I was taking it. My head was pounding and it felt like it was going to explode (literally). At the same time my chest felt like it was collapsing. I thought I was really going to die and I was entirely coming undone in my mind. I called a friend at 2:30 AM and asked him (who is religious) if he knew any prayers for those who are about to die. I truly felt this was it - the end. No one told me about Levaquin's side effects until the other day when I was reading on the internet. I now have a pulsating sound in my ears that sounds like it is linked to my heartbeat. Never heard this sound before. Its been there for almost a week and it started a few days after I stopped taking the levaquin. I also have been noticing I have a shortness of breath and I am trying to move in a week. I keep getting very fatigued and have to lay down. Find myself falling asleep quite frequently.

My 90 year old, very mentally sound, grandmother was admitted to the hospital 2 days ago after complaining of severe pain in her back. While in the emergency room, after being diagnosed with a pinched nerve, her blood pressure rose and the staff doctor decided to admit her and put her on this horrible drug! He started her out with 100mg 2 times a day. My grandmother went from her usual calm perfectly sane self to a combative, babbling, lunatic within 6 hours of her first dose! It scared my aunt so bad that she started calling everyone to come say goodbye while there was still a chance that grandma would recognize us! I just knew that there was no way my completely lucid grandmother could go into dementia overnight so I told her to find out if the doctors had administered a new medication since they admitted her. They had and it was toprol XL. The stupid doctor tried to tell us that her behavior was related to a very low dose of prednisone that she taking for 2 years. We immediately demanded that the toprol be stopped and within 8 hours she started to return to us. She had spastic tremors, severe dementia, hallucinations, shallow breathing, agitation(went from laughing to combative in the space of 10 minutes!), dehydration, very frequent urination, extreme mood swings, brain fog/confusion, eyesight and hearing loss, her tongue swelled up, and her eyes were rolling back. It has been 36 hours since her last 100 mg dose and she is still fading in and out. We pulled her out of the hospital and brought her home today where the side effects have decreased but continue none the less. Since 11 this morning she has had bouts of not recognizing her own home and asking us to do things like take things out of the oven that she said she put in it, which of course she had not. I am praying to God that this medicine does not leave permanent damage. My grandmother is an unusual case for mental soundness at her age and it would be so unfair for that to be stolen away from her because of some stupid medicine that she was not only forced to take but over dosed with as well! DO NOT TAKE THIS MEDICINE WITHOUT RESEARCHING IT THOROUGHLY!

My husband, a 55 year old diabetic who is currently on dialysis was initially prescribed 20 mg Lipitor about 5 years ago. He began experiencing leg pains, but continued to take the drug. In May 2007 in suffered a minor stroke (clot). Upon release from the hospital, the neurologist prescribed an 80 mg dose claiming studies showed those who have had a stroke benefit from the higher dosage. He recovered from the stroke and was able to return to work in August 2007. On December 31, 2007 he suffered another stroke, however this time it was a full blown cerebral hemorrhage. After he suffered this stroke, I searched Lipitor on the web and to my surprise found an article that stated the higher dosage of Lipitor could cause brain bleeds in people who have suffered a prior stroke. I truly believe this high dosage of Lipitor was the cause, however the neurologist and his regular doctor say no. Of course they would say that, since they are the ones who put him on it in the first place. They blame it on the fact that he has other health issues, however he has been on dialysis since the beginning of 2004 and was able to work and function normally. Needless to say, when he was released from the hospital, Lipitor was no longer one of his prescribed medications. They wanted to prescribe a low dose statin of a different brand, but his cholesterol levels have been excellent without them and I won't let him take another statin. The damage is done, he has difficulty walking, has lost his balance and was forced to go on permanent disbility. He was an active volunteer fire fighter for 35+ years and the fact that he can no longer do all the things he use to do depresses him.

I have been on Wellbutrin XL 150 mg for about a month and a half. I really do not feel any difference. I was put on it for mild depression and loss of energy, but I still feel like I am floating through my days and can't wait to go home and crawl into bed. I should also mention I am on a very small dose of beta blockers for my atrial fibrillation (which is meant to decrease my heart rate). Should I increase to the 300 mg dose? I am concerned about doing this, as this is my first time on any anti-depressant and I would eventually like to wean myself off.
Also, have any women noticed their periods are late or non-existent? I am a week late in my period, and I am NEVER late. I will be going to get a pregnancy test done, but I am fairly certain I am not pregnant. I also noticed very heavy cramping yesterday that would signal the start of my period, but nothing happened.
I would appreciate any feedback!
Thank you.

Within one hour after my first dose of Lisinopril I was having severe sinus congestion and mild dizziness. Since this seemed like a rather mild problem I naively continued to take my 10 mg dose every day. At first my blood pressure did drop a little, but within two weeks it had begun to climb back to the 150/90 range that I was having when it was prescribed. In addition I soon began to experience intermittent diarrhea, headache, vague moving pains in my abdomen, itching which interferred with my sleep, leg cramps, heart pain, anxiety and continuing increase in blood pressure. After calling my doctor's office and explaining all this to the nurse I received a return call telling me I was to DOUBLE my dose and assuring me that I had not been on the drug long enough for it to take effect. Especially concerning to me was the statement that the heart pain was because of my high blood pressure and that doubling the dose would resolve this. Foolishly, I did in fact double the dose for a week. During that time all of my symptoms worsened until I awoke one night with severe chest pain. My husband took my blood pressure and it was 220/120...............this as I was lying prone in bed after having just awakened from two hours sleep. At this point I was certain that my problem was more the drug than the original elevated blood pressure. I quit taking the drug immediately and within two days I was feeling better and my blood pressure was down the the original elevated level. I have now changed doctors, however I have little hope that the change will help as he has put me on a different medication ( which makes my ankles swell) and tells me that if the swelling continues he will put me on lisinopril with hydrochlorothiazide..............he does not believe that any of the symptoms I was having were related to that drug.

I have been taking 200 mg. of Lamictal (now Lamotrigine) for 5 years. I have had cognitive issues for probably about three years at least. Memory loss, sudden loss of flow in conversation, completely forgetting words and the spelling issue which was previously impeccable. It's embarrassing and frightening. I can't get through ANY given day without losing my belongings over and over again. I feel disabled (seriously) and I jokingly tell people I need an "aide". The scariest thing was last week I was going to return an item to the store and COMPLETELY forgot my PIN # for my debit card. I have been using the card nearly daily for a year and a half!!! It panicked me but I thought of course I would remember it later. NOT!!! Never again, it's gone!!! That's when I decided to search the internet for "severe memory loss" and came upon this blog. I didn't even think of the Lamictal. And I pride myself on my thorough research!!! Certainly the doctor never mentioned this side effect and I just gave it up to being 49!!! A little early for Alzheimer's!!!

The funny thing is I have also had skin problems (acne) for the first time in my life the past couple of years with it really getting bad last summer. I weaned myself off the Lamictal b/c I had read it could cause acne (another thing the doctor never told me). Well, I was completely weaned and omg, the mood issues were severe!!! So reluctantly I titrated back up to the 200 mg dose and immediately my mood was stabilized.

I don't know what the h--- to do, but something needs to change. The memory thing is terrifying!!! No wonder I am having so many problems with my job!!!

Maybe a new med, maybe not . . . My main issue was severe depression (both situational and chronic) which Lamictal seemed to stabilize. Do the benefits outweigh the side effects??? I think NOT . . .

FRUSTRATED IN MICHIGAN :(

My experience with Lisinopril is brutal! I'm 37 years old and was prescribed this drug for high blood pressure. After 2 yrs. on a 10 mg. dose per day I started having numbness in both of my arms I also had sharp pain shooting down both arms at night to the point where I couldn't sleep.And when I did fall asleep I would just wake up an hour later in tremendous pain. Ive been to three doctors. They tested me for carpal tunnal and told me I had it. But didn't schedule any plan of action, so I thought with some rest it would go away but it didn't It got worse. Then I started to have severe back pain that went clear through to my So the doctor wanted me to get an ultrasound of my testicles to check for testicular cancer. The test was negative. Since the pain was on the right side in my lower ribcage area they then thought it may be my kidneys. They then sent me to a urologist who wanted to go up my penis to scope my bladder with a camera and check for bladder cancer. Which turned out to be a very very painful experience. There was nothing wrong he said. During this time the pain was as bad as ever. Then they wanted to do exploritory kidney surgery on my right kidney. I was thinking my god am I gonna die.....I went through the surgery and the doctor said there was nothing wrong.I could not believe I was in this much pain and they couldn't find anything wrong. I thought I was dying for real. Then I decided to go on web md and try to find out anything that it could possibly be. I couldn't find anything with all the symptoms that made any seance. A few months went by with no relief... I decided one day to google my medication (Lisinopril) and joint pain, w/ arm numbness well. This site popped up and I started reading and Im glad I did. I believe that for the past year that I thought I was dying and no one could tell me why is because of this toxic poisons pill Ive been taking for two years is the reason for all of it. Ive spent thousands of dollars, had two surgery's ,went through all this pain all because of a little poison pill for blood pressure. I have flushed my pills and I,m never taking the drug again. I warn anyone who has high blood pressure if your doctor mentions the word Lisinopril tell them no!!!!!!!!! It is poison for the body.I believe it would killed me if I hadn't stopped taking it and not one doctor mentioned it may be the pill I was taking everyday for my blood pressure.

I just got a sample of 50 mg dose, but I am worried about the side effects. I am 18 and somewhat overweight but in overall decent health, but my doctor who gave the sample to me says my blood sugar & cholesterol could decrease, and there have been very rare cases of involuntary/uncontrollable facial movements. I know each patient has different side effects, but are the more severe ones more common? I don't know if I should wait to take them, or take the risk.

During the three weeks I was using 150 mg. Wellbutrin, ringing in the ears gradually increased, mild headaches on top of my head, occasional light spasms around my mouth, constipation, and bladder problems. My sleep was unaffected, and my depression did not lift. My dose was increased to 300 mg, and by the fourth day, I was having serious facial spasms, intense headaches, louder and constant ringing in the ears, almost 'round-the-clock wakefulness, anxiety, difficulty thinking and completing sentences, pounding heart, amplification of sounds, jitters and quaking. I felt like a car, perpetually idling so roughly that all my parts were about to rattle right off the chassis. On the fifth day I took nothing. I've had some chills, a little nausea, headache, neck-ache (Isn't that weird?!) and some ringing, but at a lower volume that's hardly noticeable. This is the fourth day with no Wellbutrin, and I haven't had facial spasms at all in the past couple of days, have less nausea, and the very funky smell produced in my urine from the second week I was on the meds has calmed down. If I'm still in a depression it's been overshadowed by the most awful side effects I could have imagined. It felt like the spector of death was overtaking my body by day four of that 300 mg. dose. I had been on a hefty dose of Zoloft daily for almost ten years and never experienced anything unpleasant other than weight gain, my reason for trying to switch meds because I couldn't quit putting on weight no matter what. I am going to try SAM-e, and suggest that anyone looking for a natural alternative, with the prospect of few and insignificant side effects, do an online search. Whether I find success with the SAM-e, or if it falls short of what I need, I'll post here to let you know what happens. A month ago I thought the depression was the end of the world; I think the cure was worse than the disease.

I am so thankful for this site. I thought maybe it was just me. For one, I am allergic to Sulfa. My doctor knows this, as does my pharmacy. Still, they give me Lisinopril with Hydrochlorothiazide which you should NOT take if you have a sulfa allergy. From day one, I started with anxiety, agitation, nausea and what felt like a racing heart - though my pulse was normal. Day three I called the doctor and they said this was normal as my body "adjusted" to the medication. It has been over two weeks and the same thing keeps happening. I tried taking the meds at night to hopefully sleep through the side effects but no - it just kept me awake. I put another call in today and have yet to receive a return call from my doctor. I hope the doctor calls me and NOT the front desk girl because I have a lot of questions and concerns. Other symptoms I have been experiencing since I started Lisinopril are sever muscle cramping last for over 24 hours, dizziness, heavy chest/racing heart beat, restlessness and less frequent urination. For a 37 yo female who has to "potty" constantly, even throughout the night, going once in an 8+ hour period is not normal! The worst side effect though is definitely the anger and agitation. I feel like I am going to burst out of my skin or die banging my head against the wall. Last night I tossed and turned for 2 hours in agitation. I thought I would surely have a heart attack from the stress. Oh yeah my BP has NOT dropped at all (tho it fluctuates on or off the meds) on the 20 mg dose. Go figure.

Just started today with 40 mg dose of Sortis (Swiss-branded Lipitor).
60-90 minutes later, I am very dizzy, sweating, funny taste in mouth.

I am done... no more. My cholesterol is normal, but recommended as complementary treatment with Glucophage, as I am very slightly diabetic.

I am still spaced out as I write this note. Called the MD to tell him that I the one dose is all that will enter my body.

Has anyone stayed at the 25 mg. dose? It's all they will have me taking.

Even so, after one week, I am noticing acne- I wondered about that; haven't had it in 20 years- and dry mouth.

Last week I had an issue with my INR - it has always been unstable, but this time was weird. My INR had been 6 and so I stopped the warfarin for 4 days, and went back on my regular 2 mg dose. Then we went on holiday to Washington DC for a week. 3 days in, my pee was the colour of cherry kool aid. Went to the local hospital (thank god for travel insurance). My INR was 7.89 - In the US this is considered critical and I was admitted, and treated with Vitamin K and 2 units of plasma. Within 8 hours my INR had dropped to 1.8 - now too low. The next day down to 1.25, and a week later I am still 1. I am taking fragmin now until I can get my INR theraputic again but Fragmin shots are even worse than warfarin.

An ultrasound showed now issues with my bladder or kidneys, but I do not understand why I was bleeding.

Guess that this just shows the importance of regular checking of INR levels while on warfarin.

I have been on Levaquin for 2 days. My Doctor had me take a 750 mg dose before I left his office. I am taking them due to a nasty bladder and kidney infection. I hurt more than I ever remember hurting...it is like someone used me for a punching bag and it continues to get worse, not better. I ache horribly. I cannot taste anything and I couldn't sleep more than two hours last night. I range between feeling hot and having the sweats to having the chills. If I don't feel better tomorrow, I will go to the hospital.

On lipitor for 1 1/2 years.... starting taking yoga a month ago. Had ache in knee and leg which then went to toe on other leg. Thought it was overstretching from yoga. Pain moved to hips and lower back. All very painful but worst was yet to come. Pain moved to neck and shoulders. Could not move head. Excruciating SOBBING pain. I was in so much pain for weekend. Everyone wanted me to go to emergency room but I wanted to stick it out til Monday.

PS... went on web. Saw this is lipitor side effect. never would have expected that after 1 1/2 yrs on a 10 mg dose.

Went to pain management doctor ... got Soma (muscle relaxant), an oral steroid and Percoset. Relief was almost instant.

Called my cardiologist. He says it is the Lipitor.

No more statins for me.
And back to yoga.

Just checking in after nearly a year or so, during which I cut my 10 mg Lipitor dose in HALF! I knife the little white pills down the middle and take 5 mg per day. My doctor did not notice any difference and HDL/LDL etc, are still in the range he likes. So, let's see about symptoms. The Plantar's Fasciitis is still there, but much improved, probably because I gave up full court basketball (at age 55). I have a few other symptoms that I recognize from others posting about them, such as occasional muscle ticks, general malaise, and sleep disorders, but, in general, I seem to be tolerating the 5 mg dose better than the 10 mg dose, AND, most importantly, it IS at a therapeutic level. I have not mentioned this to my Dr., and will keep it that way. If he can't tell, then my plan is working, sort of.

I really think Lipitor is poison and will eventually kill anyone who uses it, but am hoping I can cheat the hangman with the 5mg doses. I don't want to go back to cholesterol readings in the 250-plus range, because heart disease is the big killer in my family.

We'll see how 5 mg goes. I'm not suggesting anyone else necessarily should try this, but I was amazed that the numbers on my labs were almost identical as the 10mg.

Hello, I'm not sure if this is a side effect of being switched to Metoprolol Succinate ER from Toprol XL at 50 mg dose once daily or not but since I have been I've had a constant sore throat and mainly at night. If anyone else has experienced a similar problem please let me know. Thanks in advance.

I was switched to Metoprolol Succinate ER from Toprol XL at 50 mg dose once daily. I am diabetic and I was on Toprol XL which was not a problem. Now I have headaches that are horrid and I also associate them with the generic medication. I am one of the happiest persons you have ever met and now I am crying for no reason and feel depressed and angry. My feet are swelling until I can hardly get my feet in my shoes and I am having leg cramps at night because of extreme cold in my legs and feet. I am going this week to see if my doctor can get me on something else. Clearly it is this new medication that is causing the problems.

I took 20 mg of Lipitor for years with no problems, but when my doctor upped the dose to 40 mg, I had achy, flu-like symptoms, and everything tasted bad. I have stopped taking it altogether, planning to return to the 20 mg dose. But the side effects are taking so long to dissipate, I think I may not go back on it at all.

Hi, i was suffering from MCD and put on Prednisone 60 mg per day in May 2007 and after 4 weeks my Doctor asked to take alternate days and then taper by reducing 10 mg per week and it was stopped without much of side effects. But it was the beginning what i feel as in Nov 2007 again i had relapses and this time i was on 80 mg dose which i completed for 4 weeks and when it was on alternate days i started with my right hip pain which i reported to my doctor and was suggested not to go for any pain killer as it is due to Prednisone.
When pain increased i was advised to go for hip MRI and today after MRI the technician informed that my hip joint is damaged......yet i have not got the detailed report of MRI. It all caused by this drug as i have never fallen or got any other impact. Now i am on bed as i can't move and as others i am also getting swelling on face, water retention etc.

Anil

I was put on Effexor because of anxiety and panic attacks, and all I have to say is that this medication increased more so than it alleviated any of those symptoms. I was not even feeling very anxious at the time of my taking the first (37.5 mg) dose.

I took the capsule around 2 in the afternoon and by 4pm I had a severe headache. This was followed by nausea and strange thoughts. When I returned home that evening (last night) around 7pm I called my roommate a profane word (way out of character) and made her cry. We resolved the conflict, and I went to bed without any discomfort.

But I awoke around 3 am feeling strange sensations coursing through my body, anxiety, strange thoughts (again), and a sense of "overheating." I wanted to get up but I felt like I could not will myself to act, I felt as though I was in an "out of body" state. My paranoia and anxiety reached an apex at which I decided that I must not be "okay," and called my mother.

My mother assured me that I am okay and just that I must be on "too much stimulant, call the doctor tomorrow." I truly felt like I was having an awful hallucinogenic nightmare. I wanted someone to tell me that I would be okay because at certain points I had a fear that maybe I was having an allergic reaction to the stuff and might die.

Had I not researched online boards beforehand I would have called "911" no questions asked at the first onset of my symptoms last night. One of the scariest things I have been through in awhile. Still don't feel quite right, but the feeling is not as intense.