Mg tablets symptoms and conditions

I was diagnosed with a bronchial infection 8 days ago and was prescribed the generic form of Biaxin, Clarithromycin (500 MG tablets). About 3 days into treatment, I started having a bad taste in my mouth. I can brush my teeth and rinse with mouthwash, but it still lingers. When I cough, it tastes like it comes up with my cough.

I have an already sensitive stomach, but have had problems every day since starting on the Clarithromycin. I've been taking it each time with food and/or milk, so my stomach is not empty.

On Day 3 of taking this medicine, I ran a fever of 102 and thought I had the flu. However, the fever went away the next day and I was just left with the already existing croupy cough.

I'm now on Day 8 and still have the lingering bad taste and stomach issues. I can't wait to be done with this drug! In the future, I'll be sure to get something other than Biaxin/Clarithromycin!

I was diagnosed with a bronchial infection 1 week ago today. I was prescribed Clarithromycin (500 MG tablets) and Advair. About 3 days into treatment, I started having a bad taste in my mouth. In the last 4 days, the taste seems to be getting worse. I've also been feeling jittery, my heart feels like it's racing and I keep a dull headache. On the 3rd day of taking this combo, I ran a fever between 101.3 and 102.3. I thought I had the flu, but the fever broke with some Tylenol and never came back. I was told I did not have the flu, although my husband and son both got it 2 and 3 days later. After a week of taking medications for an infection, I would think I'd be feeling better, but I'm not. I have 2 more days left of the Clarithromycin, but I'm not sure I want to continue. I think I'll probably cut out the Advair first and see what effect that has on me.

My doctor prescribed Avelox 400 mg tablets to treat pneumonia. I was warned by the pharmacist not to take it with my morning vitamins, so I took it 1/2 hour before bed time - needless to say I hardly slept. I started itching all over, my arms started tingling, my heart was racing a hundred miles an hour. Believe it or not I took another one the next night, and yep it happened again, I thought I was dying. My blood pressure dropped to 99/78 and my pulse was 50 - my normal vitals are 120/60, and pulse is 95. It seemed that within minutes my pulse jumped to 115 and my pressure was 138/90. I guess that is what an anxiety attach feels like. Then to top it all off, it felt like someone was pouring water in my veins, this feeling of rushing water ran from my fingers up my arms in into my shoulders then my heart would jump again; I had weakness is my legs and felt nausea the entire next day. I contacted my doctor with no return call, so I discontinued the medication. I do not believe the benefits of this medication out weigh the side effects. I will not ever take this medicine again. I will pray for healing for all of you, God bless and keep smiling.

My 62 year old husband has had Parkinson's for about 10 years now. The other day he was prescribed Prednisone (20 mg tablets, twice a day) for 5 days. After the first day his pinched nerve problem was greatly improved, and as a side effect, his Parkinson's symptoms disappeared completely and he was like normal again! This is a miracle to us and we are looking for medical research to help prescribe Prednisone for Parkinson's', or some agent similar. Did the Prednisone make the other Parkinson's drugs more effective; or did the Prednisone fix the Parkinson's on its own. We don't know. For 5 days, it was bliss; I hope we can get someone to weigh the side effects against the miracle of being normal without any Parkinson's symptoms!

I'm a 65 year old type 2 diabetic with low-functioning thyroid. I was put on lisinopril over a year ago to prevent kidney problems. I have been on 10 mg tablets. Even before I was diagnosed with diabetes I had low blood pressure so that was not a problem.

My main side effects are hair loss, coughing, insomnia and leg cramps, joint pain. I think the lisinopril is pulling nutrients from my body. I told my family doctor about the side effects I had found but he seemed more concerned about the possibility of kidney problems than any of the side effects. I know my hair loss is not age related as both of my parents had full heads of hair when they died and my mother was also a type 2 diabetic.

My blood sugar is under control, tests usually 85-90 twice a day, last A1c was 5.5 which is quite good. I take Byetta and metformin twice a day, levothyroxine, enablex. I recently started taking magnesium as it was besides calcium plus D, a multivitamin all ordered by the doctor. I also take crestor. Feels like all I do is take pills!

My weight is 166 but I'm short, 4' 10", so still heavier than I should be for my height. I try to get exercise but have degenerative arthritis in lower spine. Funny that I developed bursitis in my right hip recently, I just thought the arthritis was spreading. Now I'm not so sure it might not be due to the lisinopril also. I stopped using it yesterday so we'll see how long it takes my body to recover from this drug.

Does anyone have any experience with how long it takes to stop coughing or for the hair to regrow after quitting lisinopril?

I am taking 500 mg. tablets (3 twice a day) and not really having any reportable side effects. My neurologist has recently added a low dose of Lamictal because I was still having occasional absence seizures. The lamictal is causing many more side effects than the Keppra (insomnia, night sweats, headache, nausea)

My doctor prescribed Avelox 400 mg tablets. I took it at night and woke up the next morning with numb feeling and tingling in my hands and feet and nausea. Anyone who is thinking of taking this drug please read these comments. I wish I read it before taking my first dose. Can someone please let me know how long this side effect will last after only one pill. Thank you.

I've been on Phentermine on and off for about 12 years. Phentermine does work really well but as with any change in eating habits or diet, you must continue to eat well when you are off of it. Because Phentermine is classified as an Amphetamine, you will gain the weight back when you get off of it and possibly gain more. Just like a drug addict who is taking Meth-Amphetamines is usually super skinny, but when they get off of the drug, they gain alot of weight back. It works great in the beginning but Phentermine is a short term diet pill and after about 3 months of taking, you should get off it for a while because your body starts to become immune to it. You may want to take more of it and the more you take, the more dangerous it could become. I read on here where someone had high blood pressure because of it. Phentermine can definitely do that. As far as the girl with the menstrual cycle problems, I have never heard of Phentermine doing that, so you might want to check to make sure something else isn't wrong. Phentermine is the generic for Adipex. Adipex actually works ALOT better but your doctor actually has to write you the prescription for Adipex. Most doctors write Phentermine on the prescription and you cannot request Adipex. Your doctor actually has to prescribe it for you. I used to get my prescription filled out Walgreens or CVS and I was paying $54 a month for it. Then I heard Costco or Sam's Club sells it "at cost". Now I only pay $13.88 a month for it. I think I mostly just take Phentermine now to stay awake when I don't get enough sleep. Also, I had read on here where someone was breaking the 37.5 mg tablets in half and just taking a half a pill. I read in a drug insert on Phentermine that you should not break or crush them because it decreases the pill's effect significantly.

Today is Christmas day 2008. And a Merry Christmas to me ha!!!!!!!! I was given a prescription for the drug Levaquin on the 19th of December for a suspicion of pneumonia. The x rays done at the hospital found no evidence of pneumonia but my doctor wanted me to take it anyway because since I have asthma and my lungs sounded so bad I was told that I was at risk for developing any secondary infection that was out there. My husband filled the prescription on the 20th which was Saturday, took the first one of a seven day supply 500 mg tablets. About 4 hours after taking just one pill was awakened by severe and agonizing pain in both of my feet and my knees that I was writhing in pain. Since I have nerve damage in my feet anyhow I know what the pain that I normally experience feels like and instantly knew that this was not normal for me. When I thought that I finally might be able to walk I hobbled into the kitchen and dug the list of side affects out of the garbage (stupid me had not read them first.) I discovered that it was one of the side affects. Called the on call doctor in the morning since it was on the weekend and he stopped it immediately and put me on something else. I only took that one pill and since Saturday night every night I wake up in agonizing knee pain and I have never had pains in my knees before. The pain is so bad that I feel like I am ready to go on a morphine drip, or cut my legs off above the knees. Six days now from one pill, how much longer can this go on? I really feel bad for the people that contined to trust their doctors and continued with the full course of the medication and I realize that what I am experiencing is minor compared to what others are going through. This drug should come with a handout that says: Take this drug at a risk to your health!!!!!! Last night the pain lasted all night and I cried all night. Have to get through this day am entertaining for the holiday and have had no sleep. Actually getting afraid to go to sleep at this point.............D.

I have been on prednisone continuously now for 15 years. I was put on it in March of 1995 for a lung condition called chronic eosinophilic pneumonia. I was 122 pounds when I first started prednisone. Now 15 years later I am 197 pounds. I am 35 years old with osteoporosis. I have dealt with depression, terrible headaches, stomach ulcers, hormonal imbalance, hair loss, swollen feet and ankles, I now wear glasses when I didn't before, I have thin skin now that looks older than my 35 years, I deal with night sweats, and in the summer out in the heat my very round moon face turns red as a beet. But, no one can get me off the prednisone. I have seen many specialists, and within 1-2 days of starting to wean past 10mg I get so sick I have to be hospitalized, I literally can't breathe or live without it. I hate this stuff and what its done to me, but I have no choice but to take it or I will die. Doctors have tried alternate medications, nothing but prednisone works. If there is ANYONE who has had to be on it as long as I have or have had success in getting off it after being on it for so long, I would love to hear from you.

I was recently prescribed Avelox for Lyme disease. I took on dose, 2- 400 mg tablets. Within an hour, i could not walk, could barely talk, i was severely dizzy, my body went limp, numbness from my head to my toes, muscle twitches and lost my eye sight for several minutes . My husband had to call 911 and have the squad pick me up and take me to the hospital. Before they got there the only thing we could think of doing was for me to take a Benadryl.....which is probably what saved me. It look over 3 hours for this to wear off and along with every thing else i had a terrible seizure.
Please be aware of this medication. If so many people have had terrible side effects from the med, why is it still on the market????
This is just CRAZY!!!!

I have been taking Ultram 50mg 3 times daily for almost 8 years. I had severe back pain that extended down my left leg. I went to a Neurologist and he performed back surgery. I did quite well for about 3 months and then was experiencing the same problems. He then prescribed Ultram ER and it has worked great. The only side affects I have recognized have been sleeplessness, hot flashes, nausea that goes away in about 1 hour after taking it, and super energy. The benefits far outway the side affects. My 34 year old brother was prescribed the 50 mg. tablets and he had to be transported to the emergency room because of a seizure. Needless to say he was advised not to ever take another pill.

After taking only 2 100 mg. tablets, I had a fever of 103, body aches and nausea. I attributed this to the bladder infection and continued the medication. After 5 tablets, I began to itch from the top of my head to the bottom of my feet and stopped taking the medication. I returned to hospital and blood tests revealed abnormal liver functions.
Please do not take this medication. It should be removed from the market.

Was prescribed Avelox 400 mg tablets for a sinus infections (second one in a row.) Became severely depressed, crying in public places (and I am not a crier), couldn't sleep, headache and just felt disconnected all together. By day four couldn't take it any more and called the doctor. Was prescribed Azithromycin pack to clear things up.

I am glad I found this website to see that other people were having these same side effects because I was starting to think I was losing my mind.

I went on Prednisone for only 3 days as treatment to a bad allergic reaction to antibiotics. I ended up in the ER for treatment of the allergic reaction and they gave me a pred IV. They put me on 80 mg tablets, which I was supposed to take for 5 days, but there was no tapering off called for by the doc. I only took it for 3 days and started bad abdominal cramps and a bad taste in my mouth. Everything tasted extremely salty--and still does almost a week later. After I was off the drug for a day or two I started bad cramping in my chest, trouble breathing even though they said my lungs were clear, and really bad anxiety, which I've never had before. I freaked out while I was driving and had to pull into a parking lot for over an hour, and still had bad anxiety trying to drive home. I felt like I was drowning and had labored breathing. It's been almost a week and I still have muscle cramping in my chest, but it's starting to subside if I stay calm. I now have headaches and am weak generally, but am starting to come out of it, I think. I don't think the docs wanted to admit that lot of this was due to the pred; it is a serious drug that should not be taken lightly. I never knew there could be such extreme side effects to a drug. I am sorry to hear that many of you have had similar experiences, but it does give me some comfort to know that these effects were real and not due to some psychosomatic problem.

I was on a Prednisone taper for 7 days (bronchitis). I have been off for 16 days now. I am still suffering from BAD headaches, head pressure and dizziness (also racing heart) - off and on??? Does anyone know how long it takes to get this stuff out of your system? My first day after finishing it my headache and dizziness got so severe that I threw up 7 times over the next 24 hours?

Is it something that I am eating or drinking that is 'reactiviting' the side effects of the Prednisone? I hate this.

Thank you.

Vanessa

I recently took 750 mg tablets of Levaquin for six days for bronchitis. The bronchitis went away but on the 7th day I had a gelastic seizure. I had never had a seizure in my life. I passed out, my wife called 911 and I went to the emergency room for help by ambulance. Enroute I threw up really bad. Once I was checked in they ran a cat-scan and found nothing. The admitted my into the hospital for more tests and observation. The next day I had an MRI with contrast, and eeg, and the tests were normal. The following morning my doctors came in and told me the results of the tests and they were going to send me home. The doctors really did not know what caused the seizure. The Doctor that prescribed it to me said he uses Levaquin all the time and none of his patients had a problem with it. I told him that since that is the only thing that changed, my opinion was it did and that I would never take it again. Unfortunately I can't drive for six months and I now take Dilantin to prevent any more seizures.

Thank-you for this site! After reading all the testimonials I was greatly helped in realizing I was not alone in the terrible side-effects I was having since being on Fosamax for the past 5 months. A week ago the pain got so crippling I could barely walk,---left hip was awful, pain going right down the leg. It was hard to even sit without pain... X-Rays ordered by our internist revealed no new fracture or injury. I was on 70 mg tablets once weekly. Fortunately a lobotomist lady told me while taking my blood that the pain she had when on a Biphosphate medication (Boniva) crippled her with such pain she had to stop working! My internist is unable to accept the fact that Fosamax is the culprit causing the horrible pain...and although he has asked me to continue it, and use acupuncture to alleviate my pain, I HAVE TAKEN THE LAST DOSE Of IT AND HAVE INFORMED THEIR OFFICE...Many of the postings reiterated what I have suffered the last few months. The capstone came yesterday when an adult doctor-student of mine told me he would not take any Biphosphate drug and feels that like Vioxx the FDA in time will HAVE TO TAKE IT off the market. In the meantime, you folks are doing a wonderful service in helping your fellow-beings make wise decisions! I feel doctors prescribe these drugs in good faith,---after all their training is drug-oriented...I am thankful there are also Natural Alternatives and this is the route I plan to take! Blessings on all you dear folks out there who are victims of drug-reactions....The good news is that I understand most symptoms will be relieved when we stop taking the drug....Also, aural surgeons will not do surgery on any patient until they have been off Fosamax or any Biphosphate drugs FOR SIX MONTHS.....THANKS AGAIN FOR THIS SITE AND ALL OF YOU WHO POSTED ON IT....You have all helped me make a wise decision...Thanks again and God bless!

Hi Everyone,

Doctor put me on Geodon about 3 months ago. I started out 60 mg in the sample package the Doctor gave me. After using the sample pack I was prescribed 2 60 mg tablets (120mg) at night. It worked well for awhile and all of a sudden it seemed to stop working for me. I read a lot about how this drug is a nasty one and decided to cut down to 1 tablet (60 mg at night) The very next day I was trembling and having hot and cold flashes along with "brain zaps" and heart palpitations. I was hoping the Lamictal would cushion the side effects of the Geodon. Well it sure didn't do that and I know as the day goes I will have the same symptoms as I did yesterday.
The Geodon website makes this drug sound like a miracle drug but does state that heart related issues are there especially for the elderly people. This is a nasty drug that I hope I can get off and maybe go back to Lexapro because I have ADHD and not Bi-Polar.

I have been taking the initial dose of Niaspan for 4 weeks, one 500 mg tablet at bedtime. I really experienced no side effects at all. This week I started on the second step and increased the dose to two 500 mg tablets at bedtime. Every night I have been waking up with diareaha. It always seems to subisde during the day, but after taking my bedtime dose, I'm up again in the middle of the night. Any suggestions?

This website may not have saved my life, but it has certainly saved my sanity. Beginning in May 2007 I was prescribed Toprol XL for a supposed heart condition. I was instructed to begin with 50 mg per day and go to 100 mg per day after 10 days. Since I already had the 50 mg tablets, I simply started taking 2 of them together when I raised the dosage. On July 25 I ran out of the 50 mg tabs and filled a prescription for 100 mg tabs. Immediately upon starting the 100 mg tabs I began experiencing side effects which increased in severity daily. By Monday July 30 I was convinced I was losing my mind. Then I discovered this website, and read that many other people had suffered in the same way. What I have trouble grasping is why the same dosage had different effects. I tolerated the 100 mg/day dose just fine when taking 2 50 mg tabs, but the 100 mg was dreadful. I've checked the pills, and both the 50 mg and 100 mg are Astra-Zeneca products, not generic. The markings, shape and size are consistent with 100 mg tabs, so I haven't been inadvertently given an overdose. I immediately backed off the dosage, and am gradually going to reduce and stop the medication. I urge anyone who is having these problems not to stop at reporting them here, but also to contact Astra-Zeneca at www.astrazeneca.com, and to report them to the FDA's Medwatch website, www.fda.gov/medwatch. It may seem fruitless to contact Astra Zeneca, but they need to be made aware of these problems.

I just recently found this site and am very thankful I did. Has anyone ever even heard of someone being prescribed 1000mg oral prednisone for 7 days, followed by 500 mg oral prednisone for 7 days for a one day occurance of optic neuritis. It happened to my father and he died 3 weeks later. I would appreciate hearing from anyone who can help me make sense of this dosage.

I took Levaquin 750 mg for 2 days. The first night it made me sleepy and drowsy. The second night I took it, I was high. I felt like I was a zombie. I sat in front of my computer rocking back and forward. And al I wanted to do while I sat there was take more and more and more levaquin. I wanted sit there and eat them like they were candy. That urge was so overwhelming. So, I hurried up and I flushed them down the toilet except for 3. Knowing that they were there, I wanted to eat those 3, so I flushed them.
That was the worst night of my life. I said to myself if this is how high suppose to feel. I don't ever be high.
This drug need to be taken off the market.

My wife has been way overtaking on tenuate, up to 10 per day instead of the prescibed 35 mg tablets. Skin is itching and scalp is itching badly. Can this condition be caused by the continual overtaking of this medicine?

Can this drug cause a rash on my shin?