Three times a day symptoms and conditions

My perscription is to take two tablets, three times a day after the second dose I have such a painful stomach ache! I have a feeling that the pain is actually in the lining of the stomach ......

I was put on a 5-day dose of Levaquin, and am on my 4th day. After the first dose, I started to get severe itching and pain in my vaginal area. I know it's a yeast infection because I had it once before. I have also had really bad insomnia for the past two days. Called my doc; she told me to continue the medicine and perscribed Diflucan and monistat 3-day. She also said to take Benadryl for itching, but I am feeling really tired already, and I think the Benadryl would just make it worse. I am very tempted to stop taking this med right now, but not sure if it's ok to do that. Has anyone else gotten a yeast infection from this? Thanks, and I hope everyone starts to feel better soon.

I got poison ivy for the first time. It wasn't bad like my brother, but lotion didn't help. I wanted out of my misery, so I went to the doctor and he gave me the option of a steroid three times a day for two weeks, or the shot (which would give me relief in a day or two, instead of towards the end). I took the shot, and it worked WELL. I also had some energy, and it helped my sinuses, which constantly feel swollen inside (despite prescription medication). I'd say if you get poison ivy, get yourself out of misery by getting the shot.

I started lamictal about 4-5 years ago,50 mgs three times a day, I was always tired,depressed, and found it to be very hard to do anything at all. I started to gain alot of weight and had diarrhea.Went to see the Dr..I was told I had hep-A for two years.I asked my doc to send me to a specialist to make sure I did'nt have cancer of the liver, the specialist told me I had celiac disease.So I went on the gluten free diet for almost another two yrs. My psychiatrist then decreased my clonazapan and put me on another 75 mgs a day of lamictal. I broke out in such a rash I went to the hospital 2 days in a row, they did'nt know what was wrong. I went for my next appt. to see my shrink,i told her about my problems, she said "I told you if you break out in a rash stop taking the drug" she(or I don't remember) never told me that! I have been lamictal free for about two months now. I now have a whole new set of Dr.s ,they can't find any signs of either hep-a or celiac. I have so much energy now,my head is clear and feel almost normal again! Still working on the weight, slowly but surely it' Is going down. I was always a size 1 at 105 lbs,and went up to 140. I am 50 years old and it is much harder to lose the weight . has anyone else had any of these symptoms? Please let me know. Thanks!

Discontinuing Lisinopril:

Like many of you good folks that have been taking Lisinopril, I have discontinued taking the med after 10 days usage.

ONE WORD OF CAUTION: Please, please, please, go to a local drug store and purchase a blood pressure cuff. It doesn't have to be anything fancy... the manual-inflate, analog-dial type costs around $15 at CVS. If you don't know how to take your own BP, then let either a nurse or your local rescue squad show you how.... It's really quite simple. Different people act differently to meds and there is a real possibility that your BP could go very high. You need to check it several times a day. Also, after discontinuing many BP meds (including Lisinopril), your potassium (and possibly calcium) levels may drop, causing some really nasty side effects.

I've been an EMT for 25+ years and have seen quite a few patients (including my mother) "stroke out" due to HBP.... please don't let it happen to you. Discuss it with your doctor; there are many other HBP meds out there and one of them will no doubt work for you without causing side effects. Just don't disregard your HBP.

(Disclaimer: the above is a personal opinion and not offered as any type of medical advice.)

I have been on Levothyroxene for 14 months now. I have been experiencing nightmares, a "butterfly" feeling between my chest and stomach, itchy skin, dizziness, and am still fatigued. My dose is 50mcg. once a day. that was upped from 25 mcg. a day as my TSH level was not within the normal range. Sometimes I feel like I'm feeling WORSE after being put on Levothyroxene. I also am still gaining weight and am constantly bloated, having bouts of diarrhea, and my blood pressure won't stay regulated. I am currently recuperating from a bad cold and the cough is hanging on. My other meds I take are Atenolol-12.5 mg. once a day and Xanax-.25 mg. two to three times a day. Is there an interaction between all these meds(I take them at different intervals thruout the day to avoid interactions)?

I took a Kenalog injection for allergies 9 years ago and swore I would never take another one. I had anxiety, depression, heart palpations, mood swings, high b/p and on and on...thought I was loosing my mind. Blood work showed I was post menapause and was put on hormones as well as anxiety meds and b/p meds. It took a few months to get somewhat back to normal. I could never get a medical professional to say the shot did it...but my "gut" said it did.

Nov. 15, 2006 I took another one, how STUPID. I had had strep throat, upper respiratory infection, seasonal asthma and was having a hard time bouncing back, before I knew it I had taken it again. It didn't seem to bother me for the first two weeks but then the blood pressure increase ( I was already taking a mild b/p pill), more anxiety than usual, rapid heart beat, mood swings, depression etc. returned. It took me a couple of days to figure out what was going on. My medical professional thought stress from the last few months was the contributing factor ( both my parents have died in the last 6 months and I had been caring for them for 2 years). I did not think that had caused the onset of all the above. I contacted my pharmacist who agreed with me that the shot was most likely the cause. Now I am stuck with all these horrible feelings until the shot wears off. I have been put on a much stronger b/p medication, which isn't working to it's full potential and I am taking zanax three times a day just to keep the anxiety at bay. Needless to say I have had them mark my medical chart..."ALLERGIC TO KENALOG". I will NEVER take another one.

I was prescribed Geodon for schizpophrenia and it has had little impact on the illness. I was told to take it three times a day, 20mg capsules. At 60mg I experience somewhat strange physiological changes, like severe weakness, dizziness, and an increase in visual and auditory hallucinations. Orthostatic Hypotension is one of the major contraindications of the medicine which I have experienced. My use of the drug has been no more than 15 days and I have not finished the bottle. I could be highly sensitive to drugs which would mean having to increase the dose slightly over longer period of time. In my experience with many of these drugs I have had few positive results with mostly negative side effects that have only served to limit my physical and mental powers. I would recomend that anyone considering the use of typical or atypical antipsychotics should reconsider and look into other options. Especially when prescribed for youth or children under the age of 10 years. The permanent changes that could occur are not positive in terms of mental development, and also the possibilty of developing Tardive Dyskinesia a serious neorological abnormality that can last for the rest of one's life. My experience has ended with Geodon because I derived little benefit from its use. I would not recomend others use of the drug.

I have been taking 20 mmg of prednisone three times a day. I'm taking it for lupus, and I have gained over 10 pounds in a week. It makes me feel wonderful, but I hate the side effects. I am gaining so much weight, my face is so fat and people continuously ask me if I'm pregnant. Also it stops me from staying asleep but not from going to sleep. However, that doesn't bother me so much.

I just started taking this two days ago. Unlike many of you I am taking this for nerve damage in my leg instead of migraines. I have previously taken Neurontin and Lyrica and had to discontinue because I am apparently very sensitive to this kind of medication. I am only taking FIFTEEN mg (the pharmacy had to special order it for me) and only right before I go to bed, but I am OUT of it. I am very, very tired, nauseous, and just not all there. I have no attention span whatsoever (it just took me like, thirty seconds to think of the phrase 'attention span'). I just called the pharmacy to ask them if these side effects last, or disappear as your body gets used to the meds. They told me to give it a couple of weeks if I can. I'd like to give it a chance- but I'm supposed to increase to three times a day, and I don't think THAT'S gonna happen anytime soon.

Re my post #14305 on Nov. 15, 2005: SAW MY PSYCHIATRIST RIGHT AWAY ABOUT ALL MY SIDE EFFECTS. SHE CHANGED MY LAMICTAL DOSAGE TIMES TO 100 MG IN THE PM AND 100 MG IN THE PM, NOT ALL AT ONCE, AND TOLD ME TO TAKE CLONAZEPAM .5 MG THREE TIMES A DAY TO CALM ME DOWN. THIS WORKED! ALMOST ALL SIDE EFFECTS ARE GONE! EXCEPT THAT I STILL WAKE MYSELF BY YELLING. SHE THINKS I AM HAVING VIVID DREAMS I DON'T REMEMBER AND THAT THIS IS CAUSING THE YELLING WHILE I'M ASLEEP. I AM HOPING IT WILL SUBSIDE. OTHERWISE, I FEEL ABSOLUTELY WONDERFUL!!!!

FOR GOD'S SAKE, READ THE LITERATURE THAT COMES WITH LAMICTAL OR GET SOME LITERATURE FROM YOUR PHARMACIST IF YOU DON'T HAVE IT. THE RASHES SOME PEOPLE GET ARE REALLY TERRIBLY DANGEROUS AND SHOULD BE REPORTED TO THE DOCTOR IMMEDIATELY! THEY CAN BE FATAL! IF YOUR DOCTOR DISMISSES IT, FIND ANOTHER DOCTOR WHO KNOWS WHAT THEY ARE DOING AND GO IMMEDIATELY TO THE E.R. OR AN URGENT CARE CLINIC, AND MAKE SURE THE DR. YOU SEE KNOWS ABOUT LAMICTAL AND THE SIDE EFFECTS! THE MEDS SHOULD BE STOPPED IF YOU GET A RASH. NOT ACNE, BUT AN ACTUAL RASH, LIKE HIVES OR ANYTHING THAT APPEARS TO BE A RASH! BE SURE YOU SEE A DR. WHO KNOWS ALL ABOUT LAMICTAL OR WILL AT LEAST READ UP ON IT. I HAD ONE TRIP TO THE E.R. (BECAUSE MY DR. WAS NOT AVAILABLE AND HAD NO BACKUP) ABOUT TERRIBLE SEVERE SIDE EFFECTS OF LITHIUM I WAS ON AT THE TIME AND HE DIDN'T KNOW S--T ABOUT LITHIUM, I WAS TREATED TERRIBLE BY THE NURSES AND I JUST GOT UP AND WALKED OUT. THEY BILLED MEDICARE $958 FOR MY 2 MINUTES WITH THE DOCTOR. I FILED A COMPLAINT WITH THE HOSPITAL AND GOT NO RESPONSE WHATSOEVER. IF THIS EVER HAPPENS AGAIN, I WILL NOT GO TO THE E.R., BUT TO AN URGENT CARE CLINIC. EDUCATE YOURSELF! DON'T JUST HANG OUT THERE IN THE WIND, WONDERING....

hi everyone. i bought a report (which i probably shouldn't post here lest i get into trouble!) that specifies dosages for quercetin with bromelain for children and adults. we tried it with my son after taking him off singulair and he did great. in fact, we're just down to a little bit of throat clearing now--no other allergy symptoms and no asthma attacks yet (knock wood). it's REALLY hard to do with the littler kids because they can't swallow the pills and it then has to be put into a food or drink and it's not the most pleasant thing. my son was able to drink it in pineapple orange juice through a straw. he had to do it three times a day. we've since stopped, but would do it again if his allergies start acting up because i do think it works. if you can get your child to take it somehow i think you will find it helpful.

good luck!
(and i'm not at all, in any way, associated with the person who wrote the report--i actually feel kind of stupid for buying the thing because i'm sure the information is available free somewhere online!)

I went to the doctor as I have IBS and stomach problems and have had for some years now. She put me on Reglan 10mg three times a day. I took it for about a week and had severe drowsiness to the point I could not stay awake at all. Also it made my nausea and vomiting worse instead of helping. I experianced trouble breathing and finally just stopped taking it all together. I would strongly caution anyone who is thinking of taking this medication.

I began taking prednisone a week ago for a severe case of poison ivy. prior to taking it, i did a little research and heard all of the horror stories, so i was very anxious. the doctor prescribed 20 mg three times a day to start, with a taper-off beginning three days later. my wife, who is a nurse, was shocked at the high dose, consulted with a friend who is a nurse practitioner and we all agreed to cut the dosage by 60%. I began to take the drug, and relief was almost immediate. My hand was so swollen with the ivy, i couldn't make a fist. in 24 hours, the swelling had gone down, in a few days, the itching was gone and the ivy was drying up. In addition, i have had zero negative side effects. Contrary to what I have read, I actually have a decrease in appetite and a bit of weight loss. I have more energy and feel wide awake until about midnight every night. It takes a bit longer than usual to fall asleep, but I feel great upon waking up in the morning. All in all, I have had a very positive experience with prednisone, and that is a lot for me to say, as I despise pharmaceutical companies, and take no prescription drugs at all (well, except for an occasional prescription decongestant when allergies flare up.) But I shudder to think of what would have happened if I had started on the massive dose the doctor originally prescribed.

hi a am a 30 year old single mom of a ten year old. I have been on clonazepam for over five years. I developed panic attacks shortly after having a surgery to correct my heart. I was born with two electrical pathways, and would have heart palpitations that lead me to the emergeny room several times. I am currently taking 1mg three times a day. I would like to get off the drug, and have heard from a friend that I causes damage to your liver. Has anyone heard of that? If anyone has heard please let me know.

Lisinopril, yet another med prescribed blithely by our doctors...and yet another drug with side effects beyond those listed. Lisinopril made me extremely tired and yes, the dry cough came with it, moods swings too. But the BP can't be ignored, you gotta do something, right? SO, a LONG story made short, someone with credibility I knew had me try CAYENNE pepper, one teaspoon in water three times a day and was CHALLENGED to check my blood pressure by the second day to see how much lower it would be, After reading on the internet about it (there is much info) I tried it, AND IT WORKS without the bad sides. It's not as horrible as it seems like it would, less firey than jalapenos, for example, and the burning lasts only a few seconds. Side effects? Seriously, my erections seem to be better. No kidding.

i have been on elavil for about 4 months 50mg three times a day, ive had intense stomach pains, overheating and panic attacks and i have had severe thoughts of suicide. they are weening me off of it and switching me to welbutrin.

I am a 55year old female. Had total thyroid removed on March 2 because of papillary carcinoma. I take 25mcg of Cytomel, three times a day. I have been on it for a week.
I get very bad muscle aches, and slight headaches mainly at night. They are however, beginning to ease up a bit. I will have a radioactive iodine treatment in about five weeks. I don't know what to expect. Help!

I have been taking 10mg three times a day for anxiety. I've noticrd that I've needed more. But If I don't take it, I feel spacey andnervous. Anyone else going thru this????

I started dating a guy that takes neurontin, thus the reason I am researching this drug. He is taking it for mood swings and a.d.d. He doesn't take it constitently. He takes various doses depending on the circumstances (sometimes he takes it like a party drug and he drinks). I can tell right away when he has taken a higher dose. He is lethargic, he drools, he is off balance, and actually seems somewhat slow (mildly retarded). I know he is intellegent, however, this drug is making him into a person that he should not want to be. I don't know if I can continue a relationship with someone that seems to be drugging himself to a complete stupor.
He said he was going to cut down to one pill, three times a day, however, I think he is having a very difficult time doing that. He is very addicted to his MEDS as he calls them. This drug seems to be destroying his life and he doesn't even know it.
He continually has to urinate, has a low sex drive and he experiences stomach problems along with back problems. This is the only drug that he takes. After what I have seen I wouldn't prescribe this to my worst enemy.

Experienced distorted vision, extreme drowsyness, dizziness. Seemed to work on tension headaches, but I was sleeping it off most of the time. Works well if you don't have anything to do with your day but lay down. I have stopped taking my morning dosage in order to be able to drive and function at work. Having a severe headache is still more functional than sleeping half the day off. The dosage was one pill three times a day as needed. This was in combination with Vioxx (anti-inflamatory/ pain reliever) once a day.

I started taking Neurontin about 4 years ago.My neuroligist started me on it for Polyneuropathy(nerve damage in my feet and legs)He started me out on 300 mgs. (taking 2 three times a day) It was a miracle drug at first,since my feet had been hurting(burning,stinging,numb toes and balls of feet felt like I had been walking on sharp rocks bare footed and they were bruised)for 2 years.Then they started hurting again after I had been on it for 2 weeks.So he increased the dosage to 400mg taking it 2 three times a day and same thing happened.So he increased it to 800 mg. 2 three times a day.I started getting blisters on my tongue and alot of swelling in my feet,ankles and legs,so he decreased it and that all went away.So he slowing started increasing it and those didn't come back.
I went to another dr. because I moved and he decreased it because thought I was taking too much.And the pain became worse.Well I had ins. whenever I was taking it before and then I didn't have it anymore after about 8 months of being on it.It is so expensive so I had to cut way back on it because I couldn't afford to take the full dosage I was suppose to take.And that is how I know it works for the pain.While I was cut back on it,the pain was almost unbareable.I am taking 300 mg. 3 in the am,2 at noon and 3 at bedtime and my feet and legs still hurt,but I know from experience that if I wasn't on it I would be in unbearable pain.
I am on alot of various drugs.I also take Lamictal 25 mg. 1 four times a day for the neuropathy.And I also have fibromylgia.I seen where alot of people have fibro and it is being treated with this drug.It doesn't seem to help my fibro.Or maybe it would be alot worse if I wasn't on it.Don't know.I take Elavil 100mg. 1 at bedtime,Zanaflex 4mg. 1 at bedtime for the pain and fibro,Synthroid 0.1 mg. 1 a day,Pravachol 40 mg. 1 a day for high cholesterol,Metaglip 2.5-500 mg. 1 a day and Avandia 4 mg. 1 a day for diabeties and Vicoden 5 mg. & apap. 1 every 6 hours for pain.
The Neurontin seems to interact well with all these drugs.
I have dry mouth and some confusion which affects my ability to think and carry on multi-tasks.I am trying to get on my diability.I applied twice and was denied and I got a lawyer and we went to court before the judge 2 weeks ago and it will be 3 to 4 months before I hear if I am getting on it or not.

worked great for me for my anxiety. No side effects except drowsiness in the first week taking it, which later subsided. I take .25 three times a day.

I have had the noticeable fatigue, depression and dizziness. I take 5 mg three times a day and 10 at bedtime. I have been taking Metoclopramide since Thanksgiving. I noticed last week that I have begun lactating and leaking.