I was prescribed these tablets last year to treat my acne and they worked for a while I was clear but in the last month or two I have started getting my acne back again and don't know what to do as am taking two tablets a day already. Do I go back to the doctors and ask for another referral or can someone help as its getting me down as it's on my face.
View 6 RepliesI was quite shocked when my gp recommended antibiotics for my hacking dry cough. I have the flu too. I started taking Clarithromycin yesterday morning. So far I have taken 3 tablets, so far so good! My violent cough which was totally debilitating and exhausting (non-stop) and causing me nearly to throw up has slightly improved, thanks definitely to the antibiotics I'm taking. I came here to check out other's opinions on taking this antibiotic. I don't like taking any tablets and what I read on this site nearly put me off starting the course. But luckily, I read a couple of good reviews on here so decided to bite the bullet. So far, I'm glad to have taken three tablets as already I'm starting to come back to life. Still got a fairly raging cough but have found it easier to cope and control. The only noticeable side-effects so far have been with a tummy ache, but otherwise it's all positive! If symptoms persist or side effects increase, I will come back and report!
View 1 RepliesI visited a hospital on 5/15/14 with symptoms of a swollen and severe sore throat (a lot of pain when swallowing) and a 100 f temperature; my throat also had white patches on it. When the doctor saw my throat he said it looks like you have strep. Then he did the 5-10 minute strep swab test but it came back negative. Nevertheless, he still thought I most likely had it and that I should start treatment. We also tested for mono on that day and since then they haven't called back for that (if they don't call back assume negative they say).
He prescribed Amoxicillin 500 MG X2 daily for ten days. So far I have taken 2,000 MG (over the course of 2 days) and my throat still seems the same in regard to pain. The only thing that consistently seems to help my pain is Ibuprofen.
Should I worry? Should I go back to the hospital to see what's going on?
I've been on mirt for 6 months. All going well until past 2 weeks. Now experiencing the dark lows, burst into tears over nothing, increased energy & weight loss. I strongly feel that meds are no longer working. Has anyone had this experience?
View 30 RepliesI am on week 8 on 20mg of flu. I was feeling EXCELLENT back to my old self even forgot I felt sad at one point..I thought it was all over.......5 days ago I started getting anxiety again, feeling depressed and the "doom" feelings again. Has this happened to anyone? Should I ask Dr to up dose is that the only solution?
View 11 RepliesI have been taking 25mg of Sertaline for 6 months and I have been great.The past week I have felt anxious and afraid.On two seperate ocassions I felt light headed like I may pass out and weak.My questions are the following:do you think my prescription needs to be increased?Do you think my period could play a part in this?Lastly,is this a form of a panic attack?
View 3 RepliesHas anyone else had this experience? I started out on a low dose and had great results. Now I am up to 1,800mg/day and it doesn't seem to be having much effect. I am actually ok if I am not doing anything, but as soon as I use my foot, it gets so hot I could probably fry an egg on it!
My story: was in a car/bike accident and ended up with the car parked on my foot. Broke all my metatarsals in multiple places, but things were not that bad until...SURGERY. After finally starting weight bearing I found I couldn't really feel my foot, but it worked. Then I had oral surgery and my world exploded. Insane nerve pain in my face and jaw which then transferred to my foot. Anyone else here with CRPS?
Oh yes, and shooting pains up and down my thigh and calf whenever I stand or walk.
Thanks to anyone who responds. Especially interested in those who found the gabapentin working at first and then not and those who are suffering from CRPS.
I am 50 and have been taking Tibolone since May 2015. The first few months it was brilliant. I could sleep better, no hot flashes or night sweats and libido was amazing. But the last 3 months things started changing. It seems that my body got used to it and I have bad insomnia again, night sweats are back , libido gone low. I am still taking it and hopping that it will work again. I did put on a stone in weight, lots of facial hair and in my legs too. My hair roots on my head have gone really curly . Has anyone experienced that ?
View 29 RepliesMy daughter's spleen has stopped working. She has sharp pain the the middle of where the rib cages meet(not at all where the spleen is. She has a high white blood cell count. Do you know what might cause a spleen to working. She is 28 and is otherwise great health,non smoker and no drugs either. They have her on morphine and gravel,also hooked up to an IV bag as she is not eating. No blood problems in the family history. She is a vegetarian so she may be low in iron. The hospital is at a loss for what to treat her for but ill next do a CT. They have done multiple blood works but nothing yet. Thank you for reading this and hope that you know something about why her spleen has stopped working.
View 1 RepliesI have been on flu 40 mg for 12 weeks now and it seems that in the last week I have been feeling worse again.
It's a strange feeling but I feel indifferent to myself and seem to not care at the moment about my actions and thinking that what I do is not a problem?
I was just wondering is it possible with depression to still have days when you feel down and want to give up?
Has anyone had their Klonopin stop working? I had antibiotics Augmentin in early June and it stopped my Klonopin from doing any good. It still hasn't started working again and I'm a nervous wreck.
View 4 RepliesI have been using Clomid for the last 5 month to try and repair my low test levels. I have been having to self diagnose and medicate as my doctor will not take me seriously as my levels just scrape the normal range, I know myself that my levels are not right. Before going on Clomid I had no sex drive, no morning wood, ever!! tense and irritable and lethargic. A week after I started on Clomid my sex drive was back, morning wood every day really felt back to normal. unfortunately the positive effects have slowly diminished over the last few weeks to a point that I feel as bad if not worse than before, morning wood gone, no energy and feeling pretty miserable.
I am wondering, does anyone else have this experience of Clomid working for a time and then just stopping all of a sudden?
After 5 good months of taking Venlafaxine and getting my life back together, being back at work etc my depressive symptoms seem to be creeping back in along with increased anxiety levels, i feel like I'm back on that downward spiral to go back to where I was 12 months ago!
I've had to take some more time off work as I feel so bad these last few days, got a Dr's appt next Monday couldn't get in any sooner unfortunately.
Is this an early poop out from the Venlafaxine? I don't know what to do I didn't think I'd be here again so soon. Currently on 150mg XR with 10mg of Abilify I know they will be reluctant to increase the Ven as I suffer from bipolar disorder and they are worried about mania but I've never had mania.
Has anyone else had any experience of Venlafaxine pooping out after so little time? Would an increase help me?
I have been really happy on this drug for three years now and envisaged staying on it for ever because it suited me so well. I was on 15mg at first which stopped working after a few weeks and then went up to 30 mg which I have been on for three years. My depression has been controlled and I was sleeping really well. Before the mirt, I had to take temazepam every night, but for the past three years I have only had to take it once a fortnight or so, but it is very difficult to get doctors to prescribe it now. Anyway, I have suddenly stopped being able to get to sleep. I have frequent need to urinate and my heart is beating too fast when I can't sleep. This used to be only a couple of nights a month, now it is every night virtually. Also, my depression and anxiety have suddenly worsened.
Do you think the mirt has stopped working? I am reluctant to up the dose if it is going to poop out again, as it will make it more difficult to withdraw from it should I need to. Has anyone else been on this drug long term and had similar experience? I have a doctors appointment a week tomorrow, but was wanting to hear others' experiences before I go.
I was on many Hypertension medicine for 3 years but nothing could lower my BP. Finally Dr. Prescribed Edarbyclor and miracle happened.
in fact it got so low that was hard to function but i was happy anyway.
Now 4 month later my BP starts to rise again.
Hello all and good wishes to all to find your cure for WED/RLS. Willis Ekbom Disease is really what this RLS is.
Anyways I started on .25 mg of requip then it was upped each week (cos it only worked for about 4 to 5 days) then up to 1 mg. of requip. Now it's horrendous and I rarely sleep. I found through research that Yes! they do use the benzos and gabapentin (neurontin), and opioids for WED/RLS. Last night I was at the end of my rope and used my ativan and low dosage of dilaudid and actually slept for 4 hours without interruption!! My doc doesn't understand and wants to try me now on Mirapex witch is another DA (dopamine agonist) and may or more than likely NOT work. It's a rough road, and I have done a lot of meds. I hope and Pray when I go to my doc next week I get some answers. As well he will NOT give me a ferritin test nor refer me to a neurologist.
I'm 28 and have crohn's disease. I have been on humira for 2 years which had worked well. The past few months, however, I have been suffering from a debilitating flair up. My Dr upped my dosage but it hasn't made a difference and am now back on steroids. I was wondering if anyone else had experienced this with humira? And if anyone had had success with any alternative medications?
View 7 RepliesI have been on Prozac 4 months and 2 of them were better and now I'm going back to the way I was before. What do I do now? I'm so miserable and don't understand why this is happening plus I'm pregnant.
View 37 RepliesI had terrible hot flashes at night, over 15 times a night waking up sweating. Over a year ago I started using Estroven Nighttime and within a month they were all gone. Now lately after over a year later , I'm am getting hot flashes again. Should I try taking something else.
View 3 RepliesI'm 28. I am capable of getting proper erection any time of the day except for being in bed with a girl. After clinical check and running tests the doctor confirmed that my sex drive is healthy and functioning and that my problem is purely psychological. Performance medications help sometimes help (sildenafil, tadalafil, vardenafil, .. ). But in other times they just don't have any effect. I have been told that as long as I have performance anxiety, all the viagra in the world will not help.
To overcome the problem, my doctor prescribed me Trazodone Hydrochloride 100mg every night. I have to say that after taking Trazodone for a couple of weeks I could have healthy sex with or without viagra. I took Trazodone for a bit more than 3 months and then gradually stopped. for the following 4 months I could also have good sex ONLY when taking viagra. But now (after 6 months of stopping Trazodone) viagra stopped working again.
My question is: Did the doctor tell me to stop taking it too soon? should I start taking trazodone again for a longer time? How long should I keep taking the Trazodone to completely overcome the performance anxiety?
I feel confused because I read that Trazodone sometimes have a reversed effect if taken for too long.
i have been taking for over a month 20mg of carbimazole (5mg 4 times a day) the edno said i have hyper and a quite big nodule which is toxic.
i have been suffering the last two years with weight loss and tachycardia,agony and had that worrying feeling all the time.
After taking carbimazole for one month i start to feel BETTER but yesterday i had hyper symptoms again.how is this possible the blood test have showed that I AM NO LONGER HYPER!!!!
i know that eventually i have to choose between RAI or surgery but i m scared that the symptoms will come back.Does carbimazole stopped working? is it normal to have symptoms while taking it?
the edno prescribe me also propranolol but i took it once and it scared the hell out of me!