have been prescribed Oxytetracycline for my cystic acne. 250mg thrice a day for 20 days and then 250 mg twice a day.
I have read on internet that it causes vision loss or impairment in some patients and scared to start the treatment.
I have been on Oxytetracycline for the past 3 months to treat acne on my back. It seems to be beginning to work now but I have a problem in that my sight has degraded quite rapidly in the past 4 months. My optician did say there is a chance this could be linked. I have done a bit of research and sight variation is a rare side effect of this medication. Does anyone know if this would be a temporary variation on a permanent deterioration?
View 1 RepliesJust started taking the tablets and wondering how long the side effects last for, Particularly the nausea.
View 1 RepliesI have been taking oxytetracycline for the last 5 months or so to clear up spots on my chest and back.But lately i have had pains in my knees,pains in my back and sometimes slight pain in my stomach area.I have noticed my legs,from the knees down especially around my ankles are full of fluid after my work.I was wondering if this is due to something else or has anyone else out there had anything like this after taking oxytetracycline.I have noticed my eyes are a bit blurry at times.But it's the pains and the fluid i would like to find out about.
View 1 RepliesHi, I have been reading this forum for a very long time. I have been on Gabapentin since October 2011. I injured my neck January 2011. Lost the use of my left arm. Had C6-C7 acdf September 2012, fell 3 weeks later due to ataxia that came on after the surgery. X-ray showed everything in place, Cervical MRI showed C5 disk herniated minimally. For the last couple of months I've been losing sensation feeling in my hands sometimes up to my elbows. It goes to one side and the other or both at the same time. My doctor thinks it's a side effect of Gabapentin and my gut says it's not it. Has anyone heard of this side effect? I have not found this loss of sensation as a side effect in my research.
View 14 RepliesI have been using a lotion called dalacin t topical lotion from about october 2007, it really improved the big spots i used to get on my back, and it helped my face a little, but not much.So i went back to the doctors and she prescribed me with Oxytetracycline, which i take 2 tablets 2 times a day, so in total 4 a day. I have been on them for a month on this monday coming up (18th), that will then be a month, i think the doctor told me they would take about 3 weeks to a month to have a visual effect, im just hoping they do work! how has everyone's experience been with this medication? how long did it take for it to start working?
View 2 RepliesI am a 25 year old male and have recently been diagnosed with Cholesteatoma in my left ear. My case is a bit different it seems as until July 2015 I had a perfectly good left ear. I picked up a cold and ear infection while on holiday in Spain in July 2015 to which a week or so later I was hearing bells going off in my ear constantly. I was put on three different doses of antibiotics and ear drops between July and October. I began to get white discharge from my ear about a month after I had the infection and this discharge turned yellow a month or so later. It was not until January 2016 that I was able to see a ENT specialist who diagnosed me and this was confirmed with a recent CT scan. I have not had any hearing (besides the bells going off in my ear) since I first got the infection back in July. After I had the CT scan and hearing tests I have been told that my ossicles have been eroded and I am very unlikely to get hearing in my left ear again. The infection has dried a little bit from some ear drops which the ENT specialist gave me and I have an MRI scan this week as they want to determine if surgery is absolutely necessary before going ahead. I have seen two ENT specialists at this NHS hospital. This morning I woke to find my ear slightly wet again and with a tiny bit of blood which prompted me to go and see the hospital to which they assured me that this was normal and can happen.
It it seems as though a lot of people have problems with their ears in childhood which leads to cholesteatoma. Has anyone been in a similar situation to myself? The more information the better.
Note: I had sinus surgery in February 2014 and the CT scan I had in preparation to that operation has shown no signs of cholesteatoma.
I might have had 2 or 3 mild headaches in my life.
6 months ago i had most of my pituitary gland removed due to Cushing's Disease.
3 months ago i had a visual field test that showed possible swelling around the optic nerve.
6 weeks ago i started waking with headaches at about 4.30am ! i would sleep more then wake later with less of a headache but when i stood up i would get a whooshing sound in my ears and a throbbing in the top of my head. i told me GP. She said its normal when you first stand up ( Normal My #$$, if it was normal wouldnt it have been happening all my life, anyway i digress lol ). So i had these headaches, i got blurred vision and my blood pressure went up to 234/127. So off i go to hospital for 4 days.They played around with my blood pressure meds and sent me home. I still had headaches, blurred vision and my BP was 180/105( now on 4 different BP meds ).
2 weeks ago i went and had a repeat of my visual field test. The Opthmalogist wasnt too happy, basically told me one quadrant of my vision in my left eye was gone. Said he would speak to my Endocrinologist !
2 days later i noticed what i can only describe as a smudge in my vision...very annoying, but not painful and yes i can still see. but im not driving, im too scared to. I drove one day and as it got darker i couldnt tell where the other cars on the road were, kind of a distortion thing i guess
My Endocrinologist rang the next day and said i need to go for an urgent MRI...so i did.
That was 1 week ago. i have had no results, no phone calls. But i did get a letter advising me i have a Neurology outpatient appointment on 13th october ! i rang to confirm as i was waiting for an endocrine appointment. Hospital said, yes, the neurosurgeon refered you to neurolgy following your MRI. Hmmm thanks for that.
So now im trying to guess whats going on. Did my MRI show up something, if so what?, if not then why am i being referred to neurology?
I hate being in the dark. Yes i know i only have 2 weeks til i find out, but 2 weeks is hell when your second guessing.
Summary : i still have headaches ( they are for the most part mild, throbbing when i stand followed by whooshing in ears), vision has maybe slightly improved in last 2 days but still not normal. Blood pressure is still sitting around 180/105
18 months ago I started getting blurry central vision in both eyes at the same time - it wasn't there all the time but when it was happening I found it very hard to do fine work.
I saw an ophthalmologist who did an OCT and retinal exam and found nothing. He suggested it was neurological so I had an MRI of my brain and orbits but nothing was found to explain the problem.
In the last three months I found that the problem had become permanent in my right eye - I could now see a faint central ring that pulsated with my heartbeat on that side. I went back to the ophthalmologist and he diagnosed a stage one macular hole. He didn't think the previous loss of vision was connected to this. He has advised me to wait and see if it gets worse but I am considering doing the surgery anyway - maybe trying the new drug Jetrea first which is very expensive but which is said to help a small number of patients.
Has anybody had a similar experience - with the visual loss coming and going? Anybody tried or considered trying Jetrea?
I used the tablets for 5 months and a bit, should be taking it for 6 months but i decide to give into not taking them due to really bad side effects.
When i started, i took 2 TWICE a day for 4 months but, rashes appeared on my cheeks, completely red and skin dried also on my nose. I couldn't bear the suffering, i applied creams like E45 (made things worse for me) then i switched to sudocrem, applying it to my face where the rashes were. this seemed to help stop the rash from getting any worse. I went to see the doctor who said i should cut down on the tabs to 1 Twice a day so i finally started to heal from the rashes. I carried on using the tabs this way until the rashes appeared on my nose again, it was really bad.
To those who suffer from Eczema, be warned as this course may effect it, making it really bad. This is the reason why i have to quit from this 6 month course (am finishing on 5 and a bit months) As for acne, it helped clear it up nicely even old scars until a point where my skin could heal no further ( i stayed the same after the 3rd month) so hopefully, changes are permanent and my side effects will go away from stopping this course.
I had a heart attack 5 weeks ago and since have been on various medicines one of which is 5mg Ramipril every night. I read the booklet which explained that a side effect is a cough but agree with other inputs here that the cough is very depressing. It constantly disrupts my sleep pattern and it's so dry ! Im off to the GPs Tomorrow and hopefully he can prescibe something else. Is there anyway else of stopping the cough ?
View 1 RepliesDoes anyone seem to sweat more on venlafaxine. I know it is a side effect but how common is it
View 55 RepliesCan someone tell me how to stop trembling on lithium as a side effect? My whole body shakes. I can stop
View 12 Repliesa have been on sertraline 50mg for 4 weeks now into my second week on 100mg a feel things are getting a lot better it is just the headaches at times are quite severe am having to take strong painkillers a know it is a side effect but are they meant to be so severe or should i go to the doctors ?
View 4 RepliesHi all,been put on Neurontin / Gabapentin for a vestibular problem.Just 300mg a day (Built up over three weeks from 100mg to 300mg a day) . Just wondered as i have a side effect i believe as it started around the same time i started the tablets . I have a low level headache along with a mild flu like feeling . Did anyone else have similar?
View 4 Repliesis that true that the tubal ligation can make her dry or without fluids if they made love? what the possible common side effect of the tubal ligation? please find me the answer. thanks.
View 1 RepliesI have been taking Ramipril 10mg for a few months now.
I have experienced the tickly cough, but not often so that's ok, the one problem I'm worried by is joint pain.
I went from 5mg to 7.5mg to 10mg it has been whilst I have been on this higher dose that my arm joint to my shoulder have started to hurt, with sometimes sharp pain, also a sharp pain in the base of my index finger but again very occasionally.
I worry that if I go and talk to my doctor he may try and treat the joint pain with yet another drug which itself might have side effects, and the spiral then goes on into old age.
I am only 51 and will continue to take the medication but will monitor my problems and eventually have a chat with my GP.
I have suffered with depression for some time. I used to take Citalopram but my Doctor recently changed my prescription to Fluoxetine. I had some very weird side effects at first - very strange thoughts - almost like hallucinations and felt quite 'spaced out'. However, after reading the leaflet, I saw that this can happen and will generally disappear with continued use. So I persevered.
I have been taking it now for about 8 weeks. I did stop for about a week when I was away on holiday. I hurt my back and had to take anti-inflammatory medicine. I was worried about the risk of stomach bleed that this can cause when interacting with fluoxetine so I stopped taking it. This was about 5 weeks ago. I became extremely low with thoughts of harming myself. I resumed the fluoxetine and these thoughts have subsided.
My problem is that I feel constantly tired with no motivation to do anything; I have difficulty concentrating and feel generally lethargic and lacklustre.
Does anyone else feel like this while taking Fluoxetine? I recently had a general health 'MOT' with blood tests for liver/kidney function, thyroid, blood sugar etc so it is unlikely there is a different underlying cause. Or is it just a symptom of my age/state of mind? I am 58, generally fit and active.
I had a heart attack in mid October due to a congenital enlarged artery. The stent was unsuccessful and I lost 10-15% of my heart. My EF is around 46/48 and the doctor has never mentioned heart failure, but I know I need to do all I can to try to prevent that from happening.
Anyway I am on metoprolol tartrate (beta) 12.5 twice a day, plavix, aspirin, lipitor, and in December the dr put me on a very low dose of lisinopril (Ace) 5 mg.
Lately my back has been aching as the day goes on and I feel like I can't take a deep breath. Let me clarify, when I sleep and when I first wake up I feel good and normal. But as the day goes on I start to get some muscle aches and my breathing seems weird. I don't feel like I'm about to suffocate and I can breath normally fine, but it's like I feel the need every few minutes to take a big deep breath and when I try I can't totally get a full really deep breath like I used to.
Could this be the lipitor or the lisinopril or maybe it's anxiety and it's all in my head because sometimes I don't even notice it. I take the lipitor and the lisinopril at bedtime and sleep well and wake up feeling well, this usually happens about mid-day or so.
I know dreams are a common side effect of fluoxetine, but do they ever settle down?
I seem to be having quite a few vivid and realistic dreams per night, usually about things that are worrying me which then makes me question myself as to whether it was a dream or not!
Has anyone experienced this and did it settle for you? Or is there anything we can do to ease it?
Can anyone tell me if dizzy spells are a side effect of coming off Citalopram. I have been reducing from 10mg to 5mg for the last 2 weeks and it has been going ok with a few moments of anxiety. But tonight I had to pull over on my way home after becoming dizzy at the wheel. Is this normal or might it be something else?
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