Mirtazapine Helped - A Miraculous Drug
Sep 19, 2015
I appear for the defence , M'Lud.
I was on SSRI antidepressants for some time. They countered my extreme anxiety well, but I had bad insomnia probably caused by the AD. I tried various drugs for the insomnia (zopiclone, amitriptyline etc) but with little success. My doctor suggested mirtazapine but I declined as I had read about its weight gain side effect. However eventually I changed my mind out of desperation. The mirt was miraculous: it completely solved the insomnia. I felt "normal" for the first time in months.
"But what about the side effects" I hear you say. Well, I did get back my appetite - but no more than it was before I became ill. I gained a little weight, but no more than I had lost.
I did have difficulty getting up in the morning and feeling groggy after that, but those lessened with time. I take the minimum mirt that allows me to get to sleep - about 11 mg, and I think that keeps the side effects down.
Mirtazapine is like a knife in that it is not evil in itself, it is how it is used that matters. The people who say it is evil have perhaps been on the wrong dose. Mirt tends to be more sedative at low doses; more activating at high doses. Do not throw out the baby with the bath water!
I get the impression from reading posts on this forum that mirt is best used (at low dose) to counter insomnia or where an SSRI antidepressant has not been tolerated.
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I have been taking this tablet now for my 4th week, I have had a lot of teething problems BUT this week was my due date for my periods and usually for 2 days I get almighty migraines but this tablet has most definitely helped just cut to a headache Nothing at all what I used to experience!!!. I have heard a lot of people not liking this drug But for me it has helped and will continue taking it, right so I have a question for 4 weeks I have been taking Half Beta Prograne 80mg, but called to pick up a new prescription and have been given Bedranol is this the same drug? .
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I'm a bit worried. I had a urine test at work but forgot to mention that I had some antibiotics about 3/4weeks (maybe more) prior to the test, the antibiotic was penicillin VK.
I've read most antibiotics stay in your system for up to around 4-8 hours, especially penicillin VK. Some other sources reckoned between 7-10 days max. Although most said up to about 8hours max.
So I'm wondering if this would show up in the test at all?
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I have just started on the 30m Mirtazapine and it's my 3rd night taking them ans i have read up on a lot of different forums that there are patients gaining weight off these? well i would like to know what the odds are of gaining weight because i have always had problems with weight gain, i can never put on any weight, no matter how much i eat, i have a fast metabolism and i am wondering, will the mirtazapine surpass my high metabolism. also in some cases i've heard it slows your metabolism down too.. but it would actually be a benefit for me to gain some extra weight.
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For the first time in a very long time, I'm finally in a good enough place to make the step in coming off my Anti-depressant. I've been on Mirtazapine 45mg for the last 4/5 years and before that a string of various of medications.
Despite my anxiety been kind of excessive at the moment, after a discussion with my GP, he was happy to let me begin tapering down the dose. The problem is with my anxiety I feel it mainly physically rather than mentally so it makes me a little oversensitive to any changes that take place in my body.
I guess what I am searching for is some reassurance so I can stop driving myself up the wall, exhausting google search on mirtazapine withdrawal. 6 nights ago I started my first reduction so 45 mg to 30mg. In all honesty it's not been that bad, a few waves of nausea, headaches and random aches and pains. Those I was expecting so don't mind too much. The trouble is that for the last 3 days, I've found myself a little short of breath for most of the day. It's nothing that's outwardly noticeable at the moment, but it's there and is slightly concerning. Has anyone else experienced this when tapering?
I'm kind of freaked out a little because one of my fears that's arisen since the mirtazapine is the that i will develop random allergies and my brain is wondering if I've suddenly developed an allergy to my meds (ridiculous, I know!) The other thing is that the rest of my family has had either viral chest problems lately so maybe I've just picked up that and it's a coincidence? Or it could just be the anxiety.
I'm totally spinning myself in circles at the moment so any wise words are most welcome at this point. If I know it is just withdrawal and nothing that can actually hurt me then I'm fine with whatever effects it throws at me.
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I first noticed my hair loss at around 19. I am now 26 and it seems to to have gotten worse.
I don't lose hair in big amounts and there's never a lot of hair loss in my hair brush so I don't understand why I'm losing hair.
I Went to my doctor about it but just got put on iron tablets which have not worked.
Is there anything that can help stop the hair loss and maybe regrow the hair i've already lost.
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I have posted a few times in this about feeling better and every time a did a ended up taking a dip but a did read in a post on here to give it up to 12 weeks so here i am going into week 12 and apart from headaches a must say that everyday that goes by a feel better when a think back to before and after that is when a realized just how much they have helped me as a was dwelling to much into the nasty side effects the negative side but now am more on the positive and feeling better wishing everyone well.
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I've had PMR symptoms since Dec, which was finally diagnosed in April. I've been on 20mg of pred since the beginning of April and mostly feel great. I'm running, biking, and actually took my kayak out to see if it would bother my shoulders, and it didn't. I'm a 68 year old male, who has always been active and in good shape.
When I read all these chats about people who are tired all the time I wonder if I am normal or if I can expect things to get worse. Is it the pred or the PMR that cause the tiredness?. My energy level seems good. I feel a little more tired during the day, but it passes. Sometimes I do take a nap when I do feel really tired. Functioning pretty normally with some awareness of mild muscle issues.
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I wondered if anyone here has become healthier following a gluten-free diet.
I am 35 and female. I am diagnosed Type 1 diabetes, have psoriasis and psoriatic arthritis, & Hashimoto thyroiditis (Hashi not treated prior to now). Recently, my TSH came back at 9.2 and my thyroid antibodies 213. I was then placed on Levothyroxin 25mcg and in six weeks my TSH is now at 3.70, so it appears I am responding pretty well to treatment.
A genetics test a few years ago indicated I am at high risk for developing celiac disease. Since then I have went gluten-free for short amounts of time and always felt better and digestive issues solved, but finding gluten-free food in my rural area is difficult and I tend to lapse on the diet.
However, I have been gluten-free now for 5 days and feeling somewhat better already. I intend to make this a lifestyle change for good this time.
I guess my real question to persons here is, has following a strict gluten-free diet greatly improved your autoimmune illnesses?
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Well Suboxone did help me with the Methadone but now I am hooked on Suboxone. I traded 1 drug for another, I tried to taper off and only got so far. I want help getting off but there is NONE. I mean other then tapering off there are NO treatment centers and the active drug is Suboxone Buprenorphine .....
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Personally I used to have severe stomach problems for years; confirmed gallbladder sludge & gastroscope illustrating peptic ulcers in my tummy.
Rather than surgical options or taking medication long term, I've been attempting to get daily requirement of fiber. Attempting to consume fiber before consuming necessary fatty food that initiate digestion, and eating plenty of green vegetable with vitamin K have resulted in what seems to be a full recovery of stomach enzymes over the years.
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Been taking Mirapex since late Oct. Have been on 1mg for about a month or so now. Doing great falling asleep, but wake up some nights at 4 or 5 and can't get back to sleep many times. Anyone find that an increase in Mirapex or starting Sinemet helped? Dr said he'll decide in February.
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In the book i am reading Kate took aloe vera juice and she said it helped her, i think i might give it ago as anybody any thoughts on this before i try it?
I am learning a lot from her, still have my panic attacks, like for instance i have been have funny feelings in my head, it does not hurt but now i am thinking twice before panicking and go back to her book for reference
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One of the guests below on this site recommended using baby wipes and Aloe Vera gel. I do already use baby wipes but hadn't tried the Aloe Vera gel. I bought some and I can say yes, it does help a lot. It doesn't cure it - but the itching has reduced hugely at night.
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I suffer from VLS and OLP.
After washing morning and night I use pure aloe vera gel on my vulva which may sting a little but really soothes. After half hour I use aqueous cream to moisturise.
When I have sore burning tongue or mouth ulcers I use pure aloe vera gel in my mouth. It really heals.
What about the emotional aspect associated with this disease. I find I suffer from lowered feelings as I feel unable to cope with the physical pain and daily maintenance. I have great difficulty accepting that my own body is attacking itself and I have no control over it.
I have great difficulty trying to sleep and am obsessed with the condition as the raw pain never eases and I know it will never get better. My dermatologist suggested anti-depressants but I disagree as my lowered feelings are caused by the presence of the disease and there is no cure for this. I read "the power of now" which helps me to live in the moment.
I would call on the women/men who have had this condition for numerous years to post and give those newly diagnosed some hope that there will be life after tomorrow.
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I used to smoke a lot. I won’t exaggerate if I say that I smoked almost 2 packs of cigarettes daily. My friend got me into quitting smoking. At the end I agreed to try with hypnosis. And I must admit that a hypnotist helped me to stop smoking. Are there any similar people here?
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have had frozen right shoulder since dec. this really is a debilitating condition and it is good to find somewhere to vent frustrations and get advice. had cortisone inj in feb, this has helped a little bit, but still in pain. i started acupuncture 6 weeks ago and am finding that it keeps the pain at a manageable level. am aware now that this is not going to be a short road to recovery, but would love to put on my bra the normal way, get undressed myself, brush and style hair at back of head and take off a jacket without first going through the rigmarole of shaking the left arm til jacket fall off. sorry lowercase but can't hold down shift.
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I would like to first off say i did not relapse on opiates. HOWEVER i ended up taking some tramadol after a few surgeries. I asked for NON OPIATE pain relief afterwards. That is what he gave me. I took them did not get high i thought that was great! However a few months later i found myself dependent on it without the high its a stupid drug. So i gradually cut back..i went back to my doc and told him it was not easy to come off of and could he help me. He gave me a taper plan to work so i started working it. I noticed as i reduced my dosage is was worse and worse like usual.. So i do smoke pot from time to time and the last time i got off subs Marijuana really helped me get off.
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I just wanted to share with everyone that I have tried Magnesium Citrate and Vitamin D for my TMJ pain and if anything, they actually made it worse. My wife recommended that instead of Advil (which does take the edge off a little) to try Aleve. I took (2) 220 mg pills right after dinner on a full stomach and noticed a big difference about 1-2 hours later. It kept me out of pain almost completely all night and I didn't even need to take more yet, knock on wood. I also noticed that a medical journal online posted that Naproxen had proven to be more effective than Ibuprofen or Tylenol for TMJ pain. Anyone else find this to be true for them too?
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3 days ago I decided to stop taking mirtazapine 45 mg but since then I have not had any appetite for any foods at all. Is this a normal symptom.
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So I've been reading a lot of posts that say they've been drug tested while they've been pregnant? When exactly do they do that right before you give birth or right after?
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