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How effective is Klonopin for Ptsd (Post-traumatic stress disorder)?





Summary: 16 Klonopin users have rated its effectiveness for Ptsd.

Overall ratings: 4.1/5
Long term ratings: 4.3/5

This is a review of how effective Klonopin (clonazepam) is for Ptsd and for what kind of people. The study is created by eHealthMe and is updated continuously.

You are not alone: join a mobile support group for people who take Klonopin for Ptsd >>>

What is Klonopin

Klonopin has active ingredients of clonazepam. It is often used in stress and anxiety. (latest outcomes from Klonopin 31,277 users)

Ptsd

Ptsd (post-traumatic stress disorder) can be treated by Zoloft, Prazosin Hydrochloride, Clonazepam, Xanax, Sertraline Hydrochloride, Klonopin. (latest reports from Ptsd 5,821 patients)

On Dec, 22, 2014: 16 people are studied for taking Klonopin in Ptsd




Klonopin effectiveness for Ptsd


Long term Klonopin effectiveness for Ptsd

Klonopin effectiveness for Ptsd (number of people):

not at allsomewhatmoderatehighvery high
Overall00475
Long term
(1+ years)
00235

Gender of people who take Klonopin for Ptsd * :

FemaleMale
Ptsd81.25%18.75%

Age of people who take Klonopin for Ptsd * :

0-12-910-1920-2930-3940-4950-5960+
Ptsd0.00%0.00%0.00%12.50%56.25%0.00%31.25%0.00%

Who find Klonopin more effective for Ptsd?

Gender of people who find Klonopin more effective * :

FemaleMale
Ptsd75.00%25.00%

Age of people who find Klonopin more effective * :

0-12-910-1920-2930-3940-4950-5960+
Ptsd0.00%0.00%0.00%16.67%58.33%0.00%25.00%0.00%

* Approximation only. Some reports may have incomplete information.

Find out which drug is more effective in real world to treat:

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Can you answer these questions (Ask a question):

  • Can i take cialis and klonopin
    I've been taking klonopin and it's making it hard for me to have an erection. Can I take cialis while on klonopin?
  • I had bladder cancer and my doctor put me on metformin should i get off this
    I do not want to take this metformin if it may cause my bladder cancer to come badk
  • Can nuvigil (vs adderall) be used simultaneously to help wean off 60mg/day of adderall? (1 answer)
    I have been on Adderall 30mg 2x daily for years!! I've had it lowered to 20mg, I've TRIED to go months without it (when not working) however I feel I've built up a tolerance level to the point that it's not as effective as it once was. My personal life has detoured WAY past anything an ADHD medication can possibly help as far as focusing on NEEDED tasks etc. I end up feeling wrapped up in what I'm doing at the moment that my anxiety increases due to all that I haven't been able to accomplish. I take various medications for various reasons, depression, anxiety, bulimia etc., and for the most part the doses have varied based on circumstances and current need at said time of prescription.. MY FAMILY HAS A HISTORY OF HEART DISEASE, And realizing that I'm already on the highest Adderall dosage scares me (and THEN as I think about it, it makes my heart race!). I've also noticed increased muscle spasms as well as extreme and intense pressure on my jaw (TMJ). MY QUESTION IS: does anyone have any experience LOWERING their Adderall dosage AND adding Nuvigil? The research I've done to date gives me impression that it could help balance out the more extreme effects of Adderall (60mg/day) but that the nuvigil would or could potentially help with the EXTREME exhaustion I feel as Adderall wears off. Some days I just crash, some days I sleep fine and others no matter how hard I tryyyy, I just CAN'T fall asleep, therefore making the next day worse! IDEALLY I'D LIKE TO BE MED FREE, right now I need them, but am hoping maybe I can speak with my doctor to lower Adderall and add Nuvigil to help wean me off the amphetamines as well as lower dosage intake. YES, a lot of the anxiety, sleeplessness and depression are related to current circumstances in my life, however, where I am is not where I want to be or where I'm headed.. Life is a journey, and all my meds have become a part of a journey I never thought I'd find myself taking. I don't want life/meds to define me, or create a me I no longer recognize, because scarily enough that seems to be a common pattern. As I overcome each and every daily obstacle, I also don't want to be "hooked" on my meds or needing "more" to wake up/sleep/function.. I'd like to work on finding a solution towards weaning off my meds NOW, and work my way off slowly, primarily the Adderall. I'm hoping by suggesting to my doctor and showing him my research he may agree (IF ITS EVEN A LOGICAL COMBO, CLEARLY IM NOT A DOCTOR) nuvigil could help me. I've already started taking less of my anti depressants, trazadone and xanax without discussing with doc because he is always busy.. My next appt I want to go in fully prepared with a plan and an overall goal to REDUCE my Adderall dose, but overall, I'm clueless!!! I have no idea what other meds other than nuvigil "could" potentially help if at all. I could be entirely wrong, Anyone with any experience using one vs other or both simultaneously, or anyone with constructive input, PLEASE COMMENT/SHARE!!
  • Can my eye twitch be because of lexapro?
    So I have had symptoms of anxiety and depression due to a lot of stressors and disasters that happened in my life over the past two years. As my anxiety got worse after a breast biopsy, I started freaking out and thinking I may have MS because my sister has MS. So I went to my GP and she decided my symptoms do not follow the symptoms of MS or any similar problem and it should most likely be anxiety. She put me on Lexapro and Clonazepam. At first I was very hesitant to take medication but as my symptoms got worse I decided to give it a try. I was on Lexopro 5 mg for about two months and then I went to 10 mg, and I would take 1 or 2 Clonazepam a day. And this all started 5 months ago. And things seemed to be working just fine.Until about two months ago I started having this freaking annoying eye twitch on my upper left eyelid. I have had eye twitches before but they always go away after a couple of days or a week top. This one has been lasting for 2 months now and seems to be just getting worse. I went to the GP and my eye doctor and they still found no cause and said it's probably stress and anxiety. I have not been overly stressed and I get plenty of sleep, 10 hrs or more! and I stopped taking caffeine and alcohol after the twitch started. Any idea? Could it be because of medication? I also need to add I have had thumb twitching and severe spasms in my muscles around my right thumb starting in May (before taking any medication).
  • Why would doctor prescribe meclizine when otc med available? stronger?
    Gastric bypass. After years found should not be prescribed extended release medications-- they do not work because stomach (duodenum) releases enzymes and acids to release XR. Suffer from GAD, MAD, PTSD, ADHD, Insomnia. I've driven away my best friend-- I'm tired of life-- alone.

More questions for: Klonopin, Ptsd

You may be interested at these reviews (Write a review):

  • Panic after using flonase
    I was diagnosed with nasal polyps and put on Flonase (a steroid nose spray). It worked well to dry up post-nasal drip but I ended up with a bad case of panic and fear. I had overcome episodes of these nervous disorders but the Flonase brought it all back. I still suffer from panic even though I stopped the Flonase months ago. I had a bad attack on a bridge and also inside a grocery store. Personnel had to take me to the store office to calm me down. I am nearly agoraphobic now. I do go out alone but try to avoid after-dark. My life has been turned into daily dread of another attack. To think that I was more than ten years FREE of panic until I took the Flonase makes me feel so regretful that I ever took that stuff. It should be banned as there is enough evidence to do so from many people who now suffer debilitating and recurring panic.
  • A life of depression and fatigue
    1) Family history of depression, 2) Diagnosed depression 1964-not treated until 1973, 3) Worked in medical field 35 years, 4) Emergency on-call 24/7, 5) Hospital 15 times major depression, 6) Tried nearly all MAOI, TCA, SSRI, SNRI, and ECT. 7) 100% Disability in 1998 for depression. Now at age 70 I have dysthymia, chronic fatigue, COPD, and PTSD. My recommendation to younger people - do not over stress,
    do not smoke, avoid horrific or traumatic situations and try to find some enjoyment in life. If you have symptoms like mine seek early treatment put balance in your life. The often heard recommendations - get plenty of sleep, eat properly, learn to relax and avoid bad habits should not be ignored, they are critical to good physical and mental health.
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  • 3 strong drugs together against neuropathic pain
    Neuropathic pain debuted when I was 24, now I'm 50. Received diagnosed with Ehler-Danlos syndrome (EDS), joint hypermobility type, when I was 35 years old. So it can take some time to get a diagnose. And as EDS-patient I do not belong to any clinic. Orthopedics says that EDS is not orthopedic, rheumatology says that EDS is not an autoimmune disease, GPs say that EDS is too difficult, and so on. Sooner or later we all end up at Psychiatry, even if we are not depressed.

    The first kind of pain I got when I was 24 came from low back, but I experienced as pelvic pain and leg pain. It was clearly a neuropathic pain, but it took years to find out. Later it was treated by a pain clinic with cortisone around the genitofemoral nerves (both sides). Since this treatment didn't result in lasting freedom from pain, the pain clinic started to give me RF (radio frequency) treatment. This made the pain disappeared after one year, and I was 80% free from it between 2002 and 2014, 12 years. The pain doctors said pain could return after 10 years.

    The other kind of neuropathic pain started 2003 with intense stomach pain. During 6 months I could hardly eat nothing due to nausea and vomiting. After this 6 months, stomach pain changed to almost unbearable pain in upper back.
    What happened 2003, and what all the doctors missed, was that the right lowest ribs slid up over the sternum. This rib dislocation is till there today, but now with a lot of cartilage formed around the rib where it is stuck in the lower end of the sternum. The dislocation is clearly visible on X-ray. This has greatly affected the thoracic spine. I have a scoliosis which I had not before 2003. And I still have severe pain in the thoracic spine.

    It was initially treated with morphine daily, and later with Durogesic (fentanyl), but this didn't help much. 2005 I was hospitalized because I had too much pain to take care of myself and my hygiene. After some months the doctors started to give me clonazepam because the muscles along the spine was in a chronic seizures. Clonazepam helped, but I could still have a lot of pain in two vertebrae in the thoracic spine. It felt as if someone drilled into the vertebrae without anesthesia. After a few months, doctors also prescribed me methadone. Then the pain disappeared almost completely. Since 2006, I have eaten clonazepam and methadone every day, and I need to sleep in an armchair to not get more pain because of moving during sleep.

    There are side effects. After 1,5 years with clonazepam and methadone I started to have panic attacks. Or rather one long panic attack which didn't stop before I got treatment with amitryptilin and pregabalin (Lyrica). These 2 medicines stopped the panic disorder completely after some hours, and the panic was then gone. Then I got side effects of these 2 medicines, amitryptilin & Lyrica, too. I gained a lot of weight (from 83 to 148 kg) and got much water (edema) in both my legs under the knees and in both feet. The feet could swallow to the double size. 2012 I stopped with amitryptilin and started to loose weight again (in Aug 2014 below 80 kg) and get less water in my legs. Today I eat as little medicines I can, but I have to take methadone, clonazepam and Lyrica every day, twice. If I try to take away one of these 3 medicines, I got pain problems at once. Lyrica is the most painful one to take away. In Sept-Dec 2013 I lowered Lyrica from 300 mg daily, to 150, then to 75 and finally 0 mg. The pain I had was extremely difficult to handle. It didn't help to take more methadone or anything else. I have checked on Internet and found that many people got pain from quitting with Lyrica. Most people start eating it again. So did I. But 2006 and 2007 it was enough to treat the pain with methadone and clonazepam, I got the Lyrica against anxiety not pain. But today I take Lyrica against pain.

    Beside weight gain and leg edema, clonazepam and Lyrica significantly affect the sexual desire. And Lyrica alone makes it almost impossible to ejaculate. All four drugs together (clonazepam, methadone, amitryptiline and Lyrica), make one forget all about sex life. You don't even miss it. When I stopped with amitryptiline and lowered Lyrica (still taking clonazepam and methadone), I could suddenly easily get erections again, feel desire, but not getting orgasms. This is quite difficult to deal with.

    The pain pattern is greatly affected, by pain and by the medicines. So is the mood. I get something which feels like heavy depression, especially if I take the medicines late that day. I should take a medicine like methadone 3 times a day, because the effects of the tablet lasts around 8 hours. But I take them every 12 hours, to have a low consumption in case doctors prescribe them too late (which happens, and then it's good to have a spouse going to the pharmacy buying them for you, because you have too much pain to go yourself).

    Since methadone is also used for treating heroine addicts, medical staff treat you with disrespect when they see that it says "methadone" in your health record. I need to show a certificate that says that I deal with chronic neuropathic pain, that I never have had problems with drug addiction, to get normal respect.

    I wanted to share this because I think I am alone in the world with these medicines in combination against neuropathic pain caused by hypermobile joints, joint dislocation and muscle spasms. After trying almost everything else, including surgery cutting nerves, methadone, clonazepam and Lyrica seems to be the only way to kill my pain. But it's a life where you always is questioned, because of the use of methadone. I can guarantee that everybody in the world should accept these medicines if they had experienced the unbearable pain I had in upper back before they started to give me clonazepam and methadone.
  • Lexapro and memory loss
    I actually have no idea what other medicine I was on the week I took Lexapro, it was back at the end of February 2014 right before I checked myself into the psych hospital. I formed no memory for a whole week just because of one drug! My friends and family tell me what happened that week and I have called them a liar because there is no recall from that week! I have been on psychiatric drugs for over 14 years and have never had such a horrible reaction as I did with Lexapro! The side effects do not include this reaction, but I didn't sleep at all that week or so I am told and there is just nothing, not even a little memory. Take this as you will I am not saying everyone gets this side effect I am just saying it is not impossible. I learned a lesson I don't remember, but will never take Lexapro again! It was dangerous for me!

More reviews for: Klonopin, Ptsd

Comments from related studies:

  • From this study (10 months ago):

  • I need to know what is causing this condition! Is it the drugs I am taking, could I have Lupus as in Urticarial Vasculitis as I do come up in big lumps, mainly on my arms! I get extremely tired to the point where I may have had a good nights sleep, have made my breakfast and whilst enjoying my coffee I feel as though I have literally been given an anaesthetic and have to lie down! I can then sleep all day!! Once I slept through the day and into the following day!
    I was diagnosed years ago with Urticarial Vasculitis, however the Specialist who diagnosed me, has suddenly done a 'back flip' and says there is nothing wrong with me!!
    Due to her 'new opinion' my Physciatrist now says there is also nothing wrong!! He is the person I have been seeing for many many years for a diagnosis of severe Post Traumatic Stress probably since I was a small child and from Multiple Trauma!!
    I AM GUTTED!! HE WAS THE ONLY 'GO TO' PERSON IN MY LIFE AND HAD PREVIOUSLY ALWAYS BELIEVED ME UNTIL THE OTHER SPECIALIST WROTE TO HIM SAYING NOTHING IS WRONG!!
    It is the worst feeling in the world to lose ones INTEGRITY!! I feel totally lost and very confused!!

    Reply

  • From this study (10 months ago):

  • For about 6 weeks I have had these symptoms. After much internet research
    I feel as though I am histamine intolerant. I have been on a low histamine
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  • From this study (11 months ago):

  • I am worried about prevacid having an interaction with my clonazeoam and/or my other meds as far as plasma concentrations or any bad interactions at all.
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    Jonathan hart

    Reply

    Nauldian on Feb, 16, 2014:

    I have been prescribed clonazepam for PTSD for 3 years. I saw my Gastro Doc, Had a Endo/colonoscopy and I was put on Dexilant (dexlansoprazole)and have an interaction that could increase the amount of clonazepam in my blood. Is this true? do I need to find a new medication for GERD?

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