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Review: could Clonazepam cause Nausea?

Summary: Nausea is found among people who take Clonazepam, especially for people who are female, 60+ old, have been taking the drug for 1 - 6 months, also take medication Aspirin, and have Depression.

We study 38,829 people who have side effects while taking Clonazepam from FDA and social media. Among them, 2,490 have Nausea. Find out below who they are, when they have Nausea and more.

You are not alone: join a mobile support group for people who take Clonazepam and have Nausea >>>

 

 

 

 

Clonazepam

Clonazepam has active ingredients of clonazepam. It is often used in stress and anxiety. (latest outcomes from 41,341 Clonazepam users)

Nausea

Nausea (feeling of having an urge to vomit) has been reported by people with type 2 diabetes, quit smoking, depression, high blood pressure, pain. (latest reports from 264,742 Nausea patients)

On Feb, 5, 2015: 38,806 people reported to have side effects when taking Clonazepam. Among them, 2,490 people (6.42%) have Nausea.

Trend of Nausea in Clonazepam reports

Time on Clonazepam when people have Nausea * :

< 1 month1 - 6 months6 - 12 months1 - 2 years2 - 5 years5 - 10 years10+ years
Nausea18.18%30.91%14.55%9.09%11.82%13.64%1.82%

Gender of people who have Nausea when taking Clonazepam * :

FemaleMale
Nausea76.37%23.63%

Age of people who have Nausea when taking Clonazepam * :

0-12-910-1920-2930-3940-4950-5960+
Nausea0.13%0.18%2.07%8.56%15.49%21.67%24.93%26.96%

Severity of Nausea when taking Clonazepam ** :

leastmoderateseveremost severe
Nausea17.95%61.54%20.51%0.00%

How people recovered from Nausea ** :

while on the drugafter off the drugnot yet
Nausea6.25%18.75%75.00%

Top conditions involved for these people * :

  1. Depression (345 people, 13.86%)
  2. Anxiety (320 people, 12.85%)
  3. Pain (256 people, 10.28%)
  4. Smoking cessation therapy (189 people, 7.59%)
  5. Hypertension (170 people, 6.83%)

Top co-used drugs for these people * :

  1. Aspirin (279 people, 11.20%)
  2. Lorazepam (208 people, 8.35%)
  3. Nexium (208 people, 8.35%)
  4. Neurontin (207 people, 8.31%)
  5. Zoloft (191 people, 7.67%)

* Approximation only. Some reports may have incomplete information.

** Reports from social media are used.

How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.

Get connected: join our support group of clonazepam and nausea on

Do you have Nausea while taking Clonazepam?

You are not alone! Join a mobile support group:
- support group for people who take Clonazepam and have Nausea
- support group for people who take Clonazepam
- support group for people who have Nausea

Drugs in real world that are associated with:

Could your condition cause:

Can you answer these questions (Ask a question):

  • I have heard that taking clonazepam and diltiazem can cause bronchitis anyone have this reaction
    I have bronchitis at least once a year, excess mucus and throat clearing. Tightening of the airways, mostly at night.was wondering if drug interactions could be the cause.
  • Does clonazapam cause tinnitus or ringing in the ears?
    Patient fell a year ago and injured her neck and broke a bone in her arm. Has had severe pain in her neck. Getting acupuncture frequently. Recently tried to change medication from Valium to Clonazepam, and developed severe tinnitus. She said she only missed two days of Valium. She also says she has skipped days without taking valium and never had a problem. She says Clonazepam caused the tinnitus. I can't find anything that states a side effect of clonazepam is tinnitus.
  • I suffer from hypotension after taking meal along with breathlessness and itching
    after eating I fell as if I will faint n hav dyspnea n headache.. n if I try to walk then I hav severe itching all over the body ... if I don't take meal then I am fine
  • Can you stop trileptal cold turkey?
    I ran outta my Trileptal, the last time I took it was in the hospital on Saturday I was there for 2 days and I was normally taking 300mg 2x daily and the hospital gave me 600mg 4x on Saturday and the day before I took the one 300mg I had left in the morning. Since the hospital I have not had any Trileptal to be able to take because they didn't send me home with any because I'm from another State and I'm not sure if that's why but I should have my medicine tomorrow but I feel horrible and I just wanna know if physically I will be alright? Thank you so much and would appreciate a quick responce.
  • I take klonopin and diltiazem (calcium channel blocker blood pressure medicine) and am concerned about side effects. my accupuncturist recommends the ashwagandha. anyone have any issues with this?
    I take these prescription medications but have been going to an accupuncturist since 2012. I have trouble sleeping at night without my clonazepam and take naps during the day and am having trouble losing weight. She thinks that my adrenal glands may be fatigued and told me to try something called Adrenal Response which contains Sensoril Ashwagandha. When I looked up Ashwaganda it said that it could interact with the Clonazepam or Klonopin and also with High blood pressure medication. I am a little concerned. I mentioned this to her and she said they both are metabolized by the liver and it should be ok to take it, just to take it an hour or more after I take the Clonazepam. Has anyone had any issues with interactions with their prescribed meds while taking Ashwagandha? I don't want to have to monitor my blood pressure because my blood pressure medication works good for me. Any help would be appreciated because I want to try it but I am a little scared too. Thanks, Crystal

More questions for: Clonazepam, Nausea

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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.

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