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Review: could Flagyl cause Sweating?

Summary: there is no Sweating reported by people who take Flagyl yet.

We study 9,851 people who have side effects while taking Flagyl from FDA and social media. Find out below who they are, when they have Sweating and more.

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

 

 

 

 

Flagyl

Flagyl has active ingredients of metronidazole. It is often used in vaginitis bacterial. (latest outcomes from 10,488 Flagyl users)

Sweating

Sweating has been reported by people with migraine, depression - elderly, gastroesophageal reflux disease, birth control, acne. (latest reports from 38 Sweating patients)

On Feb, 2, 2015: No report is found

Do you have Sweating while taking Flagyl?

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Drugs in real world that are associated with:

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Can you answer these questions (Ask a question):

  • Looking for other testimonies who have had more severe side effects than those listed from taking metronidazole & alcohol? (1 answer)
    Had 4 beers over 4 hour period on last day of taking Metronidazole. Was vomiting & basically acting totally out of character as in wild & argumentative - similar to being bad drunk. Went to sleep & woke up with basically no memory of what happened.
  • Is it safe to take methadone(52mg daily), metoprolol extended release(75mg daily) & xanax(1mg twice daily) (2 answers)
    I'm just wanting to know if its safe to take all 3. I've been on methadone for 7yrs and about a yr ago i started tapering and started at 130mg, but am now at 52mg. I've been on the Metoprolol(extended release) for about a yr now taking 50mg in AM, and 25mg in PM. I just started taking the Xanax about 3wks ago .5mg twice daily/as needed. Stopped taking birth control 3months ago, so wondering if some side effects are because of the birth control, and not the other meds. Thanks!
  • I have pouchitis.is there any cure for it.antibiotics do not help.is there any chance that imuran will help or something else?help please! (1 answer)
    Since I was 16 years old I strugle with Ulcerative Colitis.Year and a half ago my colon was removed.So, now I have J-pouch and it seems that colon removement caused severe pouchitis.When I use antibiotics it seems that everything is good,but when i stop using them ,everything gets even worse.

    I tried low dose of corticosteroides,colifoam but nothing seems to be working,so I am desperate.

    Now for a two and a half months I have been using Imuran(Azathioprine).Can you tell is it going to help me, or should I try something else.

    Please!Can somebody help me?

    Thank you in advance.
  • What has miralax done to my body? please help me... (2 answers)
    Years ago after multiple surgeries, I ended up with chronic constipation. GI doctor told me to take 4 doses of miralax everyday. About a year into the medication, I completely changed as a person. I experienced brain fog, anxiety, meltdowns, blowups, sexual dysfunction, and worst of all excessive sweating. I discontinued it about a month and a half ago.



    For the first week after ending the medication, I would wake up and feel like I was having brain spasms. I would be extremely confused, scared, felt like crying, and wanted someone to hold me. The next 2 weeks after that, I had severe headaches every morning. I did some research and found that article about how the ingredient is similar to antifreeze and there's a few cases reported of it causing psychotic episodes in people. Additionally, it somehow ruins your intestines, possibly causing some condition called dysbiosis (which I have a few symptoms of and a few websites claim also can cause sweating). Apparently it also weakens your colon, making it more prone to cancer, which my GI disease already gives a big enough threat to!!! Additionally to the list of symptoms, I've noticed that my immune system is significantly weaker - I've gotten infections and colds for the first time in years.



    I've gone to the ER, talked to doctors, and they (of course) doubt me, accuse me of being dishonest, and try to send me to a head doctor. The symptoms might be gradually improving... but the sweating isn't... and it's really concerning me and ruining my life. I'm disabled and I don't have much to do with my time and I don't like watching TV but I can't do anything else now with my time. My palms are constantly soaked so I can't hold anything and my feet constantly ruin my socks. The sweat on the palms get so intense at times that it's literally uncomfortable beyond words to the point where I almost feel like screaming or crying about it.



    Is this temporary? Did miralax really ruin my body? Do I possibly have dysbiosis? They are trying to send me to a dermatologist but I believe the underlying problem is GI/miralax related. Oh, also, I've noticed that I sweat worse after I eat - ESPECIALLY if I have sugar/carbs. I don't like dermatologist methods for curing sweat and I don't really believe it's hyperhydrosis. I just want this to stop so I can go back to doing things with my hands to keep myself distracted and so I can hold my girlfriends hand without embarrassing myself but I can't. I've been doing nothing but watching TV for the past month or two and it's driving me crazy because I haven't spent time with a TV in years and years. I can't even begin to describe how it feels that I was given a product that caused me additional problems and all the doctors are calling me a liar and I have no way of getting help.



    Someone please help me.
  • Is anyone here being treated for h pylori? (2 answers)
    Diagnosed with H-pylori and am challenged with pharmophobia (which is a phobia for taking any kind of medication in any form)also anxiety, and agoraphobia which extends to too many things such as driving, going out alone, chocolate, cherries and the list goes on. Can anyone tell me if they are or has taken these medicines together and what was the out come? Side affects, how long it took to get better, and if the weight came back after treatment. I have gone from 156 pds to 140 and it gets lower some days. haven't taken the meds yet and am seeing a counselor to help get me to that point.

More questions for: Flagyl, Sweating

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

  • Cdifficile treatment
    I had drug (cipro) induced cdifficile for three and a half years and was hospitalized 3 times and went through absolute hell until my Dr. finally agreed to do a fecal transplant. Even then the first transfer done via a lower bowel infusion didnt work. Two weeks after the first one he did a full colonoscopy transfer going up as high as my appendix and that one worked immediatly and I have had no furthur bowel problems, no diarrea at all and its' now been well over a year. I took every type of cdiff drug imaginable prior to that. I had to stay on Vancomyicin all the time or I would be spending all my time going back and forth to the john 20 or 30 times a day. I was so ill that I could bearly keep my head up. I couldnt eat without an urgent bathroom trip. I had to wear Depends all the time, my skin was raw and sore from constant wiping. I was given Tinture of Morphine to slow me down. That helped some. My veins collapsed from all the test shots and from the many pints of saline to keep me hydrated. My heart stopped from a lowering of my potassium level and I had to get a pacemaker to control my heart rate. I spent a fortune on the drugs,some costing as much as $1200.00 a month, more than I make working and working was rough. I would have to go to the restroom so often and I work outside where there were frequently no facilities. I would have to bring a complete change of clothes and a disinfecting kit with me to cleanup the restroom. I washed my hands raw. You cant leave that for someone else or they might get sick too as it is highly infectious. Hospitals are not that meticulous either. I once had to go to a Long Island Hospital that failed the precautions test miserably. They assigned me to a room with another patient whose family wanted to eat their meals in our shared room and then use the bathroom. I pitched a fit on them and told them no way were they going to eat in that room or use the bathroom. I can't imagine what that hospital was thinking. Anyway you get the idea....3 years of expensive treatment and all I needed was some healthy donor poop and someone willing to mix it up in a blender and put it in syringe and put it up the wassoo and I was done. Dont let them give you all the expensive treatment if you have a resistant case of cdiff, insist on the fecal transplant right off, you will be very glad you did. The donor should be someone in your family, preferably someone young with lots of good flora for digestion. Someone without other gut problems...they need to test them too. Bring it in the afternoon before and Bingo,you will be back on track the next day. I am open to answer questions or be tested orhelp with anything else you might want to know, just ask me.
  • Tingling feet and hands
    I have used flagyl 3 times and after stopping the use of this medication my feet and hands have became so tingly and itchy That its becoming unbearable.
  • Still ill after several years (1 response)
    I became ill several years ago.
    It all started with a head cold that lasted a few months and left me with Tinnitus and chronic sinusitis.

    After a nose operation and many visits to the doc and hospital, I am no closer to felling better or being cured.
    My doc gave me Beconase Aq at first and this made me very unwell, causing me fatigue which would last for a few days. I'm still searching for help.
  • Flagl helped my depression
    After taking Flagl for two weeks (Two per day) My depression vanished. It is now three months since I had a depression episode. Thank God for the doctor who prescribed it he saved my life. Thank you Flagl
  • Too much sleep/sleeping past 12+ hours
    Caused me to sleep and to the point where I slept 12+ hours and still didn't want to wake up

More reviews for: Flagyl, Sweating

Comments from related studies:

  • From this study (2 years ago):

  • Developed a hematoma after total hysterectomy. Started on antibiotics for hematoma. Been on opiate pain meds (fentanyl, dialudid, etc) for two years due to low back injury. Pain management doctor increased fentanyl from 100 mcg/ 48 hr to 125and mcg/ 48 hr and increased breakthrough pain medicine from dilaudid 4mg/ 8 hrs to 8mgs/ 8 hrs. Developed severe hallucinations four years days post hysterectomy. What is causing hallucinations, nausea, vomiting, sweating and no appetite?

    Reply

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