Review: could Lactulose cause Constipation?
Summary: Constipation is found among people who take Lactulose, especially for people who are female, 60+ old, have been taking the drug for < 1 month, also take medication Oxycontin, and have Pain.
We study 13,987 people who have side effects while taking Lactulose from FDA and social media. Among them, 946 have Constipation. Find out below who they are, when they have Constipation and more.
You are not alone: join a mobile support group for people who take Lactulose and have Constipation >>>
Lactulose has active ingredients of lactulose. It is often used in constipation. (latest outcomes from Lactulose 14,073 users)
Constipation has been reported by people with osteoporosis, pain, high blood pressure, depression, high blood cholesterol.(latest reports from Constipation 81,299 patients)
On Dec, 27, 2014: 13,987 people reported to have side effects when taking Lactulose. Among them, 946 people (6.76%) have Constipation.
Time on Lactulose when people have Constipation * :
|< 1 month||1 - 6 months||6 - 12 months||1 - 2 years||2 - 5 years||5 - 10 years||10+ years |
Gender of people who have Constipation when taking Lactulose * :
Age of people who have Constipation when taking Lactulose * :
Severity of Constipation when taking Lactulose ** :
|least||moderate||severe||most severe |
How people recovered from Constipation ** :
Top conditions involved for these people * :
- Pain (134 people, 14.16%)
- Constipation (129 people, 13.64%)
- Schizophrenia (87 people, 9.20%)
- Hypertension (72 people, 7.61%)
- Urinary tract infection (72 people, 7.61%)
Top co-used drugs for these people * :
- Oxycontin (172 people, 18.18%)
- Furosemide (159 people, 16.81%)
- Aspirin (158 people, 16.70%)
- Omeprazole (135 people, 14.27%)
- Folic acid (131 people, 13.85%)
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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Do you have Constipation while taking Lactulose?
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- support group for people who take Lactulose and have Constipation
- support group for people who take Lactulose
- support group for people who have Constipation
Drugs in real world that are associated with:
Could your condition cause:
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- Cymbalta r/t autonomic neuropathy
losartan 20 mg
tired all the time, dizziness, chronic constipation, stomach pains, pins and needles, diabetic type 2 hx alcoholism resolved, gerd, early satiety
- Can mrsa cause chronic intestinal pseudo obstruction?
I had a small bowel obstruction caused by adhesions from an appendectomy carried out 20yrs previously and had grumbling pain ever since but been labelled a malingerer by my family GP until one day at work when I started with terrible tummy ache and sickness like I'd never known, fetching up bile with force. I hated going to hospital after yrs of being called a moaner but after a day of rolling round in pain, temperature of 103 an dehydration, my Mammy insisted we go and I was seen straight away - to my shock I was in theatre within 3hrs with a serious obstruction.
I never really recovered... The obstruction returned after 2 days and a portion of necrotic bowel was removed, then further fever and cellulitis then MRSA and deaths door.... Isolation in high dependency (intensive care) wound break down, ventilated and all related issues that come with that - chest infection, pneumonia, bed sores. Total time in hospital 8 months. Negative pressure dressing on laparotomy wound, colostomy, picc, 4 rounds of vancomycin, minor flirt with heart failure (just water related) an eventually everything healed. Had a large incisional hernia to repair and some corrective work to the horrific scarring but then the neuropathy started plus problems eating, spewing up after any solid food, more than a few forks, diarrhoea and sickness or constipation nausea and pain driving me mad, tried all manner of drugs, nerve blocks, physio, floating tank, acupuncture, opiates, non opiates, spinal cord stimulation, an now a consultant just had a 'eureka' moment and said were you treated with vancomycin when you had MRSA? If so I'm pretty sure you have chronic intestinal pseudo obstruction and is 90% sure but wants to take a muscle biopsy to be certain. I've had so much surgery and bad news in the last 10yrs I'm terrified of germs, hospital acquired bugs and anaesthetics, is there any other way? Or can I have this test done awake - conscious sedation? I had it before during spinal cord surgery so I know what's involved and it's better than GA as I know what's going on, who is doing what to me etc...
Does anyone with a medical background know about this ailment/disease? Does it sound feasible that MRSA or it's treatment could have caused this? I was surgically debrided up to every other day when the vac pac/negative pressure machine and dressings were changed and the doctors told me I lost a great deal of tissue and had a lot of nerve damage due to the infection.
Any patient perspectives on this illness would also be very much valued in helping me make a decision, moving forward. If all this is going to accomplish is to attach a label to the pain but not actually change anything, after fighting it for 10yrs now, avoiding hospital as much as I can, I really can't see the point of exploratory surgerys and biopsys now when it is known that I have this propensity towards adhesions and a new wound means a potentially new adhesion growth site.
If it helps, the appendectomy happened when I was 10yrs old, the MRSA when I was 30 and I am now 40.
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what is easiest on guts had small bowel blockage recently and have diverticulitis
- Gastro with constipation in a 4 year old only cause pain at night?
In childrens hospital now have given the tag virus for stomach pain at night that is relieved by morphine
- Can my symptoms actually pinpoint a cause/condition? (1 answer)
I would just like insight on this. I'm on pain management right now, but it's just to manage the pain. Every thing else has really been not taken serious by any physican it office I've been to. Is this normal stuff many woman go through? I'm just sick of feeling like this between the constant pain & the daily having to pluck hairs it's insane. I'm in fantastic shape(used to be double my weight & now I'm 100lbs), the best looking I've ever been with a incredibly good looking husband & a wonderful family. My issues seem to detour a lot of things & while I'm young I'd like to get this solved or some type of solution to even maintain myself, not looking for a miracle, but would really appreciate answers.
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The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
- Trying to figure out my diagnosis . no doctor can figure it out (3 responses)
I have been having these fainting spells since I was 12 .. It starts with lower abdominal pain followed by feeling light headed then I black out and my body shakes kind of like a seizure but last a few seconds then I come to ..then I feel nausea and also I have chills
- Lithium constipation and tremor
After taking Lithium Carb for about three months, I realize I've been moderately constipated for several weeks. I also have been nauseous and suddenly realize that it's probably related to the nausea and maybe the cause of it.
- Epilepsy and depression drug side effects (2 responses)
42yo male having infrequent seizures since he was 19yo.
Was recently placed on Neurontin and Topamax after a single seizure. This combination of meds appeared to increase the frequency of seizures ( from 1 every few years unmedicated, to 1 every month ). Dosage being increased after each seizure. No seizure control achieved.
Changed Neurologist, had a 48hr EEG and was changed to Sodium Valproate.
Have not had a Tonic Clinic seizure since. Suffer myoclnic seizures every day, Lamotrogine and Lacitimal? and Topamx introduced to try a stop the myoclonus... Lamotrogine made them far worse and dizzyness caused by Lacitimal was un-bearable even at very small dose.
Over the last 3yrs I have noticed and my family even commented on my changed personality - from a care free to someone that is easily aggitated and angry...even when I know things like young children being noisey etc shouldn't make me snap, they do... I know its wrong, but can't help myself... and then hate myself for being so "short" or intolerant of petty things.
My weight increased by 30kg with 4 months... more than 40% increase in weight.
My hair just falling out, by the 1000's every day... my bike helmet is full of hair and when washing, hair is visible in the shampoo bubbles.
My gums bleed very easily and they no longer grow up around the base of my teeth - they seem to be retracting away ( believe this message s called attrophy ).
Have researched quite extensively to see the likely hood of all these medical problem I have now being associated with the medications I take for my primary condition ( epilepsy ).. And given the frequency of seizure off medication is every few years, seeking advice from or to hear from anyone with similar conditions about how they addressed them and if they remained on the medications.
From this web site, all my symptoms seems to affect a very low % of people taking the meds... am I trying to link medical concerns to the medications unjustly... the likely hood of suffering all these side effects is extremely remote when most affect only 2 or 3 in100 people.
( likely hood of suffering all 5 conditions = approx 1 in 40,000,000
- more likey to be hypercondriact aren't I?
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