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Polyethylene Glycol 3350

Average User Review Score
* Based on 31 reviews from across the web.
Wikipedia

Polyethylene glycol (PEG) is a polyether compound with many applications from industrial manufacturing to medicine. The structure of PEG is (note the repeated element in parentheses):

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  Please use Workbench for in-depth research on Polyethylene Glycol 3350.

* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

Tell us about your Experience with Polyethylene Glycol 3350

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Druginformer Identified Side Effects: None

Posted By Happy consumer in fdb.rxlist.com on August 25, 2015 @ 12:00 am

I have suffered constipation all my life, including childhood. Doctor prescribed polyethylene glycol 3350 NF six years ago and I have not been constipated since unless I forget to take it. I dissolve ...

Druginformer Identified Side Effects: Flatulence, Coordination abnormal, Muscular weakness

Posted By AJEET (INDIA) in fdb.rxlist.com on July 20, 2015 @ 12:00 am

... on you for any thing. 3. Developing confusion in him. 4. Made him slow and indecisive in his thought.(always require your help) 5. Handing the effects like Vomiting/GAS/Weakness of this medicine using...

Druginformer Identified Side Effects: Flatulence, Nausea, Abdominal distension, Drug ineffective

Posted By Laura in fdb.rxlist.com on February 17, 2015 @ 12:00 am

Took recommended dosage of 1x daily by doctor instruction. took it for several weeks, Produced gas, abdominal distension and nausea. Seemed to relax the colon and did not allow fecal matter to move...

Druginformer Identified Side Effects: Pain, Disturbance in attention, Neurological symptom

Posted By HATE MIROLAX in fdb.rxlist.com on September 22, 2014 @ 12:00 am

SENT ME TO THE HOSPITAL AFTER 3 DAYS OF USE BY CAUSING NEUROLOGICAL SIDE EFFECTS: PAIN, FIBROMYALGIA BRAIN FOG. STOPPED TAKING IT AND ONE MONTH LATER TRIED IT AGAIN WITH THE SAME NEUROLOGICAL PROBLEMS...

Druginformer Identified Side Effects: None

Posted By kipper1 in fdb.rxlist.com on August 30, 2014 @ 12:00 am

I just started my regimen. It worked great the first day and then nothing ever since. I will continue it for maybe another week and see if it kicks in.

Druginformer Identified Side Effects: Flatulence, Abdominal pain, Diarrhoea, Irritability

Posted By Daffy Duck in fdb.rxlist.com on August 17, 2014 @ 12:00 am

... in order to treat chronic constipation due to lag time between beginning treatment and loose bowel movement. Long term usage studies at varying dosage level are needed. Get gas buildup after 4-5 days ...

Druginformer Identified Side Effects: Convulsion, Discomfort

Posted By doll0422 in fdb.rxlist.com on August 8, 2014 @ 12:00 am

... it makes me wonder?? The two ingredients in antifreeze are ethylene glycol, and propylene glycol which are also used in some dog treats as a preservative, and gave my dog seizures, the names sounds to...

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on May 21, 2014 @ 12:00 am

Druginformer Identified Side Effects: None

Posted By Anonymous in fdb.rxlist.com on March 5, 2014 @ 12:00 am

Druginformer Identified Side Effects: Flatulence, Abdominal discomfort, Abdominal distension, Dry mouth, Throat tightness, Pruritus generalised, Decreased appetite, Adverse drug reaction

Posted By concern caregiver in fdb.rxlist.com on October 31, 2013 @ 12:00 am

Loss of appetite, stomach pain, bloated, gas, dry mouth, all over skin itches, breathing shallow, more difficulty swallowing, no bm for 8 days! I think this medicine made it worse, I would not recomme...


* Warning: The facts and figures contained in these reports are accurate to the best of our capability; however, our metrics are only meant to augment your medical knowledge, and should never be used as the sole basis for selecting a new medication. As with any medical decision, be sure to work with your doctor to ensure the best choices are made for your condition.

* About FAERS: The FDA Adverse Event Reporting System (FAERS) is used by FDA for activities such as looking for new safety concerns that might be related to a marketed product, evaluating a manufacturer's compliance to reporting regulations and responding to outside requests for information. Reporting of adverse events is a voluntary process, and not every report is sent to FDA and entered into FAERS. The FAERS database may contain duplicate reports, the report quality is variable, and many factors may influence reporting (e.g., media attention, length of time a drug is marketed, market share). For these reasons, FAERS case reports cannot be used to calculate incidence or estimates of risk for a particular product or compare risks between products.