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Polyethylene Glycol 3350; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride; Sodium Sulfate Anhydrous Related Palpitations

Official FDA Reports19
Social Media Events2
Active Ingredients
  • Polyethylene Glycol 3350; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride; Sodium Sulfate Anhydrous
Additional Terms for Palpitations
  • Palpitation
  • Heart Palpatations
  • Pounding Heart
  • Fast Heart Rate
  • Higher Heart Rate
Show more

  This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Golytely.


Explanation

The quarterly trend chart illustrates changing levels of adverse events over time. Results from both the FDA Adverse Event Database (AERS) and adverse events extracted from social media by Druginformer are plotted side-by-side for easy comparison.


List of Possible Side Effects Reported

Report Date Dosage Indication Outcome Country Gender Age Weight (lbs)

* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.


Social Media Comments From Around the Web

The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride

Golytely

Side Effects: Seizures, migraines, head sensations, vertigo, bloating, nausea, bowel pain, cool chills, high pulse , low bloat pressure, rash.

I have had over 29+ gallons of this liquid nigh...


Source:" GOLYTELY: Side effects, ratings, and p...

View full report on drug related palpitations

Did the author experience palpitations while taking golytely?

What is this?

Golytely

... were to take 4 Dulcolax tablets at the outset. Well within 90 minutes of that dosing, I began to feel faint, crampy and passed out. When I came to I was shaky, had palpitations and my husband called...


Source:" GOLYTELY: Side effects, ratings, and p...

View full report on drug related palpitations

Did the author experience palpitations while taking golytely?

What is this?

Tell us about your Experience with Polyethylene Glycol 3350; Potassium Chloride; Sodium Bicarbonate; Sodium Chloride; Sodium Sulfate Anhydrous Related Palpitations

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Abdominal pain, Nausea, Chills, Vertigo, Hypersensitivity, Nightmare, Palpitations, Abdominal distension, Convulsion, Migraine, Rash, Meningitis

Posted By Anonymous in askapatient.com on July 19, 2010 @ 12:00 am

Side Effects: Seizures, migraines, head sensations, vertigo, bloating, nausea, bowel pain, cool chills, high pulse, low bloat pressure, rash. I have had over 29+ gallons of this liquid nigh...

Druginformer Identified Side Effects: Tremor, Dizziness, Vertigo, Loss of consciousness, Palpitations, No adverse event, Menstrual discomfort

Posted By Anonymous in askapatient.com on July 26, 2009 @ 12:00 am

Side Effects: I didn't even get to take the Golytely portion of the prep. My instructions were to take 4 Dulcolax tablets at the outset. Well within 90 minutes of that dosing, I began to feel faint...



* 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.