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Propofol Related Renal Failure

Official FDA Reports496
Social Media Events3
Active Ingredients
  • Propofol
Additional Drug Brands and Names
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Additional Terms for Renal Failure
  • Kidneys Have Almost Shut Down
  • Kidney Failure

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


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

Propofol

Side Effects: acute kidney failure ,cardiac collaspe,multiorgan failure, the propfol infusion syndrome came on the fourth day death came on the sixth day.This is what happens when drug companys overse...


Source:" DIPRIVAN PROPOFOL: Side effects, ratin...

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Did the author experience renal failure while taking propofol?

What is this?

Propofol

Side Effects: took it for 10 days straight w/out a drug holiday. didn't wake up when it was time to. caused severe case of Rhabdomyolosis,acute renal failure .which has left my son totally disabled a...


Source:" DIPRIVAN PROPOFOL: Side effects, ratin...

View full report on drug related renal failure

Did the author experience renal failure while taking propofol?

What is this?

Propofol

Side Effects: Apnea, agitation, kidney failure , sepsis

My husband was given this medication for surgery. When he awoke in recovery he tried to pull out his vent tube and was put under agai...


Source:" DIPRIVAN PROPOFOL: Side effects, ratin...

View full report on drug related renal failure

Did the author experience renal failure while taking propofol?

What is this?

Tell us about your Experience with Propofol Related Renal Failure

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: Renal failure, Death, Infusion

Posted By Anonymous in askapatient.com on September 22, 2010 @ 12:00 am

Side Effects: acute kidney failure,cardiac collaspe,multiorgan failure, the propfol infusion syndrome came on the fourth day death came on the sixth day.This is what happens when drug companys overse...

Druginformer Identified Side Effects: Renal failure, Disability

Posted By Anonymous in askapatient.com on January 24, 2008 @ 12:00 am

Side Effects: took it for 10 days straight w/out a drug holiday. didn't wake up when it was time to. caused severe case of Rhabdomyolosis,acute renal failure.which has left my son totally disabled a...

Druginformer Identified Side Effects: Agitation, Renal failure, Sepsis, Sudden death, Endocarditis, Coma, Staphylococcal infection, Brain injury

Posted By Anonymous in askapatient.com on July 27, 2007 @ 12:00 am

Side Effects: Apnea, agitation, kidney failure, sepsis My husband was given this medication for surgery. When he awoke in recovery he tried to pull out his vent tube and was put under agai...



* 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.