This report is for all products sharing this active ingredient. For more details, please use our Workbench for research on individual brands like Propofol.
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.
Report Date | Dosage | Indication | Outcome | Country | Gender | Age | Weight (lbs) |
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* DrugInformer calculates alarm using a proprietary algorithm. Alarm should not be taken as an ofiicial signal from the FDA or other regulatory entity.
Druginformer Identified Side Effects: Pain, Hypotension, Oropharyngeal pain
Posted By Anonymous in drugs.com on January 3, 2014 @ 12:00 am
“... this time with Propofol (Diprivan) and it went much better than the first one ten years earlier with a different sedative (when I woke up in the middle of the procedure in considerable pain). It was ...”
Druginformer Identified Side Effects: Burning sensation, Hypotension, Adverse event, Asthma, Vision blurred
Posted By Anonymous in askapatient.com on February 13, 2010 @ 12:00 am
“Side Effects: Very SLIGHT burning sensation (I'm a small person!) which lasted a few seconds and then my eyes got a little blurry, then I woke up feeling wonderful. The good feeling only lasted a few...”
* 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.
Social Media Comments From Around the Web
The following are comments from users that experienced side effects while taking Milnacipran Hydrochloride
Propofol
“... room and I couldn't believe it was over. The only side effects were a sore throat (I had on an oxygen mask so that may have been a contributing factor) and very low blood pressure for about thirty mi...”
Source:" comments/propofol/for-anesthesia.html&...
View full report on drug related hypotension
Did the author experience hypotension while taking propofol?
What is this?Propofol
“... a recovering benzodiazepine dependent, and this drug is very safe. Even with a bolus dose and Asthma, I didn't even come close to being apneic or having low blood pressure . My anesthesiologist agrees ...”
Source:" DIPRIVAN PROPOFOL: Side effects, ratin...
View full report on drug related hypotension
Did the author experience hypotension while taking propofol?
What is this?