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User Voices for Mannitol

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

Cerebrovascular Accident

Acute stroke of the MCA.


Source: mannitol 20 % intravenous : User Ratin...

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Vaginal Haemorrhage

... know if it is on your paper or not. There were other red flags too that she didn't want to even read to me because they were too many. She was not too worried about the vaginal bleeding . But she sa...


Source: Broke out in hives, I must be allergic...

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Breath Odour

... toothaches! Benefit: Gum can help freshen the breath after eating stinky foods such as onions and garlic, and relieve dry mouth, which also can promote gross mouth odors. (Bad breath that is present...


Source: hildebrandhealthysmiles/posts/67569949...

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Drug Ineffective

... g. Avoid hypovolemia and hyperosmolality if mannitol is used. Bolus therapy (0.5–1.0 gm/kg) should be used with observed effect in 20 to 60 minutes. Repeat dosing if no effect within 20 minutes....


Source: seict/posts/520387224709145

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Hypoxia

... posttraumatic hematomas. A CT scan should be obtained with any abrupt increase in ICP or worsening of the neurologic examination. GCS declines by two or more or the patient develops hypoxia . f. B...


Source: seict/posts/520387224709145

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Amnesia

There are a lot of bad side effects associated with artificial sweeteners, including headaches, diarrhea, memory loss , and certain types of cancer. They can shut off the hormone that tells you you are...


Source: Artificial Sweeteners?

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Diarrhoea

There are a lot of bad side effects associated with artificial sweeteners, including headaches, diarrhea , memory loss, and certain types of cancer. They can shut off the hormone that tells you you are...


Source: Artificial Sweeteners?

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* 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.