Overdose on zolpidem tartrate

Zolpidem Tartrate Overdose Reports - DrugInformer

05:33 | Author: Nick Jenkins

Can i overdose on zolpidem
Zolpidem Tartrate Overdose Reports - DrugInformer

View detailed reports from patients taking zolpidem tartrate who experienced overdose. Reports are from official medical reports as well as online extractions.

Overdosed on it, still couldn't sleep... ”

Did the author experience overdose while taking zolpidem tartrate ?

“ Side Effects: Amnesia, overdose Every once in a while I post about the dangers. I am a terrible sleeper and have cycled through meds. I was never a fan of Ambien but every 9 months or so I... ”

Did the author experience overdose while taking zolpidem tartrate ?

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

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

Did the author experience overdose while taking zolpidem tartrate ?

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

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.

“ i was overdosing on it so 10mg went to 20, then 30, then 40, then 50 then i was taken off of it ”

* 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.

Comments (0)