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Teril

Ingredients: Carbamazepine
Average User Review Score
* Based on 0 reviews from across the web.
Wikipedia

Carbamazepine (CBZ), sold under the tradename Tegretol among others, is a medication used primarily in the treatment of epilepsy and neuropathic pain. For seizures it works as well as phenytoin and valproate. It is not effective for absence seizures or myoclonic seizures. It may be used in schizophrenia along with other medications and as a second line agent in bipolar disorder. It is taken two to four times per day. A controlled release formulation is available for which there is tentative evidence showing fewer side effects.

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Common adverse events from online conversations
Common adverse events from FDA database
* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

Tell us about your Experience with Teril

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Druginformer Identified Side Effects: None

Posted By xxdusxxxx in twitter.com on July 15, 2014 @ 12:00 am

Teril gotta chill I got no chill

Druginformer Identified Side Effects: None

Posted By ImTh4tDud3 in twitter.com on July 15, 2014 @ 12:00 am

Teril gotta chill I got no chill

Druginformer Identified Side Effects: None

Posted By ImTh4tDud3 in twitter.com on July 15, 2014 @ 12:00 am

Teril did not put my momma as his aviiii

Druginformer Identified Side Effects: None

Posted By xxdusxxxx in twitter.com on July 15, 2014 @ 12:00 am

Teril did not put my momma as his aviiii


* 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.