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Ingredients: Doxepin Hydrochloride
Average User Review Score
* Based on 3 reviews from across the web.

Doxepin is a tricyclic antidepressant marketed worldwide. Brand names of oral formulations include Deptran and Sinequan, and brand names of topical (cream) formulations include Prudoxin.

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* Extracted from FDA Adverse Event Reports for all drugs with the same active ingredients.

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Druginformer Identified Side Effects: Hangover, Somnolence, Thought blocking, Balance disorder

Posted By Anonymous in askapatient.com on August 27, 2009 @ 12:00 am

Side Effects: makes me extremely drowsy within minutes of taking, and inability to stand up straight, cannot even think straight! hangover feelings! in addition to it making me extremely dr...

Druginformer Identified Side Effects: Dizziness, Syncope, Somnolence

Posted By Anonymous in askapatient.com on May 25, 2008 @ 12:00 am

Side Effects: KNOCKED ME OUT. Dizziness. I used this "as needed" a few years ago for about 3-4 weeks? Anyway, it was a cream applied to the skin. This was an EXPENSIVE little tube of cre...

Druginformer Identified Side Effects: Weight increased

Posted By Anonymous in askapatient.com on August 24, 2004 @ 12:00 am

Side Effects: Has anyone experienced weight gain on doxepin?

Druginformer Identified Side Effects: None

Posted By Meph in healingwell.com on June 11, 2007 @ 12:00 am

Marji,I use Elidel on a small patch on my face, twice a day. I have had no side effects from it but obviously you are covering much, much larger area of your skin. I am so sorry you are having these...

* 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.