DrugInformer Search

Remeron Soltab

Ingredients: Mirtazapine
Average User Review Score
* Based on 23 reviews from across the web.
Wikipedia

Mirtazapine (brand names: Avanza, Axit, Calixta, Mirtaz, Mirtazon, Remeron, Zispin) is a noradrenergic and specific serotonergic antidepressant (NaSSA) introduced by Organon International in the United States in 1996, and is used primarily in the treatment of depression. It is also commonly used as an anxiolytic, hypnotic, antiemetic and appetite stimulant. In structure, mirtazapine can also be classified as a tetracyclic antidepressant (TeCA) and is the 6-aza analogue of mianserin. It is also racemic—occurs as a combination of both (R)- and (S)-stereoisomers, both of which are active.

Read more on Wikipedia
Share

  Please use Workbench for in-depth research on Remeron Soltab.

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

Tell us about your Experience with Remeron Soltab

Thank you for sharing your experience with us!

Share Your Experience

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on May 30, 2013 @ 12:00 am

Side Effects: No reduction in depression or anxiety

Druginformer Identified Side Effects: Drug withdrawal syndrome

Posted By Anonymous in askapatient.com on March 9, 2012 @ 12:00 am

I was never disappointed in the drug until I stopped taking it. It has some severe withdrawal symptoms. I stopped taking it because my GP more or less told me to; some recent blood tes...

Druginformer Identified Side Effects: Abnormal dreams, Amnesia, Disturbance in attention, Adverse drug reaction

Posted By Anonymous in askapatient.com on December 22, 2011 @ 12:00 am

Side Effects: Not 100% sure how long i was taking it, meds have ruined my memory a bit. Vivid/erradic/relistic dreams, stopped taking it a year or so ago (i think) and still have the problem. Makes ...

Druginformer Identified Side Effects: Weight increased, Psychotic disorder

Posted By Anonymous in askapatient.com on December 21, 2011 @ 12:00 am

Side Effects: Lack of mental clarity & major weight gain.

Druginformer Identified Side Effects: Syncope

Posted By Anonymous in askapatient.com on March 24, 2011 @ 12:00 am

Side Effects: i knock out in the night and wake up fresh in the morning

Druginformer Identified Side Effects: None

Posted By Jen in fdb.rxlist.com on January 15, 2011 @ 12:00 am

I am on 37.5 mg after 6 months of lower doses. It definitely helps sleep and the depression lifted after adding the latest 7.5mg. I have watched my calorie intake carefully and have not gained weight...

Druginformer Identified Side Effects: None

Posted By Anonymous in everydayhealth.com on January 8, 2011 @ 12:00 am

given to help sleeplessness as well as depressio

Druginformer Identified Side Effects: None

Posted By Anonymous in askapatient.com on September 30, 2010 @ 12:00 am

Side Effects: no side effects yet i was addicted to benzodiazepines but my doc tried Remeron to ease the withdrawl. it helped

Druginformer Identified Side Effects: Hunger, Restless legs syndrome, Somnolence

Posted By Anonymous in askapatient.com on September 27, 2010 @ 12:00 am

Side Effects: restless legs, hunger, sleepy Remeron is the closest thing to a wonder drug that we have. I have tried just about everything out there. I have fired 2 pdocs. A kind GP finally...

Druginformer Identified Side Effects: Restless legs syndrome, Somnolence, Dizziness, Hunger

Posted By Anonymous in askapatient.com on September 16, 2010 @ 12:00 am

Side Effects: hunger, sleepy, restless leg, dizzy wonderful drug. keeps ocd away.


* 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.