Originally Posted by
Utah49er
I will be starting 20mgs tomorrow...and then my clock starts counting towards recovery...correct? Does the clock reset if I up the dose?
Yes, and no. However, there may be a temporary increase in side-effects after dose increases, although they are usually not as severe as at the beginning.
from your posts to me, you seem to view Mirtazapine as little more than a sleep aid or anti-histamine.
Yes, because this is all it is. It is about 1,000 times more effective at blocking the histamine HI receptor than any other. It is not a classic antidepressant, neither significantly inhibiting neurotransmitter reuptake, or promoting neurogenesis.
I have read, it was found to be at least as effective as many older anti-depressants (especially for agitated depression with insomnia).
Yes, it can be effective for both because of its sedative effects, particularly at lower doses. It can, however, become agitating at the upper end of the dose range.
was wondering your opinion on Mirtazapine.
I think it can be a better longer term option than benzodiazepines as a sedative for anxiety, as a sleep aid (but when available trazodone is better, imho) and it may speed up SSRI kick-in a little.
But I'm not a fan because it also has some potential serious long-term side-effects such as diabetes due to the large weight-gains it often causes by stimulating carbohydrate cravings, and there is also a risk of liver injury with about 10% of those taking the drug showing liver abnormalities, although usually these are not significant. However, a small number may develop blood dyscrasias (PDF) which is the medical term for a wide range of blood abnormalities such as the white blood cell disorders neutropenia and agranulocytosis. While rare, these should be watched for. Typical symptoms are fever, sore throats and other signs of infection.
Mirtazapine is derived from the older antidepressant mianserin which was initially popular, particularly in Europe until doctors realised it was slightly less effective than an equivalent dose of M&Ms. So the makers rejigged the chemistry a little to create mirtazapine which they claimed was a much more potent alpha 2-adrenoceptor (a2) and serotonin 5-HT2a receptor antagonist. Both claims are untrue. The mianserin a2 binding potential is between 23-73 *Ki, that of mirtazapine 58-141 Ki. For 5-HT2a the binding potentials are mianserin: 0.36-7.0 Ki, mirtazapine 2.0-17 Ki. Mirtazapine remains popular while mianserin is rarely prescribed these days because the makers spend a lot of money marketing the drug to doctors.
* The Ki value is based on the amount of the drug needed to occupy 50% of the target receptors, so the lower the Ki the more potent the med.