Mirtazapinedosage

mirtazapine 30 MG Oral Tablet [Remeron]

Dosage and administration

Starting dose: 15-mg once daily; may increase up to maximum recommended dose of 45 mg once daily. Administer orally once daily, preferably in the evening prior to sleep. Administer REMERONSolTab immediately after removal from blister pack. Reduce dose gradually when discontinuing REMERON/REMERONSolTab.

2.1 Recommended

Dosage The recommended starting dose of REMERON/REMERONSolTab is 15 mg once daily, administered orally, preferably in the evening prior to sleep. If patients do not have an adequate response to the initial 15 mg dose, increase the dose up to a maximum of 45 mg per day. Dose changes should not be made in intervals of less than 1 to 2 weeks to allow sufficient time for evaluation of response to a given dose.

2.2 Administration of REMERONSolTab

The tablet should remain in the blister pack until the patient is ready to take it. The patient or caregiver should use dry hands to open the blister. As soon as the blister is opened, the tablet should be removed and placed on the patient's tongue. Use REMERONSolTab immediately after removal from its blister; once removed, it cannot be stored. The whole tablet should be placed on the tongue and allowed to disintegrate without chewing or crushing. Do not attempt to split the tablet. The tablet will disintegrate in saliva so that it can be swallowed.

2.3 Screen for

Bipolar Disorder Prior to Starting REMERON/REMERONSolTab Prior to initiating treatment with REMERON/REMERONSolTab or another antidepressant, screen patients for a personal or family history of bipolar disorder, mania, or hypomania.

2.4 Switching

Patients to or from a Monoamine Oxidase Inhibitor Antidepressant At least 14 days must elapse between discontinuation of a monoamine oxidase inhibitor (MAOI) antidepressant and initiation of REMERON/REMERONSolTab. In addition, at least 14 days must elapse after stopping REMERON/REMERONSolTab before starting an MAOI antidepressant.

2.5 Dosage Modifications

Due to Drug Interactions Strong CYP3A Inducers An increase in dosage of REMERON/REMERONSolTab may be needed with concomitant strong CYP3A inducer (e.g., carbamazepine, phenytoin, rifampin) use. Conversely, a decrease in dosage of REMERON/REMERONSolTab may be needed if the CYP3A inducer is discontinued. Strong CYP3A Inhibitors A decrease in dosage of REMERON/REMERONSolTab may be needed with concomitant use of strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin). Conversely, an increase in dosage of REMERON/REMERONSolTab may be needed if the CYP3A4 inhibitor is discontinued. Cimetidine A decrease in dosage of REMERON/REMERONSolTab may be needed with concomitant use of cimetidine. Conversely, an increase in dosage of REMERON/REMERONSolTab may be needed if cimetidine is discontinued.

2.6 Discontinuation of REMERON/REMERONSolTab

Treatment Adverse reactions may occur upon discontinuation or dose reduction of REMERON/REMERONSolTab. Gradually reduce the dosage of REMERON/REMERONSolTab rather than stopping abruptly whenever possible.

Text above is quoted in full from the FDA-approved drug label published by openFDA, effective August 6, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.

This page reproduces regulatory text for reference. It is not medical advice, and KenyRx is not a pharmacy or a prescriber. Talk to a doctor or pharmacist about whether a medicine is right for you.

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