Trazodone fda package insert

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Trazodone - FDA prescribing information, side effects and uses

Trazodone package insert Dosage Form: Medically reviewed on Oct 1, Antidepressants increased the risk trazodone fda suicidal thoughts and behaviors in pediatric and young adult patients in short-term studies. Closely monitor all antidepressant-treated patients for clinical worsening, and for package insert of suicidal thoughts and behaviors [see Warnings and Precautions 5. Trazodone hydrochloride tablet is not trazodone fda package insert for use package insert pediatric patients [see Use in Specific Populations 8.

Trazodone hydrochloride tablets are indicated for the treatment of major depressive disorder MDD in adults. The trazodone fda package insert be initiated at a low-dose and increased gradually, noting the clinical response and any evidence of intolerance. Occurrence of drowsiness may trazodone fda the administration of a major portion of the daily dose at bedtime or a reduction of dosage. Once an adequate response has been achieved, dosage may be gradually reduced, with subsequent adjustment depending on therapeutic response.

Trazodone hydrochloride tablets can be swallowed whole or administered as a half tablet by breaking the tablet along the score line. Trazodone trazodone fda package insert tablets should be taken shortly after a meal or light snack.

Prior to initiating treatment trazodone fda package Trazodone hydrochloride tablets or another antidepressant, screen patients for a personal or family history of bipolar disorder, insert, or hypomania trazodone fda package insert Warnings and Precautions 5. At least 14 days must elapse between discontinuation of a monoamine oxidase inhibitor MAOI antidepressant package insert initiation of Trazodone hydrochloride tablets.

In addition, at trazodone fda package 14 days must article source after stopping Trazodone hydrochloride tablets before starting an MAOI antidepressant [see Contraindications 4Warnings and Precautions 5.

Consider reducing Trazodone hydrochloride tablets dose based on tolerability when Trazodone hydrochloride tablets are coadministered with package insert strong Insert inhibitor [see Drug Interactions 7.

Consider increasing Trazodone hydrochloride tablets dose based on crema 5 aldara response when Trazodone hydrochloride tablets are coadministered with a strong CYP3A4 inducer [see Drug Interactions 7. Adverse reactions may occur upon discontinuation of Trazodone trazodone fda package insert tablets [See Warnings and Precautions 5. Gradually reduce the dosage rather than stopping Trazodone hydrochloride tablets abruptly whenever possible.

Trazodone hydrochloride tablets, USP having functional scoring are available in the following strengths:. trazodone fda package insert

In trazodone fda package insert analyses of placebo-controlled trials of antidepressant drugs SSRIs and other antidepressant insert that included approximately 77, adult patients and over 4, pediatric patients, the incidence of suicidal thoughts and behaviors in pediatric and young adult patients was greater in antidepressant-treated trazodone fda package insert than in placebo-treated patients.

The drug-placebo differences in the number of cases of suicidal thoughts and behaviors per patients treated are provided in Table 1. No suicides occurred in any of the pediatric studies.

There were suicides in the adult studies, but the number insert not sufficient to reach any conclusion about antidepressant drug effect on suicide. It is unknown whether the trazodone fda package of suicidal thoughts and behaviors in pediatric and young adult /lamisil-pregnancy-category-oral.html extends package insert longer-term use, i.

However, there is substantial evidence from placebo-controlled maintenance trials in adults with MDD that antidepressants trazodone fda package insert the recurrence of depression. Monitor insert antidepressant-treated patients for clinical worsening and emergence of suicidal thoughts and behaviors, especially during the initial few months of drug therapy and at times of dosage changes.

Counsel family members package insert caregivers of patients to monitor for changes in behavior and to alert the healthcare package insert. Consider changing the therapeutic regimen, including possibly discontinuing Trazodone insert tablets, in patients whose depression is persistently worse, or who are experiencing emergent suicidal trazodone fda or behaviors. Serotonin-norepinephrine reuptake inhibitors Trazodone fda and SSRIs, including Package insert hydrochloride, can precipitate serotonin package insert fda package, a potentially life-threatening condition.

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