Reviews Nortriptyline Hydrochloride


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Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008




Nortriptyline Hydrochloride Drug Description
Nortriptyline Hydrochloride
(nortriptyline hydrochloride) Capsules

Suicidality and Antidepressant Drugs
Antidepressants increased the risk compared to placebo of suicidal thinking
and behavior (suicidality) in children, adolescents, and young adults in short
term studies of major depressive disorder (MDD) and other psychiatric disorders.
Anyone considering the use of nortriptyline hydrochloride or any other antidepressant
in a child, adolescent or young adult must balance this risk with the clinical
need. Short term studies did not show an increase in the risk of suicidality
with antidepressants compared to placebo in adults aged 65 an older. Depression
and certain other psychiatric disorders are themselves associated with increases
in the risk of suicide. Patients of all ages who are started on therapy should
be monitored appropriately and observed closely for clinical worsening, suicidality,
or unusual changes in behavior. Families and caregivers should be advised
of the need for close observation and communication with the prescriber. Nortriptyline
hydrochloride is not approved for use in pediatric patients. (See WARNINGS:
Clinical Worsening and Suicide Risk, PRECAUTIONS: INFORMATION
FOR PATIENTS, and PRECAUTIONS:
Pediatric Use)

DRUG DESCRIPTION
Nortriptyline hydrochloride is 1-Propanamine, 3-(10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-ylidene)-N-methyl-,
hydrochloride. The structural formula is represented below:








Nortriptyline Hydrochloride Capsules USP (equivalent to 10 mg, 25 mg, 50 mg
and 75 mg Nortriptyline), for oral administration, contain the following inactive
ingredients: colloidal silicon dioxide, magnesium stearate, pregelatinized starch
and sodium lauryl sulfate. The 10 mg, 25 mg, 50 mg and 75 mg capsule shells
contain: gelatin, methylparaben, propylparaben, sodium lauryl sulfate and titanium
dioxide. They may also contain: benzyl alcohol, butylparaben, edetate calcium
disodium, silicon dioxide or sodium propionate.
The 10 mg, 25 mg and 75 mg capsule shells also contain D&C Yellow No. 10
and FD&C Blue No. 1.Last reviewed on RxList: 4/17/2008





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Other reviews about Nortriptyline Hydrochloride on web:

Nortriptyline Hydrochloride professional patient advice. Specific and up to date information about Nortriptyline Hydrochloride. Complete Nortriptyline Hydrochloride information from Drugs.com


Nortriptyline is a second-generation tricyclic antidepressant (TCA) marketed as the hydrochloride salt under the trade names Sensoval, Aventyl, Pamelor, Norpress, Allegron ... Nortriptyline - Wikipedia, the free encyclopedia


Learn about the prescription medication Nortriptyline Hydrochloride (Nortriptyline Hydrochloride Capsules), drug uses, dosage, side effects, drug interactions, warnings ... Nortriptyline Hydrochloride (Nortriptyline Hydrochloride Capsules ...


Anyone considering the use of nortriptyline hydrochloride or any other antidepressant in a child, adolescent, or young adult must balance this risk with the clinical need. Pamelor (Nortriptyline HCl) Drug Information: Uses, Side Effects ...


Nortriptyline may also be used for other purposes not listed in this medication guide. ... Nortriptyline hydrochloride 10 mg Nortriptyline Information from Drugs.com


nor·trip·ty·line hydrochloride (nôr-tr p t-l n) n. A tricyclic compound used as an antidepressant. nortriptyline hydrochloride [nôrtrip′tilēn] nortriptyline hydrochloride - definition of nortriptyline ...


nortriptyline hydrochloride ... What is online pharmacy? Since about the year 2000, hundreds of pharmacies ... Nortriptyline


Nortriptyline (Aventyl, Pamelor) drug information, dosage, side effects, drug interactions, and warnings. Nortriptyline hydrochloride, brand name drugs include Aventyl nand Pamelor Nortriptyline


Safe use of Nortriptyline hydrochloride during pregnancy and lactation has not been established; therefore, when the drug is administered to pregnant patients, nursing mothers, or ... Nortriptyline FDA


Nortriptyline Hydrochloride Oral solution To return to the main entry click here . What is this medicine? NORTRIPTYLINE (nor TRIP ti leen) is used to Nortriptyline Hydrochloride Oral solution: Information from ...





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