Reviews Tofranil


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Tofranil Drug Description
Tofranil®
(imipramine hydrochloride) Tablets USP (10 mg, 25 mg, and 50 mg)


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 imipramine 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 beyond age 24; there was
a reduction in risk with antidepressants compared to placebo in adults aged
65 and 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 antidepressant 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. Imipramine 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



What are the possible side effects of imipramine (Tofranil, Tofranil-PM)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.
Call...
Read All Potential Side Effects for Tofranil »




Tofranil is supplied in tablet form for oral administration.
Tofranil, imipramine hydrochloride USP, the original tricyclic antidepressant,
is a member of the dibenzazepine group of compounds. It is designated 5-3-(Dimethylamino)propyl-10,11-dihydro-5H-dibenz[b,f]-azepine
monohydrochloride. Its structural formula is:








Imipramine hydrochloride USP is a white to off-white, odorless, or practically
odorless crystalline powder. It is freely soluble in water and in alcohol, soluble
in acetone, and insoluble in ether and in benzene. Inactive Ingredients:
Calcium phosphate, cellulose compounds, docusate sodium, iron oxides, magnesium
stearate, polyethylene glycol, povidone, sodium starch glycolate, sucrose, talc,
and titanium dioxide.Last reviewed on RxList: 12/27/2007




Tofranil Drug Description
Tofranil®
(imipramine hydrochloride) Tablets USP (10 mg, 25 mg, and 50 mg)


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 imipramine 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 beyond age 24; there was
a reduction in risk with antidepressants compared to placebo in adults aged
65 and 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 antidepressant 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. Imipramine 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



What are the possible side effects of imipramine (Tofranil, Tofranil-PM)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.
Call...
Read All Potential Side Effects for Tofranil »




Tofranil is supplied in tablet form for oral administration.
Tofranil, imipramine hydrochloride USP, the original tricyclic antidepressant,
is a member of the dibenzazepine group of compounds. It is designated 5-3-(Dimethylamino)propyl-10,11-dihydro-5H-dibenz[b,f]-azepine
monohydrochloride. Its structural formula is:








Imipramine hydrochloride USP is a white to off-white, odorless, or practically
odorless crystalline powder. It is freely soluble in water and in alcohol, soluble
in acetone, and insoluble in ether and in benzene. Inactive Ingredients:
Calcium phosphate, cellulose compounds, docusate sodium, iron oxides, magnesium
stearate, polyethylene glycol, povidone, sodium starch glycolate, sucrose, talc,
and titanium dioxide.Last reviewed on RxList: 12/27/2007




Tofranil Drug Description
Tofranil®
(imipramine hydrochloride) Tablets USP (10 mg, 25 mg, and 50 mg)


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 imipramine 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 beyond age 24; there was
a reduction in risk with antidepressants compared to placebo in adults aged
65 and 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 antidepressant 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. Imipramine 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



What are the possible side effects of imipramine (Tofranil, Tofranil-PM)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.
Call...
Read All Potential Side Effects for Tofranil »




Tofranil is supplied in tablet form for oral administration.
Tofranil, imipramine hydrochloride USP, the original tricyclic antidepressant,
is a member of the dibenzazepine group of compounds. It is designated 5-3-(Dimethylamino)propyl-10,11-dihydro-5H-dibenz[b,f]-azepine
monohydrochloride. Its structural formula is:








Imipramine hydrochloride USP is a white to off-white, odorless, or practically
odorless crystalline powder. It is freely soluble in water and in alcohol, soluble
in acetone, and insoluble in ether and in benzene. Inactive Ingredients:
Calcium phosphate, cellulose compounds, docusate sodium, iron oxides, magnesium
stearate, polyethylene glycol, povidone, sodium starch glycolate, sucrose, talc,
and titanium dioxide.Last reviewed on RxList: 12/27/2007




Tofranil Drug Description
Tofranil®
(imipramine hydrochloride) Tablets USP (10 mg, 25 mg, and 50 mg)


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 imipramine 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 beyond age 24; there was
a reduction in risk with antidepressants compared to placebo in adults aged
65 and 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 antidepressant 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. Imipramine 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



What are the possible side effects of imipramine (Tofranil, Tofranil-PM)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.
Call...
Read All Potential Side Effects for Tofranil »




Tofranil is supplied in tablet form for oral administration.
Tofranil, imipramine hydrochloride USP, the original tricyclic antidepressant,
is a member of the dibenzazepine group of compounds. It is designated 5-3-(Dimethylamino)propyl-10,11-dihydro-5H-dibenz[b,f]-azepine
monohydrochloride. Its structural formula is:








Imipramine hydrochloride USP is a white to off-white, odorless, or practically
odorless crystalline powder. It is freely soluble in water and in alcohol, soluble
in acetone, and insoluble in ether and in benzene. Inactive Ingredients:
Calcium phosphate, cellulose compounds, docusate sodium, iron oxides, magnesium
stearate, polyethylene glycol, povidone, sodium starch glycolate, sucrose, talc,
and titanium dioxide.Last reviewed on RxList: 12/27/2007




Tofranil Drug Description
Tofranil®
(imipramine hydrochloride) Tablets USP (10 mg, 25 mg, and 50 mg)


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 imipramine 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 beyond age 24; there was
a reduction in risk with antidepressants compared to placebo in adults aged
65 and 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 antidepressant 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. Imipramine 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



What are the possible side effects of imipramine (Tofranil, Tofranil-PM)?

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.
Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, anxiety, panic attacks, trouble sleeping, or if you feel impulsive, irritable, agitated, hostile, aggressive, restless, hyperactive (mentally or physically), more depressed, or have thoughts about suicide or hurting yourself.
Call...
Read All Potential Side Effects for Tofranil »




Tofranil is supplied in tablet form for oral administration.
Tofranil, imipramine hydrochloride USP, the original tricyclic antidepressant,
is a member of the dibenzazepine group of compounds. It is designated 5-3-(Dimethylamino)propyl-10,11-dihydro-5H-dibenz[b,f]-azepine
monohydrochloride. Its structural formula is:








Imipramine hydrochloride USP is a white to off-white, odorless, or practically
odorless crystalline powder. It is freely soluble in water and in alcohol, soluble
in acetone, and insoluble in ether and in benzene. Inactive Ingredients:
Calcium phosphate, cellulose compounds, docusate sodium, iron oxides, magnesium
stearate, polyethylene glycol, povidone, sodium starch glycolate, sucrose, talc,
and titanium dioxide.Last reviewed on RxList: 12/27/2007





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Other reviews about Tofranil on web:

Learn about the prescription medication Tofranil (Imipramine), drug uses, dosage, side effects, drug interactions, warnings, reviews and patient labeling. Tofranil (Imipramine) Drug Information: Uses, Side Effects, Drug ...


Tofranil information from Drugs.com. Tofranil is used to treat depression. It is a member of the family of drugs called tricyclic antidepressants. Tofranil is also used on a short ... Tofranil patient advice including side effects


Imipramine (sold as Antideprin, Deprimin, Deprinol, Depsonil, Dynaprin, Eupramin, Imipramil, Irmin, Janimine, Melipramin, Surplix, Tofranil), also known as melipramine, is an ... Imipramine - Wikipedia, the free encyclopedia


Tofranil-PM™ 75 mg Coral Body/Coral Cap Coral body imprinted in black with 'M' and coral cap imprinted in black 'Tofranil-PM 75 mg' Covidien Pharmaceuticals - Tofranil-PM™ 75 mg


All about Tofranil Tablets. View complete and up to date Tofranil information - part of the Drugs.com trusted medication database. Tofranil Tablets Facts and Comparisons at Drugs.com


Learn about the prescription medication Tofranil-PM (Imipramine Pamoate), drug uses, dosage, side effects, drug interactions, warnings, reviews and patient labeling. Tofranil-PM (Imipramine Pamoate) Drug Information: Uses, Side ...


Tofranil side effects, dosage, and drug interactions. All accurate, up-to-date information is written for the consumer by healthcare professionals. Tofranil Oral Uses and How to Use


Find patient medical information for Tofranil Oral on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings. Tofranil Oral : Uses, Side Effects, Interactions, Pictures ...


Learn about Tofranil from the publishers of the Physicians Desk Reference. Find prescription drug information resources including interactions, side effects, symptoms, treatment ... Tofranil | Prescription Drug Information, Side Effects | PDRHealth


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