FLUOXETINE 20-EXIR

Capsule Fluoxetine 20mg

Generic Name of ProductBrand NameDosage Form StrengthPharmacologic GroupTherapeutic GroupUnit Per Pack
FluoxetineLorazac®Capsule20 mgSelective serotonin reuptake inhibitorNervous system100

Indications And Usage
  • Major Depressive Disorder
  • Obsessive Compulsive Disorder
  • Bulimia Nervosa
  • Panic Disorder

Lorazac and Olanzapine in Combination: Depressive Episodes Associated with Bipolar I Disorder

Administration

Major Depressive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose.

Pediatric: Treatment should be initiated with a dose of 10 or 20 mg/day. After 1 week at 10 mg/day, the dose should be increased to 20 mg/day.

Obsessive Compulsive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose. The full therapeutic effect may be delayed until 5 weeks of treatment or longer.

Pediatric: In adolescents and higher weight children, treatment should be initiated with a dose of 10 mg/day. After 2 weeks, the dose should be increased to 20 mg/day. Experience with daily doses greater than 20 mg is very minimal, and there is no experience with doses greater than 60 mg.

Bulimia Nervosa:

The recommended dose is 60 mg/day, administered in the morning.

Panic Disorder:

Treatment should be initiated with a dose of 10 mg/day. After one week, the dose should be increased to 20 mg/day.

Contraindications

Monoamine Oxidase Inhibitors, Pimozide, Thioridazine

Precautions

Clinical Worsening and Suicide Risk, Serotonin Syndrome or Neuroleptic Malignant Syndrome (NMS)-Like Reactions, Allergic Reactions and Rash, Screening Patients for Bipolar Disorder and Monitoring for Mania/Hypomania, Seizures, Altered Appetite and Weight, Abnormal Bleeding, Hyponatremia, Anxiety and Insomnia, Use in Patients With Concomitant Illness, Potential for Cognitive and Motor Impairment, Long Elimination Half-Life, Discontinuation of Treatment, Lorazac and Olanzapine in Combination

Adverse Reactions

More common: Hives, itching, or skin rash, inability to sit still, restlessness

Less common: Chills or fever, joint or muscle pain

Pregnancy and lactation

C

Renal and liver Impairment

Renal impairment: Use caution; drug accumulation may occur with severe renal impairment

Hepatic impairment (cirrhosis): Decreased clearance of parent drug and active metabolite (norfluoxetine); lower or less frequent dose recommended

Laboratory Tests
There are no specific laboratory tests recommended.

Indications And Usage
  • Major Depressive Disorder
  • Obsessive Compulsive Disorder
  • Bulimia Nervosa
  • Panic Disorder

Lorazac and Olanzapine in Combination: Depressive Episodes Associated with Bipolar I Disorder

Administration

Major Depressive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose.

Pediatric: Treatment should be initiated with a dose of 10 or 20 mg/day. After 1 week at 10 mg/day, the dose should be increased to 20 mg/day.

Obsessive Compulsive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose. The full therapeutic effect may be delayed until 5 weeks of treatment or longer.

Pediatric: In adolescents and higher weight children, treatment should be initiated with a dose of 10 mg/day. After 2 weeks, the dose should be increased to 20 mg/day. Experience with daily doses greater than 20 mg is very minimal, and there is no experience with doses greater than 60 mg.

Bulimia Nervosa:

The recommended dose is 60 mg/day, administered in the morning.

Panic Disorder:

Treatment should be initiated with a dose of 10 mg/day. After one week, the dose should be increased to 20 mg/day.

Contraindications

Monoamine Oxidase Inhibitors, Pimozide, Thioridazine

Precautions

Clinical Worsening and Suicide Risk, Serotonin Syndrome or Neuroleptic Malignant Syndrome (NMS)-Like Reactions, Allergic Reactions and Rash, Screening Patients for Bipolar Disorder and Monitoring for Mania/Hypomania, Seizures, Altered Appetite and Weight, Abnormal Bleeding, Hyponatremia, Anxiety and Insomnia, Use in Patients With Concomitant Illness, Potential for Cognitive and Motor Impairment, Long Elimination Half-Life, Discontinuation of Treatment, Lorazac and Olanzapine in Combination

Adverse Reactions

More common: Hives, itching, or skin rash, inability to sit still, restlessness

Less common: Chills or fever, joint or muscle pain

Pregnancy and lactation

C

Renal and liver Impairment

Renal impairment: Use caution; drug accumulation may occur with severe renal impairment

Hepatic impairment (cirrhosis): Decreased clearance of parent drug and active metabolite (norfluoxetine); lower or less frequent dose recommended

Laboratory Tests
There are no specific laboratory tests recommended.

Indications And Usage
  • Major Depressive Disorder
  • Obsessive Compulsive Disorder
  • Bulimia Nervosa
  • Panic Disorder

Lorazac and Olanzapine in Combination: Depressive Episodes Associated with Bipolar I Disorder

Administration

Major Depressive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose.

Pediatric: Treatment should be initiated with a dose of 10 or 20 mg/day. After 1 week at 10 mg/day, the dose should be increased to 20 mg/day.

Obsessive Compulsive Disorder:

Adult: A dose of 20 mg/day, administered in the morning, is recommended as the initial dose. The full therapeutic effect may be delayed until 5 weeks of treatment or longer.

Pediatric: In adolescents and higher weight children, treatment should be initiated with a dose of 10 mg/day. After 2 weeks, the dose should be increased to 20 mg/day. Experience with daily doses greater than 20 mg is very minimal, and there is no experience with doses greater than 60 mg.

Bulimia Nervosa:

The recommended dose is 60 mg/day, administered in the morning.

Panic Disorder:

Treatment should be initiated with a dose of 10 mg/day. After one week, the dose should be increased to 20 mg/day.

Contraindications

Monoamine Oxidase Inhibitors, Pimozide, Thioridazine

Precautions

Clinical Worsening and Suicide Risk, Serotonin Syndrome or Neuroleptic Malignant Syndrome (NMS)-Like Reactions, Allergic Reactions and Rash, Screening Patients for Bipolar Disorder and Monitoring for Mania/Hypomania, Seizures, Altered Appetite and Weight, Abnormal Bleeding, Hyponatremia, Anxiety and Insomnia, Use in Patients With Concomitant Illness, Potential for Cognitive and Motor Impairment, Long Elimination Half-Life, Discontinuation of Treatment, Lorazac and Olanzapine in Combination

Adverse Reactions

More common: Hives, itching, or skin rash, inability to sit still, restlessness

Less common: Chills or fever, joint or muscle pain

Pregnancy and lactation

C

Renal and liver Impairment

Renal impairment: Use caution; drug accumulation may occur with severe renal impairment

Hepatic impairment (cirrhosis): Decreased clearance of parent drug and active metabolite (norfluoxetine); lower or less frequent dose recommended

Laboratory Tests
There are no specific laboratory tests recommended.