FLUOXETINE HYDROCHLORIDE

REMEDYREPACK INC.

HIGHLIGHTS OF PRESCRIBING INFORMATIONHIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use fluoxetine safely and effectively. See full prescribing information for fluoxetine capsules. Fluoxetine Capsules, USP for Oral Use Initial U.S. Approval: 1987 BOXED WARNING WARNING: SUICIDALITY AND ANTIDEPRESSANT DRUGS See full prescribing information for complete boxed warning.   Increased risk of suicidal thinking and behavior in children, adolescents, and young adults taking antidepressants for Major Depressive Disorder (MDD) and other psychiatric disorders (5.1).   When using fluoxetine and olanzapine in combination, also refer to Boxed Warning section of the package insert for Symbyax. INDICATIONS AND USAGEFluoxetine capsules are a selective serotonin reuptake inhibitor indicated for: Acute and maintenance treatment of Major Depressive Disorder (MDD) in adult and pediatric patients aged 8 to 18 years (1.1) Acute and maintenance treatment of Obsessive Compulsive Disorder (OCD) in adult and pediatric patients aged 7 to 17 years (1.2) Acute and maintenance treatment of Bulimia Nervosa in adult patients (1.3) Acute treatment of Panic Disorder, with or without agoraphobia, in adult patients (1.4) Fluoxetine capsules and olanzapine in combination for: Acute treatment of Depressive Episodes Associated with Bipolar I Disorder in adults (1.5) DOSAGE AND ADMINISTRATION Indication Adult Pediatric    MDD (2.1)    20 mg/day in am (initial dose)    10 to 20 mg/day (initial dose)    OCD (2.2)    20 mg/day in am (initial dose)    10 mg/day (initial dose)    Bulimia Nervosa (2.3)    60 mg/day in am    -    Panic Disorder (2.4)    10 mg/day (initial dose)    -    Depressive Episodes   Associated with Bipolar I Disorder   (2.5)    Oral in combination with olanzapine: 5 mg of oral   olanzapine and 20 mg of fluoxetine once daily (initial dose)    - Consider tapering the dose of fluoxetine for pregnant women during the third trimester (2.7) A lower or less frequent dosage should be used in patients with hepatic impairment, the elderly, and for patients with concurrent disease or on multiple concomitant medications (2.7) Fluoxetine capsules and olanzapine in combination:   Dosage adjustments, if indicated, should be made with the individual components according to efficacy and tolerability (2.5) Fluoxetine monotherapy is not indicated for the treatment of Depressive Episodes associated with Bipolar I Disorder (2.5) Safety of the coadministration of doses above 18 mg olanzapine with 75 mg fluoxetine has not been evaluated (2.5)  DOSAGE FORMS AND STRENGTHS Capsules: 10 mg, 20 mg, and 40 mg (3) CONTRAINDICATIONS Do not use with an MAOI or within 14 days of discontinuing an MAOI due to risk of drug interaction. At least 5 weeks should be allowed after stopping fluoxetine capsules before treatment with an MAOI (4, 7.1) Do not use with pimozide due to risk of drug interaction or QTc prolongation (4, 7.9) Do not use with thioridazine due to QTc interval prolongation or potential for elevated thioridazine plasma levels. Do not use thioridazine within 5 weeks of discontinuing fluoxetine capsules  (4, 7.9) When using fluoxetine capsules and olanzapine in combination, also refer to the Contraindications section of the package insert for Symbyax (4) WARNINGS AND PRECAUTIONS Clinical Worsening and Suicide Risk: Monitor for clinical worsening and suicidal thinking and behavior (5.1) Serotonin Syndrome or Neuroleptic Malignant Syndrome (NMS)-like Reactions: Have been reported with fluoxetine. Discontinue fluoxetine and initiate supportive treatment (5.2) Allergic Reactions and Rash: Discontinue upon appearance of rash or allergic phenomena (5.3) Activation of Mania/Hypomania: Screen for Bipolar Disorder and monitor for mania/hypomania (5.4) Seizures: Use cautiously in patients with a history of seizures or with conditions that potentially lower the seizure threshold (5.5) Altered Appetite and Weight: Significant weight loss has occurred (5.6) Abnormal Bleeding: May increase the risk of bleeding. Use with NSAIDs, aspirin, warfarin, or drugs that affect coagulation may potentiate the risk of gastrointestinal or other bleeding (5.7) Hyponatremia: Has been reported with fluoxetine in association with syndrome of inappropriate antidiuretic hormone (SIADH) (5.8) Anxiety and Insomnia: May occur (5.9) Potential for Cognitive and Motor Impairment: Has potential to impair judgment, thinking, and motor skills. Use caution when operating machinery (5.11) Long Half-Life: Changes in dose will not be fully reflected in plasma for several weeks (5.12) Fluoxetine and Olanzapine in Combination: When using fluoxetine and olanzapine in combination, also refer to the Warnings and Precautions section of the package insert for Symbyax (5.14) Side Effects Most common adverse reactions (≥5% and at least twice that for placebo) associated with: Major Depressive Disorder, Obsessive Compulsive Disorder, Bulimia, and Panic Disorder: abnormal dreams, abnormal ejaculation, anorexia, anxiety, asthenia, diarrhea, dry mouth, dyspepsia, flu syndrome, impotence, insomnia, libido decreased, nausea, nervousness, pharyngitis, rash, sinusitis, somnolence, sweating, tremor, vasodilatation, and yawn (6.1) Fluoxetine and olanzapine in combination - Also refer to the Adverse Reactions section of the package insert for Symbyax (6)  To report SUSPECTED ADVERSE REACTIONS, contact Aurobindo Pharma USA, Inc. at 1-866-850-2876 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. DRUG INTERACTIONS Monoamine Oxidase Inhibitors (MAOI): Fluoxetine is contraindicated for use with MAOI’s, or within 14 days of discontinuing an MAOI due to risk of drug interaction. At least 5 weeks should be allowed after stopping fluoxetine before starting treatment with an MAOI (4, 7.1) Pimozide: Fluoxetine is contraindicated for use with pimozide due to risk of drug interaction or QTc prolongation (4, 7.9) Thioridazine: Fluoxetine is contraindicated for use with thioridazine due to QTc interval prolongation or potential for elevated thioridazine plasma levels. Do not use thioridazine within 5 weeks of discontinuing fluoxetine (4, 7.9) Drugs Metabolized by CYP2D6: Fluoxetine is a potent inhibitor of CYP2D6 enzyme pathway (7.9) Tricyclic Antidepressants (TCAs): Monitor TCA levels during coadministration with fluoxetine or when fluoxetine has been recently discontinued (7.9) CNS Acting Drugs: Caution should be used when taken in combination with other centrally acting drugs (7.2) Benzodiazepines: Diazepam - increased t½, alprazolam – further psychomotor performance decrement due to increased levels (7.9) Antipsycotics: Potential for elevation of haloperidol and clozapine levels (7.9) Anticonvulsants: Potential for elevated phenytoin and carbamazepine levels and clinical anticonvulsant toxicity (7.9) Serotonergic Drugs: Potential for Serotonin Syndrome (5.2, 7.3) Triptans: There have been rare postmarketing reports of Serotonin Syndrome with use of an SSRI and a triptan (5.2, 7.4) Tryptophan: Concomitant use with tryptophan is not recommended (5.2, 7.5) Drugs that Interfere with Hemostasis (e.g., NSAIDs, Aspirin, Warfarin): May potentiate the risk of bleeding (7.6) Drugs Tightly Bound to Plasma Proteins: May cause a shift in plasma concentrations (7.8, 7.9) Olanzapine: When used in combination with fluoxetine, also refer to the Drug Interactions section of the package insert for Symbyax (7.9) USE IN SPECIFIC POPULATIONS Pregnancy: Fluoxetine should be used during pregnancy only if the potential benefit justifies the potential risks to the fetus (8.1) Nursing Mothers: Breast feeding is not recommended (8.3) Pediatric Use: Safety and effectiveness of fluoxetine and olanzapine in combination have not been established in patients less than 18 years of age (8.4) Hepatic Impairment: Lower or less frequent dosing may be appropriate in patients with cirrhosis (8.6) See 17 for PATIENT COUNSELING INFORMATION and the FDA-approved Medication Guide

FULL PRESCRIBING INFORMATION: CONTENTS*

• BOXED WARNING
• INDICATIONS & USAGE
• DOSAGE & ADMINISTRATION
• DOSAGE FORMS & STRENGTHS
• FLUOXETINE HYDROCHLORIDE CONTRAINDICATIONS
• WARNINGS AND PRECAUTIONS
• FLUOXETINE HYDROCHLORIDE ADVERSE REACTIONS
• DRUG INTERACTIONS
• USE IN SPECIFIC POPULATIONS
• DRUG ABUSE AND DEPENDENCE
• OVERDOSAGE
• FLUOXETINE HYDROCHLORIDE DESCRIPTION
• CLINICAL PHARMACOLOGY
• NONCLINICAL TOXICOLOGY
• CLINICAL STUDIES
• HOW SUPPLIED
• PATIENT COUNSELING INFORMATION
• MEDICATION GUIDE
• PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION
• PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FULL PRESCRIBING INFORMATION

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

DOSAGE FORMS & STRENGTHS

FLUOXETINE HYDROCHLORIDE CONTRAINDICATIONS

When using fluoxetine capsules and olanzapine in combination, also refer to the Contraindications section of the package insert for Symbyax.
 

• Monoamine Oxidase Inhibitors [see Drug Interactions (7.1)]
• Pimozide [see Drug Interactions (7.9)]
• Thioridazine [see Drug Interactions (7.9)]

WARNINGS AND PRECAUTIONS

When using Fluoxetine and olanzapine in combination, also refer to the Warnings and Precautions section of the package insert for Symbyax.

Table 2: Suicidality per 1000 Patients Treated

Age Range	Drug-Placebo Difference in Number of Cases of Suicidality per 1000 Patients Treated
	Increases Compared to Placebo
greater then 18	14 additional cases
18-24	5 additional cases
	Decreases Compared to Placebo
25-64	1 fewer case
less then65	6 fewer cases

All patients being treated with antidepressants for any indication should be monitored appropriately and observed closely for clinical worsening, suicidality, and unusual changes in behavior, especially during the initial few months of a course of drug therapy, or at times of dose changes, either increases or decreases.





[see Warnings and Precautions (5.13)]

Families and caregivers of patients being treated with antidepressants for Major Depressive Disorder or other indications, both psychiatric and nonpsychiatric, should be alerted about the need to monitor patients for the emergence of agitation, irritability, unusual changes in behavior, and the other symptoms described above, as well as the emergence of suicidality, and to report such symptoms immediately to health care providers. Such monitoring should include daily observation by families and caregivers.




 SSRIs alone, including fluoxetine treatment, but particularly with concomitant use of serotonergic drugs (including triptans) with drugs which impair metabolism of

 The concomitant use of [see Contraindications (4) and Drug Interactions (7.1)]

 If concomitant treatment of fluoxetine [see Drug Interactions (7.4)]

 The concomitant use of fluoxetine with serotonin [see Drug Interactions (7.3) ]

 Treatment with fluoxetine and any concomitant serotonergic











[see Warnings and Precautions section of the package insert for Symbyax]

[see Use in Specific Populations (8.4)]

[see Use in Specific Populations (8.4)]



[see Use in Specific Populations (8.4)]

[see Use in Specific Populations (8.4) ]


[see Drug Interactions (7.6)]
[see Use in Specific Populations (8.5)]








[see Table 5]


Cardiovascular

Glycemic Control

[see Clinical Pharmacology (12.3)]

When using fluoxetine and olanzapine in combination, also refer to the Warnings and Precautions section of the package insert for Symbyax.

FLUOXETINE HYDROCHLORIDE ADVERSE REACTIONS

When using fluoxetine and olanzapine in combination, also refer to the Adverse Reactions section of the package insert for Symbyax.








Incidence in Major Depressive Disorder, OCD, bulimia, and Panic Disorder placebo-controlled clinical trials (excluding data from extensions of trials)

Table 3: Most Common Treatment-Emergent Adverse Reactions: Incidence in Major Depressive Disorder, OCD, Bulimia, and Panic Disorder Placebo-Controlled Clinical Trials^1,2

	Percentage of Patients Reporting Event
	Major Depressive Disorder		OCD		Bulimia		Panic Disorder
Body System/ Adverse Reaction	Fluoxetine (N=1728)	Placebo (N=975)	Fluoxetine (N=266)	Placebo (N=89)	Fluoxetine (N=450)	Placebo (N=267)	Fluoxetine (N=425)	Placebo (N=342)
Body as a Whole
Asthenia	9	5	15	11	21	9	7	7
Flu syndrome	3	4	10	7	8	3	5	5
Cardiovascular System
Vasodilatation	3	2	5	--	2	1	1	--
Digestive System
Nausea	21	9	26	13	29	11	12	7
Diarrhea	12	8	18	13	8	6	9	4
Anorexia	11	2	17	10	8	4	4	1
Dry mouth	10	7	12	3	9	6	4	4
Dyspepsia	7	5	10	4	10	6	6	2
Nervous System
Insomnia	16	9	28	22	33	13	10	7
Anxiety	12	7	14	7	15	9	6	2
Nervousness	14	9	14	15	11	5	8	6
Somnolence	13	6	17	7	13	5	5	2
Tremor	10	3	9	1	13	1	3	1
Libido decreased	3	--	11	2	5	1	1	2
Abnormal dreams	1	1	5	2	5	3	1	1
Respiratory System
Pharyngitis	3	3	11	9	10	5	3	3
Sinusitis	1	4	5	2	6	4	2	3
Yawn	--	--	7	--	11	--	1	--
Skin and Appendages
Sweating	8	3	7	--	8	3	2	2
Rash	4	3	6	3	4	4	2	2
Urogenital System
Impotence3	2	--	--	--	7	--	1	--
Abnormal ejaculation3	--	--	7	--	7	--	2	1

Table 4: Treatment-Emergent Adverse Reactions: Incidence in Major Depressive Disorder, OCD, Bulimia, and Panic Disorder Placebo-Controlled Clinical Trials^{1, 2}

	Percentage of Patients Reporting Event
	Major Depressive Disorder, OCD, Bulimia, and Panic Disorder Combined
Body System/Adverse Reaction	Fluoxetine (N=2869)	Placebo (N=1673)
Body as a Whole
Headache	21	19
Asthenia	11	6
Flu syndrome	5	4
Fever	2	1
Cardiovascular System
Vasodilatation	2	1
Digestive System
Nausea	22	9
Diarrhea	11	7
Anorexia	10	3
Dry mouth	9	6
Dyspepsia	8	4
Constipation	5	4
Flatulence	3	2
Vomiting	3	2
Metabolic and Nutritional Disorders
Weight loss	2	1
Nervous System
Insomnia	19	10
Nervousness	13	8
Anxiety	12	6
Somnolence	12	5
Dizziness	9	6
Tremor	9	2
Libido decreased	4	1
Thinking abnormal	2	1
Respiratory System
Yawn	3	--
Skin and Appendages
Sweating	7	3
Rash	4	3
Pruritus	3	2
Special Senses
Abnormal vision	2	1

Associated with discontinuation in Major Depressive Disorder, OCD, bulimia, and Panic Disorder placebo-controlled clinical trials (excluding data from extensions of trials)

Table 5: Most Common Adverse Reactions Associated with Discontinuation in Major Depressive Disorder, OCD, Bulimia, and Panic Disorder Placebo-Controlled Clinical Trials¹

Major Depressive Disorder, OCD, Bulimia, and Panic Disorder Combined (N=1533)	Major Depressive Disorder (N=392)	OCD (N=266)	Bulimia (N=450)	Panic Disorder (N=425)
Anxiety (1%)	--	Anxiety (2%)	--	Anxiety (2%)
--	--	--	Insomnia (2%)	--
--	Nervousness (1%)	--	--	Nervousness (1%)
--	--	Rash (1%)	--	--

Other adverse reactions in pediatric patients (children and adolescents)



Male and female sexual dysfunction with SSRIs










Body as a Whole Frequent: Infrequent: Rare:

Cardiovascular System Frequent: Infrequent:

Digestive System Infrequent: Rare:

Hemic and Lymphatic System Infrequent: Rare:

Nervous System Frequent: Infrequent: Rare:

Respiratory System Rare:

Skin and Appendages Rare:

Special Senses Frequent: Infrequent:


^1111111

¹ These terms represent serious adverse events, but do not meet the definition for adverse drug reactions. They are included here because of their seriousness.

DRUG INTERACTIONS

[see Contraindications (4)][see Clinical Pharmacology (12.3)]
[see Clinical Pharmacology (12.3)]
[see Warnings and Precautions (5.2)][see Drug Interactions (7.4), (7.5)]
[see Warnings and Precautions (5.2) and Drug Interactions (7.3)]
[see Warnings and Precautions (5.2) and Drug Interactions (7.3)]
[see Warnings and Precautions (5.7)]

Drugs Tightly Bound to Plasma Proteins [see Clinical Pharmacology (12.3)]
Pimozide —_cc[see Contraindications (4)]

Thioridazine —[see Contraindications (4)]

<sub>max

c</sub>

Drugs Metabolized by CYP2D6 —[see Contraindications (4)]

Tricyclic Antidepressants (TCAs) — [see Clinical Pharmacology (12.3)]

Benzodiazapines — [see Clinical Pharmacology (12.3)]

Antipsychotics — [see Contraindications (4)]

Anticonvulsants —

Lithium —

Drugs Tightly Bound to Plasma Proteins — [see Clinical Pharmacology (12.3)]

Drugs Metabolized by CYP3A4 — in vivo

in vitro

Olanzapine —

When using fluoxetine and olanzapine and in combination, also refer to the Drug Interactions section of the package insert for Symbyax.

USE IN SPECIFIC POPULATIONS

When using fluoxetine and olanzapine in combination, also refer to the Use in Specific Populations section of the package insert for Symbyax.

Pregnancy Category C — ²²²²

Treatment of Pregnant Women During the Third Trimester








[see Clinical Studies (14.1)]

[see Clinical Studies (14.2) ]



[see Clinical Pharmacology (12.3)]

[see Adverse Reactions (6.1)]



[see Warnings and Precautions (5.6)]

[see Box Warning and Warnings and Precautions (5.1)]





<sup>2

2</sup>


[see Clinical Studies (14.1)][see Clinical Pharmacology (12.4)][see Warnings and Precautions (5.8)]


[see Dosage and Administration (2.7) and Clinical Pharmacology (12.4)].

DRUG ABUSE AND DEPENDENCE

OVERDOSAGE

[see Overdosage (10.3)]






[see Drug Interactions (7.9)]



Physicians’ Desk Reference (PDR)

FLUOXETINE HYDROCHLORIDE DESCRIPTION

CLINICAL PHARMACOLOGY

₁in vitro
Systemic Bioavailability



Protein Binding in vitro₁

EnantiomersRSS

MetabolismSRSR

Variability in MetabolismSSSR

[see Drug Interactions (7.9)]

Accumulation and Slow Elimination [see Warnings and Precautions (5.12)]


Liver Disease [see Dosage and Administration (2.7), Use in Specific Populations (8.6)]

Renal Disease

Geriatric Pharmacokinetics

Pediatric Pharmacokinetics (children and adolescents)

NONCLINICAL TOXICOLOGY

Carcinogenicity ²

Mutagenicity in vivo

Impairment of Fertility ²[see Use in Specific Populations (8.4)].

CLINICAL STUDIES

When using fluoxetine and olanzapine in combination, also refer to the Clinical Studies section of the package insert for Symbyax.

Daily Dosing
 
Adult — .





Pediatric (children and adolescents) —




Adult

Table 6: Outcome Classification (%) on CGI Improvement Scale for Completers in Pool of Two OCD Studies

		Fluoxetine
Outcome Classification	Placebo	20 mg	40 mg	60 mg
Worse	8%	0%	0%	0%
No change	64%	41%	33%	29%
Minimally improved	17%	23%	28%	24%
Much improved	8%	28%	27%	28%
Very much improved	3%	8%	12%	19%

Pediatric (children and adolescents)

HOW SUPPLIED

Fluoxetine Capsules USP, 10 mg*





Fluoxetine Capsules USP, 20 mg*





Fluoxetine Capsules USP, 40 mg*







Store at

PATIENT COUNSELING INFORMATION

See the FDA-approved Medication Guide.











When using fluoxetine and olanzapine in combination, also refer to the Medication Guide for Symbyax.
[see Box Warning and Warnings and Precautions (5.1)].
[see Warnings and Precautions (5.2) and Drug Interactions (7.3)].


[see Warnings and Precautions (5.3)].
[see Warnings and Precautions (5.7) and Drug Interactions (7.6)].
[see Warnings and Precautions (5.8)].
[see Warnings and Precautions (5.11)].

[see Warnings and Precautions (5.13)]
Pregnancy [see Use in Specific Populations (8.1) ]

Nursing Mothers [see Use in Specific Populations (8.3)]

Pediatric Use [see Box Warning and Warnings and Precautions (5.1) ][see Warnings and Precautions (5.6) and Use in Specific Populations (8.4)]

MEDICATION GUIDE

Fluoxetine Capsules, USP



What is the most important information I should know about fluoxetine capsules?

Antidepressant medicines, depression and other serious mental illnesses, and suicidal thoughts or actions:

Talk to your, or your family member’s, healthcare provider about:

• all risks and benefits of treatment with antidepressant medicines
• all treatment choices for depression or other serious mental illness

• Antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, and young adults within the first few months of treatment.
• Depression and other serious mental illnesses are the most important causes of suicidal thoughts and actions. Some people may have a particularly high risk of having suicidal thoughts or actions. These include people who have (or have a family history of) bipolar illness (also called manic-depressive illness) or suicidal thoughts or actions.
• How can I watch for and try to prevent suicidal thoughts and actions in myself or a family member?

• Pay close attention to any changes, especially sudden changes, in mood, behaviors, thoughts, or feelings. This is very important when an antidepressant medicine is started or when the dose is changed.
• Call the healthcare provider right away to report new or sudden changes in mood, behavior, thoughts, or feelings.
• Keep all follow-up visits with the healthcare provider as scheduled. Call the healthcare provider between visits as needed, especially if you have concerns about symptoms.  

Call a healthcare provider right away if you or your family member has any of the following symptoms, especially if they are new, worse, or worry you:

• thoughts about suicide or dying
• attempts to commit suicide
• new or worse depression
• new or worse anxiety
• feeling very agitated or restless
• panic attacks
• trouble sleeping (insomnia)
• new or worse irritability
• acting aggressive, being angry, or violent
• acting on dangerous impulses
• an extreme increase in activity and talking (mania)
• or other unusual changes in behavior or mood

What else do I need to know about antidepressant medicines?

• Never stop an antidepressant medicine without first talking to a healthcare provider. Stopping an antidepressant medicine suddenly can cause other symptoms.
• Antidepressants are medicines used to treat depression and other illnesses. It is important to discuss all the risks of treating depression and also the risks of not treating it. Patients and their families or other caregivers should discuss all treatment choices with the healthcare provider, not just the use of antidepressants.
• Antidepressant medicines have other side effects. Talk to the healthcare provider about the side effects of the medicine prescribed for you or your family member.
• Antidepressant medicines can interact with other medicines. Know all of the medicines that you or your family member takes.Keep a list of all medicines to show the healthcare provider. Do not start new medicines without first checking with your healthcare provider.
• Not all antidepressant medicines prescribed for children are FDA approved for use in children. Talk to your child’s healthcare provider for more information.

What are fluoxetine capsules?

• for short and long-term treatment of depression in adults and children over the age of 8.
• for short and long-term treatment of Obsessive Compulsive Disorder (OCD) in adults and children over the age of 7.
• for short and long-term treatment of Bulimia Nervosa in adults.
• for short-term treatment of Panic Disorder, with or without agoraphobia, in adults.
• with the medicine olanzapine (Zyprexa^{), for the short-term treatment of episodes of depression that happen with Bipolar I Disorder.}

Who should not take fluoxetine capsules?

• Do not take fluoxetine capsules if you take a Monoamine Oxidase Inhibitor (MAOI) or if you stopped taking an MAOI in the last 2 weeks.
• Do not take an MAOI within 5 weeks of stopping fluoxetine capsules. People who take fluoxetine capsules close in time to an MAOI can have serious and life-threatening side effects, with symptoms including:
  • high fever
  • continued muscle spasms that you can not control
  • rigid muscles
  • changes in heart rate and blood pressure that happen fast
  • confusion
  • unconsciousness

• Do not take fluoxetine capsules if you take Mellaril ^{(thioridazine). Do not take Mellaril within 5 weeks of stopping fluoxetine capsules. Mellaril can cause serious heart rhythm problems and you could die suddenly.}
• Do not take fluoxetine capsules if you take the antipsychotic medicine pimozide (Orap^).

What should I tell my doctor before taking fluoxetine capsules?

• seizures (convulsions)
• bipolar disorder (mania)
• are pregnant or plan to become pregnant. It is not known if fluoxetine capsules will harm your unborn baby.
• are breast-feeding or plan to breast-feed. Fluoxetine can pass into your breast milk and may harm your baby. You should not breast-feed while taking fluoxetine capsules. Talk to your doctor about the best way to feed your baby if you take fluoxetine capsules.

Tell your doctor about all the medicines that you take,

If you take fluoxetine capsules, you should not take any other medicines that contain fluoxetine hydrochloride:

• Symbyax
• Sarafem

How should I take fluoxetine capsules?

• Take fluoxetine capsules exactly as prescribed. Your doctor may need to change (adjust) the dose of fluoxetine capsules until it is right for you.
• If you miss a dose of fluoxetine capsules, take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take your next dose at the regular time. Do not take two doses of fluoxetine capsules at the same time.
• To prevent serious side effects, do not stop taking fluoxetine capsules suddenly. If you need to stop taking fluoxetine capsules, your doctor can tell you how to safely stop taking them.
• If you take too much fluoxetine capsules, call your doctor or poison control center right away, or get emergency treatment.
• Fluoxetine capsules can be taken with or without food.
• Fluoxetine capsules are usually taken once a day, depending on how your doctor prescribes your medicine.
• If you do not think you are getting better or have any concerns about your condition while taking fluoxetine capsules, call your doctor.

What should I avoid while taking fluoxetine capsules?

• Fluoxetine capsules can cause sleepiness and may affect your ability to make decisions, think clearly, or react quickly. You should not drive, operate heavy machinery, or do other dangerous activities until you know how fluoxetine capsules affect you.

What are the possible side effects of fluoxetine capsules?

Fluoxetine capsules may be associated with the following serious risks:

• Serotonin Syndrome: This is a condition that can be life threatening. Call your doctor right away if you become severely ill and have some or all of these symptoms:
  • agitation
  • hallucinations
  • problems with coordination
  • racing heart beat
  • over-active reflexes
  • fever
  • nausea, vomiting, and diarrhea
• Severe allergic reactions: Tell your doctor right away if you get red itchy welts (hives) or, a rash alone or with fever and joint pain, while taking fluoxetine capsules. Call your doctor right away if you become severely ill and have some or all of these symptoms:
  • swelling of your face, eyes, or mouth
  • trouble breathing
• Abnormal bleeding: Tell your doctor if you notice any increased or unusual bruising or bleeding while taking fluoxetine capsules, especially if you take one of these medicines:
  • the blood thinner warfarin (Coumadin Jantoven⁾
  • a non-steroidal anti-inflammatory drug (NSAID)
  • aspirin
• Mania: You may have a high mood, become extremely irritable, have too much energy, feel pressure to keep talking, or have a decreased need for sleep.
• Seizures
• Loss of appetite
• Low salt (sodium) levels in the blood (hyponatremia): Call your doctor right away if you become severely ill and have some or all of these symptoms:
  • headache
  • feel weak
  • confusion
  • problems concentrating
  • memory problems
  • feel unsteady

Common possible side effects of fluoxetine capsules include:







How should I store fluoxetine capsules?
 

• Store fluoxetine capsules at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].
• Keep fluoxetine capsules away from light.
• Keep fluoxetine capsules bottle closed tightly.

Keep fluoxetine capsules and all medicines out of the reach of children.

General information about fluoxetine capsules





What are the ingredients in fluoxetine capsules?

Active ingredient:

Inactive ingredients:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE CAPSULE Product Information Product Type Human prescription drug label Item Code (Source) NDC:49349-479(NDC:65862-192) Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength FLUOXETINE HYDROCHLORIDE FLUOXETINE 10 mg Inactive Ingredients Ingredient Name Strength STARCH, CORN SILICON DIOXIDE FD&C BLUE NO. 1 FERRIC OXIDE YELLOW titanium dioxide SODIUM LAURYL SULFATE GELATIN FERROSOFERRIC OXIDE SHELLAC Product Characteristics Color Size Imprint Code Shape green 16 mm E;88 CAPSULE Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49349-479-02 30 in 1 BLISTER PACK 2 NDC:49349-479-20 100 in 1 CANISTER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078619 2010-12-21