PAROXETINE tablet, film coated, extended release

PAROXETINE by

Drug Labeling and Warnings

PAROXETINE by is a Prescription medication manufactured, distributed, or labeled by Lupin Pharmaceuticals, Inc., LUPIN LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: SUICIDAL THOUGHTS AND BEHAVIORS

    Antidepressants increased the risk of 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 emergence of suicidal thoughts and behaviors [see Warnings and Precautions (5.1)]. Paroxetine extended-release tablets are not approved for use in pediatric patients [see Use in Specific Populations (8.4)].

  • 1 INDICATIONS AND USAGE

    Paroxetine extended-release tablets USP are indicated in adults for the treatment of:

    • Major depressive disorder (MDD)
    • Panic disorder (PD)
    • Social anxiety disorder (SAD)
    • Premenstrual dysphoric disorder (PMDD)
  • 2 DOSAGE AND ADMINISTRATION

    2.1 Important Administration Instructions

    Administer paroxetine extended-release tablets as a single daily dose in the morning, with or without food. Swallow tablets whole and do not chew or crush.

    2.2 Dosage In Patients With Major Depressive Disorder, Panic Disorder, And Social Anxiety Disorder

    The recommended initial dosage and maximum dosage of paroxetine extended-release tablets in patients with MDD, PD, and SAD are presented in Table 1.

    In patients with an inadequate response, dosage may be increased in increments of 12.5 mg per day at intervals of at least 1 week, depending on tolerability.

    Table 1: Recommended Daily Dosage Of Paroxetine Extended-Release Tablets In Patients With MDD, PD, and SAD
    Indication
    		Starting Dose
    		Maximum Dose
    MDD
    		 25 mg
    		 62.5 mg
    PD
    		 12.5 mg
    		 75 mg
    SAD
    		 12.5   mg
    		 37.5mg

    2.3 Dosage in Patients with Premenstrual Dysphoric Disorder

    The recommended starting dosage in women with PMDD is 12.5 mg per day. Paroxetine extended-release tablets may be administered either continuously (every day throughout the menstrual cycle) or intermittently (only during the luteal phase of the menstrual cycle, i.e., starting the daily dosage 14 days prior to the anticipated onset of menstruation and continuing through the onset of menses).

    Intermittent dosing is repeated with each new cycle.

    In patients with an inadequate response, the dosage may be increased to the maximum recommended dosage of 25 mg per day, depending on tolerability. Institute dosage adjustments at intervals of at least 1 week.

    2.4 Screen For Bipolar Disorder Prior To Starting Paroxetine Extended-Release Tablets

    Prior to initiating treatment with paroxetine extended-release tablets or another antidepressant, screen patients for a personal or family history of bipolar disorder, mania, or hypomania [see Warnings and Precautions (5.6)].

    2.5 Dosage Modifications For Elderly Patients, Patients With Severe Renal Impairment And Patients With Severe Hepatic Impairment

    The recommended initial dose of paroxetine extended-release tablets is 12.5 mg per day for elderly patients, patients with severe renal impairment, and patients with severe hepatic impairment. Reduce initial dose and increase up-titration intervals if necessary. Dosage should not exceed 50 mg per day for MDD or PD and should not exceed 37.5 mg per day for SAD [see Use in Specific Populations (8.5, 8.6)].

    2.6 Switching Patients To Or From A Monoamine Oxidase Inhibitor Antidepressant

    At least 14 days must elapse between discontinuation of a monoamine oxidase inhibitor (MAOI) antidepressant and initiation of paroxetine extended-release tablets. In addition, at least 14 days must elapse after stopping paroxetine extended-release tablets before starting an MAOI antidepressant [see Contraindications (4), Warnings and Precautions (5.2)].

    2.7 Discontinuation Of Treatment With Paroxetine Extended-Release Tablets

    Adverse reactions may occur upon discontinuation of paroxetine extended-release tablets [see Warnings and Precautions (5.6)]. Gradually reduce the dosage rather than stopping paroxetine extended-release tablets abruptly whenever possible.

  • 3 DOSAGE FORMS AND STRENGTHS

    Paroxetine extended-release tablets USP are available as:

    • 12.5 mg yellow colored, round shaped, biconvex, film coated tablets imprinted with "L067" on one side and plain on other side.
    • 25 mg pink colored, round shaped, biconvex, film coated tablets imprinted with "L068" on one side and plain on other side.
    • 37.5 mg blue colored, round shaped, biconvex tablets imprinted with "L069" on one side and plain on other side.
  • 4 CONTRAINDICATIONS

    Paroxetine extended-release tablets are contraindicated in patients:

    • Taking, or within 14 days of stopping, MAOIs (including the MAOIs linezolid and intravenous methylene blue) because of an increased risk of serotonin syndrome [SeeWarnings and Precautions (5.2), Drug Interactions (7)].
    • Taking thioridazine because of risk of QT prolongation [see Warnings and Precautions(5.3), Drug Interactions (7)].
    • Taking pimozide because of risk of QT prolongation [see Warnings and Precautions (5.3), Drug Interactions (7)].
    • With known hypersensitivity (e.g., anaphylaxis, angioedema, Stevens-Johnson syndrome) to paroxetine or to any of the inactive ingredients in paroxetine extended-release tablets [see Adverse Reactions (6.1,6.2)] .
  • 5 WARNINGS AND PRECAUTIONS

    5.1 Suicidal Thoughts and Behaviors in Adolescents and Young Adults

    In pooled analyses of placebo-controlled trials of antidepressant drugs (SSRIs and other antidepressant classes) that included approximately 77,000 adult patients and 4,500 pediatric patients, the incidence of suicidal thoughts and behaviors in antidepressant-treated patients age 24 years and younger was greater than in placebo-treated patients. There was considerable variation in risk of suicidal thoughts and behaviors among drugs, but there was an increased risk identified in young patients for most drugs studied. There were differences in absolute risk of suicidal thoughts and behaviors across the different indications, with the highest incidence in patients with MDD. The drug-placebo differences in the number of cases of suicidal thoughts and behaviors per 1000 patients treated are provided in Table 2.

    Table 2: Risk Differences Of The Number Of Patients Of Suicidal Thoughts And Behaviors In The Pooled Placebo-Controlled Trials Of Antidepressants In Pediatric And Adult Patients

    Age Range
    		Drug-Placebo Difference in Number of Patients of Suicidal Thoughts and Behaviors per 1,000 Patients Treated
    Increases Compared to Placebo
    <18 years old
    		 14 additional patients
    18-24 years old
    		 5 additional patients
    Decreases Compared to Placebo
    25-64 years old
    		 1 fewer patient
    ≥65 years old
    		 6 fewer patients

    It is unknown whether the risk of suicidal thoughts and behaviors in children, adolescents, and young adults extends to longer-term use, i.e., beyond four months. However, there is substantial evidence from placebo-controlled maintenance trials in adults with MDD that antidepressants delay the recurrence of depression and that depression itself is a risk factor for suicidal thoughts and behaviors.

    Monitor all antidepressant-treated patients for any indication 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 or caregivers of patients to monitor for changes in behavior and to alert the healthcare provider. Consider changing the therapeutic regimen, including possibly discontinuing paroxetine extended-release tablets, in patients whose depression is persistently worse, or who are experiencing emergent suicidal thoughts or behaviors.

    5.2 Serotonin Syndrome

    Serotonin-norepinephrine reuptake inhibitors (SNRIs) and SSRIs, including paroxetine extended-release tablets, can precipitate serotonin syndrome, a potentially life-threatening condition. The risk is increased with concomitant use of other serotonergic drugs (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines, and St. John's Wort) and with drugs that impair metabolism of serotonin, i.e., MAOIs [see Contraindications (4), Drug Interactions (7.1)]. Serotonin syndrome can also occur when these drugs are used alone.

    Serotonin syndrome signs and symptoms may include mental status changes (e.g., agitation, hallucinations, delirium, and coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea).

    The concomitant use of paroxetine extended-release tablets with MAOIs is contraindicated. In addition, do not initiate paroxetine extended-release tablets in a patient being treated with MAOIs such as linezolid or intravenous methylene blue. No reports involved the administration of methylene blue by other routes (such as oral tablets or local tissue injection). If it is necessary to initiate treatment with an MAOI such as linezolid or intravenous methylene blue in a patient taking paroxetine extended-release tablets, discontinue paroxetine extended-release tablets before initiating treatment with the MAOI [see Contraindications (4), Drug Interactions (7.1)].

    Monitor all patients taking paroxetine extended-release tablets for the emergence of serotonin syndrome. Discontinue treatment with paroxetine extended-release tablets and any concomitant serotonergic agents immediately if the above symptoms occur, and initiate supportive symptomatic treatment. If concomitant use of paroxetine extended-release tablets with other serotonergic drugs is clinically warranted, inform patients of the increased risk for serotonin syndrome and monitor for symptoms.

    5.3 Drug Interactions Leading To Qt Prolongation

    The CYP2D6 inhibitory properties of paroxetine can elevate plasma levels of thioridazine and pimozide. Since thioridazine and pimozide given alone produce prolongation of the QTc interval and increase the risk of serious ventricular arrhythmias, the use of paroxetine extended-release tablets is contraindicated in combination with thioridazine and pimozide [see Contraindications (4), Drug Interactions (7), Clinical Pharmacology (12.3)].

    5.4 Embryofetal And Neonatal Toxicity

    Paroxetine extended-release tablets can cause fetal harm when administered to a pregnant woman. Epidemiological studies have shown that infants exposed to paroxetine in the first trimester of pregnancy have an increased risk of cardiovascular malformations. Exposure to paroxetine in late pregnancy may lead to an increased risk for persistent pulmonary hypertension of the newborn (PPNH) and/or neonatal complications requiring prolonged hospitalization, respiratory support, and tube feeding.

    If paroxetine extended-release tablets is used during pregnancy, or if the patient becomes pregnant while taking paroxetine extended-release tablets, the patient should be apprised of the potential hazard to the fetus [see Use in Specific Populations (8.1)].

    5.5 Increased Risk Of Bleeding

    Drugs that interfere with serotonin reuptake inhibition, including paroxetine extended-release tablets, increase the risk of bleeding events. Concomitant use of aspirin, nonsteroidal anti-inflammatory drugs (NSAIDS), other antiplatelet drugs, warfarin, and other anticoagulants may add to this risk. Case reports and epidemiological studies (case-control and cohort design) have demonstrated an association between use of drugs that interfere with serotonin reuptake and the occurrence of gastrointestinal bleeding. Bleeding events related to drugs that interfere with serotonin reuptake have ranged from ecchymoses, hematomas, epistaxis, and petechiae to life-threatening hemorrhages.

    Inform patients about the increased risk of bleeding associated with the concomitant use of paroxetine extended-release tablets and antiplatelet agents or anticoagulants. For patients taking warfarin, carefully monitor the international normalized ratio.

    5.6 Activation Of Mania Or Hypomania

    In patients with bipolar disorder, treating a depressive episode with paroxetine extended-release tablets or another antidepressant may precipitate a mixed/manic episode. During controlled clinical trials of immediate-release paroxetine hydrochloride, hypomania or mania occurred in approximately 1% of paroxetine-treated unipolar patients compared to 1.1% of active-control and 0.3% of placebo-treated unipolar patients. Prior to initiating treatment with paroxetine extended-release tablets, screen patients for any personal or family history of bipolar disorder, mania, or hypomania.

    5.7 Discontinuation Syndrome

    Adverse reactions after discontinuation of serotonergic antidepressants, particularly after abrupt discontinuation, include: nausea, sweating, dysphoric mood, irritability, agitation, dizziness, sensory disturbances (e.g., paresthesia, such as electric shock sensations), tremor, anxiety, confusion, headache, lethargy, emotional lability, insomnia, hypomania, tinnitus, and seizures. A gradual reduction in dosage rather than abrupt cessation is recommended whenever possible [See Dosage and Administration (2.8)].

    Adverse reactions have been reported upon discontinuation of treatment with paroxetine in pediatric patients. The safety and effectiveness of paroxetine extended-release tablets in pediatric patients have not been established [see Boxed Warning, Warnings and Precautions (5.1), Use in Specific Populations (8.4)].

    5.8 Seizures

    Paroxetine extended-release tablets has not been systematically evaluated in patients with seizure disorders. Patients with history of seizures were excluded from clinical studies. Paroxetine extended-release tablets should be prescribed with caution in patients with a seizure disorder and should be discontinued in any patient who develops seizures.

    5.9 Angle-Closure Glaucoma

    The pupillary dilation that occurs following use of many antidepressant drugs including paroxetine extended-release tablets may trigger an angle closure attack in a patient with anatomically narrow angles who does not have a patent iridectomy. Cases of angle-closure glaucoma associated with use of paroxetine hydrochloride tablets have been reported. Avoid use of antidepressants, including paroxetine extended-release tablets, in patients with untreated anatomically narrow angles.

    5.10 Hyponatremia

    Hyponatremia may occur as a result of treatment with SNRIs and SSRIs, including paroxetine extended-release tablets. Cases with serum sodium lower than 110 mmol/L have been reported. Signs and symptoms of hyponatremia include headache, difficulty concentrating, memory impairment, confusion, weakness, and unsteadiness, which may lead to falls. Signs and symptoms associated with more severe and/or acute cases have included hallucination, syncope, seizure, coma, respiratory arrest, and death. In many cases, this hyponatremia appears to be the result of the syndrome of inappropriate antidiuretic hormone secretion (SIADH).

    In patients with symptomatic hyponatremia, discontinue paroxetine extended-release tablets and institute appropriate medical intervention. Elderly patients, patients taking diuretics, and those who are volume- depleted may be at greater risk of developing hyponatremia with SNRIs and SSRIs. [see Use in Specific Populations (8.5)].

    5.11 Reduction Of Efficacy Of Tamoxifen

    Some studies have shown that the efficacy of tamoxifen, as measured by the risk of breast cancer relapse/mortality, may be reduced with concomitant use of paroxetine as a result of paroxetine's irreversible inhibition of CYP2D6 and lower blood levels of tamoxifen [see Drug Interactions (7.3)]. One study suggests that the risk may increase with longer duration of coadministration.

    However, other studies have failed to demonstrate such a risk. When tamoxifen is used for the treatment or prevention of breast cancer, prescribers should consider using an alternative antidepressant with little or no CYP2D6 inhibition.

    5.12 Bone Fracture

    Epidemiological studies on bone fracture risk during exposure to some antidepressants, including SSRIs, have reported an association between antidepressant treatment and fractures. There are multiple possible causes for this observation and it is unknown to what extent fracture risk is directly attributable to SSRI treatment.

    5.13 Risk of Allergic Reactions due to Tartrazine

    Paroxetine extended-release tablets, 12.5 mg contain FD&C Yellow No. 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

  • 6 ADVERSE REACTIONS

    The following adverse reactions are included in more detail in other sections of the prescribing information:

    • Hypersensitivity reactions to paroxetine [see Contraindications(4)]
    • Suicidal Thoughts and Behaviors [see Warnings and Precautions (5.1)]
    • Serotonin Syndrome [see Warnings and Precautions (5.2)]
    • Embryofetal and Neonatal Toxicity [see Warnings and Precautions (5.4)]
    • Increased Risk of Bleeding [see Warnings and Precautions (5.5)]
    • Activation of Mania/Hypomania [seeWarnings and Precautions (5.6)]
    • Discontinuation Syndrome [seeWarnings and Precautions (5.7)]
    • Seizures [see Warnings and Precautions (5.8)]
    • Angle-closure Glaucoma [see Warnings and Precautions (5.9)]
    • Hyponatremia [see Warnings and Precautions (5.10)]
    • Bone Fracture [see Warnings and Precautions (5.12)]

    6.1 Clinical Trials Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.

    Safety data for paroxetine extended-release tablet is from 11 short-term, placebo-controlled clinical trials including 3 studies in patients with major depressive disorder (MDD) (Studies 1, 2, and 3), 3 studies in patients with panic disorder (PD) (Studies 4, 5, and 6), 1 study in patients with social anxiety disorder (SAD) (Study 7), and 4 studies in female patients with premenstrual dysphoric disorder (PMDD) (Studies 8, 9, 10, and 11) [see Clinical Studies (14)]. These 11 trials included 1627 patients treated with paroxetine extended-release tablets.

    • Studies 1 and 2 were 12-week studies that enrolled patients 18 to 65 years old who received paroxetine extended-release tablets at doses ranging from 25 mg to 62.5 mg once daily. Study 3 was a 12-week study in patients 60 to 88 years old who received paroxetine extended-release tablets at doses ranging from 12.5 mg to 50 mg once daily.
    • Studies 4, 5, and 6 were 10-week studies in patients 19 to 72 years old who received paroxetine extended-release tablets at doses ranging from 12.5 mg to 75 mg once daily.
    • Study 7 was a 12-week study that enrolled adult patients who received paroxetine extended-release tablets at doses ranging from 12.5 mg to 37.5 mg once daily.
    • Studies 8, 9, and 10 were 12-week, placebo-controlled trials in female patients 18 to 46 years old who received paroxetine extended-release tablets at doses of 12.5 mg or 25 mg once daily.  Study 11 was a 12-week placebo-controlled trial in patients 18 to 46 years old who received paroxetine extended-release tablets 2 weeks prior to the onset of menses (luteal phase dosing) at doses of 12.5 mg or 25 mg once daily.

    Adverse Reactions Leading to Discontinuation in Patients with MDD, PD, SAD, and PMDD 

    In pooled studies in patients with MDD, PD and SAD, the most common adverse reactions leading to study withdrawal were: nausea (up to 4% of patients), asthenia, headache, depression, insomnia, and abnormal liver function tests (each occurring in up to 2% of patients), and dizziness, somnolence, and diarrhea (each occurring in up to 1% of patients).

    In pooled studies for PMDD, the most common adverse reactions leading to study withdrawal were: nausea (occurring in up to 6% of patients), asthenia (occurring in up to 5% of patients), somnolence (occurring in up to 4% of patients), insomnia (occurring in approximately 2% of patients); and impaired concentration, dry mouth, dizziness, decreased appetite, sweating, tremor, yawn and diarrhea (occurring in less than or equal to 2% of patients).

    Adverse Reactions in MDD, PD, and SAD

    Table 3 presents the most common adverse reactions in paroxetine extended-release tablets -treated patients (incidence ≥5% and greater than placebo within at least 1 of the indications) in controlled trials in patients with MDD, PD, and SAD.

    Table 3. Adverse Reactions (≥5% of Patients Treated with Paroxetine Extended-Release Tablets and Greater than Placebo) in 10 to 12 Week Studies of MDD, PD, and SAD
    MDD
    18 to 65 year olds
    		MDD
    ≥60 years old
    		Panic Disorder
    		Social Anxiety Disorder
    Body System/ Adverse Reaction
    		 Paroxetine extended-release tablets (N=212)
    %
    		 Placebo (N=211)
    %
    		 Paroxetine extended-release tablets (N=104)
    %
    		 Placebo (N=109
    %
    		 Paroxetine extended-release tablets (N=444)
    %
    		 Placebo (N=445)
    %
    		 Paroxetine extended-release tablets (N=186)
    %
    		 Placebo (N=184)
    %
    Body as a Whole
    Headache
    		 27
    		 20
    		 17
    		 13
    		 NA
    		 NA
    		 23
    		 17
    Asthenia
    		 14
    		 9
    		 15
    		 14
    		 15
    		 10
    		 18
    		 7
    Abdominal Pain
    		 7
    		 4
    		 -
    		 -
    		 6
    		 4
    		 5
    		 4
    Back Pain
    		 5
    		 3
    		 -
    		 -
    		 NA
    		 NA
    		 4
    		 1
    Digestive System
    Nausea
    		 22
    		 10
    		 -
    		 -
    		 23
    		 17
    		 22
    		 6
    Diarrhea
    		 18
    		 7
    		 15
    		 9
    		 12
    		 9
    		 9
    		 8
    Dry Mouth
    		 15
    		 8
    		 18
    		 7
    		 13
    		 9
    		 3
    		 2
    Constipation
    		 10
    		 4
    		 13
    		 5
    		 9
    		 6
    		 5
    		 2
    Flatulence
    		 6
    		 4
    		 -
    		 -
    		 NA
    		 NA
    		 NA
    		 NA
    Decreased Appetite
    		 2
    		 12
    		 5
    		 8
    		 6
    		 1
    		 <1
    Dyspepsia
    		 NA
    		 NA
    		 13
    		 10
    		 NA
    		 NA
    		 2
    		 <1
    Musculoskel etal System
    Myalgia
    		 NA
    		 NA
    		 -
    		 -
    		 5
    		 3
    		 NA
    		 NA
    Nervous System
    Somnolence
    		 22
    		 8
    		 21
    		 12
    		 20
    		 9
    		 9
    		 4
    Insomnia
    		 17
    		 9
    		 10
    		 8
    		 20
    		 11
    		 9
    		 4
    Dizziness
    		 14
    		 4
    		 9
    		 5
    		 NA
    		 NA
    		 7
    		 4
    Libido Decreased
    		 7
    		 3
    		 8
    		 <1
    		 9
    		 4
    		 1
    Nervousness
    		 NA
    		 NA
    		 -
    		 -
    		 8
    		 7
    		 NA
    		 NA
    Tremor
    		 7
    		 1
    		 7
    		 0
    		 8
    		 2
    		 4
    		 2
    Anxiety
    		 NA
    		 NA
    		 -
    		 -
    		 5
    		 4
    		 2
    		 1
    Respiratory System
    Sinusitis
    		 NA
    		 NA
    		 -
    		 -
    		 8
    		 5
    		 NA
    		 NA
    Yawn
    		 0
    		 -
    		 -
    		 3
    		 0
    		 2
    		 0
    Skin and Appendages
    Sweating
    		 6
    		 2
    		 10
    		 <1
    		 7
    		 2
    		 14
    		 3
    Special Senses
    Abnormal Visiona
    		5
    		 1
    		 -
    		 -
    		 3
    		 <1
    		 2
    		 0
    Urogenital System
    Abnormal Ejaculationb,c
    		26
    		 1
    		 17
    		 3
    		 27
    		 3
    		 15
    		 1
    Female Genital Disorderb,d
    		10
    		 <1
    		 -
    		 -
    		 7
    		 1
    		 3
    		 0
    Impotenceb
    		5
    		 3
    		 9
    		 3
    		 10
    		 1
    		 9
    		 0

    Hyphen = the reaction listed occurred in <5% of patients treated with paroxetine extended-release tablets NA = the adverse reaction listed did not occur in this group of patients

    aMostly blurred vision

    b Based on the number of males or females

    c Mostly anorgasmia or delayed ejaculation

    d Mostly anorgasmia or delayed orgasm

    Other Adverse Reactions Observed During the Premarketing Evaluation of Paroxetine Extended-Release Tablets

    Adverse reactions from studies in MDD (not including Study 3 in elderly patients), PD, and SAD that occurred between 1% and 5% of patients treated with paroxetine extended-release tablets and at a rate greater than  in placebo-treated patients include:, allergic reaction, tachycardia, vasodilatation, hypertension, migraine, vomiting, weight loss, weight gain, hypertonia, paresthesia, agitation, confusion, myoclonus, concentration impaired, depression, rhinitis, cough increased, bronchitis, photosensitivity, eczema, taste perversion, UTI, menstrual disorder, urinary frequency, urination impaired, and vaginitis.

    Adverse Reactions in Patients with PMDD

    Table 4 displays adverse reactions that occurred (incidence of 5% or more and greater than placebo within at least 1 of the studies) in patients treated with paroxetine extended-release tablets in Studies 8, 9, 10, and 11.

    Table 4. Adverse reactions (≥ 5% of patients treated with paroxetine extended-release tablets and greater than placebo) in pooled studies PMDD (studies 8, 9, 11), and in study 10a,b,c
    Body System/Adverse Reaction
    		% Reporting Adverse Reaction
    Continuous Dosing Studies 8, 9, and 10
    		Luteal Phase Dosing Study 11
    Paroxetine extended-release tablets
    (n = 681)
    %
    		Placebo
    (n = 349) %
    		Paroxetine extended-release tablets
    (n = 246)
    %
    		Placebo
    (n = 120) %
    Body as a Whole
    Asthenia
    Headache
    Infection
    		17
    15
    6
    		6
    12
    4
    		15
    NA
    NA
    		4
    NA
    NA
    Digestive System
    Nausea
    Diarrhea
    Constipation
    		17
    6
    5
    		 7
    2
    1
    		 18
    6
    2
    		 2
    0
    <1
    Nervous System
    Libido Decreased
    Somnolence
    Insomnia
    Dizziness
    Tremor
    		12
    9
    8
    7
    4
    		 5
    2
    2
    3
    <1
    		9
    3
    7
    6
    5
    		 6
    <1
    3
    3
    0
    Skin and Appendages
    Sweating
    		7
    		 <1
    		 6
    		 <1
    Urogenital System
    Female Genital
    Disordersc
    		8
    		 1
    		 2
    		 0

    NA= the adverse reaction information is not available in this population.

    a <1% means greater than zero and less than 1%.

    b The luteal phase and continuous dosing PMDD trials were not designed for making direct comparisons between the 2 dosing regimens.

    cMostly anorgasmia or difficulty achieving orgasm.

    Dose Dependent Adverse Reactions

    Comparison of the incidence of adverse reactions (placebo vs. 12.5 mg paroxetine extended-release tablets vs. 25 mg paroxetine extended-release tablets) from studies 8, 9, 10 showed the following adverse reactions to be dose-related: Nausea, somnolence, sweating, dry mouth, dizziness, decreased appetite, tremor, impaired concentration, yawn, paresthesia, hyperkinesia, and vaginitis.

    Male and Female Sexual Dysfunction

    Although changes in sexual desire, sexual performance, and sexual satisfaction often occur as manifestations of a psychiatric disorder, they may also be a consequence of SSRI treatment. However, reliable estimates of the incidence and severity of untoward experiences involving sexual desire, performance, and satisfaction are difficult to obtain, in part because patients and healthcare providers may be reluctant to discuss them. Accordingly, estimates of the incidence of untoward sexual experience and performance cited in labeling may underestimate their actual incidence.

    The percentage of patients reporting symptoms of sexual dysfunction in the Studies 1 and 2 (nonelderly patients with MDD), 4, 5, 6, 7, 8, 9, 10, and 11 are presented in Table 5:

    Table 5. Adverse Reactions Related to Sexual Dysfunction in Patients Treated With Paroxetine Extended-Release Tablets in Pooled 10-12 Week Studies of MDD, PD, SAD, and PMDD
    Studies 1 and 2
    %
    		Studies 4, 5, and 6
    %
    		Study 7
    %
    		Studies 8, 9, and 11 (Continuous Dosing)
    %
    		Study 10 (Luteal Phase Dosing)
    %
    Paroxetine Extended-Release Tablets
    		Placebo
    		Paroxetine Extended-Release Tablets
    		Placebo
    		Paroxetine Extended-Release Tablets
    		Placebo
    		Paroxetine Extended-Release Tablets
    		Placebo
    		Paroxetine Extended-Release Tablets
    		Placebo
    n (males)
    		78
    		78
    		162
    		194
    		88
    		97
    		NA
    		NA
    		NA
    		NA
    Decreased Libido
    		 10
    		 5
    		 9
    		 6
    		 13
    		 1
    		 NA
    		 NA
    		 NA
    		 NA
    Abnormal ejaculation
    		 26
    		 1
    		 27
    		 3
    		 15
    		 1
    		 NA
    		 NA
    		 NA
    		 NA
    Impotence
    		 5
    		 3
    		 10
    		 1%
    		 9
    		 0
    		 NA
    		 NA
    		 NA
    		 NA
    n (females)
    		134
    		133
    		282
    		251
    		98
    		87
    		681
    		349
    		246
    		120
    Decreased Libido
    		 4
    		 2
    		 8
    		 2
    		 4
    		 1
    		 12
    		 5
    		 9
    		 6
    Orgasmic Disturbance
    		 10
    		 <1
    		 7
    		 1
    		 3
    		 0
    		 8
    		 1
    		 2
    		 0

    NA = the adverse reaction listed did not occur in this group of patients.

    Paroxetine treatment has been associated with several cases of priapism. In those cases with a known outcome, patients recovered without sequelae.

    Less Common Adverse Reactions

    The following adverse reactions occurred during the clinical studies of paroxetine extended-release tablets and are not included elsewhere in the labeling.

    Reactions are categorized by body system and listed in order of decreasing frequency according to the following definitions: Frequent adverse reactions are those occurring on 1 or more occasions in at least 1/100 patients; infrequent adverse reactions are those occurring in 1/100 to 1/1,000 patients; rare reactions are those occurring in fewer than 1/1,000 patients.

    Cardiovascular System: Infrequent was postural hypotension.

    Hemic and Lymphatic System: Rare was thrombocytopenia.

    Metabolic and Nutritional Disorders: Infrequent were generalized edema and hypercholesteremia.

    Nervous System: Infrequent were convulsion, akathisia, and manic reaction.

    Psychiatric: Infrequent were hallucinations.

    Skin and Appendages: Frequent was rash; infrequent was urticaria; rare was angioedema and erythema multiforme.

    Urogenital System: Infrequent was urinary retention; rare was urinary incontinence.

    6.2 Postmarketing Experience

    The following reactions have been identified during post approval use of paroxetine. Because these reactions are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Acute pancreatitis, elevated liver function tests (the most severe cases were deaths due to liver necrosis, and grossly elevated transaminases associated with severe liver dysfunction), Guillain-Barr¡SR syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, priapism, syndrome of inappropriate ADH secretion (SIADH), prolactinemia and galactorrhea; extrapyramidal symptoms which have included akathisia, bradykinesia, cogwheel rigidity, dystonia, hypertonia, trismus; status epilepticus, acute renal failure, pulmonary hypertension, allergic alveolitis, anaphylaxis, eclampsia, laryngismus, optic neuritis, porphyria, restless legs syndrome (RLS), ventricular fibrillation, ventricular tachycardia (including torsade de pointes), hemolytic anemia, events related to impaired hematopoiesis (including aplastic anemia, pancytopenia, bone marrow aplasia, and agranulocytosis), and vasculitic syndromes (such as Henoch-Schönlein purpura).

  • 7 DRUG INTERACTIONS

    7.1 Clinically Significant Drug Interactions

    Table 6: Clinically Significant Drug Interactions with Paroxetine Extended-Release Tablets
    Monoamine Oxidase Inhibitors (MAOIs)
    Clinical Impact
    		The concomitant use of SSRIs, including paroxetine extended-release tablets, and MAOIs increases the risk of serotonin syndrome.
    Intervention
    		Paroxetine extended-release tablets are contraindicated in patients taking MAOIs, including MAOIs such as linezolid or intravenous methylene blue [see Dosage and Administration (2.6), Contraindications (4), Warnings and Precautions (5.2)] .
    Examples
    		selegiline, tranylcypromine, isocarboxazid, phenelzine, linezolid, methylene blue
    Pimozide and Thioridazine
    Clinical Impact
    		Increased plasma concentrations of pimozide and thioridazine, drugs with a narrow therapeutic index, may increase the risk of QTc prolongation and ventricular arrhythmias.
    Intervention
    		Paroxetine extended-release tablets are contraindicated in patients taking pimozide or thioridazine [see Contraindications (4)].
    Other Serotonergic Drugs
    Clinical Impact
    		The concomitant use of serotonergic drugs with paroxetine extended-release tablet increases the risk of serotonin syndrome.
    Intervention
    		Monitor patients for signs and symptoms of serotonin syndrome, particularly during treatment initiation and dosage increases. If serotonin syndrome occurs, consider discontinuation of paroxetine extended-release tablets and/or concomitant serotonergic drugs [see Warnings and Precautions (5.2)] .
    Examples
    		other SSRIs, SNRIs, triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, St. John's Wort
    Drugs that Interfere with Hemostasis (antiplatelet agents and anticoagulants)
    Clinical Impact
    		The concurrent use of an antiplatelet agent or anticoagulant with paroxetine extended-release tablets may potentiate the risk of bleeding.
    Intervention
    		Inform patients of the increased risk of bleeding associated with the concomitant use of paroxetine extended-release tablets and antiplatelet agents and anticoagulants. For patients taking warfarin, carefully monitor the international normalized ratio [see Warnings and Precautions (5.5)] .
    Examples
    		aspirin, clopidogrel, heparin, warfarin
    Drugs Highly Bound to Plasma Protein
    Clinical Impact
    		Paroxetine extended-release tablets are highly bound to plasma protein. The concomitant use of paroxetine extended-release tablets with another drug that is highly bound to plasma protein may increase free concentrations of paroxetine extended-release tablets or other tightly-bound drugs in plasma.
    Intervention
    		Monitor for adverse reactions and reduce dosage of paroxetine extended-release tablets or other protein-bound drugs as warranted.
    Examples
    		warfarin
    Drugs Metabolized by CYP2D6
    Clinical Impact
    		Paroxetine extended-release tablets are a CYP2D6 inhibitor [see Clinical Pharmacology (12.3)]. The concomitant use of paroxetine extended-release tablets with a CYP2D6 substrate may increase the exposure of the CYP2D6 substrate.
    Intervention
    		Decrease the dosage of a CYP2D6 substrate if needed with concomitant paroxetine extended-release tablets use. Conversely, an increase in dosage of a CYP2D6 substrate may be needed if paroxetine extended-release tablets are discontinued.
    Examples
    		propafenone, flecainide, atomoxetine, desipramine, dextromethorphan, metoprolol, nebivolol, perphenazine, tolterodine, venlafaxine, risperidone.
    Tamoxifen
    Clinical Impact
    		Concomitant use of tamoxifen with paroxetine extended-release tablets may lead to reduced plasma concentrations of the active metabolite (endoxifen) and reduced efficacy of tamoxifen
    Intervention
    		Consider use of an alternative antidepressant little or no CYP2D6 inhibition [see Warnings and Precautions (5.11)].
    Fosamprenavir/Ritonavir
    Clinical Impact
    		Co-administration of fosamprenavir/ritonavir with paroxetine significantly decreased plasma levels of paroxetine.
    Intervention
    		Any dose adjustment should be guided by clinical effect (tolerability and efficacy).
  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Category D [see Warnings and Precautions (5.14)]

    Epidemiological studies have shown that infants exposed to paroxetine in the first trimester of pregnancy have an increased risk of congenital malformations, particularly cardiovascular malformations. If paroxetine is used during pregnancy, or if the patient becomes pregnant while taking paroxetine, advise the patient of the potential hazard to the fetus.

    • A study based on Swedish national registry data demonstrated that infants exposed to paroxetine during pregnancy (n = 815) had an increased risk of cardiovascular malformations (2% risk in paroxetine-exposed infants) compared to the entire registry population (1% risk), for an odds ratio (OR) of 1.8 (95% confidence interval 1.1 to 2.8). No increase in the risk of overall congenital malformations was seen in the paroxetine-exposed infants. The cardiac malformations in the paroxetine-exposed infants were primarily ventricular septal defects (VSDs) and atrial septal defects (ASDs). Septal defects range in severity from those that resolve spontaneously to those which require surgery.
    • A separate retrospective cohort study from the United States (United Healthcare data) evaluated 5,956 infants of mothers dispensed antidepressants during the first trimester (n = 815 for paroxetine). This study showed a trend towards an increased risk for cardiovascular malformations for paroxetine (risk of 1.5%) compared to other antidepressants (risk of 1%), for an OR of 1.5 (95% confidence interval 0.8 to 2.9). Of the 12 paroxetine-exposed infants with cardiovascular malformations, 9 had VSDs. This study also suggested an increased risk of overall major congenital malformations including cardiovascular defects for paroxetine (4% risk) compared to other (2% risk) antidepressants (OR 1.8; 95% confidence interval 1.2 to 2.8).
    • Two large case-control studies using separate databases, each with >9,000 birth defect cases and >4,000 controls, found that maternal use of paroxetine during the first trimester of pregnancy was associated with a 2- to 3-fold increased risk of right ventricular outflow tract obstructions. In one study the OR was 2.5 (95% confidence interval, 1.0 to 6.0, 7 exposed infants) and in the other study the OR was 3.3 (95% confidence interval, 1.3 to 8.8, 6 exposed infants).

    Other studies have found varying results as to whether there was an increased risk of overall, cardiovascular, or specific congenital malformations. A meta-analysis of epidemiological data over a 16-year period (1992 to 2008) on first trimester paroxetine use in pregnancy and congenital malformations included the above-noted studies in addition to others (n = 17 studies that included overall malformations and n = 14 studies that included cardiovascular malformations; n = 20 distinct studies). While subject to limitations, this meta-analysis suggested an increased occurrence of cardiovascular malformations (prevalence odds ratio [POR] 1.5; 95% confidence interval 1.2 to 1.9) and overall malformations (POR 1.2; 95% confidence interval 1.1 to 1.4) with paroxetine use during the first trimester. It was not possible in this meta-analysis to determine the extent to which the observed prevalence of cardiovascular malformations might have contributed to that of overall malformations, nor was it possible to determine whether any specific types of cardiovascular malformations might have contributed to the observed prevalence of all cardiovascular malformations.

    Unless the benefits of paroxetine to the mother justify continuing treatment, consideration should be given to either discontinuing paroxetine therapy or switching to another antidepressant [see Warnings and Precautions (5.7)]. For women who intend to become pregnant or are in their first trimester of pregnancy, paroxetine should only be initiated after consideration of the other available treatment options [see Warnings and Precautions (5.4)].

    Treatment of Pregnant Women During Their Third Trimester: Neonates exposed to SSRIs or serotonin and norepinephrine reuptake inhibitors (SNRIs), including paroxetine extended-release tablets, late in the third trimester have developed complications requiring prolonged hospitalization, respiratory support, and tube feeding. Such complications can arise immediately upon delivery. Reported clinical findings have included respiratory distress, cyanosis, apnea, seizures, temperature instability, feeding difficulty, vomiting, hypoglycemia, hypotonia, hypertonia, hyperreflexia, tremor, jitteriness, irritability, and constant crying. These features are consistent with either a direct toxic effect of SSRIs and SNRIs or, possibly, a drug discontinuation syndrome. It should be noted that, in some cases, the clinical picture is consistent with serotonin syndrome [see Warnings and Precautions (5.2)].

    Exposure to SSRIs in late pregnancy may have an increased risk for persistent pulmonary hypertension of the newborn (PPHN). PPHN occurs in 1 – 2 per 1,000 live births in the general population and is associated with substantial neonatal morbidity and mortality. In a retrospective case-control study of 377 women whose infants were born with PPHN and 836 women whose infants were born healthy, the risk for developing PPHN was approximately six-fold higher for infants exposed to SSRIs after the 20th week of gestation compared to infants who had not been exposed to antidepressants during pregnancy.

    There have also been postmarketing reports of premature births in pregnant women exposed to paroxetine or other SSRIs.

    When treating a pregnant woman with paroxetine during the third trimester, the physician should carefully consider both the potential risks and benefits of treatment [see Dosage and Administration (2.5)]. A prospective longitudinal study of 201 women with a history of major depression who were euthymic at the beginning of pregnancy. The women who discontinued antidepressant medication during pregnancy were more likely to experience a relapse of major depression than women who continued antidepressant medication.

    Animal Findings: Reproduction studies were performed at doses up to 50 mg/kg/day in rats and 6 mg/kg/day in rabbits administered during organogenesis. These doses are approximately 6 (rat) and less than 2 (rabbit) times the maximum recommended human dose (MRHD – 75 mg) on an mg/m2 basis. These studies have revealed no evidence of malformations. However, in rats, there was an increase in pup deaths during the first 4 days of lactation when dosing occurred during the last trimester of gestation and continued throughout lactation. This effect occurred at a dose of 1 mg/kg/day or approximately one-thirteens of the MRHD on an mg/m2 basis. The no-effect dose for rat pup mortality was not determined. The cause of these deaths is not known.

    8.3 Nursing Mothers

    Like many other drugs, paroxetine is secreted in human milk. Because of the potential for serious adverse reactions in nursing infants from paroxetine extended-release tablets, a decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.

    8.4 Pediatric Use

    The safety and effectiveness of paroxetine extended-release tablets in pediatric patients have not been established [see Boxed Warning, Warnings and Precautions (5.1)].

    Three placebo-controlled trials in 752 pediatric patients with MDD have been conducted with immediate-release paroxetine, and effectiveness was not established in pediatric patients.

    Decreased appetite and weight loss have been observed in association with the use of SSRIs.

    In placebo-controlled clinical trials conducted with pediatric patients, the following adverse reactions were reported in at least 2% of pediatric patients treated with immediate-release paroxetine hydrochloride and at a rate at least twice that for pediatric patients receiving placebo: emotional lability (including self-harm, suicidal thoughts, attempted suicide, crying, and mood fluctuations), hostility, decreased appetite, tremor, sweating, hyperkinesia, and agitation.

    Adverse reactions upon discontinuation of treatment with immediate-release paroxetine hydrochloride in the pediatric clinical trials that included a taper phase regimen, which occurred in at least 2% of patients and at a rate at least twice that of placebo, were: emotional lability (including suicidal ideation, suicide attempt, mood changes, and tearfulness), nervousness, dizziness, nausea, and abdominal pain.

    8.5 Geriatric Use

    SSRIs and SNRIs, including paroxetine extended-release tablets, have been associated with cases of clinically significant hyponatremia in elderly patients, who may be at greater risk for this adverse reaction [see Warnings and Precautions (5.9)].

    In premarketing clinical trials with immediate-release paroxetine hydrochloride, 17% of paroxetine treated patients (approximately 700) were 65 years or older. Pharmacokinetic studies revealed a decreased clearance in the elderly, and a lower starting dose is recommended; however, no overall differences in safety or effectiveness were observed between these subjects and younger subjects [see Dosage and Administration (2.5), Clinical Pharmacology (12.3)].

    8.6 Renal And/Or Hepatic Impairment

    Increased plasma concentrations of paroxetine occur in patients with renal and hepatic impairment. The initial dosage should be reduced in patients with severe renal impairment and patients with severe hepatic impairment [see Dosage and Administration (2.5) and Clinical Pharmacology (12.3)].

  • 10 OVERDOSAGE

    Human Experience

    Since the introduction of immediate-release paroxetine hydrochloride in the United States, spontaneous cases of deliberate or accidental overdosage during paroxetine treatment have been reported worldwide. These include overdoses with paroxetine alone and in combination with other substances. There are reports of fatalities that appear to involve paroxetine alone.

    Commonly reported adverse reactions associated with paroxetine overdosage include somnolence, coma, nausea, tremor, tachycardia, confusion, vomiting, and dizziness. Other notable signs and symptoms observed with overdoses involving paroxetine (alone or with other substances) include mydriasis, convulsions (including status epilepticus), ventricular dysrhythmias (including torsade de pointes), hypertension, aggressive reactions, syncope, hypotension, stupor, bradycardia, dystonia, rhabdomyolysis, symptoms of hepatic dysfunction (including hepatic failure, hepatic necrosis, jaundice, hepatitis, and hepatic steatosis), serotonin syndrome, manic reactions, myoclonus, acute renal failure, and urinary retention.

    Overdose Management

    No specific antidotes for paroxetine are known. If over-exposure occurs, all your poison control center at 1-800-222-1222 for latest recommendations.

  • 11 DESCRIPTION

    Paroxetine extended-release tablets USP contains paroxetine hydrochloride, an SSRI. It is the hydrochloride salt of a phenylpiperidine compound identified chemically as (-)-(3S, 4R)-4-(p-Fluorophenyl)-3-([(3,4 methylenedioxy) phenoxy]methyl)piperidine hydrochloride hemihydrate and has the empirical formula of C19H21ClFNO31/2H2O. The molecular weight is 374.83. The structural formula of paroxetine hydrochloride USP is:

    Image

    Paroxetine hydrochloride USP is a white or almost white, crystalline powder. 

    Paroxetine extended-release tablets USP are intended for oral administration. Each film-coated, extended-release tablet contains paroxetine hydrochloride hemihydrate USP equivalent to paroxetine 12.5 mg, 25 mg and 37.5 mg.

     

    Inactive ingredients consist of aluminum oxide, colloidal silicon dioxide, hydrogenated vegetable oil, hypromelloses, iron oxide black, lactose monohydrate, magnesium stearate, methacrylic acid co-polymer dispersion, microcrystalline cellulose, polyethylene glycols, povidone, propylene glycol, shellac glaze, talc, titanium dioxide, triacetin and triethyl citrate.

    The 12.5 mg tablets also contain D&C Yellow No. 10 Aluminum Lake, FD&C Yellow No. 5 Aluminum Lake (tartrazine) and FD&C Yellow No. 6 Aluminum Lake.

    The 25 mg tablets also contain D&C Red No. 30 Aluminum Lake and FD&C Blue No. 2 Aluminum Lake.

    The 37.5 mg tablets also contain FD&C Blue No. 1 Aluminum Lake.

    USP Dissolution Test is Pending.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    The mechanism of action of paroxetine in the treatment of major depressive disorder (MDD), panic disorder (PD), social anxiety disorder (SAD), and premenstrual dysphoric disorder (PMDD) is unknown, but is presumed to be linked to potentiation of serotonergic activity in the central nervous system resulting from inhibition of neuronal reuptake of serotonin (5-HT).

    12.2 Pharmacodynamics

    Studies at clinically relevant doses in humans have demonstrated that paroxetine blocks the uptake of serotonin into human platelets. In vitro studies in animals also suggest that paroxetine is a potent and highly selective inhibitor of neuronal serotonin reuptake (SSRI) and has only very weak effects on norepinephrine and dopamine neuronal reuptake.

    12.3 Pharmacokinetics

    Absorption

    Paroxetine extended-release tablets are completely absorbed after oral dosing of a solution of the hydrochloride salt. In a study in which normal male and female subjects (n = 23) received single oral doses of paroxetine extended-release tablets at 4 dosage strengths (12.5 mg, 25 mg, 37.5 mg, and 50 mg), paroxetine Cmax and AUC0-inf increased disproportionately with dose (as seen also with immediate-release formulations). Mean Cmax and AUC0-inf values at these doses were 2.0, 5.5, 9.0, and 12.5 ng/mL, and 121, 261, 338, and 540 ng.hr. /mL, respectively. Tmax was observed typically between 6 and 10 hours post-dose, reflecting a reduction in absorption rate compared with immediate-release formulations. The bioavailability of 25 mg paroxetine extended-release tablets is not affected by food.

    Distribution

    Paroxetine distributes throughout the body, including the CNS, with only 1% remaining in the plasma.

    Approximately 95% and 93% of paroxetine is bound to plasma protein at 100 ng/mL and 400 ng/mL, respectively. Under clinical conditions, paroxetine concentrations would normally be less than 400 ng/mL. Paroxetine does not alter the in vitro protein binding of phenytoin or warfarin.

    Elimination

    Metabolism

    The mean elimination half-life of paroxetine was 15 to 20 hours throughout a range of single doses of paroxetine extended-release tablets (12.5 mg, 25 mg, 37.5 mg, and 50 mg). During repeated administration of paroxetine extended-release tablets (25 mg once daily), steady state was reached within 2 weeks (i.e., comparable to immediate-release formulations). In a repeat-dose study in which normal male and female subjects (n = 23) received paroxetine extended-release tablets (25 mg daily), mean steady state Cmax, Cmin, and AUC0-24 values were 30 ng/mL, 20 ng/mL, and 550 ng.hr./mL, respectively.

    Based on studies using immediate-release formulations, steady-state drug exposure based on AUC0-24 was several-fold greater than would have been predicted from single-dose data. The excess accumulation is a consequence of the fact that 1 of the enzymes that metabolizes paroxetine is readily saturable.

    In steady-state dose proportionality studies involving elderly and nonelderly patients, at doses of the immediate-release formulation of 20 mg to 40 mg daily for the elderly and 20 mg to 50 mg daily for the nonelderly, some nonlinearity was observed in both populations, again reflecting a saturable metabolic pathway (Figure 3).

    Paroxetine is extensively metabolized after oral administration. The principal metabolites are polar and conjugated products of oxidation and methylation, which are readily cleared.

    Conjugates with glucuronic acid and sulfate predominate, and major metabolites have been isolated and identified. Data indicate that the metabolites have no more than 1/50 the potency of the parent compound at inhibiting serotonin uptake. The metabolism of paroxetine is accomplished in part by CYP2D6. Saturation of this enzyme at clinical doses appears to account for the nonlinearity of paroxetine kinetics with increasing dose and increasing duration of treatment. The role of this enzyme in paroxetine metabolism also suggests potential drug-drug interactions [see Drug Interactions (7.3)].

    Excretion

    Approximately 64% of a 30-mg oral solution dose of paroxetine was excreted in the urine with 2% as the parent compound and 62% as metabolites over a 10-day post-dosing period. About 36% was excreted in the feces (probably via the bile), mostly as metabolites and less than 1% as the parent compound over the 10-day post-dosing period.

    The elimination half-life is approximately 15 to 20 hours after a single dose of paroxetine extended-release tablets. Paroxetine metabolism is mediated in part by CYP2D6, and the metabolites are primarily excreted in the urine and to some extent in the feces. Pharmacokinetic behavior of paroxetine has not been evaluated in subjects who are deficient in CYP2D6 (poor metabolizers).

    Drug Interaction Studies

    There are clinically significant, known drug interactions between paroxetine and other drugs [see Drug Interactions (7)].

    Figure 1. Impact of Paroxetine on the Pharmacokinetics of Co-Administered Drugs (log scale)

    Image

    Figure 2. Impact of Co-Administered Drugs on the Pharmacokinetics of Paroxetine

    Image

    Theophylline: Reports of elevated theophylline levels associated with immediate-release paroxetine treatment have been reported. While this interaction has not been formally studied, it is recommended that theophylline levels be monitored when these drugs are concurrently administered.

    Drugs Metabolized by Cytochrome CYP3A4

    An in vivo interaction study involving the coadministration under steady-state conditions of paroxetine and terfenadine, a substrate for CYP3A4, revealed no effect of paroxetine on terfenadine pharmacokinetics. In addition, in vitro studies have shown ketoconazole, a potent inhibitor of CYP3A4 activity, to be at least 100 times more potent than paroxetine as an inhibitor of the metabolism of several substrates for this enzyme, including terfenadine, astemizole, cisapride, triazolam, and cyclosporine. Paroxetine's extent of inhibition of CYP3A4 activity is not expected to be of clinical significance.

    Specific Populations

    The impact of specific populations on the pharmacokinetics of paroxetine are shown in Figure 3.

    Figure 3. Impact of Specific Population on the Pharmacokinetics of Paroxetine (log scale)

    Image
  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis

    Two-year carcinogenicity studies were conducted in rodents given paroxetine in the diet at 1, 5, and 25 mg/kg/day (mice) and 1, 5, and 20 mg/kg/day (rats). These doses are up to approximately 1.6 (mouse) and 2.5 (rat) times the MRHD on an mg/m2 basis. There was a significantly greater number of male rats in the high-dose group with reticulum cell sarcomas (1/100, 0/50, 0/50, and 4/50 for control, low-, middle-, and high-dose groups, respectively) and a significantly increased linear trend across dose groups for the occurrence of lymphoreticular tumors in male rats.

    Female rats were not affected. Although there was a dose-related increase in the number of tumors in mice, there was no drug-related increase in the number of mice with tumors. The relevance of these findings to humans is unknown.

    Mutagenesis

    Paroxetine produced no genotoxic effects in a battery of 5 in vitro and 2 in vivo assays that included the following: Bacterial mutation assay, mouse lymphoma mutation assay, unscheduled DNA synthesis assay, and tests for cytogenetic aberrations in vivo in mouse bone marrow and in vitro in human lymphocytes and in a dominant lethal test in rats.

    Impairment of Fertility

    Some clinical studies have shown that SSRIs (including paroxetine) may affect sperm quality during SSRI treatment, which may affect fertility in some men.

    A reduced pregnancy rate was found in reproduction studies in rats at a dose of paroxetine of 15 mg/kg/day, which is approximately twice the MRHD on an mg/m2 basis. Irreversible lesions occurred in the reproductive tract of male rats after dosing in toxicity studies for 2 to 52 weeks. These lesions consisted of vacuolation of epididymal tubular epithelium at 50 mg/kg/day and atrophic changes in the seminiferous tubules of the testes with arrested spermatogenesis at 25 mg/kg/day (approximately 6 and 3 times the MRHD on an mg/m2 basis).

  • 14 CLINICAL STUDIES

    14.1 Major Depressive Disorder

    The efficacy of paroxetine extended-release tablets as a treatment for major depressive disorder (MDD) was established in two 12-week, multicenter, randomized, double-blind, placebo-controlled, flexible dose studies with paroxetine extended-release tablets (Study 1 and Study 2) in adult patients who met Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV criteria for MDD. Study 1 and 2 included patients 18 to 65 years old who received paroxetine extended-release tablets doses of 25 to 62.5 mg/day (N= 212) or placebo (N= 211) once daily compared to immediate-release paroxetine 20 to 50 mg (N=217). A third 12-week, multicenter, randomized, double-blind, placebo-controlled, flexible dose study with paroxetine extended-release tablets (Study 3) included elderly patients, ranging in age from 60 to 88 years old and used paroxetine extended-release tablets doses of 12.5 to 50 mg/day (N=104) or placebo (N=109) once daily compared to immediate- release paroxetine 10 to 40 mg (N=106). In all three studies, paroxetine extended-release tablets was statistically superior to placebo in improving depressive symptoms as measured by the following: the mean change from baseline in the Hamilton Depression Rating Scale (HDRS) total score at Week 12, the mean change from baseline in the Hamilton Depressed Mood item score at Week 12, and the mean change from baseline in the Clinical Global Impression (CGI)–Severity of Illness score.

    Long-term efficacy of paroxetine for treatment of MDD in outpatients was established with one randomized withdrawal study with immediate-release paroxetine. Patients who responded to immediate-release paroxetine (HDRS total score <8) during an initial 8-week open-label treatment phase were then randomized to continue immediate-release paroxetine or placebo, for up to 1 year. Patients treated with immediate-release paroxetine demonstrated a statistically significant lower relapse rate during the withdrawal phase (15%) compared to those on placebo (39%). Effectiveness was similar for male and female patients.

    14.2 Panic Disorder

    The effectiveness of paroxetine extended-release tablets in the treatment of panic disorder (PD) was evaluated in three 10-week, multicenter, flexible-dose studies (Studies 4, 5, and 6) comparing paroxetine extended-release tablets (12.5 to 75 mg daily) to placebo in adult outpatients 19 to 72 years of age who met panic disorder (with or without agoraphobia) criteria according to DSM-IV. These trials were assessed on the basis of their outcomes on 3 variables: (1) the proportions of patients free of full panic attacks at Week 10; (2) change from baseline to Week 10 in the median number of full panic attacks; and (3) change from baseline to Week 10 in the median Clinical Global Impression Severity score. For Studies 4 and 5, paroxetine extended-release tablets was superior to placebo on 2 of these 3 variables. Study 6 failed to consistently demonstrate a statistically significant difference between paroxetine extended-release tablets and placebo on any of these variables.

    For all 3 studies, the mean dose of paroxetine extended-release tablets for completers at Week 10 was approximately 50 mg/day. Subgroup analyses did not indicate that there were any differences in treatment outcomes as a function of age or gender.

    Long-term maintenance effects of paroxetine in patients with PD were demonstrated in a randomized-withdrawal study using immediate-release paroxetine. Patients who were responders during a 10-week, double-blind trial (followed by a 3-month double-blind maintenance phase) of immediate-release paroxetine were re-randomized to continue immediate-release paroxetine or placebo in a 3-month, double-blind withdrawal phase. Patients randomized to immediate-release paroxetine were statistically significantly less likely to relapse than placebo-treated patients.

    14.3 Social Anxiety Disorder

    The efficacy of paroxetine extended-release tablets as a treatment for social anxiety disorder (SAD) was established, in part, on the basis of extrapolation from the established effectiveness of immediate-release paroxetine in the treatment of SAD. In addition, the effectiveness of paroxetine extended-release tablets in the treatment of SAD was demonstrated in one 12-week, multicenter, double-blind, flexible-dose, placebo-controlled study of adult outpatients with a primary diagnosis of SAD by DSM-IV criteria (Study 7). In Study 7, the effectiveness of paroxetine extended-release tablets (12.5 to 37.5 mg daily) compared to placebo was evaluated on the basis of (1) change from baseline in the Liebowitz Social Anxiety Scale (LSAS) total score at Week 12 and (2) the proportion of responders who scored 1 or 2 (very much improved or much improved) on the CGI Global Improvement score at Week 12.

    In Study 7, paroxetine extended-release tablets demonstrated statistically significant superiority over placebo on both the change on LSAS total score at Week 12 and the CGI Improvement responder criterion at Week 12. For patients who completed the trial, 64% of patients treated with paroxetine extended-release tablets compared to 35% of patients treated with placebo were CGI Improvement responders at Week 12.

    Subgroup analyses did not indicate that there were any differences in treatment outcomes as a function of gender. Subgroup analyses of studies utilizing the immediate-release formulation of paroxetine generally did not indicate differences in treatment outcomes as a function of age, race, or gender.

    14.4 Premenstrual Dysphoric Disorder

    The effectiveness of paroxetine extended-release tablets for the treatment of Premenstrual Dysphoric Disorder (PMDD) utilizing a continuous dosing regimen has been established in 2 placebo-controlled trials in female patients ages 18 to 46 (Studies 8 and 9 [N=672]). Patients in these trials met DSM-IV criteria for PMDD. Of 1,030 patients including Study 10, who were treated with daily doses of paroxetine extended-release tablets 12.5 or 25 mg/day, or placebo continuously throughout the menstrual cycle for a period of 3 menstrual cycles, the mean duration of the PMDD symptoms was approximately 11 ± 7 years. Patients on systemic hormonal contraceptives were excluded from these trials. Therefore, the efficacy of paroxetine extended-release tablets in combination with systemic (including oral) hormonal contraceptives for the continuous daily treatment of PMDD is unknown.

    The VAS score is a patient-rated instrument that mirrors the diagnostic criteria of PMDD as identified in the DSM-IV, and includes assessments for mood, physical symptoms, and other symptoms associated with PMDD. In Studies 8 and 9, 12.5 mg/day and 25 mg/day of paroxetine extended-release tablets were statistically significantly more effective than placebo as measured by change from baseline to Month 3 on the luteal phase VAS score.

    In an additional study employing luteal phase dosing (Study 11), patients (N = 366) were treated for the 2 weeks prior to the onset of menses with 12.5 or 25 mg/day of paroxetine extended-release tablets or placebo for a period of 3 months. In this trial,12.5 mg/day and 25 mg/day of paroxetine extended-release tablets, as luteal phase dosing, was statistically significantly more effective than placebo as measured by change from baseline to luteal phase VAS score at Month 3.

    There is insufficient information to determine the effect of race or age on outcome in Studies 8, 9, 10, and 11.

  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    Paroxetine extended-release tablets USP, 12.5 mg are supplied as yellow colored, round shaped, biconvex, film coated tablets imprinted with "L067" on one side and plain on other side. They are available as follows:

    Bottle of 30 tablets (NDC: 68180-647-06)

    Bottle of 100 tablets (NDC: 68180-647-01)

    Bottle of 500 tablets (NDC: 68180-647-02)

    Bottle of 1000 tablets (NDC: 68180-647-03)

    Paroxetine extended-release tablets USP, 25 mg are supplied as pink colored, round shaped, biconvex, film coated tablets imprinted with "L068" on one side and plain on other side. They are available as follows:

    Bottle of 30 tablets (NDC: 68180-646-06)

    Bottle of 100 tablets (NDC: 68180-646-01)

    Bottle of 500 tablets (NDC: 68180-646-02)

    Bottle of 1000 tablets (NDC: 68180-646-03)

    Paroxetine extended-release tablets USP, 37.5 mg are supplied as blue colored, round shaped, biconvex tablets imprinted with "L069" on one side and plain on other side. They are available as follows:

    Bottle of 30 tablets (NDC: 68180-645-06)

    Bottle of 100 tablets (NDC: 68180-645-01)

    Bottle of 500 tablets (NDC: 68180-645-02)

    Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

  • 17 PATIENT COUNSELING INFORMATION

    Advise the patient to read the FDA-approved patient labeling (Medication Guide).

    Suicidal Thoughts and Behaviors

    Advise patients and caregivers to look for the emergence of suicidality, especially early during treatment and when the dosage is adjusted up or down, and instruct them to report such symptoms to the healthcare provider [see Boxed Warning and Warnings and Precautions (5.1)].

    Important Administration Instructions

    Instruct patients to swallow paroxetine extended-release tablets whole and to not chew or crush the tablets [see Dosage and Administration (2.1)].

    Serotonin Syndrome

    Caution patients about the risk of serotonin syndrome, particularly with the concomitant use of paroxetine extended-release tablets with other serotonergic drugs including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines, St. John's Wort, and with drugs that impair metabolism of serotonin (in particular, MAOIs, both those intended to treat psychiatric disorders and also others, such as linezolid). Instruct patients to contact their health care provider or report to the emergency room if they experience signs or symptoms of serotonin syndrome [see Warnings and Precautions (5.2), Drug Interactions (7.1)].

    Concomitant Medications

    Advise patients to inform their physician if they are taking, or plan to take, any prescription or over-the-counter drugs, since there is a potential for drug-drug interactions [see Warning and Precautions (5.3), Drug Interactions (7)].

    Increased Risk of Bleeding

    Inform patients about the concomitant use of paroxetine extended-release tablets with aspirin, NSAIDs, other antiplatelet drugs, warfarin, or other anticoagulants because the combined use has been associated with an increased risk of bleeding. Advise patients to inform their health care providers if they are taking or planning to take any prescription or over-the counter medications that increase the risk of bleeding [see Warnings and Precautions (5.5)].

    Activation of Mania/Hypomania

    Advise patients and their caregivers to observe for signs of activation of mania/hypomania and instruct them to report such symptoms to the healthcare provider [see Warnings and Precautions (5.6)].

    Discontinuation Syndrome

    Advise patients not to abruptly discontinue paroxetine extended-release tablets and to discuss any tapering regimen with their healthcare provider. Inform patients that adverse reactions can occur when paroxetine extended-release tablets is discontinued [See Warnings and Precautions (5.7)].

    Allergic Reactions

    Advise patients to notify their healthcare provider if they develop an allergic reaction such as rash, hives, swelling, or difficulty breathing [see Adverse Reactions (6.1, 6.2)].

    Embryo-Fetal Toxicity

    Advise women of the potential risk to the fetus [see Warnings and Precautions (5.4), Use in Specific Populations (8.1)]. Advise patients to notify their healthcare provider if they become pregnant or intend to become pregnant during therapy because of the risk to the fetus.

    Nursing

    Advise women to notify their healthcare provider if they are breastfeeding an infant [see Use in Specific Populations (8.3)].

    Manufactured for:

    Lupin Pharmaceuticals, Inc.

    Baltimore, Maryland 21202

    United States.

    Manufactured by:

    Lupin Limited

    Pithampur (M.P.) 454 775, INDIA

    Revised: December 2019                                                                                ID#: 262623

  • MEDICATION GUIDE

    Medication Guide
    PAROXETINE (pa rox' e teen) EXTENDED-RELEASE TABLETS, USP
    Paroxetine extended-release tablets, 12.5 mg contain FD&C Yellow No. 5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible persons. Although the overall incidence of FD&C Yellow No. 5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.
    What is the most important information I should know about paroxetine extended-release tablets?
    Paroxetine extended-release tablets can cause serious side effects, including:
    Increased risk of suicidal thoughts or actions. Antidepressant medicines may increase suicidal thoughts and actions in some children and young adults within the first few months of treatment or when the dose is changed. Paroxetine extended-release tablets is not for use in people younger than 18 years of age.
    How can I watch for and try to prevent suicidal thoughts and actions?
    ο  Depression or other serious mental illnesses are the most important causes of suicidal thoughts and actions.
    ο  Pay close attention to any changes, especially sudden changes in mood, behavior, thoughts or feelings or if you develop suicidal thoughts or actions. This is very important when an antidepressant medicine is started or when the dose is changed.
    ο  Call your healthcare provider right away to report new or sudden changes in mood, behavior, thoughts or feelings or if you develop suicidal thoughts or actions.
    ο  Keep all follow-up visits with your healthcare provider as scheduled. Call your healthcare provider between visits as needed, especially if you have concerns about symptoms.
    Call your healthcare provider or get emergency medical help right away if you have any of the following symptoms, especially if they are new, worse, or worry you:
    ο  attempts to commit suicide
    ο  acting aggressive or violent
    ο  new or worse depression
    ο  feeling agitated, restless, angry, or irritable
    ο  an increase in activity and talking more than what is normal for you
    ο  acting on dangerous impulses
    ο  thoughts about suicide or dying
    ο  new or worse anxiety or panic attacks
    ο  trouble sleeping
    ο  other unusual changes in behavior or mood
    What is Paroxetine Extended-Release Tablets?
    Paroxetine extended-release tablets is a prescription medicine used in adults to treat:
    A certain type of depression called Major Depressive Disorder (MDD)
    Panic Disorder
    Social Anxiety Disorder (SAD)
    Premenstrual Dysphoric Disorder (PMDD)
    Do not take paroxetine extended-release tablets if you:
    take a monoamine oxidase inhibitor (MAOI)
    have stopped taking an MAOI in the last 14 days
    are being treated with the antibiotic linezolid or intravenous methylene blue
    are taking thioridazine
    are taking pimozide
    are allergic to paroxetine or any of the ingredients in paroxetine extended-release tablets. See the end of this Medication Guide for a complete list of ingredients in paroxetine extended-release tablets.
    Ask your healthcare provider or pharmacist if you are not sure if you take an MAOI or one of these medicines, including intravenous methylene blue.
    Do not start taking an MAOI for at least 14 days after you stop treatment with paroxetine extended-release tablets.
    Before taking paroxetine extended-release tablets, tell your healthcare provider about all your medical conditions, including if you:
    have heart problems
    have or had bleeding problems
    have, or have a family history of bipolar disorder, mania or hypomania
    have or had seizures or convulsions
    have glaucoma (high pressure in the eye)
    have low sodium levels in your blood
    have bone problems
    have kidney or liver problems
    are pregnant or plan to become pregnant. Paroxetine may harm your unborn baby. Talk to your healthcare provider about the risks to your unborn baby if you take paroxetine extended-release tablets during pregnancy. Tell your healthcare provider right away if you become pregnant or think you are pregnant during treatment with paroxetine extended-release tablets.
    are breastfeeding or plan to breastfeed. Paroxetine passes into your breast milk. Talk to your healthcare provider about the best way to feed your baby during treatment with paroxetine extended-release tablets.
    Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements.
    Paroxetine extended-release tablets and some other medicines may affect each other causing possible serious side effects. Paroxetine extended-release tablets may affect the way other medicines work and other medicines may affect the way paroxetine extended-release tablets works.
    Especially tell your healthcare provider if you take:
    medicines used to treat migraine headaches called triptans
    tricyclic antidepressants
    fentanyl
    lithium
    tramadol
    tryptophan
    buspirone
    amphetamines
    St. John's Wort
    medicines that can affect blood clotting such as aspirin, nonsteroidal anti-inflammatory drugs (NSAIDs), or warfarin
    diuretics
    tamoxifen
    Ask your healthcare provider if you are not sure if you are taking any of these medicines. Your healthcare provider can tell you if it is safe to take paroxetine extended-release tablets with your other medicines.
    Do not start or stop any other medicines during treatment with paroxetine extended-release tablets without talking to your healthcare provider first. Stopping paroxetine extended-release tablets suddenly may cause you to have serious side effects. See, "What are the possible side effects of paroxetine extended-release tablets?"
    Know the medicines you take. Keep a list of them to show to your healthcare provider and pharmacist when you get a new medicine.
    How should I take paroxetine extended-release tablets?
    Take paroxetine extended-release tablets exactly as your healthcare provider tell you to. Your healthcare provider may need to change the dose of paroxetine extended-release tablets until it is the right dose for you.
    Take paroxetine extended-release tablets one time each day in the morning.
    Paroxetine extended-release tablets may be taken with or without food.
    Swallow paroxetine extended-release tablets tablets whole. Do not chew or crush paroxetine extended-release tablets tablets.
    If you take too much paroxetine extended-release tablets, call your poison control center at 1-800-222-1222 or got to the nearest hospital emergency room right away.
    What are possible side effects of paroxetine extended-release tablets?
    Paroxetine extended-release tablets can cause serious side effects, including:
    See, "What is the most important information I should know about paroxetine extended-release tablets?"
    Serotonin syndrome. A potentially life-threatening problem called serotonin syndrome can happen when you take paroxetine extended-release tablets with certain other medicines. See, "Who should not take paroxetine extended-release tablets?" Call your healthcare provider or go to the nearest hospital emergency room right away if you have any of the following signs and symptoms of serotonin syndrome:
    ο  agitation
    ο  seeing or hearing things that are not real (hallucinations)
    ο  confusion
    ο  coma
    ο  fast heart beat
    ο  changes in blood pressure
    ο  dizziness
    ο  sweating
    ο  flushing
    ο  high body temperature (hyperthermia)
    ο  shaking (tremors), stiff muscles, or muscle twitching
    ο  loss of coordination
    ο  seizures
    ο  nausea, vomiting, diarrhea
    Medicine interactions. Taking paroxetine extended-release tablets with certain other medicines including thioridazine and pimozide may increase the risk of developing a serious heart problem called QT prolongation.
    Abnormal bleeding. Taking paroxetine extended-release tablets with aspirin, NSAIDs, or blood thinners may add to this risk. Tell your healthcare provider about any unusual bleeding or bruising.
    Manic episodes. Manic episodes may happen in people with bipolar disorder who take paroxetine extended-release tablets. Symptoms may include:
    ο  greatly increased energy
    ο  racing thoughts
    ο  unusually grand ideas
    ο  talking more or faster than usual
    ο  severe problems sleeping
    ο  reckless behavior
    ο  excessive happiness or irritability
    Discontinuation syndrome. Suddenly stopping paroxetine extended-release tablets may cause you to have serious side effects. Your healthcare provider may want to decrease your dose slowly. Symptoms may include:
    ο  nausea
    ο  sweating
    ο  changes in your mood
    ο  irritability and agitation
    ο  dizziness
    ο  electric shock feeling (paresthesia)
    ο  tremor
    ο  anxiety
    ο  confusion
    ο  headache
    ο  tiredness
    ο  problems sleeping
    ο  ringing in your ears (tinnitus)
    ο  seizures
    Seizures (convulsions).
    Eye problems (angle-closure glaucoma). Paroxetine extended-release tablets may cause a type of eye problem called angle-closure glaucoma in people with certain other eye conditions. You may want to undergo an eye examination to see if you are at risk and receive preventative treatment if you are.
    Low sodium levels in your blood (hyponatremia). Low sodium levels in your blood that may be serious and may cause death, can happen during treatment with paroxetine extended-release tablets. Elderly people and people who take certain medicines may be at a greater risk for developing low sodium levels in your blood. Signs and symptoms may include:
    ο  headache
    ο  difficulty concentrating
    ο  memory changes
    ο  confusion
    ο  weakness and unsteadiness on your feet which can lead to falls
    In more severe or more sudden cases, signs and symptoms include:
    ο  seeing or hearing things that are not real (hallucinations)
    ο  fainting
    ο  seizures
    ο  coma
    ο  stopping breathing (respiratory arrest)
    Bone fractures.
    The most common side effects paroxetine extended-release tablets include:
    male and female sexual function problems
    blurred vision
    weakness (asthenia)
    constipation
    decreased appetite
    diarrhea
    dry mouth
    problems sleeping
    nausea
    sleepiness
    sweating
    tremor
    dizziness
    These are not all the possible side effects of paroxetine extended-release tablets.
    Call your doctor for medical advice about side effects. You may report side effects to FDA at
    1-800-FDA-1088.
    How should I store paroxetine extended-release tablets?
    Store paroxetine extended-release tablets at room temperature between 68°F to 77°F (20°C to 25°C).
    Keep paroxetine extended-release tablets and all medicines out of the reach of children.
    General information about the safe and effective use of paroxetine extended-release tablets.
    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not take paroxetine extended-release tablets for a condition for which it was not prescribed. Do not give paroxetine extended-release tablets to other people, even if they have the same symptoms that you have. It may harm them. You may ask your healthcare provider or pharmacist for information about paroxetine extended-release tablets that is written for healthcare professionals.
    What are the ingredients in paroxetine extended-release tablets?
    Active ingredient: paroxetine hydrochloride hemihydrate USP
    Inactive ingredients: aluminum oxide, colloidal silicon dioxide, hydrogenated vegetable oil, hypromelloses, iron oxide black, lactose monohydrate, magnesium stearate, methacrylic acid co-polymer dispersion, microcrystalline cellulose, polyethylene glycols, povidone, propylene glycol, shellac glaze, talc, titanium dioxide, triacetin and triethyl citrate.
    The 12.5 mg tablets also contain D&C Yellow No. 10 Aluminum Lake, FD&C Yellow No. 5 Aluminum Lake (tartrazine) and FD&C Yellow No. 6 Aluminum Lake.
    The 25 mg tablets also contain D&C Red No. 30 Aluminum Lake and FD&C Blue No. 2 Aluminum Lake.
    The 37.5 mg tablets also contain FD&C Blue No. 1 Aluminum Lake.
    Manufactured for:
    Lupin Pharmaceuticals, Inc.
    Baltimore, Maryland 21202
    United States.
    Manufactured by:
    Lupin Limited
    Pithampur (M.P.) 454 775, INDIA
    Revised: December 2019                                                                                ID#:262624
    For more information about paroxetine extended-release tablets go to www.lupinpharmaceuticals.com or call Lupin Pharmaceuticals, Inc. at 1-800-399-2561.
    This Medication Guide has been approved by the U.S. Food and Drug Administration.
  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Paroxetine Extended-Release Tablets USP, 12.5 mg

    NDC: 68180-647-06

    BOTTLE LABEL - 30 TABLETS

    12.5

    Paroxetine Extended-Release Tablets USP, 25 mg

    NDC: 68180-646-06

    BOTTLE LABEL - 30 TABLETS

    25

    Paroxetine Extended-Release Tablets USP, 37.5 mg

    NDC: 68180-645-06

    BOTTLE LABEL - 30 TABLETS

    37.5
  • INGREDIENTS AND APPEARANCE
    PAROXETINE 
    paroxetine tablet, film coated, extended release
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 68180-647
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAROXETINE HYDROCHLORIDE HEMIHYDRATE (UNII: X2ELS050D8) (PAROXETINE - UNII:41VRH5220H) PAROXETINE12.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE K30 (UNII: U725QWY32X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIACETIN (UNII: XHX3C3X673)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Product Characteristics
    ColorYELLOWScoreno score
    ShapeROUND (biconvex) Size8mm
    FlavorImprint Code L067
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 68180-647-0630 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    2NDC: 68180-647-01100 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    3NDC: 68180-647-02500 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    4NDC: 68180-647-031000 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20413403/06/2017
    PAROXETINE 
    paroxetine tablet, film coated, extended release
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 68180-646
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAROXETINE HYDROCHLORIDE HEMIHYDRATE (UNII: X2ELS050D8) (PAROXETINE - UNII:41VRH5220H) PAROXETINE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    FD&C BLUE NO. 2 (UNII: L06K8R7DQK)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE K30 (UNII: U725QWY32X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIACETIN (UNII: XHX3C3X673)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Product Characteristics
    ColorPINKScoreno score
    ShapeROUND (biconvex) Size8mm
    FlavorImprint Code L068
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 68180-646-0630 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    2NDC: 68180-646-01100 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    3NDC: 68180-646-02500 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    4NDC: 68180-646-031000 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20413403/06/2017
    PAROXETINE 
    paroxetine tablet, film coated, extended release
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 68180-645
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PAROXETINE HYDROCHLORIDE HEMIHYDRATE (UNII: X2ELS050D8) (PAROXETINE - UNII:41VRH5220H) PAROXETINE37.5 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    CASTOR OIL (UNII: D5340Y2I9G)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE K30 (UNII: U725QWY32X)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIACETIN (UNII: XHX3C3X673)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Product Characteristics
    ColorBLUEScoreno score
    ShapeROUND (biconvex) Size8mm
    FlavorImprint Code L069
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 68180-645-0630 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    2NDC: 68180-645-01100 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    3NDC: 68180-645-02500 in 1 BOTTLE; Type 0: Not a Combination Product03/06/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20413403/06/2017
    Labeler - Lupin Pharmaceuticals, Inc. (089153071)
    Registrant - LUPIN LIMITED (675923163)
    Establishment
    NameAddressID/FEIBusiness Operations
    LUPIN LIMITED863645527MANUFACTURE(68180-645, 68180-646, 68180-647) , PACK(68180-645, 68180-646, 68180-647)
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