`
`These highlights do not include all the information needed to use
`INVEGA SUSTENNA® safely and effectively. See full prescribing
`
`information for INVEGA SUSTENNA®.
`INVEGA SUSTENNA® (paliperidone palmitate) extended-release
`injectable suspension, for intramuscular use
`Initial U.S. Approval: 2006
`
`WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS
`
`WITH DEMENTIA-RELATED PSYCHOSIS
`
`See full prescribing information for complete boxed warning.
`
`Elderly patients with dementia-related psychosis treated with
`
`antipsychotic drugs are at an increased risk of death. (5.1)
`
`
` INVEGA SUSTENNA® is not approved for use in patients with
`
`
`dementia-related psychosis. (5.1)
`
`x
`
`x
`
`
`
`----------------------------RECENT MAJOR CHANGES-------------------------
`Dosage and Administration (2.5)
`06/2017
`Warnings and Precautions (5.8)
`02/2017
`
`Warnings and Precautions (5.10)
`06/2017
`
`
`----------------------------INDICATIONS AND USAGE---------------------------
`INVEGA SUSTENNA® is an atypical antipsychotic indicated for
`x Treatment of schizophrenia. (1)
`x Treatment of schizoaffective disorder as monotherapy and as an adjunct to
`
`
`
`
`mood stabilizers or antidepressants. (1)
`
`-----------------------DOSAGE AND ADMINISTRATION----------------------
`x For intramuscular injection only. (2.1)
`
`
`x Each injection must be administered only by a health care professional.
`
`
`
`(2.1)
`x For deltoid injection, use 1-inch 23G needle for patients weighing less than
`
`90 kg or 1½-inch 22G needle for patients weighing 90 kg or more. For
`
`
`
`gluteal injection, use 1½-inch 22G needle regardless of patient weight.
`
`
`(2.1)
`
`Initiation Dosing
`(deltoid)
`Day 1
`Day 8
`
`Monthly
`Maintenance Dosea
`
`(deltoid or gluteal)
`
`Maximum
`
`Monthly
`Dose
`
`234 mg
`
`156 mg
`
`39-234 mgb
`
`234 mg
`
`Indication
`
`Schizophrenia
`
`(2.2)
`
`234 mg
`
`156 mg
`
`78-234 mgc
`
`
`234 mg
`
`Schizoaffective
`
`disorder (2.2)
`
` Administered 5 weeks after the first injection.
`
`
`The recommended maintenance dose for treatment of schizophrenia is 117
`mg. Some patients may benefit from lower or higher maintenance doses
`
`
`
`
`
`within the additional available strengths (39 mg, 78 mg, 156 mg, and 234
`mg).
`
`
`Adjust dose based on tolerability and/or efficacy using available strengths.
`
`
`The 39 mg strength was not studied in the long-term schizoaffective
`disorder study.
`
`
`a
`b
`
`c
`
`x For patients naïve to oral paliperidone or oral or injectable risperidone,
`
`establish tolerability with oral paliperidone or oral risperidone prior to
`
`initiating treatment with INVEGA SUSTENNA®. (2.2)
`x Missed Doses: To manage either a missed second initiation dose or a
`
`
`
`missed monthly maintenance dose, refer to the Full Prescribing
`
`Information. (2.3)
`x Moderate to severe renal impairment (creatinine clearance < 50 mL/min):
`
`INVEGA SUSTENNA® is not recommended. (2.5)
`x Mild renal impairment (creatinine clearance t 50 mL/min to < 80 mL/min):
`
`
`Administer 156 mg on treatment day 1 and 117 mg one week later, both
`
`
`administered in the deltoid muscle. Follow with monthly injections of 78
`
`
`
`
`mg in either the deltoid or gluteal muscle. (2.5)
`
`Reference ID: 4119109
`
`--------------------DOSAGE FORMS AND STRENGTHS---------------------
`
`Extended-release injectable suspension: 39 mg, 78 mg, 117 mg, 156 mg, or
`234 mg (3)
`
`-------------------------------CONTRAINDICATIONS------------------------------
`Known hypersensitivity to paliperidone, risperidone, or to any excipients in
`
`
`
`INVEGA SUSTENNA®. (4)
`
`---------------------------WARNINGS AND PRECAUTIONS-------------------
`x Cerebrovascular Adverse Reactions, Including Stroke, in Elderly Patients
`
`with Dementia-Related Psychosis: Increased incidence of cerebrovascular
`
`adverse reactions (e.g. stroke, transient ischemic attack, including
`
`
`fatalities). INVEGA SUSTENNA® is not approved for use in patients with
`
`
`dementia-related psychosis (5.2)
`x Neuroleptic Malignant Syndrome: Manage with immediate discontinuation
`of drug and close monitoring (5.3)
`x QT Prolongation: Avoid use with drugs that also increase QT interval and
`
`in patients with risk factors for prolonged QT interval (5.4)
`
`x Tardive Dyskinesia: Discontinue drug if clinically appropriate (5.5)
`x Metabolic Changes: Atypical antipsychotic drugs have been associated
`
`with metabolic changes that may increase cardiovascular/cerebrovascular
`
`
`risk. These metabolic changes include:
`
`o Hyperglycemia and Diabetes Mellitus: Monitor for symptoms of
`hyperglycemia including polydipsia, polyuria, polyphagia, and
`
`weakness. Monitor glucose regularly in patients with diabetes or at
`
`risk for diabetes. (5.6)
`o Dyslipidemia: Undesirable alterations have been observed. (5.6)
`o Weight Gain: Significant weight gain has been reported. Monitor
`
`
`weight gain. (5.6)
`x Orthostatic Hypotension and Syncope: Use with caution in patients with
`
`
`
`known cardiovascular or cerebrovascular disease and patients predisposed
`
`to hypotension (5.7)
`x Leukopenia, Neutropenia, and Agranulocytosis: Monitor complete blood
`
`count in patients with a history of a clinically significant low white blood
`
`cell count (WBC) or a drug-induced leukopenia/neutropenia. Consider
`
`
`
`
`discontinuation if clinically significant decline in WBC in the absence of
`
`
`other causative factors (5.9)
`x Hyperprolactinemia: Prolactin elevations occur and persist during chronic
`administration (5.10)
`x Potential for Cognitive and Motor Impairment: Use caution when
`
`
`operating machinery (5.11)
`x Seizures: Use cautiously in patients with a history of seizures or with
`
`
`
`conditions that lower the seizure threshold (5.12)
`
`------------------------------ADVERSE REACTIONS-----------------------------
`The most common adverse reactions LQFLGHQFH DQG RFFXUring at least
`
`
`twice as often as placebo) were injection site reactions, somnolence/sedation,
`
`dizziness, akathisia, and extrapyramidal disorder. (6)
`
`To report SUSPECTED ADVERSE REACTIONS, contact Janssen
`
`Pharmaceuticals, Inc. at 1-800-JANSSEN (1-800-526-7736) or FDA at
`
`
`
`1-800-FDA-1088 or www.fda.gov/medwatch
`
`---------------------------------DRUG INTERACTIONS---------------------------
`x Drugs that may cause orthostatic hypotension: An additive effect may
`
`
`occur when co-administered with INVEGA SUSTENNA®. (7.1)
`x Strong CYP3A4/P-glycoprotein (P-gp) inducers: Avoid using a strong
`inducer of CYP3A4 and/or P-gp (e.g., carbamazepine, rifampin, St John’s
`
`Wort) during a dosing interval for INVEGA SUSTENNA®. If
`
`
`
`administering a strong inducer is necessary, consider managing the patient
`
`
`using paliperidone extended release tablets. (2.5, 7.1, 12.3)
`
`
`-----------------------USE IN SPECIFIC POPULATIONS----------------------
`Pregnancy: May cause extrapyramidal and/or withdrawal symptoms in
`
`
`neonates with third trimester exposure. (8.1)
`
`See 17 for PATIENT COUNSELING INFORMATION and FDA-
`
`
`approved patient labeling.
`
`Revised: 06/2017
`
`1
`
`
`
`
`
` FULL PRESCRIBING INFORMATION: CONTENTS*
`
`
`
` WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS
`
`WITH DEMENTIA-RELATED PSYCHOSIS
`
`
`1
`INDICATIONS AND USAGE
`
`
`2 DOSAGE AND ADMINISTRATION
`
`
`Administration Instructions
`
`2.1
`
`
`Schizophrenia and Schizoaffective Disorder
`
`2.2
`
`
`2.3
`Missed Doses
`
`
`
`2.4
`Use with Risperidone or with Oral Paliperidone
`
`
`
`
`2.5
`Dosage Adjustments
`
`
`
`2.6
`Switching from Other Antipsychotics
`
`
`
`
`2.7
`Instructions for Use
`
`
`
`3 DOSAGE FORMS AND STRENGTHS
`
`
`
`4 CONTRAINDICATIONS
`
`
`5 WARNINGS AND PRECAUTIONS
`
`Increased Mortality in Elderly Patients with
`
`5.1
`
`
`Dementia-Related Psychosis
`
`
`5.2
`Cerebrovascular Adverse Reactions, Including
`
`Stroke, in Elderly Patients with Dementia-
`
`
`Related Psychosis
`
`
`
`Neuroleptic Malignant Syndrome
`
`5.3
`
`
`QT Prolongation
`
`5.4
`
`
`Tardive Dyskinesia
`
`5.5
`
`
`Metabolic Changes
`
`5.6
`
`
`Orthostatic Hypotension and Syncope
`
`5.7
`
`
`Falls
`
`5.8
`
`
`Leukopenia, Neutropenia, and Agranulocytosis
`
`5.9
`
`
`5.10 Hyperprolactinemia
`
`
`
`5.11 Potential for Cognitive and Motor Impairment
`
`
`
`5.12 Seizures
`
`
`
`5.13 Dysphagia
`
`
`
`5.14 Priapism
`
`
`
`5.15 Disruption of Body Temperature Regulation
`
`
`
`
`6 ADVERSE REACTIONS
`
`
`Clinical Trials Experience
`
`6.1
`
`
`
`Postmarketing Experience
`
`6.2
`
`
`7 DRUG INTERACTIONS
`
`
`Drugs Having Clinically Important Interactions
`
`7.1
`
`
`with INVEGA SUSTENNA®
`
`
`
`
` Drugs Having No Clinically Important
`
`7.2
`
`Interactions with INVEGA SUSTENNA®
`
`
`
`8 USE IN SPECIFIC POPULATIONS
`
`
`8.1
`Pregnancy
`
`
`
`8.2
`Labor and Delivery
`
`
`
`8.3
`Nursing Mothers
`
`
`
`8.4
`Pediatric Use
`
`
`
`8.5
`Geriatric Use
`
`
`
`8.6
`Renal Impairment
`
`
`
`8.7
`Hepatic Impairment
`
`
`8.8
`Patients with Parkinson’s Disease or Lewy Body
`
`
`Dementia
`
`
`
`9 DRUG ABUSE AND DEPENDENCE
`
`
`Controlled Substance
`
`9.1
`
`
`9.2
`Abuse
`
`
`
`9.3
`Dependence
`
`
`
`10 OVERDOSAGE
`
`
`10.1 Human Experience
`
`
`
`10.2 Management of Overdosage
`
`
`
`11 DESCRIPTION
`
`
`12 CLINICAL PHARMACOLOGY
`
`
`12.1 Mechanism of Action
`
`
`
`
`12.2 Pharmacodynamics
`
`
`12.3 Pharmacokinetics
`
`
`
`13 NONCLINICAL TOXICOLOGY
`
`13.1 Carcinogenesis, Mutagenesis, Impairment of
`
`
`
`
`Fertility
`
`
`
`14 CLINICAL STUDIES
`
`
`14.1 Schizophrenia
`
`
`
`14.2 Schizoaffective Disorder
`
`
`
`16 HOW SUPPLIED/STORAGE AND HANDLING
`
`
`17 PATIENT COUNSELING INFORMATION
`
`*Sections or subsections omitted from the full prescribing information are not
`
`listed.
`
`Reference ID: 4119109
`
`2
`
`
`
`FULL PRESCRIBING INFORMATION
`
`
`WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA
`RELATED PSYCHOSIS
`x Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at
`
`
`an increased risk of death [see Warnings and Precautions (5.1)].
` INVEGA SUSTENNA® is not approved for use in patients with dementia-related
`psychosis [see Warnings and Precautions (5.1)].
`
`
`
`x
`
`INDICATIONS AND USAGE
`1
`INVEGA SUSTENNA® (paliperidone palmitate) is indicated for the treatment of:
`x Schizophrenia [see Clinical Studies (14.1)].
`
` x Schizoaffective disorder as monotherapy and as an adjunct to mood stabilizers or
`antidepressants [see Clinical Studies (14.2)].
`
`
`
`2 DOSAGE AND ADMINISTRATION
`
`2.1 Administration Instructions
`Each injection must be administered only by a healthcare professional.
`
`Parenteral drug products should be inspected visually for foreign matter and discoloration prior
`
`
`
`to administration, whenever product and container permit.
`
`INVEGA SUSTENNA® is intended for intramuscular use only. Do not administer by any other
`
`
`
`route. Avoid inadvertent injection into a blood vessel. Administer the dose in a single injection;
`do not administer the dose in divided injections. Inject slowly, deep into the deltoid or gluteal
`muscle.
`
`INVEGA SUSTENNA® must be administered using only the needles that are provided in the
`
`INVEGA SUSTENNA® kit.
`
`The recommended needle size for administration of INVEGA SUSTENNA® into the deltoid
`
`
`muscle is determined by the patient’s weight:
`
`x For patients weighing less than 90 kg, the 1-inch, 23 gauge needle is recommended.
`
`x For patients weighing 90 kg or more, the 1½-inch, 22 gauge needle is recommended.
`
`Deltoid injections should be alternated between the two deltoid muscles.
`
`The recommended needle size for administration of INVEGA SUSTENNA® into the gluteal
`
`
`muscle is the 1½-inch, 22 gauge needle regardless of patient weight.
`
`
`
`
`Administer into the upper-outer quadrant of the gluteal muscle. Gluteal injections should be
`
`
`3
`
`Reference ID: 4119109
`
`
`
`alternated between the two gluteal muscles.
`
`2.2 Schizophrenia and Schizoaffective Disorder
`For patients who have never taken oral paliperidone or oral or injectable risperidone, it is
`
`recommended to establish tolerability with oral paliperidone or oral risperidone prior to initiating
`
`treatment with INVEGA SUSTENNA®.
`
`The recommended dosing of INVEGA SUSTENNA® for each approved indication is displayed
`
`in Table 1. The recommended initiation of INVEGA SUSTENNA® is with a dose of 234 mg on
`
`
`
`
`treatment day 1 and 156 mg one week later, both administered in the deltoid muscle. Following
`
`the second initiation dose, monthly maintenance doses can be administered in either the deltoid
`or gluteal muscle.
`
`Table 1:
`
`Indication
`
`Recommended Dosing of INVEGA SUSTENNA for Adults with Schizophrenia or
`Schizoaffective Disorder
`Initiation Dosing
`(deltoid)
`Day 1
`Day 8
`
`Schizophrenia
`
`234 mg
`
`156 mg
`
`Schizoaffective disorder
`
`234 mg
`
`156 mg
`
`78-234 mgc
`
`
`Monthly
`Maintenance Dosea
`(deltoid or gluteal)
`39-234 mgb
`
`Maximum Monthly
`
`Dose
`
`234 mg
`
`234 mg
`
` a Administered 5 weeks after the first injection.
`
`
`b
`The recommended maintenance dose for treatment of schizophrenia is 117 mg. Some patients may benefit from
`
`
`
`lower or higher maintenance doses within the additional available strengths (39 mg, 78 mg, 156 mg, and
`
`234 mg).
`c Adjust dose based on tolerability and/or efficacy using available strengths. The 39 mg strength was not studied
`
`
`in the long-term schizoaffective disorder study.
`
` Adjustment of the maintenance dose may be made monthly. When making dose adjustments, the
`
`prolonged-release characteristics of INVEGA SUSTENNA® should be considered [see Clinical
`Pharmacology (12.3)], as the full effect of the dose adjustment may not be evident for several
`
`months.
`
`2.3 Missed Doses
`Avoiding Missed Doses
`It is recommended that the second initiation dose of INVEGA SUSTENNA® be given one week
`
`
`
`after the first dose. To avoid a missed dose, patients may be given the second dose 4 days before
`or after the one-week time point. Similarly, the third and subsequent injections after the initiation
`
`
`regimen are recommended to be given monthly. To avoid a missed monthly dose, patients may
`be given the injection up to 7 days before or after the monthly time point.
`
`4
`
`Reference ID: 4119109
`
`
`
`Management of a Missed Second Initiation Dose
`If the target date for the second INVEGA SUSTENNA® injection (one week ± 4 days) is missed,
`
` the recommended reinitiation depends on the length of time which has elapsed since the patient's
` first injection. In case of a missed second initiation dose follow the dosing instructions provided
`
`in Table 2.
`
`Table 2:
`
`Management of a Missed Second Initiation Dose
`
`DOSING
`
`TIMING OF MISSED SECOND
`INITIATION DOSE
`
`
`
`Less than 4 weeks since first injection
`
`
`
`4 to 7 weeks since first injection
`
`Administer the second initiation dose of 156 mg in the deltoid
`
`muscle as soon as possible.
`
`It is recommended to administer a third injection of 117 mg in
`1.
`
`either the deltoid or gluteal muscle 5 weeks after the first injection
`(regardless of the timing of the second injection).
`
`2. Thereafter, resume regular monthly dosing in either the deltoid or
`gluteal muscle.
`
`Resume dosing with two injections of 156 mg in the following
`manner:
`1. Administer a deltoid injection as soon as possible.
`2. Administer a second deltoid injection 1 week later.
`
`3. Thereafter, resume regular monthly dosing in either the
`deltoid or gluteal muscle.
`More than 7 weeks since first injection Restart dosing with recommended initiation (see Section 2.2,
`Table 1):
`1. Administer a 234 mg deltoid injection on Day 1.
`
`2. Administer a 156 mg deltoid injection 1 week later.
`
`3. Thereafter, resume regular monthly dosing in either the
`deltoid or gluteal muscle.
`
`Management of a Missed Maintenance Dose
`
` In case of a missed maintenance dose follow the dosing instructions provided in Table 3.
`
`Management of a Missed Maintenance Dose
`Table 3:
`TIMING OF MISSED
`MAINTENANCE DOSE
`
`
`4 to 6 weeks since last injection
`
`DOSING
`
`Resume regular monthly dosing as soon as possible at the patient’s
`
`
`previously stabilized dose, followed by injections at monthly
`
`intervals.
`
`Resume the same dose the patient was previously stabilized on
`(unless the patient was stabilized on a dose of 234 mg, then the first
`
`5
`
`
`
`More than 6 weeks to 6 months since
`last injection
`
`Reference ID: 4119109
`
`
`
`2 injections should each be 156 mg) in the following manner:
`1. Administer a deltoid injection as soon as possible.
`
`
`2. Administer a second deltoid injection 1 week later at the same
`dose.
`
`3. Thereafter, resume administering the previously stabilized
`
`
`
`
`dose in the deltoid or gluteal muscle 1 month after the second
`injection.
`More than 6 months since last injection Restart dosing with recommended initiation (see Section 2.2,
`
`Table 1):
`1. Administer a 234 mg deltoid injection on Day 1.
`
`2. Administer a 156 mg deltoid injection 1 week later.
`
`3. Thereafter, resume administering the previously stabilized
`
`
`
`
`dose in the deltoid or gluteal muscle 1 month after the second
`injection.
`
` 2.4 Use with Risperidone or with Oral Paliperidone
`
`
`Since paliperidone is the major active metabolite of risperidone, caution should be exercised
`when INVEGA SUSTENNA® is coadministered with risperidone or with oral paliperidone for
`
`
`extended periods of time. Safety data involving concomitant use of INVEGA SUSTENNA® with
`
`other antipsychotics is limited.
`
`2.5 Dosage Adjustments
`Renal Impairment
`INVEGA SUSTENNA® has not been systematically studied in patients with renal impairment
`[see Clinical Pharmacology (12.3)]. For patients with mild renal impairment (creatinine
`
`
`FOHDUDQFH P/PLQ WR P/PLQ [Cockcroft-Gault Formula]), initiate INVEGA
`SUSTENNA® with a dose of 156 mg on treatment day 1 and 117 mg one week later. Administer
`
`
`
`both doses in the deltoid muscle. Thereafter, follow with monthly injections of 78 mg in either
`the deltoid or gluteal muscle [see Use in Specific Populations (8.6) and Clinical Pharmacology
`(12.3)].
`
`INVEGA SUSTENNA® is not recommended in patients with moderate or severe renal
`
`
`impairment (creatinine clearance < 50 mL/min) [see Use in Specific Populations (8.6) and
`
`Clinical Pharmacology (12.3)].
`
`Coadministration with Strong CYP3A4/P-glycoprotein (P-gp) Inducers
`Avoid using a strong inducer of CYP3A4 and/or P-gp (e.g., carbamazepine, rifampin, St John’s
`
`
` Wort) during the 1-month dosing interval for INVEGA SUSTENNA®, if possible. If
` administering a strong inducer is necessary, consider managing the patient using paliperidone
`
`extended release tablets [see Drug Interactions (7.1) and Clinical Pharmacology (12.3)].
`
`6
`
`Reference ID: 4119109
`
`
`
`
` 2.6 Switching from Other Antipsychotics
`
`
` There are no systematically collected data to specifically address switching patients with
`
`schizophrenia or schizoaffective disorder from other antipsychotics to INVEGA SUSTENNA®,
`or concerning concomitant administration with other antipsychotics.
`
`Switching from Oral Antipsychotics
` For patients who have never taken oral paliperidone or oral or injectable risperidone, tolerability
`
`should be established with oral paliperidone or oral risperidone prior to initiating treatment with
`INVEGA SUSTENNA®.
`
`
`
`
`Previous oral antipsychotics can be gradually discontinued at the time of initiation of treatment
`with INVEGA SUSTENNA®. Recommended initiation of INVEGA SUSTENNA® is with a
`
`
`
`dose of 234 mg on treatment day 1 and 156 mg one week later, both administered in the deltoid
`muscle [see Dosage and Administration (2.2)]. Patients previously stabilized on different doses
`
`
`of INVEGA® Extended-Release tablets can attain similar paliperidone steady-state exposure
`during maintenance treatment with INVEGA SUSTENNA® monthly doses as depicted in
`
`Table 4.
`
`Table 4:
`
`Doses of INVEGA and INVEGA SUSTENNA Needed to Attain Similar Steady-State
`Paliperidone Exposure During Maintenance Treatment
`INVEGA®
`Formulation
`Extended-Release Tablet
`Once Daily
`12
`9
`6
`3
`
`Dosing Frequency
`
`Dose (mg)
`
`INVEGA SUSTENNA®
`Injection
`Once every 4 weeks
`234
`156
`117
`39-78
`
`Switching from Long-Acting Injectable Antipsychotics
` For patients who have never taken oral paliperidone or oral or injectable risperidone, tolerability
`
`should be established with oral paliperidone or oral risperidone prior to initiating treatment with
`INVEGA SUSTENNA®.
`
`
`When switching patients currently at steady-state on a long-acting injectable antipsychotic,
`initiate INVEGA SUSTENNA® therapy in place of the next scheduled injection. INVEGA
`SUSTENNA® should then be continued at monthly intervals. The one-week initiation dosing
`
`
`
`regimen as described in Section 2.2 is not required. See Table 1 above for recommended
`
`monthly maintenance dosing. Based on previous clinical history of tolerability and/or efficacy,
`some patients may benefit from lower or higher maintenance doses within the available strengths
`(39 mg, 78 mg, 117 mg, 156 mg, and 234 mg). The 39 mg strength was not studied in the
`
`7
`
`Reference ID: 4119109
`
`
`
`
`
` long-term schizoaffective disorder study. Monthly maintenance doses can be administered in
`
` either the deltoid or gluteal muscle [see Dosage and Administration (2.2)].
`
`
`
`
`If INVEGA SUSTENNA® is discontinued, its prolonged-release characteristics must be
`considered. As recommended with other antipsychotic medications, the need for continuing
`existing extrapyramidal symptoms (EPS) medication should be re-evaluated periodically.
`
`Instructions for Use
`2.7
`Each injection must be administered only by a healthcare professional.
`
`The kit contains a prefilled syringe and 2 safety needles (a 1 ½-inch 22 gauge needle and a
`1-inch 23 gauge needle) for intramuscular injection.
`
`INVEGA SUSTENNA® is for single use only.
`
`
`a. Shake the syringe vigorously for a minimum of 10 seconds to ensure a homogeneous
`suspension.
`
`Reference ID: 4119109
`
`8
`
`
`
`b. Select the appropriate needle.
`
`For DELTOID injection:
`
`x
`
`x
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`If the patient weighs less than 90 kg, use the 1-inch 23 gauge needle (needle with blue
`colored hub).
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`If the patient weighs 90 kg or more, use the 1 ½-inch 22 gauge needle (needle with gray
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`colored hub).
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`For GLUTEAL injection:
`
`Use the 1 ½-inch 22 gauge needle (needle with gray colored hub) regardless of patient’s
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`weight.
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`c. While holding the syringe upright, remove the rubber tip cap with an easy clockwise twisting
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`motion.
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`Reference ID: 4119109
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` d. Peel the safety needle pouch half way open. Grasp the needle sheath using the plastic peel
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` pouch. Attach the safety needle to the luer connection of the syringe with an easy clockwise
`twisting motion.
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`
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`e. Pull the needle sheath away from the needle with a straight pull. Do not twist the sheath as
`the needle may be loosened from the syringe.
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` f. Bring the syringe with the attached needle in upright position to de-aerate. De-aerate the
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` syringe by moving the plunger rod carefully forward.
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`
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`g. Inject the entire contents intramuscularly slowly, deep into the selected deltoid or gluteal
`muscle of the patient. Do not administer by any other route.
`
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`h. After the injection is complete, use either thumb or finger of one hand (h1, h2) or a flat
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` surface (h3) to activate the needle protection system. The needle protection system is fully
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` activated when a ‘click’ is heard. Discard the syringe with needle appropriately.
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`h1
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`h2
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`h3
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` 3 DOSAGE FORMS AND STRENGTHS
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`INVEGA SUSTENNA® is available as a white to off-white aqueous extended-release injectable
`
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`suspension for intramuscular injection in dose strengths of 39 mg, 78 mg, 117 mg, 156 mg, and
`234 mg paliperidone palmitate.
`
`4 CONTRAINDICATIONS
`INVEGA SUSTENNA® is contraindicated in patients with a known hypersensitivity to either
`paliperidone or risperidone, or to any of the excipients in the INVEGA SUSTENNA®
`
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`formulation. Hypersensitivity reactions, including anaphylactic reactions and angioedema, have
`
`been reported in patients treated with risperidone and in patients treated with paliperidone.
`Paliperidone palmitate is converted to paliperidone, which is a metabolite of risperidone.
`
`5 WARNINGS AND PRECAUTIONS
`
`
`5.1
`Increased Mortality in Elderly Patients with Dementia-Related Psychosis
`
`Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an
`
`increased risk of death. Analyses of 17 placebo-controlled trials (modal duration of 10 weeks),
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`largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated
`patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course
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`of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%,
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`compared to a rate of about 2.6% in the placebo group. Although the causes of death were
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`varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death)
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`or infectious (e.g., pneumonia) in nature. Observational studies suggest that, similar to atypical
`
`antipsychotic drugs, treatment with conventional antipsychotic drugs may increase mortality.
`
`The extent to which the findings of increased mortality in observational studies may be attributed
`
`to the antipsychotic drug as opposed to some characteristic(s) of the patients is not clear.
`
`INVEGA SUSTENNA® is not approved for the treatment of patients with dementia-related
`
`psychosis [see Boxed Warning and Warnings and Precautions (5.2)].
`
`5.2 Cerebrovascular Adverse Reactions, Including Stroke, in Elderly Patients
`with Dementia-Related Psychosis
`In placebo-controlled trials with risperidone, aripiprazole, and olanzapine in elderly subjects with
`
`dementia, there was a higher incidence of cerebrovascular adverse reactions (cerebrovascular
`accidents and transient ischemic attacks) including fatalities compared to placebo-treated
`subjects. No studies have been conducted with oral paliperidone, INVEGA SUSTENNA®, or the
`
`3-month paliperidone palmitate extended-release injectable suspension in elderly patients with
`
`dementia. These medicines are not approved for the treatment of patients with dementia-related
`psychosis [see Boxed Warning and Warnings and Precautions (5.1)].
`
`5.3 Neuroleptic Malignant Syndrome
`
`A potentially fatal symptom complex sometimes referred to as Neuroleptic Malignant Syndrome
`(NMS) has been reported in association with antipsychotic drugs, including paliperidone.
`
`Clinical manifestations of NMS are hyperpyrexia, muscle rigidity, altered mental status, and
`evidence of autonomic instability (irregular pulse or blood pressure, tachycardia, diaphoresis,
`and cardiac dysrhythmia). Additional signs may include elevated creatine phosphokinase,
`myoglobinuria (rhabdomyolysis), and acute renal failure.
`
`
`The diagnostic evaluation of patients with this syndrome is complicated. In arriving at a
`
`diagnosis, it is important to identify cases in which the clinical presentation includes both serious
`
`medical illness (e.g., pneumonia, systemic infection, etc.) and untreated or inadequately treated
`
`extrapyramidal signs and symptoms (EPS). Other important considerations in the differential
`
`diagnosis include central anticholinergic toxicity, heat stroke, drug fever, and primary central
`nervous system pathology.
`
`The management of NMS should include: (1) immediate discontinuation of antipsychotic drugs
`
`and other drugs not essential to concurrent therapy; (2) intensive symptomatic treatment and
`
`medical monitoring; and (3) treatment of any concomitant serious medical problems for which
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`specific treatments are available. There is no general agreement about specific pharmacological
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`treatment regimens for uncomplicated NMS.
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`If a patient appears to require antipsychotic drug treatment after recovery from NMS,
`
`
`
`reintroduction of drug therapy should be closely monitored, since recurrences of NMS have been
`
`reported.
`
`5.4 QT Prolongation
`Paliperidone causes a modest increase in the corrected QT (QTc) interval. The use of
`
`
`paliperidone should be avoided in combination with other drugs that are known to prolong QTc
`
`including Class 1A (e.g., quinidine, procainamide) or Class III (e.g., amiodarone, sotalol)
`
`antiarrhythmic medications, antipsychotic medications (e.g., chlorpromazine, thioridazine),
`
`antibiotics (e.g., gatifloxacin, moxifloxacin), or any other class of medications known to prolong
`
`the QTc interval. Paliperidone should also be avoided in patients with congenital long QT
`
`syndrome and in patients with a history of cardiac arrhythmias.
`
`
`Certain circumstances may increase the risk of the occurrence of Torsades de pointes and/or
`
`sudden death in association with the use of drugs that prolong the QTc interval, including
`(1) bradycardia; (2) hypokalemia or hypomagnesemia; (3) concomitant use of other drugs that
`
`prolong the QTc interval; and (4) presence of congenital prolongation of the QT interval.
`
`The effects of oral paliperidone on the QT interval were evaluated in a double-blind,
`
`active-controlled (moxifloxacin 400 mg single dose), multicenter QT study in adults with
`
`schizophrenia and schizoaffective disorder, and in three placebo- and active-controlled 6-week,
`
`fixed-dose efficacy trials in adults with schizophrenia.
`
`In the QT study (n=141), the 8 mg dose of immediate-release oral paliperidone (n=50) showed a
`
`mean placebo-subtracted increase from baseline in QTcLD of 12.3 msec (90% CI: 8.9; 15.6) on
`
`day 8 at 1.5 hours post-dose. The mean steady-state peak plasma concentration for this 8 mg
`
`dose of paliperidone immediate release (Cmax ss = 113 ng/mL) was more than 2-fold the exposure
`observed with the maximum recommended 234 mg dose of INVEGA SUSTENNA®
`
`administered in the deltoid muscle (predicted median Cmax ss = 50 ng/mL). In this same study, a
`
`for which
`immediate-release oral
`4 mg dose of
`the
`formulation of paliperidone,
`
`Cmax ss = 35 ng/mL, showed an increased placebo-subtracted QTcLD of 6.8 msec (90% CI: 3.6;
`10.1) on day 2 at 1.5 hours post-dose.
`
`In the three fixed-dose efficacy studies of oral paliperidone extended release in subjects with
`
`schizophrenia, electrocardiogram (ECG) measurements taken at various time points showed only
`
`
`one subject in the oral paliperidone 12 mg group had a change exceeding 60 msec at one time-
`point on Day 6 (increase of 62 msec).
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`
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`In the four fixed-dose efficacy studies of INVEGA SUSTENNA® in subjects with schizophrenia
`and in the long-term study in subjects with schizoaffective disorder, no subject experienced a
`
`change in QTcLD exceeding 60 msec and no subject had a QTcLD value of > 500 msec at any
`
`time point. In the maintenance study in subjects with schizophrenia, no subject had a QTcLD
`
`
`change > 60 msec, and one subject had a QTcLD value of 507 msec (Bazett’s QT corrected
`
`interval [QTcB] value of 483 msec); this latter subject also had a heart rate of 45 beats per
`
`
`minute.
`
`5.5 Tardive Dyskinesia
`A syndrome of potentially irreversible, involuntary, dyskinetic movements may develop in
`
`patients treated with antipsychotic drugs. Although the prevalence of the syndrome appears to be
`
`
`highest among the elderly, especially elderly women, it is impossible to predict which patients
`
`
`
`will develop the syndrome. Whether antipsychotic drug products differ in their potential to cause
`
`tardive dyskinesia is unknown.
`
`The risk of developing tardive dyskinesia and the likelihood that it will become irreversible
`
`appear to increase as the duration of treatment and the total cumulative dose of antipsychotic
`drugs administered to the patient increase, but the syndrome can develop after relatively brief
`treatment periods at low doses, although this is uncommon.
`
`There is no known treatment for established tardive dyskinesia, although the syndrome may
`
`remit, partially or completely, if antipsychotic treatment is withdrawn. Antipsychotic treatment
`itself may suppress (or partially suppress) the signs and symptoms of the syndrome and may thus
`mask the underlying process. The effect of symptomatic suppression on the long-term course
`
`of the syndrome is unknown.
`
`Given these considerations, INVEGA SUSTENNA® should be prescribed in a manner that is
`
`
`
`most likely to minimize the occurrence of tardive dyskinesia. Chronic antipsychotic treatment
`
`should generally be reserved for pati