XEPLION 50 mg prolonged release suspension for injection
XEPLION 75 mg prolonged release suspension for injection
XEPLION 100 mg prolonged release suspension for injection
XEPLION 150 mg prolonged release suspension for injection
Each pre-filled syringe contains 78 mg paliperidone palmitate equivalent to 50 mg paliperidone.
Each pre-filled syringe contains 117 mg paliperidone palmitate equivalent to 75 mg paliperidone.
Each pre-filled syringe contains 156 mg paliperidone palmitate equivalent to 100 mg paliperidone.
Each pre-filled syringe contains 234 mg paliperidone palmitate equivalent to 150 mg paliperidone.
For the full list of excipients, see section 6.1.
Prolonged release suspension for injection.
The suspension is white to off-white. The suspension is pH neutral (approximately 7.0).
XEPLION is indicated for maintenance treatment of schizophrenia in adult patients stabilised with paliperidone or risperidone.
In selected adult patients with schizophrenia and previous responsiveness to oral paliperidone or risperidone, XEPLION may be used without prior stabilisation with oral treatment if psychotic symptoms are mild to moderate and a long-acting injectable treatment is needed.
Posology
Recommended initiation of XEPLION is with a dose of 150 mg on treatment day 1 and 100 mg one week later (day 8), both administered in the deltoid muscle in order to attain therapeutic concentrations rapidly (see section 5.2). The recommended monthly maintenance dose is 75 mg; some patients may benefit from lower or higher doses within the recommended range of 25 to 150 mg based on individual patient tolerability and/or efficacy. Patients who are overweight or obese may require doses in the upper range (see section 5.2). Following the second dose, monthly maintenance doses can be administered in either the deltoid or gluteal muscle.
Adjustment of the maintenance dose may be made monthly. When making dose adjustments, the prolonged release characteristics of XEPLION should be considered (see section 5.2), as the full effect of maintenance doses may not be evident for several months.
Switching from oral paliperidone or oral risperidone
Previous oral paliperidone or oral risperidone can be discontinued at the time of initiation of treatment with XEPLION. XEPLION should be initiated as described at the beginning of section 4.2 above.
Switching from risperidone long acting injection
When switching patients from risperidone long acting injection, initiate XEPLION therapy in place of the next scheduled injection. XEPLION should then be continued at monthly intervals. The one-week initiation dosing regimen including the intramuscular injections (day 1 and 8, respectively) as described in section 4.2 above is not required.
Patients previously stabilised on different doses of risperidone long acting injection can attain similar paliperidone steady-state exposure during maintenance treatment with XEPLION monthly doses according to the following:
Doses of risperidone long acting injection and XEPLION needed to attain similar paliperidone exposure at steady-state
Previous risperidone long acting injection dose
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XEPLION injection
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25 mg every 2 weeks
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50 mg monthly
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37.5 mg every 2 weeks
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75 mg monthly
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50 mg every 2 weeks
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100 mg monthly
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Discontinuation of antipsychotic medicinal products should be made in accordance with appropriate prescribing information. If XEPLION is discontinued, its prolonged release characteristics must be considered. As recommended with other antipsychotic medicinal products, the need for continuing existing extrapyramidal symptoms (EPS) medicine should be re-eva luated periodically.
Missed doses
Avoiding missed doses
It is recommended that the second initiation dose of XEPLION 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 (day 8) 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.
If the target date for the second XEPLION injection (day 8 ± 4 days) is missed, the recommended reinitiation depends on the length of time which has elapsed since the patient's first injection.
Missed second initiaton dose (< 4 weeks from first injection)
If less than 4 weeks have elapsed since the first injection, then the patient should be administered the second injection of 100 mg in the deltoid muscle as soon as possible. A third XEPLION injection of 75 mg in either the deltoid or gluteal muscles should be administered 5 weeks after the first injection (regardless of the timing of the second injection). The normal monthly cycle of injections in either the deltoid or gluteal muscle of 25 mg to 150 mg based on individual patient tolerability and/or efficacy should be followed thereafter.
Missed second initiation dose (4-7 weeks from first injection)
If 4 to 7 weeks have elapsed since the first injection of XEPLION, resume dosing with two injections of 100 mg in the following manner: