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Is Perseris the Same as Risperdal Consta? A Detailed Comparison

4 min read

Medication non-adherence rates in schizophrenia are estimated to be around 50%, making long-acting injectables a crucial treatment option [1.6.3]. While both medications contain the same active drug, the answer to 'Is Perseris the same as Risperdal Consta?' lies in their significant differences in administration and formulation.

Quick Summary

Perseris and Risperdal Consta are both long-acting injectable forms of risperidone used to treat schizophrenia. They are not the same; they differ in injection frequency, administration route, and the need for oral supplementation.

Key Points

  • Active Ingredient: Both Perseris and Risperdal Consta use risperidone as their active medication [1.2.3].

  • Key Difference: They are not the same; they differ significantly in administration route, dosing frequency, and formulation technology [1.2.5, 1.2.6].

  • Dosing Frequency: Perseris is injected once a month, while Risperdal Consta is injected every two weeks [1.2.7].

  • Administration Route: Perseris is a subcutaneous (under the skin) injection, whereas Risperdal Consta is an intramuscular (into the muscle) injection [1.5.5].

  • Oral Supplementation: Perseris does not require oral risperidone supplementation upon initiation; Risperdal Consta requires a three-week oral overlap [1.2.6, 1.4.1].

  • Therapeutic Onset: Perseris reaches therapeutic levels within hours of the first injection, while Risperdal Consta has a three-week lag before its main release phase [1.2.6, 1.4.1].

  • Indication: Both are used for schizophrenia in adults, while Risperdal Consta is also approved for maintenance treatment of Bipolar I Disorder [1.3.1, 1.4.6].

In This Article

The Role of Long-Acting Injectables in Schizophrenia Management

Schizophrenia is a chronic and complex mental health condition that requires long-term management [1.6.1]. A significant challenge in treatment is medication adherence, with studies indicating that non-adherence rates can be as high as 50% [1.6.3]. This non-adherence is a primary predictor of relapse, which can lead to hospitalization and a decline in quality of life [1.6.7, 1.6.9]. To address this, long-acting injectable (LAI) antipsychotics were developed. LAIs provide a steady release of medication over an extended period, which can improve adherence, reduce relapse rates, and offer convenience for both patients and healthcare providers [1.5.8].

Among the available LAIs are different formulations of the atypical antipsychotic risperidone. Two prominent brand names are Perseris and Risperdal Consta. While they share the same active ingredient, they are not interchangeable due to fundamental differences in their delivery systems, dosing schedules, and initiation protocols [1.2.5].

Understanding the Active Ingredient: Risperidone

Risperidone is a second-generation (atypical) antipsychotic medication first approved in 1993 [1.2.3]. Its therapeutic effects are believed to come from its activity on dopamine and serotonin receptors in the brain [1.5.8]. It is used to treat the symptoms of psychiatric disorders, primarily schizophrenia [1.2.7]. Risperdal Consta is also indicated for the maintenance treatment of Bipolar I Disorder [1.4.6]. Before starting any long-acting injectable form of risperidone, it is typically recommended to first establish that a patient can tolerate the oral version of the medication [1.4.1, 1.3.3].

A Closer Look at Perseris (risperidone)

Perseris is a newer formulation of long-acting risperidone, administered as a subcutaneous (under the skin) injection once a month [1.2.6, 1.2.7]. It is indicated for the treatment of schizophrenia in adults [1.3.1].

Key Features of Perseris:

  • Administration Route: Perseris is injected subcutaneously, typically in the abdomen or the back of the upper arm, by a healthcare professional [1.3.4]. The injection uses a smaller, 5/8-inch needle [1.3.9].
  • Dosing Frequency: It is administered once monthly [1.3.3]. This less frequent dosing may help improve patient adherence [1.2.6].
  • Formulation: It utilizes the Atrigel® delivery system. After injection, the liquid solution forms a solid biodegradable implant, which gradually releases risperidone over the month [1.5.8].
  • Initiation: A significant advantage of Perseris is that it does not require a loading dose or a period of oral risperidone supplementation [1.3.5]. Therapeutic blood levels are reached within 4 to 6 hours after the first injection [1.2.6].
  • Dosages: Perseris is available in 90 mg and 120 mg single-dose kits [1.3.1]. The 90 mg dose corresponds to 3 mg/day of oral risperidone, and the 120 mg dose corresponds to 4 mg/day of oral risperidone [1.3.5].

A Closer Look at Risperdal Consta (risperidone)

Risperdal Consta was the first long-acting atypical antipsychotic to become available [1.5.8]. It is administered via a deep intramuscular (into the muscle) injection every two weeks [1.4.4]. It is approved for schizophrenia and as a maintenance treatment for Bipolar I disorder [1.4.6].

Key Features of Risperdal Consta:

  • Administration Route: It is given as a deep intramuscular injection in either the deltoid (upper arm) or gluteal (buttocks) muscle [1.4.1]. The needle used is longer (1-inch for deltoid, 2-inch for gluteal) to reach the muscle tissue [1.4.1].
  • Dosing Frequency: Injections are administered once every two weeks [1.4.4].
  • Formulation: It uses a microsphere technology, where risperidone is contained within a biodegradable polymer that breaks down slowly to release the drug [1.5.6].
  • Initiation: Risperdal Consta has a 3-week lag time after the first injection before the main release of the medication begins [1.4.1]. Because of this, patients must continue to take an oral antipsychotic for the first three weeks of treatment to ensure adequate therapeutic coverage [1.4.1].
  • Dosages: Risperdal Consta is available in a wider range of doses: 12.5 mg, 25 mg, 37.5 mg, and 50 mg [1.4.3]. The recommended dose for most patients is 25 mg every two weeks, though some may benefit from higher doses [1.4.2].

Perseris vs. Risperdal Consta: Head-to-Head Comparison

The decision between Perseris and Risperdal Consta depends on various clinical factors, including patient preference, the need for rapid therapeutic onset, and tolerability.

Feature Perseris Risperdal Consta
Active Ingredient Risperidone [1.3.2] Risperidone [1.4.3]
Administration Route Subcutaneous (under the skin) [1.3.4] Intramuscular (into the muscle) [1.4.4]
Dosing Frequency Once per month [1.2.7] Once every 2 weeks [1.2.7]
Need for Oral Supplement? No [1.2.6] Yes, for the first 3 weeks [1.4.1]
Time to Therapeutic Levels 4 to 6 hours [1.2.6] 3 weeks (main release begins) [1.4.1]
Injection Sites Abdomen, back of upper arm [1.3.4] Deltoid (arm), gluteal (buttocks) [1.4.1]
Available Doses 90 mg, 120 mg [1.3.1] 12.5 mg, 25 mg, 37.5 mg, 50 mg [1.4.3]

Efficacy and Side Effects

Currently, there are no head-to-head clinical trials directly comparing the efficacy and safety of Perseris and Risperdal Consta [1.2.5]. As both are forms of risperidone, they are expected to have similar overall efficacy and side effect profiles. Common side effects of risperidone include weight gain, sedation or drowsiness, musculoskeletal pain, and elevated prolactin levels [1.2.6, 1.3.6]. Injection site reactions, such as pain and redness, are also possible with both medications [1.2.6]. The choice between them often comes down to the practical differences in their administration. A patient may prefer a once-monthly injection (Perseris) over a bi-weekly one (Risperdal Consta), or they may find a subcutaneous injection more tolerable than an intramuscular one. Conversely, the need for oral supplementation with Risperdal Consta can be a drawback for some patients [1.5.8].

Conclusion: Not the Same, but Both are Options

In conclusion, Perseris is not the same as Risperdal Consta. Although they both deliver the same active medication, risperidone, they are distinct products with different technologies, administration schedules, and initiation requirements. Perseris offers the convenience of a once-monthly subcutaneous injection without the need for oral supplementation. Risperdal Consta, an older formulation, requires a bi-weekly intramuscular injection and a three-week oral overlap. The selection of one over the other is a clinical decision that should be made by a healthcare provider in consultation with the patient, taking into account the patient's medical history, needs, and preferences.


For more detailed information, consult the official prescribing information from the manufacturer or a healthcare professional. An authoritative source for drug information is the U.S. Food and Drug Administration (FDA): https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/210655s000lbl.pdf

Frequently Asked Questions

No, Perseris and Risperdal Consta are not interchangeable or substitutable generics. They have different dosing schedules, administration routes, and initiation protocols [1.2.5].

Perseris is administered as a subcutaneous injection once a month [1.2.7].

Risperdal Consta is administered as an intramuscular injection once every two weeks [1.2.7].

No, a loading dose or supplemental oral risperidone is not recommended when starting Perseris. Therapeutic levels are reached quickly after the first injection [1.2.6, 1.3.5].

Yes, oral risperidone or another antipsychotic must be taken for the first three weeks after the initial Risperdal Consta injection to ensure adequate medication levels [1.4.1].

A key advantage of Perseris is its once-monthly dosing and the fact that it does not require an oral supplementation period, as it reaches therapeutic blood concentrations within 4 to 6 hours of the first injection [1.2.6, 1.5.8].

Perseris is injected subcutaneously (under the skin) in the abdomen or back of the upper arm [1.3.4]. Risperdal Consta is injected intramuscularly (into the muscle) in the deltoid (arm) or gluteal (buttocks) muscle [1.4.1].

Both are indicated for the treatment of schizophrenia in adults. Risperdal Consta is also indicated for the maintenance treatment of Bipolar I Disorder [1.3.1, 1.4.6].

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.