Q1 2023 Non-GAAP Operating Income
UZEDY™ (risperidone) Now Approved
2
RAPID ABSORPTION
Achieves therapeutic levels in plasma within 6 to 24 hours of administration 1,2
STREAMLINED INITIATION
No loading dose or oral supplementation is required²
FLEXIBLE 1- AND 2-MONTH DOSING INTERVALS
Two dosing intervals and 8 dosing options²
SUBCUTANEOUS INJECTION
Administered as a single-dose, prefilled syringe with a short, 5/8-inch needle²
DEMONSTRATED EFFICACY and KNOWN SAFETY PROFILE
Significant reductions in the risk of relapse vs placebo²
Safety profile expected to be similar to that of corresponding oral risperidone doses*
UZEDY.
(risperidone)
extended-release
injectable suspension
~$4B
LAI 2022 Market size
1 month dosing
UZEDY.
(risperidone)
FOR SUBCUTANEOUS USE ONLY
2 month dosing
UZEDY
(risperidone)
FOR SUBCUTANEOUS USE ONLY
For administration by a leathcare professional
Rx Only
NDC 51750-900-10
One side-dose predige
250mg/0.7mL
at every two
For administration by a healthcare professional
NDC 51759-630-10
Rx Only
One single-dose prefed syringe
125mg/0.35 mL
astered every are th
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References: 1. Data on file. Parsippany, NJ: Teva Neuroscience, Inc. 2. UZEDYTM (risperidone) extended-release injectable suspension Current Prescribing Information. Parsippany, NJ: Teva Neuroscience, Inc.
* The most common adverse reactions with risperidone (≥5% and greater than placebo) were parkinsonism, akathisia, dystonia, tremor, sedation, dizziness, anxiety, blurred vision, nausea, vomiting, upper abdominal pain, stomach
discomfort, dyspepsia, diarrhea, salivary hypersecretion, constipation, dry mouth, increased appetite, increased weight, fatigue, rash, nasal congestion, upper respiratory tract infection, nasopharyngitis, and pharyngolaryngeal pain. The most
common injection site reactions with UZEDY (25% and greater than placebo) were pruritus and nodule.
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