Details for: PRO-RISPERIDONE
Company: PRO DOC LIMITEE
| DIN | DIN name | Active Ingredient(s) | Strength | Dosage Form | Route of Administration |
|---|---|---|---|---|---|
| 02312700 | PRO-RISPERIDONE | RISPERIDONE | 0.25 MG | TABLET | ORAL |
| 02312719 | PRO-RISPERIDONE | RISPERIDONE | 0.5 MG | TABLET | ORAL |
| 02312727 | PRO-RISPERIDONE | RISPERIDONE | 1.0 MG | TABLET | ORAL |
| 02312735 | PRO-RISPERIDONE | RISPERIDONE | 2.0 MG | TABLET | ORAL |
| 02312743 | PRO-RISPERIDONE | RISPERIDONE | 3.0 MG | TABLET | ORAL |
| 02312751 | PRO-RISPERIDONE | RISPERIDONE | 4.0 MG | TABLET | ORAL |
Summary Reports
Summary Safety Review - Atypical antipsychotics - Assessing the Potential Risk of Sleep Apnoea
Summary Safety Review - Atypical antipsychotics - Assessing the Potential Risk of Urinary Retention
Summary Safety Review - Atypical Antipsychotics - Liver failure
Summary Safety Review - Atypical antipsychotics - Assessing the potential risk of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)
Summary Safety Review - Atypical antipsychotics - Assessing the Potential Risk of Urinary Retention
Summary Safety Review - Atypical Antipsychotics - Liver failure
Summary Safety Review - Atypical antipsychotics - Assessing the potential risk of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS)
Consumer Information
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