Details for: SANDOZ QUETIAPINE XRT
Company: SANDOZ CANADA INCORPORATED
| DIN | DIN name | Active Ingredient(s) | Strength | Dosage Form | Route of Administration |
|---|---|---|---|---|---|
| 02407671 | SANDOZ QUETIAPINE XRT | QUETIAPINE (QUETIAPINE FUMARATE) | 50 MG | TABLET (EXTENDED-RELEASE) | ORAL |
| 02407698 | SANDOZ QUETIAPINE XRT | QUETIAPINE (QUETIAPINE FUMARATE) | 150 MG | TABLET (EXTENDED-RELEASE) | ORAL |
| 02407701 | SANDOZ QUETIAPINE XRT | QUETIAPINE (QUETIAPINE FUMARATE) | 200 MG | TABLET (EXTENDED-RELEASE) | ORAL |
| 02407728 | SANDOZ QUETIAPINE XRT | QUETIAPINE (QUETIAPINE FUMARATE) | 300 MG | TABLET (EXTENDED-RELEASE) | ORAL |
| 02407736 | SANDOZ QUETIAPINE XRT | QUETIAPINE (QUETIAPINE FUMARATE) | 400 MG | TABLET (EXTENDED-RELEASE) | 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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