QUZYTTIR
Details
- Status
- Prescription
- First Approved
- 2019-10-04
- Routes
- INTRAVENOUS
- Dosage Forms
- SOLUTION
QUZYTTIR Approval History
What QUZYTTIR Treats
1 indicationsQUZYTTIR is approved for 1 conditions since its original approval in 2019. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Urticaria
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Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
QUZYTTIR FDA Label Details
ProIndications & Usage
FDA Label (PDF)QUZYTTIR ® is indicated for the treatment of acute urticaria in adults and children 6 months of age and older. QUZYTTIR ® is a histamine-1 (H 1 ) receptor antagonist indicated for the treatment of acute urticaria in adults and children 6 months of age and older Limitations of Use : Not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function Limitations of use: QUZYTTIR ® is not recommended in pediatric patients less than 6 years of age with impaired renal or hepatic function.
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Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.