Quercus alba pollen
- Generic Name
- Quercus alba pollen
- Drug Type
- Biotech
- Unique Ingredient Identifier
- Z4Y9ZSV4KK
Overview
Quercus alba pollen, or oak white pollen, is a non-standardized allergen extract used for the diagnosis and treatment of allergic disease to grass pollen. It can be subcutaneously administered to initiate an immune response in case of an allergic reaction. Diagnostic allergenic extracts are primarily indicated for establishing clinical relevance of specific allergens to which the patient has been exposed and the degree of sensitivity the patient has toward that allergen.
Background
Quercus alba pollen, or oak white pollen, is a non-standardized allergen extract used for the diagnosis and treatment of allergic disease to grass pollen. It can be subcutaneously administered to initiate an immune response in case of an allergic reaction. Diagnostic allergenic extracts are primarily indicated for establishing clinical relevance of specific allergens to which the patient has been exposed and the degree of sensitivity the patient has toward that allergen.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
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No clinical trials found
No clinical trials found for this drug
FDA Approved Products
Product Name | Manufacturer | Route | Strength | Approved | NDC Code |
|---|---|---|---|---|---|
INTRADERMAL, SUBCUTANEOUS | 0.005 g in 1 mL | 2011/02/03 | 49288-0836 | ||
SUBCUTANEOUS, INTRADERMAL | 0.01 g in 1 mL | 2011/02/03 | 49288-0837 | ||
SUBCUTANEOUS, INTRADERMAL | 0.1 g in 1 mL | 2009/11/19 | 49288-0350 | ||
SUBCUTANEOUS, INTRADERMAL | 0.00008 g in 1 mL | 2011/01/13 | 49288-0801 | ||
SUBCUTANEOUS, INTRADERMAL | 0.00008 g in 1 mL | 2010/12/01 | 49288-0799 | ||
PERCUTANEOUS, SUBCUTANEOUS | 0.20 g in 20 mL | 2011/03/15 | 54575-954 | ||
SUBCUTANEOUS, INTRADERMAL | 0.00008 g in 1 mL | 2012/05/11 | 49288-0852 | ||
INTRADERMAL, SUBCUTANEOUS | 0.0004 g in 1 mL | 2012/05/11 | 49288-0850 | ||
INTRADERMAL, SUBCUTANEOUS | 10000 [PNU] in 1 mL | 2009/12/03 | 36987-2894 | ||
SUBCUTANEOUS, INTRADERMAL | 0.005 g in 1 mL | 2009/12/02 | 49288-0665 |
EMA Approved Products
Medicine Name | EMA Number | Auth. Holder | Country | Drug Type | Status | Issued | Opinion | Revision |
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No EMA products found
No EMA products found for this drug
HSA Approved Products
Product Name | Manufacturer | Dosage Form | Strength | Approved | Approval No. |
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No HSA products found
No HSA products found for this drug
NMPA Approved Products
Product Name | Approval No. | Manufacturer | Dosage Form | Trade Name | Strength | Type | Status | Date | Import |
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No NMPA products found
No NMPA products found for this drug
PPB Approved Products
Product Name | Registration Code | Company | Category | Sale Type | Reg. Date |
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No PPB products found
No PPB products found for this drug
TGA Approved Products
Product Name | ARTG ID | Sponsor | Status | Reg. Date | Ingredient |
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No TGA products found
No TGA products found for this drug