Bassia scoparia pollen

Identification

Summary

Bassia scoparia pollen is an extract from Bassia scoparia pollen used in allergy testing.

Generic Name
Bassia scoparia pollen
DrugBank Accession Number
DB10928
Background

Bassia scoparia pollen is the pollen of the Bassia scoparia plant. Bassia scoparia pollen is mainly used in allergenic testing.

Type
Biotech
Groups
Approved
Biologic Classification
Allergenics
Allergen Extract
Synonyms
  • burning bush pollen extract
  • Kochia scoparia pollen

Pharmacology

Indication

Not Available

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Pharmacodynamics

Not Available

Mechanism of action
Not Available
Absorption

Not Available

Volume of distribution

Not Available

Protein binding

Not Available

Metabolism
Not Available
Route of elimination

Not Available

Half-life

Not Available

Clearance

Not Available

Adverse Effects
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Toxicity

Not Available

Pathways
Not Available
Pharmacogenomic Effects/ADRs
Not Available

Interactions

Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
Not Available
Food Interactions
Not Available

Products

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Brand Name Prescription Products
NameDosageStrengthRouteLabellerMarketing StartMarketing EndRegionImage
Burning Bush PollenInjection0.05 g/1mLCutaneous; Intradermal; SubcutaneousAllermed Laboratories, Inc.1974-03-12Not applicableUS flag
Center-AL - Kochia Scoparia PollenInjection, suspension10000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1975-01-152023-05-11US flag
Firebush KochiaSolution40000 [PNU]/1mLIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Firebush KochiaSolution0.05 g/1mLIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Firebush KochiaSolution20000 [PNU]/1mLIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing EndRegionImage
Central Western Weed MixBassia scoparia pollen (0.0003333 g/1mL) + Chenopodium album pollen (0.0003333 g/1mL) + Salsola kali pollen (0.0003333 g/1mL)SolutionIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Central Western Weed MixBassia scoparia pollen (0.016666 g/1mL) + Chenopodium album pollen (0.016666 g/1mL) + Salsola kali pollen (0.016666 g/1mL)SolutionIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Central Western Weed MixBassia scoparia pollen (6666.6666 [PNU]/1mL) + Chenopodium album pollen (6666.6666 [PNU]/1mL) + Salsola kali pollen (6666.6666 [PNU]/1mL)SolutionIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Number Four Weed MixtureBassia scoparia pollen (0.0036 g/1mL) + Amaranthus retroflexus pollen (0.0036 g/1mL) + Amaranthus tuberculatus pollen (0.0036 g/1mL) + Artemisia californica pollen (0.0036 g/1mL) + Artemisia dracunculus pollen (0.0036 g/1mL) + Artemisia frigida pollen (0.0036 g/1mL) + Artemisia tridentata pollen (0.0036 g/1mL) + Artemisia vulgaris pollen (0.0036 g/1mL) + Chenopodium album pollen (0.0036 g/1mL) + Iva axillaris pollen (0.0036 g/1mL) + Rumex acetosella pollen (0.0036 g/1mL) + Rumex crispus pollen (0.0036 g/1mL) + Salsola kali pollen (0.0036 g/1mL) + Xanthium strumarium pollen (0.0036 g/1mL)Injection, solutionIntradermal; SubcutaneousAntigen Laboratories, Inc.1974-03-23Not applicableUS flag
Number Three Weed MixtureBassia scoparia pollen (0.0125 g/1mL) + Amaranthus retroflexus pollen (0.0125 g/1mL) + Chenopodium album pollen (0.0125 g/1mL) + Rumex acetosella pollen (0.0125 g/1mL)Injection, solutionIntradermal; SubcutaneousAntigen Laboratories, Inc.1996-07-11Not applicableUS flag

Categories

Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
07A108ZKW5
CAS number
Not Available

References

General References
Not Available
PubChem Substance
347911026
RxNav
852593

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
FormRouteStrength
SolutionIntradermal; Percutaneous; Subcutaneous0.05 g/ml
SolutionIntradermal; Percutaneous; Subcutaneous0.1 g/ml
InjectionCutaneous; Intradermal; Subcutaneous0.05 g/1mL
Injection, suspensionSubcutaneous10000 [PNU]/1mL
SolutionIntradermal; Percutaneous; Subcutaneous
SolutionIntradermal; Percutaneous; Subcutaneous0.001 g/1mL
SolutionIntradermal; Percutaneous; Subcutaneous0.05 g/1mL
SolutionIntradermal; Percutaneous; Subcutaneous0.1 g/1mL
SolutionIntradermal; Percutaneous; Subcutaneous20000 [PNU]/1mL
SolutionIntradermal; Percutaneous; Subcutaneous40000 [PNU]/1mL
Injection, solutionPercutaneous; Subcutaneous1 g/20mL
Injection, solutionIntradermal; Subcutaneous0.05 g/1mL
Injection, solutionIntradermal; Subcutaneous0.1 g/1mL
Injection, solutionIntradermal; Subcutaneous10000 [PNU]/1mL
Injection, solutionIntradermal; Subcutaneous20000 [PNU]/1mL
Injection, solutionIntradermal; Subcutaneous40000 [PNU]/1mL
Injection, solutionIntradermal; Subcutaneous0.02 g/1mL
Injection, solutionIntradermal1000 [PNU]/1mL
Injection, solutionPercutaneous0.05 g/1mL
Injection, solutionSubcutaneous0.05 g/1mL
Injection, solutionSubcutaneous0.10 g/1mL
Injection, solutionSubcutaneous20000 [PNU]/1mL
Injection, solutionSubcutaneous40000 [PNU]/1mL
PatchCutaneous
Injection, solutionIntradermal500 [PNU]/1mL
Injection, solutionPercutaneous; Subcutaneous0.05 g/1mL
Injection, solutionPercutaneous; Subcutaneous0.1 g/1mL
Injection, solutionIntradermal; Subcutaneous
Injection, solutionSubcutaneous
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available

Drug created at December 01, 2015 20:04 / Updated at June 12, 2020 16:53