Ambrosia artemisiifolia pollen

Identification

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Name
Ambrosia artemisiifolia pollen
Accession Number
DB10385  (DB05583)
Type
Biotech
Groups
Approved
Biologic Classification
Allergenics
Allergen Extract
Description

Ambrosia artemisiifolia pollen is the pollen of the Ambrosia artemisiifolia plant. Ambrosia artemisiifolia pollen is mainly used in allergenic testing.

Synonyms
  • Ambrosia artemisiifolia
  • short ragweed pollen extract
  • short ragweed pollen extracts
  • Standardized short ragweed pollen allergenic extract
Prescription Products
NameDosageStrengthRouteLabellerMarketing StartMarketing End
Ambrosia Artemisiifolia PollenInjection, solution0.10 g/1mLSubcutaneousAlk Abello, Inc.1965-01-01Not applicableUs
Ambrosia Artemisiifolia PollenInjection, solution40000 [PNU]/1mLSubcutaneousAlk Abello, Inc.1965-01-01Not applicableUs
Ambrosia Artemisiifolia PollenInjection, solution20000 [PNU]/1mLSubcutaneousAlk Abello, Inc.1965-01-01Not applicableUs
Ambrosia Artemisiifolia PollenInjection, solution0.05 g/1mLSubcutaneousAlk Abello, Inc.1965-01-01Not applicableUs
Center-AL - Ambrosia Artemisiifolia PollenInjection, suspension10000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUs
Center-AL - Ambrosia Artemisiifolia PollenInjection, suspension20000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUs
Pollens - Weeds and Garden Plants, Short Ragweed, Ambrosia artemisiifoliaInjection, solution500 [PNU]/1mLIntradermalJubilant Hollisterstier Llc1977-10-18Not applicableUs
Pollens - Weeds and Garden Plants, Short Ragweed, Ambrosia artemisiifoliaInjection, solution0.05 g/1mLPercutaneous; SubcutaneousJubilant Hollisterstier Llc1977-10-18Not applicableUs
RagwitekTablet12 [Amb'a'1'U]/1SublingualMerck Sharp & Dohme Limited2014-04-172018-05-08Us
RagwitekTablet12 [Amb'a'1'U]/1SublingualALK-Abelló A/S2014-04-17Not applicableUs
Additional Data Available
  • Application Number
    Application Number

    A unique ID assigned by the FDA when a product is submitted for approval by the labeller.

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  • Product Code
    Product Code

    A governmentally-recognized ID which uniquely identifies the product within its regulatory market.

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Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing End
3-ragweed Mix, Giant/short/western PollenAmbrosia artemisiifolia pollen (0.34 g/20mL) + Ambrosia psilostachya pollen (0.33 g/20mL) + Ambrosia trifida pollen (0.33 g/20mL)Injection, solutionPercutaneous; SubcutaneousAllergy Laboratories, Inc.1967-12-07Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (0.1 g/1mL) + Ambrosia trifida pollen (0.1 g/1mL)Injection, solutionPercutaneous; SubcutaneousAlk Abello, Inc.2015-05-03Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (20000 [PNU]/1mL) + Ambrosia trifida pollen (20000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (10000 [PNU]/1mL) + Ambrosia trifida pollen (10000 [PNU]/1mL)Injection, solutionSubcutaneousAlk Abello, Inc.1965-01-01Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (10000 [PNU]/1mL) + Ambrosia trifida pollen (10000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (0.1 g/1mL) + Ambrosia trifida pollen (0.1 g/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (40000 [PNU]/1mL) + Ambrosia trifida pollen (40000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (0.05 g/1mL) + Ambrosia trifida pollen (0.05 g/1mL)Injection, solutionPercutaneousAlk Abello, Inc.1998-02-23Not applicableUs
Mixed RagweedAmbrosia artemisiifolia pollen (20000 [PNU]/1mL) + Ambrosia trifida pollen (20000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUs
National Weed MixAmbrosia artemisiifolia pollen (0.01 g/1mL) + Amaranthus retroflexus pollen (0.01 g/1mL) + Ambrosia trifida pollen (0.01 g/1mL) + Chenopodium album pollen (0.01 g/1mL) + Xanthium strumarium pollen (0.01 g/1mL)SolutionIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUs
Unapproved/Other Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing End
Allergen Pack Gs Ragweed MixAmbrosia artemisiifolia pollen (1 g/20mL) + Sodium chloride (0.9 g/1mL)KitIntradermal; SubcutaneousAlvix Laboratories2015-07-092018-03-08Us
Categories
UNII
9W34L2CQ9A
CAS number
Not Available

Pharmacology

Indication
Not Available
Pharmacodynamics
Not Available
Mechanism of action
Not Available
Additional Data Available
Adverse Effects

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Additional Data Available
Contraindications

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Additional Data Available
Blackbox Warnings

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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
Toxicity
Not Available
Affected organisms
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

References

General References
Not Available
External Links
PubChem Substance
347910560
RxNav
1347557
AHFS Codes
  • 92:05.00* — Allergenic Extracts

Clinical Trials

Clinical Trials
Not Available

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage forms
FormRouteStrength
Injection, solutionPercutaneous; Subcutaneous
KitIntradermal; Subcutaneous
Injection, solutionSubcutaneous0.05 g/1mL
Injection, solutionSubcutaneous0.10 g/1mL
Injection, solutionSubcutaneous20000 [PNU]/1mL
Injection, solutionSubcutaneous40000 [PNU]/1mL
Injection, suspensionSubcutaneous10000 [PNU]/1mL
Injection, suspensionSubcutaneous20000 [PNU]/1mL
Injection, solutionPercutaneous
Injection, solutionSubcutaneous
SolutionIntradermal; Percutaneous; Subcutaneous
Injection, solutionIntradermal500 [PNU]/1mL
Injection, solutionPercutaneous; Subcutaneous0.05 g/1mL
Injection, solutionIntradermal
TabletSublingual12 [Amb'a'1'U]/1
Tablet, orally disintegratingSublingual12 unit
InjectionCutaneous; Intradermal; Subcutaneous1 g/10mL
Injection, solutionPercutaneous0.05 g/1mL
Injection, solutionIntradermal; Subcutaneous0.05 g/1mL
Injection, solutionIntradermal; Subcutaneous0.1 g/1mL
Injection, solutionIntradermal; Subcutaneous20000 [PNU]/1mL
Injection, solutionIntradermal; Subcutaneous40000 [PNU]/1mL
SolutionIntradermal; Percutaneous; Subcutaneous0.05 g/1mL
Injection, solutionIntradermal; Subcutaneous100000 [AU]/1mL
Injection, solutionPercutaneous; Subcutaneous1 g/10mL
Injection, solutionIntradermal; Subcutaneous
Prices
Not Available
Patents
Not Available

Properties

State
Not Available
Experimental Properties
Not Available

Taxonomy

Classification
Not classified

Drug created on December 01, 2015 13:03 / Updated on February 23, 2020 23:03