Identification

Summary

Ambrosia artemisiifolia pollen is an extract from Ambrosia artemisiifolia pollen used in allergy testing.

Brand Names
Ragwitek
Generic Name
Ambrosia artemisiifolia pollen
DrugBank Accession Number
DB10385
Background

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

Type
Biotech
Groups
Approved
Biologic Classification
Allergenics
Allergen Extract
Synonyms
  • Ambrosia artemisiifolia
  • short ragweed pollen extract
  • short ragweed pollen extracts
  • Standardized short ragweed pollen allergenic extract

Pharmacology

Indication

Not Available

Pharmacology
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Contraindications & Blackbox Warnings
Contraindications
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Avoid life-threatening adverse drug events & improve clinical decision support.
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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
Adverseeffects
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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

Products2
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Brand Name Prescription Products
NameDosageStrengthRouteLabellerMarketing StartMarketing EndRegionImage
Ambrosia Artemisiifolia PollenInjection, solution0.10 g/1mLSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Ambrosia Artemisiifolia PollenInjection, solution20000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Ambrosia Artemisiifolia PollenInjection, solution0.05 g/1mLSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Ambrosia Artemisiifolia PollenInjection, solution40000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1965-01-012021-11-30US flag
Center-AL - Ambrosia Artemisiifolia PollenInjection, suspension20000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUS flag
Center-AL - Ambrosia Artemisiifolia PollenInjection, suspension10000 [PNU]/1mLSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUS flag
Pollens - Weeds and Garden Plants, Short Ragweed, Ambrosia artemisiifoliaInjection, solution0.05 g/1mLPercutaneous; SubcutaneousJubilant Hollisterstier Llc1977-10-18Not applicableUS flag
Pollens - Weeds and Garden Plants, Short Ragweed, Ambrosia artemisiifoliaInjection, solution500 [PNU]/1mLIntradermalJubilant Hollisterstier Llc1977-10-18Not applicableUS flag
RagwitekTablet, orally disintegrating12 unitSublingualAlk Abello A/S2014-04-29Not applicableCanada flag
RagwitekTablet12 [Amb'a'1'U]/1SublingualALK-Abello A S2014-04-17Not applicableUS flag
Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing EndRegionImage
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 flag
Mixed RagweedAmbrosia artemisiifolia pollen (20000 [PNU]/1mL) + Ambrosia trifida pollen (20000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (20000 [PNU]/1mL) + Ambrosia trifida pollen (20000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (10000 [PNU]/1mL) + Ambrosia trifida pollen (10000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (0.1 g/1mL) + Ambrosia trifida pollen (0.1 g/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (10000 [PNU]/1mL) + Ambrosia trifida pollen (10000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1975-01-15Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (0.05 g/1mL) + Ambrosia trifida pollen (0.05 g/1mL)Injection, solutionPercutaneousALK-Abello, Inc.1998-02-23Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (40000 [PNU]/1mL) + Ambrosia trifida pollen (40000 [PNU]/1mL)Injection, solutionSubcutaneousALK-Abello, Inc.1965-01-01Not applicableUS flag
Mixed RagweedAmbrosia artemisiifolia pollen (0.1 g/1mL) + Ambrosia trifida pollen (0.1 g/1mL)Injection, solutionPercutaneous; SubcutaneousALK-Abello, Inc.2015-05-03Not applicableUS flag
National Weed MixAmbrosia artemisiifolia pollen (0.02 g/1mL) + Amaranthus retroflexus pollen (0.02 g/1mL) + Ambrosia trifida pollen (0.02 g/1mL) + Chenopodium album pollen (0.02 g/1mL) + Xanthium strumarium pollen (0.02 g/1mL)SolutionIntradermal; Percutaneous; SubcutaneousGreer Laboratories, Inc.1981-09-15Not applicableUS flag
Unapproved/Other Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing EndRegionImage
Allergen Pack Gs Ragweed MixAmbrosia artemisiifolia pollen (1 g/20mL) + Sodium chloride (0.9 g/1mL)KitIntradermal; SubcutaneousAlvix Laboratories2015-07-092018-03-08US flag

Categories

Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
9W34L2CQ9A
CAS number
Not Available

References

General References
Not Available
PubChem Substance
347910560
RxNav
1347557

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

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
Tablet, orally disintegratingSublingual
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
PowderOral
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

Drug created at December 01, 2015 20:03 / Updated at November 28, 2021 11:56