Amaranthus retroflexus whole

This drug entry is a stub and has not been fully annotated. It is scheduled to be annotated soon.

Identification

Summary

Amaranthus retroflexus whole is an extract from Amaranthus retroflexus whole used in allergy testing.

Generic Name
Amaranthus retroflexus whole
DrugBank Accession Number
DB10930
Background

Amaranthus retroflexus whole allergenic extract is used in allergenic testing.

Type
Biotech
Groups
Approved
Biologic Classification
Allergenics
Allergen Extract
Synonyms
  • Amaranthus bulgaricus whole
  • Amaranthus bullatus whole
  • Amaranthus curvifolius whole
  • Amaranthus delilei whole
  • Amaranthus johnstonii whole
  • Amaranthus recurvatus whole
  • Amaranthus retroflexus
  • Amaranthus retroflexus whole
  • Amaranthus rigidus whole
  • Amaranthus spicatus whole
  • Careless weed whole
  • Galliaria retroflexa whole
  • Galliaria scabra whole
  • Red-root amaranth whole
  • Redroot amaranth whole
  • Redroot pigweed whole
  • Rough pigweed whole

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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Active Moieties
NameKindUNIICASInChI Key
Amaranthus retroflexus pollenunknown73B14PX5FWNot AvailableNot applicable
Mixture Products
NameIngredientsDosageRouteLabellerMarketing StartMarketing EndRegionImage
Treatment Set TS345380Amaranthus retroflexus whole (0.002 g/1mL) + Acer negundo pollen (0.002 g/1mL) + Ambrosia artemisiifolia pollen (160 [AU]/1mL) + Betula populifolia pollen (0.01 g/1mL) + Chenopodium album pollen (0.002 g/1mL) + Cynodon dactylon pollen (400 [BAU]/1mL) + Fraxinus americana pollen (0.0004 g/1mL) + Pascopyrum smithii pollen (0.002 g/1mL) + Plantago lanceolata pollen (0.002 g/1mL) + Populus deltoides pollen (0.002 g/1mL) + Quercus alba pollen (0.002 g/1mL) + Rumex acetosella pollen (0.004 g/1mL) + Sorghum halepense pollen (0.0004 g/1mL) + Ulmus americana pollen (0.0004 g/1mL)Injection, solutionIntradermal; SubcutaneousAntigen Laboratories, Inc.1986-10-31Not applicableUS flag

Categories

Drug Categories
Classification
Not classified
Affected organisms
Not Available

Chemical Identifiers

UNII
55W4M8149I
CAS number
Not Available

References

General References
Not Available
RxNav
1306882

Clinical Trials

Clinical Trials
PhaseStatusPurposeConditionsCount

Pharmacoeconomics

Manufacturers
Not Available
Packagers
Not Available
Dosage Forms
FormRouteStrength
Injection, solutionIntradermal; Subcutaneous
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