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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

ATRIPLEX CANESCENS POLLEN: 10 Adverse Event Reports & Safety Profile

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10
Total FAERS Reports
0
Deaths Reported
0
Hospitalizations
10
As Primary/Secondary Suspect
DNA Labs, Inc.
Manufacturer

Drug Class: Allergens [CS] · Route: SUBLINGUAL · Manufacturer: DNA Labs, Inc. · HUMAN OTC DRUG · FDA Label: Available

First Report: 20210809 · Latest Report: 20211018

What Are the Most Common ATRIPLEX CANESCENS POLLEN Side Effects?

#1 Most Reported
Urticaria
8 reports (80.0%)
#2 Most Reported
Anaphylactic reaction
6 reports (60.0%)
#3 Most Reported
Throat tightness
2 reports (20.0%)

All ATRIPLEX CANESCENS POLLEN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Urticaria 8 80.0% 0 0
Anaphylactic reaction 6 60.0% 0 0

Who Reports ATRIPLEX CANESCENS POLLEN Side Effects? Age & Gender Data

Gender: 20.0% female, 80.0% male. Average age: 33.0 years. Most reports from: US. View detailed demographics →

Is ATRIPLEX CANESCENS POLLEN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2021 10 0 0

View full timeline →

Other Drugs in Same Class: Allergens [CS]

Official FDA Label for ATRIPLEX CANESCENS POLLEN

Official prescribing information from the FDA-approved drug label.

FDA Approved Uses (Indications)

INDICATIONS Allergies.

Dosage & Administration

SUGGESTED DOSAGE Normal dose for the first week is 2-3 drops in water T.I.D. Add one drop per dose per week until a total of ten drops is reached.

Warnings

Warnings Use only if cap seal is unbroken. If pregnant or breastfeeding, ask a healthcare professional before use. Keep this and all medication out of the reach of children.

Active Ingredient

INGREDIENTS ACTIVE Allscale 6/12/30x, Lenscale 6/12/30x, Wingscale 6/12/30x INACTIVE 20% alcohol in purified water.

Inactive Ingredients

INACTIVE 20% alcohol in purified water.