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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.

QUERCUS RUBRA POLLEN: 22 Adverse Event Reports & Safety Profile

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22
Total FAERS Reports
0
Deaths Reported
0
Hospitalizations
22
As Primary/Secondary Suspect
ALK-Abello, Inc.
Manufacturer

Drug Class: Allergens [CS] · Manufacturer: ALK-Abello, Inc. ·

First Report: 20150323 · Latest Report: 20210914

What Are the Most Common QUERCUS RUBRA POLLEN Side Effects?

#1 Most Reported
Throat irritation
9 reports (40.9%)
#2 Most Reported
Rash
5 reports (22.7%)
#3 Most Reported
Cough
5 reports (22.7%)

All QUERCUS RUBRA POLLEN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Throat irritation 9 40.9% 0 0
Cough 5 22.7% 0 0
Rash 5 22.7% 0 0

Who Reports QUERCUS RUBRA POLLEN Side Effects? Age & Gender Data

Gender: 52.6% female, 47.4% male. Average age: 34.2 years. Most reports from: US. View detailed demographics →

Is QUERCUS RUBRA POLLEN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2015 2 0 0
2016 10 0 0
2019 1 0 0
2021 1 0 0

View full timeline →

Other Drugs in Same Class: Allergens [CS]

Official FDA Label for QUERCUS RUBRA POLLEN

Official prescribing information from the FDA-approved drug label.