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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 ALBA POLLEN: 56 Adverse Event Reports & Safety Profile

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56
Total FAERS Reports
0
Deaths Reported
5
Hospitalizations
56
As Primary/Secondary Suspect
1
Life-Threatening
ALK-Abello, Inc.
Manufacturer

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

First Report: 20160504 · Latest Report: 20240409

What Are the Most Common QUERCUS ALBA POLLEN Side Effects?

#1 Most Reported
Anaphylactic reaction
16 reports (28.6%)
#2 Most Reported
Injection site urticaria
8 reports (14.3%)
#3 Most Reported
Injection site erythema
8 reports (14.3%)

All QUERCUS ALBA POLLEN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Anaphylactic reaction 16 28.6% 0 2
Injection site erythema 8 14.3% 0 1
Injection site urticaria 8 14.3% 0 1
Injection site reaction 7 12.5% 0 0
Pruritus 7 12.5% 0 0
Urticaria 7 12.5% 0 0
Local reaction 6 10.7% 0 1
Dyspnoea 5 8.9% 0 2
False negative investigation result 5 8.9% 0 1
Injection site swelling 5 8.9% 0 0

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

Gender: 39.3% female, 60.7% male. Average age: 35.0 years. Most reports from: US. View detailed demographics →

Is QUERCUS ALBA POLLEN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2016 7 0 0
2017 4 0 0
2018 2 0 0
2020 5 0 1
2021 4 0 0
2022 16 0 2
2023 5 0 0
2024 1 0 1

View full timeline →

What Is QUERCUS ALBA POLLEN Used For?

IndicationReports
Product used for unknown indication 14
Skin test 8
Rhinitis allergic 6

Other Drugs in Same Class: Allergens [CS]

Official FDA Label for QUERCUS ALBA POLLEN

Official prescribing information from the FDA-approved drug label.