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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.

MORUS RUBRA POLLEN: 50 Adverse Event Reports & Safety Profile

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50
Total FAERS Reports
0
Deaths Reported
4
Hospitalizations
50
As Primary/Secondary Suspect
2
Life-Threatening
ALK-Abello, Inc.
Manufacturer

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

First Report: 20160112 · Latest Report: 20250604

What Are the Most Common MORUS RUBRA POLLEN Side Effects?

#1 Most Reported
Anaphylactic reaction
12 reports (24.0%)
#2 Most Reported
Dyspnoea
11 reports (22.0%)
#3 Most Reported
Throat irritation
9 reports (18.0%)

All MORUS RUBRA POLLEN Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Anaphylactic reaction 12 24.0% 0 1
Dyspnoea 11 22.0% 0 1
Cough 9 18.0% 0 1
Throat irritation 9 18.0% 0 0
Injection site reaction 7 14.0% 0 0
Pruritus 6 12.0% 0 0
Urticaria 6 12.0% 0 0
Dizziness 5 10.0% 0 0
Flushing 5 10.0% 0 0
Headache 5 10.0% 0 0
Injection site erythema 5 10.0% 0 1

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

Gender: 69.6% female, 30.4% male. Average age: 40.7 years. Most reports from: US. View detailed demographics →

Is MORUS RUBRA POLLEN Getting Safer? Reports by Year

YearReportsDeathsHosp.
2016 6 0 0
2017 4 0 0
2018 4 0 0
2019 2 0 0
2020 9 0 1
2021 4 0 0
2023 6 0 0
2024 1 0 1
2025 3 0 0

View full timeline →

What Is MORUS RUBRA POLLEN Used For?

IndicationReports
Product used for unknown indication 5
Seasonal allergy 5

Other Drugs in Same Class: Allergens [CS]

Official FDA Label for MORUS RUBRA POLLEN

Official prescribing information from the FDA-approved drug label.