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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.

ECHOTHIOPHATE IODIDE: 87 Adverse Event Reports & Safety Profile

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87
Total FAERS Reports
4 (4.6%)
Deaths Reported
9
Hospitalizations
87
As Primary/Secondary Suspect
Approved Prior to Jan 1, 1982
FDA Approved
Prescription
Status

FDA Application: 011963 ·

First Report: 2013 · Latest Report: 20250602

What Are the Most Common ECHOTHIOPHATE IODIDE Side Effects?

#1 Most Reported
Visual impairment
15 reports (17.2%)
#2 Most Reported
Intraocular pressure increased
14 reports (16.1%)
#3 Most Reported
Drug ineffective
9 reports (10.3%)

All ECHOTHIOPHATE IODIDE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Visual impairment 15 17.2% 0 1
Intraocular pressure increased 14 16.1% 0 0
Drug ineffective 9 10.3% 0 0
Eye pain 8 9.2% 0 0
Blindness 6 6.9% 0 1
Blindness unilateral 5 5.8% 0 0
Headache 5 5.8% 0 0

Who Reports ECHOTHIOPHATE IODIDE Side Effects? Age & Gender Data

Gender: 64.1% female, 35.9% male. Average age: 62.2 years. Most reports from: US. View detailed demographics →

Is ECHOTHIOPHATE IODIDE Getting Safer? Reports by Year

YearReportsDeathsHosp.
2013 1 0 0
2014 5 0 0
2015 2 0 0
2016 1 0 0
2017 2 0 0
2018 2 0 2
2019 1 0 0
2020 1 0 0
2021 1 0 0
2022 2 0 0
2023 5 0 0
2024 2 0 0
2025 1 0 1

View full timeline →

What Is ECHOTHIOPHATE IODIDE Used For?

IndicationReports
Glaucoma 31
Intraocular pressure increased 10
Open angle glaucoma 9
Strabismus 5

Official FDA Label for ECHOTHIOPHATE IODIDE

Official prescribing information from the FDA-approved drug label.