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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.

PROPANTHELINE: 24 Adverse Event Reports & Safety Profile

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24
Total FAERS Reports
4 (16.7%)
Deaths Reported
5
Hospitalizations
24
As Primary/Secondary Suspect
Approved Prior to Jan 1, 1982
FDA Approved
Discontinued
Status
Yes
Generic Available

Active Ingredient: PROPANTHELINE BROMIDE · FDA Application: 008732 ·

First Report: 2005 · Latest Report: 2016

What Are the Most Common PROPANTHELINE Side Effects?

#1 Most Reported
Off label use
5 reports (20.8%)
#2 Most Reported
Drug ineffective
4 reports (16.7%)
#3 Most Reported
Drug hypersensitivity
4 reports (16.7%)

All PROPANTHELINE Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Off label use 5 20.8% 0 0

Who Reports PROPANTHELINE Side Effects? Age & Gender Data

Gender: 36.0% female, 64.0% male. Average age: 62.4 years. Most reports from: US. View detailed demographics →

Is PROPANTHELINE Getting Safer? Reports by Year

YearReportsDeathsHosp.
2005 2 0 0
2012 1 0 0
2014 1 0 1
2015 1 0 1
2016 1 0 0

View full timeline →

What Is PROPANTHELINE Used For?

IndicationReports
Hyperhidrosis 5

Official FDA Label for PROPANTHELINE

Official prescribing information from the FDA-approved drug label.