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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.

BUTABARBITAL: 14 Adverse Event Reports & Safety Profile

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14
Total FAERS Reports
5 (35.7%)
Deaths Reported
4
Hospitalizations
14
As Primary/Secondary Suspect
Approved Prior to Jan 1, 1982
FDA Approved
Discontinued
Status
Yes
Generic Available

FDA Application: 000793 ·

First Report: 1980 · Latest Report: 2015

What Are the Most Common BUTABARBITAL Side Effects?

#1 Most Reported
Rhabdomyolysis
5 reports (35.7%)
#2 Most Reported
Metabolic acidosis
5 reports (35.7%)
#3 Most Reported
Leukocytosis
5 reports (35.7%)

All BUTABARBITAL Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Acute kidney injury 5 35.7% 5 2
Coagulopathy 5 35.7% 5 2
Hepatotoxicity 5 35.7% 5 2
Hypotension 5 35.7% 5 2
Leukocytosis 5 35.7% 5 2
Metabolic acidosis 5 35.7% 5 2
Rhabdomyolysis 5 35.7% 5 2

Who Reports BUTABARBITAL Side Effects? Age & Gender Data

Gender: 90.9% female, 9.1% male. Average age: 56.6 years. Most reports from: US. View detailed demographics →

Is BUTABARBITAL Getting Safer? Reports by Year

YearReportsDeathsHosp.
2015 1 0 0

View full timeline →

What Is BUTABARBITAL Used For?

IndicationReports
Product used for unknown indication 7

Official FDA Label for BUTABARBITAL

Official prescribing information from the FDA-approved drug label.