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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.

MIVACURIUM: 99 Adverse Event Reports & Safety Profile

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99
Total FAERS Reports
2 (2.0%)
Deaths Reported
32
Hospitalizations
99
As Primary/Secondary Suspect
25
Life-Threatening
23
Disabilities
Apr 30, 2009
FDA Approved
Discontinued
Status
Yes
Generic Available

Active Ingredient: MIVACURIUM CHLORIDE · FDA Application: 020098 ·

First Report: 1999 · Latest Report: 20240930

What Are the Most Common MIVACURIUM Side Effects?

#1 Most Reported
Heart rate increased
25 reports (25.3%)
#2 Most Reported
Dyspnoea
25 reports (25.3%)
#3 Most Reported
Performance status decreased
23 reports (23.2%)

All MIVACURIUM Side Effects by Frequency

Side Effect Reports % of Total Deaths Hosp.
Dyspnoea 25 25.3% 0 0
Heart rate increased 25 25.3% 0 0
Cardiovascular disorder 23 23.2% 0 0
General physical health deterioration 23 23.2% 0 0
Performance status decreased 23 23.2% 0 0
Asthenia 18 18.2% 0 0
Chest discomfort 18 18.2% 0 0
Chest pain 18 18.2% 0 0
Flatulence 18 18.2% 0 0
Hyperventilation 18 18.2% 0 0
Oropharyngeal discomfort 18 18.2% 0 0
Oropharyngeal pain 18 18.2% 0 0
Somnolence 18 18.2% 0 0
Speech disorder 18 18.2% 0 0
Visual impairment 18 18.2% 0 0
Weight bearing difficulty 18 18.2% 0 0
Blood pressure measurement 17 17.2% 0 0
Dizziness 17 17.2% 0 0
Vision blurred 17 17.2% 0 0
Impaired work ability 16 16.2% 0 0

Who Reports MIVACURIUM Side Effects? Age & Gender Data

Gender: 58.7% female, 41.3% male. Average age: 40.1 years. Most reports from: FR. View detailed demographics →

Is MIVACURIUM Getting Safer? Reports by Year

YearReportsDeathsHosp.
2009 2 0 0
2014 3 2 0
2016 3 0 0
2017 16 0 10
2018 7 0 7
2019 21 0 2
2020 2 0 2
2021 5 0 0
2022 4 0 0
2024 2 0 2

View full timeline →

What Is MIVACURIUM Used For?

IndicationReports
General anaesthesia 27
Product used for unknown indication 19
Surgery 19
Anaesthesia 11
Skin test 5

Official FDA Label for MIVACURIUM

Official prescribing information from the FDA-approved drug label.