Levothyroxine Sodium

According to the FDA label: Hypothyroidism Levothyroxine sodium tablets are indicated in adult and pediatric patients, including neonates, as a replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism.

97,346 adverse event reports submitted to the FDA (1997–2026)

This data reflects voluntary reports submitted to the FDA's Adverse Event Monitoring System (AEMS), formerly the FDA Adverse Event Reporting System (FAERS). A report does not mean the medication caused the event. Data may be incomplete or contain errors. Learn more about AEMS. New to this data? Read our guide on how to interpret FDA adverse event reports →
New to FDA adverse event data? Here's how to read these reports →

Top Reported Adverse Events

The most frequently reported events in association with Levothyroxine Sodium in the FAERS database. These are events reported by patients taking this medication, not necessarily caused by it. A single report may include multiple events.

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Ranked by frequency of reports, not severity. The most-reported event is not necessarily the most dangerous or the most common in patients taking this drug.

Who Is Reporting

Demographics of patients in FAERS reports that included this information. Not all reports include patient demographics.

By Sex

View reporter sex data as a table
Levothyroxine Sodium adverse event reports by reporter sex
SexReports
Female68,831
Male21,832
Unknown88

By Age Group

View age group data as a table
Levothyroxine Sodium adverse event reports by reporter age group
Age groupReports
0-171,354
18-342,618
35-497,554
50-6417,618
65-7415,766
75+17,550

This shows who filed reports, reflecting who takes this drug and who tends to report, not who is at greatest risk.

Reported Outcomes

Outcomes recorded in FAERS reports that included Levothyroxine Sodium. A single report may involve multiple reactions, each with a different outcome. These categories are defined by FDA reporting guidelines, not by PillSignal.

View outcome data as a table
Levothyroxine Sodium adverse event reports by reported outcome
OutcomeReports
Other Serious40,007
Hospitalization37,832
Non-Serious29,276
Death8,118
Life-Threatening5,856
Disability3,633

Serious outcomes are far more likely to be reported than mild ones, so this overstates how often outcomes are serious. A recorded death does not mean the drug caused it.

Number of FAERS reports received per quarter for Levothyroxine Sodium. Changes in volume may reflect shifts in prescribing rates, media attention, or reporting behavior, not changes in the medication's safety profile.

View report trend as a table
Levothyroxine Sodium adverse event reports by year
YearReports
19971
20042,045
20052,017
20062,182
20072,755
20084,016
20093,825
20104,304
20116,148
20126,820
20131,402
20141,710
20152,373
20163,135
20173,605
20184,128
20194,001
20205,435
20215,796
20227,383
20236,968
20247,330
20258,216
2026 (partial)1,751

The steep increase around 2004 reflects the FDA's move to electronic submission, not a change in this drug's safety. Trends track reporting volume, not risk.

Medications commonly reported with Levothyroxine Sodium

In FDA adverse event reports that mention Levothyroxine Sodium, these medications appeared most often in the same report.

This reflects co-occurrence in submitted reports, not evidence of drug interaction or combined risk. People often report several medications taken for the same condition or for unrelated reasons. Talk to a doctor or pharmacist about your specific medications.

Other medications with similar adverse event profiles in FDA FAERS reports.

Data Source

This data is sourced from the FDA's Adverse Event Monitoring System (AEMS), formerly FAERS, via the OpenFDA API. PillSignal is not affiliated with the FDA.

View this data on the FDA website →

Data last updated: June 2026