Vivelle-dotestradiol

According to the FDA label: Estradiol Vaginal Cream, 0.01% is indicated in the treatment of moderate to severe symptoms of vulvar and vaginal atrophy due to menopause.

45,427 adverse event reports submitted to the FDA (1993–2026)

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 →
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Top Reported Adverse Events

The most frequently reported events in association with Vivelle-dot 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
Vivelle-dot adverse event reports by reporter sex
SexReports
Female41,479
Male763
Unknown87

By Age Group

View age group data as a table
Vivelle-dot adverse event reports by reporter age group
Age groupReports
0-17389
18-341,064
35-494,365
50-6411,749
65-744,853
75+2,405

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 Vivelle-dot. 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
Vivelle-dot adverse event reports by reported outcome
OutcomeReports
Non-Serious23,108
Other Serious17,563
Hospitalization7,080
Disability1,229
Death878
Life-Threatening844

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 Vivelle-dot. 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
Vivelle-dot adverse event reports by year
YearReports
19931
2004543
2005600
2006444
20071,504
2008494
2009682
20101,065
2011960
20121,281
2013939
20141,160
20152,067
20162,638
20172,336
20182,604
20192,999
20203,033
20212,868
20223,162
20233,617
20243,775
20255,296
2026 (partial)1,359

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 Vivelle-dot

In FDA adverse event reports that mention Vivelle-dot, 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