Vitamin C Serumvitamin c

According to the FDA label: INDICATIONS & USAGE SECTION INDICATIONS & USAGE SECTION INDICATIONS & USAGE SECTION

89,184 adverse event reports submitted to the FDA (2003–2026)

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 Vitamin C Serum 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.

Show these terms with plain-language definitions

Tap any term below for a plain-language definition.

Browse the full glossary →

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
Vitamin C Serum adverse event reports by reporter sex
SexReports
Female57,038
Male25,678
Unknown46

By Age Group

View age group data as a table
Vitamin C Serum adverse event reports by reporter age group
Age groupReports
0-171,158
18-343,511
35-499,567
50-6417,323
65-7414,416
75+13,211

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 Vitamin C Serum. 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
Vitamin C Serum adverse event reports by reported outcome
OutcomeReports
Other Serious36,900
Non-Serious36,671
Hospitalization24,069
Death7,592
Disability6,367
Life-Threatening5,074

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 Vitamin C Serum. 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
Vitamin C Serum adverse event reports by year
YearReports
20034
2004675
2005213
20069
200711
200825
200955
2010898
2011308
20121,069
20132,661
20143,347
20156,079
20167,018
20176,154
20186,140
20196,200
20207,679
20217,630
20228,193
20237,422
20247,738
20258,078
2026 (partial)1,578

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 Vitamin C Serum

In FDA adverse event reports that mention Vitamin C Serum, 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