Ciprociprofloxacin
According to the FDA label: Ciprofloxacin Ophthalmic Solution is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions listed below: Corneal Ulcers: Pseudomonas aeruginosa Serratia marcescens * Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumoniae Streptococcus (Viridans Group) * Conjunctivitis: Haemophilus influenzae Staphylococcus aureus Staphylococcus epidermidis Streptococcus pneumoniae *Efficacy for this organism was studied in…
95,252 adverse event reports submitted to the FDA (1997–2026)
Top Reported Adverse Events
The most frequently reported events in association with Cipro 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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Drug Hypersensitivity 6,143 reports
An allergic-type reaction to a medication.
Full definition in the glossary →Pain 6,063 reports
A general report of physical discomfort, used when no more specific location is given.
Full definition in the glossary →Fatigue 5,995 reports
Extreme tiredness or lack of energy that does not improve with rest.
Full definition in the glossary → See all drugs reporting this event →Diarrhoea 5,809 reports
Loose or watery bowel movements, often frequent. Also spelled diarrhea in American English.
Full definition in the glossary → See all drugs reporting this event →Nausea 5,806 reports
The feeling of sickness in your stomach that often comes before vomiting.
Full definition in the glossary → See all drugs reporting this event →Arthralgia 5,531 reports
Drug Ineffective 5,044 reports
A report that the medication did not work as expected for the person taking it. This is a reporting category, not a sign the drug is defective. It simply means someone felt it was not helping their condition.
Full definition in the glossary →Acute Kidney Injury 4,711 reports
A sudden drop in how well the kidneys are working. It is often temporary and can have many causes.
Full definition in the glossary →Dyspnoea 4,619 reports
Shortness of breath or difficulty breathing. Also spelled dyspnea in American English.
Full definition in the glossary → See all drugs reporting this event →Off Label Use 4,541 reports
Using a medication for a condition or in a way that the FDA has not officially approved. This is common and often legal, and a report of it does not mean something went wrong. Doctors sometimes prescribe drugs off label based on their judgment.
Full definition in the glossary →Chronic Kidney Disease 4,540 reports
A long-term, gradual loss of kidney function over months or years.
Full definition in the glossary →Vomiting 4,333 reports
Throwing up the contents of the stomach.
Full definition in the glossary → See all drugs reporting this event →Pyrexia 4,223 reports
The medical term for fever, meaning a raised body temperature.
Full definition in the glossary → See all drugs reporting this event →Anxiety 4,146 reports
A feeling of worry, nervousness, or unease.
Full definition in the glossary → See all drugs reporting this event →Headache 4,039 reports
Pain in the head or upper neck.
Full definition in the glossary → See all drugs reporting this event →
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
| Sex | Reports |
|---|---|
| Female | 50,337 |
| Male | 36,413 |
| Unknown | 321 |
By Age Group
View age group data as a table
| Age group | Reports |
|---|---|
| 0-17 | 2,956 |
| 18-34 | 8,377 |
| 35-49 | 11,611 |
| 50-64 | 18,319 |
| 65-74 | 14,398 |
| 75+ | 12,078 |
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 Cipro. 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
| Outcome | Reports |
|---|---|
| Other Serious | 52,424 |
| Hospitalization | 37,031 |
| Non-Serious | 15,807 |
| Death | 9,610 |
| Disability | 6,870 |
| Life-Threatening | 5,810 |
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.
Report Volume Over Time
Number of FAERS reports received per quarter for Cipro. 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
| Year | Reports |
|---|---|
| 1997 | 1 |
| 1999 | 3 |
| 2001 | 1 |
| 2002 | 1 |
| 2003 | 3 |
| 2004 | 1,014 |
| 2005 | 1,123 |
| 2006 | 1,306 |
| 2007 | 1,287 |
| 2008 | 1,819 |
| 2009 | 1,993 |
| 2010 | 2,251 |
| 2011 | 3,342 |
| 2012 | 3,227 |
| 2013 | 3,178 |
| 2014 | 3,521 |
| 2015 | 4,870 |
| 2016 | 6,922 |
| 2017 | 5,600 |
| 2018 | 8,113 |
| 2019 | 9,945 |
| 2020 | 7,217 |
| 2021 | 6,601 |
| 2022 | 5,321 |
| 2023 | 5,613 |
| 2024 | 5,343 |
| 2025 | 4,715 |
| 2026 (partial) | 922 |
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 Cipro
In FDA adverse event reports that mention Cipro, these medications appeared most often in the same report.
- Ciprofloxacin And Hydrocortisone (20,456 reports)
- Omeprazole (11,021 reports)
- Metronidazole (10,730 reports)
- Prednisone (10,046 reports)
- Furosemide (9,325 reports)
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.
Related Drugs
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