MedDRA preferred term

Respiratory syncytial virus infection: adverse event reports recording this term

8,540 reports to FDA record it, 2004–2026; 0% of the database.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "There is no certainty that the reported event (adverse event or medication error) was actually due to the product. FDA does not require that a causal relationship between a product and event be proven, and reports do not always contain enough detail to properly evaluate an event." The information in these reports "cannot be used to estimate the incidence of these events."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

8,540
reports recording the term: 0% of all reports; 937
reports, 12 months to June 2026: 1,055 in the 12 months before; 82.9%
marked serious by the reporter: 57.4% across all reports; 6.7%
record death among outcomes, as reported: 9.1% across all reports

"Respiratory syncytial virus infection" is a MedDRA preferred term recorded in 8,540 adverse event reports received by FDA, 0% of the database, from January 2004 to June 2026. The term is chosen by whoever codes the report to match what the reporter described.

937 reports recorded it in the 12 months to June 2026, down 11% from 1,055 in the 12 months before. FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases. Of reports recording this term, 82.9% are marked serious, 6.7% include death among the outcomes and 67.7% include hospitalisation, as reported.

The drugs listed most often as suspect products in those reports are Synagis, Dupixent and Revlimid. That order mostly follows how many reports each drug has overall; the table also gives the term's share within each drug's own reports. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."

Reports by month, five years

FDA releases FAERS data quarterly, so the newest months are incomplete and grow in later releases.

Drugs listed as suspect products in these reports

Drug	Class	Reports with this term	Share of the drug's own reports
Synagis	Respiratory syncytial virus Anti-F protein monoclonal antibody	2,055	14.2%
Dupixent	Interleukin-4 receptor alpha antagonist	348	0.1%
Revlimid	Thalidomide analog	289	0.1%
Prednisone	Corticosteroid	216	0.1%
Cyclophosphamide	Alkylating drug	203	0.1%
Methotrexate	Folate analog metabolic inhibitor	180	0.1%
Humira	—	179	0%
Pomalyst	Thalidomide analog	179	0.2%
Beyfortus	Respiratory syncytial virus Anti-F protein monoclonal antibody	177	12.6%
Dexamethasone	Corticosteroid	177	0.1%
Tacrolimus	Calcineurin inhibitor immunosuppressant	174	0.2%
Mycophenolate mofetil	Antimetabolite immunosuppressant	160	0.2%
Lenalidomide	Thalidomide analog	137	0.2%
Human immunoglobulin g	Human immunoglobulin G	130	0.8%
Rituximab	CD20-directed cytolytic antibody	128	0.1%
Prednisolone	Corticosteroid	110	0.1%
Rinvoq	Janus kinase inhibitor	102	0.1%
Ambrisentan	Endothelin receptor antagonist	99	0.2%
Etoposide	Topoisomerase inhibitor	89	0.1%
Spinraza	Antisense oligonucleotide	86	1.2%
Hemangeol	beta-Adrenergic blocker	84	1.9%
Skyrizi	Interleukin-23 antagonist	82	0.1%
Fludarabine	Nucleoside metabolic inhibitor	81	0.4%
Opsumit	Endothelin receptor antagonist	79	0.2%
Xeljanz	Janus kinase inhibitor	79	0.1%

Drugs with a page on this site, ordered by the number of their reports recording this term. The last column is the term's share within that drug's own reports, against 0% across the whole database. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

By pharmacologic class

Class	Reports with this term	Share of class reports	Median drug in class
Respiratory syncytial virus Anti-F protein monoclonal antibody	2,275	13.8%	12.6%
Corticosteroid	670	0.1%	0%
Thalidomide analog	629	0.1%	0.2%
Interleukin-4 receptor alpha antagonist	365	0.1%	0.1%
Alkylating drug	355	0.1%	0%
Janus kinase inhibitor	289	0.1%	0%
Endothelin receptor antagonist	265	0.1%	0.2%
Calcineurin inhibitor immunosuppressant	259	0.1%	0%
Nucleoside metabolic inhibitor	258	0.1%	0%
Tumor necrosis factor blocker	246	0%	0%

Classes ordered by count. Class shares follow the class's overall report volume as much as anything else.

Patients in these reports

Patient age

Under 218.8%1,606

2 to 116.9%590

12 to 171.6%133

18 to 445.7%486

45 to 6413.5%1,152

65 to 749.8%837

75 and over6.7%576

Age not given37%3,160

Patient sex

Female49.4%4,222

Male37.9%3,235

Not given12.7%1,083

Grey bar: all 20,646,523 reports in the database. 71.3% of these reports give the United States as the country.

Questions about "Respiratory syncytial virus infection"

What does "Respiratory syncytial virus infection" mean in an adverse event report?

It is a MedDRA preferred term, the dictionary FDA uses to code what a reporter described. The report's own description is not published by openFDA and is not shown here.

How many reports record respiratory syncytial virus infection?

8,540 reports through June 2026 (0% of all reports), 937 of them in the latest 12 months.

Which drugs appear most often in these reports?

Synagis (2,055), Dupixent (348), Revlimid (289), Prednisone (216) and Cyclophosphamide (203). Drugs with many reports overall lead almost every term's list. FDA states that adverse event reports "represent a small percentage of total usage numbers of a product", that "common products may have a higher number of adverse events due to the higher total number of people using the product", and that the data "by themselves are not an indicator of the safety profile of the drug or biologic."

Does a drug appearing here mean it was responsible for this reaction?

No. FDA states that "a causal relationship cannot be established between product and reactions listed in a report" and that for any given report "there is no certainty that a suspected drug caused the event."

I have this symptom. What should I do?

This site cannot assess anyone. A pharmacist or clinician can; for an emergency, call the local emergency number. Nothing on this page is medical advice.

Where this comes from. Counts are built from the openFDA Drug Adverse Event (FAERS) bulk export released 28 Sep 2026, which holds reports FDA received through 30 Jun 2026. Drug names are as reported, resolved to the brand or generic name on the FDA label where openFDA's harmonisation matched them; classes are the pharmacologic class (EPC) from the label and the National Drug Code Directory of 17 Sep 2026. Terms are pooled across spelling and capitalisation variants of one MedDRA preferred term. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.

Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.