Reaction profile

The FDA adverse-event record for rhinitis

66 FDA adverse-event reports reference rhinitis (VeDDRA 869). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1606 of 2,481
by report volume (all reactions)
66
reports citing this reaction
18.2%
death-coded share
Dog
most-affected species

Release-over-release change

What changed in the latest FDA data snapshot

PlainBreed reconstructed the prior snapshot from dated openFDA partitions through 2025 Q4, then compared it with the 2026-07-27 openFDA export. Rhinitis has 66 reports now versus 63 in that prior snapshot: 3 more (4.8%).

Report change
+3
Death-coded reports
+1
Death-coded share
+0.7 pts

This compares reported-event counts in two source snapshots. It does not establish a change in real-world risk, product safety, or disease incidence.

Subscribe to Rhinitis changes

FDA AER · VeDDRA plate

Code 869 VOL-LOW

VOL-LOW · DEATH-ELEV · MID-PACK · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-LOW 66 reports
  • DEATH-ELEV 18.2%
  • MID-PACK #1606/2481
  • PHOTO-FINISH Abdominal cavity hern…
  • SPECIES-DOG Dog · 38
  • DRUG-LEAD Maropitant Citrate · 7
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Abdominal cavity hernia (±0 reports)

Instrument codes from this reaction’s FDA CVM adverse-event extract: volume band, death-coded share, corpus rank, photo-finish peer, lead species, lead drug, breed desk, and book completeness. Not a clinical diagnosis.

Report-volume neighbourhood around Rhinitis

Highest and lowest poles plus nearest volume peers, not a full 2,500-reaction corpus board reprint.

Vomiting · highest174348Abdominal cavity hern… · near66Administration device… · near66Carcinoma NOS · near66Device Complication N… · near66Rhinitis · this reaction66Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Rhinitis

What the FDA AER plate says about Rhinitis

Signature read: report volume at 66 (#1606 of 2,481) is the standout scale stamp on Rhinitis. Report volume sits in the middle third of the reaction corpus. 12 of 66 reports were death-coded (18.2% of named reports, not a population mortality rate). Nearest volume peer: Abdominal cavity hernia (±0 reports). Lead species Dog (38). Lead co-reported drug Maropitant Citrate (7).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Maropitant Citrate appears in filings alongside this reaction; that is association, not causation. Browse the full reactions index or the about page for how PlainBreed frames FDA CVM extracts.

Species Most Affected

Dog 38
Cat 21
Horse 2
Cattle 2
Human 1
Donkey 1
Turkey 1

Breeds Most Affected

Domestic Shorthair 12
Crossbred Canine/dog 4
Dog (unknown) 3
Retriever - Golden 3
Standardbred (unspecified) 2
Dachshund (unspecified) 2
Bulldog - French 2
Shepherd Dog - German 2
Ragdoll 2
Collie - Border 2

Associated Drugs

Maropitant Citrate 7
Buprenorphine 6
Gabapentin 5
Carprofen 4
Propofol 4
Cyclosporine A 4
Trilostane 4
Midazolam 4
Frunevetmab 4
Cefovecin Sodium 3
Cyclosporine 3
Pradofloxacin 3
Deracoxib 3
Enrofloxacin 3
Oclacitinib Maleate 3
Ivermectin, Praziquantel 2
Meloxicam 2
Cefovecin 2
Amoxicillin Trihydrate; Clavulanate Potassium ( K-Clavulanate) 2
Emodepside + Praziquantel 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Rhinitis, both floored at ≥50 reports so the neighborhoods stay in the advertised mass (the volume chart above is the unfloored photo-finish strip).

Similar death-coded share

Nearest other reactions by death-coded share (18.2% here), distinct from the volume row.

What to do with this reaction

A report does not prove a drug caused the reaction; consult a veterinarian before acting on this data.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

openFDA Animal & Veterinary Adverse Events (FDA CVM) for Rhinitis (#1606 of 2,481 by report volume); death-coded 18.2%. PlainBreed reaction plate · report volume stamp 66 · vintage 2025.

Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →