Reaction profile

The FDA adverse-event record for burning sensation (skin)

149 FDA adverse-event reports reference burning sensation (skin) (VeDDRA 1367). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1191 of 2,481
by report volume (all reactions)
149
reports citing this reaction
0.0%
death-coded share
Human
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. Burning sensation (skin) has 149 reports now versus 147 in that prior snapshot: 2 more (1.4%).

Report change
+2
Death-coded reports
+0
Death-coded share
+0.0 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 Burning sensation (skin) changes

FDA AER · VeDDRA plate

Code 1367 VOL-LOW

VOL-LOW · DEATH-RARE · MID-PACK · PHOTO-FINISH · SPECIES-HUMAN · DRUG-LEAD · DESK-NARROW · BOOK-FULL

  • VOL-LOW 149 reports
  • DEATH-RARE 0.0%
  • MID-PACK #1191/2481
  • PHOTO-FINISH Abnormal ECG
  • SPECIES-HUMAN Human · 149
  • DRUG-LEAD Imidacloprid + Mo… · 27
  • DESK-NARROW 1 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Abnormal ECG (±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 Burning sensation

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

Vomiting · highest174348Abnormal ECG · near149Administration device… · near149Application site skin… · near149Burning sensation (sk… · thi…149Physical product labe… · near149Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Burning sensation (skin)

Burning sensation (skin): low death-coded share in the FDA AER plate

Signature read: Burning sensation (skin)'s 0.0% death-coded share is among the lowest in the openFDA reaction corpus. Report volume sits in the middle third of the reaction corpus. Death-coded share is lower-third: 0 of 149 reports (0.0% of named reports). Nearest volume peer: Abnormal ECG (±0 reports). Lead species Human (149). Lead co-reported drug Imidacloprid + Moxidectin (27).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Imidacloprid + Moxidectin 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

Human 149

Breeds Most Affected

Unknown 149

Associated Drugs

Imidacloprid + Moxidectin 27
Selamectin 13
Selamectin;Sarolaner 8
Spinosad 7
Fluralaner Spot-On Solution 7
Enrofloxacin 5
Maropitant Citrate 5
Buprenorphine 5
Milbemycin Oxime + Spinosad 4
Emodepside + Praziquantel 3
Fluralaner Chew Tablets 3
Mirtazapine 3
Fluralaner 13.64% 12-Week Chew 3
Pyrantel Pamoate;Sarolaner 3
Prednisone 2
Toceranib Phosphate 2
Cefovecin 2
Metformin 2
Tulathromycin 2
Fenbendazol Granules 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Burning sensation (skin), 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 (0.0% 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 Burning sensation (skin) (#1191 of 2,481 by report volume); death-coded 0.0%. PlainBreed reaction plate · death-coded share stamp 0.0% · 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 →