Reaction profile

The FDA adverse-event record for lip smacking

356 FDA reports name lip smacking, a high-volume reaction in the CVM extract (VeDDRA 2118). Plate stamps and neighbourhood peers follow.

#802 of 2,481
by report volume (all reactions)
356
reports citing this reaction
3.7%
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. Lip smacking has 356 reports now versus 346 in that prior snapshot: 10 more (2.9%).

Report change
+10
Death-coded reports
+1
Death-coded share
+0.2 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 Lip smacking changes

FDA AER · VeDDRA plate

Code 2118 VOL-LOW

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

  • VOL-LOW 356 reports
  • DEATH-LOW 3.7%
  • MID-PACK #802/2481
  • PHOTO-FINISH Closed eyelid
  • SPECIES-DOG Dog · 275
  • DRUG-LEAD Milbemycin Oxime… · 54
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Closed eyelid (±0 reports)

Upper-third report volume drives the scale stamps on this plate; death-coded share and co-report peers follow. Not a clinical diagnosis.

High-volume neighbourhood around Lip smacking

Upper-third volume poles plus nearest peers, not a full reaction corpus board reprint.

Vomiting · highest174348Closed eyelid · near356Isosthenuria · near356Lip smacking · this reaction356Vasculitis · near356Skin tumour NOS · near355Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Lip smacking

Lip smacking: low death-coded share in the FDA AER plate

Signature read: Lip smacking's 3.7% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is upper-third scale: 356 named reports in the openFDA extract. Death-coded share is lower-third: 13 of 356 reports (3.7% of named reports). Nearest volume peer: Closed eyelid (±0 reports). Lead species Dog (275). Lead co-reported drug Milbemycin Oxime + Spinosad (54).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Milbemycin Oxime + Spinosad 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 275
Cat 76
Horse 5

Breeds Most Affected

Domestic Shorthair 47
Retriever - Labrador 26
Crossbred Canine/dog 21
Retriever - Golden 15
Chihuahua 14
Boxer (German Boxer) 12
Shih Tzu 11
Dog (unknown) 9
Pit Bull 9
Domestic Longhair 8

Associated Drugs

Milbemycin Oxime + Spinosad 54
Maropitant Citrate 36
Afoxolaner 33
Pyrantel Pamoate;Sarolaner 21
Sarolaner 20
Carprofen 17
Bedinvetmab 17
Oclacitinib Maleate 16
Selamectin 15
Gabapentin 15
Fluralaner 13.64% 12-Week Chew 15
Ivermectin + Pyrantel As Pamoate Salt 11
Emodepside + Praziquantel 11
Buprenorphine 10
Milbemycin Oxime + Praziquantel 10
Cyclosporine 9
Famotidine 9
Prednisone 9
Moxidectin 9
Diphenhydramine 9

Nationwide reactions with similar profiles

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

Similar report volume

Nearest other reactions by FDA report count (356 here).

Similar death-coded share

Nearest other reactions by death-coded share (3.7% 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 Lip smacking (#802 of 2,481 by report volume); death-coded 3.7%. PlainBreed reaction plate · death-coded share stamp 3.7% · 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 →