Reaction profile

The FDA adverse-event record for tingling skin

59 FDA reports name tingling skin, a lower-volume reaction in the CVM extract (VeDDRA 1842). Plate stamps and neighbourhood peers follow.

#1665 of 2,481
by report volume (all reactions)
59
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. Tingling skin has 59 reports now versus 59 in that prior snapshot: 0 the same number of (0.0%).

Report change
+0
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 Tingling skin changes

FDA AER · VeDDRA plate

Code 1842 VOL-LOW

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

  • VOL-LOW 59 reports
  • DEATH-RARE 0.0%
  • MID-PACK #1665/2481
  • PHOTO-FINISH Hypoaesthesia
  • SPECIES-HUMAN Human · 59
  • DRUG-LEAD Imidacloprid + Mo… · 11
  • DESK-NARROW 1 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hypoaesthesia (±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.

Lower-volume neighbourhood around Tingling skin

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

Vomiting · highest174348Hypoaesthesia · near59Hyposensitivity to pa… · near59Injection site fibros… · near59Loss of smell · near59Tingling skin · this reaction59Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Tingling skin

Tingling skin: low death-coded share in the FDA AER plate

Signature read: Tingling skin's 0.0% death-coded share is among the lowest in the openFDA reaction corpus. Report volume is lower-third scale: 59 named reports in the openFDA extract. Death-coded share is lower-third: 0 of 59 reports (0.0% of named reports). Nearest volume peer: Hypoaesthesia (±0 reports). Lead species Human (59). Lead co-reported drug Imidacloprid + Moxidectin (11).

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 59

Breeds Most Affected

Unknown 59

Associated Drugs

Imidacloprid + Moxidectin 11
Selamectin 11
Fluralaner Spot-On Solution 3
Moxidectin 2
Meloxicam 2
Soap 2
Fluralaner Chew Tablets 2
Tilmicosin 2
Selamectin;Sarolaner 2
Fluralaner/Moxidectin Spot-On 2
Tylosin 1
Detomidine 1
Lufenuron + Milbemycin Oxime 1
Spinosad 1
Miconazole Nitrate + Polymyxin B Sulfate + Prednisolone Acetate 1
Cephalexin 1
Amprolium Ion 1
Ivermectin + Pyrantel As Pamoate Salt 1
Phytosphingosine Salicyloyl + Pramoxine Hydrochloride 1
Flunixin Meglumine Oral Paste 1

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Tingling 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 report volume

Nearest other reactions by FDA report count (59 here).

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 Tingling skin (#1665 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 →