Reaction profile

The FDA adverse-event record for tingling sensation

168 FDA adverse-event reports reference tingling sensation (VeDDRA 1841). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#1134 of 2,481
by report volume (all reactions)
168
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 sensation has 168 reports now versus 166 in that prior snapshot: 2 more (1.2%).

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 Tingling sensation changes

FDA AER · VeDDRA plate

Code 1841 VOL-LOW

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

  • VOL-LOW 168 reports
  • DEATH-RARE 0.0%
  • MID-PACK #1134/2481
  • PHOTO-FINISH Hyperkeratosis
  • SPECIES-HUMAN Human · 168
  • DRUG-LEAD Imidacloprid + Mo… · 27
  • DESK-NARROW 1 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Hyperkeratosis (±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 Tingling sensation

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

Vomiting · highest174348Administration device… · near169Corneal oedema · near169Hyperkeratosis · near168Involuntary movement · near168Tingling sensation · this re…168Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Tingling sensation

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

Signature read: Tingling sensation'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 168 reports (0.0% of named reports). Nearest volume peer: Hyperkeratosis (±0 reports). Lead species Human (168). 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 168

Breeds Most Affected

Unknown 168

Associated Drugs

Imidacloprid + Moxidectin 27
Selamectin 19
Tilmicosin 11
Fluralaner Spot-On Solution 10
Emodepside + Praziquantel 6
Tilmicosin Phosphate 6
Nitenpyram 6
Spinosad 4
Metoprolol 4
Buprenorphine 4
Imidacloprid And Moxidectin 3
Levothyroxine 3
Mirtazapine 3
Metformin 3
Milbemycin Oxime 2
Valsartan 2
Montelukast Sodium 2
Moxidectin 2
Afoxolaner 2
Pentobarbital Sodium, Phenytoin Sodium 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Tingling sensation, 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 (168 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 sensation (#1134 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 →