Reaction profile

The FDA adverse-event record for needlestick injury

314 FDA adverse-event reports reference needlestick injury (VeDDRA 2672). Plate codes and volume neighbourhood below; species, breeds, and drugs follow.

#847 of 2,481
by report volume (all reactions)
314
reports citing this reaction
0.3%
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. Needlestick injury has 314 reports now versus 283 in that prior snapshot: 31 more (11.0%).

Report change
+31
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 Needlestick injury changes

FDA AER · VeDDRA plate

Code 2672 VOL-LOW

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

  • VOL-LOW 314 reports
  • DEATH-RARE 0.3%
  • MID-PACK #847/2481
  • PHOTO-FINISH Dry nose
  • SPECIES-HUMAN Human · 309
  • DRUG-LEAD Bedinvetmab · 116
  • DESK-MID 5 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: Dry nose (±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 Needlestick injury

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

Vomiting · highest174348Epiphora · near315Dry nose · near314Needlestick injury · this re…314Addison's disease · near312Elevated haematocrit · near311Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Needlestick injury

Needlestick injury: low death-coded share in the FDA AER plate

Signature read: Needlestick injury's 0.3% 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: 1 of 314 reports (0.3% of named reports). Nearest volume peer: Dry nose (±0 reports). Lead species Human (309). Lead co-reported drug Bedinvetmab (116).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Bedinvetmab 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 309
Dog 5

Breeds Most Affected

Unknown 309
Crossbred Canine/dog 2
Spaniel - Springer English 1
Pit Bull 1
Retriever - Labrador 1

Associated Drugs

Bedinvetmab 116
Frunevetmab 55
Maropitant Citrate 30
Moxidectin 16
Ceftiofur Crystalline Free Acid 9
Tulathromycin 9
Tilmicosin 8
Ketoprofen;Tulathromycin 7
Dinoprost Tromethamine 6
Enrofloxacin 4
Trenbolone Acetate;Estradiol Benzoate 4
Device: Syringe 4
Cefovecin 3
Melarsomine Dihydrochloride 3
Dexmedetomidine Hydrochloride 3
Alfaxalone 2
Amlodipine 2
Doramectin 2
Lotilaner 2
Milbemycin Oxime + Praziquantel 2

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Needlestick injury, 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 (314 here).

Similar death-coded share

Nearest other reactions by death-coded share (0.3% 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 Needlestick injury (#847 of 2,481 by report volume); death-coded 0.3%. PlainBreed reaction plate · death-coded share stamp 0.3% · 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 →