Reaction profile

The FDA adverse-event record for colic

762 FDA reports name colic, a high-volume reaction in the CVM extract (VeDDRA 264). Plate stamps and neighbourhood peers follow.

#479 of 2,481
by report volume (all reactions)
762
reports citing this reaction
17.8%
death-coded share
Horse
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. Colic has 762 reports now versus 748 in that prior snapshot: 14 more (1.9%).

Report change
+14
Death-coded reports
+2
Death-coded share
−0.1 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 Colic changes

FDA AER · VeDDRA plate

Code 264 VOL-MID

VOL-MID · DEATH-ELEV · UPPER-Q · PHOTO-FINISH · SPECIES-HORSE · DRUG-LEAD · DESK-WIDE · BOOK-FULL

  • VOL-MID 762 reports
  • DEATH-ELEV 17.8%
  • UPPER-Q #479/2481
  • PHOTO-FINISH INEFFECTIVE, GASTRIC…
  • SPECIES-HORSE Horse · 731
  • DRUG-LEAD Ceftiofur Crystal… · 88
  • DESK-WIDE 20 breeds
  • BOOK-FULL 8/8 fields

Nearest volume peer: INEFFECTIVE, GASTRIC ULCER(S) (±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 Colic

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

Vomiting · highest174348Application site swel… · near764Swollen eye · near763Colic · this reaction762INEFFECTIVE, GASTRIC… · near762Decreased body temper… · near760Urinary tract neoplas… · low…10
FDA AER report volume · neighbourhood around Colic

What the FDA AER plate says about Colic

Signature read: 136 death-coded reports is a heavy tail count for Colic in the CVM extract. Report volume is upper-third scale: 762 named reports in the openFDA extract. 136 of 762 reports were death-coded (17.8% of named reports, not a population mortality rate). Nearest volume peer: INEFFECTIVE, GASTRIC ULCER(S) (±0 reports). Lead species Horse (731). Lead co-reported drug Ceftiofur Crystalline Free Acid (88).

Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Ceftiofur Crystalline Free Acid 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

Horse 731
Dog 12
Cattle 10
Donkey 5
Mule 2
Other Equids 1
Alpaca 1

Breeds Most Affected

Quarter Horse 184
Horse (unknown) 132
Thoroughbred 91
Arab 45
Warmblood (unspecified) 41
Unknown 26
Paint 22
Tennessee Walking Horse 20
Warmblood - Dutch 20
Horse (other) 14

Associated Drugs

Ceftiofur Crystalline Free Acid 88
Pergolide Mesylate 62
Clodronate Disodium 59
Oxybendazole 56
Ivermectin(1.55%)/Praziquantel(7.75%) Paste 47
Detomidine Hydrochloride 36
Praziquantel;Moxidectin 30
Omeprazole 37% Oral Paste 29
Polysulfated Glycosaminoglycan 26
Praziquantel; Moxidectin 25
Moxidectin 25
Flunixin Meglumine 24
Ivermectin + Praziquantel 22
Monensin Sodium 21
Omeprazole 21
Firocoxib 19
Flunixin Meglumine Injectable 19
Phenylbutazone 17
Banamine 15
N-Butylscopolaminium Bromide 14

Nationwide reactions with similar profiles

Two openFDA-derived peer sets for Colic, 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 (17.8% 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 Colic (#479 of 2,481 by report volume); death-coded 17.8%. PlainBreed reaction plate · death-coded report count stamp 136 · 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 →