Reaction profile
The FDA adverse-event record for inappropriate schedule of drug administration
1,115 FDA reports name inappropriate schedule of drug administration, a high-volume reaction in the CVM extract (VeDDRA 99832). Plate stamps and neighbourhood peers follow.
- #360 of 2,481
- by report volume (all reactions)
- 1,115
- reports citing this reaction
- 2.1%
- 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. Inappropriate schedule of drug administration has 1,115 reports now versus 1,096 in that prior snapshot: 19 more (1.7%).
- Report change
- +19
- 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 Inappropriate schedule of drug administration changesFDA AER · VeDDRA plate
Code 99832 VOL-MID
VOL-MID · DEATH-LOW · UPPER-Q · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-WIDE · BOOK-FULL
- VOL-MID 1,115 reports
- DEATH-LOW 2.1%
- UPPER-Q #360/2481
- PHOTO-FINISH Lymphocytosis
- SPECIES-DOG Dog · 1,026
- DRUG-LEAD Oclacitinib Malea… · 590
- DESK-WIDE 20 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Lymphocytosis (±1 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 Inappropriate schedule of drug administration
Upper-third volume poles plus nearest peers, not a full reaction corpus board reprint.
Inappropriate schedule of drug administration: low death-coded share in the FDA AER plate
Signature read: 1,115 reports place Inappropriate schedule of drug administration in the upper third of FDA AER volume (#360 of 2,481). Report volume is upper-third scale: 1,115 named reports in the openFDA extract. Death-coded share is lower-third: 23 of 1,115 reports (2.1% of named reports). Nearest volume peer: Lymphocytosis (±1 reports). Lead species Dog (1,026). Lead co-reported drug Oclacitinib Maleate (590).
Read these counts as reporting volume, not risk: per our methodology, Lead co-reported drug Oclacitinib Maleate 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
Breeds Most Affected
Associated Drugs
Nationwide reactions with similar profiles
Two openFDA-derived peer sets for Inappropriate schedule of drug administration, 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 (1,115 here).
Similar death-coded share
Nearest other reactions by death-coded share (2.1% here), distinct from the volume row.
What to do with this reaction
- Compare Inappropriate schedule of drug administration's report profile against similar reactions nationwide. See similar reactions
- Read how death-coded share differs from a mortality rate before drawing conclusions. Understanding adverse events
- Browse the full reaction directory to compare report counts across reaction types. All reactions
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
Informational only. FDA adverse-event reports are voluntary and do not prove causation; consult a veterinarian before acting on them. Verify with FDA CVM →