Reaction profile
The FDA adverse-event record for plasmacytoma
10 FDA reports name plasmacytoma, a lower-volume reaction in the CVM extract (VeDDRA 2954). Plate stamps and neighbourhood peers follow.
- #2468 of 2,481
- by report volume (all reactions)
- 10
- reports citing this reaction
- 10.0%
- death-coded share
- Dog
- most-affected species
FDA AER · VeDDRA plate
Code 2954 VOL-TRACE
VOL-TRACE · DEATH-ELEV · BOTTOM-DECILE · PHOTO-FINISH · SPECIES-DOG · DRUG-LEAD · DESK-MID · BOOK-FULL
- VOL-TRACE 10 reports
- DEATH-ELEV 10.0%
- BOTTOM-DECILE #2468/2481
- PHOTO-FINISH Anoxia
- SPECIES-DOG Dog · 10
- DRUG-LEAD Oclacitinib Malea… · 4
- DESK-MID 7 breeds
- BOOK-FULL 8/8 fields
Nearest volume peer: Anoxia (±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 Plasmacytoma
Lower-third volume poles plus nearest peers, not a full reaction corpus board reprint.
What the FDA AER plate says about Plasmacytoma
Signature read: 10 reports place Plasmacytoma in the lower third of FDA AER volume (#2468 of 2,481). Report volume is lower-third scale: 10 named reports in the openFDA extract. 1 of 10 reports were death-coded (10.0% of named reports, not a population mortality rate). Nearest volume peer: Anoxia (±0 reports). Lead species Dog (10). Lead co-reported drug Oclacitinib Maleate (4).
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
What to do with this reaction
- 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 →