Animal drug adverse event reports

MSK

Reactions: Product syringe issue

Animal Owner
Foreign or domestic
Domestic
Unique aer ID number
USA-USFDACVM-2026-US-034953
Report ID
A200550
Original receive date
20260625
Primary reporter
Animal Owner
Type of information
Manufacturing/Product Defect Manufacturing Defect With no Adverse Events
Secondary reporter
Other
Health assessment prior to exposure
Assessed by
Veterinarian
Reaction
  1. Veddra version
    11
    Veddra term code
    99860
    Veddra term name
    Product syringe issue
Receiver
Organization
Food and Drug Administration Center for Veterinary Medicine
Street address
7500 Standish Place (HFV-210) Room N403
City
Rockville
State
MD
Postal code
20855
Country
USA
Drug
  1. Lot number
    XMAD
    Lot expiration
    20271030
    Brand name
    MSK
    Dosage form
    Suspension
    Atc vet code
    QM01AC06
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-A200550
    Active ingredients
    1. Name
      Meloxicam
      Dose
      Numerator
      1.50
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      Unknown
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How to read this: Each report says someone told FDA an event happened while a product was used. A report does not show the product caused it, and counts rise and fall with how many people report. Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.