Animal drug adverse event reports

MSK

Reactions: Odor, Abnormal, Solution, Abnormal, Underfilling, Tubes

Animal Owner
Unique aer ID number
USA-USFDACVM-2026-US-035237
Original receive date
20260625
Primary reporter
Animal Owner
Secondary reporter
Other
Onset date
20260624
Foreign or domestic
Domestic
Report ID
N141251
Type of information
Manufacturing/Product Defect Manufacturing Defect With no Adverse Events
Reaction
  1. Veddra version
    11
    Veddra term code
    99018
    Veddra term name
    Odor, Abnormal
  2. Veddra version
    11
    Veddra term code
    99023
    Veddra term name
    Solution, Abnormal
  3. Veddra version
    11
    Veddra term code
    99031
    Veddra term name
    Underfilling, Tubes
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
    E262155A
    Lot expiration
    2028-04
    Product NDC
    0859-2341
    Brand name
    MSK
    Dosage form
    Solution
    Atc vet code
    QP54AB52
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N141251
    Active ingredients
    1. Name
      Imidacloprid
      Dose
      Numerator
      100
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      mL
    2. Name
      Moxidectin
      Dose
      Numerator
      25
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      mL
Health assessment prior to exposure
Assessed by
Veterinarian
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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.