Animal drug adverse event reports

MSK

Dog · Reactions: Lack of efficacy (endoparasite) - heartworm

Other Health Care ProfessionalSerious
Treated for ae
false
Unique aer ID number
USA-USFDACVM-2026-US-035639
Original receive date
20260626
Number of animals affected
1
Primary reporter
Other Health Care Professional
Number of animals treated
1
Secondary reporter
Animal Owner
Onset date
20260616
Foreign or domestic
Domestic
Report ID
N141519
Type of information
Lack Of Expected Effectiveness
Serious ae
true
Reaction
  1. Veddra version
    21
    Veddra term code
    2430
    Veddra term name
    Lack of efficacy (endoparasite) - heartworm
    Number of animals affected
    1
    Accuracy
    Actual
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. First exposure date
    20250715
    Last exposure date
    20250715
    Administered by
    Veterinarian
    Route
    Subcutaneous
    Previous exposure to drug
    false
    Ae abated after stopping drug
    false
    Ae reappeared after resuming drug
    false
    Lot number
    783118
    Brand name
    MSK
    Dosage form
    Suspension
    Atc vet code
    QP54AB02
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N141519
    Active ingredients
    1. Name
      Moxidectin
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
Health assessment prior to exposure
Condition
Good
Assessed by
Veterinarian
Animal
Species
Dog
Gender
Female
Reproductive status
Neutered
Female animal physiological status
NOT APPLICABLE
Age
Min
1.91
Unit
Year
Qualifier
Measured
Weight
Min
16.329
Unit
Kilogram
Qualifier
Measured
Breed
Is crossbred
false
Breed component
Terrier - West Highland White
Outcome
  1. Medical status
    Ongoing
    Number of animals affected
    1
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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.