Animal drug adverse event reports

MSK

Dog · Reactions: Emesis (multiple)

Other
Treated for ae
false
Unique aer ID number
USA-USFDACVM-2026-US-035676
Original receive date
20260625
Number of animals affected
1
Primary reporter
Other
Number of animals treated
1
Secondary reporter
Animal Owner
Onset date
20260624
Foreign or domestic
Domestic
Report ID
N141338
Type of information
Safety Issue
Serious ae
false
Reaction
  1. Veddra version
    21
    Veddra term code
    2082
    Veddra term name
    Emesis (multiple)
    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
    20260624
    Last exposure date
    20260624
    Administered by
    Animal Owner
    Route
    Oral
    Used according to label
    true
    Lot number
    ASKED/NOT PROVIDED
    Brand name
    MSK
    Dosage form
    Tablet, chewable
    Atc vet code
    QP54AB51
    Dose
    Numerator
    1
    Numerator unit
    tablet
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N141338
    Active ingredients
    1. Name
      Milbemycin Oxime
      Dose
      Numerator
      23
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      dose
    2. Name
      Praziquantel
      Dose
      Numerator
      228
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      dose
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
1.50
Unit
Year
Qualifier
Measured
Weight
Min
24.500
Unit
Kilogram
Qualifier
Measured
Breed
Is crossbred
true
Breed component
Pit Bull, Dog (unknown)
Outcome
  1. Medical status
    Recovered/Normal
    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.