Animal drug adverse event reports

MSK

Dog · Reactions: Generalised itching, Facial swelling (see also Skin), Reddening of the skin +1

VeterinarianSerious
Treated for ae
true
Unique aer ID number
USA-USFDACVM-2026-US-035126
Original receive date
20260625
Number of animals affected
1
Primary reporter
Veterinarian
Number of animals treated
1
Secondary reporter
Animal Owner
Onset date
20260624
Foreign or domestic
Domestic
Report ID
N141519
Type of information
Safety Issue
Serious ae
true
Reaction
  1. Veddra version
    21
    Veddra term code
    1492
    Veddra term name
    Generalised itching
    Number of animals affected
    1
    Accuracy
    Actual
  2. Veddra version
    21
    Veddra term code
    517
    Veddra term name
    Facial swelling (see also Skin)
    Number of animals affected
    1
    Accuracy
    Actual
  3. Veddra version
    21
    Veddra term code
    946
    Veddra term name
    Reddening of the skin
    Number of animals affected
    1
    Accuracy
    Actual
  4. Veddra version
    21
    Veddra term code
    2241
    Veddra term name
    Hypersensitivity reaction
    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
    Other Health Care Professional
    Route
    Subcutaneous
    Used according to label
    true
    Previous exposure to drug
    false
    Ae abated after stopping drug
    false
    Ae reappeared after resuming drug
    false
    Lot number
    858081
    Brand name
    MSK
    Dosage form
    Suspension
    Atc vet code
    QP54AB02
    Dose
    Numerator
    0.35
    Numerator unit
    mL
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N141519
    Active ingredients
    1. Name
      Moxidectin
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  2. First exposure date
    20260624
    Last exposure date
    20260624
    Administered by
    Other Health Care Professional
    Route
    Unknown
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Rabies Vaccine
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  3. First exposure date
    20260624
    Last exposure date
    20260624
    Administered by
    Other Health Care Professional
    Route
    Unknown
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Dapp+L4 Vaccine
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  4. First exposure date
    20260624
    Last exposure date
    20260624
    Administered by
    Other Health Care Professional
    Route
    Unknown
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Fluralaner
      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
Unknown
Female animal physiological status
Not applicable
Age
Min
5.00
Unit
Year
Qualifier
Measured
Weight
Min
6.532
Unit
Kilogram
Qualifier
Measured
Breed
Is crossbred
false
Breed component
Dachshund - Standard Long-haired
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.