Animal drug adverse event reports

MSK

Dog · Reactions: Panting, Fever, Distress +3

VeterinarianSerious
Treated for ae
false
Unique aer ID number
USA-USFDACVM-2026-US-035746
Original receive date
20260625
Number of animals affected
1
Primary reporter
Veterinarian
Number of animals treated
1
Secondary reporter
Animal Owner
Onset date
20260625
Foreign or domestic
Domestic
Report ID
N141440
Type of information
Safety Issue
Serious ae
true
Reaction
  1. Veddra version
    21
    Veddra term code
    855
    Veddra term name
    Panting
    Number of animals affected
    1
    Accuracy
    Actual
  2. Veddra version
    21
    Veddra term code
    1032
    Veddra term name
    Fever
    Number of animals affected
    1
    Accuracy
    Actual
  3. Veddra version
    21
    Veddra term code
    114
    Veddra term name
    Distress
    Number of animals affected
    1
    Accuracy
    Actual
  4. Veddra version
    21
    Veddra term code
    2868
    Veddra term name
    Difficulty standing
    Number of animals affected
    1
    Accuracy
    Actual
  5. Veddra version
    21
    Veddra term code
    2638
    Veddra term name
    Vertical nystagmus
    Number of animals affected
    1
    Accuracy
    Actual
  6. Veddra version
    21
    Veddra term code
    645
    Veddra term name
    Seizure NOS
    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
    20260625
    Last exposure date
    20260625
    Administered by
    Veterinarian
    Route
    Auricular (Otic)
    Lot number
    E259267A
    Lot expiration
    2027-07
    Product NDC
    0859-2412
    Brand name
    MSK
    Dosage form
    Solution
    Atc vet code
    QS02CA91
    Dose
    Numerator
    1
    Numerator unit
    tube
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N141440
    Active ingredients
    1. Name
      Florfenicol
      Dose
      Numerator
      17
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      mL
    2. Name
      Mometasone Furoate
      Dose
      Numerator
      2
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      mL
    3. Name
      Terbinafine Hydrochloride
      Dose
      Numerator
      15
      Numerator unit
      Milligram
      Denominator
      1
      Denominator unit
      mL
  2. First exposure date
    20260101
    Last exposure date
    20260625
    Administered by
    Unknown
    Route
    Unknown
    Brand name
    MSK
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Oclacitinib Maleate
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  3. First exposure date
    20260625
    Last exposure date
    20260625
    Administered by
    Unknown
    Route
    Auricular (Otic)
    Brand name
    MSK
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Phytosphingosine Hydrochloride
      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
Male
Reproductive status
Neutered
Female animal physiological status
NOT APPLICABLE
Age
Min
8.00
Unit
Year
Qualifier
Measured
Weight
Min
17.500
Unit
Kilogram
Qualifier
Measured
Breed
Is crossbred
true
Breed component
Retriever - Labrador, Poodle (unspecified)
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.