Animal drug adverse event reports

MSK

Cat · Reactions: Lack of efficacy - NOS, Medication error NOS

VeterinarianSerious
Treated for ae
true
Unique aer ID number
USA-USFDACVM-2026-US-035615
Original receive date
20260625
Number of animals affected
1
Primary reporter
Veterinarian
Number of animals treated
1
Secondary reporter
Animal Owner
Onset date
20260508
Foreign or domestic
Domestic
Report ID
N012204
Type of information
Lack Of Expected Effectiveness
Serious ae
true
Reaction
  1. Veddra version
    21
    Veddra term code
    1039
    Veddra term name
    Lack of efficacy - NOS
    Number of animals affected
    1
    Accuracy
    Actual
  2. Veddra version
    21
    Veddra term code
    2282
    Veddra term name
    Medication error 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
    20260410
    Last exposure date
    20260530
    Administered by
    Unknown
    Route
    Unknown
    Used according to label
    false
    Off label use
    Indication Off-Label
    Ae abated after stopping drug
    false
    Ae reappeared after resuming drug
    false
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Suspension
    Atc vet code
    QH02AB04
    Dose
    Numerator
    10
    Numerator unit
    Milligram
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Registration number
    USA-USFDACVM-N012204
    Active ingredients
    1. Name
      Methylprednisolone Acetate
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  2. First exposure date
    20260518
    Administered by
    Animal Owner
    Route
    Topical
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Dose
    Numerator
    5
    Numerator unit
    Milligram
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Fluoxetine
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  3. First exposure date
    20260518
    Administered by
    Animal Owner
    Route
    Oral
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Frequency of administration
    Value
    12
    Unit
    Hour
    Dose
    Numerator
    100
    Numerator unit
    Milligram
    Denominator
    1
    Denominator unit
    Animal
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Gabapentin
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
  4. First exposure date
    20260518
    Administered by
    Animal Owner
    Route
    Oral
    Lot number
    not given
    Brand name
    MSK
    Dosage form
    Unassigned
    Frequency of administration
    Value
    12
    Unit
    Hour
    Manufacturer
    Name
    MSK
    Active ingredients
    1. Name
      Amantadine
      Dose
      Numerator
      1
      Numerator unit
      Unknown
      Denominator
      1
      Denominator unit
      Unknown
Health assessment prior to exposure
Condition
Unknown
Assessed by
Veterinarian
Animal
Species
Cat
Gender
Male
Reproductive status
Neutered
Female animal physiological status
NOT APPLICABLE
Age
Min
4.25
Unit
Year
Qualifier
Measured
Weight
Min
5.760
Unit
Kilogram
Qualifier
Measured
Breed
Is crossbred
false
Breed component
Domestic Shorthair
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.