Oxytetracycline Anhydrous + Polymyxin B
28 adverse event reports submitted to the FDA
Important: Adverse event reports do not establish that a drug caused or contributed to the event. Consult your veterinarian before making treatment decisions.
28
Total Reports
0
Deaths Reported
0.0%
Death Rate
Active Ingredients
Oxytetracycline AnhydrousPolymyxin B
Administration Routes
UnknownOphthalmic
Species Affected
Unknown 24
Cat 4
Most Affected Breeds
Unknown 24
Cat (other) 3
Cat (unknown) 1
Most Reported Reactions
Color, Abnormal 22
Counterfeit product 18
Suspect counterfeit product 5
Counterfeit drug administered 3
Contamination, Mold 2
Odor, Abnormal 2
Labels, Abnormal 1
Lot # and/or Expiration date incorrect 1
Underfilling, Tubes 1
Lack of efficacy (bacteria) - NOS 1
Lack of efficacy - NOS 1
Application site swelling 1
Outcome Breakdown
Ongoing
1 (25.0%)
Recovered with Sequela
1 (25.0%)
Outcome Unknown
1 (25.0%)
Recovered/Normal
1 (25.0%)
Source: FDA Center for Veterinary Medicine — Adverse Event Reports. Data reflects voluntary submissions and may not represent actual incidence rates.