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.