Reaction profile

The FDA adverse-event record for generalised congestion nos

21 FDA adverse-event reports reference generalised congestion nos (VeDDRA 3137). See the species, breeds, and drugs most associated with it below.

21
reports citing this reaction
23.8%
death-coded share
Cat
most-affected species
Fluralaner Spot-On Solution
most-associated drug
Verify with FDA CVM →
21
Total Reports
5
Deaths
23.8%
Death Rate

Species Most Affected

Cat 13
Dog 7
Human 1

Breeds Most Affected

Himalayan 4
Domestic Shorthair 4
Cat (unknown) 2
Terrier (unspecified) 1
Manx 1
Cat (other) 1
Spaniel - King Charles Cavalier 1
Bulldog - French 1
Pug 1
Dog (unknown) 1

Associated Drugs

Fluralaner Spot-On Solution 4
Cefovecin 3
Eprinomectin + Esafoxolaner + Praziquantel 2
Bordetella Bronchiseptica 92B 012992-7 Strain Boehringer Ingelheim 2
Frunevetmab 2
Bedinvetmab 2
Doxycycline 2
Trimeprazine Tartrate;Prednisolone 1
Water, Sodium Chloride, Sodium Lactate, Potassium Chloride, Calcium Chloride 1
Miconazole 2%, Chlorhexidene Gluconate 2% 1
Unknown Shampoo 1
Gabapentin 1
Unspecified Inhaler 1
Polyethylene Glycol 1
Velagliflozin Proline Monohydrate 1
Carprofen 1
Omega 3 Fatty Acids 1
Sodium Citrate/Citric Acid/Zinc Chloride 1
Glucosamine Supplement 1
S Adenosylmethionine 1

Generalised congestion NOS Reaction Insights

21 reports name Generalised congestion NOS; 5 recorded a death outcome (23.8% of reported events, not a population-level mortality rate). VeDDRA code: 3137.

By species: Cat (13 reports), Dog (7 reports), Human (1 reports). By breed: Himalayan (4), Domestic Shorthair (4), Cat (unknown) (2).

Most co-reported drugs: Fluralaner Spot-On Solution (4 reports), Cefovecin (3 reports), Eprinomectin + Esafoxolaner + Praziquantel (2 reports), Bordetella Bronchiseptica 92B 012992-7 Strain Boehringer Ingelheim (2 reports).

Read these counts as reporting volume, not risk: per our methodology, co-reporting reflects temporal association captured in voluntary submissions, not proof that a drug caused this reaction. A widely-prescribed drug will rack up more raw co-reports at an identical true rate than a rarely-used one, so compare within similar-exposure products.

Source: FDA Center for Veterinary Medicine openFDA Animal & Veterinary Adverse Events (CVM AER) · 2025

Every figure on PlainBreed is rendered directly from FDA openFDA adverse event data, no number is typed in by an editor. This page draws directly on FDA openFDA data, no figure is typed in by an editor. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.