Pet Drug Reports

Heart murmur: in adverse event reports for animal drugs

Clinical sign, a VeDDRA term

Read this first. FDA says this about the data:

An API dataset query result cannot be used to estimate the risk associated with the product or compare one drug or device product with another. When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event. This dataset should not be the sole source of information for clinical decision-making or other assumptions about the safety or effectiveness of a product. The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine publishes these words. Source: Adverse Event Reports for Animal Drugs and Devices, read on . The data have the reports that FDA received through .

This page is not veterinary advice. For an animal that is ill, speak to a veterinarian.

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From May 2003 to June 2026, FDA received 2,404 adverse event reports for animal drugs that list this sign. That is 0.2% of the 1,378,761 reports that FDA received from January 1987 to June 2026. In the 12 months to June 2026, FDA received 266 reports that list this sign.

Of the 2,404 reports, 77.5% are about dogs. A report can list more than one sign and more than one drug. A report is not proof that a drug caused a sign.

By number of reports in all years, this sign is number 238 of 1,149 clinical signs with a page. Reports that list this sign fell by 13.4% in the 12 months to June 2026, compared with the 12 months before. Reports for all animal drugs fell by 4.6% in the same periods. The newest months can get more reports in a later update. Reports about cats are 21.6% of the reports that list this sign, and 11% of all reports.

Search engines list a sign page with 3,000 reports or more in all years. The page also needs 300 reports or more in the 12 months to June 2026. This page is under one of these numbers. The site keeps the page and keeps it out of search engines.

Drug pages with reports that list this sign

The table has every drug page with 20 or more reports that list this sign, in order of name. No count decides which drug is in the table. The table has 60 drug pages.

Show the 60 drug pages
Drug pages with 20 or more reports that list this sign, in order of name
Active ingredientsReports that list the sign
Afoxolaner84
Amlodipine22
Amoxicillin23
Amoxicillin + Clavulanate Potassium25
Amoxicillin Trihydrate + Clavulanate Potassium40
Bedinvetmab150
Bexagliflozin35
Buprenorphine72
Butorphanol Tartrate39
Capromorelin35
Carprofen106
Cefovecin sodium109
Cyclosporine61
Deracoxib28
Dexamethasone31
Dexmedetomidine hydrochloride23
Diphenhydramine43
Doxycycline46
Enalapril Maleate31
Enrofloxacin41
Famotidine37
Fluralaner209
Frunevetmab84
Furosemide41
Gabapentin108
Grapiprant41
Imidacloprid + Moxidectin48
Insulin60
Isoflurane40
Ivermectin34
Ivermectin + Pyrantel Pamoate109
Ketamine Hydrochloride24
Levothyroxine sodium28
Lotilaner40
Lufenuron + Milbemycin Oxime28
Maropitant179
Melarsomine Dihydrochloride63
Meloxicam54
Metronidazole49
Midazolam31
Milbemycin Oxime33
Milbemycin Oxime + Praziquantel95
Milbemycin Oxime + Spinosad330
Mirtazapine25
Moxidectin75
Nitenpyram21
Oclacitinib129
Ondansetron21
Pimobendan60
Prednisolone25
Prednisone97
Propofol32
Pyrantel Pamoate + Sarolaner40
Robenacoxib39
Sarolaner45
Selamectin51
Spinosad83
Tramadol24
Trilostane159
Velagliflozin36

The openFDA records give the value "MSK" for the brand name and for the manufacturer name of each drug. FDA says that MSK means "masked". So the site cannot count a report for a brand. A report can name more than one drug.

An API dataset query result cannot be used to estimate the risk associated with the product or compare one drug or device product with another.

The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices

Ingredients, all combinations

The list has every active ingredient with 20 or more reports that list this sign, in order of name. It has 61 ingredients.

Show the 61 ingredients

Reports by species

The share is of the 2,404 reports that list this sign. The sign is in 0.2% of all reports about the species dog. The sign is in 0.3% of all reports about the species cat.

Reports by month and by year

Reports for each month, Jul 2021 to Jun 2026. The month is the month in which FDA received the report.

FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

Reports that list Heart murmur, by the year in which FDA received them
YearReports
2026137
2025286
2024291
2023164
2022101
2021107
2020160
2019148
2018198
2017167
2016147
2015150
2014116
2013121
201280
201120
20101
20091
20084
20071
20061
20052
20031

What these reports record

Outcome at the time of the report

  • Reports with this sign
  • All reports
  • Recovered/Normal6.4%155, All reports: 20.7%
  • Recovered with Sequela[recovered, with a lasting effect]9.9%237, All reports: 2.3%
  • Ongoing35.7%858, All reports: 17.4%
  • Died9.1%218, All reports: 4.9%
  • Euthanized13.7%329, All reports: 1.5%
  • Outcome Unknown25.6%615, All reports: 22.7%

An outcome in a report is not proof that the drug caused it. The person who sends the report gives the outcome. Each share is of the 2,404 reports that list this sign.

Age of the animal

  • Reports with this sign
  • All reports
  • Under 1 year2.6%63, All reports: 9.5%
  • 1 to 3 years9.6%231, All reports: 23.9%
  • 4 to 7 years17.1%410, All reports: 20.2%
  • 8 to 11 years33.2%798, All reports: 15.4%
  • 12 years and over35.7%859, All reports: 10.7%
  • Age not given1.8%43, All reports: 20.3%

The outcome is for the full report, not for this sign only.

Next in the A to Z list of signs

All clinical signs

Cite this page

Pet Drug Reports. Heart murmur: adverse event reports for animal drugs. https://petdrugreports.com/reaction/heart-murmur/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .

Where the data come from

The counts come from the openFDA Animal and Veterinary adverse event files, export of 30 Oct 2026. The files have the reports that the FDA Center for Veterinary Medicine received through 26 Jun 2026. The files mask brand and manufacturer names. The site counts a drug by the active ingredients that each record gives, and gives no count to a brand, an application or a company. Ingredient names and the lists of approved products follow the FDA Green Book of 2 Nov 2026. The site counts the different spellings of one VeDDRA term together.

The site does not publish report text, lot numbers or details of a reporter. FDA's record is the authority. See how the site counts reports, the data sources and the corrections page.

Questions about this sign

What does this term mean in a report?

It is a term from VeDDRA, the list of terms that FDA and drug companies use to code a report. The person who coded the report selected the term.

How does the count of the latest 12 months compare with the 12 months before?

FDA received 266 reports in the 12 months to June 2026. It received 307 reports in the 12 months before. FDA says that a report can take 3 to 6 months to reach the public data. The newest months can get more reports in a later update.

How many of these reports have a serious flag?

Of the 2,381 reports that say if the event was serious, 75.6% have the serious flag. The person who sends a report sets the flag.

Does a drug in the table cause this sign?

The reports do not show that. A report can name more than one drug. FDA states this about the data.

When looking at the results, be aware that there is no certainty that the reported drug or device caused the adverse event.

The adverse event may have been related to an underlying disease, other drugs used at the same time or other non-drug related sources.

FDA Center for Veterinary Medicine. Source: Adverse Event Reports for Animal Drugs and Devices