Moxidectin: adverse event reports in all combinations

Drug pages with moxidectin

A report names a drug by its set of active ingredients. Each set with moxidectin that has a drug page is in the table, in order of name. The table has 7 sets.

Signs that the reports list

A sign is a coded term from the report. The words in brackets are a plain gloss of the term. The percentage is the share of the 100,770 reports that list the sign. One report can list more than one sign and more than one drug.

The sign that is in the largest number of the reports comes first.

1. Vomiting15.6%15,763 reports
2. Lack of efficacy (endoparasite) - heartworm[the product did not have the expected effect: heartworm]11.2%11,270 reports
3. Lethargy[unusually tired or inactive]9%9,082 reports
4. Diarrhoea[diarrhea]6.5%6,509 reports
5. Lack of efficacy (endoparasite) - hookworm[the product did not have the expected effect: hookworms]6%6,048 reports
6. Anaphylaxis[sudden severe allergic-type reaction]5.1%5,187 reports
7. Facial swelling4.7%4,772 reports
8. Pruritus[itching]4.1%4,175 reports
9. Anorexia[not eating]3.8%3,784 reports
10. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]3.6%3,613 reports
11. Hives3.5%3,542 reports
12. Ineffective, heartworm larvae[legacy FDA term: the product did not have the expected effect (heartworm larvae)]3.2%3,199 reports
13. Behavioural disorder NOS[behaviour change, type not specified]3%3,062 reports
14. Depression[dull, quiet or withdrawn]3%3,045 reports

Download all signs (CSV)

Reports by species

• Dog76.3%76,889
• Cat11.4%11,447
• Horse1.7%1,738
• Cattle1.3%1,319
• Human exposure1%1,026
• Goat0.1%96

Reports for each month, Jul 2021 to Jun 2026

The month is the month in which FDA received the report. Each chart has its own scale. 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 by year

• Dog
• Cat
• Horse
• Other or not given

2026 has the reports that FDA received through Jun 2026. Download the years (CSV)

What the reports record

Each share of kind and age is of the 100,770 reports that name moxidectin.

FDA pages for this ingredient

• How to Report Animal Drug and Device Side Effects and Product ProblemsThe FDA page that tells an owner or a veterinarian how to send a report.
• Green Book record of NADA 141-051The FDA record of the application for ProHeart.
• Green Book record of NADA 141-189The FDA record of the application for ProHeart 6.Client Information Sheet of ProHeart 6 (PDF): a label document that FDA posts with the record.Package Insert of ProHeart 6 (PDF): a label document that FDA posts with the record.
• Green Book record of NADA 141-251The FDA record of the application for Advantage Multi for Dogs.
• Green Book record of NADA 141-417The FDA record of the application for Coraxis.
• Green Book record of NADA 141-519The FDA record of the application for ProHeart 12.Client Information Sheet of ProHeart 12 (PDF): a label document that FDA posts with the record.Package Insert of ProHeart 12 (PDF): a label document that FDA posts with the record.
• Green Book record of NADA 141-521The FDA record of the application for Simparica Trio.
• Animal Drugs @ FDAThe search page of the Green Book, the FDA list of approved animal drugs.

The site checked these addresses on 2 Oct 2026. The links open in a new tab.

Cite this page

Pet Drug Reports. Moxidectin, all combinations: adverse event reports that FDA received. https://petdrugreports.com/ingredient/moxidectin/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of 30 Oct 2026. Reports received through 26 Jun 2026.

Where the data come from

Questions about these reports

Which brand are these reports about?

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. The Green Book section of this page lists brand names with this active ingredient.

Do the reports show that the ingredient caused the signs?

No. A report can name more than one drug, and a drug can have more than one active ingredient. 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

How many reports did FDA receive in the latest 12 months?

FDA received 13,072 reports in the 12 months to June 2026. It received 9,955 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.

What kinds of report are in the count?

Of the 100,770 reports received from September 1997 to June 2026, 61.4% are about a safety issue only. 29.8% are about a lack of expected effectiveness, alone or with a safety issue. 8.6% are about a defect of the product or its package.