Pet Drug Reports

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Breed · Dog

German Shepherd Dog: adverse event reports

FDA breed label "Shepherd Dog - German" · single-breed animals only

32,587reports, 1987–20263.3% of dog reports
1,773reports, 12 months to March 20261,960 in the 12 months before
39.2%classed serious, as reportedall dogs: 38.3%
19.1%name ivermectin + pyrantel pamoateall dogs: 14.9%

FDA's database holds 32,587 reports where the animal's breed is given as "Shepherd Dog - German", shown here as German Shepherd Dog: 3.3% of reports about dogs. Reports on crossbred animals are left out of breed pages.

1,773 reports arrived in the 12 months to March 2026, down 10% from 1,960 in the 12 months before. A breed's count mostly mirrors how common the breed is; registration and ownership figures by breed are not public data, so no per-animal rate can be given.

By active ingredient, the drugs named most often are ivermectin + pyrantel pamoate, milbemycin oxime + spinosad and fluralaner. Ivermectin + Pyrantel Pamoate is named in 19.1% of this breed's reports, a larger share than in reports about all dogs (14.9%).

The terms listed most often are vomiting (14%), ineffective, heartworm larvae (13.5%) and lack of efficacy (endoparasite) - heartworm (11.2%). Vomiting appears in 14% of reports, a smaller share than in all dog reports (19.7%). 39.2% of reports stating seriousness were classed as serious, against 38.3% for dogs overall.

Drugs named most often, by active ingredient

Active ingredients recorded for the drugReportsShare of German Shepherd Dog reportsShare of all dog reports
Ivermectin + Pyrantel Pamoate6,21719.1%14.9%
Milbemycin Oxime + Spinosad3,72311.4%13.1%
Fluralaner2,0666.3%6.7%
Carprofen1,8735.7%4.8%
Afoxolaner1,7535.4%5.7%
Pyrantel Pamoate + Sarolaner1,6985.2%5.1%
Moxidectin1,5844.9%5%
Milbemycin Oxime1,3444.1%3%
Milbemycin Oxime + Praziquantel1,2733.9%3.1%
Spinosad1,1803.6%5.8%
Selamectin1,1453.5%3%
Oclacitinib1,0663.3%2.9%
Melarsomine Dihydrochloride1,0563.2%2.3%
Lufenuron + Milbemycin Oxime9953.1%2.7%
Bedinvetmab8722.7%1.9%
Deracoxib4761.5%1.1%
Ivermectin4581.4%1.3%
Sarolaner4381.3%1.7%
Cyclosporine4291.3%1.5%
Imidacloprid + Moxidectin3681.1%1.3%

Ordered by report count. Differences from the species column often come from body size (which drugs a breed is prescribed) and from how common the breed was in the years a drug sold most. FDA states that these data cannot be used to estimate risk or to compare one product with another. Brand and manufacturer names are masked by FDA in these records.

Signs listed in reports

share of German Shepherd Dog reports listing the termall dog reports

  1. Vomiting14%4,563
  2. Ineffective, heartworm larvae[legacy FDA term: the product did not have the expected effect (heartworm larvae)]13.5%4,409
  3. Lack of efficacy (endoparasite) - heartworm[the product did not have the expected effect: heartworm]11.2%3,648
  4. Diarrhoea[diarrhea]8%2,597
  5. Lethargy[unusually tired or inactive]5.7%1,847
  6. Lack of efficacy - NOS[the product did not have the expected effect]4.7%1,530
  7. Emesis[vomiting]4.5%1,478
  8. Lack of efficacy (endoparasite) - hookworm[the product did not have the expected effect: hookworms]4.5%1,462
  9. Anorexia[not eating]4.3%1,407
  10. Lack of efficacy (ectoparasite) - flea[the product did not have the expected effect: fleas]3.8%1,240
  11. Death3.4%1,100
  12. Depression[dull, quiet or withdrawn]2.9%937
  13. Death by euthanasia[the animal was euthanized]2.4%775
  14. Ataxia[unsteady, uncoordinated movement]2.2%730
  15. Ineffective, ascarids NOS[legacy FDA term: the product did not have the expected effect (ascarids nos)]2.1%696
  16. Seizure NOS[seizure, type not specified]2.1%691
  17. Cardiac disorder NOS[heart problem, type not specified]2%660
  18. Pruritus[itching]2%643
  19. Lack of efficacy (ectoparasite) - tick NOS[the product did not have the expected effect: ticks]1.9%633
  20. Digestive tract disorder NOS[digestive problem, type not specified]1.8%583
  21. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]1.7%558
  22. Lack of efficacy (bacteria) - Borrelia[the product did not have the expected effect: Borrelia (Lyme disease bacteria)]1.7%543
  23. Fever1.6%529
  24. Other abnormal test result NOS[abnormal laboratory result, type not specified]1.6%515

Age and weight

Age of the animal

Under 1 year12.4%4,050
1 to 3 years33.7%10,975
4 to 7 years27.3%8,892
8 to 11 years18%5,876
12 years and over5.6%1,821
Age not given3%973

Weight of the animal

Under 5 kg (11 lb)0.7%226
5 to 9.9 kg (11–22 lb)1.6%521
10 to 24.9 kg (22–55 lb)11%3,586
25 to 44.9 kg (55–99 lb)70.7%23,029
45 kg and over (99 lb+)11.8%3,830
Weight not given4.3%1,395

Coloured bar: German Shepherd Dog reports. Grey bar: all dog reports.

Trend and outcomes

0107213Apr 2021: 153May 2021: 154Jun 2021: 153Jul 2021: 181Aug 2021: 157Sep 2021: 121Oct 2021: 127Nov 2021: 117Dec 2021: 104Jan 2022: 752022Feb 2022: 98Mar 2022: 151Apr 2022: 141May 2022: 140Jun 2022: 106Jul 2022: 149Aug 2022: 157Sep 2022: 121Oct 2022: 111Nov 2022: 126Dec 2022: 91Jan 2023: 1332023Feb 2023: 88Mar 2023: 106Apr 2023: 132May 2023: 159Jun 2023: 154Jul 2023: 123Aug 2023: 141Sep 2023: 120Oct 2023: 141Nov 2023: 178Dec 2023: 108Jan 2024: 1322024Feb 2024: 150Mar 2024: 169Apr 2024: 213May 2024: 187Jun 2024: 154Jul 2024: 169Aug 2024: 193Sep 2024: 161Oct 2024: 182Nov 2024: 126Dec 2024: 146Jan 2025: 1612025Feb 2025: 160Mar 2025: 108Apr 2025: 181May 2025: 180Jun 2025: 182Jul 2025: 169Aug 2025: 150Sep 2025: 165Oct 2025: 164Nov 2025: 121Dec 2025: 120Jan 2026: 1272026Feb 2026: 115Mar 2026: 99

Reports by month FDA received them. The newest months are incomplete because FDA posts reports with a delay of three to six months.

Outcome recorded in the report

Recovered/Normal18.2%5,924
Recovered with Sequela4.6%1,499
Ongoing21.9%7,128
Died4.7%1,516
Euthanized1.5%477
Outcome Unknown25.9%8,427

Beside all dogs

MeasureGerman Shepherd DogAll dogs
Reports32,587985,675
Latest 12 months1,77353,292
Classed serious, of reports stating it39.2%38.3%
Death or euthanasia recorded, per 1,000 reports61.255

Questions about German Shepherd Dog reports

How many FDA adverse event reports involve German Shepherd Dogs?

32,587 reports through March 2026, 3.3% of reports about dogs; 1,773 in the latest 12 months.

Which drugs are named most often in German Shepherd Dog reports?

By active ingredient: ivermectin + pyrantel pamoate (6,217), milbemycin oxime + spinosad (3,723), fluralaner (2,066), carprofen (1,873) and afoxolaner (1,753). Brands are masked in the public data.

What signs are reported most for this breed?

vomiting (14%), ineffective, heartworm larvae (13.5%), lack of efficacy (endoparasite) - heartworm (11.2%), diarrhoea (8%) and lethargy (5.7%).

Is the German Shepherd Dog more sensitive to certain drugs?

Report counts cannot answer that. They show what was reported, not what a drug did, and they are not adjusted for how many German Shepherd Dog animals exist or were treated. Breed-related drug sensitivities that are established are described on FDA-approved labels; a veterinarian is the person to ask about an individual animal.

Why are crossbreds not included?

FDA records crossbred animals with one or more component breeds. Counting them under each component would double count, so breed pages use single-breed reports only. Crossbreds remain in the species totals.

How do I report a problem?

Call the drug company using the number on the label, or send Form FDA 1932a to FDA. See the guide on how to report.

Where this comes from. Counts are built from the openFDA Animal & Veterinary adverse event bulk files released 28 Sep 2026, which hold reports FDA's Center for Veterinary Medicine received through 31 Mar 2026. openFDA masks brand and manufacturer names in these files, so drugs are counted by the active ingredients each record discloses and no figure is attributed to a brand, application or company. Ingredient names, and the separate reference lists of approved products, follow the FDA Green Book as of 30 Sep 2026. Breed names are FDA's labels rearranged into everyday order ("Shepherd Dog - German" becomes "German Shepherd Dog"). No report text, lot numbers or reporter details are published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.