Pet Drug Reports

Gabapentinadverse event reports that FDA received

Active ingredient

The Green Book lists no brand name for exactly this active ingredient.

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.

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.

Contacting a veterinarianHow to report to FDA

From March 2011 to June 2026, FDA received 11,015 adverse event reports that name a drug with gabapentin as its active ingredient. Of the 11,015 reports, 9,023 (81.9%) are about dogs. 1,953 reports are about cats (17.7%).

In January to March 2026, FDA received 532 reports that name this drug. The signs that appear in the largest number of the 11,015 reports are "Lethargy", "Vomiting" and "Diarrhoea". A report is not proof that a drug caused a sign.

Reports that name this drug fell by 24.7% 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 dogs are 81.9% of the reports that name this drug, and 72.6% of all reports.

Since the last update of the FDA data

The site recorded an update of the FDA data on . FDA changed these counts for January to March 2026:

  • All species: from 465 to 532.
  • Dog: from 340 to 381.
  • Cat: from 125 to 151.

January to March 2026 is the latest closed quarter in the data. In that quarter FDA received 532 reports that name gabapentin: 381 dog, 151 cat, 0 horse, 0 other or not given.

All updatesFeed of updates (RSS)

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 11,015 reports that list the sign. One report can list more than one sign.

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

  1. Lethargy[unusually tired or inactive]16.8%1,846 reports
  2. Vomiting15%1,649 reports
  3. Diarrhoea[diarrhea]11.1%1,225 reports
  4. Death by euthanasia[the animal was euthanized]11%1,217 reports
  5. Not eating8.7%962 reports
  6. Lack of efficacy - NOS[the product did not have the expected effect]8.5%939 reports
  7. Decreased appetite6.6%722 reports
  8. Elevated alanine aminotransferase (ALT)[a liver enzyme above the normal range]6.5%717 reports
  9. Ataxia[unsteady, uncoordinated movement]6.2%682 reports
  10. Anorexia[not eating]5.8%634 reports
  11. Seizure NOS[seizure, type not specified]5.6%613 reports
  12. Weight loss5.5%610 reports
  13. Panting5.1%566 reports
  14. Death5%556 reports
Show the next 16 signs
  1. Pain NOS[NOS: not otherwise specified]4.9%543 reports
  2. Abnormal radiograph finding4.8%527 reports
  3. Behavioural disorder NOS[behaviour change, type not specified]4.5%496 reports
  4. Other abnormal test result NOS[abnormal laboratory result, type not specified]4.3%477 reports
  5. Elevated blood urea nitrogen (BUN)[a kidney value above the normal range]4.3%471 reports
  6. Limb weakness4.2%468 reports
  7. Polydipsia[drinking more than usual]4.1%450 reports
  8. Polyuria[passing more urine than usual]3.7%411 reports
  9. Elevated serum alkaline phosphatase (ALP)[a liver and bone enzyme above the normal range]3.5%383 reports
  10. Elevated creatinine[a kidney value above the normal range]3.1%342 reports
  11. Fever3.1%339 reports
  12. Lameness3.1%337 reports
  13. Weakness3%334 reports
  14. Neutrophilia[high neutrophil count]3%333 reports
  15. Vocalisation[crying out or unusual noise]3%331 reports
  16. Urinary incontinence3%329 reports

The list shows 30 of 1,907 coded signs. A report is not proof that a drug caused a sign. Download all signs (CSV)

Reports by species

The share is of all 11,015 reports that name gabapentin. The other reports give a different species or no species.

Reports for each month, Jul 2021 to Jun 2026

Dog6,848 reports. Largest count in one month: 255 (Jan 2025)
Cat1,752 reports. Largest count in one month: 58 (Sep 2024)
Horse3 reports

No chart: no month has 5 or more reports.

Other or not given15 reports

No chart: no month has 5 or more reports.

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
Reports that name gabapentin, by the year in which FDA received them and by species
YearDogCatHorseOther or not givenAll species
2026792243141,040
20252,094513052,612
20242,400502022,904
2023871347141,223
202248511410600
20214276305495
20204435403500
20193253703365
20183974000437
20173742203399
2016157601164
20158540493
20143930042
20137140075
20126011163
201130003

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

What the reports record

Outcome at the time of the report

  • Recovered/Normal17.2%1,899
  • Recovered with Sequela[recovered, with a lasting effect]0.4%43
  • Ongoing43.7%4,817
  • Died5.5%608
  • Euthanized11%1,214
  • Outcome Unknown22.1%2,436

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 11,015 reports that name gabapentin.

A report about more than one animal can have more than one outcome.

Kind of report

  • Safety issue84.5%9,306
  • Lack of expected effectiveness6.1%674
  • Both safety and lack of expected effectiveness8.4%926
  • Manufacturing or product defect0.9%99
  • Other0.1%10

10,979 reports say if the event was serious. 56.1% of them have the serious flag. The person who sends the report sets the flag.

Show age, weight, breed and route

Age of the animal

  • Under 1 year2.1%227
  • 1 to 3 years9.6%1,062
  • 4 to 7 years16%1,758
  • 8 to 11 years30.1%3,315
  • 12 years and over40.4%4,445
  • Age not given1.9%208

Weight of the animal

  • Under 5 kg (11 lb)13.3%1,465
  • 5 to 9.9 kg (11 to 22 lb)18.8%2,068
  • 10 to 24.9 kg (22 to 55 lb)23%2,538
  • 25 to 44.9 kg (55 to 99 lb)35.3%3,883
  • 45 kg and over (99 lb and over)5.8%639
  • Weight not given3.8%422

Breed, where the report gives one breed

A breed with many animals has many reports.

Route in the report

  • Oral47.8%5,266
  • Subcutaneous0.1%13
  • Parenteralunder 0.1%5
  • Topicalunder 0.1%5
  • Transdermalunder 0.1%4
  • Otherunder 0.1%2

Each bar is on a scale of 0 to 100%.

Approved animal drugs with this active ingredient (FDA Green Book)

This section is reference data. It has no report count.

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 lists no approved animal drug with this active ingredient. FDA also receives reports for human drugs and compounded drugs that veterinarians prescribe.

Next in the A to Z list

All drugs by active ingredient. Brand names A to Z

FDA pages for this drug

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

Cite this page

Pet Drug Reports. Gabapentin: adverse event reports that FDA received. https://petdrugreports.com/drug/gabapentin/ Source: FDA Center for Veterinary Medicine, openFDA Animal and Veterinary adverse event reports, export of . Reports received through .

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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 does not use the application number that a record has.

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 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 lists no brand name for exactly this active ingredient.

Do the reports show that the drug caused the signs?

No. 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 2,223 reports in the 12 months to June 2026. It received 2,952 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 11,015 reports received from March 2011 to June 2026, 84.5% are about a safety issue only. 14.5% are about a lack of expected effectiveness, alone or with a safety issue. 0.9% are about a defect of the product or its package.