Roxee Meds Catalog
Amoxicillin Trihydrate
Medication catalog facts with explicit FDA-approval, off-label, source-limited, and safety context.
Veterinary professional?
Data freshness
Roxee is still reviewing source support for this medication profile.
Roxee has safety or ingredient evidence for this medication, but a regulatory product/application match is still pending.
openFDA reaction terms and case summaries are supporting evidence, not proof of causality.
Source timing details
-
Storefront facts:
Source Roxee
| Refreshed May 5, 2026, 10:05 AM UTC
The storefront fact projection used for browse cards and quick facts.
- openFDA reaction terms: Source FDA openFDA | Refreshed May 5, 2026, 10:04 AM UTC
- openFDA case summaries: Source FDA openFDA | Refreshed May 5, 2026, 10:04 AM UTC
Evidence
Reviewed / Updated / Sources
Reviewed by: Not available
Last reviewed: February 12, 2026
Updated: February 12, 2026, 10:44 PM UTC
- Medication contraindications · safety_warning
- openFDA case USA-USFDACVM-2024-US-065151 · adverse_reaction
- FOI summary · document
- FOI summary · document
- FOI summary · document
Amoxicillin Trihydrate
Drug type: Generic ingredient • Generic profile • Regulatory linkage incomplete
Species: Both
Approval status: Official document linked, regulatory match incomplete. An official source document is available, but Roxee has not linked this row to a confirmed FDA animal-drug application or product record yet.
Medication Snapshot
Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.
Amoxicillin Trihydrate
For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due to Staphylococcus aureus , Streptococcus spp., Escherichia coli , and Proteus mirabilis . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections (bacterial gastroenteritis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Bacterial dermatitis due to Staphylococcus aureus , Streptococcus spp., and Proteus mirabilis . Soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . For the treatment of susceptible strains of the organisms causing the following infections: Upper respiratory tract infections due to Staphylococcus aureus , Streptococcus spp., and E. coli . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections due to E. coli . Skin and soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Pasteurella multocida . For the treatment of baby pigs under 10 pounds for porcine colibacillosis caused by Escherichia coli susceptible to amoxicillin. Species commonly shown: Both.
Indications / Uses
For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due to Staphylococcus aureus , Streptococcus spp., Escherichia coli , and Proteus mirabilis . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections (bacterial gastroenteritis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Bacterial dermatitis due to Staphylococcus aureus , Streptococcus spp., and Proteus mirabilis . Soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . For the treatment of susceptible strains of the organisms causing the following infections: Upper respiratory tract infections due to Staphylococcus aureus , Streptococcus spp., and E. coli . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections due to E. coli . Skin and soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Pasteurella multocida . For the treatment of baby pigs under 10 pounds for porcine colibacillosis caused by Escherichia coli susceptible to amoxicillin.
Warnings / Contraindications
Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
- Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Side Effects
Top reported reactions (openFDA): Lethargy (see also Central nervous system depression in 'Neurological'), Not eating, Vomiting, Death by euthanasia, Fever, Not drinking.
FAQ
Related Conditions
Source Transparency
- Verified source: https://www.roxee.ai/meds/
- Verified source: https://animaldrugsatfda.fda.gov
- Verified source: https://api.fda.gov/animalandveterinary/event.json
- Verified source: https://www.roxee.ai/conditions/
- Verified source: https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1953
- Verified source: https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1263
- Last refreshed: May 5, 2026, 10:05 a.m.
- Last verified: Feb 12, 2026, 10:44 p.m.
- Validation status: Incomplete
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Start here first for the safest next-step summary before the deeper medication detail.
Used for:
For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due to Staphylococcus aureus , Streptococcus spp., Escherichia col...
Dosing note:
Exact dosing depends on your pet's species, weight, and health status. Use your veterinarian's instructions for the exact dose and schedule.
What to watch for:
- Do not slaughter during treatment or for 15 days after latest treatment
- Do not slaughter animals during treatment or for 20 days after the latest treatment
- Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment
- Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment
- wobbly/unsteady walking (1 reports)
- trouble breathing (1 reports)
- Fever (1 reports)
When to call the vet:
- Repeated vomiting or diarrhea.
- Severe lethargy (hard to wake, very low energy).
- Collapse or fainting.
- Facial swelling or hives.
- Blood in vomit or stool.
Regulatory restrictions are shown in Vet View.
What to tell or ask your vet today:
- Is this medicine the right fit for my pet’s current symptoms?
- Which warning signs mean I should call back right away?
- How should I handle missed doses or refusal to take the medicine?
Major cautions & emergency warning signs
Side effects to monitor:
- Do not slaughter during treatment or for 15 days after latest treatment
- Do not slaughter animals during treatment or for 20 days after the latest treatment
- Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment
- Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment
- wobbly/unsteady walking
Most reported reactions:
- Unsteady walking (ataxia) (1 reports)
- Trouble breathing (dyspnea) (1 reports)
- Fever (1 reports)
Emergency warning signs:
- Repeated vomiting or diarrhea.
- Severe lethargy (hard to wake, very low energy).
- Collapse or fainting.
- Facial swelling or hives.
Quick Facts
Official label facts first, then secondary summaries. Marketing content is separated below.
Warnings / Contraindications
Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
- High: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
- https://animaldrugsatfda.fda.gov · safety_warning · Medication contraindications
Adverse Reactions
Snapshot first, detailed rows second. This section summarizes signal data and is not a diagnosis.
Tap or hover a reaction to see what it means in plain language.
Grouped by Body System
Most Reported Reactions
| Reaction | Body system | Cases | Species | Serious cases |
|---|---|---|---|---|
| Neurologic | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Cat | 1 | |
| Other | 1 | Cat | 1 | |
| Other | 1 | Cat | 1 |
Species coverage: Dog (21) Cat (11)
View detailed reaction table
| Reaction | Body system | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|---|
| Digestive | Dog | Non-serious | - | 1 | |
| Neurologic | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Digestive | Dog | Non-serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Neurologic | Cat | Non-serious | - | 1 | |
| Digestive | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Behavior | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 |
- https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2024-US-065151
Documents
Owner handouts and official technical documents open on-page first, with the original source still one click away.
Owner handouts
0Official label / PI
0SPL
0FOI
5FOI Summary oA 200-709 Approved August 18, 2021.pdf
FOI · FOI summary
FOI Summary oA 200-702 Approved April 23, 2021.pdf
FOI · FOI summary
N055101_Supp_12_23_1997.pdf
FOI · FOI summary
FOI Summary oA 200-604 Approved October 20, 2021.pdf
FOI · FOI summary
UCM524262.pdf
FOI · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/11187 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/10753 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1953 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/11403 · document · FOI summary
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/1263 · document · FOI summary
Veterinary reference (advanced)
Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.
At a Glance
Quick facts and links to official labeling and safety signals.
-
Storefront facts:
Source Roxee
| Refreshed May 5, 2026, 10:05 AM UTC
The storefront fact projection used for browse cards and quick facts.
- openFDA reaction terms: Source FDA openFDA | Refreshed May 5, 2026, 10:04 AM UTC
- openFDA case summaries: Source FDA openFDA | Refreshed May 5, 2026, 10:04 AM UTC
Counseling and Monitoring Highlights
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
- Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 32903-122-25 | 32903 | - | |
| 62157-527-01 | 62157 | - | |
| 62157-585-01 | 62157 | - | |
| 73309-210-01 | 73309 | - | |
| 73309-210-02 | 73309 | - | |
| 73309-210-03 | 73309 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
FOI Summary oA 200-709 Approved August 18, 2021.pdf
• FOI summary • Official
• April 10, 2024
FDA FOI summary for application 200709
-
FOI Summary oA 200-702 Approved April 23, 2021.pdf
• FOI summary • Official
• Dec. 12, 2023
FDA FOI summary for application 200702
-
N055101_Supp_12_23_1997.pdf
• FOI summary • Official
• Jan. 12, 2023
FDA FOI summary for application 55101
-
FOI Summary oA 200-604 Approved October 20, 2021.pdf
• FOI summary • Official
• July 25, 2022
FDA FOI summary for application 200604
-
UCM524262.pdf
• FOI summary • Official
• March 29, 2022
FDA FOI summary for application 200592
Data Sources & Change Log
Every non-trivial field is expected to include provenance and update timestamps.
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-05-05)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-05-03)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-05-02)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-29)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-28)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-27)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-26)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-25)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Clinical, 2026-04-22)
- side_effects: Top reported reactions (openFDA): Lethargy (see also Central nervous system depression in 'Neurological'), Not eating, Vomiting, Death by euthanasia, Fever, No… (Clinical, 2026-04-11)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-05-05)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-05-03)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-05-02)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-29)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-28)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-27)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-26)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-25)
- usage: For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due t… (Clinical, 2026-04-22)
- contraindications: Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. … (Official, 2026-04-30)
- side_effects updated 2026-05-05 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-05-05 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-05-05 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-05-03 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-05-03 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-05-03 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-05-02 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-04-30 10:09 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-29 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-29 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-04-29 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-28 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-28 10:05 by etl_backfill • Backfilled from existing medication fields
- usage updated 2026-04-28 10:05 by etl_backfill • Backfilled from existing medication fields
- side_effects updated 2026-04-27 10:05 by etl_backfill • Backfilled from existing medication fields
- contraindications updated 2026-04-27 10:05 by etl_backfill • Backfilled from existing medication fields
Usage
For the treatment of susceptible strains of the organisms causing the following infections: Respiratory tract infections (tonsillitis, tracheobronchitis) due to Staphylococcus aureus , Streptococcus spp., Escherichia coli , and Proteus mirabilis . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections (bacterial gastroenteritis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Bacterial dermatitis due to Staphylococcus aureus , Streptococcus spp., and Proteus mirabilis . Soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . For the treatment of susceptible strains of the organisms causing the following infections: Upper respiratory tract infections due to Staphylococcus aureus , Streptococcus spp., and E. coli . Genitourinary tract infections (cystitis) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Proteus mirabilis . Gastrointestinal tract infections due to E. coli . Skin and soft tissue infections (abscesses, lacerations, and wounds) due to Staphylococcus aureus , Streptococcus spp., E. coli , and Pasteurella multocida . For the treatment of baby pigs under 10 pounds for porcine colibacillosis caused by Escherichia coli susceptible to amoxicillin.
Contraindications
Do not slaughter during treatment or for 15 days after latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Do not slaughter animals during treatment or for 20 days after the latest treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Treated animals must not be slaughtered for food during treatment and for 25 days after the last treatment. Milk from treated cows must not be used for human consumption during treatment or for 96 hours (8 milkings) after last treatment. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Top Reported Reactions (openFDA)
De-duplicated reaction terms grouped by body system from FDA openFDA reports (not verified; does not prove causation).
Showing top 5 for Digestive.
Showing top 5 for Neurologic.
Showing top 5 for Behavior.
Show more (21)
Showing top 5 for Other.
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Adverse Event Case Summaries (openFDA)
These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.
Dog, Bulldog - French, Male, 4.96 month, 6.57 kilogram • Drug: MSK, Suspension, Unknown • Reactions: Anal and rectal disorder NOS • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-075322
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Age: 4.96 Month
- Weight: 6.570 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Suspension
Dog, ['Hound (unspecified)', 'Dog (unknown)'], Male, 14.5 year, 35.83 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Aspiration pneumonia, Lack of efficacy - NOS, Medication error NOS, Anaemia NOS, Mass NOS… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-074245
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Age: 14.50 Year
- Weight: 35.830 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Unassigned
Dog, Bulldog - English, Female, 1 day, 34.473 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Offspring only event, Rigidity, Stiffness NOS, Falling, Death… • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-072861
- Serious AE: Yes
- Treated For AE: No
- Sex: Female
- Age: 1.00 Day
- Weight: 34.473 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Unassigned
Dog, Dachshund - Miniature, Male, 5.25 year, 6.07 kilogram • Drug: MSK, Powder, Unknown • Reactions: Haemorrhagic gastroenteritis, Lack of efficacy (endoparasite) - roundworm NOS, Diarrhea, Ear infection NOS, Hypochloraemia… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-075298
- Serious AE: No
- Treated For AE: Yes
- Sex: Male
- Age: 5.25 Year
- Weight: 6.070 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Powder
Dog, Dachshund - Miniature, Male, 5.25 year, 6.07 kilogram • Drug: MSK, Unknown • Reactions: Haemorrhagic gastroenteritis, Lack of efficacy (endoparasite) - roundworm NOS, Diarrhea, Ear infection NOS, Hypochloraemia… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-069774
- Serious AE: No
- Treated For AE: Yes
- Sex: Male
- Age: 5.25 Year
- Weight: 6.070 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Dog, ['Sheepdog (unspecified)', 'Poodle (unspecified)'], Male, 4 year, 49.895 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Injection site swelling, Abnormal cytology, Injection site abscess, Painful urination, Vocalisation… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-068758
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Male
- Age: 4.00 Year
- Weight: 49.895 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Unassigned
Cat, Cat (unknown), Female, 18 year, 2.72 kilogram • Drug: MSK, Unknown • Reactions: Grand mal seizure • Outcome: Recovered/Normal
- Report ID: USA-USFDACVM-2025-US-068104
- Serious AE: Yes
- Treated For AE: No
- Sex: Female
- Age: 18.00 Year
- Weight: 2.720 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Cat, Domestic Shorthair, Male, 7 week, 0.363 kilogram • Drug: MSK, Unassigned, Oral, Dose: 1 dose per animal, Frequency: 1 per day • Reactions: Death, Dehydration • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-067003
- Serious AE: Yes
- Treated For AE: No
- Sex: Male
- Age: 7.00 Week
- Weight: 0.363 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Unassigned
- Dose: 1 dose per animal
- Frequency: 1 per day
Data source: FDA openFDA Animal & Veterinary adverse event reports.
Overdose Information
No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.
Storage & Handling
No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.
Share Your Thoughts
Let others know your experience or advice regarding this medication.
This medication has not been reviewed by a veterinarian yet.