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Roxee Medication Guide
Medication reference facts with explicit FDA-approval, off-label, source-limited, and safety context. Roxee does not sell, prescribe, or dispense medications.
Veterinary professional?
These are the reference facts Roxee uses on browse cards and quick facts.
Sponsor, product, and application records imported from Animal Drugs @ FDA.
openFDA reaction terms and case summaries are supporting evidence, not proof of causality.
Drug type: Generic ingredient • Generic profile • No FDA branded products linked
Species: Both
Manufacturer: Multiple FDA sponsors
Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.
For treatment of external eye infections and inflammation in dogs. For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (tonsillitis, pneumonia, tracheobronchitis), skin and soft tissue (pyodermatitis, wounds, lacerations, peritonitis). For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (pneumonitis pneumonia, upper respiratory tract infections), skin and soft tissue (wounds, lacerations, peritonitis), and as supportive therapy for secondary bacterial infections associated with panleucopenia. Species commonly shown: Both, Poults 1 to 3 Day Old, 1 day-old broiler chicks.
For treatment of external eye infections and inflammation in dogs. For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (tonsillitis, pneumonia, tracheobronchitis), skin and soft tissue (pyodermatitis, wounds, lacerations, peritonitis). For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (pneumonitis pneumonia, upper respiratory tract infections), skin and soft tissue (wounds, lacerations, peritonitis), and as supportive therapy for secondary bacterial infections associated with panleucopenia.
If response is not noted after 7 days, the antibiotic sensitivity of the infecting organism should be retested. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Not for use in horses intended for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Top reported reactions (openFDA): Loss of hearing, Lack of efficacy - NOS, Vomiting, Deafness, Lack of efficacy (bacteria) - NOS, Lethargy (see also Central nervous system depression in Neurological).
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Used for:
For prevention of early mortality caused by Escherichia coli. Salmonella typhimurium, and Pseudomonas aeruginosa that are susceptible to gentamicin.
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:
When to call the vet:
Regulatory restrictions are shown in Vet View.
What to tell or ask your vet today:
A source-aware map of what to know, what is uncertain, and what to verify with your veterinarian.
Roxee has limited cited overview evidence for Gentamicin Sulfate; use the official documents and your veterinarian's instructions for product-specific decisions.
32 tracked reaction signals; 32 reported cases; 23 serious reports; 2 species groups. These are reporting and label-derived signals for interpretation with a veterinarian.
Adverse-event reports help form a watch list, but they do not prove the medication caused the reaction and they are not a risk ranking between medications.
Official labels, package inserts, and reviewed summaries carry more weight than isolated reports.
Case reports and openFDA terms are useful for pattern awareness, but they are incomplete, can include multiple exposures, and do not estimate an individual pet's probability of harm.
Fluid in abdomen NOS (1 reports), Facial swelling (possible allergy) (1 reports), Eosinopenia (1 reports), Enlarged lymph node (1 reports), Elevated total bilirubin (1 reports)
Digestive (5), Skin & allergy (2), Other (25)
Dog (22 reports), Cat (10 reports)
Retriever - Labrador (3), ['Retriever - Golden', 'Poodle - Standard'] (1), ['Retriever - Labrador', 'Crossbred Canine/dog'] (1), Domestic Shorthair (1). These are report metadata, not proof that a breed is at higher risk.
Verify whether Gentamicin Sulfate fits the pet's species, current diagnosis, age, weight, organ status, pregnancy/lactation status, and concurrent medications.
Separate label-backed warnings from adverse-event reports and owner observations before changing the plan.
If response is not noted after 7 days, the antibiotic sensitivity of the infecting organism should b, Not for use in horses intended for food, Fluid in abdomen NOS, Facial swelling, Eosinopenia
Repeated vomiting or diarrhea. Severe lethargy (hard to wake, very low energy). Collapse or fainting.
Review status / Updated / Sources
Review status: Clinical reviewer not listed
Updated: April 15, 2026, 10:04 AM UTC
Side effects to monitor:
Most reported reactions:
Emergency warning signs:
Source-backed clinical checkpoints for quick review.
Official label facts first, then secondary summaries. Marketing content is separated below.
If response is not noted after 7 days, the antibiotic sensitivity of the infecting organism should be retested. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Not for use in horses intended for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
Snapshot first, detailed rows second. This section summarizes signal data and is not a diagnosis.
Filter stored openFDA reports by pet and report attributes. Counts describe reports in this data set, not risk.
Received 2026-02-19 · MSK · MSK
Received 2025-10-22 · MSK · MSK
Tap or hover a reaction to see what it means in plain language.
| Reaction | Body system | Cases | Species | Serious cases |
|---|---|---|---|---|
| Other | 1 | Dog | 1 | |
| Skin & allergy | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 | |
| Other | 1 | Dog | 1 |
Species coverage: Dog (22) Cat (10)
| Reaction | Body system | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|---|
| Digestive | Cat | Non-serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Skin & allergy | Dog | Serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | 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 | |
| Other | Dog | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Digestive | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Digestive | Cat | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 | |
| Skin & allergy | Dog | Non-serious | - | 1 | |
| Digestive | Cat | Serious | - | 1 | |
| Digestive | Cat | Serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 | |
| Other | Cat | Serious | - | 1 | |
| Other | Cat | Non-serious | - | 1 | |
| Other | Dog | Serious | - | 1 | |
| Other | Dog | Non-serious | - | 1 |
The most useful source links appear first; full previews and metadata stay in the veterinary/professional layer.
Use original documents to confirm product-specific warnings, ingredients, and handling details with your veterinarian.
Full source previews and metadata remain in the veterinary/professional layer.
Official label / PI · EA
Official label / PI · FONSI
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
As an aid in the prevention of early mortality due to Arizona paracolon infections susceptible to gentamicin sulfate.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
For the prevention of early mortality in day-old chickens associated with Escherichia coli, Salmonella typhimurium, and Pseudomonas aeruginosa susceptible to gentamicin sulfate.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
For the control and treatment of colibacillosis in neonatal pigs 1-3 days of age, caused by strains of E. coli sensitive to gentamicin.
Administer 1 mL of pig pump oral solution (5 mg of gentamicin) orally per pig one time.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
For the control and treatment of colibacillosis in weaning swine caused by strains of Escherichia coli sensitive to gentamicin.
25 mg gentamicin per gallon (1 level scoop/240 gallons) of drinking water, for three consecutive days to provide 0.5 mg/lb/day. (Note: the jar contains a scoop that provides approximately 18 g of product when level full.) For proportioner use, add 1 level scoop to 2 gallons stock solution and dispense at the rate of 1 oz/gal drinking water (25 mg/gal).
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
For the control and treatment of swine dysentery associated with Treponema hyodysenteriae.
50 mg gentamicin per gallon (1 level scoop/120 gallons) for three consecutive days to ensure a gentamicin dosage of approximately 1.0 mg/lb/day. (Note: the jar contains a scoop that provides approximately 18 g of product when level full.)
For proportioner use, add 1 level scoop to 1 gallons stock solution and dispense at the rate of 1 oz/gal drinking water (50 mg/gal).
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water.
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
For control and treatment of colibacillosis in weanling swine caused by strains of Escherichia coli sensitive to gentamicin.
Administer gentamicin sulfate equivalent to 25 milligrams of gentamicin per gallon of drinking water to provide 0.5 milligram per pound of body weight per day for 3 consecutive days.
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water for 3 consecutive days. Do not slaughter treated swine for food for at least 10 days following treatment. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.
For control and treatment of swine dysentery associated with Brachyspira hyodysenteriae.
Administer gentamicin sulfate equivalent to 50 milligrams of gentamicin per gallon of drinking water to provide 1.0 milligram per pound of body weight per day for 3 consecutive days. Treatment may be repeated if dysentery recurs.
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water for 3 consecutive days. Do not slaughter treated swine for food for at least 10 days following treatment. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
SPL · SPL
Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.
FOI · FOI
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Canonical medication sections are above. This legacy block remains available for deeper cross-reference without cluttering the primary workflow.
Quick facts and links to official labeling and safety signals.
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 0061-0100-01 | 0061 | - | |
| 0061-0134-01 | 0061 | - | |
| 0061-0387-01 | 0061 | - | |
| 0061-0387-02 | 0061 | - | |
| 0061-0387-03 | 0061 | - | |
| 0061-0387-08 | 0061 | - | |
| 0061-0387-17 | 0061 | - | |
| 0061-1246-01 | 0061 | - | |
| 0061-1246-02 | 0061 | - | |
| 0061-1246-04 | 0061 | - | |
| 0061-1246-05 | 0061 | - | |
| 11695-4153-1 | 11695 | - | |
| 11695-4153-2 | 11695 | - | |
| 11695-7009-1 | 11695 | - | |
| 11695-7009-2 | 11695 | - | |
| 11695-7009-3 | 11695 | - | |
| 13985-566-12 | 13985 | - | |
| 13985-566-24 | 13985 | - | |
| 13985-566-60 | 13985 | - | |
| 13985-701-07 | 13985 | - |
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
Every non-trivial field is expected to include provenance and update timestamps.
Official sponsor/proprietary-name/application-status records linked by active ingredient.
| Product | Sponsor | Application | Status | Published |
|---|---|---|---|---|
|
Garasol®
RX
Gentamicin Sulfate
Liquid (Solution)
• Subcutaneous
|
Intervet, Inc. | NADA 101-862 | Approved | Feb 3, 2026 |
|
GentaPoult Genta-Ject®
RX
Gentamicin Sulfate
Liquid (Solution)
• Subcutaneous
|
Huvepharma EOOD | ANADA 200-147 | Approved | Jul 3, 2024 |
|
Gentamicin Sulfate Ophthalmic Solution
RX
Gentamicin Sulfate
Ophthalmic Solution
• Ophthalmic
|
Domes Pharma S.A. | ANADA 200-576 | Approved | Dec 14, 2023 |
|
Gentasol
OTC
Gentamicin Sulfate
Liquid (Solution)
• Immersion
|
Med-Pharmex, Inc. | ANADA 200-191 | W | Aug 25, 2023 |
|
GentaMed™-P
RX
Gentamicin Sulfate
Injection
• Subcutaneous
|
Bimeda Animal Health Ltd. | ANADA 200-468 | Approved | Apr 26, 2023 |
|
Gentamicin Piglet Injection
RX
Gentamicin Sulfate
Liquid (Solution)
• Intramuscular
|
Sparhawk Laboratories, Inc. | ANADA 200-394 | Approved | Apr 26, 2023 |
|
Gentamicin Sulfate Pig Pump Oral Solution
RX
Gentamicin Sulfate
Liquid (Solution)
• Oral
|
Huvepharma EOOD | ANADA 200-174 | Approved | Apr 26, 2023 |
|
Vetro-Gen™ Veterinary Ophthalmic Ointment
OTC
Gentamicin Sulfate
Ointment
• Topical
|
Dechra Veterinary Products LLC | ANADA 200-273 | Approved | Oct 1, 2019 |
|
GentaMed™
RX
Gentamicin Sulfate
Soluble Powder
• Oral
|
Bimeda Animal Health Ltd. | ANADA 200-494 | Approved | Oct 2, 2018 |
|
Gentamex™ 100
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Bimeda Animal Health Ltd. | ANADA 200-115 | Approved | Oct 2, 2018 |
|
GEN-GARD®
RX
Gentamicin Sulfate
Soluble Powder
• Oral
|
Huvepharma EOOD | ANADA 200-185 | Approved | Jul 2, 2018 |
|
Legacy Sterile Solution Gentamicin Sulfate Solution
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Huvepharma EOOD | ANADA 200-037 | Approved | Jul 2, 2018 |
|
GentaMax® 100
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Elanco US Inc. | ANADA 200-137 | Approved | Jun 19, 2018 |
|
Gentamicin Sulfate Solution 100 mg/ml
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Cronus Pharma Specialities India Private Ltd. | ANADA 200-023 | Approved | Feb 1, 2018 |
|
Gentaglyde™ Solution
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Zoetis Inc. | ANADA 200-102 | Approved | Jul 19, 2017 |
|
Gentamicin Sulfate Solution
RX
Gentamicin Sulfate
Liquid (Solution)
• Intrauterine
|
Sparhawk Laboratories, Inc. | ANADA 200-395 | Approved | Jun 1, 2016 |
Data source: FDA Animal Drugs @ FDA (public search export).
Extracted from FDA Animal Drugs @ FDA product labeling. Always confirm details with your veterinarian.
As an aid in the prevention of early mortality due to Arizona paracolon infections susceptible to gentamicin sulfate.
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
For the prevention of early mortality in day-old chickens associated with Escherichia coli, Salmonella typhimurium, and Pseudomonas aeruginosa susceptible to gentamicin sulfate.
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
For the control and treatment of colibacillosis in neonatal pigs 1-3 days of age, caused by strains of E. coli sensitive to gentamicin.
Administer 1 mL of pig pump oral solution (5 mg of gentamicin) orally per pig one time.
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
For the control and treatment of colibacillosis in weaning swine caused by strains of Escherichia coli sensitive to gentamicin.
25 mg gentamicin per gallon (1 level scoop/240 gallons) of drinking water, for three consecutive days to provide 0.5 mg/lb/day. (Note: the jar contains a scoop that provides approximately 18 g of product when level full.) For proportioner use, add 1 level scoop to 2 gallons stock solution and dispense at the rate of 1 oz/gal drinking water (25 mg/gal).
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
For the control and treatment of swine dysentery associated with Treponema hyodysenteriae.
50 mg gentamicin per gallon (1 level scoop/120 gallons) for three consecutive days to ensure a gentamicin dosage of approximately 1.0 mg/lb/day. (Note: the jar contains a scoop that provides approximately 18 g of product when level full.)
For proportioner use, add 1 level scoop to 1 gallons stock solution and dispense at the rate of 1 oz/gal drinking water (50 mg/gal).
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water.
Federal law restricts this drug to use by or on the order of a licensed veterinarian.
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
For control and treatment of colibacillosis in weanling swine caused by strains of Escherichia coli sensitive to gentamicin.
Administer gentamicin sulfate equivalent to 25 milligrams of gentamicin per gallon of drinking water to provide 0.5 milligram per pound of body weight per day for 3 consecutive days.
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water for 3 consecutive days. Do not slaughter treated swine for food for at least 10 days following treatment. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.
For control and treatment of swine dysentery associated with Brachyspira hyodysenteriae.
Administer gentamicin sulfate equivalent to 50 milligrams of gentamicin per gallon of drinking water to provide 1.0 milligram per pound of body weight per day for 3 consecutive days. Treatment may be repeated if dysentery recurs.
For use in swine drinking water only. Do not store or offer medicated drinking water in rusty containers since the drug is quickly destroyed in such containers. Medicated drinking water should be prepared daily and be the sole source of drinking water for 3 consecutive days. Do not slaughter treated swine for food for at least 10 days following treatment. Federal Law restricts this drug to use by or on the order of a licensed veterinarian.
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
FDA page: Open in Animal Drugs @ FDA
For treatment of external eye infections and inflammation in dogs. For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (tonsillitis, pneumonia, tracheobronchitis), skin and soft tissue (pyodermatitis, wounds, lacerations, peritonitis). For the treatment of infections of urinary tract (cystitis, nephritis), respiratory tract (pneumonitis pneumonia, upper respiratory tract infections), skin and soft tissue (wounds, lacerations, peritonitis), and as supportive therapy for secondary bacterial infections associated with panleucopenia.
Source: FDA Animal Drugs @ FDA • Reference
If response is not noted after 7 days, the antibiotic sensitivity of the infecting organism should be retested. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Not for use in horses intended for food. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
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 Skin & allergy.
Showing top 5 for Other.
Data source: FDA openFDA Animal & Veterinary adverse event reports.
These are individual FDA adverse event reports. They are unverified and do not prove the medication caused the reaction.
Dog, Retriever - Labrador, Female, 4 year, 33.75 kilogram • Drug: MSK, Unknown • Reactions: Vomiting bile • Outcome: Recovered/Normal
Dog, ['Retriever - Golden', 'Poodle - Standard'], Unknown, 1.08 year, 25.49 kilogram • Drug: MSK, Oral • Reactions: Cough, Heavy breathing, Respiratory sound, Abnormal radiograph finding, Eosinophilia… • Outcome: Ongoing
Dog, ['Retriever - Labrador', 'Crossbred Canine/dog'], Male, 2.25 year • Drug: MSK, Unknown • Reactions: Diarrhea, Lack of efficacy (endoparasite) - heartworm, Otitis NOS, Cystitis, Crust… • Outcome: Outcome Unknown
Cat, Domestic Shorthair, Male, 7.07 year, 6.26 kilogram • Drug: MSK, Topical • Reactions: Other abnormal test result NOS, Lack of efficacy - NOS • Outcome: Ongoing
Dog, ['Retriever - Labrador', 'Dog (unknown)'], Male, 12 year, 17.69 kilogram • Drug: MSK, Unassigned, Topical • Reactions: Vomiting, Not eating, Weight loss, Icterus, Leucopenia NOS… • Outcome: Euthanized
Dog, Retriever - Labrador, Female, 8.75 year, 30.11 kilogram • Drug: MSK, Unknown • Reactions: Lying down, Sedation, Tongue protrusion • Outcome: Ongoing
Dog, Shepherd Dog - German, Female, 4 year, 27.66 kilogram • Drug: MSK, Spray, Unknown • Reactions: Licking at injection site, Injection site pain, Injection site lump, Injection site erythema, Injection site alopecia… • Outcome: Ongoing
Dog, Retriever - Labrador, Male, 2.5 year, 45.359 kilogram • Drug: MSK, Auricular (Otic) • Reactions: Head shake - ear disorder, Lack of efficacy (bacteria) - Ehrlichia, Obesity/adipositas, Lack of efficacy (endoparasite) - heartworm • Outcome: Outcome Unknown
Data source: FDA openFDA Animal & Veterinary adverse event reports.
No approved overdose-management text is linked yet. If overdose is suspected, contact a veterinarian or emergency clinic immediately.
No approved storage guidance is linked yet for this ingredient. Use manufacturer packaging and veterinary guidance for handling/storage.
Let others know your experience or advice regarding this medication.
This medication has not been reviewed by a veterinarian yet.