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Roxee Meds Catalog

Tigilanol Tiglate

Medication catalog facts with explicit FDA-approval, off-label, source-limited, and safety context.

Both Catalog complete FDA data linked Rx required Injection Virbac AH Inc Official label facts Owner quick guide first
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Data freshness

Storefront facts
Catalog refreshed
May 5, 2026, 10:00 a.m.

These are the storefront facts Roxee uses on browse cards and quick facts.

FDA applications
FDA application data refreshed
May 5, 2026, 10:00 a.m.

Sponsor, product, and application records imported from Animal Drugs @ FDA.

Safety reports
Safety data refreshed
May 5, 2026, 10:01 a.m.

openFDA reaction terms and case summaries are supporting evidence, not proof of causality.

Source timing details
Source timing details
  • Storefront facts: Source Roxee | Refreshed May 5, 2026, 10:00 AM UTC
    The storefront fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Applications/products are imported from FDA export data.
  • Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
    Label highlights/doc links are fetched from FDA preview endpoints.
  • Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • 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

Sources:
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Tigilanol Tiglate

Tigilanol Tiglate

Drug type: Generic ingredient • Branded profile • FDA branded products available

Both Injection Rx required 100% storefront ready

Species: Both

Manufacturer: Virbac AH Inc

Medication Snapshot

Merged from the current Roxee medication system with field-level provenance, freshness, and completeness tracking.

Tigilanol Tiglate

For use in dogs for the treatment of: non-metastatic cutaneous mast cell tumors non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock Species commonly shown: Both, Dog, No Use Class Stated Or Implied.

Generic name
Tigilanol Tiglate
Brand names
STELFONTA®, STELFONTA 1 mg/mL
Manufacturer
Virbac AH Inc
Species
Both, Dog, No Use Class Stated Or Implied
Dosage forms
Injection, Injectable Solution
Prescription
Prescription required
Completeness
100%
Validation
Complete
Brand names
STELFONTA® STELFONTA 1 mg/mL
Dosage forms
Injection Injectable Solution

Indications / Uses

For use in dogs for the treatment of: non-metastatic cutaneous mast cell tumors non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock

Side Effects

Top reported reactions (openFDA): Lack of efficacy - NOS, Injection site swelling, Wound, Injection site pain, Swelling NOS, Pain NOS.

FAQ

Both, Dog, No Use Class Stated Or Implied

Yes. Roxee shows this as prescription-only.

Injection, Injectable Solution

Related Conditions

Mast Cell Tumor (MCT)

Source Transparency

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Pet Owner Quick Guide

Start here first for the safest next-step summary before the deeper medication detail.

Used for:

For use in dogs for the treatment of: non-metastatic cutaneous mast cell tumors non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock

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:

  • trouble breathing (1 reports)
  • Loss of appetite (1 reports)
  • Generalised skin slough (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.

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:

  • trouble breathing
  • Loss of appetite
  • Generalised skin slough

Most reported reactions:

  • Trouble breathing (dyspnea) (1 reports)
  • Loss of appetite (1 reports)
  • Generalised skin slough (1 reports)

Emergency warning signs:

  • Repeated vomiting or diarrhea.
  • Severe lethargy (hard to wake, very low energy).
  • Collapse or fainting.
  • Facial swelling or hives.
Talk to a Vet / Find a Vet Near You Start Symptom Intake

Quick Facts

Official label facts first, then secondary summaries. Marketing content is separated below.

Species: Both
Manufacturer: Virbac AH Inc
Form: Injectable Solution
Identifiers:
NADA: 141541 NDC Package: 51311-993-02 NDC Product: 51311
Source metadata:

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.

Tracked signals
32
Reported cases
32
Serious reports
30
Species represented
2
Grouped by Body System
Digestive (3) · Loss of appetite, Drooling, Diarrhea Neurologic (1) · Convulsion Other (28) · Trouble breathing (dyspnea), Generalised skin slough, General pain
Most Reported Reactions
Reaction Body system Cases Species Serious cases
Other 1 Dog 1
Digestive 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 (29) Cat (3)

View detailed reaction table
Reaction Body system Species Seriousness Frequency Reports
Other Dog Serious - 1
Digestive Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Digestive Dog Serious - 1
Other Dog Serious - 1
Digestive Dog Non-serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Cat Serious - 1
Other Dog Serious - 1
Neurologic Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Cat Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Cat Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Other Dog Non-serious - 1
Other Dog Serious - 1
Other Dog Serious - 1
Source metadata:

Documents

Owner handouts and official technical documents open on-page first, with the original source still one click away.

Owner handouts

0
No owner handouts linked yet.

Official label / PI

2

SPL

2

FOI

1

STELFONTA N141541G0008.pdf

Official label / PI · Labeling

Open original

STELFONTA N141541G0008.pdf

Official label / PI · Labeling

Open original

STELFONTA®

SPL · SPL

Open original
FDA Structured Product Label

STELFONTA®

Rendered from Roxee's cached FDA SPL package contents for on-page reading. Use Open original for the raw FDA ZIP/XML source.

Sponsor
QBiotics Group Ltd.
NADA
141-541
Status
RX
Form
Injectable Solution
Route
Intratumoral
Species
Dog, No Use Class Stated Or Implied
Composition / specifications
1 mg/mL

Dogs

Indication

For use in dogs for the treatment of:

  • non-metastatic cutaneous mast cell tumors
  • non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock
Dosage

Administer as an intratumoral injection at a dose of 0.5 mL per cm3 of tumor volume, as determined by the following calculations:

  • Determine the Tumor Volume in cm3:
    0.5 x [length (cm) x width (cm) x height (cm)]
  • Confirm the Tumor Volume does not exceed 10 cm3. Do not use STELFONTA® if tumor volume is > 10 cm3.
  • Calculate the Dose volume (mL) of STELFONTA® to inject: Tumor Volume x 0.5 mL
  • Confirm the dose of STELFONTA® does not exceed 0.25 mL/kg body weight.
  • Do not exceed 5 mL per dog, regardless of tumor volume or body weight.
  • The minimum dose of STELFONTA® is 0.1 mL, regardless of tumor volume or body weight. If the calculated dose is less than 0.1 mL, administer 0.1 mL.

STELFONTA 1 mg/mL SPL

SPL · Structured Product Label

Open original
FDA Structured Product Label XML for STELFONTA 1 mg/mL. Use the source link for the full official labeling record.

FOI Summary oN 141-541 Approved November 16, 2020.pdf

FOI · FOI

Open original
Source metadata:
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.

Data freshness
  • Storefront facts: Source Roxee | Refreshed May 5, 2026, 10:00 AM UTC
    The storefront fact projection used for browse cards and quick facts.
  • Animal Drugs @ FDA: Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Applications/products are imported from FDA export data.
  • Animal Drugs @ FDA previews: Source FDA | Refreshed Feb 9, 2026, 3:05 AM UTC
    Label highlights/doc links are fetched from FDA preview endpoints.
  • Animal Drug Product Listing Directory (NDC): Source FDA | Refreshed May 5, 2026, 10:00 AM UTC
    Package/product NDCs from FDA’s electronic listing directory (XLS).
  • 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
Official (FDA)
Identity: Generic ingredient • FDA branded products available
Official FDA brands: STELFONTA 1 mg/mL
Manufacturer mapping: Virbac AH Inc
Case-reported brands (openFDA): MSK
Catalog species: Both • FDA-labeled species: Dog
Rx/OTC: RX
Form/route: Injectable Solution • Intratumoral
Applications: NADA 141-541
NDC: Packages 51311-993-02 • Products 51311
Documents: 3 (FOI: 1) • SPL: 1 • Label highlights • Official documents
Safety (openFDA)
Top reactions: Dog 38 • Cat 0 • View
Case summaries: 10 (showing 8) • View
openFDA reports are unverified and do not prove causation.
Explore
Related conditions: Mast Cell Tumor (MCT)
Linked using: Fda_Label (0.95)
Diagnosis Codes
ICD10_CM: C96.A
Mast cell neoplasm

Counseling and Monitoring Highlights

Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.

Top reaction signals
Trouble breathing (dyspnea) (1) Loss of appetite (1) Generalised skin slough (1) General pain (1) Fixed pupil (1) Enlarged lymph node (1) Elevated triglyceride (1) Elevated temperature (1)

Identifiers & Packages

Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.

Identifiers
NADA: 141541 NDC Package: 51311-993-02 NDC Product: 51311
Package NDC Product NDC Form / Route Status
51311-993-02 51311 -

Enriched Documents

Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.

Data Sources & Change Log

Every non-trivial field is expected to include provenance and update timestamps.

Official 45 Clinical 1 Manufacturer 0 Marketing 0
Current Field Facts
  • side_effects: Top reported reactions (openFDA): Lack of efficacy - NOS, Injection site swelling, Wound, Injection site pain, Swelling NOS, Pain NOS. (Clinical, 2026-04-11)
  • dosage_forms: Injection (Official, 2026-05-05)
  • dosage_forms: Injection (Official, 2026-05-03)
  • dosage_forms: Injection (Official, 2026-05-02)
  • dosage_forms: Injection (Official, 2026-04-29)
  • dosage_forms: Injection (Official, 2026-04-28)
  • dosage_forms: Injection (Official, 2026-04-27)
  • dosage_forms: Injection (Official, 2026-04-26)
  • dosage_forms: Injection (Official, 2026-04-25)
  • dosage_forms: Injection (Official, 2026-04-22)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-05-05)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-05-03)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-05-02)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-29)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-28)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-27)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-26)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-25)
  • indications: For use in dogs for the treatment of:non-metastatic cutaneous mast cell tumorsnon-metastatic subcutaneous mast cell tumors located at or distal to the elbow or… (Official, 2026-04-22)
  • manufacturer_name: Virbac AH Inc (Official, 2026-05-05)
Recent Revisions
  • side_effects updated 2026-04-12 10:05 by etl_backfill • Backfilled from existing medication fields
  • usage updated 2026-04-12 10:05 by etl_backfill • Backfilled from existing medication fields
  • side_effects updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
  • usage updated 2026-04-11 10:05 by etl_backfill • Backfilled from existing medication fields
  • side_effects updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
  • usage updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields

FDA Products & Applications (Animal Drugs @ FDA)

Official sponsor/proprietary-name/application-status records linked by active ingredient.

Product Sponsor Application Status Published
STELFONTA®
RX
Tigilanol tiglate
Injectable Solution • Intratumoral
Label highlights
Official documents
QBiotics Group Ltd. NADA 141-541 Approved Oct 26, 2023

Data source: FDA Animal Drugs @ FDA (public search export).

What It's For (FDA Label Highlights)

Extracted from FDA Animal Drugs @ FDA product labeling. Always confirm details with your veterinarian.

Species: Dog, No Use Class Stated Or Implied
Composition / specifications
1 mg/mL
Dogs
Indication

For use in dogs for the treatment of:

  • non-metastatic cutaneous mast cell tumors
  • non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock
Dosage

Administer as an intratumoral injection at a dose of 0.5 mL per cm3 of tumor volume, as determined by the following calculations:

  • Determine the Tumor Volume in cm3:
    0.5 x [length (cm) x width (cm) x height (cm)]
  • Confirm the Tumor Volume does not exceed 10 cm3. Do not use STELFONTA® if tumor volume is > 10 cm3.
  • Calculate the Dose volume (mL) of STELFONTA® to inject: Tumor Volume x 0.5 mL
  • Confirm the dose of STELFONTA® does not exceed 0.25 mL/kg body weight.
  • Do not exceed 5 mL per dog, regardless of tumor volume or body weight.
  • The minimum dose of STELFONTA® is 0.1 mL, regardless of tumor volume or body weight. If the calculated dose is less than 0.1 mL, administer 0.1 mL.
Limitations

FDA page: Open in Animal Drugs @ FDA

Usage

For use in dogs for the treatment of: non-metastatic cutaneous mast cell tumors non-metastatic subcutaneous mast cell tumors located at or distal to the elbow or the hock

Source: FDA Animal Drugs @ FDA • Reference

Top Reported Reactions (openFDA)

De-duplicated reaction terms grouped by body system from FDA openFDA reports (not verified; does not prove causation).

Digestive
Loss of appetite (1) • Dog Drooling (1) • Dog Diarrhea (1) • Dog

Showing top 5 for Digestive.

Neurologic
Convulsion (1) • Dog

Showing top 5 for Neurologic.

Other
Trouble breathing (1) • Dog Generalised skin slough (1) • Dog General pain (1) • Dog Fixed pupil (1) • Dog Enlarged lymph node (1) • Dog
Show more (23)
Elevated triglyceride (1) • Dog Elevated temperature (1) • Dog Elevated serum alkaline phosphatase (1) • Dog Elevated cholesterol (1) • Dog Dilated pupils (1) • Dog Dermal nodule (1) • Dog Death by euthanasia (1) • Dog Death (1) • Cat Cyanotic mucous membranes (1) • Dog Coma (1) • Dog Cellulitis (1) • Dog Cardiorespiratory arrest (1) • Dog Cardiac arrest (1) • Cat Bruising (1) • Dog Breathing difficulty (1) • Dog Bradycardia (1) • Cat Bacterial skin infection NOS (1) • Dog Asystole (1) • Dog Arthritis (1) • Dog Application site skin slough (1) • Dog Application site scar (1) • Dog Application site dry skin (1) • Dog Acid-base disorder (1) • Dog

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, ['Spitz - German Pomeranian', 'Spitz - American Eskimo Dog'], Female, 6 year, 6.35 kilogram • Drug: MSK, Solution, Parenteral, Dose: 0.25 Milligram per kilogram, Frequency: 1 per day • Reactions: Injection site swelling, Reluctant to move, Swollen limb, Partial anorexia, Injection site skin discolouration… • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-075335
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 6.00 Year
  • Weight: 6.350 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 0.25 Milligram per kilogram
  • Frequency: 1 per day
Reactions Reported:
Injection site swelling Reluctant to move Swollen limb Partial anorexia Injection site skin discolouration Injection site ulcer Injection site bleeding Uncomfortable Limb non-weight bearing Reddening of the skin Local swelling Walking slowly Localised oedema Bruising
Outcomes: Outcome Unknown

Dog, Bulldog - French, Female, 11 year, 12.066 kilogram • Drug: MSK, Solution, Parenteral, Dose: 0.28 mL per dose, Frequency: 1 per day • Reactions: Lack of efficacy, Swollen limb, Wound, Local erythema, Bruising • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-074617
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 11.00 Year
  • Weight: 12.066 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 0.28 mL per dose
  • Frequency: 1 per day
Reactions Reported:
Lack of efficacy Swollen limb Wound Local erythema Bruising
Outcomes: Outcome Unknown

Dog, Pug, Female, 6 year, 9.344 kilogram • Drug: MSK, Solution, Parenteral, Dose: 1.50 mL per dose, Frequency: 1 per day • Reactions: Swollen limb, Limb non-weight bearing, Pain NOS, Bruising, Local erythema… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-073872
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 6.00 Year
  • Weight: 9.344 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 1.50 mL per dose
  • Frequency: 1 per day
Reactions Reported:
Swollen limb Limb non-weight bearing Pain NOS Bruising Local erythema Injection site skin discolouration
Outcomes: Ongoing

Dog, Bulldog - French, Female, 5 year, 11.34 kilogram • Drug: MSK, Solution, Parenteral, Dose: 1.30 mL per dose, Frequency: 1 per day • Reactions: Injection site swelling, Local swelling, Local skin slough, Enlarged lymph node, Application site skin slough… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-074498
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 5.00 Year
  • Weight: 11.340 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 1.30 mL per dose
  • Frequency: 1 per day
Reactions Reported:
Injection site swelling Local swelling Local skin slough Enlarged lymph node Application site skin slough Injection site reaction NOS Wound Injection site skin change NOS Injection site mucopurulent discharge Skin reaction NOS Pain NOS Injection site bleeding
Outcomes: Ongoing

Dog, Shepherd Dog - Australian, Male, 5 year, 21.772 kilogram • Drug: MSK, Solution, Parenteral, Dose: 0.70 mL per dose, Frequency: 1 per day • Reactions: Swollen limb, Limb non-weight bearing, Injection site reaction NOS • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-074096
  • Serious AE: Yes
  • Treated For AE: No
  • Sex: Male
  • Age: 5.00 Year
  • Weight: 21.772 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 0.70 mL per dose
  • Frequency: 1 per day
Reactions Reported:
Swollen limb Limb non-weight bearing Injection site reaction NOS
Outcomes: Ongoing

Dog, ['Pointing Dog - Hungarian Short-haired (Vizsla)', 'Retriever - Labrador'], Male, 8 year, 40.415 kilogram • Drug: MSK, Solution, Parenteral, Dose: 0.10 mL per dose, Frequency: 1 per day • Reactions: Application site scar, Injection site alopecia, Injection site reaction NOS, Injection site nodule, Mast cell tumour… • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-073513
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 8.00 Year
  • Weight: 40.415 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 0.10 mL per dose
  • Frequency: 1 per day
Reactions Reported:
Application site scar Injection site alopecia Injection site reaction NOS Injection site nodule Mast cell tumour Lack of efficacy
Outcomes: Outcome Unknown

Dog, Retriever - Labrador, Male, 12 year, 28.576 kilogram • Drug: MSK, Intralesional, Dose: 4.90 mL per other • Reactions: Application site dry skin, Lack of efficacy, Injection site hair loss, Injection site scab, Mast cell tumour… • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-074135
  • Serious AE: Yes
  • Treated For AE: No
  • Sex: Male
  • Age: 12.00 Year
  • Weight: 28.576 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Intralesional
  • Dose: 4.90 mL per other
Reactions Reported:
Application site dry skin Lack of efficacy Injection site hair loss Injection site scab Mast cell tumour Local swelling Swollen eye
Outcomes: Outcome Unknown

Dog, Retriever - Labrador, Female, 6.5 year, 29.484 kilogram • Drug: MSK, Solution, Parenteral, Dose: 1 dose per animal, Frequency: 1 per day • Reactions: Lack of efficacy • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2025-US-069220
  • Serious AE: Yes
  • Treated For AE: No
  • Sex: Female
  • Age: 6.50 Year
  • Weight: 29.484 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Parenteral
  • Form: Solution
  • Dose: 1 dose per animal
  • Frequency: 1 per day
Reactions Reported:
Lack of efficacy
Outcomes: Outcome Unknown

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.

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