Meds A-Z
Propofol
Detailed information about Propofol
Pet Owner Quick Guide
Start here: what this medicine is for, what it does, and when it's usually needed.
Usually used for:
For induction of anesthesia. For maintenance of general anesthesia by intermittent bolus injections for short procedures. For induction of general anesthesia where maintenance is provided by inhalant anesthetics.
What it does:
The drug is indicated for use as an anesthetic as follows: As a single injection to provide general anesthesia for short procedures, for induction and maintenance of general anesthesia using incremental doses to effect,...
When it's needed:
Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the ord...
Call your vet sooner if you notice:
- Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Adequate data concerning safe use of propofol in pregnant and breeding dogs have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. Administer by intravenous injection only. Rapid bolus administration (induction or maintenance) or accidental overdosage of propofol may cause undesirable cardiorespiratory depression including hypotension and oxygen desaturation. Respiratory arrest (apnea) could occur. When using propofol, dogs should be continuously monitored and facilities for the maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available. The use of propofol in pregnant and breeding dogs has not been evaluated. Propofol crosses the placenta and, as with other general anesthetic agents, the administration of propofol may be associated with neonatal depression. Propofol has not been evaluated in dogs less than 10 weeks of age
Commonly reported reactions:
- (2 reports)
- (1 reports)
- (1 reports)
What to 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?
Propofol
Drug type: Generic ingredient • Branded profile • FDA branded products available
Species: Both
Manufacturer: MSK
Quick Facts
Official label facts first, then secondary summaries. Marketing content is separated below.
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200793 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/141070 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov · fda_animal_drugs · Medication usage source
Warnings / Contraindications
Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Adequate data concerning safe use of propofol in pregnant and breeding dogs have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. Administer by intravenous injection only. Rapid bolus administration (induction or maintenance) or accidental overdosage of propofol may cause undesirable cardiorespiratory depression including hypotension and oxygen desaturation. Respiratory arrest (apnea) could occur. When using propofol, dogs should be continuously monitored and facilities for the maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available. The use of propofol in pregnant and breeding dogs has not been evaluated. Propofol crosses the placenta and, as with other general anesthetic agents, the administration of propofol may be associated with neonatal depression. Propofol has not been evaluated in dogs less than 10 weeks of age
- High: Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Adequate data concerning safe use of propofol in pregnant and breeding dogs have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. Administer by intravenous injection only. Rapid bolus administration (induction or maintenance) or accidental overdosage of propofol may cause undesirable cardiorespiratory depression including hypotension and oxygen desaturation. Respiratory arrest (apnea) could occur. When using propofol, dogs should be continuously monitored and facilities for the maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available. The use of propofol in pregnant and breeding dogs has not been evaluated. Propofol crosses the placenta and, as with other general anesthetic agents, the administration of propofol may be associated with neonatal depression. Propofol has not been evaluated in dogs less than 10 weeks of age
- https://animaldrugsatfda.fda.gov · fda_animal_drugs · Contraindication source
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.
Most Reported Reactions
| Reaction | Cases | Species | Serious cases |
|---|---|---|---|
| 2 | Cat, Dog | 2 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Cat | 1 | |
| 1 | Cat | 1 | |
| 1 | Cat | 1 | |
| 1 | Dog | 1 |
Species coverage: Dog (21) Cat (11)
View detailed reaction table
| Reaction | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|
| Dog | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 |
- https://api.fda.gov/animalandveterinary/event.json · adverse_reaction · openFDA case USA-USFDACVM-2025-US-055950
Storage & Handling
No storage/handling guidance is linked yet.
Documents
Official label facts are separated from secondary summaries.
Official documents: 11 • Secondary summaries: 0
- FOI Summary oA 200-793 Approved November 18, 2024.pdf · FOI
- PropofolVet Multidose · SPL
- ucm116781.pdf · FOI
- UCM488658.pdf · FOI
- Rapanofal® · SPL
- UCM248263.pdf · FOI
- UCM355533.pdf · FOI
- PropoFlo™ 28 · SPL
- PropoFlo™ · SPL
- UCM224476.pdf · FOI
- PropoClear™ · SPL
No source yet.
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/16265 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/16596/PropofolVet%20Multidose · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/611 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/610 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/1823/Rapanofal%C2%AE · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/631 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/630 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/1363/PropoFlo%E2%84%A2%2028 · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/1362/PropoFlo%E2%84%A2 · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/867 · document · FOI
Promotional Materials (Marketing)
This content is marketing material and not clinical guidance.
No marketing assets are linked yet.
No source yet.
Technical appendix (vet reference)
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.
- Medication catalog: Source PetWisePlus | Refreshed Feb 12, 2026, 10:44 PM UTC
-
Animal Drugs @ FDA:
Source FDA
| Refreshed Feb 16, 2026, 11:00 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 Feb 16, 2026, 11:00 AM UTC
Package/product NDCs from FDA’s electronic listing directory (XLS).
- openFDA reaction terms: Source FDA openFDA | Refreshed Feb 16, 2026, 11:02 AM UTC
- openFDA case summaries: Source FDA openFDA | Refreshed Feb 9, 2026, 3:20 AM UTC
Diagnosis-code mappings are not available for this medication yet.
Counseling and Monitoring Highlights
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
- Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Adequate data concerning safe use of propofol in pregnant and breeding dogs have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. Administer by intravenous injection only. Rapid bolus administration (induction or maintenance) or accidental overdosage of propofol may cause undesirable cardiorespiratory depression including hypotension and oxygen desaturation. Respiratory arrest (apnea) could occur. When using propofol, dogs should be continuously monitored and facilities for the maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available. The use of propofol in pregnant and breeding dogs has not been evaluated. Propofol crosses the placenta and, as with other general anesthetic agents, the administration of propofol may be associated with neonatal depression. Propofol has not been evaluated in dogs less than 10 weeks of age (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 11695-2801-1 | 11695 | - | |
| 11695-7036-1 | 11695 | - | |
| 13985-740-23 | 13985 | - | |
| 54771-4944-1 | 54771 | - | |
| 54771-4944-2 | 54771 | - | |
| 54771-5206-1 | 54771 | - | |
| 68504-008-01 | 68504 | - | |
| 86064-001-20 | 86064 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
FOI Summary oA 200-793 Approved November 18, 2024.pdf
• FOI summary • Official
• Dec. 2, 2024
FDA FOI summary for application 200793
-
UCM488658.pdf
• FOI summary • Official
• April 29, 2022
FDA FOI summary for application 141070
-
ucm116781.pdf
• FOI summary • Official
• April 29, 2022
FDA FOI summary for application 141070
-
UCM355533.pdf
• FOI summary • Official
• Dec. 18, 2017
FDA FOI summary for application 141098
-
UCM248263.pdf
• FOI summary • Official
• Dec. 18, 2017
FDA FOI summary for application 141098
-
UCM224476.pdf
• FOI summary • Official
• June 1, 2016
FDA FOI summary for application 141303
Data Sources & Revision History
Every non-trivial field is expected to include provenance and update timestamps.
- contraindications: Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated pati… (Official, 2026-02-12)
- side_effects: Top reported reactions (openFDA): Death, Vomiting, Lack of efficacy - NOS, Bradycardia, Seizure NOS, Diarrhoea. (Official, 2026-02-12)
- usage: The drug is indicated for use as an anesthetic as follows: As a single injection to provide general anesthesia for short procedures, for induction and maintena… (Official, 2026-02-12)
- side_effects updated 2026-02-12 22:44 by etl_backfill • Backfilled from existing medication fields
- contraindications 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 |
|---|---|---|---|---|
|
PropofolVet Multidose
RX
Propofol
Injectable emulsion
• Intravenous
|
Parnell Technologies Pty. Ltd. | ANADA 200-793 | Approved | Dec 2, 2024 |
|
Rapanofal®
RX
Propofol
Liquid (Emulsion)
• Intravenous
|
Ivaoes Animal Health | NADA 141-070 | Approved | Apr 29, 2022 |
|
PropoFlo™ 28 PropoFlo™
RX
Propofol
Liquid (Emulsion)
• Intravenous
|
Zoetis Inc. | NADA 141-098 | Approved | Dec 18, 2017 |
|
PropoClear™
RX
Propofol
Microemulsion
• Intravenous
|
Zoetis Inc. | NADA 141-303 | Approved | Jun 1, 2016 |
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.
Composition / specifications
For induction of anesthesia. For maintenance of general anesthesia by intermittent bolus injections for short procedures. For induction of general anesthesia where maintenance is provided by inhalant anesthetics.
For induction of general anesthesia without the use of preanesthetics, the dosage is 7.6 milligrams per kilogram titrated against the response of the patient over 60-90 seconds or until clinical signs show the onset of anesthesia (5.0 to 7.6 mg/kg/min).The use of preanesthetic medication reduces propofol dose requirements. For the maintenance of general anesthesia without the use of preanesthetics, the dosage is 3.2 milligrams per kilogram The use of preanesthetic medication reduces propofol dose requirements. Due to the rapid metabolism of propofol, additional low doses of propofol, similar to those used for maintenance with propofol, may be required to complete the transition to inhalant maintenance anesthesia.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Official Documents (FDA)
Direct links to FDA-hosted PDFs and SPL packages (when available).
-
Summary
For induction of anesthesia. For maintenance of general anesthesia by intermittent bolus injections for short procedures. For induction of general anesthesia where maintenance is provided by inhalant anesthetics.
- PropofolVet Multidose (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI ucm116781.pdf
Summary
1. The supplement supports the addition of a new species, cats, to the original approved dog application for the same anesthetic indications.
2. The supplement also contains changes to the original canine portions of the label and FOI Summary as follows:
a. Information concerning the use of medetomidine prior to propofol anesthesia in dogs will appear on the label as well as in the FOI Summary. Medetomidine is approved for use in dogs for sedation and analgesia.
b. The recommended preanesthetic medetomidine dose will be lowered from 10-40 ug/kg IM/IV to 5-10 ug/kg IM based on data already contained in the original new animal drug application (NADA) approval for propofol in dogs. -
FOI UCM488658.pdf
Summary
Rapinovet®is an anesthetic injection for use in dogs as follows: a) as a single injection to provide general anesthesia for procedures lasting up to five minutes; b) for induction and maintenance of general anesthesia using incremental doses to effect; and c) for induction of general anesthesia where maintenance is provided by inhalant anesthetics.
- Rapanofal® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM248263.pdf
Summary
The effect of the supplement is to add a preservative (benzyl alcohol) for a multidose presentation in a 20 mL vial.. -
FOI UCM355533.pdf
Summary
a. For induction of anesthesia.
b. For maintenance of general anesthesia for up to 20 minutes.
c. For induction of general anesthesia where maintenance is provided by inhalant anesthetics.
- PropoFlo™ 28 (ZIP)
- PropoFlo™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM224476.pdf
Summary
For the induction and maintenance of anesthesia and for induction followed by maintenance with an inhalant anesthetic, in cats and dogs.
- PropoClear™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
Usage
The drug is indicated for use as an anesthetic as follows: As a single injection to provide general anesthesia for short procedures, for induction and maintenance of general anesthesia using incremental doses to effect, and for induction of general anesthesia where maintenance is provided by inhalant anesthetics. The drug is indicated for use as an anesthetic as follows: As a single injection to provide general anesthesia for procedures lasting up to 5 minutes; for induction and maintenance of general anesthesia using incremental doses to effect; for induction of general anesthesia where maintenance is provided by inhalant anesthetics. For induction of anesthesia. For maintenance of general anesthesia for up to 20 minutes. For induction of general anesthesia where maintenance is provided by inhalant anesthetics.
Source: FDA Animal Drugs @ FDA • Reference
Contraindications
Adequate data concerning safe use of propofol in pregnant and breeding cats have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal law restricts this drug to use by or on the order of a licensed veterinarian. Adequate data concerning safe use of propofol in pregnant and breeding dogs have not been obtained. Doses may need adjustment for geriatric or debilitated patients. Federal (USA) law restricts this drug to use by or on the order of a licensed veterinarian. Administer by intravenous injection only. Rapid bolus administration (induction or maintenance) or accidental overdosage of propofol may cause undesirable cardiorespiratory depression including hypotension and oxygen desaturation. Respiratory arrest (apnea) could occur. When using propofol, dogs should be continuously monitored and facilities for the maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available. The use of propofol in pregnant and breeding dogs has not been evaluated. Propofol crosses the placenta and, as with other general anesthetic agents, the administration of propofol may be associated with neonatal depression. Propofol has not been evaluated in dogs less than 10 weeks of age
Side Effects
No approved side-effect narrative is linked yet.
openFDA reaction signals are available for Dog 56 and Cat 56 (view top reported reactions).
Top Reported Reactions (openFDA)
Aggregated reaction terms from FDA openFDA reports (not verified; does not prove causation).
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, ['Shepherd Dog - German', 'Dog (unknown)'], Female, 2.5 year • Drug: MSK, Intravenous, Dose: 7 mL per animal • Reactions: Neutropenia, Eosinophilia, Lymphocytosis, Enamel disorder, Tooth disorder • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-055809
- Serious AE: Yes
- Treated For AE: No
- Sex: Female
- Age: 2.50 Year
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Intravenous
- Dose: 7 mL per animal
Cat, Domestic Shorthair, Female, 10 month, 3.629 kilogram • Drug: MSK, Injection, suspension, Intravenous, Dose: 1.50 mL per animal • Reactions: Shaking, Overdose, Medication error NOS, Increased heart rate, Intentional misuse • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-054487
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 10.00 Month
- Weight: 3.629 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Intravenous
- Form: Injection, suspension
- Dose: 1.50 mL per animal
Dog, ['Dachshund - Standard Long-haired', 'Dog (unknown)'], Female, 12 year, 5.942 kilogram • Drug: MSK, Emulsion, Intravenous, Dose: 2 mL per animal • Reactions: Localised pain NOS, Intervertebral disc disease, Excessive chewing, licking and/or grooming, Skin necrosis, Reddening of the skin… • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-054276
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 12.00 Year
- Weight: 5.942 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Intravenous
- Form: Emulsion
- Dose: 2 mL per animal
Cat, Domestic Mediumhair, Female, 19 week, 2.06 kilogram • Drug: MSK, Unknown • Reactions: Sleepiness - neurological disorder, Temporary blindness, Tiredness (lethargy), Reduced responses, Mydriasis… • Outcome: Euthanized
- Report ID: USA-USFDACVM-2025-US-055689
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 19.00 Week
- Weight: 2.060 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Dog, ['Dog (unknown)', 'Poodle (unspecified)'], Male, 8 month, 21.863 kilogram • Drug: MSK, Intravenous, Dose: 10 mL per unknown, Frequency: 31 per day • Reactions: Hyperthermia, Tachycardia, Abnormal electrocardiogram, Tachypnoea • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-055950
- Serious AE: No
- Treated For AE: Yes
- Sex: Male
- Age: 8.00 Month
- Weight: 21.863 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Intravenous
- Dose: 10 mL per unknown
- Frequency: 31 per day
Dog, Dog (unknown), Male, 10 year, 32.659 kilogram • Drug: MSK, Unknown • Reactions: Mass NOS, Lymph node abscess, Lymphadenopathy, Tachycardia, Drooling… • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-055759
- Serious AE: Yes
- Treated For AE: No
- Sex: Male
- Age: 10.00 Year
- Weight: 32.659 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
Dog, Pug, Female, 6 year, 7.8 kilogram • Drug: MSK, Unknown, Dose: 3 mL per unknown • Reactions: Diarrhea, Vomiting, Haematochezia • Outcome: Recovered/Normal
- Report ID: GBR-USFDACVM-2025-GB-000062
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 6.00 Year
- Weight: 7.800 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Dose: 3 mL per unknown
Cat, Domestic Shorthair, Male, 20 week, 3 kilogram • Drug: MSK, Unknown • Reactions: Dysphoria, Sedation, Decreased blood urea nitrogen (BUN) or creatinine, Intentional misuse • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-053968
- Serious AE: Yes
- Treated For AE: No
- Sex: Male
- Age: 20.00 Week
- Weight: 3.000 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: 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.
Share Your Thoughts
Let others know your experience or advice regarding this medication.
This medication has not been reviewed by a veterinarian yet.