Meds A-Z
Cyclosporine
Detailed information about Cyclosporine
Pet Owner Quick Guide
Start here: what this medicine is for, what it does, and when it's usually needed.
Usually used for:
For the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), miliary dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3...
What it does:
For the management of chronic keratoconjunctivitis sicca (KCS) and chronic superficial keratitis (CSK) in dogs. For the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight. For the control...
When it's needed:
Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis drug to use...
Call your vet sooner if you notice:
- Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis 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.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For use only in cats. The safety and effectiveness of ATOPICA for Cats has not been established in cats less than 6 months of age or less than 3 lbs (1.4 kg) body weight. ATOPICA for Cats is not for use in breeding cats, pregnant or lactating queens. Cats should be tested and found to be negative for FeLV and FIV infections before treatment.
Commonly reported reactions:
- (1 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?
Cyclosporine
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/200744 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov/adafda/views/#/home/previewsearch/200743 · official_label · FDA application profile
- https://animaldrugsatfda.fda.gov · fda_animal_drugs · Medication usage source
Warnings / Contraindications
Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis 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.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For use only in cats. The safety and effectiveness of ATOPICA for Cats has not been established in cats less than 6 months of age or less than 3 lbs (1.4 kg) body weight. ATOPICA for Cats is not for use in breeding cats, pregnant or lactating queens. Cats should be tested and found to be negative for FeLV and FIV infections before treatment.
- High: Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis 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.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For use only in cats. The safety and effectiveness of ATOPICA for Cats has not been established in cats less than 6 months of age or less than 3 lbs (1.4 kg) body weight. ATOPICA for Cats is not for use in breeding cats, pregnant or lactating queens. Cats should be tested and found to be negative for FeLV and FIV infections before treatment.
- 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 |
|---|---|---|---|
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 | |
| 1 | Dog | 1 |
Species coverage: Dog (24) Cat (8)
View detailed reaction table
| Reaction | Species | Seriousness | Frequency | Reports |
|---|---|---|---|---|
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Cat | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Dog | Serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Cat | Non-serious | - | 1 | |
| Dog | 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-055514
Storage & Handling
No storage/handling guidance is linked yet.
Documents
Official label facts are separated from secondary summaries.
Official documents: 19 • Secondary summaries: 0
- FOI Summary oA 200-744 Approved March 29, 2023.pdf · FOI
- Modulis® for Cats · SPL
- FOI Summary oA 200-743 Approved March 21, 2023.pdf · FOI
- MODULIS® for Dogs · SPL
- FOI Summary oA 200-692 Approved October 29, 2020.pdf · FOI
- CYCLAVANCE A200692.pdf · Labeling
- CYCLAVANCE A200692.pdf · Labeling
- Cyclavance® · SPL
- FOI Summary oA 200-627 Approved November 1, 2018.pdf · FOI
- Sporimune™ · SPL
- UCM287922.pdf · FOI
- ATOPICA N141329C0033.pdf · Labeling
- ATOPICA N141329C0033.pdf · Labeling
- Atopica™ for Cats · SPL
- ucm118025.pdf · FOI
- Atopica™ · SPL
- N141052 Supp_8_26_1997.pdf · FOI
- UCM488646.pdf · FOI
- Optimmune® · SPL
No source yet.
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/13676 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/13894/Modulis%C2%AE%20for%20Cats · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/13657 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/13854/MODULIS%C2%AE%20for%20Dogs · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/9928 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/884 · document · Labeling
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadLabeling/885 · document · Labeling
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/10010/Cyclavance%C2%AE · document · SPL
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/document/downloadFoi/5781 · document · FOI
- https://animaldrugsatfda.fda.gov/adafda/app/search/public/spl/file/5608/Sporimune%E2%84%A2 · document · SPL
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
Counseling and Monitoring Highlights
Global Pet owner/Vet mode is controlled in the header. This section avoids duplicate in-page persona tabs.
- Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis 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.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For use only in cats. The safety and effectiveness of ATOPICA for Cats has not been established in cats less than 6 months of age or less than 3 lbs (1.4 kg) body weight. ATOPICA for Cats is not for use in breeding cats, pregnant or lactating queens. Cats should be tested and found to be negative for FeLV and FIV infections before treatment. (Contraindication, High)
Identifiers & Packages
Normalized identifiers (NDC/NADA/ANADA) and package metadata from regulator listings.
| Package NDC | Product NDC | Form / Route | Status |
|---|---|---|---|
| 0061-1088-01 | 0061 | - | |
| 13744-535-01 | 13744 | - | |
| 13744-535-02 | 13744 | - | |
| 13744-535-03 | 13744 | - | |
| 13744-536-01 | 13744 | - | |
| 13744-536-02 | 13744 | - | |
| 17033-261-15 | 17033 | - | |
| 17033-262-15 | 17033 | - | |
| 17033-263-15 | 17033 | - | |
| 51311-994-15 | 51311 | - | |
| 51311-994-50 | 51311 | - | |
| 58198-4351-1 | 58198 | - | |
| 58198-4352-1 | 58198 | - | |
| 58198-4353-1 | 58198 | - | |
| 58198-4354-1 | 58198 | - | |
| 58198-9725-1 | 58198 | - | |
| 58198-9725-2 | 58198 | - | |
| 62157-376-01 | 62157 | - | |
| 73377-197-01 | 73377 | - | |
| 73377-197-02 | 73377 | - |
Enriched Documents
Documents are tiered by source trust: Official, Clinical, Manufacturer, Marketing.
-
FOI Summary oA 200-744 Approved March 29, 2023.pdf
• FOI summary • Official
• Sept. 1, 2023
FDA FOI summary for application 200744
-
FOI Summary oA 200-743 Approved March 21, 2023.pdf
• FOI summary • Official
• Sept. 1, 2023
FDA FOI summary for application 200743
-
CYCLAVANCE A200692.pdf
• Official label • Official
• Sept. 29, 2022
FDA official labeling for application 200692
-
CYCLAVANCE A200692.pdf
• Official label • Official
• Sept. 29, 2022
FDA official labeling for application 200692
-
FOI Summary oA 200-692 Approved October 29, 2020.pdf
• FOI summary • Official
• Sept. 29, 2022
FDA FOI summary for application 200692
-
FOI Summary oA 200-627 Approved November 1, 2018.pdf
• FOI summary • Official
• July 6, 2022
FDA FOI summary for application 200627
-
ATOPICA N141329C0033.pdf
• Official label • Official
• May 17, 2021
FDA official labeling for application 141329
-
ATOPICA N141329C0033.pdf
• Official label • Official
• May 17, 2021
FDA official labeling for application 141329
-
UCM287922.pdf
• FOI summary • Official
• May 17, 2021
FDA FOI summary for application 141329
-
ucm118025.pdf
• FOI summary • Official
• March 15, 2019
FDA FOI summary for application 141218
-
UCM488646.pdf
• FOI summary • Official
• Dec. 7, 2017
FDA FOI summary for application 141052
-
N141052 Supp_8_26_1997.pdf
• FOI summary • Official
• Dec. 7, 2017
FDA FOI summary for application 141052
Data Sources & Revision History
Every non-trivial field is expected to include provenance and update timestamps.
- contraindications: Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not… (Official, 2026-02-12)
- side_effects: Top reported reactions (openFDA): Vomiting, Diarrhoea, Lethargy (see also Central nervous system depression in 'Neurological'), Lack of efficacy - NOS, INEFFEC… (Official, 2026-02-12)
- usage: For the management of chronic keratoconjunctivitis sicca (KCS) and chronic superficial keratitis (CSK) in dogs. For the control of atopic dermatitis in dogs we… (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 |
|---|---|---|---|---|
|
Modulis® for Cats
RX
Cyclosporine oral solution, USP Modified
Solution
• Oral
|
Ceva Sante Animale | ANADA 200-744 | Approved | Sep 1, 2023 |
|
MODULIS® for Dogs
RX
Cyclosporine
Solution
• Oral
|
Ceva Sante Animale | ANADA 200-743 | Approved | Sep 1, 2023 |
|
Cyclavance®
RX
Cyclosporine
Solution
• Oral
|
Virbac AH, Inc. | ANADA 200-692 | Approved | Sep 29, 2022 |
|
Sporimune™
RX
Cyclosporine
Oral
|
Dechra Veterinary Products LLC | ANADA 200-627 | Approved | Jul 6, 2022 |
|
Atopica™ for Cats
RX
Cyclosporine oral solution, USP Modified
Oral Solution
• Oral
|
Elanco US Inc. | NADA 141-329 | Approved | May 17, 2021 |
|
Atopica™
RX
Cyclosporine
Capsule
• Oral
|
Elanco US Inc. | NADA 141-218 | Approved | Mar 15, 2019 |
|
Optimmune®
RX
Cyclosporine
Ointment
• Ophthalmic
|
Intervet, Inc. | NADA 141-052 | Approved | Dec 7, 2017 |
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 the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), miliary dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3 lbs (1.4 kg) in body weight.
Administer 3.2 mg/lb/day (7 mg/kg/day) orally as a single daily dose for a minimum of 4 to 6 weeks or until resolution of clinical signs. Following this initial daily treatment period, the dosage may be tapered by decreasing the frequency of administration to every other day or twice weekly to maintain the desired therapeutic effect.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight.
Administer 5 mg per kilogram (mg/kg) of body weight given orally as a single daily dose for 30 days. Following this initial daily treatment period, the dosage may be tapered by decreasing the frequency of administration to every other day or two times a week, until a minimum frequency is reached which will maintain the desired therapeutic effect.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the control of atopic dermatitis in dogs weighing at least 4 lbs (1.8 kg) body weight.
Administer 5 mg per kilogram (mg/kg) of body weight given orally as a single daily dose for 30 days. Following this initial daily treatment period, the dosage may be tapered by decreasing the frequency of administration to every other day or two times a week, until a minimum frequency is reached which will maintain the desired therapeutic effect.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
Cyclosporine Capsules, USP MODIFIED are indicated for the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight.
The initial dose of Cyclosporine Capsules, USP MODIFIED is 5 mg/kg/day (3.3-6.7 mg/kg/day) as a single daily dose for 30 days. Following the initial daily treatment period, the dose of Cyclosporine Capsules, USP MODIFIED may be tapered by decreasing the frequency of dosing to every other day or twice weekly, until a minimum frequency is reached which will maintain the desired therapeutic effect. Cyclosporine Capsules, USP MODIFIED should be given at least one hour before or two hours after a meal. If a dose is missed, the next dose should be administered (without doubling) as soon as possible, but dosing should be no more frequent than once daily.
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
FDA page: Open in Animal Drugs @ FDA
Composition / specifications
For the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight.
The initial dose is 5 mg/kg/day (3.3-6.7 mg/kg/day) as a single daily dose for 30 days. Following this initial daily treatment period, the dose may be tapered by decreasing the frequency of dosing to every other day or twice weekly, until a minimum frequency is reached which will maintain the desired therapeutic effect. Atopica® should be given at least one hour before or two hours after a meal. If a dose is missed, the next dose should be administered (without doubling) as soon as possible, but dosing should be no more frequent than once daily.
Federal law restricts this drug to use by or on the order of a licensed veterinarian.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened.
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 the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), miliary dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3 lbs (1.4 kg) in body weight.
- Modulis® for Cats (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
For the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight.
- MODULIS® for Dogs (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
For the control of atopic dermatitis in dogs weighing at least 4 lbs (1.8 kg) body weight.
-
Labeling CYCLAVANCE A200692.pdf
-
Labeling CYCLAVANCE A200692.pdf
- Cyclavance® (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
Cyclosporine Capsules, USP MODIFIED are indicated for the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight.
- Sporimune™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI UCM287922.pdf
Summary
Atopica® for Cats is indicated for the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), military dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3 lbs (1.4 kg) in body weight. -
Labeling ATOPICA N141329C0033.pdf
-
Labeling ATOPICA N141329C0033.pdf
- Atopica™ for Cats (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
FOI ucm118025.pdf
Summary
For the control of atopic dermatitis in dogs weighing at least 4 lbs body weight.
- Atopica™ (ZIP)
FDA page: Open in Animal Drugs @ FDA
-
Summary
To add the label claim for the management of chronic superficial keratitis (CSK) in dogs. In addition, the label claim for treatment of chronic keratoconjunctivis sicca (KCS) was changed to management of chronic KCS. The term management reflects the complexity of therapy for the two diseases.
-
FOI UCM488646.pdf
Summary
For the treatment of chronic keratoconjunctivitis sicca (KCS) in dogs.
- Optimmune® (ZIP)
FDA page: Open in Animal Drugs @ FDA
Usage
For the management of chronic keratoconjunctivitis sicca (KCS) and chronic superficial keratitis (CSK) in dogs. For the control of atopic dermatitis in dogs weighing at least 4 lbs. (1.8 kg) body weight. For the control of feline allergic dermatitis as manifested by excoriations (including facial and neck), miliary dermatitis, eosinophilic plaques, and self-induced alopecia in cats at least 6 months of age and at least 3 lbs (1.4 kg) in body weight.
Source: FDA Animal Drugs @ FDA • Reference
Contraindications
Place ointment directly on cornea or into the conjunctival sac. For ophthalmic use in dogs only. Safety of use in puppies, pregnant or breeding animals has not been determined. US Federal law restricts thiis 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.ATOPICA is contraindicated for use in dogs with a history of neoplasia.For use in dogs only.Capsules should not be broken or opened. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For use only in cats. The safety and effectiveness of ATOPICA for Cats has not been established in cats less than 6 months of age or less than 3 lbs (1.4 kg) body weight. ATOPICA for Cats is not for use in breeding cats, pregnant or lactating queens. Cats should be tested and found to be negative for FeLV and FIV infections before treatment.
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.
Cat, Burmese, Female, 2 year • Drug: MSK, Solution, Oral, Dose: 0.90 mL per animal • Reactions: Vomiting, Foaming at the mouth, Hyperactivity, Hiding, Not eating… • Outcome: Recovered/Normal
- Report ID: USA-USFDACVM-2025-US-055773
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 2.00 Year
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Solution
- Dose: 0.90 mL per animal
Cat, Cat (unknown), Unknown • Drug: MSK, Capsule, Unknown • Reactions: Unclassifiable adverse event • Outcome: Outcome Unknown
- Report ID: USA-USFDACVM-2025-US-054375
- Serious AE: No
- Treated For AE: No
- Sex: Unknown
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Unknown
- Form: Capsule
Cat, Domestic Longhair, Female, 4 year, 3.856 kilogram • Drug: MSK, Capsule, Oral • Reactions: Application site scab, Application site hair loss • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-054544
- Serious AE: No
- Treated For AE: Yes
- Sex: Female
- Age: 4.00 Year
- Weight: 3.856 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Capsule
Cat, Cat (unknown), Female, 12 year, 4.36 kilogram • Drug: MSK, Solution, Oral, Dose: 100 Milligram per ml • Reactions: Not eating, Not defecating, Seizure NOS, Digestive tract stenosis and obstruction NOS, Not urinating… • Outcome: Died
- Report ID: USA-USFDACVM-2025-US-054337
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 12.00 Year
- Weight: 4.360 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Solution
- Dose: 100 Milligram per ml
Cat, Domestic Shorthair, Female, 5 year, 4.98 kilogram • Drug: MSK, Capsule, Oral, Dose: 1 tablet per animal, Frequency: 2 per day • Reactions: Vomiting, UNPALATABLE, Intentional misuse • Outcome: Recovered/Normal
- Report ID: USA-USFDACVM-2025-US-055560
- Serious AE: No
- Treated For AE: No
- Sex: Female
- Age: 5.00 Year
- Weight: 4.980 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Capsule
- Dose: 1 tablet per animal
- Frequency: 2 per day
Dog, Havanese, Female, 4 year, 9.616 kilogram • Drug: MSK, Capsule, Oral • Reactions: Loose stool, Vomiting, Abnormal posture NOS, Unsteady gait, Lack of efficacy - NOS… • Outcome: Euthanized
- Report ID: USA-USFDACVM-2025-US-055514
- Serious AE: Yes
- Treated For AE: Yes
- Sex: Female
- Age: 4.00 Year
- Weight: 9.616 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Capsule
Dog, ['Schnauzer (unspecified)', 'Mixed (Dog)'], Female, 3 year, 17.23 kilogram • Drug: MSK, Capsule, Oral, Dose: 1 tablet per animal, Frequency: 1 per day • Reactions: Skin lesion NOS, Dermal thickening • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-055513
- Serious AE: No
- Treated For AE: Yes
- Sex: Female
- Age: 3.00 Year
- Weight: 17.230 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Capsule
- Dose: 1 tablet per animal
- Frequency: 1 per day
Dog, ['Shih Tzu', 'Dog (unknown)'], Male, 10.83 year, 7.394 kilogram • Drug: MSK, Capsule, Oral, Dose: 1 tablet per animal, Frequency: 1 per day • Reactions: Elevated serum alkaline phosphatase, Diarrhea • Outcome: Ongoing
- Report ID: USA-USFDACVM-2025-US-054258
- Serious AE: No
- Treated For AE: No
- Sex: Male
- Age: 10.83 Year
- Weight: 7.394 Kilogram
- Case-reported brand: MSK
- Case-reported manufacturer: MSK
- Route: Oral
- Form: Capsule
- Dose: 1 tablet 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.
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This medication has not been reviewed by a veterinarian yet.