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Meds A-Z

Desoxycorticosterone Pivalate

Detailed information about Desoxycorticosterone Pivalate

Official label facts Owner quick guide first Marketing clearly labeled
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Pet Owner Quick Guide

Start here: what this medicine is for, what it does, and when it's usually needed.

Usually used for:

For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency.

What it does:

For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency. For use as replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism...

When it's needed:

For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Call your vet sooner if you notice:

  • For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Commonly reported reactions:

  • (2 reports)
  • (2 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?
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Desoxycorticosterone Pivalate

Desoxycorticosterone Pivalate

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.

Species: Both
Manufacturer: MSK
Form: Injectable Suspension, Liquid (Suspension)
Identifiers:
NADA: 141029 NADA: 141444 NDC Package: 17033-382-04 NDC Package: 58198-6450-0 NDC Product: 17033 NDC Product: 58198
Source metadata:

Warnings / Contraindications

For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

  • High: For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian.
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
25
Species represented
2
Most Reported Reactions
Reaction Cases Species Serious cases
2 Cat, Dog 2
2 Cat, Dog 1
1 Dog 1
1 Cat 1
1 Cat 1
1 Dog 1
1 Cat 1
1 Cat 1

Species coverage: Cat (21) Dog (11)

View detailed reaction table
Reaction Species Seriousness Frequency Reports
Cat Serious - 1
Dog Serious - 1
Cat Serious - 1
Dog Serious - 1
Cat Serious - 1
Cat Serious - 1
Cat Serious - 1
Cat Serious - 1
Dog Serious - 1
Cat Serious - 1
Dog Non-serious - 1
Cat Serious - 1
Dog Serious - 1
Cat Non-serious - 1
Dog Non-serious - 1
Cat Serious - 1
Cat Serious - 1
Cat Serious - 1
Dog Serious - 1
Cat Serious - 1
Cat Non-serious - 1
Cat Serious - 1
Dog Serious - 1
Cat Serious - 1
Cat Serious - 1
Dog Non-serious - 1
Dog Serious - 1
Cat Non-serious - 1
Cat Serious - 1
Cat Non-serious - 1
Cat Serious - 1
Dog Serious - 1
Source metadata:

Storage & Handling

No storage/handling guidance is linked yet.

Source metadata: No source yet.

Documents

Official label facts are separated from secondary summaries.

Promotional Materials (Marketing)

This content is marketing material and not clinical guidance.

No marketing assets are linked yet.

No source yet.

Source metadata: No source yet.
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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.

Data freshness
  • 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 9, 2026, 3:13 AM UTC
  • openFDA case summaries: Source FDA openFDA | Refreshed Feb 9, 2026, 3:21 AM UTC
Official (FDA)
Identity: Generic ingredient • FDA branded products available
Official FDA brands: Percorten™-V Zycortal® Suspension
Case-reported brands (openFDA): MSK
Catalog species: Both FDA-labeled species: Dog
Rx/OTC: RX
Form/route: Injectable Suspension, Liquid (Suspension) Intramuscular, Subcutaneous
Applications: NADA 141-029 • NADA 141-444
Documents: 2 (FOI: 2) • SPL: 2 Label highlights Official documents
Safety (openFDA)
Top reactions: Dog 8 Cat 8 View
Case summaries: 10 (showing 8) View
openFDA reports are unverified and do not prove causation.

Explore
Linked using: Fda_Label (0.95), Fda_Label (0.95)

Diagnosis Codes
ICD10_CM: E27.1
Primary adrenocortical insufficiency

Counseling and Monitoring Highlights

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

Owner-facing counseling points
  • For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian. (Contraindication, High)
Top reaction signals
Abnormal ultrasound finding (1) Addison's disease (1) Anorexia (1) Coprophagia (1) Decreased appetite (1) Dehydration (1) Disorientation (1) Drug administration error (1) Drunken gait (1) Falling (1) Fever (1) Gastrointestinal foreign body NOS (1) High sodium-potassium ratio (Na:K ratio) (1) High sodium-potassium ratio (Na:K ratio) (1) Hyperactivity (1) Hyperalbuminaemia (1)

Identifiers & Packages

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

Identifiers
NADA: 141029 NADA: 141444 NDC Package: 17033-382-04 NDC Package: 58198-6450-0 NDC Product: 17033 NDC Product: 58198
Package NDC Product NDC Form / Route Status
17033-382-04 17033 -
58198-6450-0 58198 -

Enriched Documents

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

  • N141029 Org_1_12_1998.pdf • FOI summary • Official • June 18, 2018
    FDA FOI summary for application 141029
  • UCM488818.pdf • FOI summary • Official • June 1, 2016
    FDA FOI summary for application 141444

Data Sources & Revision History

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

Official 5 Clinical 0 Manufacturer 0 Marketing 0
Current Field Facts
  • contraindications: For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts th… (Official, 2026-02-12)
  • side_effects: Top reported reactions (openFDA): Immediate pain upon injection, High sodium-potassium ratio (Na:K ratio), Lethargy (see also Central nervous system depression… (Official, 2026-02-12)
  • usage: For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency. For use as replacement therapy for mineralo… (Official, 2026-02-12)
Recent Revisions
  • 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
Percorten™-V
RX
Desoxycorticosterone Pivalate
Liquid (Suspension) Intramuscular
Elanco US Inc. NADA 141-029 Approved Jun 18, 2018
Zycortal® Suspension
RX
Desoxycorticosterone Pivalate
Injectable Suspension Subcutaneous
Dechra, Ltd. NADA 141-444 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.

Species: Dog, Restricted During Pregnancy
Composition / specifications
Each milliliter of sterile aqueous suspension contains 25 milligrams of desoxycorticosterone pivalate.
Dogs
Indication
For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency.
Dosage
Dosage requirements are variable and must be individualized on the basis of the response of the patient to therapy. Initial dose of 1 milligram per pound (0.45 kilogram) of body weight every 25 days, intramuscularly. Usual dose is 0.75 to 1.0 milligram per pound of body weight every 21 to 30 days.
Limitations
For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Species: Dog, No Use Class Stated Or Implied
Composition / specifications
25 mg/mL
Dogs
Indication
For use as replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism (Addison’s disease).
Dosage
Administer an initial dose of 2.2 mg/kilogram (1 mg/lb) body weight by subcutaneous injection. Subsequent dosages should be individualized according to label instructions based on patient response to therapy.
Limitations
For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

FDA page: Open in Animal Drugs @ FDA

Official Documents (FDA)

Direct links to FDA-hosted PDFs and SPL packages (when available).

Documents
  • Summary

    For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency.

SPL Packages

FDA page: Open in Animal Drugs @ FDA

Documents
  • Summary
    For use as replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism (Addison’s disease).
SPL Packages

FDA page: Open in Animal Drugs @ FDA

Usage

For use as replacement therapy for the mineralocorticoid deficit in dogs with primary adrenocortical insufficiency. For use as replacement therapy for mineralocorticoid deficiency in dogs with primary hypoadrenocorticism (Addison’s disease).

Source: FDA Animal Drugs @ FDA • Reference

Contraindications

For intramuscular use only. Do not use in pregnant dogs, dogs suffering from congestive heart disease, severe renal disease, or edema. Federal law restricts this drug to use by or on the order of a licensed veterinarian. For subcutaneous use in dogs only. Federal law restricts this drug to use by or on the order of a licensed veterinarian.

Side Effects

No approved side-effect narrative is linked yet.

openFDA reaction signals are available for Dog 8 and Cat 8 (view top reported reactions).

Top Reported Reactions (openFDA)

Aggregated reaction terms from FDA openFDA reports (not verified; does not prove causation).

Dog
Digestive
Vomiting (111) Diarrhea (77)
Neurologic
Tiredness (lethargy) (122)
Other
Immediate pain upon injection (208) High sodium-potassium ratio (136) Polyuria (93) Polydipsia (90) Vocalisation (78)
Cat
Digestive
Loss of appetite (3) Decreased appetite (1)
Other
Dehydration (2) Hyperglycaemia (2) Weight loss (2) Abnormal ultrasound finding (1) Disorientation (1) Drug administration error (1)

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, Maltese, Female, 7 year, 6.486 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Shaking • Outcome: Recovered/Normal

  • Report ID: USA-USFDACVM-2025-US-030815
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 7.00 Year
  • Weight: 6.486 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Unassigned
Reactions Reported:
Shaking
Outcomes: Recovered/Normal

Dog, ['Spitz - German Pomeranian', 'Poodle (unspecified)'], Female, 15 month, 4.5 kilogram • Drug: MSK, Unknown • Reactions: Fever, Hyperactivity, Vomiting, Itching • Outcome: Recovered/Normal

  • Report ID: USA-USFDACVM-2025-US-025357
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 15.00 Month
  • Weight: 4.500 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Fever Hyperactivity Vomiting Itching
Outcomes: Recovered/Normal

Dog, Cattle Dog - Australian (blue heeler, red heeler, Queensland cattledog), Female, 7 year, 21.319 kilogram • Drug: MSK, Unassigned, Unknown • Reactions: Trauma NOS, Paraplegia, Hyposensitivity to pain, Unable to walk, Drunken gait… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-019689
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 7.00 Year
  • Weight: 21.319 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Unassigned
Reactions Reported:
Trauma NOS Paraplegia Hyposensitivity to pain Unable to walk Drunken gait Pain NOS
Outcomes: Ongoing

Dog, ['Shepherd Dog - German', 'Dog (unknown)'], Female, 10 year, 31.75 kilogram • Drug: MSK, Unknown • Reactions: Coprophagia, Lack of efficacy (endoparasite) - whipworm, Addison's disease • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-010338
  • Serious AE: Yes
  • Treated For AE: No
  • Sex: Female
  • Age: 10.00 Year
  • Weight: 31.750 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
Reactions Reported:
Coprophagia Lack of efficacy (endoparasite) - whipworm Addison's disease
Outcomes: Ongoing

Dog, Crossbred Canine/dog, Female, 4 year, 27.7 kilogram • Drug: MSK, Unknown, Dose: 2.30 mL per animal • Reactions: High sodium-potassium ratio, Hypochloraemia, Weight gain, Vulvar oedema, Polyphagia… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2025-US-010109
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Female
  • Age: 4.00 Year
  • Weight: 27.700 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Dose: 2.30 mL per animal
Reactions Reported:
High sodium-potassium ratio Hypochloraemia Weight gain Vulvar oedema Polyphagia Poor coat condition
Outcomes: Ongoing

Cat, Domestic Shorthair, Male, 5 year, 5.41 kilogram • Drug: MSK, Injection, suspension, Subcutaneous, Dose: 1.85 Milligram per kilogram • Reactions: Vomiting, Gastrointestinal foreign body NOS, Abnormal ultrasound finding, Loss of appetite, Hyperglycaemia… • Outcome: Ongoing

  • Report ID: USA-USFDACVM-2021-US-000678
  • Serious AE: Yes
  • Treated For AE: Yes
  • Sex: Male
  • Age: 5.00 Year
  • Weight: 5.410 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Subcutaneous
  • Form: Injection, suspension
  • Dose: 1.85 Milligram per kilogram
Reactions Reported:
Vomiting Gastrointestinal foreign body NOS Abnormal ultrasound finding Loss of appetite Hyperglycaemia Weight loss Dehydration Reduced faecal output Hyperalbuminaemia Increased red blood cell count Increased packed cell volume Lymphopenia Other abnormal test result NOS
Outcomes: Ongoing

Cat, Birman (Sacred Birman), Female, 8 year • Drug: MSK, Injection, suspension, Unknown • Reactions: Loss of appetite, Lack of efficacy - NOS • Outcome: Recovered/Normal

  • Report ID: USA-USFDACVM-2019-US-052741
  • Serious AE: No
  • Treated For AE: No
  • Sex: Female
  • Age: 8.00 Year
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Unknown
  • Form: Injection, suspension
Reactions Reported:
Loss of appetite Lack of efficacy - NOS
Outcomes: Recovered/Normal

Cat, Domestic Shorthair, Male, 14 year, 6.23 kilogram • Drug: MSK, Injection, suspension, Intramuscular, Dose: 4.01 Milligram per kilogram • Reactions: Hypoglycaemia, High sodium-potassium ratio, Medication error • Outcome: Outcome Unknown

  • Report ID: USA-USFDACVM-2019-US-024335
  • Serious AE: No
  • Treated For AE: No
  • Sex: Male
  • Age: 14.00 Year
  • Weight: 6.230 Kilogram
  • Case-reported brand: MSK
  • Case-reported manufacturer: MSK
  • Route: Intramuscular
  • Form: Injection, suspension
  • Dose: 4.01 Milligram per kilogram
Reactions Reported:
Hypoglycaemia High sodium-potassium ratio Medication error
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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