Cosyntropin Dosage
Medically reviewed by Drugs.com. Last updated on Jul 16, 2024.
Applies to the following strengths: 0.25 mg; 0.25 mg/mL
Usual Adult Dose for:
Usual Pediatric Dose for:
Additional dosage information:
Usual Adult Dose for Adrenocortical Insufficiency
Rapid Screening Test for Adrenal Function: 0.25 mg IV or IM once
- Dose range of 0.25 to 0.75 mg has been used in clinical studies; maximal response occurred with 0.25 mg dose
- At 30 minutes post-dose, a rise of at least 7 mcg/100 mL is expected; stimulated plasma cortisol levels less than 18 to 20 mcg/dL at 30 to 60 minutes post dose are suggestive of adrenocortical insufficiency.
Comments:
- Patients should omit pre-test doses of cortisone, hydrocortisone, or spironolactone to avoid diagnostic inaccuracies.
- An IV infusion has also been used to provide a greater stimulus to the adrenal glands; same dose infused over 4 to 8 hours with adrenal response measured by urinary steroid excretion before and after treatment or measuring plasma cortisol levels before and at the end of the infusion (preferred).
- Test results can be affected by concomitant medications and certain medical conditions.
Use: As a diagnostic drug in screening patients presumed to have adrenocortical insufficiency.
Usual Pediatric Dose for Adrenocortical Insufficiency
Rapid Screening Test for Adrenal Function:
0 to 2 years: 0.125 mg IV or IM once
3 years or older: 0.25 mg IV or IM once
- Dose range of 0.25 to 0.75 mg has been used in clinical studies; maximal response occurred with 0.25 mg dose
At 30 minutes post-dose, a rise of at least 7 mcg/100 mL is expected; stimulated plasma cortisol levels less than 18 to 20 mcg/dL at 30 to 60 minutes post dose are suggestive of adrenocortical insufficiency.
Comments:
- Patients should omit pre-test doses of cortisone, hydrocortisone, or spironolactone to avoid diagnostic inaccuracies.
- An IV infusion has also been used to provide a greater stimulus to the adrenal glands; same dose infused over 4 to 8 hours with adrenal response measured by urinary steroid excretion before and after treatment or measuring plasma cortisol levels before and at the end of the infusion (preferred).
- Test results can be affected by concomitant medications and certain medical conditions.
Use: As a diagnostic drug in screening patients presumed to have adrenocortical insufficiency.
Renal Dose Adjustments
Use caution in patients with nephrotic syndrome
- Cortisol binding globulin levels can be low in patients with nephrotic syndrome; for these patients, cortisol binding globulin levels should be measured
Liver Dose Adjustments
Use caution in patients with cirrhosis
- Cortisol binding globulin levels can be low in patients with cirrhosis; for these patients, cortisol binding globulin levels should be measured
Precautions
CONTRAINDICATIONS:
- Hypersensitivity to active substance, synthetic ACTH, or any product excipients
Consult WARNINGS section for additional precautions.
Dialysis
Data not available
Other Comments
Administration advice:
May be administered IM or IV; however, some products for IV administration only
IV administration:
- IV injection: Add dose to 2 to 5 mL of 0.9% sodium chloride injection; administer over 2-minutes
- IV infusion: Add dose to glucose or saline solution and give at approximately 40 mcg/hour for 6 hours
IM administration:
- Reconstitute 0.25 mg with 1 mL of 0.9% sodium chloride injection; inject IM
ACTH Stimulation Test:
- Collect blood sample (6 to 7 mL) prior to injection
- Administer dose
- Collect second blood sample 30 and/or 60 minutes postdose
Storage requirements:
- Protect from light
- Store refrigerated 36F to 46F (2C to 8C); protect from freezing
General:
- Plasma cortisol levels less than 18 to 20 mcg/dL at 30 or 60 minutes post injection are suggestive of adrenocortical insufficiency.
- Test results may be affected by concomitant medications (e.g. cortisone, hydrocortisone, synthetic glucocorticoids [oral, inhaled, or injectable], spironolactone, and estrogens) or certain medical conditions (e.g., cirrhosis, nephrotic syndrome).
- Concurrent measurement of cortisol binding globulin levels is recommended; if cortisol binding globulin levels are elevated, plasma total cortisol levels should be considered inaccurate.
Monitoring:
- Monitor for hypersensitivity reactions
Patient advice:
- Read the US FDA-approved patient labeling
- Patients should understand that hypersensitivity reactions may occur.
More about cosyntropin
- Check interactions
- Compare alternatives
- Pricing & coupons
- Side effects
- During pregnancy
- Drug class: corticotropin
- En español
Patient resources
Other brands
Professional resources
Other brands
Related treatment guides
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.