this site is intended for U.S. healthcare professionals only.

By clicking continue, you certify that you are a U.S. healthcare professional.

this site is intended for U.S. healthcare professionals only.

By clicking continue, you certify that you are a U.S. healthcare professional.

this site is intended for U.S. healthcare professionals only.

By clicking continue, you certify that you are a U.S. healthcare professional.

Note that DTE products, including amerithroid, have not been reviewed by the FDA for safety or efficacy.

Indications and Usage 

Thyroid Tablets, USP are indicated for:

  • Replacement or supplemental therapy in hypothyroidism of any etiology (except transient hypothyroidism during recovery from subacute thyroiditis) 

  • TSH suppression in the management of certain goiters and in thyroid cancer 

contraindications

  • Uncorrected adrenal cortical insufficiency

  • Untreated thyrotoxicosis

  • Known hypersensitivity to thyroid hormone preparations or excipients 

IMPORTANT RISK INFORMATION

BOXED WARNING

WARNING: NOT FOR TREATMENT OF OBESITY OR FOR WEIGHT LOSS

  • THYROID HORMONES, ALONE OR IN COMBINATION, SHOULD NOT BE USED FOR WEIGHT LOSS OR OBESITY TREATMENT. 

  • IN EUTHYROID PATIENTS, DOSES WITHIN NORMAL HORMONAL REQUIREMENTS ARE INEFFECTIVE FOR WEIGHT REDUCTION. 

  • LARGER DOSES MAY PRODUCE SERIOUS OR LIFE‑THREATENING TOXICITY, PARTICULARLY WHEN USED WITH SYMPATHOMIMETIC AMINES. 

Warnings and Precautions

Cardiovascular Risk
  • Use with extreme caution in:  

    • Patients with coronary artery disease or angina 

    • Elderly patients 

  • Therapy should be initiated at low doses and titrated carefully, as thyroid hormones may precipitate:

    • Angina

    • Arrhythmias

    • Myocardial infarction

Risk of Over‑Replacement (Hyperthyroidism) 
  • Excess dosing may result in symptoms of hyperthyroidism, including:

    • Palpitations

    • Tachycardia

    • Nervousness 

    • Heat intolerance 

  • Liothyronine (T3) content may produce more rapid and pronounced effects 

Endocrine Effects 
  • May worsen:  

    • Diabetes mellitus (increased insulin/oral hypoglycemic requirements) 

    • Adrenal insufficiency (must be corrected prior to therapy) 

  • Requires careful monitoring and dose adjustment 

Anticoagulant Sensitivity 
  • Thyroid hormones may increase response to oral anticoagulants

  • Monitor prothrombin time/INR and adjust anticoagulant dose as needed 

Special Populations 

  • Pediatric patients: Excess dosing may cause craniosynostosis

  • Pregnancy: Continue therapy; dose adjustments may be required 

  • Lactation: Use with caution 

Adverse Reactions 

  • Adverse reactions are generally due to overdosage and resemble hyperthyroidism: 

    • Palpitations

    • Tachycardia

    • Arrhythmias

    • Nervousness

    • Insomnia

    • Tremor

    • Heat intolerance

  • Other reactions are rare when properly dosed 

Drug Interactions

  • Decreased absorption:

    • Cholestyramine (separate dosing by 4–5 hours) 

  • Increased anticoagulant effects 

  • Altered glycemic control with insulin or oral hypoglycemics 

  • Estrogens/oral contraceptives:  

    • May increase thyroid hormone requirements 

Dosage and Administration  

  • Dosage must be individualized based on clinical response and laboratory monitoring (TSH, T4, T3)

  • Typically initiated at low doses and titrated gradually, especially in patients with cardiovascular disease 

  • Administer orally; consistency in administration is important 

This is the most important safety information you should know about AMERITHROID®. For more information see full Prescribing Information, including BOXED WARNING.

To report SUSPECTED ADVERSE REACTIONS, contact Oliva Therapeutics, LLC at 1-877-200-6088, or FDA at 1-800-FDA-1088 or www.fda.gov/MedWatch.


All patient and physician images are representative only.

Note that DTE products, including amerithroid, have not been reviewed by the FDA for safety or efficacy.

Indications and Usage 

Thyroid Tablets, USP are indicated for:

  • Replacement or supplemental therapy in hypothyroidism of any etiology (except transient hypothyroidism during recovery from subacute thyroiditis) 

  • TSH suppression in the management of certain goiters and in thyroid cancer 

IMPORTANT RISK INFORMATION (CONT’D)

contraindications

  • Uncorrected adrenal cortical insufficiency

  • Untreated thyrotoxicosis

  • Known hypersensitivity to thyroid hormone preparations or excipients 

IMPORTANT RISK INFORMATION

BOXED WARNING

WARNING: NOT FOR TREATMENT OF OBESITY OR FOR WEIGHT LOSS

  • THYROID HORMONES, ALONE OR IN COMBINATION, SHOULD NOT BE USED FOR WEIGHT LOSS OR OBESITY TREATMENT. 

  • IN EUTHYROID PATIENTS, DOSES WITHIN NORMAL HORMONAL REQUIREMENTS ARE INEFFECTIVE FOR WEIGHT REDUCTION. 

  • LARGER DOSES MAY PRODUCE SERIOUS OR LIFE‑THREATENING TOXICITY, PARTICULARLY WHEN USED WITH SYMPATHOMIMETIC AMINES. 

Warnings and Precautions

Cardiovascular Risk
  • Use with extreme caution in:  

    • Patients with coronary artery disease or angina 

    • Elderly patients 

  • Therapy should be initiated at low doses and titrated carefully, as thyroid hormones may precipitate:

    • Angina

    • Arrhythmias

    • Myocardial infarction

Risk of Over‑Replacement (Hyperthyroidism) 
  • Excess dosing may result in symptoms of hyperthyroidism, including:

    • Palpitations

    • Tachycardia

    • Nervousness 

    • Heat intolerance 

  • Liothyronine (T3) content may produce more rapid and pronounced effects 

Endocrine Effects 
  • May worsen:  

    • Diabetes mellitus (increased insulin/oral hypoglycemic requirements) 

    • Adrenal insufficiency (must be corrected prior to therapy) 

  • Requires careful monitoring and dose adjustment 

Anticoagulant Sensitivity 
  • Thyroid hormones may increase response to oral anticoagulants

  • Monitor prothrombin time/INR and adjust anticoagulant dose as needed 

Special Populations 

  • Pediatric patients: Excess dosing may cause craniosynostosis

  • Pregnancy: Continue therapy; dose adjustments may be required 

  • Lactation: Use with caution 

Adverse Reactions 

  • Adverse reactions are generally due to overdosage and resemble hyperthyroidism: 

    • Palpitations

    • Tachycardia

    • Arrhythmias

    • Nervousness

    • Insomnia

    • Tremor

    • Heat intolerance

  • Other reactions are rare when properly dosed 

Drug Interactions

  • Decreased absorption:

    • Cholestyramine (separate dosing by 4–5 hours) 

  • Increased anticoagulant effects 

  • Altered glycemic control with insulin or oral hypoglycemics 

  • Estrogens/oral contraceptives:  

    • May increase thyroid hormone requirements 

Dosage and Administration  

  • Dosage must be individualized based on clinical response and laboratory monitoring (TSH, T4, T3)

  • Typically initiated at low doses and titrated gradually, especially in patients with cardiovascular disease 

  • Administer orally; consistency in administration is important 

This is the most important safety information you should know about AMERITHROID®. For more information see full Prescribing Information, including BOXED WARNING.

To report SUSPECTED ADVERSE REACTIONS, contact Oliva Therapeutics, LLC at 1-877-200-6088, or FDA at 1-800-FDA-1088 or www.fda.gov/MedWatch.


All patient and physician images are representative only.

Note that DTE products, including amerithroid, have not been reviewed by the FDA for safety or efficacy.

Indications and Usage 

Thyroid Tablets, USP are indicated for:

  • Replacement or supplemental therapy in hypothyroidism of any etiology (except transient hypothyroidism during recovery from subacute thyroiditis) 

  • TSH suppression in the management of certain goiters and in thyroid cancer 

IMPORTANT RISK INFORMATION (CONT’D)

contraindications

  • Uncorrected adrenal cortical insufficiency

  • Untreated thyrotoxicosis

  • Known hypersensitivity to thyroid hormone preparations or excipients 

IMPORTANT RISK INFORMATION

BOXED WARNING

WARNING: NOT FOR TREATMENT OF OBESITY OR FOR WEIGHT LOSS

  • THYROID HORMONES, ALONE OR IN COMBINATION, SHOULD NOT BE USED FOR WEIGHT LOSS OR OBESITY TREATMENT. 

  • IN EUTHYROID PATIENTS, DOSES WITHIN NORMAL HORMONAL REQUIREMENTS ARE INEFFECTIVE FOR WEIGHT REDUCTION. 

  • LARGER DOSES MAY PRODUCE SERIOUS OR LIFE‑THREATENING TOXICITY, PARTICULARLY WHEN USED WITH SYMPATHOMIMETIC AMINES. 

Warnings and Precautions

Cardiovascular Risk
  • Use with extreme caution in:  

    • Patients with coronary artery disease or angina 

    • Elderly patients 

  • Therapy should be initiated at low doses and titrated carefully, as thyroid hormones may precipitate:

    • Angina

    • Arrhythmias

    • Myocardial infarction

Risk of Over‑Replacement (Hyperthyroidism) 
  • Excess dosing may result in symptoms of hyperthyroidism, including:

    • Palpitations

    • Tachycardia

    • Nervousness 

    • Heat intolerance 

  • Liothyronine (T3) content may produce more rapid and pronounced effects 

Endocrine Effects 
  • May worsen:  

    • Diabetes mellitus (increased insulin/oral hypoglycemic requirements) 

    • Adrenal insufficiency (must be corrected prior to therapy) 

  • Requires careful monitoring and dose adjustment 

Anticoagulant Sensitivity 
  • Thyroid hormones may increase response to oral anticoagulants

  • Monitor prothrombin time/INR and adjust anticoagulant dose as needed 

Special Populations 

  • Pediatric patients: Excess dosing may cause craniosynostosis

  • Pregnancy: Continue therapy; dose adjustments may be required 

  • Lactation: Use with caution 

Adverse Reactions 

  • Adverse reactions are generally due to overdosage and resemble hyperthyroidism: 

    • Palpitations

    • Tachycardia

    • Arrhythmias

    • Nervousness

    • Insomnia

    • Tremor

    • Heat intolerance

  • Other reactions are rare when properly dosed 

Drug Interactions

  • Decreased absorption:

    • Cholestyramine (separate dosing by 4–5 hours) 

  • Increased anticoagulant effects 

  • Altered glycemic control with insulin or oral hypoglycemics 

  • Estrogens/oral contraceptives:  

    • May increase thyroid hormone requirements 

Dosage and Administration  

  • Dosage must be individualized based on clinical response and laboratory monitoring (TSH, T4, T3)

  • Typically initiated at low doses and titrated gradually, especially in patients with cardiovascular disease 

  • Administer orally; consistency in administration is important 

This is the most important safety information you should know about AMERITHROID®. For more information see full Prescribing Information, including BOXED WARNING.

To report SUSPECTED ADVERSE REACTIONS, contact Oliva Therapeutics, LLC at 1-877-200-6088, or FDA at 1-800-FDA-1088 or www.fda.gov/MedWatch.


All patient and physician images are representative only.

Amerithroid logo

Amerithroid is a registered trademark of Oliva Therapeutics and is manufactured by Jerome Stevens Pharmaceuticals, Inc.

© 2026 Oliva Therapeutics. All rights reserved.  US-AME-26009-10/26
This site is intended for U.S. healthcare professionals only.

Amerithroid logo

Amerithroid is a registered trademark of Oliva Therapeutics and is manufactured by Jerome Stevens Pharmaceuticals, Inc.
© 2026 Oliva Therapeutics. All rights reserved.  US-AME-26009-10/26
This site is intended for U.S. healthcare professionals only.

Amerithroid logo

Amerithroid is a registered trademark of Oliva Therapeutics and is manufactured by Jerome Stevens Pharmaceuticals, Inc.
© 2026 Oliva Therapeutics. All rights reserved.  US-AME-26009-10/26
This site is intended for U.S. healthcare professionals only.

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