|
| U.S. Brand
Names |
|
| Thytropar® |

|
|
| Generic
Available |
|
|
No |

|
|
| Synonyms |
|
|
Thyroid Stimulating Hormone; Thyrotropic Hormone; TSH |

|
|
| Pharmacological Index |
|
|
Diagnostic Agent, Thyroid Function |

|
|
| Use |
|
|
Diagnostic aid to differentiate thyroid failure; diagnosis of decreased
thyroid reserve, to differentiate between primary and secondary hypothyroidism
and between primary hypothyroidism and euthyroidism in patients receiving
thyroid replacement |

|
|
| Pregnancy Risk
Factor |
|
|
C |

|
|
| Contraindications |
|
|
Coronary thrombosis, untreated Addison's disease, hypersensitivity to
thyrotropin or any component |

|
|
| Warnings/Precautions |
|
|
Use with caution in patients with angina pectoris or cardiac failure,
patients with hypopituitarism, adrenal cortical suppression as may be seen with
corticosteroid therapy; may cause thyroid hyperplasia |

|
|
| Adverse
Reactions |
|
|
<1%: Tachycardia, fever, headache, menstrual irregularities, nausea,
vomiting, increased bowel motility, anaphylaxis with repeated
administration |

|
|
| Overdosage/Toxicology |
|
|
Symptoms of overdose include weight loss, nervousness, sweating, tachycardia,
insomnia, heat intolerance, menstrual irregularities, headache, angina pectoris,
CHF
Acute massive overdose may require cardiac glycosides for CHF; fever should
be controlled with the help of acetaminophen; antiadrenergic agents,
particularly propranolol 1-3 mg I.V. every 6 hours or 80-160 mg/day, can be used
to treat increased sympathetic activity. |

|
|
| Drug
Interactions |
|
|
No data reported |

|
|
| Stability |
|
|
Refrigerate at 2°C to 8°C
(36°F to 46°F) after reconstitution;
use within 2 weeks |

|
|
| Mechanism of
Action |
|
|
Stimulates formation and secretion of thyroid hormone, increases uptake of
iodine by thyroid gland |

|
|
| Pharmacodynamics/Kinetics |
|
|
Half-life: 35 minutes, dependent upon thyroid state
Elimination: Rapidly by the kidney in the urine |

|
|
| Usual Dosage |
|
|
Adults: I.M., S.C.: 10 units/day for 1-3 days; follow by a radioiodine study
24 hours past last injection, no response in thyroid failure, substantial
response in pituitary failure |

|
|
| Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
|
|
No information available to require special precautions |

|
|
| Dental Health:
Effects on Dental Treatment |
|
|
No effects or complications reported |

|
|
| Patient
Information |
|
|
You will receive this medication for 3 days prior to the radiologic studies.
You may experience some nausea or vomiting. Report dizziness, faintness,
palpitations, or any respiratory difficulties. Pregnancy precautions:
Inform prescriber if you are or intend to be pregnant. |

|
|
| Dosage Forms |
|
|
Injection: 10 units |

|
|
Copyright © 2007 Drugs Area
|