Synthroid (levothyroxine) is a replacement for a hormone normally produced by your thyroid gland to regulate the body’s energy and metabolism. Levothyroxine is given when the thyroid does not produce enough of this hormone on its own.
Synthroid treats hypothyroidism (low thyroid hormone). Synthroid is also used to treat or prevent goiter (enlarged thyroid gland), which can be caused by hormone imbalances, radiation treatment, surgery, or cancer.
Thyroxine tablets are important in managing hypothyroidism, but treatment may be sub-optimal if they are used incorrectly. The tablets have pharmaceutical properties which can impair the patients management. Discussing the correct use and storage of the tablets is an important part of prescribing thyroxine.
Thyroxine is variably absorbed from the gut following oral administration. It has a bioavailability of 40–80%. Absorption may decrease with age.1,2
The extent of thyroxine absorption is increased in the fasting state and is influenced by the content of the gastrointestinal tract. Some substances bind the thyroxine, making it unavailable for diffusion across the gut wall. Concurrent administration with iron salts, antacids, calcium carbonate (including milk), sucralfate, cholestyramine and soy-based formulas may therefore decrease absorption of thyroxine.
Patients should be instructed to take thyroxine 30–60 minutes before breakfast in order to maximise absorption. If this is too difficult or threatens compliance, the patient may try taking the thyroxine last thing at night on an empty stomach. Patients who still decide to take their tablets with, rather than before, breakfast need to do this consistently, to avoid fluctuating thyroxine concentrations. Depending on the fibre and milk content of the meal, taking thyroxine with food may require a larger dose to maintain euthyroidism, because of the decreased bioavailability.
While most patients take a daily dose, the long half-life of thyroxine lends itself to longer dosing intervals, such as alternate daily dosing. Once-weekly dosing is also possible although a slightly larger dose than seven times the normal daily dose may be required. This regimen may be suitable for poorly compliant patients who require supervised dosing.3
For patients, particularly children, who cannot swallow tablets, the tablets may be crushed in 10–20 mL of water, breast milk or non-soybean formula. The resulting mixture should be used immediately and any remainder discarded.2 Breast milk contains only 20–30% of the calcium concentration of cows milk, making the likelihood of decreased thyroxine bioavailability less likely. Nonetheless, if breast milk is used to deliver the thyroxine, it should be used consistently, in order to minimise any variation in absorption.
Onset and duration of action
The half-life of thyroxine in euthyroidism is 6–7 days. This is reduced to 3–4 days in hyperthyroidism and prolonged to 9–10 days in hypothyroidism. Thyroxine has a full therapeutic effect 3–4 weeks after starting treatment and will continue to have a therapeutic action for 1–3 weeks after treatment stops. In view of the long half-life, dose changes should only be made every 3–4 weeks. Despite undergoing both hepatic and renal clearance, there is no evidence that dose adjustment is required for patients with liver or kidney disease.1,2