Levo-T Prescribing Information
6 ADVERSE REACTIONSAdverse reactions associated with LEVO-T therapy are primarily those of hyperthyroidism due to therapeutic overdosage
- General:fatigue, increased appetite, weight loss, heat intolerance, fever, excessive sweating
- Central nervous system:headache, hyperactivity, nervousness, anxiety, irritability, emotional lability, insomnia
- Musculoskeletal:tremors, muscle weakness, muscle spasm
- Cardiovascular:palpitations, tachycardia, arrhythmias, increased pulse and blood pressure, heart failure, angina, myocardial infarction, cardiac arrest
- Respiratory:dyspnea
- Gastrointestinal:diarrhea, vomiting, abdominal cramps, elevations in liver function tests
- Dermatologic:hair loss, flushing, rash
- Endocrine:decreased bone mineral density
- Reproductive:menstrual irregularities, impaired fertility
Seizures have been reported rarely with the institution of levothyroxine therapy.
Adverse reactions associated with LEVO-T therapy are primarily those of hyperthyroidism due to therapeutic overdosage: arrhythmias, myocardial infarction, dyspnea, muscle spasm, headache, nervousness, irritability, insomnia, tremors, muscle weakness, increased appetite, weight loss, diarrhea, heat intolerance, menstrual irregularities, and skin rash.
Pseudotumor cerebri and slipped capital femoral epiphysis have been reported in children receiving levothyroxine therapy. Overtreatment may result in craniosynostosis in infants and premature closure of the epiphyses in children with resultant compromised adult height.
Hypersensitivity reactions to inactive ingredients have occurred in patients treated with thyroid hormone products. These include urticaria, pruritus, skin rash, flushing, angioedema, various gastrointestinal symptoms (abdominal pain, nausea, vomiting and diarrhea), fever, arthralgia, serum sickness, and wheezing. Hypersensitivity to levothyroxine itself is not known to occur.
7.7 SympathomimeticsConcurrent use of sympathomimetics and LEVO-T may increase the effects of sympathomimetics or thyroid hormone. Thyroid hormones may increase the risk of coronary insufficiency when sympathomimetic agents are administered to patients with coronary artery disease.
10 OVERDOSAGEThe signs and symptoms of overdosage are those of hyperthyroidism
Reduce the LEVO-T dose or discontinue temporarily if signs or symptoms of overdosage occur. Initiate appropriate supportive treatment as dictated by the patient's medical status.
For current information on the management of poisoning or overdosage, contact the National Poison Control Center at 1-800-222-1222 or www.poison.org.
LEVO-T is L-thyroxine (T
4) indicated for:
- Hypothyroidism: As replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism. ( )
1 INDICATIONS AND USAGELEVO-T is L-thyroxine (T4) indicated for:
- Hypothyroidism: As replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism.
- Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) Suppression: As an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer. Limitations of Use:
- Not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient patients.
- Not indicated for treatment of hypothyroidism during the recovery phase of subacute thyroiditis.
HypothyroidismLEVO-T is indicated as a replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism.
Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) SuppressionLEVO-T is indicated as an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer.
Limitations of Use:- LEVO-T is not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient patients as there are no clinical benefits and overtreatment with LEVO-T may induce hyperthyroidism[see Warnings and Precautions (5.4)].
- LEVO-T is not indicated for treatment of hypothyroidism during the recovery phase of subacute thyroiditis.
- Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) Suppression: As an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer. ( )
1 INDICATIONS AND USAGELEVO-T is L-thyroxine (T4) indicated for:
- Hypothyroidism: As replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism.
- Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) Suppression: As an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer. Limitations of Use:
- Not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient patients.
- Not indicated for treatment of hypothyroidism during the recovery phase of subacute thyroiditis.
HypothyroidismLEVO-T is indicated as a replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism.
Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) SuppressionLEVO-T is indicated as an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer.
Limitations of Use:- LEVO-T is not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient patients as there are no clinical benefits and overtreatment with LEVO-T may induce hyperthyroidism[see Warnings and Precautions (5.4)].
- LEVO-T is not indicated for treatment of hypothyroidism during the recovery phase of subacute thyroiditis.
Limitations of Use:
- Not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient patients.
- Not indicated for treatment of hypothyroidism during the recovery phase of subacute thyroiditis.
- Administer once daily, preferably on an empty stomach, one-half to one hour before breakfast. ( )
2.1 General Administration InformationTake LEVO-T with a full glass of water as the tablet may rapidly disintegrate
.Administer LEVO-T as a single daily dose, on an empty stomach, one-half to one hour before breakfast.
Administer LEVO-T at least 4 hours before or after drugs known to interfere with LEVO-T absorption
[see Drug Interactions (7.1)].Evaluate the need for dose adjustments when regularly administering within one hour of certain foods that may affect LEVO-T absorption
[see Drug Interactions (7.9)andClinical Pharmacology (12.3)].Administer LEVO-T to infants and children who cannot swallow intact tablets by crushing the tablet, suspending the freshly crushed tablet in a small amount (5 to 10 mL or 1 to 2 teaspoons) of water and immediately administering the suspension by spoon or dropper. Do not store the suspension. Do not administer in foods that decrease absorption of LEVO-T, such as soybean-based infant formula
[see Drug Interactions (7.9)]. - Administer at least 4 hours before or after drugs that are known to interfere with absorption. ( )
2.1 General Administration InformationTake LEVO-T with a full glass of water as the tablet may rapidly disintegrate
.Administer LEVO-T as a single daily dose, on an empty stomach, one-half to one hour before breakfast.
Administer LEVO-T at least 4 hours before or after drugs known to interfere with LEVO-T absorption
[see Drug Interactions (7.1)].Evaluate the need for dose adjustments when regularly administering within one hour of certain foods that may affect LEVO-T absorption
[see Drug Interactions (7.9)andClinical Pharmacology (12.3)].Administer LEVO-T to infants and children who cannot swallow intact tablets by crushing the tablet, suspending the freshly crushed tablet in a small amount (5 to 10 mL or 1 to 2 teaspoons) of water and immediately administering the suspension by spoon or dropper. Do not store the suspension. Do not administer in foods that decrease absorption of LEVO-T, such as soybean-based infant formula
[see Drug Interactions (7.9)]. - Evaluate the need for dose adjustments when regularly administering within one hour of certain foods that may affect absorption. ( )
2.1 General Administration InformationTake LEVO-T with a full glass of water as the tablet may rapidly disintegrate
.Administer LEVO-T as a single daily dose, on an empty stomach, one-half to one hour before breakfast.
Administer LEVO-T at least 4 hours before or after drugs known to interfere with LEVO-T absorption
[see Drug Interactions (7.1)].Evaluate the need for dose adjustments when regularly administering within one hour of certain foods that may affect LEVO-T absorption
[see Drug Interactions (7.9)andClinical Pharmacology (12.3)].Administer LEVO-T to infants and children who cannot swallow intact tablets by crushing the tablet, suspending the freshly crushed tablet in a small amount (5 to 10 mL or 1 to 2 teaspoons) of water and immediately administering the suspension by spoon or dropper. Do not store the suspension. Do not administer in foods that decrease absorption of LEVO-T, such as soybean-based infant formula
[see Drug Interactions (7.9)]. - Starting dose depends on a variety of factors, including age, body weight, cardiovascular status, and concomitant medications. Peak therapeutic effect may not be attained for 4-6 weeks. ( )
2.2 General Principles of DosingThe dose of LEVO-T for hypothyroidism or pituitary TSH suppression depends on a variety of factors including: the patient's age, body weight, cardiovascular status, concomitant medical conditions (including pregnancy), concomitant medications, co-administered food and the specific nature of the condition being treated
[see Dosage and Administration (2.3), Warnings and Precautions (5), andDrug Interactions (7)]. Dosing must be individualized to account for these factors and dose adjustments made based on periodic assessment of the patient's clinical response and laboratory parameters[see Dosage and Administration (2.4)].The peak therapeutic effect of a given dose of LEVO-T may not be attained for 4 to 6 weeks.
- See full prescribing information for dosing in specific patient populations. ( )
2.3 Dosing in Specific Patient PopulationsPrimary Hypothyroidism in Adults and in Adolescents in Whom Growth and Puberty are CompleteStart LEVO-T at the full replacement dose in otherwise healthy, non-elderly individuals who have been hypothyroid for only a short time (such as a few months). The average full replacement dose of LEVO-T is approximately 1.6 mcg per kg per day (for example: 100 to 125 mcg per day for a 70 kg adult).
Adjust the dose by 12.5 to 25 mcg increments every 4 to 6 weeks until the patient is clinically euthyroid and the serum TSH returns to normal. Doses greater than 200 mcg per day are seldom required. An inadequate response to daily doses of greater than 300 mcg per day is rare and may indicate poor compliance, malabsorption, drug interactions, or a combination of these factors.
For elderly patients or patients with underlying cardiac disease, start with a dose of 12.5 to 25 mcg per day. Increase the dose every 6 to 8 weeks, as needed until the patient is clinically euthyroid and the serum TSH returns to normal. The full replacement dose of LEVO-T may be less than 1 mcg per kg per day in elderly patients.
In patients with severe longstanding hypothyroidism, start with a dose of 12.5 to 25 mcg per day. Adjust the dose in 12.5 to 25 mcg increments every 2 to 4 weeks until the patient is clinically euthyroid and the serum TSH level is normalized.
Secondary or Tertiary HypothyroidismStart LEVO-T at the full replacement dose in otherwise healthy, non-elderly individuals. Start with a lower dose in elderly patients, patients with underlying cardiovascular disease or patients with severe longstanding hypothyroidism as described above. Serum TSH is not a reliable measure of LEVO-T dose adequacy in patients with secondary or tertiary hypothyroidism and should not be used to monitor therapy. Use the serum free-T4 level to monitor adequacy of therapy in this patient population. Titrate LEVO-T dosing per above instructions until the patient is clinically euthyroid and the serum free-T4 level is restored to the upper half of the normal range.
Pediatric Dosage - Congenital or Acquired HypothyroidismThe recommended daily dose of LEVO-T in pediatric patients with hypothyroidism is based on body weight and changes with age as described in Table 1. Start LEVO-T at the full daily dose in most pediatric patients. Start at a lower starting dose in newborns (0-3 months) at risk for cardiac failure and in children at risk for hyperactivity (see below). Monitor for clinical and laboratory response
[see Dosage and Administration (2.4)].Table 1. LEVO-T Dosing Guidelines for Pediatric Hypothyroidism AGE Daily Dose Per Kg Body Weight 0-3 months 10-15 mcg/kg/day 3-6 months 8-10 mcg/kg/day 6-12 months 6-8 mcg/kg/day 1-5 years 5-6 mcg/kg/day 6-12 years 4-5 mcg/kg/day Greater than 12 years but growth and puberty incomplete 2-3 mcg/kg/day Growth and puberty complete 1.6 mcg/kg/day a - The dose should be adjusted based on clinical response and laboratory parameters [see Dosage and Administration (2.4) and Use in Specific Populations (8.4)] .Newborns (0-3 months) at risk for cardiac failure: Consider a lower starting dose in newborns at risk for cardiac failure. Increase the dose every 4 to 6 weeks as needed based on clinical and laboratory response.Children at risk for hyperactivity: To minimize the risk of hyperactivity in children, start at one-fourth the recommended full replacement dose, and increase on a weekly basis by one-fourth the full recommended replacement dose until the full recommended replacement dose is reached.PregnancyPre-existing Hypothyroidism:LEVO-T dose requirements may increase during pregnancy. Measure serum TSH and free-T4 as soon as pregnancy is confirmed and, at minimum, during each trimester of pregnancy. In patients with primary hypothyroidism, maintain serum TSH in the trimester-specific reference range. For patients with serum TSH above the normal trimester-specific range, increase the dose of LEVO-T by 12.5 to 25 mcg/day and measure TSH every 4 weeks until a stable LEVO-T dose is reached and serum TSH is within the normal trimester-specific range. Reduce LEVO-T dosage to pre-pregnancy levels immediately after delivery and measure serum TSH levels 4 to 8 weeks postpartum to ensure LEVO-T dose is appropriate.New Onset Hypothyroidism: Normalize thyroid function as rapidly as possible. In patients with moderate to severe signs and symptoms of hypothyroidism, start LEVO-T at the full replacement dose (1.6 mcg per kg body weight per day). In patients with mild hypothyroidism (TSH < 10 IU per liter) start LEVO-T at 1.0 mcg per kg body weight per day. Evaluate serum TSH every 4 weeks and adjust LEVO-T dosage until a serum TSH is within the normal trimester specific range[see Use in Specific Populations (8.1)].TSH Suppression in Well-differentiated Thyroid CancerGenerally, TSH is suppressed to below 0.1 IU per liter, and this usually requires a LEVO-T dose of greater than 2 mcg per kg per day. However, in patients with high-risk tumors, the target level for TSH suppression may be lower.
- Adequacy of therapy determined with periodic monitoring of TSH and/or T4 as well as clinical status. ( )
2.4 Monitoring TSH and/or Thyroxine (T4) LevelsAssess the adequacy of therapy by periodic assessment of laboratory tests and clinical evaluation. Persistent clinical and laboratory evidence of hypothyroidism despite an apparent adequate replacement dose of LEVO-T may be evidence of inadequate absorption, poor compliance, drug interactions, or a combination of these factors.
AdultsIn adult patients with primary hypothyroidism, monitor serum TSH levels after an interval of 6 to 8 weeks after any change in dose. In patients on a stable and appropriate replacement dose, evaluate clinical and biochemical response every 6 to 12 months and whenever there is a change in the patient's clinical status.
PediatricsIn patients with congenital hypothyroidism, assess the adequacy of replacement therapy by measuring both serum TSH and total or free-T4. Monitor TSH and total or free-T4 in children as follows: 2 and 4 weeks after the initiation of treatment, 2 weeks after any change in dosage, and then every 3 to 12 months thereafter following dose stabilization until growth is completed. Poor compliance or abnormal values may necessitate more frequent monitoring. Perform routine clinical examination, including assessment of development, mental and physical growth, and bone maturation, at regular intervals.
While the general aim of therapy is to normalize the serum TSH level, TSH may not normalize in some patients due to in utero hypothyroidism causing a resetting of pituitary-thyroid feedback. Failure of the serum T4 to increase into the upper half of the normal range within 2 weeks of initiation of LEVO-T therapy and/or of the serum TSH to decrease below 20 IU per liter within 4 weeks may indicate the child is not receiving adequate therapy. Assess compliance, dose of medication administered, and method of administration prior to increasing the dose of LEVO-T
[see Warnings and Precautions (5.1)andUse in Specific Populations (8.4)].Secondary and Tertiary HypothyroidismMonitor serum free-T4 levels and maintain in the upper half of the normal range in these patients.
LEVO-T tablets are available as follows:
| Tablet Strength | Tablet Color/Shape | Tablet Markings |
|---|---|---|
| 25 mcg | Orange/Caplet | "25" and "GG/331" |
| 50 mcg | White/ Caplet | "50" and "GG/332" |
| 75 mcg | Violet/ Caplet | "75" and "GG/333" |
| 88 mcg | Olive Green/ Caplet | "88" and "GG/334" |
| 100 mcg | Yellow/ Caplet | "100" and "GG/335" |
| 112 mcg | Rose/ Caplet | "112" and "GG/336" |
| 125 mcg | Brown/ Caplet | "125" and "GG/337" |
| 137 mcg | Turquoise/ Caplet | "137" and "GG/330" |
| 150 mcg | Blue/ Caplet | "150" and "GG/338" |
| 175 mcg | Lilac/ Caplet | "175" and "GG/339" |
| 200 mcg | Pink/ Caplet | "200" and "GG/340" |
| 300 mcg | Green/ Caplet | "300" and "GG/341" |
Pregnancy may require the use of higher doses of LEVO-T. (
2.3 Dosing in Specific Patient PopulationsStart LEVO-T at the full replacement dose in otherwise healthy, non-elderly individuals who have been hypothyroid for only a short time (such as a few months). The average full replacement dose of LEVO-T is approximately 1.6 mcg per kg per day (for example: 100 to 125 mcg per day for a 70 kg adult).
Adjust the dose by 12.5 to 25 mcg increments every 4 to 6 weeks until the patient is clinically euthyroid and the serum TSH returns to normal. Doses greater than 200 mcg per day are seldom required. An inadequate response to daily doses of greater than 300 mcg per day is rare and may indicate poor compliance, malabsorption, drug interactions, or a combination of these factors.
For elderly patients or patients with underlying cardiac disease, start with a dose of 12.5 to 25 mcg per day. Increase the dose every 6 to 8 weeks, as needed until the patient is clinically euthyroid and the serum TSH returns to normal. The full replacement dose of LEVO-T may be less than 1 mcg per kg per day in elderly patients.
In patients with severe longstanding hypothyroidism, start with a dose of 12.5 to 25 mcg per day. Adjust the dose in 12.5 to 25 mcg increments every 2 to 4 weeks until the patient is clinically euthyroid and the serum TSH level is normalized.
Start LEVO-T at the full replacement dose in otherwise healthy, non-elderly individuals. Start with a lower dose in elderly patients, patients with underlying cardiovascular disease or patients with severe longstanding hypothyroidism as described above. Serum TSH is not a reliable measure of LEVO-T dose adequacy in patients with secondary or tertiary hypothyroidism and should not be used to monitor therapy. Use the serum free-T4 level to monitor adequacy of therapy in this patient population. Titrate LEVO-T dosing per above instructions until the patient is clinically euthyroid and the serum free-T4 level is restored to the upper half of the normal range.
The recommended daily dose of LEVO-T in pediatric patients with hypothyroidism is based on body weight and changes with age as described in Table 1. Start LEVO-T at the full daily dose in most pediatric patients. Start at a lower starting dose in newborns (0-3 months) at risk for cardiac failure and in children at risk for hyperactivity (see below). Monitor for clinical and laboratory response
| AGE | Daily Dose Per Kg Body Weight |
|---|---|
| 0-3 months | 10-15 mcg/kg/day |
| 3-6 months | 8-10 mcg/kg/day |
| 6-12 months | 6-8 mcg/kg/day |
| 1-5 years | 5-6 mcg/kg/day |
| 6-12 years | 4-5 mcg/kg/day |
| Greater than 12 years but growth and puberty incomplete | 2-3 mcg/kg/day |
| Growth and puberty complete | 1.6 mcg/kg/day |
| a - The dose should be adjusted based on clinical response and laboratory parameters [see Dosage and Administration (2.4) and Use in Specific Populations (8.4)] . | |
Generally, TSH is suppressed to below 0.1 IU per liter, and this usually requires a LEVO-T dose of greater than 2 mcg per kg per day. However, in patients with high-risk tumors, the target level for TSH suppression may be lower.
8.1 PregnancyRisk Summary
Experience with levothyroxine use in pregnant women, including data from post-marketing studies, have not reported increased rates of major birth defects or miscarriages
The estimated background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.
Clinical Considerations
Maternal hypothyroidism during pregnancy is associated with a higher rate of complications, including spontaneous abortion, gestational hypertension, pre-eclampsia, stillbirth, and premature delivery. Untreated maternal hypothyroidism may have an adverse effect on fetal neurocognitive development.
Pregnancy may increase LEVO-T requirements. Serum TSH levels should be monitored and the LEVO-T dosage adjusted during pregnancy. Since postpartum TSH levels are similar to preconception values, the LEVO-T dosage should return to the pre-pregnancy dose immediately after delivery
Data
Levothyroxine is approved for use as a replacement therapy for hypothyroidism. There is a long experience of levothyroxine use in pregnant women, including data from post-marketing studies that have not reported increased rates of fetal malformations, miscarriages or other adverse maternal or fetal outcomes associated with levothyroxine use in pregnant women.
LEVO-T is contraindicated in patients with uncorrected adrenal insufficiency
5.3 Acute Adrenal Crisis in Patients with Concomitant Adrenal InsufficiencyThyroid hormone increases metabolic clearance of glucocorticoids. Initiation of thyroid hormone therapy prior to initiating glucocorticoid therapy may precipitate an acute adrenal crisis in patients with adrenal insufficiency. Treat patients with adrenal insufficiency with replacement glucocorticoids prior to initiating treatment with LEVO-T