Levothyroxine sodium
Levothyroxine, the active substance of Levothyroxine Accord, is a synthetic thyroid hormone intended for the treatment of thyroid diseases and disorders. It has the same effect as the thyroid hormones that occur naturally in the body. Levothyroxine Accord is used:
Levothyroxine Accord 25 micrograms, 50 micrograms, 75 micrograms, 88 micrograms, and 100 micrograms are also used to adjust thyroid hormone levels in patients who are taking antithyroid drugs due to excessive thyroid hormone production. Levothyroxine Accord 100 micrograms, 150 micrograms, and 200 micrograms may also be used in tests to assess thyroid function. Levothyroxine Accord, 12.5 micrograms:
Levothyroxine Accord should not be used in combination with antithyroid drugs if the patient is pregnant (see "Pregnancy and breastfeeding" below).
Before starting treatment with Levothyroxine Accord, inform your doctor about the presence of any of the following heart diseases:
Treatment of these disorders is necessary before starting treatment with Levothyroxine Accord and before performing a thyroid suppression test. During treatment with Levothyroxine Accord, it is necessary to frequently monitor thyroid hormone levels. In case of doubts about the presence of any of the above diseases or if they are not treated, you should consult a doctor. The doctor will perform the necessary tests to determine if the patient has adrenal or pituitary disorders or a certain type of thyroid disorder with uncontrolled excessive thyroid hormone production (autonomous thyroid function), as in such cases, appropriate treatment may be necessary before starting treatment with Levothyroxine Accord and before performing a thyroid suppression test. After starting levothyroxine treatment in premature infants with very low birth weight, it is necessary to regularly monitor blood pressure, as a sudden drop in blood pressure (called circulatory collapse) may occur. If it is necessary to change the medicine to another levothyroxine-containing medicine, a disruption of thyroid hormone balance may occur. You should consult a doctor if you have any questions about changing medicines. During the transition period, close monitoring of clinical and biochemical parameters is necessary. You should inform your doctor if you experience any side effects, as it may be necessary to increase or decrease the dose.
Tell your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take, as Levothyroxine Accord may affect the action of these medicines:
It is necessary to ensure that the recommended time intervals are followed if you are taking any of the following medicines:
These medicines may weaken the action of Levothyroxine Accord, so you should inform your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take:
These medicines may enhance the action of Levothyroxine Accord, so you should inform your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take:
These medicines may affect the action of Levothyroxine Accord, so you should inform your doctor or pharmacist about all medicines you are taking or have recently taken, as well as any medicines you plan to take:
In this situation, it may be necessary to regularly perform thyroid hormone tests and change the dose of the medicine. If you are taking amiodarone (a medicine used to treat heart rhythm disorders), you should inform your doctor, as this medicine may affect thyroid function. You should inform your doctor about taking Levothyroxine Accord if it is necessary to undergo a diagnostic or imaging test with a contrast agent containing iodine, as this test involves the administration of an injection that affects thyroid function. You should inform your doctor or pharmacist about all medicines you are taking or have recently taken, including those that are available without a prescription. Thyroid hormones should not be used to lose weight. Taking them will not cause weight loss if thyroid hormones are at the proper level. Increasing the dose without consulting a doctor may lead to serious and life-threatening side effects, especially when taking other weight loss medicines. If you are currently taking or have recently taken biotin, you must inform your doctor or laboratory staff if you are to undergo thyroid hormone laboratory tests. Biotin may affect laboratory test results (see "Warnings and precautions").
If your diet includes soy products, you should inform your doctor, especially if you change the amount of these products you consume. Soy products may reduce the absorption of Levothyroxine Accord from the gut, and it may be necessary to modify the dose of Levothyroxine Accord accordingly.
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine. Adequate amounts of thyroid hormone are necessary for the proper course of pregnancy. Therefore, during pregnancy, you should continue taking Levothyroxine Accord. During pregnancy, you should not take Levothyroxine Accord if you are taking antithyroid drugs (medicines used to treat excessive thyroid hormone levels). If necessary, your doctor may adjust the dose. If you become pregnant, you should contact your doctor. There is no evidence to suggest that Levothyroxine Accord is harmful to the baby if the mother is breastfeeding and has normal thyroid function. You should not take Levothyroxine Accord if you are breastfeeding and taking antithyroid drugs (medicines used to treat hyperthyroidism).
Levothyroxine sodium should not affect your ability to drive or use machines.
This medicine contains less than 1 mmol (23 mg) of sodium per tablet, which means it is essentially "sodium-free". The 25 microgram tablet contains orange yellow S (E 110), which may cause allergic reactions. The 75 microgram tablet contains indigo carmine (E 132) and Allura red AC (E 129), which may cause allergic reactions. The 88 microgram tablet contains tartrazine (E 102), which may cause allergic reactions. The 100 microgram tablet contains tartrazine (E 102) and orange yellow S (E 110), which may cause allergic reactions. The 125 microgram tablet contains orange yellow S (E 110) and Allura red AC (E 129), which may cause allergic reactions.
Always take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, ask your doctor or pharmacist. Your doctor will determine the appropriate dose for each patient individually based on clinical evaluation and laboratory tests. Treatment usually starts with a small dose, which is increased every 2 to 4 weeks until the full dose, adjusted individually for each patient, is reached. In the first weeks of treatment, laboratory tests will be necessary to allow the doctor to adjust the appropriate dose. If a child is born with a thyroid disease that involves insufficient production of thyroid hormones, it is essential to supplement them quickly. Therefore, the doctor may recommend a higher initial dose of 10 to 15 micrograms per kilogram of body weight per day for the first 3 months. Then, the doctor will adjust the dose individually. Typical dose ranges are shown in the table below. Smaller, individually adjusted doses may be sufficient for:
Administration of Levothyroxine Accord | Recommended daily dose of Levothyroxine Accord | |
Treatment of mild goiter in patients with normal thyroid function |
| |
Prevention of goiter recurrence after surgery |
| |
Supplementation of lack of natural thyroid hormones when their production by the thyroid gland is insufficient
| Adults
| Children and adolescents 12.5 – 50 micrograms
|
Inhibition of tumor growth in patients with thyroid cancer |
| |
Adjustment of thyroid hormone levels during treatment of excessive thyroid hormone production with antithyroid drugs |
| |
In tests to assess thyroid function | Levothyroxine Accord, 100 micrograms: Start 2 weeks before the test – 200 micrograms (2 tablets) Levothyroxine Accord, 150 micrograms: Start 4 weeks before the test – 75 micrograms (½ tablet) for 2 weeks, and then 150 micrograms (1 tablet) until the test Levothyroxine Accord, 200 micrograms: Start 2 weeks before the test – 200 micrograms (1 tablet) |
Method of administration
Levothyroxine Accord is intended for oral use.
The single daily dose should be taken in the morning, on an empty stomach (at least half an hour before breakfast), preferably with a small amount of liquid, e.g., half a glass of water.
Infants should be given the entire daily dose of Levothyroxine Accord at one time, at least half an hour before the first meal of the day. Immediately before administration, the tablet should be crushed and mixed with a small amount of water, and the resulting suspension, which should be prepared freshly each time, should be given with a small additional amount of liquid.
Duration of treatment
The duration of treatment may vary depending on the reason for taking Levothyroxine Accord. Your doctor will discuss with you individually how long you should take the medicine. Most patients need to take Levothyroxine Accord for the rest of their lives.
If you take a higher dose than recommended, you may experience symptoms such as rapid heartbeat, nervousness, agitation, or involuntary movements. In patients with neurological disorders, such as epilepsy, single seizures have been observed. In patients with psychotic disorders, symptoms of acute psychosis may occur. In such cases, you should consult a doctor.
Do not take a double dose of the medicine to make up for a missed dose. The next day, take the usual dose of the medicine. If you have any doubts about taking Levothyroxine Accord, consult your doctor or pharmacist.
Like all medicines, Levothyroxine Accord can cause side effects, although not everybody gets them. All medicines can cause allergic reactions, but severe allergic reactions are rare. If you experience sudden symptoms such as wheezing, difficulty breathing, swelling of the eyelids, face, or lips, rash, and itching (especially all over the body), you should contact your doctor immediately. If you experience poor tolerance to the recommended dose or take a higher dose of Levothyroxine Accord than recommended, you may experience symptoms similar to hyperthyroidism, especially if the dose is increased too quickly at the beginning of treatment. The following side effects have been observed (frequency not known):
If you experience any of the above symptoms, you should contact your doctor. The symptoms usually disappear after changing the dose.
If you experience any side effects, including those not listed in this package leaflet, you should inform your doctor, pharmacist, or nurse. You can report side effects directly to the Department of Drug Safety Monitoring of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel: +48 22 49 21 301, Fax: +48 22 49 21 309, website: https://smz.ezdrowie.gov.pl. You can also report side effects to the marketing authorization holder. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children. Do not use Levothyroxine Accord after the expiry date stated on the blister, bottle, and carton after EXP. The expiry date refers to the last day of the month stated. Store below 25°C. HDPE bottle: discard 180 days after first opening. Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
The active substance of Levothyroxine Accord is levothyroxine sodium. Each tablet contains 12.5 micrograms, 25 micrograms, 50 micrograms, 75 micrograms, 88 micrograms, 100 micrograms, 112 micrograms, 125 micrograms, 137 micrograms, 150 micrograms, 175 micrograms, or 200 micrograms of levothyroxine sodium. The other ingredients are microcrystalline cellulose, microcrystalline cellulose (type 112), light magnesium oxide, sodium carboxymethylcellulose (type A), sodium stearyl fumarate. The 25 microgram tablet contains orange yellow S (E 110), aluminum lake. The 75 microgram tablet contains indigo carmine (E 132), aluminum lake, and Allura red AC (E 129), aluminum lake. The 88 microgram tablet contains tartrazine (E 102), aluminum lake, and indigo carmine (E 132), aluminum lake. The 100 microgram tablet contains tartrazine (E 102), aluminum lake, and orange yellow S (E 110), aluminum lake. The 125 microgram tablet contains orange yellow S (E 110), aluminum lake, and Allura red AC (E 129), aluminum lake.
12.5 micrograms
Round, flat, uncoated white tablets with "P" and "13" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm.
25 micrograms
Round, flat, uncoated orange tablets with a score line on both sides and "P" and "1" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
50 micrograms
Round, flat, uncoated white tablets with a score line on both sides and "P" and "2" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
75 micrograms
Round, flat, uncoated purple tablets with a score line on both sides and "P" and "3" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
88 micrograms
Round, flat, uncoated green tablets with a score line on both sides and "P" and "4" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
100 micrograms
Round, flat, uncoated yellow tablets with a score line on both sides and "P" and "14" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
112 micrograms
Round, flat, uncoated pink tablets with a score line on both sides and "P" and "6" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
125 micrograms
Round, flat, uncoated brown tablets with a score line on both sides and "P" and "7" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
137 micrograms
Round, flat, uncoated turquoise tablets with a score line on both sides and "P" and "8" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
150 micrograms
Round, flat, uncoated blue tablets with a score line on both sides and "P" and "9" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
175 micrograms
Round, flat, uncoated lilac tablets with a score line on both sides and "P" and "10" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
200 micrograms
Round, flat, uncoated pink tablets with a score line on both sides and "P" and "11" embossed on one side and smooth on the other. The diameter of the tablet is approximately 7 mm. The tablet can be divided into equal doses.
12.5 micrograms
Orange-colored blister pack of PVC/EVOH/Aclar/Aluminum containing 10, 50, 100, or 200 tablets in a carton.
25/50/100 micrograms
Orange-colored blister pack of PVC/EVOH/Aclar/Aluminum containing 10, 30, 50, 56, 90, 100, or 200 tablets in a carton.
75/88/112/125/137/150/175/200 micrograms
Orange-colored blister pack of PVC/EVOH/Aclar/Aluminum containing 10, 30, 50, 90, 100, or 200 tablets in a carton.
25/50/75/88/100/112/125/137/150/175/200 micrograms
White HDPE bottle with a white, non-transparent polypropylene child-resistant closure with an induction seal, containing 90 tablets. Not all pack sizes may be marketed.
Accord Healthcare Polska Sp. z o.o.
ul. Taśmowa 7
02-677 Warsaw
Tel: +48 22 577 28 00
LABORATORI FUNDACIÓ DAU
C/C, 12-14 Pol. Ind. Zona Franca
08040 Barcelona
Spain
Accord Healthcare Polska Sp. z o.o.
ul. Lutomierska 50
96-200 Pabianice
Netherlands
Levothyroxine Accord 12.5/25/50/75/88/100/112/125/137/150/175/200 microgram tablets
Austria
Levothyroxin natrium Accord 12.5/25/50/75/88/100/112/125/137/150/175/200 micrograms tablets
Estonia
Levothyroxine Accord
Latvia
Levothyroxine Accord 12.5/25/50/75/88/100/112/125/137/150/175/200 micrograms tablets
Lithuania
Levothyroxine Accord 12.5/25/50/75/88/100/112/125/137/150/175/200 micrograms tablets
Poland
Levothyroxine Accord
Cyprus
Levothyroxine Accord 25/50/100 microgram tablets
Greece
Levothyroxine/Accord
Date of last revision of the package leaflet: November 2024
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