Specialty medicines • Bangladesh

LuciSemag 3 MG & 7 MG & 14 MG (Semaglutide)

LuciSemag — Semaglutide. Manufactured by Lucius Pharmaceuticals (Lao) Co., Ltd.

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Description

Semaglutide

Each film-coated tablet contains: Semaglutide … 3mg.

INDICATIONS

LuciSemag is a glucagon-like peptide-1 (GLP- 1) Receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in a dults with type 2 diabetes mellitus. Limitations of Use • Has not been studied in patients with a history of pancreatitis. • Not for treatment of type 1 diabetes mellitus.

DOSAGE AND USE

• Instruct patients to take LuciSemag at least 30 minutes before the first food, beverage, or other oral medications of the day with no more than 4 ounces of plain water only. Waiting less than 3 0 minutes, or taking with food, beverages (other than plain wa ter) or other oral medications will lessen the effect of LuciSemag. Waiting more than 30 minutes to eat may increase the absorptio n of LuciSemag. • Swallow tablets whole. Do not split, crush, or chew tablets. • Start LuciSemag with 3 mg once daily for 30 days. After 30 days on the 3 mg dosage, increase the dosage to 7 mg once daily. • Dosage may be increased to 14 mg once daily if additional glycemic control is needed after at least 30 days on the 7 mg dosage.

STORAGE

In a dry place and store at 20°C to 25°C.

MANUFACTURED AND MARKETED BY

LUCIUS PHARMACEUTICALS(LAO) CO., LTD No.26, Thongmang village, Xaythany district, Vientiane Capital, Laos

WARNINGS

• Pancreatitis: Has been reported in clinical trials. Discontinue promptly if pancreatitis is suspected. Do not restart if pancreatitis is confirmed. • Hypoglycemia: Concomitant use with an insulin secretagogue or insulin may increase the risk of hypoglycemia, including severe hypoglycemia. Reducing the dose of insulin secretagogue or insulin may be necessary. • Acute Kidney Injury: Monitor renal function in patients with renal impairment reporting severe adverse gastrointestinal reactions. • Hypersensitivity Reactions: Serious hypersensitivity reactions (e.g., anaphylaxis and angioedema) have been reported. Discontinue LuciSemag if suspected and promptly seek medical advice. • Acute Gallbladder Disease: If cholelithiasis or cholecystitis are suspected, gallbladder studies are indicated.

Semaglutide

Each film-coated tablet contains: Semaglutide … 7mg.

INDICATIONS

LuciSemag is a glucagon-like peptide-1 (GLP- 1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in a dults with type 2 diabetes mellitus. Limitations of Use •Has not been studied in patients with a history of pancreatitis. •Not for treatment of type 1 diabetes mellitus.

DOSAGE AND USE

• Instruct patients to take LuciSemag at least 30 minutes before the first food, beverage, or other oral medications of the day with no more than 4 ounces of plain water only. Waiting less than 3 0 minutes, or taking with food, beverages (other than plain wa ter) or other oral medications will lessen the effect of LuciSemag. Waiting more than 30 minutes to eat may increase the absorptio n of LuciSemag. • Swallow tablets whole. Do not split, crush, or chew tablets . • Start LuciSemag with 3 mg once daily for 30 days. After 30 days on the 3 mg dosage, increase t he dosage to 7 mg once daily. • Dosage may be increased to 14 mg once daily if additional glycemic control is needed after at l east 30 days on the 7 mg dosage.

STORAGE

In a dry place and store at 20°C to 25°C.

MANUFACTURED AND MARKETED BY

LUCIUS PHARMACEUTICALS(LAO) CO., LTD No.26, Thongmang village, Xaythany district, Vientiane Capital, Laos

WARNINGS

• Pancreatitis: Has been reported in clinical trials. Discontinue promptly if pancreatitis is suspected. Do not restart if pancreatitis is confirmed. • Hypoglycemia: Concomitant use with an insulin secretagogue or insulin may increase the risk of hypoglycemia, including severe hypoglycemia. Reducing dose of insulin secretagogue or insulin may be necessary. • Acute Kidney Injury: Monitor renal function in patients with renal impairment reporting severe adverse gastrointestinal reactions. • Hypersensitivity Reactions: Serious hypersensitivity reactions (e.g., anaphylaxis and angioedema) have been reported. Discontinue LuciSemag if suspected and promptly seek medical advice. • Acute Gallbladder Disease: If cholelithiasis or cholecystitis are suspected, gallbladder studies are indicated.

Semaglutide

Each film-coated tablet contains: Semaglutide … 14mg.

INDICATIONS

LuciSemag is a glucagon-like peptide-1 (GLP- 1) receptor agonist indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. Limitations of Use •Has not been studied in patients with a history of pancreatitis. •Not for treatment of type 1 diabetes mellitus.

DOSAGE AND USE

• Instruct patients to take LuciSemag at least 30 minutes before the first food, beverage, or other oral medications of the day with no more than 4 ounces of plain water only. Waiting less than 3 0 minutes, or taking with food, beverages (other than plain wa ter) or other oral medications will lessen the effect of LuciSemag. Waiting more than 30 minutes to eat may increase the absorption of LuciSemag. • Swallow tablets whole. Do not split, crush, or chew tablets. • Start LuciSemag with 3 mg once daily for 30 days. After 30 days on the 3 mg dosage, increase the dosage to 7 mg once daily. • Dosage may be increased to 14 mg once daily if additional glycemic control is needed after at least 30 days on the 7 mg dosage.

STORAGE

In a dry place and store at 20°C to 25°C.

MANUFACTURED AND MARKETED BY

LUCIUS PHARMACEUTICALS(LAO) CO., LTD No.26, Thongmang village, Xaythany district, Vientiane Capital, Laos

WARNINGS

• Pancreatitis: Has been reported in clinical trials. Discontinue promptly if pancreatitis is suspected. Do not restart if pancreatitis is confirmed. • Hypoglycemia: Concomitant use with an insulin secretagogue or insulin may increase the risk of hypoglycemia, including severe hypoglycemia. Reducing dose of insulin secretagogue or insulin may be necessary. • Acute Kidney Injury: Monitor renal function in patients with renal impairment reporting severe adverse gastrointestinal reactions. • Hypersensitivity Reactions: Serious hypersensitivity reactions (e.g., anaphylaxis and angioedema) have been reported. Discontinue LuciSemag if suspected and promptly seek medical advice. Acute Gallbladder Disease: If cholelithiasis or cholecystitis are suspected, gallbladder studies are indicated.

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