
MBBS

MBBS, DNB (OBGY)
Semaglutide is available in different forms, including subcutaneous injection (pre-filled pen) and oral tablets.
Semaglutide is primarily approved for adults. Certain formulations for weight management may be used in adolescents ≥12 years in specific indications and countries.
Semaglutide is contraindicated in patients with known hypersensitivity to Semaglutide. It should not be used in patients with a personal or family history of medullary thyroid carcinoma or in patients with multiple endocrine neoplasia syndrome type 2. It is also contraindicated in patients with a history of serious hypersensitivity reactions to GLP-1 receptor agonists.
Semaglutide may interact with insulin and insulin secretagogues (e.g., sulfonylureas), hormone replacement therapy (e.g., levothyroxine), anticoagulants (warfarin), diuretics (e.g., furosemide), and corticosteroids (e.g., prednisolone). Before using any prescription or over-the-counter medicines, you must talk to your doctor first.
Semaglutide does not usually affect the ability to drive or operate machinery. However, caution is advised when used with other antidiabetic medicines due to the risk of hypoglycaemia.
Semaglutide is not recommended during pregnancy and breastfeeding.
Frequently asked questions
Semaglutide begins to lower blood glucose levels within the first week of initiation, although full therapeutic effects may take several weeks as the dose is gradually increased.
Avoid using Semaglutide if you have a history of medullary thyroid carcinoma or multiple endocrine neoplasia syndrome type 2. Monitor for symptoms of pancreatitis such as severe abdominal pain. Regular follow-up is recommended to assess glycaemic control and tolerance.
Do not discontinue Semaglutide without consulting your doctor. Stopping treatment may lead to loss of glycaemic control or weight regain.
Patients with kidney or liver impairment should use Semaglutide with caution and under medical supervision, as dose adjustments or monitoring may be required.







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