"Metformin hydrochloride 

Metformin hydrochloride 
SEIZMET is the chemical name for the active ingredient in the medication commonly known as metformin. SEIZMET is an oral antidiabetic medication used in the management of type 2 diabetes mellitus.
SEIZMET works primarily by reducing the production of glucose in the liver and improving insulin sensitivity in peripheral tissues. SEIZMET helps lower blood sugar levels by reducing the amount of glucose released into the bloodstream and enhancing the uptake of glucose by the cells.
SEIZMET is available in various forms, including immediate-release tablets, extended-release tablets, and oral solutions. SEIZMET choice of formulation depends on factors such as the individual's specific needs, response to treatment, and the prescribing physician's recommendation.
SEIZMET is typically taken two to three times daily with meals. The dosage is adjusted based on the individual's blood sugar levels and response to treatment. SEIZMET is often prescribed as part of a comprehensive treatment plan that includes diet and exercise.
Common side effects of SEIZMET may include gastrointestinal symptoms such as nausea, diarrhea, and abdominal discomfort. These side effects are usually mild and transient. In rare cases, SEIZMET can cause a serious side effect called lactic acidosis, which requires immediate medical attention.
Steris deals in Generic medicine refers to a medication that contains the same active ingredient(s), dosage form, strength, route of administration, and intended use as a brand-name drug. However, it is typically sold under its chemical or active ingredient name, rather than a specific brand name.
Here are some key points about generic medicines:
Active Ingredient: Generic medicines have the same active ingredient(s) as their brand-name counterparts. The active ingredient is the specific chemical component responsible for the therapeutic effect of the medication.
Bioequivalence: Generic medicines must demonstrate bioequivalence to the brand-name drug. This means that they must have similar pharmacokinetic properties, such as the rate and extent of absorption, in the body. Regulatory authorities set specific criteria for bioequivalence to ensure that generic medicines perform similarly to the brand-name drugs.
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