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Insuget N is a human insulin isophane suspension (NPH insulin) used for the treatment of diabetes mellitus. It is an intermediate-acting insulin designed to control blood glucose levels by promoting glucose uptake in tissues and inhibiting glucose production in the liver. It is supplied in a 10 ml multi-dose vial for subcutaneous injection.
Active Ingredient: Human Insulin Isophane (NPH Insulin) – 100 IU/ml
Excipients: Zinc chloride, glycerol, phenol or m-cresol (preservative), protamine sulfate, sodium phosphate buffer, water for injection (may vary by manufacturer).
Intermediate-acting insulin
Antidiabetic agent
Injectable suspension in 10 ml vial (multi-dose)
Strength: 100 IU/ml
Treatment of diabetes mellitus (Type 1 and Type 2) when insulin therapy is required
Provides basal glycemic control (covers glucose needs between meals and during the night)
May be used in combination with short-acting insulins or oral antidiabetic drugs for better control
Individualized based on blood glucose monitoring, diet, and physician’s guidance
Typical starting total daily insulin dose: 0.2 – 0.6 IU/kg body weight/day (combined regimen)
Insuget N is often administered once or twice daily via subcutaneous injection
Should not be administered intravenously
Overdose can lead to severe hypoglycemia with symptoms such as sweating, tremor, confusion, palpitations, seizures, or loss of consciousness
Immediate management:
Give fast-acting carbohydrate orally if the patient is conscious
If unconscious: administer glucagon injection or IV glucose
Continuous monitoring until recovery
If a dose is missed, monitor blood glucose and take corrective action per doctor’s advice
Never double the next dose to compensate, as this may cause hypoglycemia
Roll the vial gently between palms before use (do not shake vigorously).
Inspect suspension; it should appear uniformly cloudy/white after mixing.
Inject subcutaneously (abdomen, thigh, upper arm, or buttock); rotate injection sites to avoid lipodystrophy.
Do not inject into a vein or muscle unless specifically advised.
Use sterile syringes and needles; do not share.
Known hypersensitivity to human insulin or formulation components
During episodes of hypoglycemia
IV administration is contraindicated
Common:
Injection site reactions (pain, redness, swelling)
Hypoglycemia (most frequent adverse effect)
Less common / serious:
Lipodystrophy at injection sites
Allergic reactions (rash, itching, swelling)
Rare systemic allergic reactions including anaphylaxis
Monitor blood glucose regularly; adjust dose with changes in diet, activity, or illness
Use with caution in patients with renal or hepatic impairment
Avoid alcohol intake (may worsen hypoglycemia)
Pregnancy & lactation: insulin requirements may change; medical supervision required
Carry glucose tablets or sugar in case of hypoglycemia
Increased hypoglycemic effect: oral antidiabetic drugs, ACE inhibitors, beta-blockers, MAO inhibitors, sulfonamides, alcohol
Decreased effect: corticosteroids, diuretics, thyroid hormones, oral contraceptives, sympathomimetics
Beta-blockers may mask hypoglycemia symptoms (e.g., rapid heartbeat)
Store at 2°C – 8°C (refrigerated); do not freeze
Protect from direct heat and light
Once in use, may be kept at room temperature (<25°C) for up to 28 days (follow label instructions)
Discard vial after 28 days of opening or if suspension looks abnormal
Dispose of needles/syringes in sharps container
Prescription only medicine
Must be used under the supervision of a healthcare professional
Always check vial appearance before use; insulin should look evenly cloudy when mixed
Rotate injection sites to prevent skin complications
Keep a blood glucose monitoring diary and carry emergency sugar at all times
Do not stop insulin suddenly without medical advice
Inform doctor before surgery, illness, or changes in diet/exercise
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