What is ACTRAPID HM PENFILL 100 Units/ml
ACTRAPID HM PENFILL 100 Units/ml is a fast-acting human soluble insulin preparation provided in 3ml cartridges compatible with insulin pen devices. It is designed to help individuals with diabetes mellitus manage their blood glucose levels effectively. Being a biosynthetic human insulin, it has the same amino acid sequence as naturally occurring insulin in the human body, ensuring predictable pharmacological effects and minimizing allergic reactions compared to animal-derived insulins.
This medication is particularly useful in controlling postprandial blood sugar spikes, making it suitable for use before meals. It is widely used in both type 1 diabetes (where the body produces little or no insulin) and type 2 diabetes (where the body’s insulin production or effectiveness is impaired). The penfill format offers convenience, dose accuracy, and portability, enhancing patient adherence to insulin therapy.
- Formulation: Human soluble insulin in a 3ml cartridge for pen injectors.
- Indications: Management of type 1 and type 2 diabetes mellitus requiring rapid-acting insulin.
- Pharmacological class: Short-acting insulin analogue.
- Administration: Subcutaneous injection using insulin pens.
- Benefits: Precise dosing, ease of use, and rapid onset of action.
How to use ACTRAPID HM PENFILL 100 Units/ml
Proper use of ACTRAPID HM PENFILL is vital to maintain optimal glycemic control and minimize adverse effects.
- Device compatibility: Use only with compatible insulin pen devices designed for 3ml cartridges.
- Injection technique: Inject subcutaneously into the abdomen, thigh, or upper arm. Rotate injection sites regularly to prevent lipodystrophy.
- Timing: Administer approximately 30 minutes before meals to align insulin action with food absorption.
- Preparing the pen: Before each injection, check that insulin appears clear and colorless. Do not use if cloudy or discolored.
- Dose setting: Turn the dose selector on the pen to the prescribed units.
- Injection: Insert the needle fully, press the injection button, and hold for 5-10 seconds to ensure full dose delivery.
- Needle disposal: Use a new sterile needle for every injection and dispose of used needles in appropriate sharps containers.
- Monitoring: Regular blood glucose monitoring is essential to adjust doses and avoid hypo- or hyperglycemia.
Mode of Action ACTRAPID HM PENFILL 100 Units/ml
ACTRAPID HM PENFILL contains human soluble insulin, which acts to regulate blood glucose by facilitating cellular glucose uptake and metabolism.
- Receptor binding: Insulin binds to insulin receptors on muscle, fat, and liver cells, activating intracellular signaling cascades.
- Glucose uptake: Promotes translocation of glucose transporter proteins (GLUT4) to the cell surface, increasing glucose entry into cells.
- Glycogen synthesis: Stimulates conversion of glucose into glycogen in the liver and muscle for storage.
- Inhibits glucose production: Suppresses hepatic gluconeogenesis and glycogenolysis, reducing glucose release into the bloodstream.
- Lipid metabolism: Promotes lipogenesis and inhibits lipolysis, impacting energy storage and utilization.
- Protein metabolism: Enhances amino acid uptake and protein synthesis, preventing muscle breakdown.
- Pharmacokinetics: Rapid onset within 30 minutes, peak activity between 1 to 3 hours, duration of action approximately 6 to 8 hours.
ACTRAPID HM PENFILL 100 Units/ml Interactions ACTRAPID HM PENFILL 100 Units/ml
ACTRAPID HM PENFILL’s effects on blood glucose can be altered by concomitant medications, necessitating close monitoring and possible dose adjustments.
- Beta-blockers: May mask hypoglycemia symptoms like tremors and palpitations and reduce insulin sensitivity.
- Corticosteroids and thyroid hormones: Often increase blood glucose levels, requiring increased insulin doses.
- Diuretics: Some, especially thiazides and loop diuretics, can impair glucose tolerance.
- Alcohol: Can potentiate hypoglycemic effects or cause delayed hypoglycemia, especially with irregular intake.
- ACE inhibitors: May improve insulin sensitivity, lowering insulin requirements.
- Salicylates and anabolic steroids: Can potentiate insulin’s hypoglycemic effect.
- Sympathomimetics and calcium channel blockers: May cause variable effects on glucose metabolism.
Patients should inform healthcare providers about all medications to optimize insulin therapy safely.
Dosage of ACTRAPID HM PENFILL 100 Units/ml
The dosage of ACTRAPID HM PENFILL is individualized according to the patient's metabolic needs, lifestyle, and blood glucose monitoring results.
- Initial dosing: Usually 0.5 to 1 unit/kg/day in type 1 diabetes, divided into basal and mealtime insulin doses.
- Administration timing: Inject approximately 30 minutes before meals to cover postprandial glucose.
- Titration: Adjust doses based on frequent blood glucose measurements and clinical response.
- Special populations: Dosage adjustments are necessary for elderly patients, renal or hepatic impairment, or during illness.
- Missed dose: If a dose is missed, administer as soon as possible unless it is close to the next scheduled dose.
- Consult healthcare provider: Never change doses without professional guidance.
Possible side effects of ACTRAPID HM PENFILL 100 Units/ml
While ACTRAPID HM PENFILL is effective, it may cause side effects that patients should be aware of:
- Hypoglycemia: Most common adverse effect characterized by sweating, shaking, confusion, dizziness, and in severe cases, seizures or loss of consciousness.
- Injection site reactions: Including pain, redness, swelling, or lipodystrophy (localized fat atrophy or hypertrophy).
- Allergic reactions: Rare but may range from mild rash to anaphylaxis.
- Weight gain: Insulin therapy may promote weight gain due to anabolic effects.
- Hypokalemia: Insulin drives potassium into cells, possibly leading to low blood potassium.
- Edema and fluid retention: Occasionally observed in some patients.
Prompt recognition and management of side effects are essential for safe insulin therapy.
ACTRAPID HM PENFILL 100 Units/ml Contraindications ACTRAPID HM PENFILL 100 Units/ml
Contraindications for ACTRAPID HM PENFILL use include:
- Hypoglycemia: Insulin must never be administered during episodes of low blood sugar.
- Hypersensitivity: Known allergy to insulin or any excipients present in the formulation.
- Diabetic ketoacidosis: Should be treated with insulin only under close medical supervision alongside fluid and electrolyte replacement.
- Severe hypokalemia: Insulin can worsen potassium depletion.
Use with caution in pregnancy and lactation; consult healthcare providers for risk-benefit assessment.
Storage of ACTRAPID HM PENFILL 100 Units/ml
Proper storage of insulin is essential to maintain potency and safety.
- Unopened cartridges: Store refrigerated at 2°C to 8°C; do not freeze.
- In-use cartridges: Can be kept at room temperature (below 25°C) for up to 28 days once inserted into the pen device.
- Protection: Keep away from direct sunlight and extreme temperatures.
- Inspection: Before use, check insulin clarity; do not use if cloudy, discolored, or containing particles.
- Disposal: Dispose of used cartridges and needles according to local medical waste regulations.
Adhering to recommended storage conditions ensures therapeutic effectiveness and patient safety.
ACTRAPID HM PENFILL 100 Units/ml features an exceptional active ingredient renowned for its potent effects, comprising Insulin - Soluble (human). This powerful formulation provides a superior solution for addressing diverse health concerns. With 100 Units/ml concentration and an easily manageable Injection, it remains a preferred option for countless individuals seeking effective treatment.
Introduction
All you need to know about ACTRAPID HM PENFILL 100 Units/ml .
Welcome to Dwaey, specifically on ACTRAPID HM PENFILL 100 Units/ml page.
This medicine contains an important and useful components, as it consists of Insulin - Soluble (human).
ACTRAPID HM PENFILL 100 Units/ml is available in the market in concentration 100 Units/ml and in the form of Injection.
NOVO NORDISK A/S is the producer of ACTRAPID HM PENFILL 100 Units/ml and it is imported from DENMARK,
The most popular alternatives of ACTRAPID HM PENFILL 100 Units/ml are listed downward .
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Active Substance
Insulin - Soluble (human)
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Size
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Indications
- No indications available.
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Type
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Company
Frequently Asked Questions
ACTRAPID HM PENFILL 100 Units/ml should be stored according to the instructions provided by NOVO NORDISK A/S.
In general, it is recommended to store ACTRAPID HM PENFILL 100 Units/ml in a cool, dry place, away from direct sunlight
and out of the reach of children.
The duration of treatment with ACTRAPID HM PENFILL 100 Units/ml may vary depending on the condition being treated
and the guidance of your healthcare provider. It is important to follow the prescribed treatment
plan and continue taking ACTRAPID HM PENFILL 100 Units/ml for the recommended duration, even if your symptoms improve.
If you have any concerns or questions about the duration of treatment, consult your healthcare provider.
It is important to check with your healthcare provider or read the medication label for specific
instructions regarding alcohol consumption while taking ACTRAPID HM PENFILL 100 Units/ml. Some medications, including
ACTRAPID HM PENFILL 100 Units/ml, may have interactions with alcohol that can reduce effectiveness, increase side
effects, or pose other risks to your health. It is best to follow the guidance provided by your
healthcare professional.
If you miss a dose of ACTRAPID HM PENFILL 100 Units/ml, take it as soon as you remember. However, if it is close
to the time for your next scheduled dose, skip the missed dose and continue with your regular dosing
schedule. Do not take a double dose to make up for a missed one unless advised by your healthcare provider.
No, do not stop taking ACTRAPID HM PENFILL 100 Units/ml without consulting your healthcare provider, even if your
symptoms improve. It is important to complete the full course of treatment as prescribed. Stopping
the medication prematurely may lead to a relapse or incomplete resolution of the condition. If you
have concerns about the duration of treatment, consult your healthcare provider for guidance.
It is important to consult your healthcare provider before taking ACTRAPID HM PENFILL 100 Units/ml if you are
pregnant or breastfeeding. They will be able to assess the potential risks and benefits based on your
specific situation. Please note that the safety and suitability of ACTRAPID HM PENFILL 100 Units/ml during pregnancy
or breastfeeding may depend on the active substance [Active Substance], concentration 100 Units/ml,
and the specific recommendations of NOVO NORDISK A/S.
The effects of ACTRAPID HM PENFILL 100 Units/ml on your ability to drive or operate machinery can vary depending on
the active substance [Active Substance], concentration 100 Units/ml, and individual factors.
Some medications may cause drowsiness, dizziness, or other side effects that can impair your judgment
or coordination. It is important to read the medication label or consult your healthcare provider to
understand any potential effects on your ability to perform tasks that require alertness.
The instructions for taking ACTRAPID HM PENFILL 100 Units/ml with or without food may vary depending on the medication
and the recommendations of NOVO NORDISK A/S. Some medications may be more effective when taken with
food to enhance absorption or reduce stomach irritation, while others may need to be taken on an empty
stomach for optimal absorption. Read the medication label or consult your healthcare provider for specific instructions.
The use of ACTRAPID HM PENFILL 100 Units/ml in children or elderly individuals may depend on various factors, including
the specific medication, type Injection, and the recommendations of NOVO NORDISK A/S. Some
medications may have specific dosing instructions or precautions for these age groups. Consult your
healthcare provider or read the medication label for information regarding the safe and appropriate use
of ACTRAPID HM PENFILL 100 Units/ml in children or elderly individuals.
Dwaey
All medical information published on the Dwaey website aims to increase medical awareness and health education among users. However, it is not a substitute for professional medical advice. Always consult with a specialist doctor. We strongly advise against using any information or medicine found on the site without referring to your healthcare provider.
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