Humatrope 36IU (12mg)
Humatrope 36IU (12mg) is a prescription somatropin product manufactured by Eli Lilly and Company. It contains recombinant human growth hormone and is supplied as a 12 mg cartridge, equivalent to 36 IU, for use with the compatible HumatroPen 12 mg delivery device. Humatrope is intended for medically diagnosed growth hormone-related conditions and should be used only under the supervision of a qualified healthcare professional.
General Information
Product Name: Humatrope 36IU (12mg)
Active Ingredient: Somatropin
Strength: 12 mg, equivalent to 36 IU
Dosage Form: Powder for solution for injection supplied in a cartridge
Delivery System: Designed for use with HumatroPen 12 mg
Manufacturer: Eli Lilly and Company
Product Type: Recombinant human growth hormone
Route of Administration: Subcutaneous injection after correct preparation
Prescription Status: Prescription medicine; requirements vary by country
Product Overview
Humatrope 36IU (12mg) contains somatropin, a laboratory-produced form of human growth hormone. The medicine is manufactured using recombinant DNA technology and has the same 191-amino-acid sequence as naturally occurring human growth hormone.
The 12 mg cartridge is one of the established Humatrope cartridge strengths. Other cartridge presentations have included 6 mg and 24 mg. The 12 mg presentation contains the equivalent of 36 IU of somatropin and is intended for use with the matching HumatroPen 12 mg injection device.
Patients should not interchange cartridge or pen strengths without instructions from their healthcare professional. The appropriate dose of Humatrope is individualized according to the medical condition being treated, clinical response, body weight or body surface area where applicable, and ongoing medical monitoring.
Medical Uses of Humatrope
Humatrope is used for specific medically diagnosed growth hormone-related conditions in children and adults.
Depending on the approved labeling in the relevant country, Humatrope may be prescribed to children with growth failure caused by inadequate production of endogenous growth hormone and for certain other recognized causes of short stature or impaired growth.
Humatrope may also be prescribed to adults with confirmed growth hormone deficiency when the diagnosis has been established by an appropriate healthcare professional.
Humatrope 36IU (12mg) should not be used for general bodybuilding, anti-aging purposes, athletic-performance enhancement, or unsupervised weight loss. Treatment should follow the indication, dose, monitoring schedule, and instructions provided by the prescribing healthcare professional.
Humatrope 12mg Cartridge
Humatrope 36IU (12mg) is supplied in cartridge form containing 12 mg of somatropin. The cartridge is designed for use with the corresponding HumatroPen 12 mg delivery system.
The Humatrope cartridge must be prepared using the specified diluent according to the manufacturer’s instructions before administration. Patients or caregivers should carefully follow the official preparation instructions supplied with the medicine.
Once prepared, the solution should be visually inspected before injection. Do not use the product if the solution appears cloudy, discolored, or contains visible particles.
The HumatroPen should also be used only after the patient or caregiver has received appropriate instructions from a healthcare professional.
Administration Information
Humatrope is administered by subcutaneous injection. The exact amount required is determined by the prescribing healthcare professional.
Do not change the prescribed dose, cartridge strength, injection schedule, or delivery device without medical advice.
Injection sites should be rotated as instructed to reduce the risk of localized tissue changes at repeatedly used injection sites.
Patients should read the HumatroPen instructions and the patient information supplied with Humatrope before using a new cartridge.
Storage and Handling
Proper storage is important for maintaining the quality of Humatrope 36IU (12mg).
Humatrope cartridges should be stored under refrigeration according to the manufacturer’s instructions and protected from light.
After preparation, Humatrope cartridges are generally stored refrigerated at 2°C to 8°C. The cartridge should not be frozen.
The prepared cartridge should not remain at room temperature for longer than permitted by the official product instructions.
Before use, check:
- The product packaging
- Expiration date
- Cartridge condition
- Supplied diluent
- Storage conditions
- Appearance of the prepared solution
Do not use a cartridge that is damaged, expired, improperly stored, or shows an unusual appearance after preparation.
Important Safety Information
Humatrope 36IU (12mg) is a prescription medicine and is not suitable for every patient.
Humatrope is contraindicated in certain medical circumstances, including active malignancy and some forms of acute critical illness. Other conditions may require additional medical assessment or monitoring.
Patients should inform their healthcare professional if they have or previously had conditions involving:
- Diabetes or problems with blood glucose
- Thyroid disease
- Previous tumors or malignancy
- Intracranial hypertension
- Scoliosis
- Severe respiratory problems
- Allergies to medicine ingredients
- Other significant medical conditions
Somatropin treatment may require regular clinical examinations, laboratory testing, and dose adjustments.
Patients should also inform their healthcare provider about all prescription medicines, over-the-counter medicines, vitamins, supplements, and other products they are currently using.
Seek medical advice promptly if serious or unexpected symptoms develop during treatment.
Before Using Humatrope 36IU (12mg)
Before obtaining or using Humatrope 36IU (12mg), confirm that the 12 mg / 36 IU cartridge is the exact strength prescribed and that it matches the appropriate HumatroPen delivery device.
The medicine should be used only where legally permitted and with a valid prescription whenever required under local regulations.
Packaging, availability, prescribing requirements, and regulatory status may differ between countries. Always check the product packaging and official patient information supplied with the medicine.
Humatrope 36IU (12mg) is a specialist prescription somatropin product intended for medically supervised treatment. Use it exactly as directed by the prescribing healthcare professional and follow the official Humatrope and HumatroPen instructions supplied with the product.
