This site is provided for patients and families dealing with growth hormone deficiency
and growth disorders. Humatrope is a man-made form of human growth hormone and was first approved in 1987
to treat children who are growing slowly because they do not make enough growth hormone on their own. Since that time, Humatrope has also been approved for the treatment of several additional growth disorders
(idiopathic short stature, Turner syndrome, small for gestational age, SHOX deficiency) and for growth hormone deficiency in adults. Humatrope is available in cartridges for use in a HumatroPen® injection device and in vials for use with a syringe and needle.
Indications for Humatrope
Humatrope® (somatropin [rDNA origin] for injection) is used to treat children who are short or growing slowly because they:
- Do not make enough growth hormone on their own.
- Have Turner syndrome.
- Have idiopathic short stature, which means they are shorter than 98.8% of other children of the same age and sex,
are growing at a rate not likely to allow them to reach normal adult height, and for whom no other cause of short stature can be found.
- Have SHOX deficiency.
- Were born smaller than normal for the number of weeks of pregnancy and do not catch up in height by 2 to 4 years of age.
Humatrope is used to treat adults who have growth hormone deficiency that began either in:
- Adulthood (as a result of pituitary disease, hypothalamic disease, surgery, radiation therapy, or trauma); or
- Childhood. Patients treated for growth hormone deficiency in childhood whose bones have stopped growing should be reevaluated.
Important Safety Information for Humatrope
WHO SHOULD NOT TAKE HUMATROPE?
- You should not take Humatrope if you are having serious complications after undergoing open heart surgery, abdominal surgery, serious injuries involving many body systems, or life-threatening breathing problems. Deaths have been reported in such cases.
- Somatropin should not be used in children with Prader-Willi syndrome who are severely obese or have a history of severe breathing problems. Deaths have been reported in children with Prader-Willi syndrome who are severely obese, have a history of blocked upper airways, sleep apnea (pauses in breathing during sleeping), or other severe breathing problems. Humatrope has not been approved for the treatment of patients with Prader-Willi syndrome.
- Humatrope should not be used if you have active cancer. Because growth hormone deficiency can be an early sign of some tumors in the brain or pituitary gland, the presence of these types of tumors should be ruled out by your doctor before you start Humatrope.
- Humatrope should not be used in children whose growth plates in their bones have closed.
- Humatrope should not be used in adults or children with diabetic retinopathy.
- If you are allergic to metacresol or glycerin, you should not mix Humatrope with the supplied diluent. Reactions at the injection site are the most common allergic reactions. If you have had an allergic reaction to somatropin, you should not take Humatrope.
WHAT SHOULD I TELL MY DOCTOR BEFORE TAKING HUMATROPE?
- Tell your doctor if you take cyclosporine, hormone replacement therapy, insulin or other diabetes medications, drugs containing steroids, or drugs for seizures. These medications may need to be adjusted while taking Humatrope.
- There have been reports of death in children with Prader-Willi syndrome who recently started somatropin therapy and had one or more of the following risk factors: obesity, history of severe breathing problems or sleep apnea (pauses in breathing during sleeping), or unidentified respiratory infection. Boys with one or more of these risk factors may be at greater risk than girls. A child with Prader-Willi syndrome should be evaluated by a doctor for signs of severe breathing problems or sleep apnea before starting somatropin therapy.
- If you have pre-existing tumors or growth hormone deficiency caused by abnormal tissue in the brain, you should be watched closely for worsening or returning of this condition. If you had cancer as a child, an increased risk of a new tumor, particularly certain brain tumors, has been reported in patients taking somatropin.
- Your doctor should check your blood sugar regularly while you are taking Humatrope, especially if you have risk factors for diabetes. If you have diabetes or impaired glucose tolerance, your doctor should monitor your blood sugar closely during Humatrope therapy. New cases of type 2 diabetes have been reported in patients taking Humatrope.
- Cases of pancreatitis (inflammation of the pancreas) have been reported rarely in children and adults receiving somatropin. Consult a doctor if you develop abdominal pain while taking Humatrope.
- Tell your doctor if you have any visual changes accompanied by headache, nausea, and/or vomiting while taking Humatrope. This may be a sign of increased pressure in the brain.
- Adults may retain water during therapy with Humatrope. This may be brief but may increase with higher doses of Humatrope.
- If you have hypopituitarism and are on standard hormone replacement therapy, your doctor should monitor your hormone replacement therapy closely while taking Humatrope.
- You should have your thyroid function tested periodically during Humatrope therapy. Thyroid hormone treatment may need to be started or adjusted.
- Slipped capital femoral epiphysis (fracture in the ball of the hip joint) can occur in children who have endocrine problems and in children who have rapid growth. Any child taking Humatrope who develops a limp or complains of hip or knee pain should be seen by a doctor to check for this.
- Progression of scoliosis (curvature of the spine) can occur in children who have rapid growth. Humatrope has not been shown to increase the occurrence of this condition.
- Children with Turner syndrome should be monitored closely by a doctor for ear infections and cardiovascular problems while taking Humatrope.
- You should rotate your injection sites to avoid breakdown of skin and fat. Seek prompt medical attention for any allergic reaction you experience to the injection of Humatrope.
- If you are pregnant or nursing, you should talk to your doctor before using Humatrope. It is not known whether Humatrope is excreted in human milk. Humatrope should be used during pregnancy only when clearly needed.
- Clinical studies in patients over 65 years of age have not been done. Elderly patients may be more sensitive to Humatrope and may experience more side effects.
- Because Humatrope may affect how two hormones, cortisol and cortisone, are processed in the body, people may discover they have hypoadrenalism after starting Humatrope therapy. In these cases, glucocorticoid replacement therapy would need to be started.
WHAT ARE THE POSSIBLE SIDE EFFECTS OF HUMATROPE?
- Common side effects reported in adults and children taking Humatrope include injection site reactions, allergic reactions to the diluent, and hypothyroidism. Additional common side effects in adults include swelling, joint pain, muscle pain, carpal tunnel syndrome, unusual skin sensations, and high blood sugar. You are encouraged to report negative side effects of prescription drugs to the FDA. Visit or call 1-800-FDA-1088.
HOW SHOULD I STORE HUMATROPE?
- Humatrope must be kept refrigerated (36° to 46°F [2° to 8°C]) before and after it is mixed. Do not freeze. Once Humatrope has been mixed and is in liquid form, cartridges must be used within 28 days and vials must be used within 14 days. Throw away any unused Humatrope in a cartridge after 28 days and in a vial after 14 days. Before giving an injection, check the manufacturer’s expiration date on the cartridge or vial. Do not use the cartridge or vial if it has expired.
For more information, please see Patient Information-Cartridge,
Patient Information-Vial, and
Full Prescribing Information.
See Full Pen User Manual that accompanies the HumatroPen® 6 mg, 12 mg, and 24 mg.
HG CON ISI 04242012