ZOMACTON - Ferring Pharmaceuticals, Inc.
Contents
1. Figure U If no blood appears in the syringe slowly push down plunger all the way until the syringe is completely empty See Figure V Figure V Quickly remove the needle from the skin and apply pressure to the injection site with a dry sterile gauze pad or cotton ball A drop of blood may appear Apply a small bandage if needed Throw away the needle and syringe in your puncture resistant disposal container Do not share your syringes needles or vials with anyone else You may give them or get an infection from them Step 4 Disposing of used syringes needles and vials To prevent needle stick injury and spread of infection do not try to re cap the needle Place used needles syringes and vials in a closeable puncture resistant container You may use a Sharps container such as a red biohazard container hard plastic container Such as a detergent bottle or metal container such as an empty coffee can Do not use glass or clear plastic containers Ask your healthcare provider for instructions on the right way to throw away dispose of the container There may be state and local laws about how you should throw away used needles and syringes If you do not have a FDA cleared sharps disposal container you may use a household container that is e made of a heavy duty plastic e can be closed with a tight fitting puncture resistant lid without sharps being able to come out e upright and stable during use e leak2. concurrently develop these illnesses has not been established Therefore the potential benefit of treatment continuation with somatropin in patients experiencing acute critical illnesses should be weighed against the potential risk There have been reports of fatalities after initiating therapy with somatropin in pediatric patients with Prader Willi syndrome who had one or more of the following risk factors severe obesity history of upper airway obstructions or sleep apnea or unidentified respiratory infection Male patients with one or more of these factors may be at greater risk than females Patients with Prader Willi syndrome should be evaluated for signs of upper airway obstruction and sleep apnea before initiation of treatment with somatropin If during treatment with somatropin patients show signs of upper airway obstruction including onset of or increased snoring and or new onset sleep apnea treatment should be interrupted All patients with Prader Willi syndrome treated with somatropin should also have effective weight control and be monitored for signs of respiratory infection which should be diagnosed as early as possible and treated aggressively see CONTRAINDICATIONS ZOMACTON is not indicated for the treatment of pediatric patients who have growth failure due to genetically confirmed Prader Willi syndrome Cases of pancreatitis have been reported rarely in children and adults receiving somatropin treatment with some evidence su
3. during appropriate use of somatropin headaches children and adults gynecomastia children and pancreatitis children and adults See WARNINGS section As with all therapeutic proteins there is potential for immunogenicity The detection of antibody formation is highly dependent on the sensitivity and specificity of the assay Additionally the observed incidence of antibody including neutralizing antibody positivity in an assay may be influences by several factors including assay methodology sample handling timing of sample collection concomitant medications and underlying disease For these reasons comparison of the incidence of antibodies to ZOMACTON with the incidence of antibodies to other products may be misleading With respect to growth hormone antibody binding capacities below 2 mg L have not been associated with growth attenuation In some cases when binding capacity exceeds 2 mg L growth attenuation has been observed None of the patients with anti GH antibodies in the clinical studies experienced decreased linear growth response to ZOMACTON or any other associated adverse event Injection site reactions e g pain bruise occurred in 8 of the 164 treated patients Leukemia has been reported in a small number of patients treated with other growth hormone products It is uncertain whether this risk is related to the pathology of growth hormone deficiency itself growth hormone therapy or other associated treatments such a
4. not take the place of talking to your healthcare provider about your medical condition or treatment Before you use ZOMACTON for the first time make sure your healthcare provider shows you the right way to use it Supplies needed for your ZOMACTON Injection e ZOMACTON 5mg See Figure A containing o 1 vial of ZOMACTON 5mg growth hormone in a powder o 1 vial of liquid diluent containing Bacteriostatic 0 9 Sodium Chloride Injection USP 5mL This is used to mix your ZOMACTON 5mg ZOMACTON 5mg Liquid diluent Figure A or e ZOMACTON 10mg See Figure B containing o 1 vial of ZOMACTON 10mg growth hormone in a powder o 1 syringe of liquid diluent containing Bacteriostatic Water for Injection with 0 33 Metacresol as a preservative 1mL This is used to mix your ZOMACTON 10mg o 25 gauge mixing needle Syringe diluent 2 Mixing needle el 10mg Figure B The following additional supplies See Figure C will be needed e Syringe and needle for injection Your healthcare provider will tell you the size of the syringe and needle to use e Alcohol swab e Puncture resistant container See Step 4 Disposing of used syringes needles and vials ny container Syringe e gir a A aa Na es Figure C Preparing for Your ZOMACTON Injection e Place the supplies you will need on a clean flat surface in a well lit area e Wash your hands thoroughly with soap and water Important The liqu
5. out under the regular guidance of a physician who is experienced in the diagnosis and management of pediatric patients with growth hormone deficiency In childhood cancer survivors who were treated with radiation to the brain head for their first neoplasm and who developed subsequent GHD and were treated with somatropin an increased risk of a second neoplasm has been reported Intracranial tumors in particular meningiomas were the most common of these second neoplasms In adults it is unknown whether there is any relationship between somatropin replacement therapy and CNS tumor recurrence see CONTRAINDICATIONS Monitor all patients with a history of GHD secondary to an intracranial neoplasm routinely while on somatropin therapy for progression or recurrence of the tumor Because children with certain rare genetic causes of short stature have an increased risk of developing malignancies practitioners should thoroughly consider the risks and benefits of starting somatropin in these patients If treatment with somatropin is initiated these patients should be carefully monitored for development of neoplasms Monitor patients on somatropin therapy carefully for increased growth or potential malignant changes of preexisting nevi Treatment with somatropin may decrease insulin sensitivity particularly at higher doses in susceptible patients As a result previously undiagnosed impaired glucose tolerance and overt diabetes mellitus may be unmask
6. syringe is correctly filled with the liquid remove the syringe and needle from the vial and recap the needle Preparing ZOMACTON 10mg Liquid for Injection e Remove the syringe tip cap from the top of the pre filled liquid syringe and attach the 25G mixing needle that comes with your ZOMACTON See Figure J Figure J Diluting Your ZOMACTON e Only use the liquid that comes with the 5mg ZOMACTON to mix the 5mg growth hormone Only use the liquid that comes with the 10mg ZOMACTON to mix the 10mg growth hormone e Remove the hard plastic cap of the growth hormone vial See Figure K Figure K e Clean the top of the growth hormone vial with an alcohol swab See Figure L Figure L e Remove the needle cap from the syringe filled with liquid and insert the needle into the center of the rubber stopper on the growth hormone vial See Figure M Figure M Point the needle toward the side of the vial and slowly push the plunger so that the liquid squirts onto the side of the vial and not directly onto the powder When all the liquid is in the growth hormone vial remove the needle from the vial See Figure N Figure N Recap the needle and throw away the syringe Mixing ZOMACTON Hold the vial between your hands and gently roll it until the mixture is clear Do not shake the vial Your ZOMACTON is ready for injection Sometimes the vial may need to sit a few seconds before the mixture becomes clear Do not us
7. D was 80 50 ng mL which occurred approximately 7 hours post injection and the apparent elimination half life was approximately 2 7 hours Compared to intravenous administration the extent of systemic availability from subcutaneous administration was approximately 70 INDICATION AND USAGE ZOMACTON is indicated for the treatment of children who have growth failure due to an inadequate secretion of normal endogenous growth hormone CONTRAINDICATIONS ZOMACTON 5 mg reconstituted with bacteriostatic 0 9 sodium chloride injection USP normal saline benzyl alcohol preserved should not be administered to patients with a known sensitivity to benzyl alcohol see WARNINGS ZOMACTON 10 mg reconstituted with bacteriostatic water for injection containing 0 33 metacresol should not be used if the patient is allergic to metacresol Somatropin should not be used for growth promotion in pediatric patients with closed epiphyses Somatropin is contraindicated in patients with active proliferative or severe non proliferative diabetic retinopathy In general somatropin is contraindicated in the presence of active malignancy Any preexisting malignancy should be inactive and its treatment complete prior to instituting therapy with somatropin Somatropin should be discontinued if there is evidence of recurrent activity Since growth hormone deficiency may be an early sign of the presence of a pituitary tumor or rarely other brain tumors the presen
8. TON is equivalent in its therapeutic effectiveness and in its pharmacokinetic profile to those of human growth hormone of pituitary origin somatropin ZOMACTON stimulates linear growth in children who lack adequate levels of endogenous growth hormone Treatment of growth hormone deficient children with ZOMACTON produces increased growth rates and IGF 1 Insulin Like Growth Factor 1 concentrations that are similar to those seen after therapy with human growth hormone of pituitary origin Both ZOMACTON and somatropin have also been shown to have other actions including A Tissue Growth 1 Skeletal Growth ZOMACTON stimulates skeletal growth in patients with growth hormone deficiency The measurable increase in body length after administration of ZOMACTON results from its effect on the epiphyseal growth plates of long bones Concentration of IGF 1 which may play a role in skeletal growth are low in the serum of growth hormone deficient children but increase during treatment with ZOMACTON Mean serum alkaline phosphatase concentrations are increased 2 Cell Growth It has been shown that there are fewer skeletal muscle cells in short statured children who lack endogenous growth hormone as compared with normal children Treatment with somatropin results in an increase in both the number and size of muscle cells 3 Organ Growth Somatropin influences the size of internal organs and it also increases red cell mass B Protein Metabol
9. ZOMACTON somatropin rDNA origin for Injection 5 mg and 10 mg DESCRIPTION ZOMACTON somatropin rDNA origin for Injection a polypeptide of recombinant DNA origin has 191 amino acid residues and a molecular weight of about 22 124 daltons It has an amino acid sequence identical to that of human growth hormone of pituitary origin ZOMACTON is a strain of Escherichia coli modified by insertion of the human growth hormone gene ZOMACTON is a sterile white lyophilized powder intended for subcutaneous administration after reconstitution with the accompanying diluent ZOMACTON 5 mg vial contains recombinant somatropin 5 mg and mannitol 30 mg The 5 mg vial is supplied in a combination package with an accompanying 5 mL vial of diluting solution The diluent contains bacteriostatic 0 9 sodium chloride injection USP normal saline 0 9 benzyl alcohol as a preservative and water for injection ZOMACTON 10 mg vial contains recombinant somatropin 10 mg mannitol 10 mg disodium phosphate dodecahydrate 3 57 mg and sodium dihydrogen phosphate dehydrate 0 79 mg The 10 mg vial is supplied in a combination package with an accompanying 1 mL syringe of diluting solution The diluent contains bacteriostatic water for injection with 0 33 metacresol as a preservative ZOMACTON is a highly purified preparation Reconstituted solutions have a pH in the range of 7 0 to 9 0 CLINICAL PHARMACOLOGY Clinical trials have demonstrated that ZOMAC
10. ays when reconstituted with 1 mL syringe of bacteriostatic water for injection containing 0 33 metacresol as a preservative and stored in a refrigerator at 36 to 46 F 2 to 8 C Do not freeze the reconstituted solution HOW SUPPLIED ZOMACTON somatropin rDNA origin for injection is supplied as 5 mg and 10 mg of lyophilized sterile somatropin per vial ZOMACTON 5 mg carton NDC 55566 1801 1 contains one vial of ZOMACTON 5 mg per vial and one vial of diluent 5 mL of bacteriostatic 0 9 sodium chloride for injection USP benzyl alcohol preserved and is supplied in single cartons ZOMACTON 10 mg carton NDC 55566 1901 1 contains one vial of ZOMACTON 10 mg per vial one syringe of diluent 1 mL of bacteriostatic water for injection with 0 33 metacresol as preservative and a 25G reconstitution needle and is supplied in single cartons ZOMACTON 10 mg carton NDC 55566 1902 1 contains one vial of ZOMACTON 10mg per vial one syringe of diluent 1 mL of bacteriostatic water for injection with 0 33 metacresol as preservative 1 vial adapter and is supplied in single cartons Rx only Manufactured for Ferring Pharmaceuticals Inc Parsippany NJ 07054 Rev 03 15 Instructions for Use ZOMACTON zoh MACK ton somatropin rDNA origin for Injection Read the Instructions for Use that come with your ZOMACTON before you start using it and each time you get a refill There may be new information This leaflet does
11. ce of such tumors should be ruled out prior to initiation of treatment Somatropin should not be used in patients with any evidence of progression or recurrence of an underlying intracranial tumor Treatment with pharmacologic amounts of somatropin is contraindicated in patients with acute critical illness due to complications following open heart surgery abdominal surgery or multiple accidental trauma or those with acute respiratory failure Two placebo controlled clinical trials in non growth hormone deficient adult patients n 522 with these conditions in intensive care units revealed a significant increase in mortality 41 9 vs 19 3 among somatropin treated patients doses 5 3 to 8 mg day compared to those receiving placebo see WARNINGS Somatropin is contraindicated in patients with Prader Willi syndrome who are severely obese or have severe respiratory impairment see WARNINGS ZOMACTON is not indicated for the treatment of pediatric patients who have growth failure due to genetically confirmed Prader Willi syndrome WARNINGS Increased mortality in patients with acute critical illness due to complications following open heart surgery abdominal surgery or multiple accidental trauma or those with acute respiratory failure has been reported after treatment with pharmacologic doses of somatropin see CONTRAINDICATIONS The safety of continuing somatropin treatment in patients receiving replacement doses for approved indications who
12. ct on growth Limited published data indicate that somatropin treatment increases cytochrome P450 CP450 mediated antipyrine clearance in man These data suggest that somatropin administration may alter the clearance of compounds known to be metabolized by CP450 liver enzymes e g corticosteroids sex steroids anticonvulsants cyclosporine Careful monitoring is advisable when somatropin is administered in combination with other drugs known to be metabolized by CP450 liver enzymes Carcinogenesis Mutagenesis Impairment of Fertility Carcinogenesis mutagenesis and reproduction studies have not been conducted with ZOMACTON Pregnancy Pregnancy Category C Animal reproduction studies have not been conducted with ZOMACTON It is also not known whether ZOMACTON can cause fetal harm when administered to a pregnant woman or can affect reproductive capacity ZOMACTON should be given to a pregnant woman only if clearly needed Nursing Mothers It is not known whether this drug is excreted in human milk Because many drugs are excreted in human milk caution should be exercised when ZOMACTON is administered to a nursing woman Geriatric Use The safety and effectiveness of somatropin in patients aged 65 and over has not been evaluated in clinical studies Elderly patients may be more sensitive to the action of somatropin and may be more prone to develop adverse reactions ADVERSE REACTIONS The following adverse reactions have been observed
13. e the mixture in the vial if it remains cloudy or you see particles floating in the mixture If air bubbles appear let the growth hormone sit for a while until they disappear Write the date you mixed the growth hormone on the vial label The 5 mg vial must be used within 14 days The 10mg vial must be used within 28 days Store your mixed growth hormone and all unopened vials of growth hormone in the refrigerator at 36 F to 46 F 2 C to 8 C Do not freeze Step 1 Preparing the Injection You are now ready for your ZOMACTON injection Wash your hands thoroughly with soap and water Check that the vial of growth hormone you are using is clear and that the date of mixing is within 14 days if you are using ZOMACTON 5mg or 28 days if you are using ZOMACTON 10mg Clean the top of the growth hormone vial with an alcohol swab Do not touch the rubber stopper after cleaning See Figure O Figure O e Remove the needle cap from the syringe and insert the needle into the center of the rubber stopper on the growth hormone vial See Figure P Figure P e Gently pull back the plunger until the amount of growth hormone solution your healthcare provider has prescribed is in the syringe See Figure Q Figure Q e Remove the needle from the vial when the syringe is correctly filled with the solution See Figure R Recap the needle Figure R Step 2 Choosing an Injection Site e There are different sites you can use for y
14. ed during somatropin treatment New onset type 2 diabetes mellitus has been reported in patients Therefore glucose levels should be monitored periodically in all patients treated with somatropin especially in those with risk factors for diabetes mellitus such as obesity Turner syndrome or a family history of diabetes mellitus Patients with preexisting type or type 2 diabetes mellitus or impaired glucose tolerance should be monitored closely during somatropin therapy The doses of antihyperglycemic drugs i e insulin or oral agents may require adjustment when somatropin therapy is instituted in these patients In patients with hypopituitarism multiple hormone deficiencies standard hormonal replacement therapy should be monitored closely when somatropin therapy is administered Undiagnosed untreated hypothyroidism may prevent an optimal response to somatropin in particular the growth response in children Patients with Turner syndrome have an inherently increased risk of developing autoimmune thyroid disease and primary hypothyroidism In patients with growth hormone deficiency central secondary hypothyroidism may first become evident or worsen during somatropin treatment Therefore patients treated with somatropin should have periodic thyroid function tests and thyroid hormone replacement therapy should be initiated or appropriately adjusted when indicated Patients with endocrine disorders including growth hormone deficiency may ha
15. ids are different for the 5mg and 10mg vials e Do not use the 5mg liquid with the 10mg ZOMACTON e Do not use the 10mg liquid with the 5mg ZOMACTON Preparing ZOMACTON 5mg Liquid for I njection e Remove the hard plastic cap from the top of the liquid vial by gently pushing up on the edge of the cap See Figure D Do not remove the rubber stopper Figure D e Use an alcohol swab to wipe off the top of the liquid vial See Figure E After cleaning do not touch the rubber stopper Figure E e Remove the needle cap from the syringe while making sure you do not touch the needle See Figure F Do not throw away the needle cap Figure F e Hold the barrel of the syringe with 1 hand and pull back on the plunger with the other hand until you have drawn up the amount of air that is the same as the amount of liquid your healthcare provider has prescribed See Figure G Figure G e Insert the needle into the liquid vial through the center of the clean rubber stopper Push down on the plunger until all the air is released into the vial See Figure H Figure H e Hold the vial with 1 hand and carefully turn the vial upside down making sure the syringe needle stays in the vial The tip of the needle should be below the surface of the liquid e With your other hand gently pull back the plunger until the amount of liquid your healthcare provider prescribed is in the syringe See Figure Figure e When the
16. ism Linear growth is facilitated in part by increased cellular protein synthesis Nitrogen retention as demonstrated by decreased urinary nitrogen excretion and serum urea nitrogen results from treatment with somatropin C Carbohydrate Metabolism Children with hypopituitarism sometimes experience fasting hypoglycemia that is improved by treatment with somatropin Large doses of somatropin may impair glucose tolerance D Lipid Metabolism Administration of somatropin to growth hormone deficient patients mobilizes lipid reduces body fat stores and increases plasma fatty acids E Mineral Metabolism Sodium potassium and phosphorous are conserved by somatropin Serum concentrations of inorganic phosphates increased in patients with growth hormone deficiency after therapy with ZOMACTON or somatropin Serum calcium concentrations are not significantly altered in patients treated with either somatropin or ZOMACTON F Connective Tissue Metabolism Somatropin stimulates the synthesis of chondroitin sulfate and collagen as well as the urinary excretion of hydroxyproline PHARMACOKINETICS Following intravenous administration of 0 1 mg kg of ZOMACTON the elimination half life was about 0 42 hours approximately 25 minutes and the mean plasma clearance SD was 133 16 mL min in healthy male volunteers In the same volunteers after a subcutaneous injection of 0 1 mg kg ZOMACTON to the forearm the mean peak serum concentration S
17. oncomitant thyroid hormone replacement therapy Under these circumstances epiphyseal maturation may progress rapidly When somatropin is administered subcutaneously at the same site over a long period of time tissue atrophy may result This can be avoided by rotating the injection site As is the case with any protein local or systemic allergic reactions may occur Parents Patient should be informed that such reactions are possible and that prompt medical attention should be sought if allergic reactions occur Information for Patients Patients being treated with ZOMACTON and or their caregivers should be informed about the potential benefits and risks associated with treatment See the patient information included with the product and or injection device This information is intended to aid in the safe and effective administration of the medication It is not a disclosure of all possible adverse or intended effects Patients and caregivers who will administer ZOMACTON should receive appropriate training and instruction on the proper use of ZOMACTON from the physician or other suitable qualified health care professional A puncture resistant container for the disposal of used needles and syringes should be strongly recommended Patients and or caregivers should be thoroughly instructed in the importance of proper disposal and cautioned against any reuse of needles and syringes Laboratory Tests Serum levels of inorganic phosphorus alkaline pho
18. our injections These sites should be rotated See Figure S Figure S If you notice any of the following signs contact your healthcare provider e A lump bruise or redness at the injection site that does not go away e Any sign of infection at the injection site pus redness heat or persistent pain e Severe sharp pain or ache at injection site that does not go away e Rash at the injection site Step 3 Injecting ZOMACTON e Using a circular motion clean the injection site with an alcohol swab starting at the injection site and moving outward about 2 inches Let the skin air dry Check that the correct dose is in the syringe Remove the needle cap Hold the syringe like a pencil in 1 hand With your free hand pinch the skin around the site with the thumb and forefinger of the other hand See Figure T Quickly insert the needle into the skin at a 45 90 angle with a quick dart like motion Figure T Holding the syringe in place pull back a little on the plunger and check to see if any blood flows into the syringe See Figure U If you see blood in the syringe it means that you have entered a blood vessel Do not inject ZOMACTON Withdraw the needle Throw away the syringe and needle in a puncture resistant container Do not use the same syringe or any of the other supplies that you used for this injection Repeat the steps to prepare a new syringe for injection Choose and clean a new injection site
19. pporting a greater risk in children compared with adults Published literature indicates that girls who have Turner syndrome may be at greater risk than other somatropin treated children Pancreatitis should be considered in any somatropin treated patient especially a child who develops persistent severe abdominal pain Benzyl alcohol a component used to reconstitute the ZOMACTON 5 mg vial has been associated with serious adverse events and death particularly in pediatric patients The gasping syndrome characterized by central nervous system depression metabolic acidosis gasping respirations and high levels of benzyl alcohol and its metabolites found in the blood and urine has been associated with benzyl alcohol dosages gt 99 mg kg day in neonates and low birth weight neonates Additional symptoms may include gradual neurological deterioration seizures intracranial hemorrhage hematologic abnormalities skin breakdown hepatic and renal failure hypotension bradycardia and cardiovascular collapse Practitioners administering this and other medications containing benzyl alcohol should consider the combined daily metabolic load of benzyl alcohol from all sources When administering ZOMACTON 5 mg to newborns reconstitute with sterile normal saline for injection USP WHEN RECONSTITUTING WITH STERILE NORMAL SALINE USE ONLY ONE DOSE PER VIAL AND DISCARD THE UNUSED PORTION PRECAUTIONS General ZOMACTON therapy should be carried
20. resistant and e properly labeled to warn of hazardous waste inside the container When your sharps disposal container is almost full you will need to follow your community guidelines for the right way to dispose of your sharps disposal container There may be state or local laws about how you should throw away used needles and syringes For more information about safe sharps disposal and for specific information about sharps disposal in the state that you live in go to the FDA s website at http www fda gov safesharpsdisposal e Do not throw used needles syringes or vials in your household trash or recycle e Keep the disposal container needles syringes and vials of ZOMACTON out of reach of children This Instructions for Use has been approved by the Food and Drug Administration Manufactured for Ferring Pharmaceuticals Inc Parsippany NJ 07054 Manufactured in Germany Rev 03 15
21. s radiation therapy for intracranial tumors New onset type 2 diabetes mellitus has been reported OVERDOSAGE The recommended dosage of up to 0 1 mg kg of body weight 3 times per week up to 0 3 mg kg week should not be exceeded Acute overdose could cause initial hypoglycemia and subsequent hyperglycemia Repeated use of doses in excess of those recommended could result in signs and symptoms of gigantism and or acromegaly consistent with the known effects of excess human growth hormone DOSAGE AND ADMINISTRATION The recommended dose is up to 0 1 mg kg administered subcutaneously three 3 times per week up to 0 3 mg kg week ZOMACTON 5 mg should be reconstituted with 1 5 mL of bacteriostatic 0 9 sodium chloride for injection USP benzyl alcohol preserved Reconstituted ZOMACTON 5 mg vials should not be used if the patient has a known sensitivity to benzyl alcohol Benzyl alcohol as a preservative in bacteriostatic normal saline USP has been associated with toxicity in newborns WHEN ADMINISTERING ZOMACTON TO NEWBORNS RECONSTITUTE WITH STERILE NORMAL SALINE FOR INJECTION USP ZOMACTON 10 mg should be reconstituted with 1 mL syringe of bacteriostatic water for injection containing 0 33 metacresol as a preservative Reconstituted ZOMACTON 10 mg vials should not be used if the patient is allergic to metacresol The stream of normal saline should be aimed against the side of the vial to prevent foaming Swirl the vial with a GENTLE ro
22. sphatase and IGF 1 may increase after somatropin therapy Drug Interactions The microsomal enzyme 11f hydroxysteroid dehydrogenase type 1 11BHSD 1 is required for conversion of cortisone to its active metabolite cortisol in hepatic and adipose tissue Growth hormone and somatropin inhibit 11BHSD 1 Consequently individuals with untreated GH deficiency have relative increases in 11BHSD 1 and serum cortisol Introduction of somatropin treatment may result in inhibition of 11BHSD 1 and reduced serum cortisol concentrations As a consequence previously undiagnosed central secondary hypoadrenalism may be unmasked and glucocorticoid replacement may be required in patients treated with somatropin In addition patients treated with glucocorticoid replacement for previously diagnosed hypoadrenalism may require an increase in their maintenance or stress doses following initiation of somatropin treatment this may be especially true for patients treated with cortisone acetate and prednisone since conversion of these drugs to their biologically active metabolites is dependent on the activity of 11BHSD 1 Pharmacologic glucocorticoid therapy and supraphysiologic glucocorticoid treatment may attenuate the growth promoting effects of somatropin in children Therefore glucocorticoid replacement dosing should be carefully adjusted in children receiving concomitant somatropin and glucocorticoid treatments to avoid both hypoadrenalism and an inhibitory effe
23. tary motion until the contents are completely dissolved and the solution is clear DO NOT SHAKE Since ZOMACTON is a protein shaking or vigorous mixing will cause the solution to be cloudy If the resulting solution is cloudy or contains particulate matter the contents MUST NOT be injected Occasionally after refrigeration some cloudiness may occur This is not unusual for proteins like ZOMACTON Allow the product to warm to room temperature If cloudiness persists or particulate matter is noted the contents MUST NOT be used Before and after injection the septum of the vial should be wiped with rubbing alcohol or an alcoholic antiseptic solution to prevent contamination of the contents by repeated needle insertions ZOMACTON 5 mg and 10 mg can be administered using a standard sterile disposable syringe or a ZOMA Jet Needle Free injection device For proper use please refer to the User s Manual provided with the administration device STABILITY AND STORAGE Before Reconstitution Vials of ZOMACTON 5 and 10 mg are stable when refrigerated at 36 to 46 F 2 to 8 C Avoid freezing the accompanying diluent Expiration dates are stated on the labels After Reconstitution ZOMACTON 5 mg is stable for up to 14 days when reconstituted with bacteriostatic 0 9 sodium chloride normal saline USP and stored in a refrigerator at 36 to 46 F 2 to 8 C Do not freeze the reconstituted solution ZOMACTON 10 mg is stable for up to 28 d
24. ve an increased incidence of slipped capital femoral epiphysis Any child who develops a limp or complains of hip or knee pain during somatropin therapy should be evaluated Intracranial hypertension IH with papilledema visual changes headache nausea and or vomiting has been reported in a small number of patients treated with growth hormone products IH has been reported more frequently after treatment with IGF 1 Symptoms usually occur within the first eight weeks after the initiation of growth hormone therapy In all reported cases H associated signs and symptoms resolved rapidly after temporary suspension or termination of therapy Funduscopic examination should be performed routinely before initiating treatment with somatropin to exclude preexisting papilledema and periodically during the course of somatropin therapy If papilledema is observed by funduscopy during somatropin treatment treatment should be stopped If somatropin induced idiopathic IH is diagnosed treatment with somatropin can be restarted at a lower dose after H associated signs and symptoms have resolved Progression of scoliosis can occur in children who experience rapid growth Because somatropin increases growth rate patients with a history of scoliosis who are treated with somatropin should be monitored for progression of scoliosis Bone age should be monitored periodically during somatropin administration especially in patients who are pubertal and or receiving c
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