List of Drugs That Are Included in the Program

Total Page:16

File Type:pdf, Size:1020Kb

List of Drugs That Are Included in the Program MEDICAL INJECTABLE DRUG PROGRAM EFFECTIVE 09/01/2021 (additions in red) Brand Name Generic Name (billing code description) HCPCS MID Voluntary Adcetris brentuximab vedotin J9042 Alimta pemetrexed J9305 Avastin bevacizumab J9035 Erbitux cetuximab J9055 Eylea afilbercept J0178 Faslodex fulvestrant J9395 Halaven eribulin J9179 Kadcyla ado-trastuzumab emtansine J9354 Kyprolis carfilzomib J9047 Lucentis ranibizumab injection J2778 Macugen pegaptanib sodium J2503 Nplate romiplostim J2796 Oncaspar pegaspargase J9266 Opdivo nivolumab J9299 Perjeta pertuzumab J9306 Rituxan rituximab J9312 Treanda bendamustine J9033 Valstar valrubicin J9357 Velcade bortezomib J9041 Yervoy ipilimumab J9228 MID Mandatory Actimmune interferon gamma-1b J9216 Adagen pegademase bovine J2504 Aldurazyme laronidase J1931 Benlysta belimumab J0490 Betaseron interferon beta-1b J1830 Bivigam (immune globulin intravenous [human]) J1556 Botox botulinum toxin type A J0585 Carimune NF IVIG [immune globulin] (lyophilized and non-lyophilized) J1566 Cerezyme imiglucerase J1786 Copaxone glatiramer acetate J1595 Cosentyx secukinumab J3590 Durolane (preferred) hyaluronic acid J7318 Dysport abobotulinumtoxia A J0586 Elaprase idursulfase J1743 Enytivo vedolizumab J3380 Euflexxa (preferred) hyaluronate sodium injection J7323 Extavia interferon beta-1b J1830 Fabrazyme agalsidase beta J0180 Flebogamma DIF Injection, immune globulin, (flebogamma/flebogamma dif), J1572 intravenous, non-lyophilized (e.g. liquid), 500 mg Forteo teriparatide J3110 Gammagard immune globulin J1569 Gammagard S/D IVIG [immune globulin] (lyophilized and non-lyophilized) J1566 Gammaplex immune globulin J1557 Gamunex immune globulin J1561 Gamunex-C immune globulin Intravenous (Human) J1561 1 Brand Name Generic Name (billing code description) HCPCS MID Mandatory Gel-One hyaluronate hydrogel J7326 GELSYN-3 (preferred) sodium hyaluronate J7328 Genotropin somatropin [rDNA origin] J2941 GenVisc 850 sodium hyaluronate J7320 Glatopa glatiramer acetate J1595 H.P. Acthar repository corticotrophin J0800 Hizentra immune globulin [human] J1559 Humatrope somatropin [rDNA origin] J2941 Hyalgan sodium hyaluronate J7321 Hydroxyprogesterone Caproate (HPC) hydroxyprogesterone caproate J1729 Hymovis hyaluronan J7322 HyQvia Recombinant Human Hyaluronidase J1575 Ilaris canakinumab J0638 IVIG immune globulin [human] 90283 Kanuma sebelipase alfa J2840 Lemtrada alemtuzumab J0202 Lumizyme alglucosidase alfa J0221 Makena hydroxyprogesterone J1726 Monovisc high molecular weight hyaluronan J7327 Myobloc botulinum toxin type B J0587 Natpara parathyroid hormone J3590 Norditropin Growth Hormone J2941 Nucala mepolizumab J2182 Nutropin Growth Hormone J2941 Ocrevus ocrelizumab J2350 Octagam immune globulin J1568 Omnitrope somatropin J2941 Orencia abatacept J0129 Orthovisc high molecular weight hyaluronan J7324 Plegridy peginterferon beta-1a J3590 Praluent alirocumab J3590 Prialt ziconotide intrathecal infusion J2278 Privigen immune globulin [human] J1459 Rebif interferon beta-1a Q3028 Repatha evolocumab J3590 Risperdal Consta risperidone J2794 Ruconest recombinant human C1 esterase inhibitor (rhC1INH) J0596 Saizen [somatropin (rDNA origin)] J2941 Serostim somatropin J2941 Soliris eculizumab J1300 Stelara ustekinumab J3357 Stelara IV ustekinumab J3358 Supartz FX (preferred) sodium hyaluronate J7321 Supprelin LA histrelin acetate J9226 Sylvant siltuximab J2860 Synagis palivizumab 90378 Synvisc hylan GF 20 J7325 Synvisc- One hylan GF 20 J7325 Tev-Tropin [somatropin (rDNA origin)] J2941 Thyrogen thyrotropin alfa J3240 2 Brand Name Generic Name (billing code description) HCPCS MID Mandatory Tysabri natalizumab J2323 Visco-3 sodium hyaluronate J7333 Visudyne verteporfin J3396 Vivaglobin immune globulin subcutaneous J1562 & 90284 VPRIV veraglucerase J3385 Xeomin incobotulinumtoxin A J0588 Xolair omalizumab J2357 Zorbitive [somatropin (rDNA origin)] J2941 3.
Recommended publications
  • DRUGS REQUIRING PRIOR AUTHORIZATION in the MEDICAL BENEFIT Page 1
    Effective Date: 08/01/2021 DRUGS REQUIRING PRIOR AUTHORIZATION IN THE MEDICAL BENEFIT Page 1 Therapeutic Category Drug Class Trade Name Generic Name HCPCS Procedure Code HCPCS Procedure Code Description Anti-infectives Antiretrovirals, HIV CABENUVA cabotegravir-rilpivirine C9077 Injection, cabotegravir and rilpivirine, 2mg/3mg Antithrombotic Agents von Willebrand Factor-Directed Antibody CABLIVI caplacizumab-yhdp C9047 Injection, caplacizumab-yhdp, 1 mg Cardiology Antilipemic EVKEEZA evinacumab-dgnb C9079 Injection, evinacumab-dgnb, 5 mg Cardiology Hemostatic Agent BERINERT c1 esterase J0597 Injection, C1 esterase inhibitor (human), Berinert, 10 units Cardiology Hemostatic Agent CINRYZE c1 esterase J0598 Injection, C1 esterase inhibitor (human), Cinryze, 10 units Cardiology Hemostatic Agent FIRAZYR icatibant J1744 Injection, icatibant, 1 mg Cardiology Hemostatic Agent HAEGARDA c1 esterase J0599 Injection, C1 esterase inhibitor (human), (Haegarda), 10 units Cardiology Hemostatic Agent ICATIBANT (generic) icatibant J1744 Injection, icatibant, 1 mg Cardiology Hemostatic Agent KALBITOR ecallantide J1290 Injection, ecallantide, 1 mg Cardiology Hemostatic Agent RUCONEST c1 esterase J0596 Injection, C1 esterase inhibitor (recombinant), Ruconest, 10 units Injection, lanadelumab-flyo, 1 mg (code may be used for Medicare when drug administered under Cardiology Hemostatic Agent TAKHZYRO lanadelumab-flyo J0593 direct supervision of a physician, not for use when drug is self-administered) Cardiology Pulmonary Arterial Hypertension EPOPROSTENOL (generic)
    [Show full text]
  • Treatment of MDS in 2014 and Beyond Treatment Goals in MDS
    5/22/2014 Treatment of MDS in 2014 and Beyond Treatment goals in MDS • Get rid of it May 17, 2014 • If you can’t do that, make life better and longer – Improve blood counts Gail J. Roboz, M.D. – Improve quality of life Director, Leukemia Program – Decrease time to progression/leukemia Associate Professor of Medicine Hematopoietic Growth Factors: Hematopoietic Growth Factors: What are they? What are they? • Erythropoietin (EPO,Procrit®, Epogen®) – red • Synthetic versions of proteins normally • Granulocyte colony stimulating factor (GCSF, made in the body to stimulate growth of red Neupogen®) – white cells, white cells and platelets • Granulocyte-macrophage colony stimulating • Promote growth and differentiation factor (GM-CSF, Leukine®) – white • Thrombopoietin (TPO, romiplostim, Nplate®) – • Inhibitors of apoptosis (cell death) platelets • Darbepoietin (Aranesp®) • Peg-filgrastim (Neulasta®) • Note, these are not FDA-approved for MDS Erythropoietin (epo) in MDS Erythropoietin (epo) in MDS • Anemia is presents in >80% of MDS pts at dx • Often high endogenous epo levels • Transfusions help, but many issues • Many different doses and schedules • Recombinant EPO is FDA-approved for treating • Higher response rates with epo + G-CSF if anemia associated with kidney failure epo ≤500 mU/mL and transfusions <2 • Has been used since about 1990 in MDS U/month • Response rates in about 15-30% of patients • Poor probability of response if epo >500 • Many different studies including >1000 patients mU/mL and transfusions >2 U/month • Part of the NCCN MDS treatment guidelines 1. Casadevall N, et al. Blood. 2004;104:321-327. 2. Hellstrom-Lindberg E. Br J Haematol. 1995;89:67-71.
    [Show full text]
  • Saizen Prior Authorization Request Form (Page 1 of 4) DO NOT COPY for FUTURE USE
    OptumRx has partnered with CoverMyMeds to receive prior authorization requests, saving you time and often delivering real-time determinations. Visit go.covermymeds.com/OptumRx to begin using this free service. Please note: All information below is required to process this request. Mon-Fri: 5am to 10pm Pacific / Sat: 6am to 3pm Pacific ® Saizen Prior Authorization Request Form (Page 1 of 4) DO NOT COPY FOR FUTURE USE. FORMS ARE UPDATED FREQUENTLY AND MAY BE BARCODED Member Information (required) Provider Information (required) Member Name: Provider Name: Insurance ID#: NPI#: Specialty: Date of Birth: Office Phone: Street Address: Office Fax: City: State: Zip: Office Street Address: Phone: City: State: Zip: Medication Information (required) Medication Name: Strength: Dosage Form: Check if requesting brand Directions for Use: Check if request is for continuation of therapy Clinical Information (required) Select the diagnosis below: Pediatric growth hormone deficiency Growth hormone deficiency in adults Growth hormone deficiency in transition phase adolescents Isolated growth hormone deficiency in adults Pediatric growth failure associated with chronic renal insufficiency Prader-Willi syndrome Short-stature homeobox (SHOX) gene deficiency Small for gestational age (SGA) Turner syndrome or Noonan syndrome Other diagnosis: _________________________________________ ICD-10 Code(s): ___________________________________ Clinical Information: Select if the requested medication is prescribed by or in consultation with one of the following
    [Show full text]
  • September 2017 ~ Resource #330909
    −This Clinical Resource gives subscribers additional insight related to the Recommendations published in− September 2017 ~ Resource #330909 Medications Stored in the Refrigerator (Information below comes from current U.S. and Canadian product labeling and is current as of date of publication) Proper medication storage is important to ensure medication shelf life until the manufacturer expiration date and to reduce waste. Many meds are recommended to be stored at controlled-room temperature. However, several meds require storage in the refrigerator or freezer to ensure stability. See our toolbox, Medication Storage: Maintaining the Cold Chain, for helpful storage tips and other resources. Though most meds requiring storage at temperatures colder than room temperature should be stored in the refrigerator, expect to see a few meds require storage in the freezer. Some examples of medications requiring frozen storage conditions include: anthrax immune globulin (Anthrasil [U.S. only]), carmustine wafer (Gliadel [U.S. only]), cholera (live) vaccine (Vaxchora), dinoprostone vaginal insert (Cervidil), dinoprostone vaginal suppository (Prostin E2 [U.S.]), varicella vaccine (Varivax [U.S.]; Varivax III [Canada] can be stored in the refrigerator or freezer), zoster vaccine (Zostavax [U.S.]; Zostavax II [Canada] can be stored in the refrigerator or freezer). Use the list below to help identify medications requiring refrigerator storage and become familiar with acceptable temperature excursions from recommended storage conditions. Abbreviations: RT = room temperature Abaloparatide (Tymlos [U.S.]) Aflibercept (Eylea) Amphotericin B (Abelcet, Fungizone) • Once open, may store at RT (68°F to 77°F • May store at RT (77°F [25°C]) for up to Anakinra (Kineret) [20°C to 25°C]) for up to 30 days.
    [Show full text]
  • ANONYMOUS V MERCK SERONO Conduct of Representative
    CASE AUTH/2591/3/13 ANONYMOUS v MERCK SERONO Conduct of representative An anonymous, non-contactable complainant, An anonymous, non-contactable complainant, complained about the conduct of an un-named complained about the conduct of an un-named representative from Merck Serono who had representative from Merck Serono. requested a monthly visit throughout 2013. The complainant stated that he/she felt harassed as COMPLAINT such frequent meetings were unnecessary. The complainant was informed that these visits were The complainant was concerned about a meeting required to meet an instruction to have meetings that he/she had had with a Merck Serono with seven health professionals each day. representative. The complainant alleged that the representative had requested that he/she plan a The complainant noted that before this episode, monthly visit with him/her throughout 2013. The he/she had always found the representative to be complainant stated that he/she felt harassed by this very professional and an asset to the company. The request as such frequent meetings were completely complainant considered that the representatives unnecessary. When the complainant asked why the were being forced to behave in this way by representative wanted to plan so many meetings in unrealistic expectations from their managers. advance he/she was informed that these visits were required to meet an instruction to have meetings The detailed response from Merck Serono is given with seven health professionals each day. below. The complainant noted that before this episode, he/ The Panel noted that Merck Serono’s instructions to she had always found this representative to be very its representatives referred to a number of different professional and an asset to his/her company.
    [Show full text]
  • S. No. Name of the Firm Date of Permission No. Name of the Indication Dosage Form & Strength
    List of new drugs (r-DNA origin) approved for mannufacture and marketing in India for the Year 2021 S. No. Name of the firm Date of Permission No. Name of the Indication Dosage Form & Strength Rheumatoid Arthritis (RA)–Etanercept in combination with methotrexate is indicated for the treatment of moderate to severe active rheumatoid arthritis in adults when the response to disease-modifying antirheumatic drugs, including methotrexate (unless contraindicated), has been inadequate.Etanercept can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriateEtanercept is also indicated in the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate. Etanercept, alone or in combination with methotrexate, has been shown to reduce the rate of progression of joint damage as measured by X-ray and to improve physical functionJuvenile Idiopathic Arthritis (JIA) – Treatment of polyarthritis (rheumatoid factor positive or negative)and extended oligoarthritis in children and adolescents from the age of 2 years who have had aninadequate response to, or who have proved intolerant of, methotrexate.Treatment of psoriatic arthritis in adolescents from the age of 12 years who have had an inadequate response to, or who have proved intolerant of, methotrexate.Treatment of enthesitis-related arthritis in adolescents from the age of 12 years who have had an inadequate response Solution for subcutaneous Injection (single use)Pre- Mylan Pharmaceuticals to, or who have proved intolerant of, conventional therapy.Etanercept has not been studied in children aged less than 2 filled syringe:(i). 50 mg/mL in Prefilled Syringes(ii).
    [Show full text]
  • GROWTH HORMONE (Adult Therapy) Genotropin, Humatrope, Norditropin, Nutropin, Nutropin AQ, Omnitrope, Saizen, Sogroya*, Zomacton
    GROWTH HORMONE (Adult therapy) Genotropin, Humatrope, Norditropin, Nutropin, Nutropin AQ, Omnitrope, Saizen, Sogroya*, Zomacton Bolded medications are the preferred products *This medication is included in this policy but is not available in the market as of yet RATIONALE FOR INCLUSION IN PA PROGRAM Background Growth hormone deficiency (GHD) in adulthood, associated with hypothalamic-pituitary dysfunction is now widely accepted as a distinct clinical syndrome, and is linked to a substantial number of significant co-morbidities, many of which can be ameliorated with growth hormone replacement therapy (1). The FDA has approved growth hormone replacement for use in adult patients with growth hormone deficiency. Approved indications are for the treatment of adults with either adult onset or childhood onset GHD. With the exception of idiopathic adult onset GHD, GHD should be confirmed as due to pituitary disease from known causes, including pituitary tumor, pituitary surgical damage, hypothalamic disease, irradiation, trauma, or reconfirmed childhood GHD. Growth hormone should only be prescribed to patients with clinical features suggestive of adult GHD and biochemically proven evidence of adult GHD (1-9). Regulatory Status FDA approved indications: Human growth hormone is indicated for treatment of adult patients with either childhood-onset or adult-onset GH deficiency (2-9). The laboratory diagnosis of GHD in adults is determined by dynamic endocrine testing. Because growth hormone has a short half-life in blood growth hormone levels frequently are undetectable in blood samples obtained at random from normal subjects. For this reason, a stimulation test is needed to confirm the diagnosis. American Association of Clinical Endocrinologists (AACE) does not recommend growth hormone stimulation testing in patients with three or more pituitary hormone deficiencies and low IGF1 (2-9).
    [Show full text]
  • Novel Concepts of Treatment for Patients with Myelofibrosis And
    cancers Review Novel Concepts of Treatment for Patients with Myelofibrosis and Related Neoplasms Prithviraj Bose * , Lucia Masarova and Srdan Verstovsek Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; [email protected] (L.M.); [email protected] (S.V.) * Correspondence: [email protected] Received: 30 August 2020; Accepted: 1 October 2020; Published: 9 October 2020 Simple Summary: Myelofibrosis (MF) is an advanced form of a group of rare, related bone marrow cancers termed myeloproliferative neoplasms (MPNs). Some patients develop myelofibrosis from the outset, while in others, it occurs as a complication of the more indolent MPNs, polycythemia vera (PV) or essential thrombocythemia (ET). Patients with PV or ET who require drug treatment are typically treated with the chemotherapy drug hydroxyurea, while in MF, the targeted therapies termed Janus kinase (JAK) inhibitors form the mainstay of treatment. However, these and other drugs (e.g., interferons) have important limitations. No drug has been shown to reliably prevent the progression of PV or ET to MF or transformation of MPNs to acute myeloid leukemia. In PV, it is not conclusively known if JAK inhibitors reduce the risk of blood clots, and in MF, these drugs do not improve low blood counts. New approaches to treating MF and related MPNs are, therefore, necessary. Abstract: Janus kinase (JAK) inhibition forms the cornerstone of the treatment of myelofibrosis (MF), and the JAK inhibitor ruxolitinib is often used as a second-line agent in patients with polycythemia vera (PV) who fail hydroxyurea (HU). In addition, ruxolitinib continues to be studied in patients with essential thrombocythemia (ET).
    [Show full text]
  • Specialty Guideline Management
    Reference number(s) 1741-A SPECIALTY GUIDELINE MANAGEMENT GENOTROPIN (somatropin) HUMATROPE (somatropin) NORDITROPIN (somatropin) NUTROPIN AQ (somatropin) OMNITROPE (somatropin) SAIZEN (somatropin) ZOMACTON (somatropin) POLICY I. INDICATIONS The indications below including FDA-approved indications and compendial uses are considered a covered benefit provided that all the approval criteria are met and the member has no contraindications or exclusions to the prescribed therapy. A. FDA-Approved Indications 1. Pediatric patients with growth failure due to any of the following: a. Growth hormone (GH) deficiency b. Turner syndrome c. Noonan syndrome d. Small for gestational age (SGA) e. Prader-Willi syndrome f. Chronic kidney disease (CKD) g. Short stature homeobox-containing gene (SHOX) deficiency h. Idiopathic short stature (ISS)* 2. Adults with childhood-onset or adult-onset GH deficiency * ISS may not be covered by some plans B. Compendial Uses 1. Human immunodeficiency virus (HIV)-associated wasting/cachexia 2. Short bowel syndrome (SBS) 3. Growth failure associated with any of the following: a. Cerebral palsy b. Congenital adrenal hyperplasia c. Cystic fibrosis d. Russell-Silver syndrome All other indications are considered experimental/investigational and not medically necessary. II. REQUIRED DOCUMENTATION The following information is necessary to initiate the prior authorization review for both initial and continuation of therapy requests (where applicable): A. Medical records supporting the diagnosis of neonatal GH deficiency Growth Hormone With ISS 1741-A SGM P2021.docx © 2021 CVS Caremark. All rights reserved. This document contains confidential and proprietary information of CVS Caremark and cannot be reproduced, distributed or printed without written permission from CVS Caremark. This document contains prescription brand name drugs that are trademarks or registered trademarks of pharmaceutical manufacturers that are not affiliated with CVS Caremark.
    [Show full text]
  • Medicines/Pharmaceuticals of Animal Origin V3.0 November 2020
    Medicines/pharmaceuticals of animal origin V3.0 November 2020 Medicines/pharmaceuticals of animal origin - This guideline provides information for all clinical staff within Hospital and Health Services (HHS) on best practice for avoidance of issues related to animal products. Medicines/pharmaceuticals of animal origin - V3.0 November 2020 Published by the State of Queensland (Queensland Health), November 2020 This document is licensed under a Creative Commons Attribution 3.0 Australia licence. To view a copy of this licence, visit creativecommons.org/licenses/by/3.0/au © State of Queensland (Queensland Health) 2020 You are free to copy, communicate and adapt the work, as long as you attribute the State of Queensland (Queensland Health). For more information contact: Medication Services Queensland, Queensland Health, GPO Box 48, Brisbane QLD 4001, email [email protected] An electronic version of this document is available at https://www.health.qld.gov.au/__data/assets/pdf_file/0024/147507/qh-gdl-954.pdf Disclaimer: The content presented in this publication is distributed by the Queensland Government as an information source only. The State of Queensland makes no statements, representations or warranties about the accuracy, completeness or reliability of any information contained in this publication. The State of Queensland disclaims all responsibility and all liability (including without limitation for liability in negligence) for all expenses, losses, damages and costs you might incur as a result of the information being inaccurate
    [Show full text]
  • Nplate (Romiplostim)  Discard Any Unused Portion of the Single-Use Vial
    HIGHLIGHTS OF PRESCRIBING INFORMATION Do not shake during reconstitution; protect reconstituted Nplate from These highlights do not include all the information needed to use Nplate light; administer reconstituted Nplate within 24 hours. (2.2) safely and effectively. See full prescribing information for Nplate. The injection volume may be very small. Use a syringe with graduations to 0.01 mL. (2.2) ® Nplate (romiplostim) Discard any unused portion of the single-use vial. (2.2) For subcutaneous injection ---------------------DOSAGE FORMS AND STRENGTHS---------------------- 250 mcg or 500 mcg of deliverable romiplostim in single-use vials ( 3) Initial U.S. Approval: 2008 ---------------------------RECENT MAJOR CHANGES--------------------------- -------------------------------CONTRAINDICATIONS ---------------------------- Indications and Usage (1) 07/2011 None (4) Dosage and Administration, Nplate Distribution removal 12/2011 -----------------------WARNINGS AND PRECAUTIONS------------------------ Program (2) In patients with MDS, Nplate increases blast cell counts and increases Warnings and Precautions: Progression of Myelodysplastic the risk of progression to acute myelogenous leukemia. (5.1) Syndromes (5.1) 07/2011 Thrombotic/thromboembolic complications may result from increases in Warnings and Precautions: Thrombotic/Thromboembolic platelet counts with Nplate use. Portal vein thrombosis has been Events (5.2) 07/2011 reported in patients with chronic liver disease receiving Nplate. Use Warning and Precaution: Bone Marrow Reticulin Formation with additional caution in ITP patients with chronic liver disease. (5.2) and Fibrosis (5.3) 12/2011 Discontinuation of Nplate may result in worsened thrombocytopenia Warnings and Precautions: Laboratory Monitoring (5.6) 12/2011 than was present prior to Nplate therapy. Monitor complete blood Warnings and Precautions: Nplate Distribution removal 12/2011 counts (CBCs), including platelet counts, for at least 2 weeks following Program (5.7) Nplate discontinuation.
    [Show full text]
  • Saizen Prescribing Information
    HIGHLIGHTS OF PRESCRIBING INFORMATION ___________ WARNINGS AND PRECAUTIONS ___________ These highlights do not include all the information needed to use • Acute Critical Illness: Potential benefit of treatment continuation SAIZEN® safely and effectively. See full prescribing information should be weighed against the potential risk (5.1) for SAIZEN. • Prader-Willi syndrome in Children: Evaluate for signs of upper airway obstruction and sleep apnea before initiation of SAIZEN (somatropin) for injection, for subcutaneous use treatment. Discontinue treatment if these signs occur (5.2) Initial U.S. Approval: 1987 • Neoplasms: Monitor patients with preexisting tumors for progression or recurrence. Increased risk of a second neoplasm ______________ ______________ in childhood cancer survivors treated with somatropin—in INDICATIONS AND USAGE particular meningiomas as in patients treated with radiation to SAIZEN is a recombinant human growth hormone indicated for: the head for their first neoplasm (5.3) Pediatric: Treatment of children with growth failure due to growth • Impaired Glucose Tolerance and Diabetes Mellitus: May be hormone deficiency (GHD) (1.1) unmasked. Periodically monitor glucose levels in all patients Adult: Treatment of adults with either adult onset or childhood onset Doses of concurrent antihyperglycemic drugs in diabetics may GHD. (1.2) require adjustment (5.4) • Intracranial Hypertension: Exclude preexisting papilledema. ___________ DOSAGE AND ADMINISTRATION ___________ May develop and is usually reversible after discontinuation
    [Show full text]