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Pediatric Disease Annotations & Medicines



   polymyositis
  

Disease ID 115
Disease polymyositis
Definition
Diseases characterized by inflammation involving multiple muscles. This may occur as an acute or chronic condition associated with medication toxicity (DRUG TOXICITY); CONNECTIVE TISSUE DISEASES; infections; malignant NEOPLASMS; and other disorders. The term polymyositis is frequently used to refer to a specific clinical entity characterized by subacute or slowly progressing symmetrical weakness primarily affecting the proximal limb and trunk muscles. The illness may occur at any age, but is most frequent in the fourth to sixth decade of life. Weakness of pharyngeal and laryngeal muscles, interstitial lung disease, and inflammation of the myocardium may also occur. Muscle biopsy reveals widespread destruction of segments of muscle fibers and an inflammatory cellular response. (Adams et al., Principles of Neurology, 6th ed, pp1404-9)
Synonym
multiple myositis
myositides, multiple
myositis, multiple
neuromyositis
neuromyositis-retired
neuromyositis-retired (disorder)
pm - polymyositis
polymyositides
polymyositis (disorder)
polymyositis [disease/finding]
Orphanet
DOID
UMLS
C0085655
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:58)
C0024115  |  lung disease  |  12
C0206062  |  interstitial lung disease  |  12
C0026848  |  myopathy  |  5
C0019158  |  hepatitis  |  4
C0003873  |  rheumatoid arthritis  |  3
C0009782  |  connective tissue disorder  |  3
C0003864  |  arthritis  |  2
C0241910  |  autoimmune hepatitis  |  2
C0009782  |  connective tissue disorders  |  2
C0011633  |  dermatomyositis  |  2
C0027121  |  myositis  |  2
C0019163  |  hepatitis b  |  2
C0007102  |  colon cancer  |  2
C0026896  |  myasthenia gravis  |  2
C0020538  |  hypertension  |  2
C0027059  |  myocarditis  |  2
C0032285  |  pneumonia  |  2
C0206062  |  interstitial lung diseases  |  1
C0752166  |  bardet-biedl syndrome  |  1
C0008312  |  primary biliary cirrhosis  |  1
C0020676  |  hypothyroidism  |  1
C0027121  |  inflammatory myopathy  |  1
C0677607  |  hashimoto's thyroiditis  |  1
C1527336  |  sjogren's syndrome  |  1
C1145670  |  respiratory failure  |  1
C0020542  |  pulmonary hypertension  |  1
C0021053  |  immune disease  |  1
C0009782  |  connective tissue diseases  |  1
C0006142  |  breast cancer  |  1
C0442874  |  neuropathy  |  1
C0456845  |  non-secretory myeloma  |  1
C0334254  |  lymphoepithelioma  |  1
C0027121  |  inflammatory myopathies  |  1
C0010346  |  crohn's disease  |  1
C0020550  |  hyperthyroidism  |  1
C0026848  |  myopathies  |  1
C0032461  |  polycythaemia  |  1
C0027726  |  nephrotic syndrome  |  1
C0026850  |  muscular dystrophies  |  1
C0032463  |  polycythaemia vera  |  1
C0027121  |  muscle inflammation  |  1
C0242379  |  lung cancer  |  1
C0024115  |  pulmonary disease  |  1
C0018213  |  graves' disease  |  1
C0026850  |  muscular dystrophy  |  1
C0019204  |  hepatocellular carcinoma  |  1
C0024115  |  lung diseases  |  1
C0024299  |  lymphoma  |  1
C0009782  |  connective tissue disease  |  1
C0026764  |  myeloma  |  1
C0011570  |  depression  |  1
C0085278  |  antiphospholipid antibody syndrome  |  1
C0034065  |  pulmonary embolism  |  1
C0020626  |  hypoparathyroidism  |  1
C0039590  |  testicular cancer  |  1
C0026846  |  muscle atrophy  |  1
C0235974  |  pancreatic cancer  |  1
C0376545  |  hematological malignancy  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:5)
TNF  |  7124  |  CTD_human
IL6  |  3569  |  CTD_human
IL1B  |  3553  |  CTD_human
CYP27B1  |  1594  |  CTD_human
IL1A  |  3552  |  CTD_human
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 115
Disease polymyositis
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:41)
HP:0011675  |  Arrhythmia
HP:0001618  |  Dysphonia
HP:0012735  |  Cough
HP:0002239  |  Gastrointestinal hemorrhage
HP:0002829  |  Arthralgia
HP:0001635  |  Congestive heart failure
HP:0001824  |  Weight loss
HP:0002019  |  Constipation
HP:0005150  |  Abnormal atrioventricular conduction
HP:0001315  |  Reduced tendon reflexes
HP:0000934  |  Chondrocalcinosis
HP:0001633  |  Abnormality of the mitral valve
HP:0003701  |  Proximal muscle weakness
HP:0002960  |  Autoimmunity
HP:0003326  |  Myalgia
HP:0001945  |  Fever
HP:0006530  |  Interstitial pulmonary disease
HP:0004936  |  Venous thrombosis
HP:0002206  |  Pulmonary fibrosis
HP:0000091  |  Abnormality of the renal tubule
HP:0002093  |  Respiratory insufficiency
HP:0003236  |  Elevated serum creatine phosphokinase
HP:0001252  |  Muscular hypotonia
HP:0003002  |  Breast carcinoma
HP:0012544  |  Elevated aldolase level
HP:0002240  |  Hepatomegaly
HP:0003457  |  EMG abnormality
HP:0012378  |  Fatigue
HP:0002633  |  Vasculitis
HP:0001369  |  Arthritis
HP:0001701  |  Pericarditis
HP:0001658  |  Myocardial infarction
HP:0004303  |  Abnormality of muscle fibers
HP:0002875  |  Exertional dyspnea
HP:0001608  |  Abnormality of the voice
HP:0002039  |  Anorexia
HP:0002020  |  Gastroesophageal reflux
HP:0001639  |  Hypertrophic cardiomyopathy
HP:0002027  |  Abdominal pain
HP:0001288  |  Gait disturbance
HP:0001644  |  Dilated cardiomyopathy
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:47)
HP:0006530  |  Interstitial lung disease  |  11
HP:0003198  |  Myopathic changes  |  5
HP:0001324  |  Muscular weakness  |  5
HP:0012115  |  Liver inflammation  |  4
HP:0001370  |  Rheumatoid arthritis  |  3
HP:0003201  |  Rhabdomyolysis  |  3
HP:0100614  |  Muscle inflammation  |  3
HP:0002090  |  Pneumonia  |  2
HP:0003473  |  Fatigable weakness  |  2
HP:0003003  |  Colon cancer  |  2
HP:0001369  |  Arthritis  |  2
HP:0003701  |  Proximal limb muscle weakness  |  2
HP:0001297  |  Cerebral vascular events  |  2
HP:0012819  |  Myocarditis  |  2
HP:0000829  |  Hypoparathyroidism  |  1
HP:0003560  |  Muscular dystrophy  |  1
HP:0002664  |  Neoplasia  |  1
HP:0002894  |  Neoplasia of the pancreas  |  1
HP:0002092  |  Pulmonary artery hypertension  |  1
HP:0002486  |  Myotonia  |  1
HP:0002204  |  Pulmonary embolism  |  1
HP:0000836  |  Overactive thyroid  |  1
HP:0001288  |  Gait disturbance  |  1
HP:0002140  |  Ischemic stroke  |  1
HP:0003613  |  Antiphospholipid antibodies  |  1
HP:0003002  |  Breast carcinoma  |  1
HP:0012089  |  Arteritis  |  1
HP:0000822  |  Hypertension  |  1
HP:0000716  |  Depression  |  1
HP:0009071  |  Inflammatory myopathy  |  1
HP:0012531  |  Pain  |  1
HP:0012378  |  Fatigue  |  1
HP:0002665  |  Lymphoma  |  1
HP:0001402  |  Hepatocellular carcinoma  |  1
HP:0004756  |  Ventricular tachycardia  |  1
HP:0001649  |  Tachycardia  |  1
HP:0002878  |  Respiratory failure  |  1
HP:0000821  |  Underactive thyroid  |  1
HP:0000872  |  Hashimoto's thyroiditis  |  1
HP:0003202  |  Neurogenic muscle atrophy, especially in the lower limbs  |  1
HP:0002960  |  Autoimmune condition  |  1
HP:0000100  |  Nephrosis  |  1
HP:0001717  |  Coronary artery calcification  |  1
HP:0011096  |  Demyelination  |  1
HP:0100280  |  Morbus Crohn  |  1
HP:0030731  |  Carcinoma  |  1
HP:0000969  |  Dropsy  |  1
Disease ID 115
Disease polymyositis
Manually Symptom
UMLS  | Name(Total Manually Symptoms:90)
C2697391  |  rheumatoid arthritis
C2609059  |  antisynthetase syndrome
C2364133  |  infection
C2364118  |  weakness
C1963229  |  retinal detachment
C1963220  |  pulmonary hypertension
C1962972  |  proteinuria
C1962971  |  myocarditis
C1962966  |  retinopathy
C1512411  |  hepatocellular carcinoma
C1420725  |  thymoma
C1384514  |  primary aldosteronism
C1290344  |  nonspecific interstitial pneumonia
C1145670  |  respiratory failure
C1112565  |  pneumatosis intestinalis
C0878544  |  myocardial disease
C0865681  |  chronic myocarditis
C0852949  |  arteriopathy
C0748159  |  pulmonary involvement
C0549225  |  myasthenic syndrome
C0520463  |  chronic active hepatitis
C0520459  |  necrotizing enterocolitis
C0442874  |  neuropathy
C0432474  |  klinefelter's syndrome
C0403457  |  myoglobinuric acute renal failure
C0403416  |  crescentic glomerulonephritis
C0398367  |  kikuchi-fujimoto disease
C0268123  |  myoadenylate deaminase deficiency
C0264886  |  conduction disorders
C0264886  |  conduction defects
C0264886  |  cardiac conduction defects
C0264490  |  acute respiratory failure
C0242770  |  bronchiolitis obliterans organizing pneumonia
C0238183  |  atrophic thyroiditis
C0235896  |  pulmonary infiltrates
C0231443  |  musculoskeletal symptoms
C0206180  |  ki-1 lymphoma
C0206062  |  interstitial lung diseases
C0206062  |  interstitial lung disease
C0206061  |  interstitial pneumonitis
C0206061  |  interstitial pneumonia
C0205969  |  malignant thymoma
C0155686  |  acute myocarditis
C0085786  |  fibrosing alveolitis
C0042769  |  viral infection
C0042721  |  virus hepatitis
C0042338  |  herpes zoster
C0038463  |  strongyloidiasis
C0037116  |  silicosis
C0035222  |  adult respiratory distress syndrome
C0034902  |  pure red cell aplasia
C0034155  |  thrombotic thrombocytopenic purpura
C0034069  |  pulmonary fibrosis
C0032285  |  pneumonitis
C0032285  |  pneumonia
C0032266  |  pneumatosis cystoides intestinalis
C0030472  |  paraneoplastic syndrome
C0030326  |  panniculitis
C0029118  |  opportunistic infections
C0027831  |  von recklinghausen's disease
C0027122  |  muscle calcification
C0027121  |  muscle inflammation
C0026916  |  mycobacterium avium-intracellulare infection
C0025063  |  mediastinal tumor
C0024305  |  non-hodgkin's lymphoma
C0024299  |  malignant lymphoma
C0024282  |  lymphocytosis
C0024115  |  lung disease
C0023283  |  cutaneous leishmaniasis
C0023241  |  legionnaires' disease
C0022660  |  acute renal failure
C0022408  |  arthropathy
C0019829  |  hodgkin's disease
C0018802  |  congestive heart failure
C0018794  |  heart block
C0018213  |  graves' disease
C0017668  |  focal glomerulosclerosis
C0017658  |  glomerulonephritis
C0017152  |  gastritis
C0014858  |  esophageal motility disorder
C0014858  |  esophageal dysmotility
C0011168  |  dysphagia
C0010403  |  cryoglobulinemia
C0010266  |  cranial neuropathy
C0008521  |  choroidopathy
C0008312  |  primary biliary cirrhosis
C0007193  |  dilated cardiomyopathy
C0007134  |  renal cell carcinoma
C0004245  |  av block
C0003490  |  aortic arch syndrome
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:16)
C0206062  |  interstitial lung disease  |  11
C0024115  |  lung disease  |  11
C0004093  |  weakness  |  3
C0003873  |  rheumatoid arthritis  |  3
C0027059  |  myocarditis  |  2
C0032285  |  pneumonia  |  2
C0009450  |  infection  |  2
C0008312  |  primary biliary cirrhosis  |  1
C0020542  |  pulmonary hypertension  |  1
C0018213  |  graves' disease  |  1
C1145670  |  respiratory failure  |  1
C2609059  |  antisynthetase syndrome  |  1
C0027121  |  muscle inflammation  |  1
C0206061  |  interstitial pneumonia  |  1
C0442874  |  neuropathy  |  1
C0019204  |  hepatocellular carcinoma  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:15)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs10069690263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51279675CT
rs10069690263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51279675CT
rs11171739263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA1256076841CT
rs11171739263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA1256076841CT
rs1327711324632671640BLKumls:C0085655BeFreeThe C8orf13-BLK rs13277113A allele was associated with overall polymyositis/dermatomyositis (P<0.001, odds ratio [OR] 1.44, 95% confidence interval [CI] 1.19-1.73), as well as polymyositis (P = 0.011, OR 1.32, 95% CI 1.06-1.64) and dermatomyositis (P<0.001, OR 1.64, 95% CI 1.26-2.12).0.0005428842014NA811491677GA
rs132771132463267183648FAM167Aumls:C0085655BeFreeThe C8orf13-BLK rs13277113A allele was associated with overall polymyositis/dermatomyositis (P<0.001, odds ratio [OR] 1.44, 95% confidence interval [CI] 1.19-1.73), as well as polymyositis (P = 0.011, OR 1.32, 95% CI 1.06-1.64) and dermatomyositis (P<0.001, OR 1.64, 95% CI 1.26-2.12).0.0005428842014NA811491677GA
rs2292239263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015ERBB31256088396TG
rs2292239263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015ERBB31256088396TG
rs2492358263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934737831CT
rs2492358263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934737831CT
rs2853676263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51288432TC
rs2853676263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015TERT51288432TC
rs951005263205932065ERBB3umls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934743684GA
rs951005263205936366CCL21umls:C0085655BeFreeA single-nucleotide polymorphism of CCL21 rs951005 T>C is associated with susceptibility of polymyositis and such patients with interstitial lung disease in a Chinese Han population.0.0032672342015NA934743684GA
rs951005263205937015TERTumls:C0085655BeFreeChinese polymyositis (PM) patients (n =291), dermatomyositis (DM) patients (n=526) and ethnically-matched healthy controls (n =968) were genotyped for the CCL21 region SNPs (rs951005 and rs2492358), ERBB3 (rs2292239 and rs11171739), and TERT (rs2853676 and rs10069690), by using the Sequenom MassArray system.0.0002714422015NA934743684GA
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002206Pulmonary fibrosisMP:0003141cardiac fibrosis;HP:0001402Hepatocellular carcinoma
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0002206Pulmonary fibrosisMP:0002420abnormal adaptive immunity;HP:0001402Hepatocellular carcinoma
Chemical(Total Drugs:11)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0085655ampicillinD00066769-53-4polymyositisMESH:D017285marker/mechanism712173
C0085655celecoxibD000068579-polymyositisMESH:D017285marker/mechanism18583892
C0085655cimetidineD00292751481-61-9polymyositisMESH:D017285marker/mechanism6217424
C0085655ethambutolD00497774-55-5polymyositisMESH:D017285marker/mechanism18583892
C0085655methotrexateD0087271959/5/2polymyositisMESH:D017285therapeutic17400583
C0085655octreotideD01528283150-76-9polymyositisMESH:D017285marker/mechanism10509161
C0085655phenytoinD01067257-41-0polymyositisMESH:D017285marker/mechanism574201
C0085655pravastatinD01703581093-37-0polymyositisMESH:D017285marker/mechanism15199734
C0085655tioproninD0086251953/2/2polymyositisMESH:D017285marker/mechanism10360187
C0085655cholecalciferolD00276267-97-0polymyositisMESH:D017285marker/mechanism20427501
C0085655zidovudineD01521530516-87-1polymyositisMESH:D017285marker/mechanism3422706
FDA approved drug and dosage information(Total Drugs:8)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D017285celebrexcelecoxib100MGCAPSULE;ORALPrescriptionABYesNo
MESH:D017285celebrexcelecoxib100MGCAPSULE;ORALPrescriptionNoneNoNo
MESH:D017285retrovirzidovudine100MGCAPSULE;ORALPrescriptionABYesYes
MESH:D017285retrovirzidovudine50MG/5MLSYRUP;ORALPrescriptionAAYesYes
MESH:D017285retrovirzidovudine10MG/MLINJECTABLE;INJECTIONPrescriptionAPYesYes
MESH:D017285retrovirzidovudine200MGTABLET;ORALDiscontinuedNoneNoNo
MESH:D017285zidovudinezidovudine60MGTABLET;ORALDiscontinuedNoneNoNo
MESH:D017285zidovudinezidovudine60MGTABLET;ORALDiscontinuedNoneNoNo
FDA labeling changes(Total Drugs:8)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D01728512/15/2006celebrexcelecoxibRelief of the signs and symptoms of juvenile rheumatoid arthritis (JRA)New indication in 2 years and older Has not been studied in patients < 2 years, in patients with body weight < 10 kg, or in patients with active systemic features Celecoxib should be used only with caution in patients with systemic onset JRA due to the risk for serious adverse reactions including the risk of disseminated intravascular coagulation The long-term cardiovascular toxicity in children has not been evaluated; it is unknown if the long-term risk may be similar to that seen in adults New 50 mg capsule developed Information on adding contents of a capsule to applesauce. for patients with difficulty swallowing capsules Information on dose, clinical studies, PK parameters, AEsLabelingB---Pfizer08/23/2006FALSE'
MESH:D01728512/15/2006celebrexcelecoxibRelief of the signs and symptoms of juvenile rheumatoid arthritis (JRA)New indication in 2 years and older Has not been studied in patients < 2 years, in patients with body weight < 10 kg, or in patients with active systemic features Celecoxib should be used only with caution in patients with systemic onset JRA due to the risk for serious adverse reactions including the risk of disseminated intravascular coagulation The long-term cardiovascular toxicity in children has not been evaluated; it is unknown if the long-term risk may be similar to that seen in adults New 50 mg capsule developed Information on adding contents of a capsule to applesauce. for patients with difficulty swallowing capsules Information on dose, clinical studies, PK parameters, AEsLabelingB---Pfizer08/23/2006FALSE'
MESH:D0172856/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0172856/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0172856/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0172856/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'
MESH:D01728509/19/2008retrovir syrup, capsules and tabletszidovudineUsed in combination with 18 other antiretroviral agents for the treatment of HIV-1 infectionDosing and administration information provided to children 6 weeks to less than 18 years of age Macrocytosis was reported in the majority of pediatric patients receiving Retrovir 180 mg/m2 every 6 hours in open-label studies New dosing regimenLabeling-P--GlaxoSmithKline-TRUE'
MESH:D0172856/11/2009retrovirzidovudineTreatment of HIV-1 infection in combination with other antiretroviral agentsProvided dosing recommendations for patients 4 weeks to < 6 weeks of age and weighing 4 kg to < 9 kgLabeling-P--GlaxoSmithKline-TRUE'