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Pediatric Disease Annotations & Medicines



   leiomyoma
  

Disease ID 886
Disease leiomyoma
Definition
A benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. They rarely occur outside of the UTERUS and the GASTROINTESTINAL TRACT but can occur in the SKIN and SUBCUTANEOUS TISSUE, probably arising from the smooth muscle of small blood vessels in these tissues.
Synonym
[m]leiomyoma nos
[m]leiomyoma nos (morphologic abnormality)
[m]leiomyomatous neoplasm nos
[m]leiomyomatous neoplasm nos (morphologic abnormality)
[m]leiomyomatous neoplasms
[m]leiomyomatous neoplasms (morphologic abnormality)
fibroid
fibroid neoplasm
fibroid tumor
fibroid tumors
fibroids
fibroids tumor
fibroids tumors
fibromyoma
fibromyomas
leiomyofibroma
leiomyofibroma (morphologic abnormality)
leiomyoma [disease/finding]
leiomyoma, benign
leiomyoma, nos
leiomyomas
leiomyomatous neoplasm
leiomyomatous tumor
tumor fibroid
tumor, fibroid
tumors, fibroid
DOID
UMLS
C0023267
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:41)
C0042133  |  uterine leiomyoma  |  5
C0162482  |  uterine inversion  |  3
C0023267  |  leiomyomas  |  2
C0341858  |  adenomyosis  |  2
C1261473  |  sarcoma  |  2
C0087086  |  thrombi  |  1
C0259779  |  fibrous dysplasia  |  1
C0009806  |  constipation  |  1
C0023798  |  lipoma  |  1
C0014175  |  endometriosis  |  1
C0007134  |  renal cell carcinoma  |  1
C0085413  |  autosomal dominant polycystic kidney  |  1
C0206654  |  leiomyomatosis  |  1
C0346200  |  intravenous leiomyomatosis  |  1
C0003857  |  arteriovenous malformation  |  1
C0004245  |  atrioventricular block  |  1
C0023269  |  leiomyosarcoma  |  1
C0006264  |  bronchial tumor  |  1
C0021359  |  infertility  |  1
C0042133  |  uterine fibroid  |  1
C0016719  |  friedreich's ataxia  |  1
C1704327  |  bone sarcoma  |  1
C0206630  |  endometrial stromal sarcoma  |  1
C0153676  |  lung metastasis  |  1
C0037856  |  testicular torsion  |  1
C1368910  |  mature teratoma  |  1
C0022679  |  cystic kidney  |  1
C0007137  |  squamous cell carcinoma  |  1
C0085413  |  autosomal dominant polycystic kidney disease  |  1
C0016063  |  fibrous dysplasia of bone  |  1
C0025202  |  melanoma  |  1
C0032461  |  polycythaemia  |  1
C0242379  |  lung cancer  |  1
C0022593  |  keratosis  |  1
C0042133  |  uterine fibromyoma  |  1
C0032285  |  pneumonitis  |  1
C0040053  |  thrombosis  |  1
C0020437  |  hypercalcemia  |  1
C0023267  |  fibromyomas  |  1
C0007138  |  transitional cell carcinoma  |  1
C0042133  |  uterine fibroids  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:6)
SMAD3  |  4088  |  CTD_human
ESR1  |  2099  |  CTD_human
TSC2  |  7249  |  CTD_human
SFRP1  |  6422  |  CTD_human
INHBA  |  3624  |  CTD_human
WNT5B  |  81029  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:14)
51272  |  BET1L  |  infer
339799  |  EIF3FP3  |  infer
3479  |  IGF1  |  infer
23112  |  TNRC6B  |  infer
2068  |  ERCC2  |  infer
2271  |  FH  |  infer
2944  |  GSTM1  |  infer
3594  |  IL12RB1  |  infer
3606  |  IL18  |  infer
3553  |  IL1B  |  infer
3557  |  IL1RN  |  infer
3558  |  IL2  |  infer
3565  |  IL4  |  infer
7518  |  XRCC4  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:291)
401237  |  CASC15  |  DISEASES
50508  |  NOX3  |  DISEASES
7145  |  TNS1  |  DISEASES
51015  |  ISOC1  |  DISEASES
8646  |  CHRD  |  DISEASES
2099  |  ESR1  |  DISEASES
124  |  ADH1A  |  DISEASES
10454  |  TAB1  |  DISEASES
50  |  ACO2  |  DISEASES
10857  |  PGRMC1  |  DISEASES
9506  |  PAGE4  |  DISEASES
4313  |  MMP2  |  DISEASES
7249  |  TSC2  |  DISEASES
59284  |  CACNG7  |  DISEASES
3912  |  LAMB1  |  DISEASES
51384  |  WNT16  |  DISEASES
5054  |  SERPINE1  |  DISEASES
4232  |  MEST  |  DISEASES
1592  |  CYP26A1  |  DISEASES
6347  |  CCL2  |  DISEASES
1277  |  COL1A1  |  DISEASES
2798  |  GNRHR  |  DISEASES
595  |  CCND1  |  DISEASES
2026  |  ENO2  |  DISEASES
7942  |  TFEB  |  DISEASES
1839  |  HBEGF  |  DISEASES
7043  |  TGFB3  |  DISEASES
2797  |  GNRH2  |  DISEASES
27335  |  EIF3K  |  DISEASES
9098  |  USP6  |  DISEASES
968  |  CD68  |  DISEASES
1890  |  TYMP  |  DISEASES
25796  |  PGLS  |  DISEASES
2670  |  GFAP  |  DISEASES
5156  |  PDGFRA  |  DISEASES
10220  |  GDF11  |  DISEASES
1019  |  CDK4  |  DISEASES
3658  |  IREB2  |  DISEASES
4856  |  NOV  |  DISEASES
7057  |  THBS1  |  DISEASES
1588  |  CYP19A1  |  DISEASES
2660  |  MSTN  |  DISEASES
10152  |  ABI2  |  DISEASES
27190  |  IL17B  |  DISEASES
4053  |  LTBP2  |  DISEASES
4092  |  SMAD7  |  DISEASES
4087  |  SMAD2  |  DISEASES
284058  |  KANSL1  |  DISEASES
8503  |  PIK3R3  |  DISEASES
7077  |  TIMP2  |  DISEASES
10075  |  HUWE1  |  DISEASES
5595  |  MAPK3  |  DISEASES
6855  |  SYP  |  DISEASES
6801  |  STRN  |  DISEASES
2247  |  FGF2  |  DISEASES
1788  |  DNMT3A  |  DISEASES
8626  |  TP63  |  DISEASES
1462  |  VCAN  |  DISEASES
1950  |  EGF  |  DISEASES
1017  |  CDK2  |  DISEASES
5925  |  RB1  |  DISEASES
3480  |  IGF1R  |  DISEASES
9611  |  NCOR1  |  DISEASES
7157  |  TP53  |  DISEASES
207  |  AKT1  |  DISEASES
23432  |  GPR161  |  DISEASES
5546  |  PRCC  |  DISEASES
1513  |  CTSK  |  DISEASES
54539  |  NDUFB11  |  DISEASES
53336  |  CPXCR1  |  DISEASES
2796  |  GNRH1  |  DISEASES
5047  |  PAEP  |  DISEASES
133  |  ADM  |  DISEASES
6876  |  TAGLN  |  DISEASES
2697  |  GJA1  |  DISEASES
3206  |  HOXA10  |  DISEASES
221895  |  JAZF1  |  DISEASES
7345  |  UCHL1  |  DISEASES
201163  |  FLCN  |  DISEASES
760  |  CA2  |  DISEASES
7411  |  VBP1  |  DISEASES
23522  |  KAT6B  |  DISEASES
3815  |  KIT  |  DISEASES
3837  |  KPNB1  |  DISEASES
54361  |  WNT4  |  DISEASES
112950  |  MED8  |  DISEASES
23387  |  SIK3  |  DISEASES
6271  |  S100A1  |  DISEASES
112939  |  NACC1  |  DISEASES
30818  |  KCNIP3  |  DISEASES
9076  |  CLDN1  |  DISEASES
4286  |  MITF  |  DISEASES
6997  |  TDGF1  |  DISEASES
122042  |  RXFP2  |  DISEASES
7248  |  TSC1  |  DISEASES
2619  |  GAS1  |  DISEASES
3429  |  IFI27  |  DISEASES
170689  |  ADAMTS15  |  DISEASES
1381  |  CRABP1  |  DISEASES
123169  |  LEO1  |  DISEASES
5617  |  PRL  |  DISEASES
3479  |  IGF1  |  DISEASES
59350  |  RXFP1  |  DISEASES
3688  |  ITGB1  |  DISEASES
1281  |  COL3A1  |  DISEASES
649  |  BMP1  |  DISEASES
6638  |  SNRPN  |  DISEASES
2353  |  FOS  |  DISEASES
7532  |  YWHAG  |  DISEASES
23627  |  PRND  |  DISEASES
8462  |  KLF11  |  DISEASES
150353  |  DNAJB7  |  DISEASES
794  |  CALB2  |  DISEASES
9940  |  DLEC1  |  DISEASES
211  |  ALAS1  |  DISEASES
947  |  CD34  |  DISEASES
836  |  CASP3  |  DISEASES
9156  |  EXO1  |  DISEASES
7030  |  TFE3  |  DISEASES
23512  |  SUZ12  |  DISEASES
4233  |  MET  |  DISEASES
1960  |  EGR3  |  DISEASES
4684  |  NCAM1  |  DISEASES
83787  |  ARMC10  |  DISEASES
5315  |  PKM  |  DISEASES
23428  |  SLC7A8  |  DISEASES
8648  |  NCOA1  |  DISEASES
1400  |  CRMP1  |  DISEASES
222235  |  FBXL13  |  DISEASES
3039  |  HBA1  |  DISEASES
4312  |  MMP1  |  DISEASES
5021  |  OXTR  |  DISEASES
5241  |  PGR  |  DISEASES
4670  |  HNRNPM  |  DISEASES
5324  |  PLAG1  |  DISEASES
23347  |  SMCHD1  |  DISEASES
8738  |  CRADD  |  DISEASES
3855  |  KRT7  |  DISEASES
5121  |  PCP4  |  DISEASES
3009  |  HIST1H1B  |  DISEASES
5155  |  PDGFB  |  DISEASES
63827  |  BCAN  |  DISEASES
7490  |  WT1  |  DISEASES
1287  |  COL4A5  |  DISEASES
4088  |  SMAD3  |  DISEASES
682  |  BSG  |  DISEASES
3092  |  HIP1  |  DISEASES
10957  |  PNRC1  |  DISEASES
4221  |  MEN1  |  DISEASES
677  |  ZFP36L1  |  DISEASES
57820  |  CCNB1IP1  |  DISEASES
7095  |  SEC62  |  DISEASES
3091  |  HIF1A  |  DISEASES
2246  |  FGF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
4076  |  CAPRIN1  |  DISEASES
6590  |  SLPI  |  DISEASES
2100  |  ESR2  |  DISEASES
1499  |  CTNNB1  |  DISEASES
1842  |  ECM2  |  DISEASES
10516  |  FBLN5  |  DISEASES
92737  |  DNER  |  DISEASES
3767  |  KCNJ11  |  DISEASES
2335  |  FN1  |  DISEASES
2331  |  FMOD  |  DISEASES
55107  |  ANO1  |  DISEASES
5733  |  PTGER3  |  DISEASES
440738  |  MAP1LC3C  |  DISEASES
60  |  ACTB  |  DISEASES
4763  |  NF1  |  DISEASES
56980  |  PRDM10  |  DISEASES
7048  |  TGFBR2  |  DISEASES
4151  |  MB  |  DISEASES
93034  |  NT5C1B  |  DISEASES
1523  |  CUX1  |  DISEASES
3164  |  NR4A1  |  DISEASES
25942  |  SIN3A  |  DISEASES
1284  |  COL4A2  |  DISEASES
4311  |  MME  |  DISEASES
1312  |  COMT  |  DISEASES
2475  |  MTOR  |  DISEASES
114814  |  GNRHR2  |  DISEASES
800  |  CALD1  |  DISEASES
4779  |  NFE2L1  |  DISEASES
57713  |  SFMBT2  |  DISEASES
3151  |  HMGN2  |  DISEASES
1122  |  CHML  |  DISEASES
23596  |  OPN3  |  DISEASES
2271  |  FH  |  DISEASES
6000  |  RGS7  |  DISEASES
10370  |  CITED2  |  DISEASES
1805  |  DPT  |  DISEASES
6391  |  SDHC  |  DISEASES
1490  |  CTGF  |  DISEASES
1382  |  CRABP2  |  DISEASES
4288  |  MKI67  |  DISEASES
6277  |  S100A6  |  DISEASES
3713  |  IVL  |  DISEASES
5016  |  OVGP1  |  DISEASES
1586  |  CYP17A1  |  DISEASES
2564  |  GABRE  |  DISEASES
60495  |  HPSE2  |  DISEASES
5223  |  PGAM1  |  DISEASES
1791  |  DNTT  |  DISEASES
5730  |  PTGDS  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
8471  |  IRS4  |  DISEASES
1288  |  COL4A6  |  DISEASES
4318  |  MMP9  |  DISEASES
7075  |  TIE1  |  DISEASES
27328  |  PCDH11X  |  DISEASES
219738  |  C10orf35  |  DISEASES
5090  |  PBX3  |  DISEASES
8668  |  EIF3I  |  DISEASES
23633  |  KPNA6  |  DISEASES
54797  |  MED18  |  DISEASES
9968  |  MED12  |  DISEASES
367  |  AR  |  DISEASES
5698  |  PSMB9  |  DISEASES
4686  |  NCBP1  |  DISEASES
64061  |  TSPYL2  |  DISEASES
6390  |  SDHB  |  DISEASES
6392  |  SDHD  |  DISEASES
1282  |  COL4A1  |  DISEASES
1460  |  CSNK2B  |  DISEASES
5935  |  RBM3  |  DISEASES
687  |  KLF9  |  DISEASES
5987  |  TRIM27  |  DISEASES
1910  |  EDNRB  |  DISEASES
56998  |  CTNNBIP1  |  DISEASES
4609  |  MYC  |  DISEASES
55966  |  AJAP1  |  DISEASES
768  |  CA9  |  DISEASES
1906  |  EDN1  |  DISEASES
2308  |  FOXO1  |  DISEASES
6462  |  SHBG  |  DISEASES
171482  |  FAM9A  |  DISEASES
2315  |  MLANA  |  DISEASES
192668  |  CYS1  |  DISEASES
9037  |  SEMA5A  |  DISEASES
6468  |  FBXW4  |  DISEASES
238  |  ALK  |  DISEASES
6710  |  SPTB  |  DISEASES
2869  |  GRK5  |  DISEASES
29893  |  PSMC3IP  |  DISEASES
9801  |  MRPL19  |  DISEASES
65009  |  NDRG4  |  DISEASES
79868  |  ALG13  |  DISEASES
5744  |  PTHLH  |  DISEASES
1285  |  COL4A3  |  DISEASES
1286  |  COL4A4  |  DISEASES
124056  |  NOXO1  |  DISEASES
116372  |  LYPD1  |  DISEASES
29911  |  HOOK2  |  DISEASES
2047  |  EPHB1  |  DISEASES
7322  |  UBE2D2  |  DISEASES
81669  |  CCNL2  |  DISEASES
9612  |  NCOR2  |  DISEASES
8091  |  HMGA2  |  DISEASES
2199  |  FBLN2  |  DISEASES
2825  |  GPR1  |  DISEASES
3238  |  HOXD12  |  DISEASES
4052  |  LTBP1  |  DISEASES
84334  |  APOPT1  |  DISEASES
200424  |  TET3  |  DISEASES
9698  |  PUM1  |  DISEASES
3481  |  IGF2  |  DISEASES
3800  |  KIF5C  |  DISEASES
1029  |  CDKN2A  |  DISEASES
7849  |  PAX8  |  DISEASES
387836  |  CLEC2A  |  DISEASES
3491  |  CYR61  |  DISEASES
2741  |  GLRA1  |  DISEASES
1945  |  EFNA4  |  DISEASES
1967  |  EIF2B1  |  DISEASES
6513  |  SLC2A1  |  DISEASES
5890  |  RAD51B  |  DISEASES
6256  |  RXRA  |  DISEASES
55998  |  NXF5  |  DISEASES
55733  |  HHAT  |  DISEASES
200150  |  PLD5  |  DISEASES
3250  |  HPR  |  DISEASES
3939  |  LDHA  |  DISEASES
641455  |  POTEM  |  DISEASES
51741  |  WWOX  |  DISEASES
90632  |  LINC00473  |  DISEASES
401613  |  LINC00890  |  DISEASES
4553  |  MT-TA  |  DISEASES
9383  |  TSIX  |  DISEASES
7503  |  XIST  |  DISEASES
Locus(Waiting for update.)
Disease ID 886
Disease leiomyoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:42)
HP:0000131  |  Uterine leiomyoma  |  6
HP:0002664  |  Neoplasia  |  5
HP:0012531  |  Pain  |  4
HP:0100242  |  Sarcoma  |  2
HP:0000016  |  Urinary retention  |  2
HP:0000969  |  Dropsy  |  2
HP:0001541  |  Ascites  |  2
HP:0000139  |  Sagging uterus  |  1
HP:0009725  |  Bladder neoplasm  |  1
HP:0011134  |  Mild fever  |  1
HP:0012721  |  Venous malformations  |  1
HP:0100518  |  Painful or difficult urination  |  1
HP:0000074  |  Ureteropelvic junction obstruction  |  1
HP:0030127  |  Endometriosis  |  1
HP:0001978  |  Extramedullary hematopoiesis  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0001678  |  Atrioventricular block  |  1
HP:0000855  |  Insulin resistance  |  1
HP:0100749  |  Thoracic pain  |  1
HP:0002019  |  Dyschezia  |  1
HP:0002861  |  Melanoma  |  1
HP:0002304  |  Akinesia  |  1
HP:0002094  |  Dyspnea  |  1
HP:0012032  |  Lipoma  |  1
HP:0000789  |  Infertility  |  1
HP:0000132  |  Hypermenorrhea  |  1
HP:0006548  |  Pulmonary av malformation  |  1
HP:0100570  |  Carcinoid tumor  |  1
HP:0002721  |  Immunodeficiency  |  1
HP:0100243  |  Leiomyosarcoma  |  1
HP:0030016  |  Dyspareunia  |  1
HP:0005584  |  Renal cell carcinoma  |  1
HP:0002860  |  Squamous cell carcinoma  |  1
HP:0200116  |  Distal ileal atresia  |  1
HP:0011102  |  Ileal atresia  |  1
HP:0000113  |  Polycystic kidney dysplasia  |  1
HP:0100615  |  Neoplasm of the ovary  |  1
HP:0006515  |  Interstitial pneumonitis  |  1
HP:0030731  |  Carcinoma  |  1
HP:0100813  |  Testicular torsion  |  1
HP:0001945  |  Fever  |  1
HP:0003072  |  Hypercalcemia  |  1
Disease ID 886
Disease leiomyoma
Manually Symptom(Waiting for update.)
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:4)
C0341858  |  adenomyosis  |  2
C0019080  |  hemorrhage  |  1
C0032461  |  polycythaemia  |  1
C0040053  |  thrombosis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:12)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1048943205596491543CYP1A1umls:C0023267BeFreeWe concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.0.008272742011CYP1A11574720644TG,C,A
rs1048943205596491545CYP1B1umls:C0023267BeFreeWe concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.0.0053628242011CYP1A11574720644TG,C,A
rs1048943187630311543CYP1A1umls:C0023267BeFreeThese results suggest that the genotype of CYP1A1 Ile462Val was associated with the increased risk of uterine leiomyomas in Chinese women.0.008272742008CYP1A11574720644TG,C,A
rs1056836205596491543CYP1A1umls:C0023267BeFreeWe concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.0.008272742011CYP1B1238071060GC
rs1056836205596491545CYP1B1umls:C0023267BeFreeWe concluded that the carriage of CYP1A1 Ile462Val AG and CYP1B1 Leu 432Val CC genotypes predict the susceptibility to leiomyoma in Egyptian women and they are likely to contribute in the pathogenesis of leiomyoma.0.0053628242011CYP1B1238071060GC
rs1219085852461808181608FIP1L1umls:C0023267BeFreeActivated forms of the platelet derived growth factor receptor alpha (PDGFRα) have been described in various tumors, including FIP1L1-PDGFRα in patients with myeloproliferative diseases associated with hypereosinophilia and the PDGFRα(D842V) mutant in gastrointestinal stromal tumors and inflammatory fibroid polyps.0.0002714422014PDGFRA454285926AT
rs121908585246180815156PDGFRAumls:C0023267BeFreeActivated forms of the platelet derived growth factor receptor alpha (PDGFRα) have been described in various tumors, including FIP1L1-PDGFRα in patients with myeloproliferative diseases associated with hypereosinophilia and the PDGFRα(D842V) mutant in gastrointestinal stromal tumors and inflammatory fibroid polyps.0.0010857672014PDGFRA454285926AT
rs124847762146084223112TNRC6Bumls:C0023267GAD[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]0.0026384742011TNRC6B2240256869AG
rs2070874211386523565IL4umls:C0023267BeFreeAn association between polymorphisms of the IL4 gene promotor at positions -590 C/T and -33 C/T, and the risk of leiomyoma was observed.0.0005428842010IL45132674018CT
rs2172873214608423479IGF1umls:C0023267GAD[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]0.0142543932011NA12102731912GA
rs22805432146084251272BET1Lumls:C0023267GAD[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]0.0026384742011BET1L11203788CT
rs79130692146084279991OBFC1umls:C0023267GAD[A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.]0.0023670322011LOC10272435110103954641CT
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:0)
(Waiting for update.)
Chemical(Total Drugs:6)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0023267doxazosinD01729274191-85-8leiomyomaMESH:D007889therapeutic16403393
C0023267gabapentinC04002960142-96-3leiomyomaMESH:D007889therapeutic16403393
C0023267goserelinD01727365807-02-5leiomyomaMESH:D007889therapeutic16973256
C0023267leuprolideD01672953714-56-0leiomyomaMESH:D007889therapeutic10763848
C0023267progesteroneD01137457-83-0leiomyomaMESH:D007889marker/mechanism23427402
C0023267tranexamic acidD0141481197-18-8leiomyomaMESH:D007889therapeutic15229393
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:D007889neurontingabapentin100MGCAPSULE;ORALPrescriptionABYesNo
MESH:D007889neurontingabapentin600MGTABLET;ORALPrescriptionABYesNo
MESH:D007889neurontingabapentin250MG/5MLSOLUTION;ORALPrescriptionAAYesYes
MESH:D007889neurontingabapentin0SOLUTION; ORALPrescriptionNoneNoNo
MESH:D007889neurontingabapentin600MGTABLET; ORALPrescriptionNoneNoNo
MESH:D007889neurontingabapentin800MGCAPSULE; ORALPrescriptionNoneNoNo
MESH:D007889neurontingabapentin250MG/5MLSOLUTION; ORALPrescriptionNoneNoNo
MESH:D007889lystedatranexamic acid650MGTABLET;ORALPrescriptionABYesYes
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:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788912/10/2000neurontingabapentinAdjunctive therapy in the treatment of partial seizuresSafety and effectiveness established down to 3 years Neuropsychiatric AE's identified in 3-12 year olds Oral clearance normalized per body weight increased in childrenLabelingB---Parke-Davis2/2/2000FALSE'
MESH:D00788908/21/2013lystedatranexamic acidTreatment of cyclic heavy menstrual bleedingIndicated for women of reproductive age. It is not intended for use in premenarcheal girls Information on PK studyPostmarketing study-P--Ferring-FALSE'-