leukocytosis |
Disease ID | 1929 |
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Disease | leukocytosis |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | (Waiting for update.) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Chemical(Total Drugs:18) | |||||||||
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CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
C0023518 | arsenic trioxide | C006632 | 1327-53-3 | leukocytosis | MESH:D007964 | marker/mechanism | 11007035 | ||
C0023518 | azithromycin | D017963 | 83905-01-5 | leukocytosis | MESH:D007964 | therapeutic | 21195124 | ||
C0023518 | carbamazepine | D002220 | 298-46-4 | leukocytosis | MESH:D007964 | marker/mechanism | 2327680 | ||
C0023518 | chloramphenicol | D002701 | 56-75-7 | leukocytosis | MESH:D007964 | marker/mechanism | 4800729 | ||
C0023518 | ciprofloxacin | D002939 | 85721-33-1 | leukocytosis | MESH:D007964 | marker/mechanism | 11476450 | ||
C0023518 | ciprofloxacin | D002939 | 85721-33-1 | leukocytosis | MESH:D007964 | therapeutic | 19401694 | ||
C0023518 | clozapine | D003024 | 5786-21-0 | leukocytosis | MESH:D007964 | marker/mechanism | 11307364 | ||
C0023518 | erythromycin | D004917 | 114-07-8 | leukocytosis | MESH:D007964 | marker/mechanism | 8629881 | ||
C0023518 | hydroxyurea | D006918 | 127-07-1 | leukocytosis | MESH:D007964 | therapeutic | 17136541 | ||
C0023518 | indinavir | D019469 | 150378-17-9 | leukocytosis | MESH:D007964 | marker/mechanism | 12571522 | ||
C0023518 | indomethacin | D007213 | 53-86-1 | leukocytosis | MESH:D007964 | therapeutic | 16537180 | ||
C0023518 | propylthiouracil | D011441 | 51-52-5 | leukocytosis | MESH:D007964 | marker/mechanism | 1806466 | ||
C0023518 | rifampin | D012293 | 13292-46-1 | leukocytosis | MESH:D007964 | marker/mechanism | 11837753 | ||
C0023518 | rofecoxib | C116926 | - | leukocytosis | MESH:D007964 | marker/mechanism | 15892770 | ||
C0023518 | thalidomide | D013792 | 50-35-1 | leukocytosis | MESH:D007964 | marker/mechanism | 11972510 | ||
C0023518 | theophylline | D013806 | 58-55-9 | leukocytosis | MESH:D007964 | marker/mechanism | 20940509 | ||
C0023518 | tretinoin | D014212 | 302-79-4 | leukocytosis | MESH:D007964 | marker/mechanism | 10609785 | ||
C0023518 | zafirlukast | C062735 | 107753-78-6 | leukocytosis | MESH:D007964 | marker/mechanism | 18489783 |
FDA approved drug and dosage information(Total Drugs:7) | ||||||||
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DiseaseID | Drug_name | active_ingredients | strength | Dosage Form/Route | Marketing Status | TE code | RLD | RS |
MESH:D007964 | cipro | ciprofloxacin | 400MG/40ML (10MG/ML) | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
MESH:D007964 | cipro | ciprofloxacin | 400MG/40ML (10MG/ML) | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
MESH:D007964 | cipro | ciprofloxacin | 250MG/5ML | FOR SUSPENSION;ORAL | Prescription | AB | Yes | No |
MESH:D007964 | cipro | ciprofloxacin | 250MG/5ML | FOR SUSPENSION;ORAL | Prescription | AB | Yes | No |
MESH:D007964 | vioxx | rofecoxib | 12.5MG | TABLET;ORAL | Discontinued | None | No | No |
MESH:D007964 | vioxx | rofecoxib | 12.5MG/5ML | SUSPENSION;ORAL | Discontinued | None | No | No |
MESH:D007964 | vioxx | rofecoxib | 12.5MG | TABLET; ORAL | Discontinued | None | No | No |
FDA labeling changes(Total Drugs:7) | |||||||||||||
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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:D007964 | 03/25/2004 | cipro | ciprofloxacin | Complicated UTI and pyelonephritis | Indicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1 17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1 17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectively | Labeling | B | - | - | - | Bayer | 12/18/2003 | FALSE' |
MESH:D007964 | 03/25/2004 | cipro | ciprofloxacin | Complicated UTI and pyelonephritis | Indicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1 17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1 17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectively | Labeling | B | - | - | - | Bayer | 12/18/2003 | FALSE' |
MESH:D007964 | 03/25/2004 | cipro | ciprofloxacin | Complicated UTI and pyelonephritis | Indicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1 17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1 17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectively | Labeling | B | - | - | - | Bayer | 12/18/2003 | FALSE' |
MESH:D007964 | 03/25/2004 | cipro | ciprofloxacin | Complicated UTI and pyelonephritis | Indicated for the treatment of complicated urinary tract infections (cUTIs) and pyelonephritis in pediatric patients 1 17 years of age Not drug of first choice due to increased adverse events compared to controls including events related to joints and/or surrounding tissues Information on PK and dose in pediatric patients 1 17 years of age The most frequent adverse events observed within 6 weeks of treatment initiation during the cUTI clinical trial were gastrointestinal 15% compared to 9% and musculoskeletal 9.3% compared to 6% in ciprofloxacin-treated compared to control-treated patients, respectively | Labeling | B | - | - | - | Bayer | 12/18/2003 | FALSE' |
MESH:D007964 | 08/19/2004 | vioxx | rofecoxib | Pauciarticular or polyarticular course Juvenile Rheumatoid Arthritis | Merck announced a voluntary worldwide withdrawal of Vioxx (rofecoxib) due to safety concerns on September 30, 2004. | Labeling | B | - | - | - | Merck | 02/18/2004 | FALSE' |
MESH:D007964 | 08/19/2004 | vioxx | rofecoxib | Pauciarticular or polyarticular course Juvenile Rheumatoid Arthritis | Merck announced a voluntary worldwide withdrawal of Vioxx (rofecoxib) due to safety concerns on September 30, 2004. | Labeling | B | - | - | - | Merck | 02/18/2004 | FALSE' |
MESH:D007964 | 08/19/2004 | vioxx | rofecoxib | Pauciarticular or polyarticular course Juvenile Rheumatoid Arthritis | Merck announced a voluntary worldwide withdrawal of Vioxx (rofecoxib) due to safety concerns on September 30, 2004. | Labeling | B | - | - | - | Merck | 02/18/2004 | FALSE' |