hematuria |
Disease ID | 1666 |
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Disease | hematuria |
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:45) | |||||||||
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CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
C0018965 | acetylcysteine | D000111 | 616-91-1 | hematuria | MESH:D006417 | therapeutic | 6836328 | ||
C0018965 | aminocaproic acid | D015119 | 60-32-2 | hematuria | MESH:D006417 | marker/mechanism | 3812474 | ||
C0018965 | amitriptyline | D000639 | 50-48-6 | hematuria | MESH:D006417 | marker/mechanism | 6703117 | ||
C0018965 | baclofen | D001418 | 1134-47-0 | hematuria | MESH:D006417 | marker/mechanism | 17924939 | ||
C0018965 | bleomycin | D001761 | 11056-06-7 | hematuria | MESH:D006417 | marker/mechanism | 9572663 | ||
C0018965 | busulfan | D002066 | 55-98-1 | hematuria | MESH:D006417 | marker/mechanism | 12913734 | ||
C0018965 | caffeine | D002110 | 1958/8/2 | hematuria | MESH:D006417 | marker/mechanism | 2240058 | ||
C0018965 | carbenicillin | D002228 | 4697-36-3 | hematuria | MESH:D006417 | marker/mechanism | 760523 | ||
C0018965 | carboprost tromethamine | C062843 | 58551-69-2 | hematuria | MESH:D006417 | therapeutic | 2369708 | ||
C0018965 | carmustine | D002330 | 154-93-8 | hematuria | MESH:D006417 | marker/mechanism | 6134004 | ||
C0018965 | cephalexin | D002506 | 15686-71-2 | hematuria | MESH:D006417 | marker/mechanism | 1242194 | ||
C0018965 | chlorambucil | D002699 | 305-03-3 | hematuria | MESH:D006417 | marker/mechanism | 1138180 | ||
C0018965 | ciprofloxacin | D002939 | 85721-33-1 | hematuria | MESH:D006417 | marker/mechanism | 2931381 | ||
C0018965 | clozapine | D003024 | 5786-21-0 | hematuria | MESH:D006417 | marker/mechanism | 9669191 | ||
C0018965 | cyclophosphamide | D003520 | 50-18-0 | hematuria | MESH:D006417 | marker/mechanism | 10507982 | ||
C0018965 | cyclophosphamide | D003520 | 50-18-0 | hematuria | MESH:D006417 | therapeutic | 14563468 | ||
C0018965 | cyclosporine | D016572 | 59865-13-3 | hematuria | MESH:D006417 | marker/mechanism | 12913734 | ||
C0018965 | cisplatin | D002945 | 15663-27-1 | hematuria | MESH:D006417 | marker/mechanism | 9572663 | ||
C0018965 | epirubicin | D015251 | 56420-45-2 | hematuria | MESH:D006417 | marker/mechanism | 7598036 | ||
C0018965 | ethosuximide | D005013 | 77-67-8 | hematuria | MESH:D006417 | marker/mechanism | 9776542 | ||
C0018965 | fluorouracil | D005472 | 51-21-8 | hematuria | MESH:D006417 | therapeutic | 2996749 | ||
C0018965 | foscarnet | D017245 | 4428-95-9 | hematuria | MESH:D006417 | marker/mechanism | 10231404 | ||
C0018965 | glutathione | D005978 | 70-18-8 | hematuria | MESH:D006417 | therapeutic | 2773078 | ||
C0018965 | griseofulvin | D006118 | 126-07-8 | hematuria | MESH:D006417 | marker/mechanism | 2237566 | ||
C0018965 | ifosfamide | D007069 | 3778-73-2 | hematuria | MESH:D006417 | marker/mechanism | 1277203 | ||
C0018965 | ifosfamide | D007069 | 3778-73-2 | hematuria | MESH:D006417 | therapeutic | 6106781 | ||
C0018965 | indinavir | D019469 | 150378-17-9 | hematuria | MESH:D006417 | marker/mechanism | 10197375 | ||
C0018965 | indomethacin | D007213 | 53-86-1 | hematuria | MESH:D006417 | marker/mechanism | 7880236 | ||
C0018965 | ivermectin | D007559 | 70288-86-7 | hematuria | MESH:D006417 | marker/mechanism | 8555762 | ||
C0018965 | mesna | D015080 | 19767-45-4 | hematuria | MESH:D006417 | marker/mechanism | 12913734 | ||
C0018965 | mesna | D015080 | 19767-45-4 | hematuria | MESH:D006417 | therapeutic | 11450158 | ||
C0018965 | methotrexate | D008727 | 1959/5/2 | hematuria | MESH:D006417 | marker/mechanism | 12913734 | ||
C0018965 | metoprolol | D008790 | 37350-58-6 | hematuria | MESH:D006417 | marker/mechanism | 8554013 | ||
C0018965 | mitomycin | D016685 | 1950/7/7 | hematuria | MESH:D006417 | therapeutic | 2996749 | ||
C0018965 | morphine | D009020 | 57-27-2 | hematuria | MESH:D006417 | marker/mechanism | 8225663 | ||
C0018965 | nafcillin | D009254 | 147-52-4 | hematuria | MESH:D006417 | marker/mechanism | 7431606 | ||
C0018965 | ofloxacin | D015242 | 82419-36-1 | hematuria | MESH:D006417 | marker/mechanism | 8239258 | ||
C0018965 | omeprazole | D009853 | 73590-58-6 | hematuria | MESH:D006417 | marker/mechanism | 7802778 | ||
C0018965 | oxytetracycline | D010118 | 79-57-2 | hematuria | MESH:D006417 | marker/mechanism | 7364640 | ||
C0018965 | propylthiouracil | D011441 | 51-52-5 | hematuria | MESH:D006417 | marker/mechanism | 12521217 | ||
C0018965 | rifampin | D012293 | 13292-46-1 | hematuria | MESH:D006417 | marker/mechanism | 20497752 | ||
C0018965 | sulfadiazine | D013411 | 68-35-9 | hematuria | MESH:D006417 | marker/mechanism | 3389358 | ||
C0018965 | valproic acid | D014635 | 99-66-1 | hematuria | MESH:D006417 | marker/mechanism | 3124010 | ||
C0018965 | vincristine | D014750 | - | hematuria | MESH:D006417 | marker/mechanism | 12748258 | ||
C0018965 | vindesine | D014751 | 53643-48-4 | hematuria | MESH:D006417 | marker/mechanism | 8602639 |
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:D006417 | prilosec | omeprazole | 20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons | CAPSULE, DELAYED REL PELLETS;ORAL | Discontinued | None | Yes | No |
MESH:D006417 | prilosec | omeprazole | 20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons | CAPSULE, DELAYED REL PELLETS;ORAL | Discontinued | None | Yes | No |
MESH:D006417 | omeprazole | omeprazole | 20MG | TABLET, DELAYED RELEASE;ORAL | Over-the-counter | None | Yes | Yes |
MESH:D006417 | omeprazole | omeprazole | 20MG | TABLET, DELAYED RELEASE;ORAL | Over-the-counter | None | Yes | Yes |
MESH:D006417 | busulfex | busulfan | 6MG/ML | INJECTABLE;INJECTION | Prescription | AP | Yes | Yes |
MESH:D006417 | cipro | ciprofloxacin | 400MG/40ML (10MG/ML) | INJECTABLE;INJECTION | Discontinued | None | Yes | No |
MESH:D006417 | cipro | ciprofloxacin | 250MG/5ML | FOR SUSPENSION;ORAL | Prescription | AB | Yes | 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:D006417 | 12/7/2002 | prilosec | omeprazole | Gastroesophageal reflux and erosive esophagitis | Safety and effectiveness established in pediatric patients 2-16 years of age Information on dose, PK parameters, exposure/response and AE profile | Labeling | B | - | - | - | AstraZeneca | - | FALSE' |
MESH:D006417 | 03/20/2008 | prilosec | omeprazole | Maintenance healing of erosive esophagitis | Efficacy was extrapolated from adults and older children to 1 to 2 year olds and supported with an open-label trial Unique adverse reactions in pediatric patients included increased respiratory system adverse events and fever. Safety and effectiveness in children less than 1 year of age have not been established Dosing and administration information provided for patients 1 year and older weighing at least 5 kg. New dosage form | Labeling | - | - | B, P | - | AstraZeneca | 1/5/2001 | FALSE' |
MESH:D006417 | 12/7/2002 | prilosec | omeprazole | Gastroesophageal reflux and erosive esophagitis | Safety and effectiveness established in pediatric patients 2-16 years of age Information on dose, PK parameters, exposure/response and AE profile | Labeling | B | - | - | - | AstraZeneca | - | FALSE' |
MESH:D006417 | 03/20/2008 | prilosec | omeprazole | Maintenance healing of erosive esophagitis | Efficacy was extrapolated from adults and older children to 1 to 2 year olds and supported with an open-label trial Unique adverse reactions in pediatric patients included increased respiratory system adverse events and fever. Safety and effectiveness in children less than 1 year of age have not been established Dosing and administration information provided for patients 1 year and older weighing at least 5 kg. New dosage form | Labeling | - | - | B, P | - | AstraZeneca | 1/5/2001 | FALSE' |
MESH:D006417 | 01/13/2003 | busulfex | busulfan | Part of a conditioning regimen administered prior to hematopoietic progenitor cell transplantation for a variety of malignant hematologic or non-malignant diseases | The population pharmacokinetic estimates of busulfan for clearance and volume of distribution were determined in an open-label, uncontrolled PK study in 24 pediatric patients 5 months to 16 years who received busulfan as part of a conditioning regimen administered prior to hematopoietic progenitor cell transplantation for a variety of malignant hematologic or non-malignant diseases Suggested dosing regimen | Labeling | B | - | - | - | Orphan Medical | 12/3/2002 | FALSE' |
MESH:D006417 | 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:D006417 | 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' |