hemiplegia |
Disease ID | 1129 |
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Disease | hemiplegia |
Manually Symptom | (Waiting for update.) |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:8) C0030193 | pain | 6 C0026838 | spasticity | 4 C0037011 | shoulder pain | 3 C0040053 | thrombosis | 1 C0014544 | epilepsy | 1 C0023015 | language disorders | 1 C0036572 | seizures | 1 C0034931 | shoulder-hand syndrome | 1 |
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:10) | |||||||||
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CUI | ChemicalName | ChemicalID | CasRN | DiseaseName | DiseaseID | DirectEvidence | PubMedIDs | ||
C0018991 | baclofen | D001418 | 1134-47-0 | hemiplegia | MESH:D006429 | therapeutic | 12917859 | ||
C0018991 | bortezomib | D000069286 | - | hemiplegia | MESH:D006429 | marker/mechanism | 17204182 | ||
C0018991 | haloperidol | D006220 | 52-86-8 | hemiplegia | MESH:D006429 | marker/mechanism | 3683725 | ||
C0018991 | methotrexate | D008727 | 1959/5/2 | hemiplegia | MESH:D006429 | marker/mechanism | 12764767 | ||
C0018991 | methylphenidate | D008774 | 113-45-1 | hemiplegia | MESH:D006429 | marker/mechanism | 7115156 | ||
C0018991 | morphine | D009020 | 57-27-2 | hemiplegia | MESH:D006429 | marker/mechanism | 6692145 | ||
C0018991 | phenytoin | D010672 | 57-41-0 | hemiplegia | MESH:D006429 | marker/mechanism | 3117426 | ||
C0018991 | tacrolimus | D016559 | 109581-93-3 | hemiplegia | MESH:D006429 | marker/mechanism | 21321342 | ||
C0018991 | tranexamic acid | D014148 | 1197-18-8 | hemiplegia | MESH:D006429 | marker/mechanism | 7104262 | ||
C0018991 | vincristine | D014750 | - | hemiplegia | MESH:D006429 | marker/mechanism | 20363963 |
FDA approved drug and dosage information(Total Drugs:5) | ||||||||
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DiseaseID | Drug_name | active_ingredients | strength | Dosage Form/Route | Marketing Status | TE code | RLD | RS |
MESH:D006429 | daytrana | methylphenidate | 10MG/9HR (1.1MG/HR) | FILM, EXTENDED RELEASE;TRANSDERMAL | Prescription | None | Yes | No |
MESH:D006429 | daytrana | methylphenidate | 10MG/9HR (1.1MG/HR) | FILM, EXTENDED RELEASE;TRANSDERMAL | Prescription | None | Yes | No |
MESH:D006429 | daytrana | methylphenidate | 10MG/9HR (1.1MG/HR) | FILM, EXTENDED RELEASE;TRANSDERMAL | Prescription | None | Yes | No |
MESH:D006429 | lysteda | tranexamic acid | 650MG | TABLET;ORAL | Prescription | AB | Yes | Yes |
MESH:D006429 | velcade | bortezomib | 3.5MG/VIAL | INJECTABLE;INTRAVENOUS, SUBCUTANEOUS | Prescription | None | Yes | Yes |
FDA labeling changes(Total Drugs:5) | |||||||||||||
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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:D006429 | 6/4/2006 | daytrana | methylphenidate | ADHD | Summary is pending | Labeling | - | P | - | - | Shire | - | FALSE' |
MESH:D006429 | 12/14/2009 | daytrana | methylphenidate | Postmarketing safety study | Information added to Warnings and Adverse Reactions on skin reactions observed in a postmarketing dermal study in pediatric patients | Labeling | - | P | - | - | Shire | - | FALSE' |
MESH:D006429 | 06/29/2010 | daytrana | methylphenidate | ADHD | Expanded pediatric indication to include adolescent patients ages13-17 years The most commonly reported adverse reactions in a trial in patients 13-17 years included appetite decreased, nausea, insomnia, weight decreased, dizziness, abdominal pain, and anorexia. The majority of patients had erythema at the application site Information on PK parameters, Adverse Event profile and clinical studies | Labeling | - | P | - | - | Shire | - | FALSE' |
MESH:D006429 | 08/21/2013 | lysteda | tranexamic acid | Treatment of cyclic heavy menstrual bleeding | Indicated for women of reproductive age. It is not intended for use in premenarcheal girls Information on PK studyPostmarketing study | - | P | - | - | Ferring | - | FALSE' | - |
MESH:D006429 | 09/14/2015 | velcade | bortezomib | Relapsed Acute Lymphoblastic Leukemia (ALL) and Lymphoblastic Lymphoma (LL) | Effectiveness in pediatric patients with relapsed pre-B ALL has not been established. The activity and safety of Velcade in combination with intensive reinduction chemotherapy was evaluated in pediatric and young adult patients with lymphoid malignancies. There were 140 patients with ALL or LL enrolled and evaluated for safety. No new safety concerns were observed | Labeling | B | - | - | - | Millennium Pharmaceuticals, Inc. | - | FALSE |