Stem definition | Drug id | CAS RN |
---|---|---|
corticosteroids, except prednisolone derivatives | 793 | 14484-47-0 |
Dose | Unit | Route |
---|---|---|
15 | mg | O |
Property | Value | Reference |
---|---|---|
BA (Bioavailability) | 68 % | Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H |
Date | Agency | Company | Orphan |
---|---|---|---|
Feb. 9, 2017 | FDA | MARATHON PHARMACEUTICALS LLC |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Bursitis infective | 111.64 | 22.40 | 23 | 2613 | 1154 | 46682272 |
Angioedema | 72.37 | 22.40 | 38 | 2598 | 39304 | 46644122 |
Allergy test positive | 72.02 | 22.40 | 13 | 2623 | 321 | 46683105 |
Bronchiectasis | 57.03 | 22.40 | 21 | 2615 | 9295 | 46674131 |
Peripheral vascular disorder | 50.02 | 22.40 | 17 | 2619 | 5960 | 46677466 |
Drug reaction with eosinophilia and systemic symptoms | 47.18 | 22.40 | 26 | 2610 | 29522 | 46653904 |
Apraxia | 46.24 | 22.40 | 12 | 2624 | 1663 | 46681763 |
Perseveration | 42.34 | 22.40 | 8 | 2628 | 255 | 46683171 |
Urticaria | 38.60 | 22.40 | 40 | 2596 | 117852 | 46565574 |
Localised infection | 38.15 | 22.40 | 21 | 2615 | 23780 | 46659646 |
Toxic epidermal necrolysis | 33.90 | 22.40 | 19 | 2617 | 22259 | 46661167 |
Respiratory tract infection | 33.65 | 22.40 | 21 | 2615 | 29951 | 46653475 |
Hyperreflexia | 32.72 | 22.40 | 12 | 2624 | 5242 | 46678184 |
Osteoporosis | 32.41 | 22.40 | 23 | 2613 | 40585 | 46642841 |
Skin ulcer | 32.12 | 22.40 | 21 | 2615 | 32437 | 46650989 |
Bone disorder | 30.25 | 22.40 | 17 | 2619 | 20016 | 46663410 |
Tenosynovitis | 28.56 | 22.40 | 12 | 2624 | 7503 | 46675923 |
Staphylococcal infection | 27.94 | 22.40 | 20 | 2616 | 35751 | 46647675 |
Hemianopia | 27.44 | 22.40 | 7 | 2629 | 906 | 46682520 |
Skin discolouration | 27.21 | 22.40 | 19 | 2617 | 32661 | 46650765 |
Myoclonus | 23.92 | 22.40 | 13 | 2623 | 14339 | 46669087 |
Gastroenteritis bacterial | 22.47 | 22.40 | 4 | 2632 | 91 | 46683335 |
MedDRA adverse event term | Likelihood ratio | Likelihood ratio threshold | Patients taking drug having adverse event | Patients taking drug not having adverse event | Patients not taking drug having adverse event | Patients not taking drug not having adverse event |
---|---|---|---|---|---|---|
Weight increased | 283.52 | 36.39 | 133 | 2360 | 74780 | 29875205 |
Nasopharyngitis | 108.69 | 36.39 | 65 | 2428 | 58784 | 29891201 |
Influenza | 104.44 | 36.39 | 57 | 2436 | 43341 | 29906644 |
Myoglobinuria | 100.41 | 36.39 | 21 | 2472 | 763 | 29949222 |
Increased appetite | 79.08 | 36.39 | 26 | 2467 | 5591 | 29944394 |
Gastroenteritis viral | 77.68 | 36.39 | 26 | 2467 | 5907 | 29944078 |
Off label use | 76.11 | 36.39 | 98 | 2395 | 249192 | 29700793 |
Behaviour disorder | 58.72 | 36.39 | 17 | 2476 | 2395 | 29947590 |
Product dose omission issue | 57.79 | 36.39 | 53 | 2440 | 91578 | 29858407 |
Anger | 51.92 | 36.39 | 23 | 2470 | 11097 | 29938888 |
Systemic inflammatory response syndrome | 49.10 | 36.39 | 19 | 2474 | 6527 | 29943458 |
Pyrexia | 45.96 | 36.39 | 85 | 2408 | 294404 | 29655581 |
Fall | 42.44 | 36.39 | 63 | 2430 | 181809 | 29768176 |
Malaise | 40.62 | 36.39 | 59 | 2434 | 166903 | 29783082 |
Tachypnoea | 39.67 | 36.39 | 21 | 2472 | 14931 | 29935054 |
Swelling face | 37.91 | 36.39 | 23 | 2470 | 21181 | 29928804 |
Cushingoid | 36.95 | 36.39 | 12 | 2481 | 2475 | 29947510 |
Rhabdomyolysis | 36.59 | 36.39 | 35 | 2458 | 63545 | 29886440 |
Source | Code | Description |
---|---|---|
ATC | H02AB13 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS CORTICOSTEROIDS FOR SYSTEMIC USE CORTICOSTEROIDS FOR SYSTEMIC USE, PLAIN Glucocorticoids |
FDA MoA | N0000175450 | Corticosteroid Hormone Receptor Agonists |
FDA EPC | N0000175576 | Corticosteroid |
MeSH PA | D000893 | Anti-Inflammatory Agents |
MeSH PA | D007155 | Immunologic Factors |
MeSH PA | D007166 | Immunosuppressive Agents |
Disease | Relation | SNOMED_ID | DOID |
---|---|---|---|
Duchenne muscular dystrophy | indication | 76670001 | DOID:11723 |
Dissociation level | Dissociation constant | Type (acidic/basic) |
---|---|---|
pKa1 | 12.27 | acidic |
pKa2 | 7.14 | Basic |
None
Formulation strength | Trade name | Applicant | Application number | Approval date | Type | Dose form | Route | Exclusivity date | Description |
---|---|---|---|---|---|---|---|---|---|
18MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2022 | NEW CHEMICAL ENTITY |
30MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2022 | NEW CHEMICAL ENTITY |
36MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2022 | NEW CHEMICAL ENTITY |
6MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2022 | NEW CHEMICAL ENTITY |
22.75MG/ML | EMFLAZA | PTC THERAP | N208685 | Feb. 9, 2017 | RX | SUSPENSION | ORAL | Feb. 9, 2022 | NEW CHEMICAL ENTITY |
18MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2024 | TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY IN PATIENTS 5 YEARS OF AGE AND OLDER |
30MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2024 | TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY IN PATIENTS 5 YEARS OF AGE AND OLDER |
36MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2024 | TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY IN PATIENTS 5 YEARS OF AGE AND OLDER |
6MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | Feb. 9, 2024 | TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY IN PATIENTS 5 YEARS OF AGE AND OLDER |
22.75MG/ML | EMFLAZA | PTC THERAP | N208685 | Feb. 9, 2017 | RX | SUSPENSION | ORAL | Feb. 9, 2024 | TREATMENT OF DUCHENNE MUSCULAR DYSTROPHY IN PATIENTS 5 YEARS OF AGE AND OLDER |
18MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | June 7, 2026 | TREATMENT OF DUCHENE MUSCULAR DYSTROPHY IN PATIENTS 2 YEARS OF AGE TO LESS THAN 5 YEARS OF AGE |
30MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | June 7, 2026 | TREATMENT OF DUCHENE MUSCULAR DYSTROPHY IN PATIENTS 2 YEARS OF AGE TO LESS THAN 5 YEARS OF AGE |
36MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | June 7, 2026 | TREATMENT OF DUCHENE MUSCULAR DYSTROPHY IN PATIENTS 2 YEARS OF AGE TO LESS THAN 5 YEARS OF AGE |
6MG | EMFLAZA | PTC THERAP | N208684 | Feb. 9, 2017 | RX | TABLET | ORAL | June 7, 2026 | TREATMENT OF DUCHENE MUSCULAR DYSTROPHY IN PATIENTS 2 YEARS OF AGE TO LESS THAN 5 YEARS OF AGE |
22.75MG/ML | EMFLAZA | PTC THERAP | N208685 | Feb. 9, 2017 | RX | SUSPENSION | ORAL | June 7, 2026 | TREATMENT OF DUCHENE MUSCULAR DYSTROPHY IN PATIENTS 2 YEARS OF AGE TO LESS THAN 5 YEARS OF AGE |
None
ID | Source |
---|---|
D03671 | KEGG_DRUG |
13649-57-5 | SECONDARY_CAS_RN |
4036431 | VANDF |
C0593761 | UMLSCUI |
CHEBI:135720 | CHEBI |
CHEMBL1201891 | ChEMBL_ID |
DB11921 | DRUGBANK_ID |
189821 | PUBCHEM_CID |
C021988 | MESH_SUPPLEMENTAL_RECORD_UI |
C014725 | MESH_SUPPLEMENTAL_RECORD_UI |
9477 | IUPHAR_LIGAND_ID |
4323 | INN_ID |
KR5YZ6AE4B | UNII |
3081431 | PUBCHEM_CID |
T1LWN33J2P | UNII |
153100 | RXNORM |
18036 | MMSL |
d04977 | MMSL |
006032 | NDDF |
116578002 | SNOMEDCT_US |
396012006 | SNOMEDCT_US |
Product | Category | Ingredients | NDC | Form | Quantity | Route | Marketing | Label |
---|---|---|---|---|---|---|---|---|
EMFLAZA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 52856-501 | TABLET | 6 mg | ORAL | NDA | 27 sections |
EMFLAZA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 52856-502 | TABLET | 18 mg | ORAL | NDA | 27 sections |
EMFLAZA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 52856-503 | TABLET | 30 mg | ORAL | NDA | 27 sections |
EMFLAZA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 52856-504 | TABLET | 36 mg | ORAL | NDA | 27 sections |
EMFLAZA | HUMAN PRESCRIPTION DRUG LABEL | 1 | 52856-505 | SUSPENSION | 22.75 mg | ORAL | NDA | 27 sections |