LABELS · 1203ca7f-080c-4c49-e063-6294a90a90e0
SOLU-MEDROL
Open original source → · Download preserved record
Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.
- Label effective date
- 2024-02-22
- Captured
- 2026-09-09T23:37:39.774134+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- INDICATIONS & USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-MEDROL Sterile Powder is indicated as follows: Allergic states Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
Full extracted label fields
- application numbers
- NDA011856
- boxed warning exact
- brand names
- SOLU-MEDROL
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=74e5060c-8426-1b77-e053-2a91aa0a1f13
- generic names
- SOLU-MEDROL
- id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- indications and usage exact
- INDICATIONS & USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-MEDROL Sterile Powder is indicated as follows: Allergic states Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
- indications and usage tables exact
- is original packager
- manufacturer names
- HF Acquisition Co. LLC, DBA HealthFirst
- matched search terms
- cancer
- lymphomas
- tumor
- package ndcs
- 51662-1264-2
- 51662-1264-3
- 51662-1264-1
- product ndcs
- 51662-1264
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- INTRAMUSCULAR
- INTRAVENOUS
- rxcuis
- 311659
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00000.json
- meta
- disclaimer
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
- last updated
- 2026-09-09
- results
- limit
- 100
- skip
- 0
- total
- 830
- sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl effective time
- 20240222
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- substance names
- METHYLPREDNISOLONE SODIUM SUCCINATE
- uniis
- LEC9GKY20K
- verification flags
- oncology_keyword_candidate_not_clinically_classified
- spl_text_not_verified_identical_to_latest_approved_label
- individual_indications_not_split_or_reconciled
- not_identified_as_original_packager
- fda_label_posted_after_spl_effective_date_requires_version_review
Drugs@FDA application source records
- application number
- NDA011856
- payload
- all indexed label documents
- Appl No
- 011856
- Application Docs Date
- 2011-10-25 00:00:00
- Application Docs ID
- 10784
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/011856s103s104lbl.pdf
- Submission No
- 104
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2011-10-25 00:00:00
- Application Docs ID
- 33061
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2011/011856s103s104lbl.pdf
- Submission No
- 103
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2010-07-01 00:00:00
- Application Docs ID
- 33062
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2010/011856s107lbl.pdf
- Submission No
- 107
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2014-07-09 00:00:00
- Application Docs ID
- 33063
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2014/011856s123lbl.pdf
- Submission No
- 123
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2016-09-09 00:00:00
- Application Docs ID
- 45262
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/011856s124and126lbl.pdf
- Submission No
- 124
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2016-09-09 00:00:00
- Application Docs ID
- 45263
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2016/011856s124and126lbl.pdf
- Submission No
- 126
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2018-04-01 00:00:00
- Application Docs ID
- 53571
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2018/011856s131lbl.pdf
- Submission No
- 131
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2018-07-25 00:00:00
- Application Docs ID
- 54963
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2018/011856s133lbl.pdf
- Submission No
- 133
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2021-06-04 00:00:00
- Application Docs ID
- 67701
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/011856s136lbl.pdf
- Submission No
- 136
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2021-11-29 00:00:00
- Application Docs ID
- 69419
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/011856s139lbl.pdf
- Submission No
- 139
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2023-12-21 00:00:00
- Application Docs ID
- 77105
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2023/011856s141lbl.pdf
- Submission No
- 141
- Submission Type
- SUPPL
- Appl No
- 011856
- Application Docs Date
- 2024-06-06 00:00:00
- Application Docs ID
- 78675
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/011856s144lbl.pdf
- Submission No
- 144
- Submission Type
- SUPPL
- all submission records
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 144
- Submission Status
- AP
- Submission Status Date
- 2024-06-05 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 143
- Submission Status
- AP
- Submission Status Date
- 2025-11-04 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 141
- Submission Status
- AP
- Submission Status Date
- 2023-12-20 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- N/A
- Submission Class Code ID
- 4
- Submission No
- 139
- Submission Status
- AP
- Submission Status Date
- 2021-10-27 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 136
- Submission Status
- AP
- Submission Status Date
- 2021-05-27 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 133
- Submission Status
- AP
- Submission Status Date
- 2018-07-24 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 131
- Submission Status
- AP
- Submission Status Date
- 2018-03-28 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 4
- Submission No
- 127
- Submission Status
- AP
- Submission Status Date
- 2015-08-06 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 126
- Submission Status
- AP
- Submission Status Date
- 2016-09-08 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 124
- Submission Status
- AP
- Submission Status Date
- 2016-09-08 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 123
- Submission Status
- AP
- Submission Status Date
- 2014-07-03 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 011856
- Review Priority
- STANDARD
- Submission Class Code ID
- 4
- Submission No
- 122
- Submission Status
- AP
- Submission Status Date
- 2014-06-09 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- application number
- NDA011856
- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=011856
- has approved submission record
- true
- latest approved submission date
- 2025-11-04
- latest label selection rule
- max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
- latest posted label documents
- Appl No
- 011856
- Application Docs Date
- 2025-11-07 00:00:00
- Application Docs ID
- 84121
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2025/011856s143lbl.pdf
- Submission No
- 143
- Submission Type
- SUPPL
- official application record
- Appl No
- 011856
- Appl Public Notes
- Appl Type
- NDA
- Sponsor Name
- PHARMACIA AND UPJOHN
- openfda application present
- true
- products
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 003
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- EQ 40MG BASE/VIAL
- marketing status
- Prescription
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 004
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- EQ 125MG BASE/VIAL
- marketing status
- Prescription
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 005
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- EQ 500MG BASE/VIAL
- marketing status
- Prescription
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 006
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- EQ 1GM BASE/VIAL
- marketing status
- Prescription
- Active Ingredient
- METHYLPREDNISOLONE SODIUM SUCCINATE
- Appl No
- 011856
- Drug Name
- SOLU-MEDROL
- Form
- INJECTABLE;INJECTION
- Product No
- 007
- Reference Drug
- 1
- Reference Standard
- 1
- Strength
- EQ 2GM BASE/VIAL
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- explicit_positive_indication_predicate
- no_tumor_directed_keyword_in_positive_statement
- clinical review status
- pending
- content role
- positive_indication_candidate
- context span
- end
- 776
- end exclusive
- true
- exact text
- INDICATIONS & USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-MEDROL Sterile Powder is indicated as follows: Allergic states Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or s
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 0
- current approval status
- not_reconciled
- duplicate text group
- dup-8bfbfb28593219f9925f
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-18e3e0d13b32c8295afa
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- end
- 272
- end exclusive
- true
- exact text
- is indicated
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 260
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 576
- end exclusive
- true
- exact text
- INDICATIONS & USAGE When oral therapy is not feasible, and the strength, dosage form, and route of administration of the drug reasonably lend the preparation to the treatment of the condition, the intravenous or intramuscular use of SOLU-MEDROL Sterile Powder is indicated as follows: Allergic states Control of severe or incapacitating allergic conditions intractable to adequate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 0
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- non_oncology_or_unclear_candidate
Passage 2 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 943
- end exclusive
- true
- exact text
- ate trials of conventional treatment in asthma, atopic dermatitis, contact dermatitis, drug hypersensitivity reactions, perennial or seasonal allergic rhinitis, serum sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where ap
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 377
- current approval status
- not_reconciled
- duplicate text group
- dup-f232b8100816c14008ff
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-b03c0bba2b7f1cd56d32
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 743
- end exclusive
- true
- exact text
- Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome).
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 577
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 3 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 1326
- end exclusive
- true
- exact text
- sickness, transfusion reactions. Dermatologic diseases Bullous dermatitis herpetiformis, exfoliative erythroderma, mycosis fungoides, pemphigus, severe erythema multiforme (Stevens-Johnson syndrome). Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemoly
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 544
- current approval status
- not_reconciled
- duplicate text group
- dup-16b675ab735658d3a335
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-5b73f94736ad7c454b93
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 1126
- end exclusive
- true
- exact text
- Endocrine disorders Primary or secondary adrenocortical insufficiency (hydrocortisone or cortisone is the drug of choice; synthetic analogs may be used in conjunction with mineralocorticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 744
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 4 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 1475
- end exclusive
- true
- exact text
- ticoids where applicable; in infancy, mineralocorticoid supplementation is of particular importance), congenital adrenal hyperplasia, hypercalcemia associated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administr
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 927
- current approval status
- not_reconciled
- duplicate text group
- dup-2a767d6181d51c3a6a4c
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-0bf82734338ddaf13530
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 1275
- end exclusive
- true
- exact text
- Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1127
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 5 · risk or warning
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- risk_or_warning_words_without_positive_predicate
- clinical review status
- pending
- content role
- risk_or_warning
- context span
- end
- 1805
- end exclusive
- true
- exact text
- ssociated with cancer, nonsuppurative thyroiditis. Gastrointestinal diseases To tide the patient over a critical period of the disease in regional enteritis (systemic therapy) and ulcerative colitis. Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemothe
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1076
- current approval status
- not_reconciled
- duplicate text group
- dup-dc08b3d3acd568ee1edc
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-1acb13ace74817894c0f
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- context exact
- nd-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administrat
- kind
- age
- polarity
- not_inferred
- span
- end
- 1452
- end exclusive
- true
- exact text
- adults
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1446
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 1605
- end exclusive
- true
- exact text
- Hematologic disorders Acquired (autoimmune) hemolytic anemia, congenital (erythroid) hypoplastic anemia (Diamond-Blackfan anemia), idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1276
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- not_applicable
Passage 6 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2010
- end exclusive
- true
- exact text
- idiopathic thrombocytopenic purpura in adults (intravenous administration only; intramuscular administration is contraindicated), pure red cell aplasia, selected cases of secondary thrombocytopenia. Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumo
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1406
- current approval status
- not_reconciled
- duplicate text group
- dup-c2bb4f487d7e3f3f2e88
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-e29810a277f8939e09a2
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 1810
- end exclusive
- true
- exact text
- Miscellaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1606
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 7 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2088
- end exclusive
- true
- exact text
- llaneous Trichinosis with neurologic or myocardial involvement, tuberculous meningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocul
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1611
- current approval status
- not_reconciled
- duplicate text group
- dup-e7e48fb705e90adf307b
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-e24aade6541eba5d6238
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 1888
- end exclusive
- true
- exact text
- Neoplastic diseases For the palliative management of leukemias and lymphomas.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1811
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 8 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2227
- end exclusive
- true
- exact text
- ningitis with subarachnoid block or impending block when used concurrently with appropriate antituberculous chemotherapy. Neoplastic diseases For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopa
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1689
- current approval status
- not_reconciled
- duplicate text group
- dup-2b9fac38334eaafc40f1
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-d09ba1272143632261ee
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- context exact
- ltiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy.
- kind
- biomarker
- polarity
- not_inferred
- span
- end
- 2011
- end exclusive
- true
- exact text
- metastatic brain tumor
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1989
- context exact
- ltiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy.
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 2011
- end exclusive
- true
- exact text
- metastatic brain tumor
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1989
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2027
- end exclusive
- true
- exact text
- Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1889
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 9 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2355
- end exclusive
- true
- exact text
- es For the palliative management of leukemias and lymphomas. Nervous System Acute exacerbations of multiple sclerosis; cerebral edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmon
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1828
- current approval status
- not_reconciled
- duplicate text group
- dup-343fee39ef8c72d8b075
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-019586101cded69f534a
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2155
- end exclusive
- true
- exact text
- Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2028
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 10 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2486
- end exclusive
- true
- exact text
- edema associated with primary or metastatic brain tumor, or craniotomy. Ophthalmic diseases Sympathetic ophthalmia, uveitis and ocular inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptoma
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 1956
- current approval status
- not_reconciled
- duplicate text group
- dup-9fbb6837c895178e0233
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-2cc2e333dab21d0eade4
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2286
- end exclusive
- true
- exact text
- Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2156
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 11 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2702
- end exclusive
- true
- exact text
- lar inflammatory conditions unresponsive to topical corticosteroids. Renal diseases To induce diuresis or remission of proteinuria in idiopathic nephrotic syndrome or that due to lupus erythematosus. Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spon
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2087
- current approval status
- not_reconciled
- duplicate text group
- dup-d321ab32d081d2081625
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-125bdb30e7e8decd15b3
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2502
- end exclusive
- true
- exact text
- Respiratory diseases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2287
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 12 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2958
- end exclusive
- true
- exact text
- ases Berylliosis, fulminating or disseminated pulmonary tuberculosis when used concurrently with appropriate antituberculous chemotherapy, idiopathic eosinophilic pneumonias, symptomatic sarcoidosis. Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2303
- current approval status
- not_reconciled
- duplicate text group
- dup-bf3a6bac6b0740eefcad
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-b8baecffa4c3ec48e9ce
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2852
- end exclusive
- true
- exact text
- Rheumatic disorders As adjunctive therapy for short-term administration (to tide the patient over an acute episode or exacerbation) in acute gouty arthritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy).
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2503
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Passage 13 · unclassified context
- application numbers
- NDA011856
- brand names
- SOLU-MEDROL
- classification reasons
- no_unambiguous_positive_indication_predicate
- clinical review status
- pending
- content role
- unclassified_context
- context span
- end
- 2958
- end exclusive
- true
- exact text
- hritis; acute rheumatic carditis; ankylosing spondylitis; psoriatic arthritis; rheumatoid arthritis, including juvenile rheumatoid arthritis (selected cases may require low-dose maintenance therapy). For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2653
- current approval status
- not_reconciled
- duplicate text group
- dup-a019d33f39e129a34356
- extraction review status
- automated_candidate_pending_source_review
- generic names
- SOLU-MEDROL
- id
- ind-span-5dfdf305787a97f77535
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- 0dba7a040bbbf460aa9f482c5b67c9f28f75fc9df775ee1e7b345b758f780e07
- source defined aliases
- source span
- end
- 2958
- end exclusive
- true
- exact text
- For the treatment of dermatomyositis, temporal arteritis, polymyositis, and systemic lupus erythematosus.
- label id
- 1203ca7f-080c-4c49-e063-6294a90a90e0
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 00e900f60d9223601eb11bbc92ed46381adad7b793770517b64e5bb78b5264b5
- start
- 2853
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%221203ca7f-080c-4c49-e063-6294a90a90e0%22
- spl effective date
- 2024-02-22
- spl set id
- 74e5060c-8426-1b77-e053-2a91aa0a1f13
- spl version
- 8
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- unclear
Preserved source evidence · Not medical advice
Triangle