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Methylprednisolone hemisuccinate

Generic Name
Methylprednisolone hemisuccinate
Brand Names
Solu-medrol
Drug Type
Small Molecule
Chemical Formula
C26H34O8
CAS Number
2921-57-5
Unique Ingredient Identifier
5GMR90S4KN

Overview

A water-soluble ester of methylprednisolone used for cardiac, allergic, and hypoxic emergencies.

Background

A water-soluble ester of methylprednisolone used for cardiac, allergic, and hypoxic emergencies.

Indication

No indication information available.

Associated Conditions

  • Acute Gouty Arthritis
  • Ankylosing Spondylitis (AS)
  • Berylliosis
  • Congenital Adrenal Hyperplasia (CAH)
  • Congenital Hypoplastic Anemia
  • Dermatitis bullous
  • Dermatomyositis (DM)
  • Edema of the cerebrum
  • Hypercalcemia of Malignancy
  • Immune Thrombocytopenia (ITP)
  • Leukemias
  • Lymphoma
  • Multiple sclerosis exacerbation
  • Mycosis Fungoides (MF)
  • Ophthalmia, Sympathetic
  • Pemphigus
  • Polymyositis
  • Primary adrenocortical insufficiency
  • Psoriatic Arthritis
  • Pure Red Cell Aplasia
  • Refractory Uveitis
  • Regional Enteritis
  • Rheumatoid Arthritis
  • Secondary adrenocortical insufficiency
  • Secondary thrombocytopenia
  • Stevens-Johnson Syndrome
  • Systemic Lupus Erythematosus
  • Temporal Arteritis
  • Trichinosis
  • Tuberculous Meningitis
  • Ulcerative Colitis
  • Acquired immune hemolytic anemia
  • Acute rheumatic carditis
  • Disseminated Pulmonary Tuberculosis (TB)
  • Exfoliative erythroderma
  • Fulminating Pulmonary Tuberculosis
  • Idiopathic eosinophilic pneumonias
  • Non-suppurative Thyroiditis
  • Severe Allergic Reactions
  • Symptomatic Sarcoidosis

Clinical Trials

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Title
Posted
Study ID
Phase
Status
Sponsor
2020/05/29
Phase 1
Recruiting
Prevail Therapeutics
2020/05/06
Phase 2
Terminated
2020/05/05
N/A
Completed
2020/04/21
Phase 2
UNKNOWN
Auxilio Mutuo Cancer Center
2020/04/16
Phase 2
Completed
The Camelot Foundation
2020/04/14
Phase 3
UNKNOWN
2020/04/13
Phase 2
Completed
Fundação de Medicina Tropical Dr. Heitor Vieira Dourado
2020/04/10
Phase 3
UNKNOWN
Hospital Universitari de Bellvitge
2020/03/26
N/A
Completed
2020/03/24
Phase 4
Completed

FDA Approved Products

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Product Name
Manufacturer
Route
Strength
Approved
NDC Code
ORAL
32 mg in 1 1
2022/11/28
59762-0051
INTRAVENOUS, INTRAMUSCULAR
125 mg in 2 mL
2020/04/09
55154-3941
INTRAMUSCULAR, INTRASYNOVIAL, INTRALESIONAL, SOFT TISSUE
40 mg in 1 mL
2024/03/14
0781-3522
ORAL
4 mg in 1 1
2017/12/07
72162-1689
ORAL
4 mg in 1 1
2021/03/16
76420-193
ORAL
4 mg in 1 1
2023/12/27
68382-916
ORAL
8 mg in 1 1
2023/12/27
68382-917
HF Acquisition Co. LLC, DBA HealthFirst
INTRAMUSCULAR, INTRAVENOUS
125 mg in 2 mL
2024/01/29
51662-1263
INTRAVENOUS, INTRAMUSCULAR
125 mg in 2 mL
2022/12/27
52584-047
INTRAMUSCULAR, INTRASYNOVIAL, INTRALESIONAL, SOFT TISSUE
40 mg in 1 mL
2021/03/10
50090-0312

EMA Approved Products

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EMA Number
Auth. Holder
Country
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Status
Issued
Opinion
Revision

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No EMA products found for this drug

HSA Approved Products

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Approval No.

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NMPA Approved Products

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Manufacturer
Dosage Form
Trade Name
Strength
Type
Status
Date
Import

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PPB Approved Products

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Registration Code
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Category
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Reg. Date

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TGA Approved Products

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Ingredient

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