Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Methylprednisolone
Drug ID BADD_D01433
Description Methylprednisolone is a [prednisolone] derivative glucocorticoid with higher potency than [prednisone].[A188811] It was first described in the literature in the late 1950s.[A188811,A188814] Methylprednisolone was granted FDA approval on 24 October 1957.[L10785] In the outbreak of COVID-19, low dose methylprednisolone-based therapy was successful in treating COVID-19-associated pneumonia in one patient with long-term immunosuppression.[A192813] The efficacy of methylprednisolone in novel coronavirus pneumonia is being investigated further in clinical trials.[L12666]
Indications and Usage Oral and intramuscular methylprednisolone are indicated for a number of endocrine, rheumatic, collagen, dermatologic, allergic, ophthalmic, respiratory, hematologic, neoplastic, edematous, gastrointestinal, nervous system, and other disorders.[L10785,L10788] Intra-articular and soft tissue injections are indicated for short term treatment of acute gouty arthritis, acute and subactute bursitis, acute nonspecific tenosynovitis, epicondylitis, rheumatoid arthritis, and synovitis of osteoarthritis.[L10788] Intralesional injections are indicated for alopecia areata, discoid lupus erythematosus, keloids, lichen planus, lichen simplex chronicus and psoriatic plaques, necrobiosis lipoidica diabeticorum, and localized hypertrophic infiltrated inflammatory lesions of granuloma annulare.[L10788]
Marketing Status approved; vet_approved
ATC Code D07AA01; D10AA02; H02AB04
DrugBank ID DB00959
KEGG ID D00407
MeSH ID D008775
PubChem ID 6741
TTD Drug ID D08PIQ
NDC Product Code 72647-331; 0781-5022; 80425-0230; 59746-003; 59762-0049; 63187-160; 71205-453; 0603-4593; 82094-402; 60722-1003; 64958-0084; 55289-649; 59762-4440; 63629-2218; 68001-557; 68001-560; 80425-0242; 22552-0029; 0009-0056; 45865-104; 59762-0050; 59762-0051; 60760-373; 63187-802; 65162-871; 68071-5221; 70121-1000; 59746-015; 65162-982; 68001-005; 68071-4028; 68084-149; 68788-4593; 71205-054; 72189-264; 82094-401; 45865-417; 50090-3094; 59746-002; 63629-2433; 68001-558; 68180-686; 69306-400; 70518-3622; 82094-403; 59746-001; 68071-2301; 68180-687; 70518-2982; 70771-1348; 70771-1349; 80425-0255; 0009-0073; 49999-153; 53002-3120; 63629-2226; 68001-559; 68180-685; 68180-688; 68382-917; 68382-918; 68382-919; 70771-1350; 80425-0231; 0904-6914; 49452-4686; 51552-0603; 0009-0020; 42806-400; 65162-984; 68180-689; 68382-916; 68788-8276; 69306-004; 70121-1001; 70771-1351; 76420-041; 82298-118; 76420-193; 82094-404; 82094-405; 51927-0201; 0009-0022; 65162-980; 68071-2745; 68788-7833; 0009-0038; 57582-011; 0009-0176; 57582-101
UNII X4W7ZR7023
Synonyms Methylprednisolone | Metipred | 6-Methylprednisolone | 6 Methylprednisolone | Urbason | Medrol
Chemical Information
Molecular Formula C22H30O5
CAS Registry Number 83-43-2
SMILES CC1CC2C3CCC(C3(CC(C2C4(C1=CC(=O)C=C4)C)O)C)(C(=O)CO)O
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Skin discolouration23.03.03.0050.000080%Not Available
Skin disorder23.03.03.007--Not Available
Skin exfoliation23.03.07.0030.000096%Not Available
Skin hyperpigmentation23.05.01.003--
Skin hypertrophy23.01.04.002--Not Available
Skin lesion23.03.03.0100.000064%Not Available
Skin striae23.01.05.0020.000032%Not Available
Skin ulcer24.04.03.007; 23.07.03.0030.000096%
Sleep disorder19.02.04.0010.000192%Not Available
Sodium retention14.05.04.0030.000064%Not Available
Speech disorder22.12.03.027; 19.19.02.002; 17.02.08.0030.000134%Not Available
Spinal compression fracture15.08.05.004; 14.04.04.003; 12.04.04.001--Not Available
Splenomegaly01.09.02.0010.000032%Not Available
Status epilepticus17.12.03.0050.000048%Not Available
Steroid withdrawal syndrome19.04.02.014; 08.06.02.013; 05.01.02.007--Not Available
Stridor22.04.02.0030.000032%
Subarachnoid haemorrhage24.07.04.004; 17.08.01.010; 12.01.10.0110.000048%Not Available
Suffocation feeling22.12.02.0140.000032%Not Available
Suicidal ideation19.12.01.003--
Swelling08.01.03.0150.000726%Not Available
Swelling face10.01.05.018; 08.01.03.100; 23.04.01.0180.000275%Not Available
Syncope02.11.04.015; 24.06.02.012; 17.02.04.0080.000320%
Synovitis15.04.02.0010.000195%Not Available
Systemic lupus erythematosus15.06.02.003; 10.04.03.004; 23.03.02.0060.000032%Not Available
Tachycardia02.03.02.0070.000569%Not Available
Tachypnoea22.02.01.0140.000160%Not Available
Telangiectasia24.03.03.003; 23.06.03.001--
Tenderness08.01.08.0050.000086%Not Available
Tendon disorder12.01.07.019; 15.07.01.0020.000096%Not Available
Tendon rupture15.07.01.008; 12.01.07.003--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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