Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Prednisolone
Drug ID BADD_D01831
Description Prednisolone is a glucocorticoid similar to [cortisol] used for its anti-inflammatory, immunosuppressive, anti-neoplastic, and vasoconstrictive effects.[A187463] Prednisolone was granted FDA approval on 21 June 1955.[L9431]
Indications and Usage Prednisolone is indicated to treat endocrine, rheumatic, and hematologic disorders; collagen, dermatologic, ophthalmic, respiratory, and gastrointestinal diseases; allergic and edematous states; and other conditions like tuberculous meningitis.[L9542]
Marketing Status approved; vet_approved
ATC Code A01AC04; A07EA01; C05AA04; D07AA03; D07XA02; H02AB06; R01AD02; S01BA04; S01CB02; S02BA03; S03BA02
DrugBank ID DB00860
KEGG ID D00472
MeSH ID D011239
PubChem ID 5755
TTD Drug ID D0D1SG
NDC Product Code 38779-0150; 64958-0097; 82298-104; 67296-1656; 50383-042; 59651-491; 63187-466; 0527-5406; 65089-0038; 50090-0655; 57582-004; 62135-437; 73534-505; 49452-5980; 82298-105; 82298-106; 60592-911; 60722-3001; 51927-0234; 22552-0052
UNII 9PHQ9Y1OLM
Synonyms Prednisolone | Predate | Predonine | Di-Adreson-F | Di Adreson F | DiAdresonF
Chemical Information
Molecular Formula C21H28O5
CAS Registry Number 50-24-8
SMILES CC12CC(C3C(C1CCC2(C(=O)CO)O)CCC4=CC(=O)C=CC34C)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)
Altered state of consciousness19.07.01.003; 17.02.04.0010.000280%Not Available
Alveolar proteinosis10.04.04.018; 22.01.02.0090.000210%Not Available
Alveolitis22.01.01.0010.000035%Not Available
Anal fissure07.03.01.0020.000087%
Anal fistula07.11.05.0020.000070%
Anaphylactic shock24.06.02.004; 10.01.07.0020.000227%Not Available
Anaphylactoid reaction10.01.07.003; 24.06.03.007--Not Available
Aneurysm24.02.01.0010.000052%Not Available
Anger19.04.02.0010.000122%Not Available
Angioedema23.04.01.001; 10.01.05.009; 22.04.02.008--Not Available
Anisocytosis01.07.02.0080.000035%Not Available
Anosmia22.04.03.006; 17.04.04.0010.000052%
Anterior spinal artery syndrome24.04.06.015; 17.10.01.0080.000035%Not Available
Anterograde amnesia19.20.01.005; 17.03.02.0050.000035%Not Available
Anuria20.01.03.0020.000052%Not Available
Aortic valve incompetence02.07.03.0010.000105%Not Available
Aphasia19.21.01.001; 17.02.03.0010.000157%
Aplastic anaemia01.03.03.0020.000052%Not Available
Apnoea22.02.01.0010.000052%
Arachnoiditis17.06.01.001; 12.02.04.0020.000087%
Arrhythmia02.03.02.001--Not Available
Arteriosclerosis24.04.02.0010.000227%Not Available
Arteriospasm coronary12.02.01.031; 24.04.04.005; 02.02.02.0050.000052%Not Available
Arthralgia15.01.02.0010.001335%
Arthritis15.01.01.0010.000262%
Arthropathy15.01.01.003--Not Available
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.000262%
Asphyxia22.02.02.001; 12.01.08.0110.000035%Not Available
Asthma22.03.01.002; 10.01.03.0100.000367%Not Available
Ataxia17.02.02.001; 08.01.02.0040.000105%
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ADReCS-Target
Drug Name ADR Term Target
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