Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Carboplatin
Drug ID BADD_D00364
Description Carboplatin is an organoplatinum antineoplastic alkylating agent used in the treatment of advanced ovarian carcinoma.[L32253] Early clinical studies of carboplatin were performed in 1982.[A230523] Carboplatin was developed as an analog of [cisplatin] with reduced nephrotoxicity and vomiting.[A230463,A230523] Carboplatin was granted FDA approval on 3 March 1989.[L32248]
Indications and Usage Carboplatin is indicated in combination with an established combination of chemotherapeutic agents for the initial treatment of advanced ovarian carcinoma.[L32253] Carboplatin is also indicated for the palliative treatment of ovarian carcinoma, recurrent after prior chemotherapy.[L32253]
Marketing Status approved
ATC Code L01XA02
DrugBank ID DB00958
KEGG ID D01363
MeSH ID D016190
PubChem ID 426756
TTD Drug ID D0X7HM
NDC Product Code 0703-4239; 55150-386; 63323-172; 68083-191; 63592-0271; 61703-339; 0703-4244; 0703-4246; 72659-863; 50742-447; 69448-005; 61703-600; 55150-334; 61703-262; 61703-360; 71288-100; 49812-0010; 16729-295; 55150-333; 61703-150; 68083-193; 68554-0084; 68083-190; 68083-192; 53104-7570; 54875-0002; 50742-448; 55150-335; 0703-4248
UNII BG3F62OND5
Synonyms Carboplatin | cis-Diammine(cyclobutanedicarboxylato)platinum II | CBDCA | Paraplatin | Paraplatine | Platinwas | Ribocarbo | Carboplat | Neocarbo | Carbosin | Carbotec | Ercar | JM-8 | JM 8 | JM8 | Nealorin | NSC-241240 | NSC 241240 | NSC241240 | Blastocarb
Chemical Information
Molecular Formula C6H12N2O4Pt
CAS Registry Number 41575-94-4
SMILES C1CC(C1)(C(=O)O)C(=O)O.[NH2-].[NH2-].[Pt+2]
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)
General physical health deterioration08.01.03.0180.001455%Not Available
Left ventricular dysfunction02.04.02.0110.000168%
Tumour haemorrhage24.07.01.028; 16.32.03.0080.000112%
Shock haemorrhagic24.06.02.014; 14.05.05.0030.000280%Not Available
Anal sphincter atony17.05.02.009; 07.03.01.0030.000504%Not Available
Idiosyncratic drug reaction08.06.01.0020.000112%Not Available
Subileus07.13.01.0040.000224%Not Available
Lupus-like syndrome10.04.03.003; 23.03.02.004; 15.06.02.0040.000112%Not Available
Deep vein thrombosis24.01.02.0030.001623%Not Available
Lacunar infarction24.04.06.009; 17.08.01.0160.000168%Not Available
Cardiopulmonary failure22.02.06.004; 02.05.01.0040.000168%Not Available
Madarosis23.02.02.004; 06.06.04.0100.000358%Not Available
Central nervous system lesion17.02.10.0110.000280%Not Available
Systemic inflammatory response syndrome24.06.03.008; 10.02.01.008; 08.01.05.0050.000168%Not Available
Malignant neoplasm progression16.16.01.0050.006548%Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
Conjunctival hyperaemia06.04.01.0040.000112%Not Available
Metastases to peritoneum16.22.02.008; 07.21.03.0030.000280%Not Available
Cytokine release syndrome10.02.01.0100.000112%
Metabolic syndrome05.06.02.007; 24.08.02.014; 14.06.02.0070.000112%Not Available
Ear pruritus04.03.01.0110.000302%Not Available
Eye pruritus06.04.05.0060.000716%Not Available
Catheter site erythema23.03.06.014; 12.07.02.003; 08.02.02.0030.000112%Not Available
Drug tolerance decreased08.06.01.0240.000224%Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Inappropriate antidiuretic hormone secretion14.05.07.001; 05.03.03.0010.001399%Not Available
Febrile bone marrow aplasia01.03.03.007; 08.05.02.0050.000783%Not Available
Injection site swelling12.07.03.018; 08.02.03.017--Not Available
Infusion site pain12.07.05.002; 08.02.05.0140.000392%Not Available
Infusion site swelling12.07.05.003; 08.02.05.0020.000224%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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