Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Mitomycin
Drug ID BADD_D01478
Description Mitomycin is an antineoplastic antibiotic first isolated by Japanese microbiologists in the 1950s from cultures of _Streptomyces caespitosus_.[L12867,A193419] It is an alkylating agent that inhibits DNA synthesis (and, at higher concentrations, RNA and protein synthesis) by cross-linking the complementary strands of the DNA double helix.[A193419] Few other antibiotics have been discovered that work via this alkylating mechanism, making mitomycin relatively unique in the space of microbiota-derived therapies.[A193419] Mitomycin's cross-linking activity has resulted in its approval for the treatment of a variety of cancers - the most recent of which is an April 2020 approval for its use in low-grade Upper Tract Urothelial Cancer (LG-UTUC)[L12867] - as well as adjunctly to _ab externo_ glaucoma surgeries.
Indications and Usage For treatment of malignant neoplasm of lip, oral cavity, pharynx, digestive organs, peritoneum, female breast, and urinary bladder. Also used as an adjunct to ab externo glaucoma surgery.
Marketing Status Prescription; Discontinued
ATC Code L01DC03
DrugBank ID DB00305
KEGG ID D00208
MeSH ID D016685
PubChem ID 5746
TTD Drug ID D0Y0GH
NDC Product Code 0143-9279; 68254-0016; 51552-1509; 72819-152; 58623-0045; 16729-246; 38779-0553; 16729-108; 71052-644; 16729-116; 53183-7010; 16729-247; 68083-483; 68001-391; 67457-519; 73212-036; 49771-002; 62158-0005; 68001-389; 67457-520; 67457-996; 69448-002; 0143-9280; 16729-115; 69448-001; 16729-248; 68001-390; 67457-997; 67457-518; 51927-3642; 65050-0058; 67457-995; 69448-003; 72493-103; 68083-484
Synonyms Mitomycin | Mitomycin C | Mitomycin-C | Mitocin-C | Mitocin C | MitocinC | NSC-26980 | NSC 26980 | NSC26980 | Ametycine | Mutamycin
Chemical Information
Molecular Formula C15H18N4O5
CAS Registry Number 50-07-7
SMILES CC1=C(C(=O)C2=C(C1=O)N3CC4C(C3(C2COC(=O)N)OC)N4)N
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Erythema23.03.06.0010.000533%Not Available
Extravasation08.01.03.0080.002398%Not Available
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Folliculitis23.09.04.007; 11.01.12.0180.000533%
Genital ulceration23.07.03.004; 21.10.05.0010.000533%Not Available
Haematemesis07.12.02.002; 24.07.02.011--Not Available
Haematocrit13.01.05.017--Not Available
Haematuria24.07.01.047; 20.02.01.0060.002664%
Haemoglobin decreased13.01.05.0030.000533%Not Available
Haemolysis01.06.04.002--
Haemolytic anaemia01.06.03.002--Not Available
Haemolytic uraemic syndrome20.01.03.011; 01.06.02.001--
Headache17.14.01.001--
Hydrocele21.12.02.003; 03.03.01.0040.000533%Not Available
Hypersensitivity10.01.03.0030.000799%
Hypertension24.08.02.001--
Hypotony of eye06.08.03.0040.005595%Not Available
Infection11.01.08.0020.000139%Not Available
Injection site reaction12.07.03.015; 08.02.03.014--
Iris atrophy06.06.06.0040.000799%Not Available
Lacrimation increased06.08.02.0040.000533%
Leukopenia01.02.02.0010.001865%Not Available
Loss of consciousness17.02.04.004--Not Available
Lung infiltration22.01.02.004--Not Available
Maculopathy06.09.03.0070.002131%Not Available
Malaise08.01.01.003--
Malignant melanoma23.08.01.001; 16.03.01.0010.000139%Not Available
Microangiopathic haemolytic anaemia24.03.02.019; 01.06.02.002--Not Available
Mucous membrane disorder08.01.06.004--Not Available
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