Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Bevacizumab
Drug ID BADD_D00268
Description There is a great deal of evidence indicating that vascular endothelial growth factor (VEGF) is important for the survival and proliferation of cancer cells.[A192939,A192837,A192891,A193275] VEGF plays an important role in angiogenesis, lymphangiogenesis, and tumor growth, which are all factors that contribute to its attractiveness as a therapeutic target for anti-cancer therapies.[A192834,A192888,A192837,A192891,A192894] In 2004, bevacizumab (Avastin) gained FDA approval for specific types of cancer, and became the first antiangiogenic agent introduced to the market.[A193272,A193275] It is a humanized monoclonal IgG antibody, and inhibits angiogenesis by binding and neutralizing VEGF-A.[A192888,A192939] Bevacizumab is generally indicated for use in combination with different chemotherapy regimens which are specific to the type, severity, and stage of cancer.[L12648] Interestingly, researchers have identified higher VEGF expression in patients with COVID-19, which may contribute to lung pathologies including acute respiratory syndrome (ARDS) and acute lung injury (ALI).[L12699] As such, bevacizumab is being investigated for the treatment of lung complications associated with severe cases of COVID-19.[L12699]
Indications and Usage As part of combination therapy for metastatic colorectal cancer and HER2-negative metastatic breast cancer.
Marketing Status Prescription
ATC Code L01FG01; S01LA08
DrugBank ID DB00112
KEGG ID D06409
MeSH ID D000068258
PubChem ID Not Available
TTD Drug ID D04KBL
NDC Product Code 50242-060; 50242-059; 63552-113; 50242-061; 58394-095; 50242-160; 63552-114
Synonyms Bevacizumab | Mvasi | Bevacizumab-awwb | Bevacizumab awwb | Avastin
Chemical Information
Molecular Formula Not Available
CAS Registry Number 216974-75-3
SMILES Not Available
Chemical Structure
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Proteinuria20.02.01.011--
Pulmonary embolism22.06.02.001; 24.01.06.001--Not Available
Pulmonary hypertension22.06.01.001; 24.08.03.002--
Rash23.03.13.001--Not Available
Rectal haemorrhage07.12.03.001; 24.07.02.018--
Retroperitoneal haemorrhage07.07.02.002; 24.07.01.017--
Rhinitis11.01.13.004; 22.07.03.006--
Skin exfoliation23.03.07.003--Not Available
Skin ulcer23.07.03.003; 24.04.03.007--
Stomatitis07.05.06.005--
Syncope02.01.02.008; 17.02.04.008; 24.06.02.012--
Thrombocytopenia01.08.01.002--Not Available
Thrombosis24.01.01.006--Not Available
Thrombotic microangiopathy01.01.02.006; 20.01.07.004; 24.01.01.013--Not Available
Tinnitus04.04.01.002; 17.04.07.004--
Tooth abscess07.09.01.003; 11.01.04.003--Not Available
Upper respiratory tract infection11.01.13.009; 22.07.03.011--
Vaginal haemorrhage21.08.01.001; 24.07.03.005--
Venous thrombosis24.01.01.008--Not Available
Vision blurred06.02.06.007; 17.17.01.010--
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
Wound infection11.01.08.010; 12.01.08.012--
Deep vein thrombosis24.01.02.003--Not Available
Post procedural haemorrhage12.02.05.004; 24.07.01.014--
Wound complication12.01.08.010--
Haemorrhage24.07.01.002--Not Available
Neutropenic infection01.02.03.009; 11.01.08.024--Not Available
Decreased appetite08.01.09.028; 14.03.01.005--
Device related infection08.07.01.005; 11.01.08.018--
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ADReCS-Target
Drug Name ADR Term Target
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