Adverse Drug Reaction Classification System

ADR Ontology
ADR Term Amaurosis
ADR ID BADD_A00160
ADR Hierarchy
06      Eye disorders
06.02      Vision disorders
06.02.02      Blindness (excl colour blindness)
06.02.02.008      Amaurosis
Description The inability to see or the loss or absence of perception of visual stimuli. This condition may be the result of EYE DISEASES; OPTIC NERVE DISEASES; OPTIC CHIASM diseases; or BRAIN DISEASES affecting the VISUAL PATHWAYS or OCCIPITAL LOBE. [MeSH]
MedDRA Code 10001902
MeSH ID D001766
ADR Severity Grade (FAERS)
ADR Severity Grade (CTCAE) Not Available
Synonym
Amaurosis | Amaurosis unilateral | Amaurosis bilateral | Blindness | Blindness, Acquired | Acquired Blindness | Blindness, Monocular | Monocular Blindness | Blindness, Hysterical | Hysterical Blindness | Blindness, Transient | Transient Blindness | Blindness, Legal | Legal Blindness | Amauroses | Blindness, Complete | Complete Blindness
ADR Related Proteins
Protein Name UniProt AC TTD Target ID
Not AvailableNot AvailableNot Available
Drugs Leading to the ADR
Drug IDDrug NameADR Frequency (FAERS)ADR Severity Grade (FAERS)
BADD_D00121Amlodipine0.000031%
BADD_D00151Apixaban0.000265%
BADD_D00497Clomiphene--
BADD_D00504Clopidogrel0.000098%
BADD_D00535Crizotinib0.000533%
BADD_D01009Gemcitabine0.000799%
BADD_D01163Insulin glargine--
BADD_D01864Propofol0.000788%
BADD_D01871Protirelin--
BADD_D01951Risperidone0.000536%
BADD_D02209Thyrotropin releasing hormone--
BADD_D02369Voriconazole0.026622%
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