Fimasartan

DrugBank ID: DB09279


Summary

Metric Value
Total Predictions 50
KG+DL (Dual Validated) 0
DL Only 50
KG Only 0

Predictions

Indication Score Source
pulmonary hypertension owing to lung disease and/or hypoxia 0.9920 DL
pulmonary hypertension with unclear multifactorial mechanism 0.9920 DL
malignant hypertensive renal disease 0.9916 DL
malignant renovascular hypertension 0.9916 DL
hypertensive disorder 0.9913 DL
Braddock syndrome 0.9893 DL
chronic pulmonary heart disease 0.9480 DL
cerebrovascular disorder 0.9180 DL
intracerebral hemorrhage 0.8721 DL
obsolete susceptibility to ischemic stroke 0.8419 DL
brain stem infarction 0.8137 DL
stroke disorder 0.7655 DL
ABri amyloidosis 0.7455 DL
cerebral artery occlusion 0.7210 DL
MRI defined brain infarct 0.6828 DL
brain small vessel disease 1 with or without ocular anomalies 0.6759 DL
autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome 0.6750 DL
spinal cord ischemia 0.6607 DL
Prinzmetal angina 0.6490 DL
posteroinferior myocardial infarction 0.6088 DL
posterolateral myocardial infarction 0.6088 DL
septal myocardial infarction 0.5999 DL
myocardial infarction 0.5988 DL
ocular tuberculosis 0.5928 DL
congenital temporomandibular joint ankylosis 0.5923 DL
atrial flutter (disease) 0.5916 DL
primary hereditary glaucoma 0.5913 DL
polydipsia 0.5822 DL
obsolete superimposed infection 0.5802 DL
obsolete pathologic fracture 0.5795 DL
anuria 0.5747 DL
obsolete functional visual loss 0.5738 DL
obsolete breast fibroadenosis 0.5668 DL
obsolete left bundle branch block 0.5663 DL
sudden arrhythmia death syndrome 0.5639 DL
tibial adamantinoma 0.5635 DL
sunburn 0.5584 DL
pulmonary valve insufficiency 0.5481 DL
Marin-Amat syndrome 0.5411 DL
inverse Marcus-Gunn phenomenon 0.5411 DL
mitral valve prolapse, myxomatous 0.5407 DL
cerebral infarction 0.5358 DL
arteriosclerosis obliterans 0.5350 DL
spinal chordoma 0.5347 DL
guttate psoriasis 0.5328 DL
mitral valve stenosis 0.5328 DL
conduct disorder 0.5314 DL
cloacogenic carcinoma 0.5254 DL
ergotism 0.5252 DL
hypercarotenemia and vitamin A deficiency, autosomal recessive 0.5251 DL


Disclaimer
Predictions are for research purposes only and do not constitute medical advice.

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