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Drug ReportsDapagliflozin propanediol
Dapagliflozin propanediol
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Events Timeline
Commercial
Clinical
Drug
Target
Variants
Financial
Trends
Safety
Events Timeline
5D
1M
3M
6M
YTD
1Y
2Y
5Y
Max
Events
FDA approval date
EMA approval date
Patent expiration date
Study first post date
Last update post date
Start date
Primary completion date
Completion date
Results first post date
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Commercial
No data
Clinical
Clinical Trials
650 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Type 2 diabetes mellitusD003924EFO_0001360E1131197910249273
Diabetes mellitusD003920EFO_0000400E08-E131216748136212
Heart failureD006333EFO_0003144I5051521303096
Kidney diseasesD007674EFO_0003086N0822017141463
Chronic renal insufficiencyD051436N1821813101050
Type 1 diabetes mellitusD003922EFO_0001359E10661011334
Myocardial infarctionD009203EFO_0000612I21385721
InfarctionD007238EFO_0009463285720
HypertensionD006973EFO_0000537I102374318
Cardiovascular diseasesD002318EFO_0000319I98136514
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Indications Phases 2
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients24125
Diabetic ketoacidosisD016883EFO_1000897123
Pancreatic neoplasmsD010190EFO_0003860C2511
Therapeutic equivalencyD01381011
MalnutritionD044342EFO_0008572E40-E4611
Prostatic neoplasmsD011471C6111
Reperfusion injuryD01542711
Vascular ringD000073872Q25.4511
HyperinsulinismD006946E16.111
HypothyroidismD007037EFO_0004705E03.911
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Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
InfectionsD007239EFO_000054433
Urinary tract infectionsD014552EFO_0003103N39.033
Communicable diseasesD00314111
Body weight changesD00183611
Urinary bladder neoplasmsD001749C6711
Chemical and drug induced liver injuryD056486EFO_000422811
Mitochondrial diseasesD028361EFO_000059111
Systolic murmursD054160R01.111
Tricuspid valve insufficiencyD01426211
Exercise testD005080EFO_000432811
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Epidemiology
Epidemiological information for investigational and approved indications
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Drug
No data
Target
No data
Variants
No data
Financial
No data
Trends
No data
Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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15,652 adverse events reported
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