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Drug ReportsKetorolac tromethamine
Ketorolac tromethamine
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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
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Completion date
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Commercial
No data
Clinical
Clinical Trials
169 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Postoperative painD010149G89.1835612732
PainD010146EFO_0003843R52348317
CataractD002386HP_0000518H26.92137315
Macular edemaD008269324210
Acute painD059787R52123319
OsteoarthritisD010003EFO_0002506M15-M191427
Back painD001416HP_0003418M54235
Knee osteoarthritisD020370EFO_0004616M17145
Renal colicD056844EFO_1001412N2312125
AnesthesiaD000758224
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Indications Phases 3
Indications Phases 2
Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients88
MammaplastyD01646211
PharmacokineticsD01059911
Blood pressureD001794EFO_000432511
Pathologic dilatationD00410811
Ovarian neoplasmsD010051EFO_0003893C5611
Fallopian tube neoplasmsD00518511
UveitisD014605HP_0000554H20.911
Pancreatic ductal carcinomaD02144111
Pancreatic neoplasmsD010190EFO_0003860C2511
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Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
BunionD000071378M21.6111
Hammer toe syndromeD037801EFO_1001336M21.5311
Tailor's bunionD050489M21.6211
Colorectal neoplasmsD01517911
Postoperative nausea and vomitingD020250EFO_000488811
VomitingD014839HP_0002013R11.111
NauseaD009325HP_0002018R11.011
ContraceptionD00326711
Respiratory aspirationD053120EFO_100183911
Congenital heart defectsD006330HP_0001627Q24.911
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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
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 1,807 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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6,565 adverse events reported
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