Template:Valproic Acid Teratogenic Dose table: Difference between revisions

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| width=150px|'''Route'''
| width=150px|'''Route'''
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|-
| Man
| Human
| 30
| 30
| 20-30
| 20-30
| Oral
| Oral
|-bgcolor="F5FAFF"  
|-bgcolor="F5FAFF"  
| Monkey
| {{monkey}}
| not observed
| not observed
| 150
| 150
| oral
| oral
|-
|-
| Rabbit
| {{rabbit}}
| not observed
| not observed
| 150
| 150
| oral
| oral
|-bgcolor="F5FAFF"  
|-bgcolor="F5FAFF"  
| Rat
| {{rat}}
| not observed
| not observed
| 150
| 150
| oral
| oral
|-
|-
| Hamster
| {{hamster}}
| 300
| 300
| not investigated
| not investigated
| ip
| ip
|-bgcolor="F5FAFF"  
|-bgcolor="F5FAFF"  
| Mouse
| {{mouse}}
| 200
| 200
| 200, 250, 400
| 200, 250, 400

Revision as of 23:24, 6 June 2018

Species Difference for Teratogenic Dose (lowest) mg/kg/day
Species Neural tube defects Skeletal defects Route
Human 30 20-30 Oral
monkey not observed 150 oral
rabbit not observed 150 oral
rat not observed 150 oral
hamster 300 not investigated ip
mouse 200 200, 250, 400 ip, sc, oral
Table Data[1]    Links: drugs
  1. Nau H. (1986). Species differences in pharmacokinetics and drug teratogenesis. Environ. Health Perspect. , 70, 113-29. PMID: 3104022