Registration Dossier

Administrative data

Endpoint:
acute toxicity: other routes
Remarks:
Intraperitoneal
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail

Data source

Materials and methods

GLP compliance:
not specified

Administration / exposure

Route of administration:
intraperitoneal
Doses:
LD50 > 1000 mg/kg in rats

Results and discussion

Applicant's summary and conclusion

Conclusions:
Some rats at the 1000 mg/kg dose had diarrhoea.