Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Additional toxicological data

Currently viewing:

Administrative data

Endpoint:
additional toxicological information
Type of information:
not specified
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Judged as a supporting study but reliability of the data is not verifiable.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
secondary source
Title:
SAFETY DATA SHEET CANDESARTAN CILEXETIL CRS Y0001388
Year:
2011
Bibliographic source:
EDQM -European Directorate for the Quality of Medicines & Healthcare, Council of Europe

Materials and methods

Type of study / information:
hazard information related to specific target organ toxicity in case of repeated exposure.
Principles of method if other than guideline:
no data
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
CANDESARTAN CILEXETIL CRS
IUPAC Name:
CANDESARTAN CILEXETIL CRS
Test material form:
not specified
Details on test material:
no data

Results and discussion

Any other information on results incl. tables

Damage to kidneys and heart blood are signs of chronic toxicity after exposure to the substance.

Applicant's summary and conclusion

Conclusions:
Damage to kidneys and heart blood are signs of chronic toxicity after exposure to the substance.