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EC number: 200-652-8 | CAS number: 67-43-6
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- supporting study
- Study period:
- 2007
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Published data, information on methods and results is sufficient to make an assessment.
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- publication
- Title:
- Gadolinium periconceptional exposure: pregnancy and neonatal outcome
- Author:
- De Santis, M.
- Year:
- 2 007
- Bibliographic source:
- Acta Obstet Gynecol Scand. 2007; 86(1):99-101. [Acta obstetricia et gynecologica Scandinavica]
Materials and methods
- Type of study / information:
- This is a prospective cohort study of patients exposed to gadolinium in the first trimester of pregnancy to observe associated adverse events.
- Endpoint addressed:
- toxicity to reproduction / fertility
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Gadolinium salt of DTPA
- IUPAC Name:
- Gadolinium salt of DTPA
- Details on test material:
- gadolinium derivatives (salts) - gadopentetate dimeglumine, gadobene acid, gadodiamide, and gadoteridol
Constituent 1
Method
- Ethical approval:
- confirmed, but no further information available
- Details on study design:
- no data
- Exposure assessment:
- not specified
- Details on exposure:
- 26 women exposed to gadopentetate dimeglumine in the periconceptional and first trimester period who had undergone an MRI owing to other clinical indications. All pregnancies were singleton and one patient had had three MRIs with intravenous contrast agent infusion in the same pregnancy because of astrocytoma in pregnancy.
Seventeen patients were exposed to MRI of the central nervous system (CNS), five to MRI of the spine, two to MRI of the pelvis, one to MRI of the abdomen, and one to MRI of the thorax. Six patients were also exposed to x-rays, five to the thorax and one to computerized tomography (CT) of the totalbody.
Results and discussion
- Results:
- In this prospective cohort study there were no maternal or neonatal complications and only one congenital anomaly at birth.
Any other information on results incl. tables
none
Applicant's summary and conclusion
- Conclusions:
- Under the conditions of this prospective cohort study there were no maternal or neonatal complications and only one congenital anomaly at birth, however, this study represents the only prospective investigation of gadolinium derivatives in pregnancy, but more data are necessary to exclude a teratogenic risk.
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