GADOSAM
GADODIAMIDE
What it does
Gadodiamide is a contrast agent used during imaging tests to help visualize certain areas of the body more clearly.
Commonly used for: imaging tests (MRI scans)
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Source: Food and Drugs Authority · fetched 2026-04-18 08:37:11 · updated 2026-09-18 04:00:09
About this medicine
Gadodiamide is a contrast agent used during imaging tests to help visualize certain areas of the body more clearly.
What it treats
- imaging tests (MRI scans)
How it works
It enhances the contrast of images taken during scans, allowing doctors to see details more clearly.
Who it's for
It is for patients who need detailed imaging of their organs or tissues.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: gadodiamide
BNF-referencedGadodiamide is a paramagnetic contrast agent used in magnetic resonance imaging (MRI) to enhance the visibility of internal structures. It possesses a gadolinium ion that generates a magnetic moment in the presence of a magnetic field, which alters the relaxation rates of water protons in tissues, thereby increasing contrast in areas where gadodiamide accumulates.
Indications
- Magnetic resonance imaging (MRI) for the visualization of normal and pathological tissues
- Assessment of neoplasms
- Evaluation of abscesses
- Investigation of subacute infarcts
Dosage
Children: Refer to the BNF for Children for appropriate dosing information in paediatric patients.
Adults: Refer to specific guidelines or protocols for dosing in adults as provided in the BNF.
Mechanism of action
Gadodiamide acts as a paramagnetic molecule that develops a magnetic moment when exposed to a magnetic field. This magnetic moment modifies the relaxation rates of water protons nearby, allowing for improved contrast in MRI imaging of tissues where gadodiamide is present.
Pharmacodynamics
In MRI, the visualization of tissues is influenced by variations in radiofrequency signal intensity, which depend on changes in proton density and alterations in relaxation times (T1 and T2). Gadodiamide enhances the T1 relaxation time, leading to increased signal intensity in tissues where it accumulates, particularly in areas with disrupted blood-brain barriers or abnormal vascularity, such as tumors and abscesses.
Pharmacokinetics
The pharmacokinetic properties of gadodiamide in various lesions are not extensively characterized. However, as a paramagnetic agent, it is distributed in the body based on the vascularity of tissues and may accumulate in abnormal lesions. The distribution and elimination pathways of gadodiamide are influenced by its solubility and interactions with body fluids.
Adverse effects
- Headache
- Nausea
- Dizziness
- Injection site reactions
- Nephrogenic systemic fibrosis in patients with severe renal impairment
Precautions
- Use with caution in patients with renal impairment
- Monitor renal function in patients at risk for nephrogenic systemic fibrosis
- Ensure adequate hydration prior to administration
Pregnancy
Gadodiamide should only be used during pregnancy if the potential benefit justifies the potential risk to the fetus. Safety in pregnancy has not been established.
Breast-feeding
It is not known whether gadodiamide is excreted in human milk. Caution should be exercised when administering to a nursing woman.
Storage
Store at 20-25 degrees Celsius. Protect from light and keep in the original container. Do not freeze.
Formulations
- Solution for injection
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: gadodiamide
PubChem CID 153921Molecular formula: C16H26GdN5O8
Mechanism of action
Gadodiamide paramagnetic molecule that develops a magnetic moment when placed in a magnetic field. The magnetic moment alters the relaxation rates of water protons in its vicinity in the body. Its use in magnetic resonance imaging (MRI) allows to selectively increase contrast in tissues where gadodiamide accumulates.
Pharmacodynamics
In magnetic resonance imaging, visualization of normal and pathologic tissue depends in part on variations in the radiofrequency signal intensity. These variations occur due to: changes in proton density; alteration of the spin-lattice or longitudinal relaxation time (T1); and variation of the spin-spin or transverse relaxation time (T2). Gadodiamide is a paramagnetic agent with unpaired electron spins which generate a local magnetic field. As water protons move through this local magnetic field, the changes in the magnetic field experienced by the protons reorient them with the main magnetic field more quickly than in the absence of a paramagnetic agent. By increasing the relaxation rate, gadodiamide decreases both the T1 and T2 relaxation times in tissues where it is distributed. At clinical doses, the effect is primarily on the T1 relaxation time and produces an increase in signal intensity. Disruption of the blood-brain barrier or abnormal vascularity allows the accumulation of gadodiamide in lesions such as neoplasms, abscesses, and subacute infarcts. The pharmacokinetic parameters of gadodiamide in various lesions are not known.
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.
This drug in other countries
The same active ingredient registered across other registries we cover - including different brands.