ADDAVEN

This brand name is authorized in Brazil, Estonia, Finland, Hong Kong SAR China, Lithuania, Malta, New Zealand, Romania, Singapore, South Africa, UK.

Active ingredients

The drug ADDAVEN contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII KB1PCR9DMW - CHROMIC CHLORIDE
 
Read more about Chromic chloride
2
UNII P484053J2Y - CUPRIC CHLORIDE ANHYDROUS
 
Read more about Copper chloride
3
UNII U38V3ZVV3V - FERRIC CHLORIDE
 
Read more about Ferrous chloride
4
UNII QQE170PANO - MANGANESE CHLORIDE
 

Manganese is required for the synthesis of the mucopolysaccharides of cartilage, glucose utilisation, steroid biosynthesis and for the activity of pyruvate carboxylase. It is bound to arginase of the liver and activates many enzymes.

 
Read more about Manganese
5
UNII 1C4QK22F9J - POTASSIUM IODIDE
 

Potassium iodide is indicated as a thyroid-blocking agent to prevent the uptake of radioactive iodine, for example after a nuclear accident or during a nuclear medicine investigation before administering a radioiodinated compound, which is metabolised to iodide or which contains radioiodine impurities.

 
Read more about Potassium iodide
6
UNII 8ZYQ1474W7 - SODIUM FLUORIDE
 

Sodium fluoride is indicated for the prevention of dental caries in adolescents and adults, particularly amongst patients at risk from multiple caries (coronal and/or root caries). The primary mode of the caries preventative action of fluoride is post-eruptive, i.e topical action. Systemic fluoride supplements are believed also to act mainly topically (i.e during ingestion, via saliva).

 
Read more about Sodium fluoride
7
UNII 8F2SXI1704 - SODIUM MOLYBDATE DIHYDRATE
 
Read more about Sodium molybdate
8
UNII HIW548RQ3W - SODIUM SELENITE
 

Selenium is an essential trace element. In human, selenium compounds are glutathione peroxidase and a selenium protein P found in the plasma. Deficiency of selenium has been associated with an endemic form of cardiomyopathy, Keshan disease and with Kaschin-Beck disease, an endemic osteoarthropathy which causes a severe deformity of the joints.

 
Read more about Sodium selenite
9
UNII 86Q357L16B - ZINC CHLORIDE
 
Read more about Zinc chloride

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
B05XA31 Electrolytes in combination with other drugs B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05X I.V. solution additives → B05XA Electrolyte solutions
Discover more medicines within B05XA31

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 509520120028007
EE Ravimiamet 1607172
FI Lääkealan turvallisuus- ja kehittämiskeskus 497556
GB Medicines & Healthcare Products Regulatory Agency 377629
HK Department of Health Drug Office 64379
LT Valstybinė vaistų kontrolės tarnyba 1069565
MT Medicines Authority MA1123/01901
NZ Medicines and Medical Devices Safety Authority 6223
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W66283001
SG Health Sciences Authority 15302P
ZA Health Products Regulatory Authority 49/24/0996

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