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OTC

SOFABIC

23,53G/69,95G/L/Solution/CHLORURE DE SODIUM/BICARBONATE DE SODIUM
SOFARM
ManufacturerVerified lab

SOFARM

Public retail price
N/ADZD

Identification

Active ingredient (INN)
CHLORURE DE SODIUM/BICARBONATE DE SODIUM
Internal code
25 G 053
Country of Origin
Algeria
Pharmaceutical form
Solution
Prescription List
OTC
Packaging
bidon/10l
SOFABIC
Clinical View

DAWA Clinical Workbench v2.0

Information may not be accurate. Always consult a physician, pharmacist, or specialist before acting on any data shown here.

Description

Methylene blue is an oxidation-reduction agent.

The intravenous form of methylene blue is approved by the FDA for the treatment of pediatric and adult patients with acquired methemoglobinemia.

Historically, it has been widely used in Africa to treat malaria, but now it disappeared when chloroquine (CQ) and other drugs entered the market.

Its use as an urinary tract antiseptic has also been investigated.

Methylthioninium chloride (INN, or methylene blue, proposed trade name Rember) is an investigational drug being developed by the University of Aberdeen and TauRx Therapeutics that has been shown in early clinical trials to be an inhibitor of Tau protein aggregation.

The drug is of potential interest for the treatment of patients with Alzheimer's disease.

Indications

Indicated for the treatment of pediatric and adult patients with acquired methemoglobinemia.

Other clinical applications of methylene blue include improvement of hypotension associated with various clinical states, an antiseptic in urinary tract infections, treatment of hypoxia and hyperdynamic circulation in cirrhosis of liver and severe hepatopulmonary syndrome, and treatment of ifofosamide induced neurotoxicity.

Mechanism of Action

Guanylate cyclase soluble subunit alpha-2 Inhibitor Nitric oxide synthase 1 Inhibitor.

Metabolism

Following distribution into tissues, rapidly reduced to leukomethylene blue (leucomethylthioninium chloride).

Metabolism to leucomethylene blue may be less efficient in neonates than in older individuals.

Route of Elimination

Excreted in urine and bile.

About 75% of an oral dose excreted in urine, primarily as stabilized colorless leukomethylene blue.

Half-life

5–6.5 hours (after Intravenous dose).

Adverse Effects

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Alternatives