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Diuroral Brand names, Diuroral Analogs

Diuroral Brand Names Mixture

  • No information avaliable

Diuroral Chemical_Formula

C8H8Cl3N3O4S2

Diuroral RX_link

No information avaliable

Diuroral fda sheet

Diuroral msds (material safety sheet)

Diuroral MSDS

Diuroral Synthesis Reference

No information avaliable

Diuroral Molecular Weight

380.657 g/mol

Diuroral Melting Point

No information avaliable

Diuroral H2O Solubility

No information avaliable

Diuroral State

Solid

Diuroral LogP

1.023

Diuroral Dosage Forms

No information avaliable

Diuroral Indication

Used in the treatment of oedema (including that associated with heart failure) and hypertension.

Diuroral Pharmacology

Trichloromethiazide is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Trichloromethiazide has also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomer-ulonephritis, and chronic renal failure. Trichloromethiazide is also indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension. Like other thiazides, Trichloromethiazide promotes water loss from the body (diuretics). They inhibit Na+/Cl- reabsorption from the distal convoluted tubules in the kidneys. Thiazides also cause loss of potassium and an increase in serum uric acid. Thiazides are often used to treat hypertension, but their hypotensive effects are not necessarily due to their diuretic activity. Thiazides have been shown to prevent hypertension-related morbidity and mortality although the mechanism is not fully understood. Thiazides cause vasodilation by activating calcium-activated potassium channels (large conductance) in vascular smooth muscles and inhibiting various carbonic anhydrases in vascular tissue.

Diuroral Absorption

No information avaliable

Diuroral side effects and Toxicity

Oral Rat LD50 = 5600 mg/kg, oral Mouse LD50 = 2600 mg/kg

Diuroral Patient Information

No information avaliable

Diuroral Organisms Affected

Humans and other mammals