JAMP INDAPAMIDE is a brand name for Indapamide, supplied as a tablet. The medicine, its uses, side effects and dosage are the same regardless of brand.
Verbatim from this product's HC label. Tap a section to expand.
25 mg tablet per day taken in the morning as a single dose. 5 mg as a single dose taken in the morning. If the antihypertensive response to JAMP Indapamide (indapamide) is insufficient, an increase in dosage is not recommended (see Warnings).
Instead, a non-diuretic antihypertensive agent should be added to the drug regimen. Alternatively, if in the opinion of the physician, an important diuretic effect is desirable for the patient's control, a different diuretic which allows for dose titration could be tried instead of indapamide.
83 g/mol Chemical Name 4-chloro-N-[2-methyl-1-indolinyl]-3-sulfamoylbenzamide Description A white or almost white powder, practically insoluble in water, soluble in ethanol (96 per cent). 25 mg, and non-medicinal ingredients: Corn starch, D&C yellow no.
10 aluminum lake, FD&C yellow no. 6, hypromellose, lactose monohydrate, macrogol, magnesium stearate, microcrystalline cellulose, polydextrose, povidone, sodium starch glycolate, talc, titanium dioxide, and triacetin. 5 mg, and non-medicinal ingredients: Corn starch, FD&C blue no.
2, FD&C red no. 40, hypromellose, lactose monohydrate, macrogol, magnesium stearate, microcrystalline cellulose, polydextrose, povidone, sodium starch glycolate, talc, titanium dioxide, and triacetin. Stability and Storage Recommendations Store between 15-30C.
Protect from light. Keep out of reach and sight of children. 25 mg are available in bottles of 100 tablets. 25” on the other side. 5 mg are available in bottles of 100 tablets. 5” on the other side. PHARMACOLOGY Indapamide is a non-thiazide sulfonamide derivative with an indole ring, possessing antihypertensive and diuretic properties.
Antihypertensive Action In normal rats, cats and dogs, intravenous administration of 30 mcg to 30 mg/kg failed to change blood pressure or heart rate. No change in cardiac output, heart rate, peripheral or pulmonary resistance was seen.
In rats, oral doses of up to 100 mg/kg did not change blood pressure over a 96-hour measurement period. , of indapamide elicited antihypertensive activity as follows: • in desoxycorticosterone acetate (DOCA)/saline, hypertensive rats with unilateral nephrectomy, a single dose of 10 mg/kg indapamide produced a maximal fall in systolic blood pressure of 25 mmHg after 24 hours and the antihypertensive action lasted for 72 hours.
• similar results were observed in DOCA/saline rats without nephrectomy. • higher doses up to 100 mg/kg produced only small increases in activity but the blood pressure reduction continued for longer than 1 day. Following repeated oral administration of indapamide (1 mg/kg) or trichlormethiazide (3 mg/kg) to DOCA/saline nephrectomized rats for 14 days, mean systolic blood pressure fell more with indapamide (33 mmHg) than with trichlormethiazide (23 mmHg).
Not medical advice. Always read the patient information leaflet and follow your prescriber or pharmacist.
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One week after indapamide treatment, the blood pressure had only partially returned towards pre-treatment value. , produces a maximal reduction (37 mmHg) in systolic blood pressure after 48 hours and an antihypertensive effect was still evident after 4 days.
o. for 11 weeks prevented the onset of hypertension of DOCA/ saline hypertensive rats with unilateral nephrectomy, the effect was still apparent 5 weeks after interrupting treatment. ) in amyelinated or DOCA/saline hypertensive rats.
JAMP Indapamide (Indapamide Tablets) Product Monograph Page 16 of 27 Indapamide (10-5 and 10-4M) diminished vascular hyper-reactivity to epinephrine, norepinephrine and angiotensin in isolated organ preparations. Indapamide (10-6 g/mL) inhibited vascular smooth muscle cell contractility.
v. and cardiac output showed an increase after 2 hours and a slight decrease over 24 hours. Action on the Kidney Diuretic activity has been studied in rats and dogs. o. o. o. Indapamide did not alter glomerular filtration rate or renal haemodynamics in dogs, suggesting that it acts directly on renal tubules.
Studies of positive and negative free water clearance suggested that diuresis may have resulted from inhibition of water, sodium and chloride reabsorption in the proximal portion of the distal tubule of the nephron. TOXICOLOGY Acute Toxicology (LD50) Route Animals No.
) 10F ) guinea pigs 4M ) 4F ) IV mice 10M 577 (538-618) idem 48 hr 10F 635 (589-684) 611 (575-648) rats 10M 440 (412-470) 433 (404-463) 10F 394 (368-421) idem 48 hr guinea pigs 4M 358 (312-409) 272 (176-421) 4F 315 (249-397) 285 (239-341) Signs of Toxicity Piloerection, […]