Senade 13.5mg tabs 500 pcs

Description

Composition
Active substance:
Senna leaf extract …. 93.33 mg (containing calcium salts the amount of sennosides A and B, based on the sennosides C – 13.5 mg)
Excipients:
Lactose – 23.07 mg Starch – 43.56 mg methyl parahydroxybenzoate – 0.04 mg Microcrystalline cellulose – 15.0 mg talc – 11.13 mg magnesium stearate – 0.93 mg Sodium lauryl sulfate – 0.93 mg, carmellose sodium – 2.00 mg.
Description:
Flat round tablets with bevelled edges brown to dark brown in color with a splash. On one side of the tablets embossed word «CIPLA», on the other – a fault line.
Product form:
13.5 mg Tablets
20 tablets in the blister of a three-layer film (PVC / PE / PVDC), and aluminum foil.
20 tablets in a blister 25 in the blister cardboard pack with an attachment 25 on the application document.
Contraindications
Increased sensitivity to the drug, spastic constipation, ileus, abdominal pain of unknown origin, strangulated hernia, acute inflammatory diseases of the abdominal cavity, peritonitis, gastro-intestinal and uterine bleeding, cystitis, disturbances of water-electrolyte metabolism.
Precautions prescribed for liver and / or kidney disease, as well as during pregnancy and lactation, in states after abdominal operations, as well as children’s age (age 6) on the basis of the dosing regimen.
Indications
Constipation caused by hypotension and sluggish motility of the colon regulation stool with hemorrhoids, proctitis, anal fissures.
Interaction with other drugs
With prolonged use at high doses Senade® possible potentiation of cardiac glycosides and the effect on the action of antiarrhythmic drugs due to the possibility of hypokalemia.
While the use of thiazide diuretics, corticosteroids, licorice root drugs increases the risk of hypokalemia.
Overdose
The main adverse effects in overdose – diarrhea, leading to dehydration. Conservative measures – increase in fluid intake. This is usually sufficient to compensate for the loss of fluid and electrolytes. In some cases it is necessary to replenish lost fluids and electrolytes via intravenous infusion of plasma substitutes.
pharmachologic effect
Pharmacological group:
The laxative of plant origin.
Pharmacological properties:
It has a laxative effect, occurring in 8-10 hours. Laxative effect due to the action of the large intestine receptors, increases peristalsis.
Pregnancy and breast-feeding
No reports of adverse events during pregnancy or damaging effect on the fetus when using the drug in recommended doses is not published.
However, there are reports of experimental data on the risk of genotoxic effects of some natural anthranol (emodin, aloe-emodin). In this regard, it is not recommended to use the drug in the first trimester of pregnancy. In the second and third trimester of pregnancy is allowed to use the drug with caution, only in those cases where the intended benefits to the mother outweighs the potential risk to the fetus.
During breastfeeding apply the drug is not recommended as metabolites in a small amount into breast milk and may cause diarrhea in infants.
In the event that there is a need to take medication, breast-feeding is recommended to temporarily stop.
Conditions of supply of pharmacies
Without a prescription.
side effects
Laxative effect of the drug may be accompanied by colicky abdominal pain, flatulence. With prolonged use, particularly at high doses, possible violations of water-electrolyte metabolism, albuminuria, hematuria, melanin deposition in the intestinal mucosa, nausea, vomiting, diarrhea, urinary discoloration, skin rash, seizures, vascular collapse, fatigue, confusion.
special instructions
Do not use the drug for more than 2 weeks.
After ingestion urine can acquire a yellow-brown or red-violet color.
Effect on driving ability
Use of the drug has no effect on the ability to perform potentially hazardous activities that require high concentration and psychomotor speed reactions (vehicle control, work with moving machinery).
Storage conditions
Stored in a dry place at a temperature not higher than 25 ° C.
Keep out of the reach of children.
Dosing and Administration
Taken orally usually 1 time per day at night before bedtime, drinking water or any beverage.
Adults and children over 12 years: 1 tablet at the reception. In the absence of effective dose can be increased to 2-3 tablets.
Children 6-12 years: 1/2 tablet and, if necessary, increase the dose to 1-2 tablets.
In the process of selection of the same dose should be taken within a few days and gradually increase it to 1/2 tablets. If the maximum dose of defecation occurs within 3 days, you must consult your doctor.
Information
Appearance may differ from that depicted in the picture. There are contraindications. You need to read the manual or consult with a specialist