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MRP ₹158
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MRP ₹158
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Alcohol
Caution
Drinking alcohol with SUCRAKAT 1000MG SUSPENSION 200ML may cause dehydration and elevate the level of stomach acid, thereby decreasing SUCRAKAT 1000MG SUSPENSION 200ML efficacy.
Pregnancy
Safe if prescribed
SUCRAKAT 1000MG SUSPENSION 200ML should not be taken until prescribed. Your doctor will weigh the benefits and any potential risks before prescribing it to you. Please consult your doctor.
Breast Feeding
Caution
There is limited data on how SUCRAKAT 1000MG SUSPENSION 200ML affects breastfeeding. Please consult your doctor, before taking SUCRAKAT 1000MG SUSPENSION 200ML. Your doctor will weigh the benefits and any potential risks before prescribing them to you.
Driving
Caution
SUCRAKAT 1000MG SUSPENSION 200ML decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.
Liver
Caution
SUCRAKAT 1000MG SUSPENSION 200ML to be taken with caution if you had or have a history of liver disease/conditions. The dose may have to be adjusted by your doctor.
Kidney
Unsafe
SUCRAKAT 1000MG SUSPENSION 200ML contains aluminium, which is normally excreted by your kidney. Therefore, people with kidney problems may be at greater risk of high aluminium toxicity in the body. The dose adjustment is necessary for patients with kidney disease.
Children
Caution
The safety and effectiveness of SUCRAKAT 1000MG SUSPENSION 200ML in children have not been established. Please consult your doctor before giving SUCRAKAT 1000MG SUSPENSION 200ML to children.
Product Substitutes
About SUCRAKAT 1000MG SUSPENSION 200ML
SUCRAKAT 1000MG SUSPENSION 200ML belongs to a gastrointestinal class of drugs called 'ulcer protectants' primarily used to prevent or treat peptic ulcers or gastrointestinal ulcers. A peptic ulcer is a sore on the stomach's lining or the first part of the small intestine (duodenum). Ulcer or sores of the stomach region is called gastric ulcer, while ulcer of the duodenum is known as duodenal ulcer.
SUCRAKAT 1000MG SUSPENSION 200ML contains 'Sucralfate', which works by forming a protective barrier or coat over the ulcer so that digestive enzymes, acid and bile salts cannot further irritate the lining of the stomach and duodenum. This protects the ulcer from the stomach's acid, allowing it to heal.
Your doctor will advise you on how often you take SUCRAKAT 1000MG SUSPENSION 200ML based on your medical condition. Some people may experience common side effects like constipation, dizziness, sleepiness, dry mouth, blurred vision, and diarrhoea. Most of these side effects of SUCRAKAT 1000MG SUSPENSION 200ML do not require medical attention and gradually resolve over time. However, if the side effects persist or worsen, please consult your doctor.
Avoid taking any antacid like magnesium hydroxide or aluminium hydroxide within 30 minutes before or after taking SUCRAKAT 1000MG SUSPENSION 200ML. If you are known to be allergic to SUCRAKAT 1000MG SUSPENSION 200ML or active and inactive ingredients present on it, please tell your doctor. If you are pregnant or breastfeeding, it is advised to consult a doctor before using SUCRAKAT 1000MG SUSPENSION 200ML. Duodenal ulcer tends to be a recurrent disease. Try not to stop taking SUCRAKAT 1000MG SUSPENSION 200ML of your own. Stopping a sudden intake of SUCRAKAT 1000MG SUSPENSION 200ML will not influence the frequency or severity of future ulceration. Let your doctor know if you have any kidney problems. People with reduced kidney function may be more likely to experience side effects of aluminium accumulation with SUCRAKAT 1000MG SUSPENSION 200ML. The dose adjustment is necessary for patients with kidney disease and elderly patients.
Uses of SUCRAKAT 1000MG SUSPENSION 200ML
Medicinal Benefits
SUCRAKAT 1000MG SUSPENSION 200ML is a class of an anti-ulcer drugs prescribed for treating or preventing the return of duodenal ulcers (ulcers located in the first part of the small intestines). SUCRAKAT 1000MG SUSPENSION 200ML works by forming a protective barrier or coat over the ulcer to pepsin and bile and inhibits the diffusion of gastric acid. This protects the ulcer from the stomach's acid, allowing it to heal. SUCRAKAT 1000MG SUSPENSION 200ML exhibits a cytoprotective effect and forms a viscous, adhesive barrier on the surface of the intact intestinal mucosa and the stomach. SUCRAKAT 1000MG SUSPENSION 200ML stimulates the synthesis and release of gastric mucosal prostaglandins, bicarbonate, and the epidermal growth factor, which promotes healing.
Directions for Use
Side Effects of SUCRAKAT 1000MG SUSPENSION 200ML
Drug Warnings
You should avoid taking SUCRAKAT 1000MG SUSPENSION 200ML if you are allergic to SUCRAKAT 1000MG SUSPENSION 200ML or other ingredients present in it, have kidney disease, stomach/intestine problems (delayed gastric emptying), are pregnant or planning for pregnancy, and are a breastfeeding mother. Caution is required before giving SUCRAKAT 1000MG SUSPENSION 200ML to elderly patients. SUCRAKAT 1000MG SUSPENSION 200ML contains aluminium, which is normally removed by your kidney. Therefore, older adults and people with kidney problems may be at greater risk for developing high aluminium levels while using this drug with other products containing aluminium (e.g. antacids). The safety and effectiveness in children are not established; please consult your doctor before giving SUCRAKAT 1000MG SUSPENSION 200ML to children.
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Habit Forming
Special Advise
SUCRAKAT 1000MG SUSPENSION 200ML is prescribed for acute or short-term conditions of duodenal ulcer. Do not take SUCRAKAT 1000MG SUSPENSION 200ML for more than eight weeks. If still, your duodenal ulcer persists, stop taking SUCRAKAT 1000MG SUSPENSION 200ML and contact a doctor. SUCRAKAT 1000MG SUSPENSION 200ML contains aluminium, so if you are a kidney patient, let your doctor know about this before taking SUCRAKAT 1000MG SUSPENSION 200ML.
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