KREMIL-S ADVANCE Famotidine / Calcium Carbonate / Magnesium Hydroxide 10mg / 800mg / 165mg Chewable Tablet 1's
NONRXDRUG-DR-XY32411-1pc
- View all variations as list
| CODE | Dosage Strength | Drug Packaging | Availability | Price | ||
|---|---|---|---|---|---|---|
|
NONRXDRUG-DR-XY32411-1pc
|
In stock
|
₱2500 |
Discreet Packaging
We recognize that purchasing medications can be a deeply personal matter. To respect your privacy, we ensure that all orders are packaged discreetly, with no indication of the contents on the packaging. This means that even our couriers remain unaware of the package contents.
Furthermore, we uphold strict confidentiality standards. We guarantee that your order information will never be disclosed to any third party. Your trust is paramount to us, and we are committed to safeguarding your privacy at every step of the process. Our dedication to discretion and confidentiality is part of our unwavering commitment to you, our valued customer.
FDA-registered Products
FDA-licensed Pharmacies
Sellers of this product
Features
Brand
Kremil-S Advance
Full Details
Dosage Strength
10 mg / 800 mg / 165 mg
Drug Ingredients
- Calcium
- Famotidine
- Magnesium
Drug Packaging
Chewable Tablet 1's
Generic Name
Famotidine / Calcium Carbonate / Magnesium Hydroxide
Dosage Form
Chewable Tablet
Registration Number
DR-XY32411
Drug Classification
Over-The-Counter (OTC)
Description
Indications/Uses
This medicine is used for the relief of heartburn associated with acid indigestion and hyperacidity.
Dosage/Direction for Use
To relieve heartburn in adults and children 12 years and older: 1 tablet as needed.
Or, as directed by a doctor.
Chew tablet completely before swallowing.
Do not use more than 2 chewable tablets in 24 hours.
Or, as directed by a doctor.
Chew tablet completely before swallowing.
Do not use more than 2 chewable tablets in 24 hours.
Overdosage
There is no experience to date with acute over dosage of famotidine. Oral doses of up to 800 mg/day of famotidine have been given to patients with pathological hypersecretory conditions with no serious adverse effects.
There have been rare reports of milk-alkali syndrome (high levels of calcium) and tissue calcification (hardening of tissues) in patients receiving about 10 g calcium carbonate (4 g elemental calcium per day).
There have been rare reports of milk-alkali syndrome (high levels of calcium) and tissue calcification (hardening of tissues) in patients receiving about 10 g calcium carbonate (4 g elemental calcium per day).
Administration
Should be taken on an empty stomach: Take 1 hr before or 2 hr after meals. Chew tab completely before swallowing.
Special Precautions
If the patient is allergic to any ingredient in this product.
If the patient have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be due to a serious condition and require consultation with the doctor.
If patient is using other acid reducers.
Had heartburn for more than three months; this may be a sign of a more serious disease of the stomach.
Frequent chest or shoulder pain with shortness of breath, lightheadedness, sweating, or dizziness.
Stomach pain, nausea and vomiting and unexplained weight loss.
Moderate (creatinine clearance < 50 mL/min) to severe (creatinine clearance <10 mL/min) kidney disease.
Do not take more than the recommended dose or duration of treatment.
Stop use and ask doctor if the patient needs to take this product for more than 14 days.
Do not use after the expiry date on the label.
If the patient have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be due to a serious condition and require consultation with the doctor.
If patient is using other acid reducers.
Had heartburn for more than three months; this may be a sign of a more serious disease of the stomach.
Frequent chest or shoulder pain with shortness of breath, lightheadedness, sweating, or dizziness.
Stomach pain, nausea and vomiting and unexplained weight loss.
Moderate (creatinine clearance < 50 mL/min) to severe (creatinine clearance <10 mL/min) kidney disease.
Do not take more than the recommended dose or duration of treatment.
Stop use and ask doctor if the patient needs to take this product for more than 14 days.
Do not use after the expiry date on the label.
Adverse Reactions
Famotidine: Famotidine is generally well tolerated.
Undesirable effects involving stomach and intestines include: constipation, diarrhea, nausea, vomiting, abdominal and gas-related discomfort, decreased appetite, dry mouth, heartburn, and loss of taste.
Famotidine may also cause the following skin reactions: acne, itching, red, itchy patches on the skin (hives), rash and dry skin.
Headache, dizziness, weakness, fatigue, muscle weakness, seizures, insomnia, drowsiness, depression, confusion, disorientation, anxiety, decreased sexual desire, and hallucinations have been reported.
Famotidine may also cause kidney problems (e.g., increased serum creatinine concentration and abnormal amounts of protein in the urine) and liver disease such as yellowing of the skin (jaundice).
Other undesirable effects include: fever, hypertension, flushing, muscle cramps, pain in the joints, ringing in the ears (tinnitus), and community-acquired pneumonia.
Antacids: Flatulence from increased carbon dioxide may occur in some patients.
Calcium carbonate can stimulate acid rebound in some people. Acid rebound causes stomach to produce even more acid, making heartburn worse. This, however, is very rare.
Excessive doses of calcium carbonate and magnesium hydroxide may result in high calcium and magnesium levels in the blood in patients with kidney impairment.
Alkalosis (excess base in body fluids) may also occur with excessive doses of antacid.
The combination of magnesium hydroxide and calcium carbonate balances the side effects of diarrhea from magnesium hydroxide and constipation from calcium carbonate.
Undesirable effects involving stomach and intestines include: constipation, diarrhea, nausea, vomiting, abdominal and gas-related discomfort, decreased appetite, dry mouth, heartburn, and loss of taste.
Famotidine may also cause the following skin reactions: acne, itching, red, itchy patches on the skin (hives), rash and dry skin.
Headache, dizziness, weakness, fatigue, muscle weakness, seizures, insomnia, drowsiness, depression, confusion, disorientation, anxiety, decreased sexual desire, and hallucinations have been reported.
Famotidine may also cause kidney problems (e.g., increased serum creatinine concentration and abnormal amounts of protein in the urine) and liver disease such as yellowing of the skin (jaundice).
Other undesirable effects include: fever, hypertension, flushing, muscle cramps, pain in the joints, ringing in the ears (tinnitus), and community-acquired pneumonia.
Antacids: Flatulence from increased carbon dioxide may occur in some patients.
Calcium carbonate can stimulate acid rebound in some people. Acid rebound causes stomach to produce even more acid, making heartburn worse. This, however, is very rare.
Excessive doses of calcium carbonate and magnesium hydroxide may result in high calcium and magnesium levels in the blood in patients with kidney impairment.
Alkalosis (excess base in body fluids) may also occur with excessive doses of antacid.
The combination of magnesium hydroxide and calcium carbonate balances the side effects of diarrhea from magnesium hydroxide and constipation from calcium carbonate.
Drug Interactions
Food appears to slightly increase and antacids appear to slightly decrease the absorption of famotidine, but these effects do not appear to be clinically important.
Unlike cimetidine, famotidine is considered to have little effect on the actions of other drugs such as warfarin, theophylline, phenytoin, diazepam, or procainamide.
Antacids may interact with other drugs such as propranolol, isoniazid, prednisolone, diflunisal, and naproxen which may cause formation of complexes that are not absorbed.
Antacids decrease the absorption of tetracycline and iron. Take tetracycline 1 hour before or 2 hours after antacids and 2 hours before or 3 hours after iron preparations and vitamin products that contain iron.
Unlike cimetidine, famotidine is considered to have little effect on the actions of other drugs such as warfarin, theophylline, phenytoin, diazepam, or procainamide.
Antacids may interact with other drugs such as propranolol, isoniazid, prednisolone, diflunisal, and naproxen which may cause formation of complexes that are not absorbed.
Antacids decrease the absorption of tetracycline and iron. Take tetracycline 1 hour before or 2 hours after antacids and 2 hours before or 3 hours after iron preparations and vitamin products that contain iron.
Storage
Store at temperatures not exceeding 30°C.
Action
Pharmacology: This medicine contains famotidine, calcium carbonate and magnesium hydroxide. Famotidine, a histamine H2-receptor antagonist, reduces acid production in the stomach.
Calcium carbonate and magnesium hydroxide are antacids that neutralize acid in the stomach. This medicine also provides 321 mg calcium and 71 mg magnesium per chewable tablet.
Calcium carbonate and magnesium hydroxide are antacids that neutralize acid in the stomach. This medicine also provides 321 mg calcium and 71 mg magnesium per chewable tablet.
MedsGo Class
Antacids, Antireflux Agents & Antiulcerants
Please sign in so that we can notify you about a reply