ALVEDON Paracetamol 500mg Tablet 250's
NONRXDRUG-DRP-10583-250
Discreet Packaging
FDA-registered Products
FDA-licensed Pharmacies
Indications/Uses
Headache, toothache, fever associated with colds, menstrual pain, muscle pain and influenza.
Dosage/Direction for Use
Adults: 1-2 tablets every 6 to 8 hours.
Children: 1/2-1 tablet every 6 to 8 hours.
Missed Dose: If the patient misses a dose, take the next dose if still needed for pain and/or fever and the subsequent dose every 4 to 6 hours thereafter.
Do not double the dose.
Children: 1/2-1 tablet every 6 to 8 hours.
Missed Dose: If the patient misses a dose, take the next dose if still needed for pain and/or fever and the subsequent dose every 4 to 6 hours thereafter.
Do not double the dose.
Overdosage
Signs and Symptoms of Overdosage: Overdosage of paracetamol usually involves 4 phases with the following signs and symptoms: I. Eating disorder, nausea, vomiting, malaise, and excessive sweating.
II. Right upper abdominal pain or tenderness, liver enlargement which may be characterized by abdominal discomfort of "feeling full", elevated bilirubin and liver enzyme concentrations, prolongation of prothrombin time, and occasionally decreased urine output.
III. Eating disorder, nausea, vomiting, and malaise recur and signs of liver (e.g., jaundice) and possibly kidney failure.
IV. Recovery or progression to fatal complete liver failure.
When the Patient Has Taken More Than the Recommended Dosage: If the patient has taken more than the recommended dosage, consult a doctor.
II. Right upper abdominal pain or tenderness, liver enlargement which may be characterized by abdominal discomfort of "feeling full", elevated bilirubin and liver enzyme concentrations, prolongation of prothrombin time, and occasionally decreased urine output.
III. Eating disorder, nausea, vomiting, and malaise recur and signs of liver (e.g., jaundice) and possibly kidney failure.
IV. Recovery or progression to fatal complete liver failure.
When the Patient Has Taken More Than the Recommended Dosage: If the patient has taken more than the recommended dosage, consult a doctor.
Administration
May be taken with or without food.
Contraindications
If the patient is allergic to paracetamol or any ingredient in the product.
Avoid long-term use of paracetamol in patients with anemia or with heart, lung, kidney, or liver disease.
Avoid long-term use of paracetamol in patients with anemia or with heart, lung, kidney, or liver disease.
Special Precautions
Liver Warning: This product contains paracetamol. Severe liver damage may occur if: An adult or child 12 years old and above takes more than 4 g of paracetamol in 24 hours, which is the maximum daily amount; Taken with other medicines containing paracetamol (or acetaminophen); An adult has 3 or more alcoholic drinks everyday while using this product.
Do not use with any other medicine containing paracetamol (prescription or nonprescription). If the patient is not sure whether a medicine contains paracetamol, ask a doctor.
Ask a doctor before use if the patient has kidney or liver problems.
Ask a doctor before use if the patient is taking warfarin, a blood thinning medicine.
Consult a Doctor: If the patient is pregnant or breastfeeding, consult a doctor before use.
Stop use and ask a doctor if: New symptoms occur, Symptoms do not get better, Redness or swelling is present, Fever gets worse or lasts more than 3 days, Pain gets worse or lasts more than 10 days.
Do not use with any other medicine containing paracetamol (prescription or nonprescription). If the patient is not sure whether a medicine contains paracetamol, ask a doctor.
Ask a doctor before use if the patient has kidney or liver problems.
Ask a doctor before use if the patient is taking warfarin, a blood thinning medicine.
Consult a Doctor: If the patient is pregnant or breastfeeding, consult a doctor before use.
Stop use and ask a doctor if: New symptoms occur, Symptoms do not get better, Redness or swelling is present, Fever gets worse or lasts more than 3 days, Pain gets worse or lasts more than 10 days.
Use In Pregnancy & Lactation
If the patient is pregnant or breastfeeding, consult a doctor before use.
Adverse Reactions
Paracetamol, when taken within the recommended dose and duration of treatment, has low incidence of side effects.
Skin rashes, hypersensitivity reactions, changes in the number of white blood cells and platelets, and minor stomach and intestinal disturbances have been reported.
Skin rashes, hypersensitivity reactions, changes in the number of white blood cells and platelets, and minor stomach and intestinal disturbances have been reported.
Drug Interactions
The absorption of paracetamol may be accelerated by metoclopramide or domperidone and absorption reduced by cholestyramine.
Medicines which stimulate the enzymes responsible for the metabolic activation of paracetamol such as medicines for convulsion (e.g., phenobarbital) may increase susceptibility to the harmful effects to the liver.
Warfarin, a blood thinning medicine; an increase in the International Normalized Ratio (INR), which may serve as a sign of increased risk for bleeding, may be observed when using paracetamol and warfarin at the same time. Paracetamol increases the anticoagulation effect of warfarin.
Medicines which stimulate the enzymes responsible for the metabolic activation of paracetamol such as medicines for convulsion (e.g., phenobarbital) may increase susceptibility to the harmful effects to the liver.
Warfarin, a blood thinning medicine; an increase in the International Normalized Ratio (INR), which may serve as a sign of increased risk for bleeding, may be observed when using paracetamol and warfarin at the same time. Paracetamol increases the anticoagulation effect of warfarin.
Storage
Store at temperatures not exceeding 30°C.
Action
This product contains paracetamol, a fever reducer and pain reliever.
MedsGo Class
Analgesics (Non-Opioid) & Antipyretics
Features
Brand
Alvedon
Full Details
Dosage Strength
500 mg
Drug Ingredients
- Paracetamol
Drug Packaging
Tablet 250's
Generic Name
Paracetamol
Dosage Form
Tablet
Registration Number
DRP-10583
Drug Classification
Over-The-Counter (OTC)
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