Dolocatil codeina para que sirve
Some side effects may be serious. If you experience any of the following symptoms or those listed in the IMPORTANT WARNINGS section, stop taking codeine and call your doctor immediately or seek emergency medical attention:
Codeine may cause other side effects. Call your doctor if you have any unusual problems while taking this medicine.If you develop a serious side effect, you or your doctor may send a report to the Food and Drug Administration’s (FDA) MedWatch Adverse Event Reporting Program at http://www.fda.gov/Safety/MedWatch or by phone at 1-800-332-1088.How should I store or dispose of this medicine?
The administration of this drug is subject to the appearance of painful symptoms and as these disappear, the dose should be reduced and then the medication should be discontinued.
Patients with severe renal insufficiency: In case of severe renal insufficiency (creatinine clearance less than 10 ml/min), it is recommended that the interval between 2 intakes be at least 8 hours and that the total daily dose be reduced by 50%. Do not exceed 500 mg of paracetamol in each dose.
Patients with hepatic insufficiency: In case of mild or moderate hepatic insufficiency, 2 g of paracetamol/24 hours should not be exceeded and the minimum interval between doses should be 8 hours (see section 4.4). Use in patients with severe hepatic insufficiency is contraindicated (see section 4.3).
Paracetamol is hepatically metabolized, giving rise to hepatotoxic metabolites and can therefore interact with drugs that use the same metabolic pathways. These drugs are:
It crosses the placenta, so it is recommended not to administer unless necessary (FDA category C). As a precaution, codeine should not be used during the first trimester of pregnancy (see section 5.3).
Dolocatil codeine 500/15 mg
tablets have a slot that allows them to be broken in half. Each box contains 20 tablets. DOLOCATIL Codeine 650/30 mg tablets belong to the group of analgesic drugs. DOLOCATIL Codeine 650/30 mg tablets are indicated for the symptomatic treatment of pain of any cause of moderate intensity.
Severe renal insufficiency (creatinine clearance 10 ml/minute) it is recommended that the interval between two intakes be at least 8 hours and the total daily dose be reduced by 50%. In elderly patients, it is recommended to reduce the daily dose and to space the doses at least 8 hours apart.
Consult your doctor or pharmacist before using a medicine. The use of medicines during pregnancy may be dangerous for the embryo or fetus. If you are pregnant or think you may be pregnant, consult your doctor before taking DOLOCATIL 650/30 mg tablets.
Consult your doctor or pharmacist before using a medicine. Paracetamol and codeine pass into breast milk, so breastfeeding women should consult a doctor before using DOLOCATIL Codeine 650/30 mg tablets.
If you are going to undergo any analytical test (including blood tests, urine tests, skin tests using allergens, etc.) tell your doctor that you are taking Dolocatil codeine, as it may alter the results of such tests.
Use in athletes: This medicine contains codeine. As a result of its metabolism, some compounds are produced that may produce a positive result in doping control tests.
If you take more Dolocatil Codeine than you should, consult your doctor or pharmacist immediately or call the Poison Information Service, telephone 915 620 420, indicating the medicine and the amount taken. It is recommended to take the package and the package leaflet of the medicine to the health care professional.
If an overdose has been taken, a medical center should be consulted quickly even if there are no symptoms, since symptoms often do not appear until 3 days after the overdose, even in cases of severe intoxication. Treatment of overdose is most effective if started within 4 hours after ingestion of the drug.