Dotium Domesco medicine for symptoms of vomiting, nausea (10 blisters x 10 tablets)
Dosage form Box of 10 blisters x 10 tablets
Specifications Domperidon
Ingredient Vomiting/nausea
Ingredient
| Composition information | Content |
| Domperidon | 10mg |
Uses
indications
Dotium drugs are indicated: Vomiting and nausea treatment.
Pharmacokic
Domperidone is a dopamine receptor anti -receptor with anti -vomiting properties. Domperidone does not easily pass the bloody barrier. In domperidone users, especially adults, unwanted effects like the surgeon syndrome are rare, but domperidone promotes prolactin secretion in the pituitary gland.
Anti -vomiting effects may be due to the coordination of peripheral effects (gastric hyperactivity) and the Dopamine receptor resistance in the CTZ receptor sensor area (Chemoreceptor Trigger Zone) is located outside the bloodstream barrier in the vomiting area of the onion.
Through animal research shows that the concentration found in the brain is low, showing the effect of domperidone mainly on peripheral dopamine receptors.
Research in humans shows that drinking domperidone increases the lower esophageal muscle tone, improves the exercise of the duodenum and increases the stomach empty. The drug does not affect the secretion of the stomach.
pharmacokinetics
absorption:
In hungry people, the domperidone absorbs quickly after drinking with peak blood concentration achieved after 30–60 minutes. The absolute bioavailability of low oral domperidone (about 15%) is due to the broad initial metabolism in the intestinal wall and liver.
Domperidone'sDomperidone is increased in healthy people after drinking after meals, patients with digestive problems should take domperidone before eating 15–30 minutes. The decrease in acid levels in the stomach does not reduce the absorption of Domperidone Base.
The oral bioavailability of Domperidone Base does not decrease if the patient previously takes cimetidine or sodium bicarbonate. Time to reach the peak concentration will be a bit slow and the AUC will increase slightly when the drug is taken after eating.Distribution:
Domperidone is used without accumulating or creating separate metabolism, the peak concentration in plasma is achieved after 90 minutes of 21 ng/ml, after taking 30 mg/day for 2 weeks, it is almost equivalent to the peak concentration after the first dose of 18 ng/mL.
The ratio of plasma bound domeridone is 91–93 %. Researching the distribution of drugs by marking radioactivity on animals shows that the drug is widely distributed in the body tissue but low concentrations in the brain. In mice, a small amount of drugs go through the placenta.
Metabolism:
Domperidone undergo a quick and multi-liver process with liver with hydroxylation and reducing N-alkyl.
In vitro, the test of metabolism with inhibited drugs shows that CYP3A4 is a major form of Cytochrome P450 related to the de-alkyl deholes of domperidone, while CYP3A4, CYP1A2 and CYP2E1 are related to the aromatic hydroxylation of Domperidone.
Era:
Eliminate urine and fertilizer about 31% and 66% of oral dose. A small part of the drug is excreted in intact form (10% in feces and 1% in urine).
Semi -selling time in plasma after single dose is 7–9 hours in healthy but prolonged people in patients with severe kidney function.
Before taking Dotium Domesco medicine for symptoms of vomiting, nausea (10 blisters x 10 tablets)
How to use
oral medication and should be taken before meals. If taken after meals, the drug may be slowly absorbed.
Patients should take medicine at fixed time.
Dosage
always use the right dose in the prescription. Dotium should only use the lowest dose effectively in the shortest time to control vomiting and nausea. Maximum treatment time should not exceed a week.
Adults and minors (aged 12 years and older and weighing 35 kg or more):
Use 10 mg/time, can be used up to 3 times/day, a maximum dose of 30 mg/day.
infants, young children, children (under 12 years old) and adolescents weighs less than 35 kg:
Due to the exact dosage, the form of film tablets is not suitable for young children and minors weighing less than 35 kg.
Patients with liver failure:
Dotium is contraindicated to patients with medium and severe liver failure.
Patients with renal failure:
Due to the prolonged domeridone's selling time in patients with severe renal impairment, if used repeated, the number of dotium drugs should be reduced to 1–2 times/day and adjust the dose depending on the degree of renal failure.
Note: The above dose is for reference only. Specific dosage depends on the condition and level of progression of the disease. For a suitable dose, you need to consult a doctor or medical specialist.What to do when overdose?
There is no specific antidote. In the case of an overdose, it is necessary to take symptomatic treatment immediately. Should monitor the electrocardiogram due to the ability to extend the QT range.
Gastrointestinal lavage as well as using activated carbon can be helpful.
Strict medical monitoring and treatment support are encouraged.
anti -cholinergic drugs, Parkinson's treatment may be helpful in controlling foreign reactions.
What to do when you forget 1 dose?
Drink as soon as you remember. If the time is close to the next medication, skip the forgotten dose and take the next dose at the usual time. Do not use double dose to compensate for the forgotten dose.
Side Effects
When using dotium, you may experience unwanted effects (ADR).
Common, ADR> 1/100
No report.
Uncommon, 1/1000 Rare, 1/10000 Very rare, ADR Skin and subcutaneous tissue: urticaria, itching, rash. Not determined frequency Instructions on how to handle ADR Stop medication and symptomatic treatment.
Warnings
Before using the drug you need to read the instructions carefully and refer to the information below.
contraindicated
Dotium drugs contraindicated in the following cases:
Mechanical intestinal obstruction; Prolactin secretion (prolactinom); only use domeridone for no more than 12 weeks for Parkinson's patient, when other anti -vomiting measures are safer. Harmful effects in the central nervous system may appear. Renal failure: Domperidone's disposal time is prolonged in patients with severe renal impairment. In the case of repeated use, the frequency of using domperidone should be reduced to 1–2 times/day depending on the degree of renal failure. Can adjust the dose if needed. Cardiovascular effects: Epidemiological studies show that domperidone may increase the risk of severe ventricular arrhythmia or sudden cardiovascular disease. This risk is higher for patients over 60 years old, patients taking daily doses> 30 mg and patients with simultaneous use of the drug extending the QT or CYP3A4 inhibitors. Contraindicated domperidone for patients with prolonged heart impulse transmission time, especially QT interval, patients with obvious electrolyte disorders (hypotension, hyperkalemia, hypoglycemia), slow heartbeat or patients with cardiovascular disease such as congestive heart failure due to ventricular disorder. electrolyte disorders (hypotension, hyperkalemia, hypoglycemia) or slow heartbeat have been known as a factor that increases the risk of arrhythmia. Domperidone treatment should be stopped and exchanged with health workers if there are any symptoms or signs related to arrhythmia. Patients should immediately report symptoms on the heart. Patients with galactose tolerance problems, patients with enzyme deficiency lapp lactase or malcose -galactose should not be used. The drug can cause drowsiness, headache (rare). Be cautious when driving or operating machinery.
Restrict the use of domperidone in pregnant women. A study in mice shows that reproductive toxicity at high doses of toxicity in the mother mouse. The potential risks in humans are unknown. Therefore, domperidone should only be used during pregnancy when the treatment benefits have been proven. domperidone excreted through breast milk and breastfed babies receive less than 0.1% dose according to the mother's weight. The adverse effects, especially the effect on the heart can still occur after breastfeeding. Consider the benefits of breastfeeding and the benefits of treatment for mothers to decide to stop breastfeeding or stop/avoid domeridone treatment. Be careful in case of risk factors that extend the QT range in breastfed babies. The main metabolic line of domperidone via CYP3A4. The research data on in vitro shows that these drugs simultaneously inhibit the enzyme strongly can increase the concentration of domperidone in the blood. Interaction with oral ketoconazole or Erythromycin oral oral in healthy people has confirmed the indirect inhibition of the domeridone's first passing effect via CYP3A4 by these drugs. Increase the risk of extending the QT distance due to pharmacokinetic interaction or pharmacokinetic energy.
Contraindicated with the following drugs: Medications that extend the QT range: Strong CYP3A4 inhibitors (regardless of the effect of extending the QT): Protease inhibitors, Azole -group antifungal drugs, macrolide drugs (erythromycin, clarithromycin and telithromycin). Do not recommend using the following drugs: Medium CYP3A4 inhibitors such as Diltiazem, Verapamil and some macrolide drugs. Use cautiously when used simultaneously with the following drugs: Heart rate slow, hypokalemia and some macrolid drugs contribute to extending QT interval such as azithromycin, Roxithromycin (clarithromycin contraindicated as a powerful CYP3A4 inhibitor).
Levodopa: Increasing Levodopa's plasma concentrations (up to 30–40 %). Opioid can reduce the effect of domperidone in stomach empty. Cavalry of the drug: Because there is no studies on oral medications, they do not mix this drug with other drugs. Be cautious when using
The ability to drive and operate machinery
Pregnancy
breastfeeding period
Interactive drug
Storage
In the dry place, temperatures below 30 ° C, avoiding light.
Storage in the original packaging of the drug.
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