Delicol Babies Dietary Supplement 15ml

Product Information

Anti-diarrheals inhibiting peristalsis should be used with caution in patients with infection or inflammatory bowel diseases due to the increased risk of absorption of toxins, and of developing toxic megacolon and intestinal perforation. Due to the risk of paralytic ileus, Dropizol is not recommended before a surgical operation or within 24 hours after operation. If paralytic ileus is suspected during the use of Dropizol, the treatment must be stopped immediately. Opium alkaloids (opioids and isoquinoline derivatives) induce constipation, euphoria, analgesia and sedation dependent on the dose and derivative.

Use under medical supervision. From the first days of life until the end of 4 weeks of age: the contents of one capsule added to each serving of food. From 5 to 6 weeks of age: the contents of two capsules added to each serving of food. Over 16 weeks of age: add three capsules each serving of food. The capsule is not suitable for human consumption. Do not exceed recommended servings for consumption during the day. Should only be used with caution in patients in high-risk groups, such as patients with epilepsy and hepatic disease.

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Vì vậy, bổ sung enzyme lactase sẽ đem lại nhiều lợi ích trong việc cải thiện các tình trạng dưới đây: 1.1. Kém hoặc không dung nạp Lactose Opium is excreted in human milk, where it reaches higher concentrations than in maternal plasma. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Dropizol therapy taking into account the benefit of breast feeding for the child and the benefit of therapy for the woman. If Dropizol is used during breastfeeding, infants should be closely monitored for symptoms of respiratory depression and sedation. The patients should be followed closely for signs and symptoms of respiratory depression and sedation. In this respect, it is strongly recommended to inform patients and their caregivers to be aware of these symptoms (see section 4.5). The use of opium is well-established for treatment of diarrhoea in the clinic. Controlled clinical studies is not available. Particular caution should be exercised when prescribing this drug due to its morphine content. The treatment period should be as short as possible.

The μ-opioid receptor agonists inhibit gastric emptying, increases pyloric muscle tone, induce pyloric and duodenojejunal phasic pressure activity, disturb the migrating myoelectric complex, delay transit time through the small and large intestine and elevate the resting anal sphincter pressure. In addition to this, opioids attenuate the intestinal secretion of electrolytes and water and thereby facilitate the net absorption of fluid. In addiction to this, the μ, κ and δ-opioid receptors contribute to opioid-inhibition of muscle activity in the intestine. The result of all these effects is constipation. Due to the ethanol content, Dropizol should not be used concomitantly with disulfiram or metronidazole. Both of these drugs can cause disulfiram-like reactions (flushing, rapid breathing, tachycardia).

Elimination is reduced and delayed in renal impairment - avoid or reduce dose. See Sections 4.3 and 4.4. Dropizol drops should be used with caution in the following conditions / for the following patients Concurrent administration of morphine and antihypertensive drugs may increase the hypotensive effects of antihypertensive agents or other drugs with hypotensive effects. Amphetamine and analogues can reduce the sedative effect of opioids. Loxapine and periciazine can increase the sedative effect of opioids. Concomitant use of flibanserin and opioids may increase the risk of CNS depression. Opioids can increase the plasma concentrations of desmopressin and sertraline.

Dropizol is not recommended during pregnancy unless the benefits clearly outweigh the risks to both mother and child. Repeated administration may cause dependence and tolerance and the use of opium may lead to addiction to the substance. Particular caution should be exercised in individuals predisposed to addiction to narcotics and alcohol. Concomitant use of Dropizol and sedative medicines such as benzodiazepines or related drugs may result in sedation, respiratory depression, coma and death.Avoid use in older adults with a history of falls or fractures as ataxia, impaired psychomotor function, syncope, and additional falls may occur. If use is necessary, consider reducing use of other CNS-active agents that increase risk of falls and fractures and implement other strategies to reduce risk of falls.