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-25% DULCOLAX NP drops, 30 ml

DULCOLAX NP drops, 30 ml

DULCOLAX NP Tropfen

Manufacturers: Sanofi-Aventis Deutschland GmbH GB Selbstmedikation /Consumer-Ca

PZN: 04657033

Dosage: Tropfen zum Einnehmen

Content: 30 ml

Reward Points: 119

Availability: In stock

$24.13

$18.10

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-25% DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml
  • DULCOLAX NP drops, 30 ml

Instructions for use for DULCOLAX NP drops, 30 ml


Dulcolax® NP drops

Active ingredient: sodium picosulfate.

Field of use:
For use in the event of constipation and for diseases that require relieved stool emptying. Like other laxatives, Dulcolax NP drops without a medical clarification of the cause of the constipation are not taken daily or over a longer period of time.
Warning: contains sorbitol. Note leaflet! Pharmacy.

Read the package supplement and ask your doctor or pharmacist about risks and side effects.

Sanofi-Aventis Deutschland GmbH, 65926 Frankfurt am Main.
As of September 2020




Detailed instructions for DULCOLAX NP drops, 30 ml

Field of use

The active ingredient sodium picosulfate contained in Dulcolax NP drops (package size: 30 ml) develops exactly where it should work: in the large intestine. Only there is converted into its laxative form by the body's own colon bacteria.
This works twice against constipation:
1. The fluid content in the intestine is heard, which improves stool consistency and facilitates intestinal transport.
2. The natural movement of the large intestine is stimulated, which quickly and effectively resolved the constipation.

Active ingredients / ingredients / ingredients

7.5 mg sodium picosulfate
Citronic acid 1-water auxiliary material (+)
Sodium citrate 2-water auxiliary material (+)
Sorbitol 70 Hedge substance (+)
450 mg sorbitol auxiliary material (+)
Water, cleaned auxiliary material (+)
Sodium benzoat auxiliary substance (+)

Contradictions

  • The medicine must not be taken,
    • if they are hypersensitive (allergic) against sodium picosulfate, related active ingredients from the group of triarylmethanes or one of the other components of the preparation;
    • in the case of intestinal narrowing with worsened intestinal passage, with intestinal obstruction, in the case of acute abdominal problems such as appendicitis, with severe abdominal pain combined with nausea and vomiting;
    • in the case of acute inflammatory diseases of the gastrointestinal tract;
    • if the body lacks a significant lack of fluid;
    • with rare innate fructose intolerance.
  • Constipation, combined with other symptoms such as abdominal pain, vomiting and fever, can be signs of a serious disease (intestinal obstruction, acute inflammation in the abdominal area). With such symptoms, you must not take the preparation or other medicines and should see your doctor immediately.
  • In the event of diseases that are associated with disorders of the water and mineral salt balance (e.g. severely restricted kidney function), you may only take the medicine under medical control.

dosage

  • Always take the preparation exactly according to the instruction. Please ask your doctor or pharmacist if you are not quite sure.
  • Unless otherwise prescribed by the doctor, the usual single dose for adults is:
    • 10 - 18 Drops (corresponds to 5 - 10 mg sodium picosulfate).
  • As far as prescribed by the doctor, children take up a single dose of 5 - 9 drops (corresponds to 2.5 - 5 mg sodium picosulfate).
  • Please note the duration until you enter and do not try to force stool through strong pressing.
  • The drug should not be taken continuously every day or over longer periods without prior medical clarification.
  • Please speak to your doctor or pharmacist if you have the impression that the effect of the preparation is too strong or too weak.

 

  • If you have taken a larger amount of the drug than you should
    • Acute overdose of the preparation can lead to diarrhea, symptoms in the abdomen, loss of liquid, potassium and other minerals. The countermeasures are based on the symptoms. Within a short time after taking it can be done by induced inheritancecalculation or gastric flushing the effect of the drug is reduced or prevented. In the event of severe water and mineral losses, these must be compensated for according to the doctor's instructions. The administration of antispasmodic agents may be useful.
    • Furthermore, individual cases of reduced or interrupted blood flow to the large -end mucosa was reported, in which the dosage of sodium picosulfate was considerably higher than the dosage recommended to treat constipation.
    • Notice:
      • In general, it is known from the preparation as well as other laxatives that, in the event of chronic overdose, they lead to chronic diarrhea, abdominal pain, humiliated potassium values, excessive secretion of aldosterone and kidney stones. In conjunction with chronic laxative abuse, the kidney tissue damage, metabolism-related increase in base concentrations in the blood and about reduced potassium values was also reported.

Taking

  • It is best to take the preparation in the evening. The intake can take place with and without liquid. The laxative effect usually occurs after 10 - 12 hours.

Patient information

  • Particular caution when taking the drug is required,
    • if your symptoms have occurred spontaneously, last longer and/or are accompanied by symptoms such as blood in the stool or fever. In this case, you should get advice and examine your doctor before starting treatment with the preparation, because disorders or impairments of bowel movements can be signs of a serious disease.
  • The drug should not be taken continuously every day or over longer periods without prior medical clarification.
  • If the preparation is discontinued, the symptoms can be recovered. After long -term use in chronic constipation, the recurrence of the symptoms can also be associated with worsening the constipation.
  • In patients who have taken the preparation, dizziness and short -term seizures of consciousness (syncope) were reported. According to the corresponding case reports, these are presumably syncope that either go back to the laxative process itself, pressing or on circulatory reactions due to abdominal pain.
  • Children
    • The preparation should not be used in children under 4 years.
    • In older children, the medicine and a. Because of the possibility of unknown innate fructose intolerance, only used after consultation with the doctor.

 

  • Wateriness and operating machines
    • When using the drug in the intended dosage, no impairment is usually to be expected. However, if symptoms such as dizziness, short -term loss of consciousness (syncope) or abdominal cramps occur, the ability to participate in road traffic and to operate machines can be affected.

Pregnancy

  • Ask your doctor or pharmacist for advice before taking/using all drugs.
  • Pregnancy
    • There are no meaningful clinical studies on the application during pregnancy. An application during pregnancy should be avoided as far as possible.
  • Breastfeeding
    • It has been shown that the active ingredient does not transfer to breast milk. The preparation can therefore be used during breastfeeding.

Hints

Dulcolax® NP drops. Active ingredient: sodium picosulfate. Area of application: For use in the event of constipation and for diseases that require relieved stool emptying. Like other laxatives, Dulcolax® NP drops should not be taken daily or over a longer period of time. Warning: contains sorbitol. Note leaflet! Pharmacy.

Read the package supplement and ask your doctor about risks and side effects or pharmacist.

Sanofi-Aventis Deutschland GmbH, 65926 Frankfurt am Main.

As of September 2020

Read the package supplement and ask your doctor or pharmacist for risks and side effects.

Miscellaneous

- In general, drug treatment of constipation is only recommended if long-term measures such as the change in nutrition (ballast and source-rich food as well as sufficient fluid intake) and the lifestyle (e.g. sufficient physical exercise) cannot be achieved or not sufficient success .- A long-lasting application can lead to intensification of intestinal inertia. - In addition, as with high -dose use, there may be often increased losses of water, potassium and other salts in the blood. This can lead to disorders of the heart function and muscle weakness, especially when taking drained medication and cortisone preparations at the same time.

Manufacturer:  A. Nattermann & CIE GmbH, Brüningstraße 50

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