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-30% Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs

Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs

NAC-ratiopharm akut 600 mg Hustenlöser Brausetabl.

Manufacturers: ratiopharm GmbH

PZN: 06323000

Dosage: Brausetabletten

Content: 20 St

Reward Points: 60

Availability: Out of stock

$15.36

$10.73

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-30% Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs
  • Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs

Instructions for use for Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs

NAC-ratiopharm® acute 600 cough solves

Active ingredient: acetylcysteine

Application areas:
To liquefy the mucus and to facilitate the crush in acute cold bronchitis.

Notice:
Each effervescent tablet contains 20 mg aspartam as a source for phenylalanine (corresponding to 11 mg phenylalanine) and can be harmful if you have a phenyl ketonuria.
Each effervescent tablet contains 6.5 mmol (150 mg) sodium.

Detailed instructions for Nac-ratiopharm acute 600 mg cough solder brokelass., 20 pcs

Field of use

  • The preparation is a medicine for liquefaction, tough mucus in the airways.
  • The medicine is used
    • for the mucus solution and for facilitated coughing in the case of respiratory diseases with a tough mucus.

Active ingredients / ingredients / ingredients

600 mg acetylcysteine
Obesic acid auxiliary material (+)
20 mg aspartam auxiliary substance (+)
11.2 mg phenylalanine auxiliary substance (+)
Citronic acid, water -free auxiliary material (+)
Sodium hydrogen carbonate auxiliary material (+)
150.2 mg sodium ion helper (+)
Povidon K25 Hedge substance (+)
Lemon aroma hedge material (+)

Contradictions

  • The medicine must not be taken,
    • if you are allergic to acetylcysteine or one of the other components of this medicine.
  • The preparation must not be used in children under 14 years due to the high active ingredient content.

dosage

  • Always take this medicine exactly as described or exactly after the agreement made with your doctor or pharmacist. Ask your doctor or pharmacist if you are not sure.
  • The recommended dose is
    • The following information applies unless your doctor prescribed the preparation otherwise. Please adhere to the application regulations, otherwise the medicine cannot work properly!
    • Young people aged 14 and over and adults
      • Total dose:
        • 2 times a day 1/2 or 1 times a day 1 (corresponding to 600 mg acetylcysteine per day)

 

  • Total duration of the application
    • If the clinical picture worsens or no improvement occurs after 4 - 5 days, you should see a doctor.

 

  • If you have taken a larger amount than you should
    • In the event of overdose, irritation symptoms in the gastrointestinal area (e.g. abdominal pain, nausea, vomiting, diarrhea) can occur.
    • Serious side effects or symptoms have so far not been observed even after massive overdose of acetylcysteine. If you suspect an overdose with the preparation, please notify your doctor.

 

  • If you have forgotten the intake
    • Once you have forgotten to take the preparation or have taken too little, please continue taking the drug, as described in the dosage instructions.

 

  • If you cancel the intake
    • Please do not break the treatment without consulting your doctor. Your illness might worsen by this.

 

  • If you have any further questions about taking this medicine, please contact your doctor or pharmacist.

Taking

  • Take the medicine after meals.
  • Please dissolve the effervescent tablet in a glass of drinking water and drink the contents of the glass completely.

Patient information

  • Warnings and Precautions
    • Please speak to your doctor or pharmacist before taking the medicine.
    • It has been very rare about the occurrence of severe skin reactions such as Stevens-Johnson syndrome and Lyell syndrome in a temporal connection with the use of acetylcysteine. When the skin and mucous membrane changes are being recovered, ÄRcaught up and the application of acetylcysteine ended.
    • Caution is advised if you have or have had or have a stomach or intestinal ulcer in the past.
    • Caution is advised in patients with histamine intolerance. Long -term therapy should be avoided in these patients, since the preparation influences histamine metabolism and can lead to intolerance symptoms (e.g. headache, fluid snuff, itching).
    • The use of the preparation, in particular at the beginning of the treatment, can lead to liquefaction and thus an increase in volume of the bronchial secretion. If you are unable to cough this off, your doctor will carry out suitable measures for you.

 

  • Wateriness and ability to operate machines
    • There are no special features to consider.

Pregnancy

  • If you are pregnant or breastfeed, or if you suspect to be pregnant or intend to become pregnant, ask your doctor or pharmacist for advice before taking this drug.
  • Pregnancy
    • Since there is no sufficient experience with the use of acetylcysteine for pregnant women, you should only apply the medicine during pregnancy if your doctor considers this to be absolutely necessary.
  • Breastfeeding
    • There is no information on the excretion of acetylcysteine into breast milk.
    • Therefore, you should only apply the medicine during breastfeeding if your doctor considers this to be absolutely necessary.

Hints

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

Miscellaneous

- The expectorant effect of acetylcysteine is improved by hydration.

Manufacturer:  ratiopharm GmbH, Graf-Arco-Straße 3, 89079 Ulm

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