AMBROXOL 30 drops-1A Pharma, 100 ml

Instructions for use for AMBROXOL 30 drops-1A Pharma, 100 ml

Detailed instructions for AMBROXOL 30 drops-1A Pharma, 100 ml

Field of use

The preparation is a medicine for the mucus solution for respiratory diseases with tough mucus (expectorant). Application area:

• for expectorant treatment for acute chronic diseases of the bronchi and lungs with a tough mucus.

Active ingredients / ingredients / ingredients

30 mg ambroxol hydrochloride
27.36 mg ambroxol
Citronic acid 1-water auxiliary material (+)
Sodium hydroxide auxiliary substance (+)
Water, cleaned auxiliary material (+)
2.6 mg methyl 4-hydroxybenzoat auxiliary substance (+)
0.4 mg propyl 4-hydroxybenzoat auxiliary substance (+)
Raspberry aroma hedge material (+)
Saccharosis auxiliary substance (+)
Ethanol Hedge substance (+)

Contradictions

The medicine must not be taken,

• if you are hypersensitive to ambroxol hydrochloride or one of the other components.

dosage

Always take the preparation exactly according to the instruction. Please ask your doctor or pharmacist if you are not quite sure. If you do not prescribe otherwise by the doctor, the usual dose is: the following information applies, unless your doctor has prescribed the medicine otherwise. Please adhere to the application regulations, otherwise the preparation cannot work properly! Children up to 2 years:

• 1/2 Ml solution is taken twice a day, taken twice 10 drops (corresponding to 15 mg ambroxol hydrochloride/day).

Children from 2 to 5 years:

• 1/2 Ml solution is taken 3 times a day, taken 3 times 10 drops (corresponding to 22.5 mg ambroxol hydrochloride/day)

Children from 6 to 12 years:

• 1 Ml solution is taken 2-3 times a day, taken 2 - 3 times 20 drops (corresponding to 30 - 45 mg ambroxol hydrochloride/day).

Adults and adolescents from the age of 12:

• As a rule, 2ml solution is taken 3 times a day during the first 2 - 3 days, corresponding to 3 times 40 drops (corresponding to 90 mg ambroxol hydrochloride/day), after which 2ml solution is 2ml each, corresponding to a corresponding 60 mg ambroxol hydrochloride/day 2 times a day (corresponding to 60 mg of ambroxol hydro. ) taken.
• In the case of adult dosage, an increase in effectiveness may be possible due to the administration of 60mg ambroxol hydrochloride (corresponds to 120 mg ambroxol hydrochloride/day).

Treatment duration:

• If your clinical picture worsens or no improvement occurs after 4-5 days, you should see a doctor.

Please speak to your doctor or pharmacist if you have the impression that the effect of the drug is too strong or too weak. Overdosing:

• Serious symptoms of poisoning have not been observed when overdosing ambroxol, the active ingredient of the preparation. There has been reported on short -term unrest and diarrhea. In the event of accidental or intended extreme overdose, increased saliva secretion, strangling, vomiting and blood pressure drop can occur.
• Contact a doctor. Acute measures, such as triggering vomiting and gastric flushing, are not generally indicated and are only considered to be extremely overdosed. Treatment is recommended in accordance with the overdosing sign that occurs.

Forgotten intake:

• Once you have forgotten to take the medicine or have taken too little, please continue taking the preparation at the next time.

Abortion therapy:

• Please do not break the treatment with the medicine without consulting your doctor. Your illness might worsen by this.

Taking

After meals, the medicine is diluted after meals (e.g. water, tea or juice).

Patient information

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 ambroxol. When the skin and mucosa changes are being reflected, medical advice should therefore be obtained immediately and the use of ambroxol should be ended. In patients with restricted kidney and liver function:

• If you suffer from a restricted kidney function or a serious liver disease, the medicine may only be used with special caution (i.e. in larger revenue distances or in a reduced dose). In the event of severe renal insufficiency, the reduction products from ambroxol formed in the liver must be expected to accumulate in the liver.
• In some rare diseases of the bronchi, which are accompanied by excessive secretion collection (e.g. malignant zilien syndrome), the medicine should only be used under medical control due to a possible secretion.

Wateriness and operating machines:

• There are no special precautions required.

Children:

• In children under 2 years, the medicine may only be applied to medical instruction.

Store drug out of reach of children.

Pregnancy

Since there has been no sufficient experiences on humans so far, you should only take the medicine during pregnancy by ordering your doctor and only after he has carried out a careful benefit-risk assessment. Since there has been no sufficient experience in humans so far, you should only take the medicine during breastfeeding when you order your doctor.

Hints

Miscellaneous

- In the case of severe kidney dysfunction, the conservation dose should be reduced accordingly or the distance between the applications (dosage interval) should be extended.

- The expectorant effect of the drug is supported by fluid intake.

Manufacturer:  1 A Pharma GmbH, Keltenring 1+3, 82041 Oberhaching